Cytoplasmic

protein name left right site
ATP2C2 Calcium-transporting ATPase type 2C member 2 856 874 TCRSQTKLIFEIGFLRNHM
ATP2C2 Calcium-transporting ATPase type 2C member 2 927 946 KLCEKYCCSPKRVQMHPEDV
Atp2c2 Calcium-transporting ATPase type 2C member 2 149 229 QEYRSEKSLEELTKLVPPECNCLRDGKLRHMLARDLVPGDIVSLSMGDRIPADIRLTEVTDLLVDESSFTGEVEPCGKTDS
Atp2c2 Calcium-transporting ATPase type 2C member 2 854 872 SCRSQTKLIFEIGFFRNRM
Atp2c2 Calcium-transporting ATPase type 2C member 2 925 944 KLWEKFLSRARPTQMLPEAV
Atp2c2 Calcium-transporting ATPase type 2C member 2 770 802 DGPPAQSLGVEPVDRDALRRPPRSVGDTILNRA
Atp2c2 Calcium-transporting ATPase type 2C member 2 313 329 VQGKPLLSMFTIGVSLA
Atp2c2 Calcium-transporting ATPase type 2C member 2 1 104 MGRRLKFLQKLAFLGQNHRYKALERDEVETLIDEQCELKAIEREKTVAALPPGEACKCSREELARAFHVDLDSGLSEFAVAQRRLVHGWNEFVTDNAEPVWKKY
Atp2c2 Calcium-transporting ATPase type 2C member 2 1 104 MGRRFKFLQKLAFLGQNHRYKALERDEVDTLIDEQYELKAIEREKAVAALPPREACKCSKEELARTFHVDLDSGLSEFAVAQRRLVHGWNEFVTDNTEPVWKKY
Atp2c2 Calcium-transporting ATPase type 2C member 2 925 944 KLCEKFCSRAKADQMLPEAV
Atp2c2 Calcium-transporting ATPase type 2C member 2 313 329 VQGKPFLSMFTVGVSLA
Atp2c2 Calcium-transporting ATPase type 2C member 2 770 802 DGPPAQSLGVEPVDRDALKRPPRSVKDTILNRA
Atp4a Potassium-transporting ATPase alpha chain 1 162 297 KSTNIIASFKNLVPQQATVIRDGDKFQINADQLVVGDLVEMKGGDRVPADIRILSAQGCKVDNSSLTGESEPQTRSPECTHESPLETRNIAFFSTMCLEGTAQGLVVSTGDRTIIGRIASLASGVENEKTPIAIEI
Atp4a Potassium-transporting ATPase alpha chain 1 834 853 YEKAESDIMHLRPRNPKRDR
Atp4a Potassium-transporting ATPase alpha chain 1 833 852 YEKAESDIMHLRPRNPRRDR
Atp4a Potassium-transporting ATPase alpha chain 1 949 962 TRRLSVFQQGFFRN
Atp4a Potassium-transporting ATPase alpha chain 1 348 781 TVTVCLSLTAKRLASKNCVVKNLEAVETLGSTSVICSDKTGTLTQNRMTVSHLWFDNHIHTADTTEDQSGQTFDQSSETWRALCRVLTLCNRAAFKSGQDAVPVPKRIVIGDASETALLKFSELTLGNAMGYRDRFPKVCEIPFNSTNKFQLSIHTLEDPRDPRHLLVMKGAPERVLERCSSILIKGQELPLDEQWREAFQTAYLSLGGLGERVLGFCQLYLNEKDYPPGYTFDVEAMNFPSSGLCFAGLVSMIDPPRATVPDAVLKCRTAGIRVIMVTGDHPITAKAIAASVGIISEGSETVEDIAARLRMPVDQVNKKDARACVINGMQLKDMDPSELVEALRTHPEMVFARTSPQQKLVIVESCQRLGAIVAVTGDGVNDSPALKKADIGVAMGIAGSDAAKNAADMILLDDNFASIVTGVEQGRLIFDNL
Atp4a Potassium-transporting ATPase alpha chain 1 1018 1034 LGVRCCPGSWWDQELYY
ATP4A Potassium-transporting ATPase alpha chain 1 1 98 MGKAENYELYSVELGPGPGGDMAAKMSKKKKAGGGGGKRKEKLENMKKEMEINDHQLSVAELEQKYQTSATKGLSASLAAELLLRDGPNALRPPRGTP
ATP4A Potassium-transporting ATPase alpha chain 1 164 299 KSTNIIASFKNLVPQQATVIRDGDKFQINADQLVVGDLVEMKGGDRVPADIRILAAQGCKVDNSSLTGESEPQTRSPECTHESPLETRNIAFFSTMCLEGTVQGLVVNTGDRTIIGRIASLASGVENEKTPIAIEI
ATP4A Potassium-transporting ATPase alpha chain 1 350 783 TVTVCLSLTAKRLASKNCVVKNLEAVETLGSTSVICSDKTGTLTQNRMTVSHLWFDNHIHTADTTEDQSGQTFDQSSETWRALCRVLTLCNRAAFKSGQDAVPVPKRIVIGDASETALLKFSELTLGNAMGYRDRFPKVCEIPFNSTNKFQLSIHTLEDPRDPRHLLVMKGAPERVLERCSSILIKGQELPLDEQWREAFQTAYLSLGGLGERVLGFCQLYLNEKDYPPGYAFDVEAMNFPSSGLCFAGLVSMIDPPRATVPDAVLKCRTAGIRVIMVTGDHPITAKAIAASVGIISEGSETVEDIAARLRVPVDQVNRKDARACVINGMQLKDMDPSELVEALRTHPEMVFARTSPQQKLVIVESCQRLGAIVAVTGDGVNDSPALKKADIGVAMGIAGSDAAKNAADMILLDDNFASIVTGVEQGRLIFDNL
ATP4A Potassium-transporting ATPase alpha chain 1 835 854 YEKAESDIMHLRPRNPKRDR
ATP4A Potassium-transporting ATPase alpha chain 1 950 963 TRRLSAFQQGFFRN
ATP4A Potassium-transporting ATPase alpha chain 1 1019 1035 LGVRCCPGSWWDQELYY
Atp4a Potassium-transporting ATPase alpha chain 1 1017 1033 LGVRCCPGSWWDQELYY
Atp4a Potassium-transporting ATPase alpha chain 1 349 782 TVTVCLSLTAKRLASKNCVVKNLEAVETLGSTSVICSDKTGTLTQNRMTVSHLWFDNHIHTADTTEDQSGQTFDQSSETWRALCRVLTLCNRAAFKSGQDAVPVPKRIVIGDASETALLKFSELTLGNAMGYRDRFPKVCEIPFNSINKFQLSIHTLEDPRDSRHLLVMKGAPERVLERCSSILIKGQELPLDEQWREAFQTAYLSLGGLGERVLGFCQLYLNEKDYPPGYAFDVEAMNFPSSGLCFAGLVSMIDPPRATVPDAVLKCRTAGIRVIMVTGDHPITAKAIAASVGIISEGSETVEDIAARLRMPVDQVNRKDARACVINGMQLKDMDPSELVEALRTHPEMVFARTSPQQKLVIVESCQRLGAIVAVTGDGVNDSPALKKADIGVAMGIAGSDAAKNAADMILLDDNFASIVTGVEQGRLIFDNL
Atp4a Potassium-transporting ATPase alpha chain 1 163 298 KSTNIIASFKNLVPQQATVIRDGDKFQINADQLVVGDLVEMKGGDRVPADIRILSAQGCKVDNSSLTGESEPQTRSPECTHESPLETRNIAFFSTMCLEGTAQGLVVSTGDRTIIGRIASLASGVENEKTPIAIEI
Atp4a Potassium-transporting ATPase alpha chain 1 1 96 MGKENYELYSVELGTGPGGDMAAKMSKKKAGGGGGKKKEKLENMKKEMEMNDHQLSVSELEQKYQTSATKGLKASLAAELLLRDGPNALRPPRGTP
Atp4a Potassium-transporting ATPase alpha chain 1 948 961 TRRLSAFQQGFFRN
Atp4a Potassium-transporting ATPase alpha chain 1 1 97 MGKAENYELYSVELGSGPGGDMTAKMSKKKAGGGGGKKKEKLENMKKEMEINDHQLSVSELEQKYQTSATKGLKASLAAELLLRDGPNALRPPRGTP
Atp4b Potassium-transporting ATPase subunit beta 1 36 MAALQEKKSCSQRMAEFRHYCWNPDTGQMLGRTPAR
Atp4b Potassium-transporting ATPase subunit beta 1 36 MAALQEKKSCSQRMAEFRQYCWNPDTGQMLGRTPAR
ATP4B Potassium-transporting ATPase subunit beta 1 36 MAALQEKKTCGQRMEEFQRYCWNPDTGQMLGRTLSR
Atp6ap1 V-type proton ATPase subunit S1 434 463 TYGLHMILSLKTMDRFDDRKGPTITLTQIV
Atp6ap1 V-type proton ATPase subunit S1 434 463 TYGLHMILSLKTMDRFDDHKGPTITLTQIV
ATP6AP1 V-type proton ATPase subunit S1 441 470 TYGLHMILSLKTMDRFDDHKGPTISLTQIV
ATP6AP2 Renin receptor 324 350 TSYNIWNMDPGYDSIIYRMTNQKIRMD
Atp6ap2 Renin receptor 324 350 TSYNIWNMDPGYDSIIYRMTNQKIRMD
Atp6ap2 Renin receptor 324 350 TSYNIWNMDPGYDSIIYRMTNQKIRID
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 556 573 SLFNHIYFKKPLNIYFGF
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 660 725 RHQYLRKKHLGTLNFGGIRVGNGPTEEDAEIIQHDQLSTHSEDAEEPTEDEVFDFGDTMVHQAIHT
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 811 838 FQNKFYTGTGFKFLPFSFEHIREGKFDE
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 427 441 ESRILSQKNENEMFS
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 563 580 SLFNHIYFKKPLNIYFGF
ATP6V0A1 V-type proton ATPase 116 kDa subunit a 1 659 724 RRQYLRRKHLGTLNFGGIRVGNGPTEEDAEIIQHDQLSTHSEDADEPSEDEVFDFGDTMVHQAIHT
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 812 839 FQNKFYTGTGFKFLPFSFEHIREGKFDE
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 1 388 MGELFRSEEMTLAQLFLQSEAAYCCVSELEELGKVQFRDLNPDVNVFQRKFVNEVRRCEEMDRKLRFVEKEIRKANIPIMDTGENPEVPFPRDMIDLEANFEKIENELKEINTNQEALKRNFLELTELKFILRKTQQFFDEMADPDLLEESSSLLEPNEMGRGAPLRLGFVAGVINRERIPTFERMLWRVCRGNVFLRQAEIENPLEDPVTGDYVHKSVFIIFFQGDQLKNRVKKICEGFRASLYPCPETPQERKEMASGVNTRIDDLQMVLNQTEDHRQRVLQAAAKNIRVWFIKVRKMKAIYHTLNLCNIDVTQKCLIAEVWCPVTDLDSIQFALRRGTEHSGSTVPSILNRMQTNQTPPTYNKTNKFTHGFQNIVDAYGIGTYRE
ATP6V0A1 V-type proton ATPase 116 kDa subunit a 1 810 837 FQNKFYSGTGFKFLPFSFEHIREGKFEE
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 1 395 MGELFRSEEMTLAQLFLQSEAAYCCVSELGELGKVQFRDLNPDVNVFQRKFVNEVRRCEEMDRKLRFVEKEIRKANIPIMDTGENPEVPFPRDMIDLEANFEKIENELKEINTNQEALKRNFLELTELKFILRKTQQFFDEAELHHQQMADPDLLEESSSLLEPNEMGRGAPLRLGFVAGVINRERIPTFERMLWRVCRGNVFLRQAEIENPLEDPVTGDYVHKSVFIIFFQGDQLKNRVKKICEGFRASLYPCPETPQERKEMASGVNTRIDDLQMVLNQTEDHRQRVLQAAAKNIRVWFIKVRKMKAIYHTLNLCNIDVTQKCLIAEVWCPVTDLDSIQFALRRGTEHSGSTVPSILNRMQTNQTPPTYNKTNKFTHGFQNIVDAYGIGTYRE
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 434 448 ESRILSQKHENEMFS
ATP6V0A1 V-type proton ATPase 116 kDa subunit a 1 555 572 SLFNHIYFKKPLNIYFGF
ATP6V0A1 V-type proton ATPase 116 kDa subunit a 1 427 441 ESRILSQKNENEMFS
ATP6V0A1 V-type proton ATPase 116 kDa subunit a 1 1 388 MGELFRSEEMTLAQLFLQSEAAYCCVSELGELGKVQFRDLNPDVNVFQRKFVNEVRRCEEMDRKLRFVEKEIRKANIPIMDTGENPEVPFPRDMIDLEANFEKIENELKEINTNQEALKRNFLELTELKFILRKTQQFFDEMADPDLLEESSSLLEPSEMGRGTPLRLGFVAGVINRERIPTFERMLWRVCRGNVFLRQAEIENPLEDPVTGDYVHKSVFIIFFQGDQLKNRVKKICEGFRASLYPCPETPQERKEMASGVNTRIDDLQMVLNQTEDHRQRVLQAAAKNIRVWFIKVRKMKAIYHTLNLCNIDVTQKCLIAEVWCPVTDLDSIQFALRRGTEHSGSTVPSILNRMQTNQTPPTYNKTNKFTYGFQNIVDAYGIGTYRE
Atp6v0a1 V-type proton ATPase 116 kDa subunit a 1 667 726 RHQYLRKKHLGTLNFGGIRVGNGPTEEDAEIIQHDQLSTHSEDAEEFDFGDTMVHQAIHT
ATP6V0A2 V-type proton ATPase 116 kDa subunit a 2 570 587 GIFNHLHFRKKFNIYLVS
ATP6V0A2 V-type proton ATPase 116 kDa subunit a 2 432 445 ENHPRLNQSQEIMR
Atp6v0a2 V-type proton ATPase 116 kDa subunit a 2 432 445 ENHPRLSQSQEILR
ATP6V0A2 V-type proton ATPase 116 kDa subunit a 2 672 739 LWLHNGRSCFGVNRSGYTLIRKDSEEEVSLLGSQDIEEGNHQVEDGCREMACEEFNFGEILMTQVIHS
ATP6V0A2 V-type proton ATPase 116 kDa subunit a 2 825 856 FQNKFYVGAGTKFVPFSFSLLSSKFNNDDSVA
Atp6v0a2 V-type proton ATPase 116 kDa subunit a 2 672 739 LWLHNGRNCFGMSRSGYTLVRKDSEEEVSLLGNQDIEEGNSRMEEGCREVTCEEFNFGEILMTQAIHS
Atp6v0a2 V-type proton ATPase 116 kDa subunit a 2 825 856 FQNKFYVGAGTKFVPFSFSLLSSKFSNDDSIA
Atp6v0a2 V-type proton ATPase 116 kDa subunit a 2 570 587 GIFNHLHFRKKFNVYLVS
ATP6V0A2 V-type proton ATPase 116 kDa subunit a 2 1 393 MGSLFRSETMCLAQLFLQSGTAYECLSALGEKGLVQFRDLNQNVSSFQRKFVGEVKRCEELERILVYLVQEINRADIPLPEGEASPPAPPLKQVLEMQEQLQKLEVELREVTKNKEKLRKNLLELIEYTHMLRVTKTFVKRNVEFEPTYEEFPSLESDSLLDYSCMQRLGAKLGFVSGLINQGKVEAFEKMLWRVCKGYTIVSYAELDESLEDPETGEVIKWYVFLISFWGEQIGHKVKKICDCYHCHVYPYPNTAEERREIQEGLNTRIQDLYTVLHKTEDYLRQVLCKAAESVYSRVIQVKKMKAIYHMLNMCSFDVTNKCLIAEVWCPEADLQDLRRALEEGSRESGATIPSFMNIIPTKETPPTRIRTNKFTEGFQNIVDAYGVGSYRE
Atp6v0a2 V-type proton ATPase 116 kDa subunit a 2 1 393 MGSLFRSESMCLAQLFLQSGTAYECLSALGEKGLVQFRDLNQNVSSFQRKFVGEVKRCEELERILVYLVQEITRADIPLPEGEASPPAPPLKHVLEMQEQLQKLEVELREVTKNKEKLRKNLLELVEYTHMLRVTKTFLKRNVEFEPTYEEFPALENDSLLDYSCMQRLGAKLGFVSGLIQQGRVEAFERMLWRACKGYTIVTYAELDECLEDPETGEVIKWYVFLISFWGEQIGHKVKKICDCYHCHIYPYPNTAEERREIQEGLNTRIQDLYTVLHKTEDYLRQVLCKAAESVCSRVVQVRKMKAIYHMLNMCSFDVTNKCLIAEVWCPEVDLPGLRRALEEGSRESGATIPSFMNTIPTKETPPTLIRTNKFTEGFQNIVDAYGVGSYRE
Atp6v0a4 V-type proton ATPase 116 kDa subunit a 4 429 443 ERHLLAQKSTNEMWN
Atp6v0a4 V-type proton ATPase 116 kDa subunit a 4 1 390 MASVFRSEEMCLSQVFLQVEAAYCCVAELGELGLVQFKDLNANVNSFQRKFVNEVRRCESLERILRFLEDEMQNEILIQVPEKDAETPLPREMITLETTLEKLEGELQEANQSHQALKKSFLELTELKYLLKKTQDFFETETNLGEDFFVEDTSGLLELRTIPAFMTGKLGFTAGVINRERMASFERLLWRVCRGNVYLKFSEMDTLLEDPVTKEEIKKNIFIIFYQGEQLRLKIKKICDGFRATIYPCPEHAAERREMLTSVNVRLEDLITVITQTESHRQRLLQEAAANWHSWVIKVQKMKAVYHVLNMCNIDVTQQCIIAEIWFPVADTRHIKKALEQGMELSGSSMIPIMTEVETKTDPPTFNRTNKFTAGFQNIVDAYGVGSYRE
ATP6V0A4 V-type proton ATPase 116 kDa subunit a 4 429 443 ERRLLSQKTDNEIWN
ATP6V0A4 V-type proton ATPase 116 kDa subunit a 4 813 840 FQNKFYVGDGYKFSPFSFKHILDGTAEE
ATP6V0A4 V-type proton ATPase 116 kDa subunit a 4 663 727 RASHRKSQLQASRIQEDATENIEGDSSSPSSRSGQRTSADTHGALDDHGEEFNFGDVFVHQAIHT
ATP6V0A4 V-type proton ATPase 116 kDa subunit a 4 559 576 SLFNHIYFRRTLNIILQF
Atp6v0a4 V-type proton ATPase 116 kDa subunit a 4 806 833 FQNKFYEGAGSKFSPFSFKHVLEGTAEE
ATP6V0A4 V-type proton ATPase 116 kDa subunit a 4 1 390 MVSVFRSEEMCLSQLFLQVEAAYCCVAELGELGLVQFKDLNMNVNSFQRKFVNEVRRCESLERILRFLEDEMQNEIVVQLLEKSPLTPLPREMITLETVLEKLEGELQEANQNQQALKQSFLELTELKYLLKKTQDFFETETNLADDFFTEDTSGLLELKAVPAYMTGKLGFIAGVINRERMASFERLLWRICRGNVYLKFSEMDAPLEDPVTKEEIQKNIFIIFYQGEQLRQKIKKICDGFRATVYPCPEPAVERREMLESVNVRLEDLITVITQTESHRQRLLQEAAANWHSWLIKVQKMKAVYHILNMCNIDVTQQCVIAEIWFPVADATRIKRALEQGMELSGSSMAPIMTTVQSKTAPPTFNRTNKFTAGFQNIVDAYGVGSYRE
Atp6v0a4 V-type proton ATPase 116 kDa subunit a 4 559 576 SLFNHIYFRRTLNIILQF
Atp6v0a4 V-type proton ATPase 116 kDa subunit a 4 663 720 RAKHQKSQLQSFTIHEDAVEGDHSGHSSKKTAGAHGMKDGHEEEFNFGDIFVHQAIHT
Atp6v0b V-type proton ATPase 21 kDa proteolipid subunit c'' 197 205 QTSRVKMGD
Atp6v0b V-type proton ATPase 21 kDa proteolipid subunit c'' 112 137 SNMAEPFSATEPKAIGHRNYHAGYSM
Atp6v0b V-type proton ATPase 21 kDa proteolipid subunit c'' 25 51 CYTIFDLGFRFDVAWFLTETSPFMWSN
ATP6V0B V-type proton ATPase 21 kDa proteolipid subunit c'' 112 137 SNMAEPFSATDPKAIGHRNYHAGYSM
ATP6V0B V-type proton ATPase 21 kDa proteolipid subunit c'' 197 205 QTSRVKMGD
ATP6V0B V-type proton ATPase 21 kDa proteolipid subunit c'' 25 51 CYTIFDLGFRFDVAWFLTETSPFMWSN
Atp6v0c V-type proton ATPase 16 kDa proteolipid subunit c 115 131 DAGVRGTAQQPRLFVGM
ATP6V0C V-type proton ATPase 16 kDa proteolipid subunit c 34 55 TAKSGTGIAAMSVMRPEQIMKS
ATP6V0C V-type proton ATPase 16 kDa proteolipid subunit c 115 131 DAGVRGTAQQPRLFVGM
Atp6v0c V-type proton ATPase 16 kDa proteolipid subunit c 34 55 TAKSGTGIAAMSVMRPELIMKS
Atp6v0c V-type proton ATPase 16 kDa proteolipid subunit c 115 131 DAGVRGTAQQPRLFVGM
Atp6v0c V-type proton ATPase 16 kDa proteolipid subunit c 34 55 TAKSGTGIAAMSVMRPELIMKS
ATP6V0E1 V-type proton ATPase subunit e 1 29 35 PKGPNRG
Atp6v0e1 V-type proton ATPase subunit e 1 29 35 PKGPNRG
Atp6v0e1 V-type proton ATPase subunit e 1 29 35 PKGPNRG
Atp6v0e2 V-type proton ATPase subunit e 2 29 35 PKGPNRG
ATP6V0E2 V-type proton ATPase subunit e 2 29 35 PKGPNRG
Atp6v0e2 V-type proton ATPase subunit e 2 29 35 PKGPNRG
Atp7a Copper-transporting ATPase 1 1398 1492 FLKLYRKPTYDNYELRPRSHTGQRSPSEISVHVGIDDTSRNSPRLGLLDRIVNYSRASINSLLSDKRSLNSVVTSEPDKHSLLVGDFREDDDTTL
Atp7a Copper-transporting ATPase 1 795 927 GKTSEALAKLISLQATEATIVTLNSENLLLSEEQVDVELVQRGDIIKVVPGGKFPVDGRVIEGHSMVDESLITGEAMPVAKKPGSTVIAGSINQNGSLLIRATHVGADTTLSQIVKLVEEAQTSKAPIQQFAD
Atp7a Copper-transporting ATPase 1 1 645 MEPNMDANSITITVEGMTCISCVRTIEQQIGKVNGVHHIKVSLEEKSATVIYNPKLQTPKTLQEAIDDMGFDALLHNANPLPVLTNTVFLTVTAPLALPWDHIQSTLLKTKGVTGVKISPQQRSAVVTIIPSVVSANQIVELVPDLSLDMGTQEKKSGTSEEHSTPQAGEVLLKMRVEGMTCHSCTSTIEGKVGKLQGVQRIKVSLDNQEATIVYQPHLITAEEIKKQIEAVGFPAFIKKQPKYLKLGAIDVERLKSTPVKSSEGSQQKSPAYPSDSAITFTIDGMHCKSCVSNIESALSTLQYVSSIVVSLENRSAIVKYNASLVTPEILRKAIEAVSPGQYRVSISSEVESPTSSPSSSSLQKMPLNLVSQPLTQEVVININGMTCNSCVQSIEGVISKKPGVKSIHVSLTNSTGTIEYDPLLTSPEPLREAIEDMGFDAVLPADMKEPLVVIAQPSLETPLLPSTTEPENVMTPVQNKCYIQVSGMTCASCVANIERNLRREEGIYSVLVALMAGKAEVRYNPAVIQPRVIAELIRELGFGAVVMENAGEGNGILELVVRGMTCASCVHKIESTLTKHKGIFYCSVALATNKAHIKYDPEIIGPRDIIHTIGNLGFEASLVKKDRSANHLDHKREIKQWRGS
Atp7a Copper-transporting ATPase 1 794 926 GKTSEALAKLISLQATEATIVTLNSENLLLSEEQVDVELVQRGDIIKVVPGGKFPVDGRVIEGHSMVDESLITGEAMPVAKKPGSTVIAGSINQNGSLLIRATHVGADTTLSQIVKLVEEAQTSKAPIQQFAD
Atp7a Copper-transporting ATPase 1 1003 1347 VMVGTGVGAQNGILIKGGEPLEMAHKVKVVVFDKTGTITHGTPVVNQVKVLVESNKISRNKILAIVGTAESNSEHPLGAAVTKYCKKELDTETLGTCTDFQVVPGCGISCKVTNIEGLLHKSNLKIEENNIKNASLVQIDAINEQSSTSSSMIIDAHLSNAVNTQQYKVLIGNREWMIRNGLVISNDVDESMIEHERRGRTAVLVTIDDELCGLIAIADTVKPEAELAVHILKSMGLEVVLMTGDNSKTARSIASQVGITKVFAEVLPSHKVAKVKQLQEEGKRVAMVGDGINDSPALAMANVGIAIGTGTDVAIEAADVVLIRNDLLDVVASIDLSRKTVKRIR
Atp7a Copper-transporting ATPase 1 1004 1348 VMVGTGVGAQNGILIKGGEPLEMAHKVKVVVFDKTGTITHGTPVVNQVKVLVESNKISRNKILAIVGTAESNSEHPLGAAVTKYCKQELDTETLGTCTDFQVVPGCGISCKVTNIEGLLHKSNLKIEENNIKNASLVQIDAINEQSSPSSSMIIDAHLSNAVNTQQYKVLIGNREWMIRNGLVISNDVDESMIEHERRGRTAVLVTIDDELCGLIAIADTVKPEAELAVHILKSMGLEVVLMTGDNSKTARSIASQVGITKVFAEVLPSHKVAKVKQLQEEGKRVAMVGDGINDSPALAMASVGIAIGTGTDVAIEAADVVLIRNDLLDVVASIDLSRKTVKRIR
Atp7a Copper-transporting ATPase 1 726 732 AYKALKH
Atp7a Copper-transporting ATPase 1 1 644 MEPSVDANSITITVEGMTCISCVRTIEQQIGKVNGVHHIKVSLEEKSATIIYDPKLQTPKTLQEAIDDMGFDALLHNANPLPVLTNTVFLTVTAPLTLPWDHIQSTLLKTKGVTGVKISPQQRSAVVTIIPSVVSASQIVELVPDLSLDMGTQEKKSGACEEHSTPQAGEVMLKMKVEGMTCHSCTSTIEGKVGKLQGVQRIKVSLDNQEATIVFQPHLITAEEIKKQIEAVGFPAFIKKQPKYLKLGAIDVERLKNTPVKSSEGSQQKSPSYPSDSTTMFTIEGMHCKSCVSNIESALSTLQYVSSIVVSLENRSAIVKYNASLVTPEMLRKAIEAISPGQYRVSIASEVESTASSPSSSSLQKMPLNIVSQPLTQEAVININGMTCNSCVQSIEGVISKKPGVKSIHVSLANSTGTIEFDPLLTSPETLREAIEDMGFDAALPDMKEPLVVIAQPSLETPLLPSSNELENVMTSVQNKCYIQVSGMTCASCVANIERNLRREEGIYSVLVALMAGKAEVRYNPAVIQPRVIAEFIRELGFGAMVMENAGEGNGILELVVRGMTCASCVHKIESTLTKHKGIFYCSVALATNKAHIKYDPEIIGPRDIIHTIGSLGFEASLVKKDRSANHLDHKREIKQWRGS
Atp7a Copper-transporting ATPase 1 727 733 AYKALRH
ATP7A Copper-transporting ATPase 1 1 653 MDPSMGVNSVTISVEGMTCNSCVWTIEQQIGKVNGVHHIKVSLEEKNATIIYDPKLQTPKTLQEAIDDMGFDAVIHNPDPLPVLTDTLFLTVTASLTLPWDHIQSTLLKTKGVTDIKIYPQKRTVAVTIIPSIVNANQIKELVPELSLDTGTLEKKSGACEDHSMAQAGEVVLKMKVEGMTCHSCTSTIEGKIGKLQGVQRIKVSLDNQEATIVYQPHLISVEEMKKQIEAMGFPAFVKKQPKYLKLGAIDVERLKNTPVKSSEGSQQRSPSYTNDSTATFIIDGMHCKSCVSNIESTLSALQYVSSIVVSLENRSAIVKYNASSVTPESLRKAIEAVSPGLYRVSITSEVESTSNSPSSSSLQKIPLNVVSQPLTQETVINIDGMTCNSCVQSIEGVISKKPGVKSIRVSLANSNGTVEYDPLLTSPETLRGAIEDMGFDATLSDTNEPLVVIAQPSSEMPLLTSTNEFYTKGMTPVQDKEEGKNSSKCYIQVTGMTCASCVANIERNLRREEGIYSILVALMAGKAEVRYNPAVIQPPMIAEFIRELGFGATVIENADEGDGVLELVVRGMTCASCVHKIESSLTKHRGILYCSVALATNKAHIKYDPEIIGPRDIIHTIESLGFEASLVKKDRSASHLDHKREIRQWRRS
ATP7A Copper-transporting ATPase 1 735 741 AYKALKH
ATP7A Copper-transporting ATPase 1 803 936 GKTSEALAKLISLQATEATIVTLDSDNILLSEEQVDVELVQRGDIIKVVPGGKFPVDGRVIEGHSMVDESLITGEAMPVAKKPGSTVIAGSINQNGSLLICATHVGADTTLSQIVKLVEEAQTSKAPIQQFADK
ATP7A Copper-transporting ATPase 1 1012 1356 VMVGTGVGAQNGILIKGGEPLEMAHKVKVVVFDKTGTITHGTPVVNQVKVLTESNRISHHKILAIVGTAESNSEHPLGTAITKYCKQELDTETLGTCIDFQVVPGCGISCKVTNIEGLLHKNNWNIEDNNIKNASLVQIDASNEQSSTSSSMIIDAQISNALNAQQYKVLIGNREWMIRNGLVINNDVNDFMTEHERKGRTAVLVAVDDELCGLIAIADTVKPEAELAIHILKSMGLEVVLMTGDNSKTARSIASQVGITKVFAEVLPSHKVAKVKQLQEEGKRVAMVGDGINDSPALAMANVGIAIGTGTDVAIEAADVVLIRNDLLDVVASIDLSRKTVKRIR
ATP7A Copper-transporting ATPase 1 1406 1500 FLKLYRKPTYESYELPARSQIGQKSPSEISVHVGIDDTSRNSPKLGLLDRIVNYSRASINSLLSDKRSLNSVVTSEPDKHSLLVGDFREDDDTAL
Atp7a Copper-transporting ATPase 1 1397 1491 FLKLYRKPTYDNYELHPRSHTGQRSPSEISVHVGIDDTSRNSPRLGLLDRIVNYSRASINSLLSDKRSLNSVVTSEPDKHSLLVGDFREDDDTTL
Atp7b Copper-transporting ATPase 2 1358 1451 QLKCYRKPDLERYEAQAHGRMKPLSASQVSVHVGMDDRRRDSPRATPWDQVSYVSQVSLSSLTSDRLSRHGGMAEDGGDKWSLLLSDRDEEQCI
Atp7b Copper-transporting ATPase 2 1369 1462 QLKCYRKPDLERYEAQAHGRMKPLSASQVSVHIGMDDRRRDSPRATAWDQVSYVSQVSLSSLTSDRLSRHGGAAEDGGDKWSLLLSDRDEEQCI
Atp7b Copper-transporting ATPase 2 997 1319 VMVGTGVAAQNGVLIKGGKPLEMAHKIKTVMFDKTGTITHGVPRVMRFLLLADVATLPLRKVLAVVGTAEASSEHPLGVAVTKYCKEELGTETLGYSTDFQAVPGCGISCKVSNVEGILARSDLTAHPVGVGNPPTGEGAGPQTFSVLIGNREWMRRNGLTISSDISDAMTDHEMKGQTAILVAIDGVLCGMIAIADAVKPEAALAIYTLKSMGVDVALITGDNRKTARAIATQVGINKVFAEVLPSHKVAKVQELQNEGKKVAMVGDGVNDSPALAQADVGIAIGTGTDVAIEAADVVLIRNDLLDVVASIHLSKRTVRRIR
Atp7b Copper-transporting ATPase 2 788 921 SKTSEALAKLMSLQATEATVVTLGEDNLILREEQVPMELVQRGDVIKVVPGGKFPVDGKVLEGNTMADESLITGEAMPVTKKPGSIVIAGSINAHGSVLLKATHVGNDTTLAQIVKLVEEAQMSKAPIQQLADR
Atp7b Copper-transporting ATPase 2 720 726 AYKSLRH
Atp7b Copper-transporting ATPase 2 988 1310 VMVGTGVAAQNGVLIKGGKPLEMAHKIKTVMFDKTGTITHGVPRVMRFLLLVDVATLSLRKVLAVVGTAEASSEHPLGVAVTKYCKEELGTETLGYSTDFQAVPGCGISCKVSNVESILAHRGPTAHPIGVGNPPIGEGTGPQTFSVLIGNREWMRRNGLTISSDISDAMTDHEMKGQTAILVAIDGVLCGMIAIADAVKPEAALASITLKSMGVDVALITGDNRKTARAIATQVGINKVFAEVLPSHKVAKVQELQNKGKKVAMVGDGVNDSPALAQADVGIAIGTGTDVAIDAADVVLIRNDLLDVVASIHLSKRTVRRIR
Atp7b Copper-transporting ATPase 2 1 655 MDPRKNLASVGTMPEQERQVTAKEASRKILSKLALPGRPWEQSMKQSFAFDNVGYEGGLDSTSSSPAATDVVNILGMTCHSCVKSIEDRISSLKGIVNIKVSLEQGSATVRYVPSVMNLQQICLQIEDMGFEASAAEGKAASWPSRSSPAQEAVVKLRVEGMTCQSCVSSIEGKIRKLQGVVRIKVSLSNQEAVITYQPYLIQPEDLRDHICDMGFEAAIKNRTAPLRLGPIDVNKLESTNLKKETVSPVQISNHFETLGHQGSYLATLPLRIDGMHCKSCVLNIEGNIGQLPGVQNIHVSLENKTAQIQYDPSCVTPMFLQTAIEALPPGHFKVSLPDGVEENEPQSGSSQRHQEQGPGRTAVLTISGITCASSVQPIEDMLSQRKGVQQTSISLAEGTGAVLYDPSIVSLDELRTAVEDMGFEVSVNSETFTINPVRNFKSGNSVPQTMGDIAGSVQKMAPDTRGLPTHQGPGHSSETPSSPGATASQKCFVQIKGMTCASCVSNIERSLQRHAGILSVLVALMSGKAEVKYDPEIIQSPRIAQLIQDLGFEASVMEDNTVSEGDIELIITGMTCASCVHNIESKLTRTNGITYASVALATSKAHVKFDPEIVGPRDIIKIIEEIGFHASLAQRNPNAHHLDHKTEIKQWKKS
Atp7b Copper-transporting ATPase 2 711 717 AYKSLRH
Atp7b Copper-transporting ATPase 2 1 646 MPEQERKVTAKEASRKILSKLALPTRPWGQSMKQSFAFDNVGYEGGLDSTCFILQLTTGVVSILGMTCHSCVKSIEDRISSLKGIVSIKVSLEQGSATVKYVPSVLNLQQICLQIEDMGFEASAAEGKAASWPSRSSPAQEAVVKLRVEGMTCQSCVSSIEGKIRKLQGVVRVKVSLSNQEAVITYQPYLIQPEDLRDHICDMGFEAAIKNRTAPLRLGPIDINKLESTNLKRAAVPPIQNSNHLETPGHQQNHLATLPLRIDGMHCKSCVLNIEGNIGQLPGVQNIHVSLENKTAQVQYDSSCITPLFLQTAIEALPPGYFKVSLPDGLEKESGSSSVPSLGSSQRQQEPGPCRTAVLTITGIPRDSSVQPMEDMLSQMKGVQQIDISLAEGTGAVLYDPSVVSSDELRTAVEDMGFEVSVNPENITTNRVSSGNSVPQAVGDSPGSVQNMASDTRGLLTHQGPGYLSDSPPSPGGTASQKCFVQIKGMTCASCVSNIERSLQRHAGILSVLVALMSGKAEVKYDPEVIQSPRIAQLIEDLGFEAAIMEDNTVSEGDIELIITGMTCASCVHNIESKLTRTNGITYASVALATSKAHVKFDPEIIGPRDIIKVIEEIGFHASLAHRNPNAHHLDHKTEIKQWKKS
ATP7B Copper-transporting ATPase 2 1 653 MPEQERQITAREGASRKILSKLSLPTRAWEPAMKKSFAFDNVGYEGGLDGLGPSSQVATSTVRILGMTCQSCVKSIEDRISNLKGIISMKVSLEQGSATVKYVPSVVCLQQVCHQIGDMGFEASIAEGKAASWPSRSLPAQEAVVKLRVEGMTCQSCVSSIEGKVRKLQGVVRVKVSLSNQEAVITYQPYLIQPEDLRDHVNDMGFEAAIKSKVAPLSLGPIDIERLQSTNPKRPLSSANQNFNNSETLGHQGSHVVTLQLRIDGMHCKSCVLNIEENIGQLLGVQSIQVSLENKTAQVKYDPSCTSPVALQRAIEALPPGNFKVSLPDGAEGSGTDHRSSSSHSPGSPPRNQVQGTCSTTLIAIAGMTCASCVHSIEGMISQLEGVQQISVSLAEGTATVLYNPSVISPEELRAAIEDMGFEASVVSESCSTNPLGNHSAGNSMVQTTDGTPTSVQEVAPHTGRLPANHAPDILAKSPQSTRAVAPQKCFLQIKGMTCASCVSNIERNLQKEAGVLSVLVALMAGKAEIKYDPEVIQPLEIAQFIQDLGFEAAVMEDYAGSDGNIELTITGMTCASCVHNIESKLTRTNGITYASVALATSKALVKFDPEIIGPRDIIKIIEEIGFHASLAQRNPNAHHLDHKMEIKQWKKS
ATP7B Copper-transporting ATPase 2 718 724 AYKSLRH
ATP7B Copper-transporting ATPase 2 786 919 SKTSEALAKLMSLQATEATVVTLGEDNLIIREEQVPMELVQRGDIVKVVPGGKFPVDGKVLEGNTMADESLITGEAMPVTKKPGSTVIAGSINAHGSVLIKATHVGNDTTLAQIVKLVEEAQMSKAPIQQLADR
ATP7B Copper-transporting ATPase 2 995 1322 VMVGTGVAAQNGILIKGGKPLEMAHKIKTVMFDKTGTITHGVPRVMRVLLLGDVATLPLRKVLAVVGTAEASSEHPLGVAVTKYCKEELGTETLGYCTDFQAVPGCGIGCKVSNVEGILAHSERPLSAPASHLNEAGSLPAEKDAVPQTFSVLIGNREWLRRNGLTISSDVSDAMTDHEMKGQTAILVAIDGVLCGMIAIADAVKQEAALAVHTLQSMGVDVVLITGDNRKTARAIATQVGINKVFAEVLPSHKVAKVQELQNKGKKVAMVGDGVNDSPALAQADMGVAIGTGTDVAIEAADVVLIRNDLLDVVASIHLSKRTVRRIR
ATP7B Copper-transporting ATPase 2 1372 1465 QLKCYKKPDLERYEAQAHGHMKPLTASQVSVHIGMDDRWRDSPRATPWDQVSYVSQVSLSSLTSDKPSRHSAAADDDGDKWSLLLNGRDEEQYI
Atp7b Copper-transporting ATPase 2 779 912 SKTSEALAKLMSLQATEATVVTLGEDNLILREEQVPMELVQRGDIIKVVPGGKFPVDGKVLEGNTMADESLITGEAMPVTKKPGSIVIAGSINAHGSVLIKATHVGNDTTLAQIVKLVEEAQMSKAPIQQLADR
ATP8A1 Phospholipid-transporting ATPase IA 1071 1164 VIKRTAFKTLVDEVQELEAKSQDPGAVVLGKSLTERAQLLKNVFKKNHVNLYRSESLQQNLLHGYAFSQDENGIVSQSEVIRAYDTTKQRPDEW
ATP8A1 Phospholipid-transporting ATPase IA 1000 1005 TSYWTW
ATP8A1 Phospholipid-transporting ATPase IA 911 940 FERSCRKENMLKYPELYKTSQNALDFNTKV
ATP8A1 Phospholipid-transporting ATPase IA 367 857 KFTQAYFINWDLDMHYEPTDTAAMARTSNLNEELGQVKYIFSDKTGTLTCNVMQFKKCTIAGVAYGHVPEPEDYGCSPDEWQNSQFGDEKTFSDSSLLENLQNNHPTAPIICEFLTMMAVCHTAVPEREGDKIIYQAASPDEGALVRAAKQLNFVFTGRTPDSVIIDSLGQEERYELLNVLEFTSARKRMSVIVRTPSGKLRLYCKGADTVIYDRLAETSKYKEITLKHLEQFATEGLRTLCFAVAEISESDFQEWRAVYQRASTSVQNRLLKLEESYELIEKNLQLLGATAIEDKLQDQVPETIETLMKADIKIWILTGDKQETAINIGHSCKLLKKNMGMIVINEGSLDGTRETLSRHCTTLGDALRKENDFALIIDGKTLKYALTFGVRQYFLDLALSCKAVICCRVSPLQKSEVVEMVKKQVKVVTLAIGDGANDVSMIQTAHVGVGISGNEGLQAANSSDYSIAQFKYLKNLLMIHGAWNYNRVSK
ATP8A1 Phospholipid-transporting ATPase IA 116 297 EIIEDIKRHKADNAVNKKQTQVLRNGAWEIVHWEKVAVGEIVKVTNGEHLPADLISLSSSEPQAMCYIETSNLDGETNLKIRQGLPATSDIKDVDSLMRISGRIECESPNRHLYDFVGNIRLDGHGTVPLGADQILLRGAQLRNTQWVHGIVVYTGHDTKLMQNSTSPPLKLSNVERITNVQ
ATP8A1 Phospholipid-transporting ATPase IA 1 65 MPTMRRTVSEIRSRAEGYEKTDDVSEKTSLADQEEVRTIFINQPQLTKFCNNHVSTAKYNIITFL
Atp8a1 Phospholipid-transporting ATPase IA 999 1008 ETSYWTWFSH
Atp8a1 Phospholipid-transporting ATPase IA 1 75 MPTMRRTVSEIRSRAEGYEKTDDVSEKTSLADQEEVRTIFINQPQLTKFCNNHVSTAKYNVITFLPRFLYSQFRR
Atp8a1 Phospholipid-transporting ATPase IA 361 866 VTLEVVKFTQAYFINWDLDMHYEPTDTAAMARTSNLNEELGQVKYIFSDKTGTLTCNVMQFKKCTIAGVAYGHVPEPEDYGCSPDEWQSSQFGDEKTFNDPSLLDNLQNNHPTAPIICEFLTMMAVCHTAVPEREGDKIIYQAASPDEGALVRAAKQLNFVFTGRTPDSVIIDSLGQEERYELLNVLEFTSARKRMSVVVRTPSGKLRLYCKGADTVIYERLAETSKYKEITLKHLEQFATEGLRTLCFAVAEISESDFEEWRAVYHRASTSVQNRLLKLEESYELIEKNLQLLGATAIEDKLQDQVPETIETLMKADIKIWILTGDKQETAINIGHSCRLLKRNMGMIVINEGSLDGTRETLSRHCTTLGDALRKENDFALIIDGKTLKYALTFGVRQYFLDLALSCKAVICCRVSPLQKSEVVEMVKKQVKVITLAIGDGANDVSMIQTAHVGVGISGNEGLQAANSSDYSIAQFKYLKNLLMVHGAWNYNRVSKCILYCFYKN
Atp8a1 Phospholipid-transporting ATPase IA 912 939 ERSCRKENMLKYPELYKTSQNALDFNTK
Atp8a1 Phospholipid-transporting ATPase IA 122 297 KRHKADNAVNKKQTQVLRNGAWEIVHWEKVAVGEIVKVTNGEHLPADLLSLSSSEPQAMCYIETSNLDGETNLKIRQGLPATSDIKDIDSLMRISGRIECESPNRHLYDFVGNIRLDGHGTVPLGADQILLRGAQLRNTQWVHGIVVYTGHDTKLMQNSTSPPLKLSNVERITNVQ
Atp8a1 Phospholipid-transporting ATPase IA 1066 1164 DVLYKVIKRTAFKTLVDEVQELEAKSQDPGAVVLGKSLTERAQLLKNVFKKNHVNLYRSESLQQNLLHGYAFSQDENGIVSQSEVIRAYDTTKQRPDEW
ATP8A2 Phospholipid-transporting ATPase IB 1019 1028 ETTAWTKFSH
Atp8a2 Phospholipid-transporting ATPase IB 891 920 FERSCTQESMLRFPQLYRITQNAEGFNTKV
ATP8A2 Phospholipid-transporting ATPase IB 1085 1188 EDVAWRAAKHTCKKTLLEEVQELETKSRVLGKAVLRDSNGKRLNERDRLIKRLGRKTPPTLFRGSSLQQGVPHGYAFSQEEHGAVSQEEVIRAYDTTKKKSRKK
ATP8A2 Phospholipid-transporting ATPase IB 386 887 KYTQALFINWDTDMYYIGNDTPAMARTSNLNEELGQVKYLFSDKTGTLTCNIMNFKKCSIAGVTYGHFPELAREPSSDDFCRMPPPCSDSCDFDDPRLLKNIEDRHPTAPCIQEFLTLLAVCHTVVPEKDGDNIIYQASSPDEAALVKGAKKLGFVFTARTPFSVIIEAMGQEQTFGILNVLEFSSDRKRMSVIVRTPSGRLRLYCKGADNVIFERLSKDSKYMEETLCHLEYFATEGLRTLCVAYADLSENEYEEWLKVYQEASTILKDRAQRLEECYEIIEKNLLLLGATAIEDRLQAGVPETIATLLKAEIKIWVLTGDKQETAINIGYSCRLVSQNMALILLKEDSLDATRAAITQHCTDLGNLLGKENDVALIIDGHTLKYALSFEVRRSFLDLALSCKAVICCRVSPLQKSEIVDVVKKRVKAITLAIGDGANDVGMIQTAHVGVGISGNEGMQATNNSDYAIAQFSYLEKLLLVHGAWSYNRVTKCILYCFYKNV
ATP8A2 Phospholipid-transporting ATPase IB 141 316 KRHKADNAVNKKKTIVLRNGMWHTIMWKEVAVGDIVKVVNGQYLPADVVLLSSSEPQAMCYVETANLDGETNLKIRQGLSHTADMQTREVLMKLSGTIECEGPNRHLYDFTGNLNLDGKSLVALGPDQILLRGTQLRNTQWVFGIVVYTGHDTKLMQNSTKAPLKRSNVEKVTNVQ
ATP8A2 Phospholipid-transporting ATPase IB 1 94 MLNGAGLDKALKMSLPRRSRIRSSVGPVRSSLGYKKAEDEMSRATSVGDQLEAPARTIYLNQPHLNKFRDNQISTAKYSVLTFLPRFLYEQIRR
Atp8a2 Phospholipid-transporting ATPase IB 95 276 EIIEDFKRHKADNAVNKKKTIVLRNGMWHTIMWKEVAVGDIVKVLNGQYLPADMVLFSSSEPQGMCYVETANLDGETNLKIRQGLSHTTDMQTRDVLMKLSGRIECEGPNRHLYDFTGNLHLDGKSSVALGPDQILLRGTQLRNTQWVFGVVVYTGHDSKLMQNSTKAPLKRSNVEKVTNVQ
ATP8A2 Phospholipid-transporting ATPase IB 932 959 ERSCTQESMLRFPQLYKITQNGEGFNTK
Atp8a2 Phospholipid-transporting ATPase IB 980 985 TTAWTK
Atp8a2 Phospholipid-transporting ATPase IB 346 837 KYTQALFINWDMDMYYIENDTPAMARTSNLNEELGQVKYLFSDKTGTLTCNIMNFKKCSIAGVTYGHFPELAREQSSDDFCRMTSCTNDSCDFNDPRLLKNIEDQHPTAPCIQEFLTLLAVCHTVVPEKDGDEIIYQASSPDEAALVKGAKKLGFVFTGRTPYSVIIEAMGQEQTFGILNVLEFSSDRKRMSVIVRLPSGQLRLYCKGADNVIFERLSKDSKYMEETLCHLEYFATEGLRTLCVAYADLSENEYEEWLKVYQEASIILKDRAQRLEECYEIIEKNLLLLGATAIEDRLQAGVPETIATLLKAEIKIWVLTGDKQETAINIGYSCRLVSQNMALILLKEDSLDATRAAITQHCTDLGNLLGKENDVALIIDGHTLKYALSFEVRRSFLDLALSCKAVICCRVSPLQKSEIVDVVKKRVKAITLAIGDGANDVGMIQTAHVGVGISGNEGMQATNNSDYAIAQFSYLEKLLLVHGAWSYNRVTK
Atp8a2 Phospholipid-transporting ATPase IB 1050 1148 RAAKHTCKKTLLEEVQELETKSRVMGKAMLRDSNGKRMNERDRLIKRLSRKTPPTLFRTGSIQQCVSHGYAFSQEEHGAVTQEEIVRAYDTTKENSRKK
Atp8a2 Phospholipid-transporting ATPase IB 1 44 MSRATSVGDQLEAPARIIYLNQSHLNKFCDNRISTAKYSVLTFL
Atp8b1 Phospholipid-transporting ATPase IC 1 121 MNTERDSETTFDEDSQPNDEVVPYSDDETEDELEDQGPAVEPEQNRVNREVEKKKETFRKDCTWQVKANDRKFHEQPHFMNTKFFCIKESKYASNAIKTYKYNALTFLPMNLFEQFKRAAN
ATP8B1 Phospholipid-transporting ATPase IC 1 108 MSTERDSETTFDEDSQPNDEVVPYSDDETEDELDDQGSAVEPEQNRVNREAEENREPFRKECTWQVKANDRKYHEQPHFMNTKFLCIKESKYANNAIKTYKYNAFTFI
ATP8B1 Phospholipid-transporting ATPase IC 157 340 IKDLVDDVARHKMDKEINNRTCEVIKDGRFKVAKWKEIQVGDVIRLKKNDFVPADILLLSSSEPNSLCYVETAELDGETNLKFKMSLEITDQYLQREDTLATFDGFIECEEPNNRLDKFTGTLFWRNTSFPLDADKILLRGCVIRNTDFCHGLVIFAGADTKIMKNSGKTRFKRTKIDYLMNYM
ATP8B1 Phospholipid-transporting ATPase IC 412 949 RLGQSHFINWDLQMYYAEKDTPAKARTTTLNEQLGQIHYIFSDKTGTLTQNIMTFKKCCINGQIYGDHRDASQHNHNKIEQVDFSWNTYADGKLAFYDHYLIEQIQSGKEPEVRQFFFLLAVCHTVMVDRTDGQLNYQAASPDEGALVNAARNFGFAFLARTQNTITISELGTERTYNVLAILDFNSDRKRMSIIVRTPEGNIKLYCKGADTVIYERLHRMNPTKQETQDALDIFANETLRTLCLCYKEIEEKEFTEWNKKFMAASVASTNRDEALDKVYEEIEKDLILLGATAIEDKLQDGVPETISKLAKADIKIWVLTGDKKETAENIGFACELLTEDTTICYGEDINSLLHARMENQRNRGGVYAKFAPPVQESFFPPGGNRALIITGSWLNEILLEKKTKRNKILKLKFPRTEEERRMRTQSKRRLEAKKEQRQKNFVDLACECSAVICCRVTPKQKAMVVDLVKRYKKAITLAIGDGANDVNMIKTAHIGVGISGQEGMQAVMSSDYSFAQFRYLQRLLLVHGRWSYIRMCK
ATP8B1 Phospholipid-transporting ATPase IC 1003 1032 LDQDVSDKLSLRFPGLYIVGQRDLLFNYKR
ATP8B1 Phospholipid-transporting ATPase IC 1092 1097 TSYWTF
ATP8B1 Phospholipid-transporting ATPase IC 1164 1251 RFLSMTIWPSESDKIQKHRKRLKAEEQWQRRQQVFRRGVSTRRSAYAFSHQRGYADLISSGRSIRKKRSPLDAIVADGTAEYRRTGDS
Atp8b1 Phospholipid-transporting ATPase IC 1004 1032 DQDVSDKLSLRFPGLYVVGQRDLLFNYKK
Atp8b1 Phospholipid-transporting ATPase IC 1 121 MSTERDSETTFDEESQPNDEVVPYSDDETEDELEDQGSTVEPEQNRVNREAEKKRETFRKDCTWQVKANDRKFHEQPHFMNTKFFCIKESKYASNAIKTYKYNGFTFLPMNLFEQFKRAAN
Atp8b1 Phospholipid-transporting ATPase IC 407 952 SVEVIRLGQSHFINWDLQMYYAEKDTPAKARTTTLNEQLGQIHYIFSDKTGTLTQNIMTFKKCCINGTIYGDHRDASQHSHSKIELVDFSWNTFADGKLAFYDHYLIEQIQSGKEPEVRQFFFLLSICHTVMVDRIDGQINYQAASPDEGALVNAARNFGFAFLARTQNTITVSELGSERTYNVLAILDFNSDRKRMSIIVRTPEGSIRLYCKGADTVIYERLHRMNPTKQETQDALDIFASETLRTLCLCYKEIEEKEFTEWNNKFMAASVASSNRDEALDKVYEEIEKDLILLGATAIEDKLQDGVPETISKLAKADIKIWVLTGDKKETAENIGFACELLTEDTTICYGEDINSLLHTRMENQRNRGGVSAKFAPPVYEPFFPPGENRALIITGSWLNEILLEKKTKRSKILKLKFPRTEEERRMRSQSRRRLEEKKEQRQKNFVDLACECSAVICCRVTPKQKAMVVDLVKRYKKAITLAIGDGANDVNMIKTAHIGVGISGQEGMQAVMSSDYSFAQFRYLQRLLLVHGRWSYIRMCKFLR
Atp8b1 Phospholipid-transporting ATPase IC 1004 1032 DQDVSDKLSLRFPGLYVVGQRDLLFNYKR
Atp8b1 Phospholipid-transporting ATPase IC 1164 1251 RFLSMTIWPSESDKIQKHRKRLKAEEQWKRRQSVFRRGASSRRSAYAFSHQRGYADLISSGRSIRKKRSPLDAIIADGTAEYRRTVES
Atp8b1 Phospholipid-transporting ATPase IC 1093 1094 SY
Atp8b1 Phospholipid-transporting ATPase IC 1164 1251 RFLSMTIWPSESDKIQKHRKRLKAEEQWKRRQSVFRRGVSSRRSAYAFSHQRGYADLISSGRSIRKKRSPLDAIIADGTAEYRRTVES
Atp8b1 Phospholipid-transporting ATPase IC 407 952 SVEVIRLGQSHFINWDLQMYYAEKDTPAKSRTTTLNEQLGQIHYIFSDKTGTLTQNIMTFKKCCINGTIYGDHRDASQHSHSKIELVDFSWNEFADGKLAFYDHYLIEQIQSGKEPEVRQFFFLLSICHTVMVDRIDGQINYQAASPDEGALVNAARNFGFAFLARTQNTITVSELGTERTYSVLAILDFNSDRKRMSIIVRTPEGSIRLYCKGADTVIYERLHRMNPMKQETQDALDIFASETLRTLCLCYKEIEEKEFAEWNKKFMAASVASSNRDEALDKVYEEIERDLILLGATAIEDKLQDGVPETISKLAKADIKIWVLTGDKKETAENIGFACELLTEDTTICYGEDINSLLHTRMENQRNRGGVSAKFAPPAYEPFFPPGENRALIITGSWLNEILLEKKTKRSKILKLKFPRTEEERRMRSQSRRRLEEKKEQRQKNFVDLACECSAVICCRVTPKQKAMVVDLVKRYKKAITLAIGDGANDVNMIKTAHIGVGISGQEGMQAVMSSDYSFAQFRYLQRLLLVHGRWSYIRMCKFLR
Atp8b1 Phospholipid-transporting ATPase IC 166 339 RHKMDKEINNRTCEVIKDGRFKIIKWKDIQVGDVIRLKKNDFIPADILLLSSSEPNSLCYVETAELDGETNLKFKMALEITDQYLQIEDNLATFDGFIECEEPNNRLDKFTGTLFWRNQSFPLDADKILLRGCVIRNTDVCHGLVIFAGADTKIMKNSGKTRFKRTKIDYLMNY
Atp8b1 Phospholipid-transporting ATPase IC 166 339 RHKMDKEINNRTCEVIKDGRFKIIKWKDIQVGDVIRLKKNDFIPADILLLSSSEPNSLCYVETAELDGETNLKFKMALEITDQYLQIEDNLATFDGFIECEEPNNRLDKFTGTLFWKNQSFPLDADKILLRGCVIRNTDVCHGLVIFAGADTKIMKNSGKTRFKRTKIDYLMNY
Atp8b1 Phospholipid-transporting ATPase IC 1093 1094 SY
Atp8b2 Phospholipid-transporting ATPase ID 113 295 VKDATDDYFRHKSDNQVNNRHSQVLINGVLQQEQWMNVCVGDIIKLENNQFVAADLLLLSSSEPHGLCYIETAELDGETNMKVRQAIPVTSELGDVSQLARFDGEVICEPPNNKLDKFSGTLYWKENKFPLSNQNMLLRGCVLRNTEWCFGLVIFAGPDTKLMQNSGRTKFKRTSIDRLMNTL
Atp8b2 Phospholipid-transporting ATPase ID 1033 1036 GYWT
Atp8b2 Phospholipid-transporting ATPase ID 1104 1209 RFLRLSLKPDLSDTVRYTQLVRKKQKAQHRCMRRVGRTGSRRSGYAFSHQEGFGELIMSGKNMRLSSLALSSFSTRSSSSWIESLRRKKSDSANSPSGGAEKPLKG
Atp8b2 Phospholipid-transporting ATPase ID 360 898 SLYVSVEVIRLGHSYFINWDKKMFCMKKRTPAEARTTTLNEELGQVEYIFSDKTGTLTQNIMVFNKCSINGHSYGDVFDVLGHKAELGERPEPVDFSFNPLADKKFLFWDSSLLEAVKMGDPHTHEFFRLLSLCHTVMSEEKNEGELYYKAQSPDEGALVTAARNFGFVFRSRTPKTITVHELGTAITYQLLAILDFNNIRKRMSVIVRNPEGKIRLYCKGADTILLDRLHPPTQELLSSTTDHLNEYAGDGLRTLVLAYKDLDEEYYEEWARRRLQASLAQDSREDRLASIYEEVESDMMLLGATAIEDKLQQGVPETIALLTLANIKIWVLTGDKQETAVNIGYSCKMLTDDMTEVFVVTGHTVLEVREELRKARKKMVDSSHAVGNGFTYQGNLSSSKLTSVLEAVAGEYALVINGHSLAHALEADMELEFLETACACKAVICCRVTPLQKAQVVELVKKYKKAVTLAIGDGANDVSMIKTAHIGVGISGQEGIQAVLASDYSFSQFKFLQRLLLVHGRWSYLRMCKFLCYFFYKN
Atp8b2 Phospholipid-transporting ATPase ID 944 972 DQDVPEQRSMEYPKLYEPGQLNLLFNKRE
Atp8b2 Phospholipid-transporting ATPase ID 1 68 MTVPKEIPEKWARAGAPPSWSQKKPSWGTEEERRARANDREYNEKFQYASNCIKTSKYNIVTFLPVNL
ATP8B2 Phospholipid-transporting ATPase ID 1 64 MTVPKEMPEKWARAQAPPSWSRKKPSWGTEEERRARANDREYNEKFQYASNCIKTSKYNILTFL
ATP8B2 Phospholipid-transporting ATPase ID 113 295 VKDATDDYFRHKSDNQVNNRQSQVLINGILQQEQWMNVCVGDIIKLENNQFVAADLLLLSSSEPHGLCYIETAELDGETNMKVRQAIPVTSELGDISKLAKFDGEVICEPPNNKLDKFSGTLYWKENKFPLSNQNMLLRGCVLRNTEWCFGLVIFAGPDTKLMQNSGRTKFKRTSIDRLMNTL
ATP8B2 Phospholipid-transporting ATPase ID 369 889 RLGHSYFINWDKKMFCMKKRTPAEARTTTLNEELGQVEYIFSDKTGTLTQNIMVFNKCSINGHSYGDVFDVLGHKAELGERPEPVDFSFNPLADKKFLFWDPSLLEAVKIGDPHTHEFFRLLSLCHTVMSEEKNEGELYYKAQSPDEGALVTAARNFGFVFRSRTPKTITVHEMGTAITYQLLAILDFNNIRKRMSVIVRNPEGKIRLYCKGADTILLDRLHHSTQELLNTTMDHLNEYAGEGLRTLVLAYKDLDEEYYEEWAERRLQASLAQDSREDRLASIYEEVENNMMLLGATAIEDKLQQGVPETIALLTLANIKIWVLTGDKQETAVNIGYSCKMLTDDMTEVFIVTGHTVLEVREELRKAREKMMDSSRSVGNGFTYQDKLSSSKLTSVLEAVAGEYALVINGHSLAHALEADMELEFLETACACKAVICCRVTPLQKAQVVELVKKYKKAVTLAIGDGANDVSMIKTAHIGVGISGQEGIQAVLASDYSFSQFKFLQRLLLVHGRWSYLRMCK
ATP8B2 Phospholipid-transporting ATPase ID 943 972 FDQDVPEQRSMEYPKLYEPGQLNLLFNKRE
ATP8B2 Phospholipid-transporting ATPase ID 1032 1037 TGYWTA
ATP8B2 Phospholipid-transporting ATPase ID 1104 1209 RFLRLNLKPDLSDTVRYTQLVRKKQKAQHRCMRRVGRTGSRRSGYAFSHQEGFGELIMSGKNMRLSSLALSSFTTRSSSSWIESLRRKKSDSASSPSGGADKPLKG
Atp8b3 Phospholipid-transporting ATPase IK 1077 1104 SLTQSLWMYRISPKTFPFLFADYNVLFE
ATP8B3 Phospholipid-transporting ATPase IK 1 149 MGTGPAQTPRSTRAGPEPSPAPPGPGDTGDSDVTQEGSGPAGIRGGETVIRAGMGDSPGRGAPERRHKAQPGRARKYEWRPEGPTSMGSLGQREDLQDEDRNSAFTWKVQANNRAYNGQFKEKVILCWQRKKYKTNVIRTAKYNFYSFL
ATP8B3 Phospholipid-transporting ATPase IK 198 381 TRDLVDDMGRHKSDRAINNRPCQILMGKSFKQKKWQDLCVGDVVCLRKDNIVPADMLLLASTEPSSLCYVETVDIDGETNLKFRQALMVTHKELATIKKMASFQGTVTCEAPNSRMHHFVGCLEWNDKKYSLDIGNLLLRGCRIRNTDTCYGLVIYAGFDTKIMKNCGKIHLKRTKLDLLMNKL
ATP8B3 Phospholipid-transporting ATPase IK 453 995 YLGNSVFIDWDVQMYYKPQDVPAKARSTSLNDHLGQVEYIFSDKTGTLTQNILTFNKCCISGRVYGPDSEATTRPKENPYLWNKFADGKLLFHNAALLHLVRTNGDEAVREFWRLLAICHTVMVRESPRERPDQLLYQAASPDEGALVTAARNFGYVFLSRTQDTVTIMELGEERVYQVLAIMDFNSTRKRMSVLVRKPEGAICLYTKGADTVIFERLHRRGAMEFATEEALAAFAQETLRTLCLAYREVAEDIYEDWQQRHQEASLLLQNRAQALQQLLGATAIEDRLQDGVPETIKCLKKSNIKIWVLTGDKQETAVNIGFACELLSENMLILEEKEISRILETYWENSNNLLTRESLSQVKLALVINGDFLDKLLVSLRKEPRALAQNVNMDEAWQELGQSRRDFLYARRLSLLCRRFGLPLAAPPAQDSRARRSSEVLQERAFVDLASKCQAVICCRVTPKQKALIVALVKKYHQVVTLAIGDGANDINMIKTADVGVGLAGQEGMQAVQNSDFVLGQFCFLQRLLLVHGRWSYVRICK
ATP8B3 Phospholipid-transporting ATPase IK 1049 1078 FEQDVSAEQSLEKPELYVVGQKDELFNYWV
ATP8B3 Phospholipid-transporting ATPase IK 1136 1141 IKYWTA
ATP8B3 Phospholipid-transporting ATPase IK 1208 1300 RVIFPALKELRAKEEKVEEGPSEEIFTMEPLPHVHRESRARRSSYAFSHREGYANLITQGTILRRGPGVSSDIASESLDPSDEEAASSPKESQ
Atp8b3 Phospholipid-transporting ATPase IK 939 946 SAQPLYEG
Atp8b3 Phospholipid-transporting ATPase IK 1 74 MDGVHLGENLEDKDTEFTWEVKANDRTYHKQFKKKGFLCWRQKKYKSNAIHTAKYNIFSFLPLNLYEQFHRMSN
Atp8b3 Phospholipid-transporting ATPase IK 1017 1033 MVSSDMSKAGSSHDYQS
Atp8b3 Phospholipid-transporting ATPase IK 317 339 KQFKAKHYYMSPTHGRSDAMESF
ATP8B4 Probable phospholipid-transporting ATPase IM 93 276 VKDATDDYFRHKSDNQVNNRQSEVLINSKLQNEKWMNVKVGDIIKLENNQFVAADLLLLSSSEPHGLCYVETAELDGETNLKVRHALSVTSELGADISRLAGFDGIVVCEVPNNKLDKFMGILSWKDSKHSLNNEKIILRGCILRNTSWCFGMVIFAGPDTKLMQNSGKTKFKRTSIDRLMNTL
ATP8B4 Probable phospholipid-transporting ATPase IM 1014 1019 TSYWTF
ATP8B4 Probable phospholipid-transporting ATPase IM 925 954 FDQDVSDQNSVDCPQLYKPGQLNLLFNKRK
ATP8B4 Probable phospholipid-transporting ATPase IM 350 871 RLGHSYFINWDRKMYYSRKAIPAVARTTTLNEELGQIEYIFSDKTGTLTQNIMTFKRCSINGRIYGEVHDDLDQKTEITQEKEPVDFSVKSQADREFQFFDHHLMESIKMGDPKVHEFLRLLALCHTVMSEENSAGELIYQVQSPDEGALVTAARNFGFIFKSRTPETITIEELGTLVTYQLLAFLDFNNTRKRMSVIVRNPEGQIKLYSKGADTILFEKLHPSNEVLLSLTSDHLSEFAGEGLRTLAIAYRDLDDKYFKEWHKMLEDANAATEERDERIAGLYEEIERDLMLLGATAVEDKLQEGVIETVTSLSLANIKIWVLTGDKQETAINIGYACNMLTDDMNDVFVIAGNNAVEVREELRKAKQNLFGQNRNFSNGHVVCEKKQQLELDSIVEETITGDYALIINGHSLAHALESDVKNDLLELACMCKTVICCRVTPLQKAQVVELVKKYRNAVTLAIGDGANDVSMIKSAHIGVGISGQEGLQAVLASDYSFAQFRYLQRLLLVHGRWSYFRMCK
ATP8B4 Probable phospholipid-transporting ATPase IM 1 44 MFCSEKKLREVERIVKANDREYNEKFQYADNRIHTSKYNILTFL
ATP8B4 Probable phospholipid-transporting ATPase IM 1086 1192 RFLKVDLYPTLSDQIRRWQKAQKKARPPSSRRPRTRRSSSRRSGYAFAHQEGYGELITSGKNMRAKNPPPTSGLEKTHYNSTSWIENLCKKTTDTVSSFSQDKTVKL
ATP9A Probable phospholipid-transporting ATPase IIA 2 69 TDNIPLQPVRQKKRMDSRPRAGCCEWLRCCGGGEARPRTVWLGHPEKRDQRYPRNVINNQKYNFFTFL
ATP9A Probable phospholipid-transporting ATPase IIA 120 303 EAVEEIRCYVRDKEVNSQVYSRLTARGTVKVKSSNIQVGDLIIVEKNQRVPADMIFLRTSEKNGSCFLRTDQLDGETDWKLRLPVACTQRLPTAADLLQIRSYVYAEEPNIDIHNFVGTFTREDSDPPISESLSIENTLWAGTVVASGTVVGVVLYTGRELRSVMNTSNPRSKIGLFDLEVNCL
ATP9A Probable phospholipid-transporting ATPase IIA 355 841 KIVYSWVIRRDSKIPGTVVRSSTIPEQLGRISYLLTDKTGTLTQNEMIFKRLHLGTVAYGLDSMDEVQSHIFSIYTQQSQDPPAQKGPTLTTKVRRTMSSRVHEAVKAIALCHNVTPVYESNGVTDQAEAEKQYEDSCRVYQASSPDEVALVQWTESVGLTLVGRDQSSMQLRTPGDQILNFTILQIFPFTYESKRMGIIVRDESTGEITFYMKGADVVMAGIVQYNDWLEEECGNMAREGLRVLVVAKKSLAEEQYQDFEARYVQAKLSVHDRSLKVATVIESLEMEMELLCLTGVEDQLQADVRPTLETLRNAGIKVWMLTGDKLETATCTAKNAHLVTRNQDIHVFRLVTNRGEAHLELNAFRRKHDCALVISGDSLEVCLKYYEYEFMELACQCPAVVCCRCAPTQKAQIVRLLQERTGKLTCAVGDGGNDVSMIQESDCGVGVEGKEGKQASLAADFSITQFKHLGRLLMVHGRNSYKRSAA
ATP9A Probable phospholipid-transporting ATPase IIA 894 923 LDKDVKSEVAMLYPELYKDLLKGRPLSYKT
ATP9A Probable phospholipid-transporting ATPase IIA 973 978 IQTWHW
ATP9A Probable phospholipid-transporting ATPase IIA 1031 1047 KYLRRRFSPPSYSKLTS
Atp9a Probable phospholipid-transporting ATPase IIA 894 923 LDKDVKSEVAMLYPELYKDLLKGRPLSYKT
Atp9a Probable phospholipid-transporting ATPase IIA 2 69 TDSIPLQPVRHKKRVDSRPRAGCCEWLRCCGGGEPRPRTVWLGHPEKRDQRYPRNVINNQKYNFFTFL
Atp9a Probable phospholipid-transporting ATPase IIA 973 978 IQTWHW
Atp9a Probable phospholipid-transporting ATPase IIA 1031 1047 KYLRRRFSPPSYSKLTS
Atp9a Probable phospholipid-transporting ATPase IIA 120 303 EAVEEIRCYVRDKEMNSQVYSRLTSRGTVKVKSSNIQVGDLILVEKNQRVPADMIFLRTSEKNGSCFLRTDQLDGETDWKLRLPVACTQRLPTAADLLQIRSYVYAEEPNIDIHNFLGTFTREDSDPPISESLSIENTLWAGTVIASGTVVGVVLYTGRELRSVMNTSDPRSKIGLFDLEVNCL
Atp9a Probable phospholipid-transporting ATPase IIA 355 841 KIVYSWVIRRDSKIPGTVVRSSTIPEQLGRISYLLTDKTGTLTQNEMVFKRLHLGTVAYGLDSMDEVQSHIFSIYTQQSQDPPAQKGPTVTTKVRRTMSSRVHEAVKAIALCHNVTPVYESNGVTDQAEAEKQFEDSCRVYQASSPDEVALVQWTESVGLTLVGRDQSSMQLRTPGDQVLNLTILQVFPFTYESKRMGIIVRDESTGEITFYMKGADVVMAGIVQYNDWLEEECGNMAREGLRVLVVAKKSLTEEQYQDFEARYVQAKLSVHDRSLKVATVIESLEMEMELLCLTGVEDQLQADVRPTLETLRNAGIKVWMLTGDKLETATCTAKNAHLVTRNQDIHVFRLVTNRGEAHLELNAFRRKHDCALVISGDSLEVCLKYYEYEFMELACQCPAVVCCRCAPTQKAQIVRLLQERTGKLTCAVGDGGNDVSMIQESDCGVGVEGKEGKQASLAADFSITQFKHLGRLLMVHGRNSYKRSAA
Atp9b Probable phospholipid-transporting ATPase IIB 984 1012 DQDVKPEMAILYPELYKDLTKGRSLSFKT
ATP9B Probable phospholipid-transporting ATPase IIB 1 146 MADQIPLYPVRSAAAAAANRKRAAYYSAAGPRPGADRHSRYQLEDESAHLDEMPLMMSEEGFENEESDYHTLPRARIMQRKRGLEWFVCDGWKFLCTSCCGWLINICRRKKELKARTVWLGCPEKCEEKHPRNSIKNQKYNVFTFI
ATP9B Probable phospholipid-transporting ATPase IIB 197 380 EAIDEFRRFQRDKEVNSQLYSKLTVRGKVQVKSSDIQVGDLIIVEKNQRIPSDMVFLRTSEKAGSCFIRTDQLDGETDWKLKVAVSCTQQLPALGDLFSISAYVYAQKPQMDIHSFEGTFTREDSDPPIHESLSIENTLWASTIVASGTVIGVVIYTGKETRSVMNTSNPKNKVGLLDLELNRL
ATP9B Probable phospholipid-transporting ATPase IIB 432 930 KAVYGWMMMKDENIPGTVVRTSTIPEELGRLVYLLTDKTGTLTQNEMIFKRLHLGTVSYGADTMDEIQSHVRDSYSQMQSQAGGNNTGSTPLRKAQSSAPKVRKSVSSRIHEAVKAIVLCHNVTPVYESRAGVTEETEFAEADQDFSDENRTYQASSPDEVALVQWTESVGLTLVSRDLTSMQLKTPSGQVLSFCILQLFPFTSESKRMGVIVRDESTAEITFYMKGADVAMSPIVQYNDWLEEECGNMAREGLRTLVVAKKALTEEQYQDFESRYTQAKLSMHDRSLKVAAVVESLEREMELLCLTGVEDQLQADVRPTLEMLRNAGIKIWMLTGDKLETATCIAKSSHLVSRTQDIHIFRQVTSRGEAHLELNAFRRKHDCALVISGDSLEVCLKYYEHEFVELACQCPAVVCCRCSPTQKARIVTLLQQHTGRRTCAIGDGGNDVSMIQAADCGIGIEGKEGKQASLAADFSITQFRHIGRLLMVHGRNSYKRSAA
ATP9B Probable phospholipid-transporting ATPase IIB 983 1012 LDQDVKPEMAMLYPELYKDLTKGRSLSFKT
ATP9B Probable phospholipid-transporting ATPase IIB 1062 1067 VRTWHW
ATP9B Probable phospholipid-transporting ATPase IIB 1131 1147 KYLRRKLSPPSYCKLAS
Atp9b Probable phospholipid-transporting ATPase IIB 428 938 DMGKAAYGWMIMKDENIPGTVVRTSTIPEELGRLVYLLTDKTGTLTQNEMVFKRLHLGTVSYGTDTMDEIQSHVLNSYLQVHSQPSGHNPSSAPLRRSQSSTPKVKKSVSSRIHEAVKAIALCHNVTPVYEARAGITGETEFAEADQDFSDENRTYQASSPDEVALVRWTESVGLTLVSRDLASMQLKTPSGQVLTYCILQMFPFTSESKRMGIIVRDESTAEITFYMKGADVAMSTIVQYNDWLEEECGNMAREGLRTLVVAKRTLTEEQYQDFESRYSQAKLSIHDRALKVAAVVESLEREMELLCLTGVEDQLQADVRPTLEMLRNAGIKIWMLTGDKLETATCIAKSSHLVSRTQDIHVFRPVTSRGEAHLELNAFRRKHDCALVISGDSLEVCLRYYEHELVELACQCPAVVCCRCSPTQKAHIVTLLRQHTRKRTCAIGDGGNDVSMIQAADCGIGIEGKEGKQASLAADFSITQFRHIGRLLMVHGRNSYKRSAALGQFVMHRG
Atp9b Probable phospholipid-transporting ATPase IIB 194 381 AREAIDEFRRFQRDKEMNSQLYSKLTVRGKVQVKSSDIQVGDLIIVEKNQRIPSDMVFLRTSEKAGSCFIRTDQLDGETDWKLKVAVSCTQRLPALGDLFSISAYVYAQKPQLDIHSFEGTFTREDSDPPIHESLSIENTLWASTIVASGTVIGVVIYTGKETRSVMNTSNPNNKVGLLDLELNQLTK
Atp9b Probable phospholipid-transporting ATPase IIB 1129 1146 LKYLKRKLSPPSYSKLSS
Atp9b Probable phospholipid-transporting ATPase IIB 1 143 MADQIPLYPVRSAGAAASHRRAAYYSSAGPGPGADRRGRYQLEDESAHLDEMPLMMSEEGFENDESDYHTLPRARITRRKRGLEWFVCGGWKFLCTSCCDWLINVCQRKKELKARTVWLGCPEKCEEKHPRNSIKNQKYNVFT
Atp9b Probable phospholipid-transporting ATPase IIB 983 1011 DQDVKPEMAILYPELYKDLTKGRSLSFKT
Atp9b Probable phospholipid-transporting ATPase IIB 1062 1065 RTWH
Atp9b Probable phospholipid-transporting ATPase IIB 429 939 DMGKAAYGWMIMKDENIPGTVVRTSTIPEELGRLVYLLTDKTGTLTQNEMVFKRLHLGTVSYGTDTMDEIQSHVLNSYLQVHSQTSGHNPSSAPLRRSQSSTPKVKKSVSSRIHEAVKAIALCHNVTPVYEARTGITGETEFAEADQDFSDENRTYQASSPDEVALVRWTESVGLTLVSRDLASMQLKTPSGQVLTYCILQMFPFTSESKRMGIIVRDEATAEITFYMKGADVAMSTIVQYNDWLEEECGNMAREGLRTLVVAKRTLTEEQYQDFESRYSQAKLSIHDRTLKVAAVVESLEREMELLCLTGVEDQLQADVRPTLEMLRNAGIKIWMLTGDKLETATCIAKSSHLVSRTQDIHIFRPVTNRGEAHLELNAFRRKHDCALVISGDSLEVCLRYYEHELVELACQCPAVVCCRCSPTQKAHIVTLLRQHTRKRTCAIGDGGNDVSMIQAADCGIGIEGKEGKQASLAADFSITQFRHIGRLLMVHGRNSYKRSAALGQFVMHRG
Atp9b Probable phospholipid-transporting ATPase IIB 1 144 MADQIPLYPVRSAAAAAASHRRAAYYSAVGPGPGADRRGRYQLEDESAHLDEMPLMMSEEGFENDESDYHTLPRARITRRERGLEWFVCGGWKFLCTSCCDWLINVCQRKKELKARTVWLGCPEKCEEKHPRNSIKNQKYNVFT
Atp9b Probable phospholipid-transporting ATPase IIB 1063 1066 RTWH
Atp9b Probable phospholipid-transporting ATPase IIB 195 382 AREAIDEFRRFQRDKEMNSQLYSKLTVRGKVQVKSSDIQVGDLIIVEKNQRIPSDMVFLRTSEKAGSCFIRTDQLDGETDWKLKVAVSCTQRLPALGDLFSISAYVYAQKPQLDIHSFEGTFTRDDSDPPIHESLSIENTLWASTIVASGTVIGVVIYTGKETRSVMNTSNPKNKVGLLDLELNQLTK
Atp9b Probable phospholipid-transporting ATPase IIB 1130 1147 LKYLKRKLSPPSYSKLSS
atpB ATP synthase subunit a 61 99 RSVAKKATSGVPGKFQTAIELVIGFVNGSVKDMYHGKSK
atpB ATP synthase subunit a 167 219 KMKGIGGFTKELTLQPFNHWAFIPVNLILEGVSLLSKPVSLGLRLFGNMYAGE
atpB ATP synthase subunit a 263 271 YLSMASEEH
atpE ATP synthase subunit c 32 52 GGKFLEGAARQPDLIPLLRTQ
atpE ATP synthase subunit c, sodium ion specific 30 67 VGQGYAAGKAVESVARQPEAKGDIISTMVLGQAVAEST
atpI ATP synthase protein I 2 14 SVSLVSRNVARKL
atpI ATP synthase protein I 118 126 APAVINNKG
atpI ATP synthase protein I 2 14 SVSLVSRNVARKL
atpI ATP synthase protein I 59 70 WRHQAHTPAKGR
atpI ATP synthase protein I 118 126 APAVINNKG
atpI ATP synthase protein I 59 70 WRHQAHTPAKGR
atpI ATP synthase protein I 59 70 WRHQAHTPAKGR
atpI ATP synthase protein I 118 126 APAVINNKG
atpI ATP synthase protein I 2 14 SVSLVSRNVARKL
ATRAID All-trans retinoic acid-induced differentiation factor 221 229 TQRRKAKTS
Atraid All-trans retinoic acid-induced differentiation factor 215 223 TQRRKAKAS
ATRN Attractin 1301 1429 WKIKQSCWASRRREQLLREMQQMASRPFASVNVALETDEEPPDLIGGSIKTVPKPIALEPCFGNKAAVLSVFVRLPRGLGGIPPPGQSGLAVASALVDISQQMPIVYKEKSGAVRNRKQQPPAQPGTCI
Atrn Attractin 1300 1428 WKIKQSCWASRRREQLLREMQQMASRPFASVNVALETDEEPPDLIGGSIKTVPKPIALEPCFGNKAAVLSVFVRLPRGLGGIPPPGQSGLAVASALVDISQQMPIVYKEKSGAVRNRKQQPPAQPGTCI
Atrn Attractin 1304 1432 WKIKQSCWASRRREQLLREMQQMASRPFASVNVALETDEEPPDLIGGSIKTVPKPIALEPCFGNKAAVLSVFVRLPRGLGGIPPPGQSGLAVASALVDISQQMPIVYKEKSGAVRNRKQQPPAQPGTCI
Atrnl1 Attractin-like protein 1 1251 1378 WKIKQTCWASRRREQLLRERQQMASRPFASVDVALEVGAEQTDFLRGPLEGAPKPIAIEPCAGNRAAVLTVFLCLPRGSSGAPPPGQSGLAIASALIDISQQKPSDNKDKTSGVRNRKHLSTRQGTCV
ATRNL1 Attractin-like protein 1 1252 1379 WKIKQTCWASRRREQLLRERQQMASRPFASVDVALEVGAEQTEFLRGPLEGAPKPIAIEPCAGNRAAVLTVFLCLPRGSSGAPPPGQSGLAIASALIDISQQKASDSKDKTSGVRNRKHLSTRQGTCV
AUP1 Lipid droplet-regulating VLDL assembly factor AUP1 42 410 RLFLGIHVFLVSCALPDSVLRRFVVRTMCAVLGLVARQEDSGLRDHSVRVLISNHVTPFDHNIVNLLTTCSTPLLNSPPSFVCWSRGFMEMNGRGELVESLKRFCASTRLPPTPLLLFPEEEATNGREGLLRFSSWPFSIQDVVQPLTLQVQRPLVSVTVSDASWVSELLWSLFVPFTVYQVRWLRPVHRQLGEANEEFALRVQQLVAKELGQTGTRLTPADKAEHMKRQRHPRLRPQSAQSSFPPSPGPSPDVQLATLAQRVKEVLPHVPLGVIQRDLAKTGCVDLTITNLLEGAVAFMPEDITKGTQSLPTASASKFPSSGPVTPQPTALTFAKSSWARQESLQERKQALYEYARRRFTERRAQEAD
AUP1 Lipid droplet-regulating VLDL assembly factor AUP1 1 20 MELPSGPGPERLFDSHRLPG
Aup1 Lipid droplet-regulating VLDL assembly factor AUP1 1 20 MEPPPAPGPERLFDSHRLPS
Aup1 Lipid droplet-regulating VLDL assembly factor AUP1 42 410 RLFLGLHVFLVSCALPDSVLRRFVVRTMCAVLGLVARQEDSGLRDHRVRVLISNHVTPFDHNIVNLLTTCSTPLLNSPPSFVCWSRGFMEMDRRVELVESLKKFCASTRLPPTPLLLFPEEEATNGREGLLRFSSWPFSIQDVVQPLTLQVQRPLVSVTVSDASWVSELLWSLFVPFTVYQVRWLHPIRRQLGEESEEFALRVQQLVAKELGQIGTRLTPADKAEHMKRQRHPRLRPQSVQSSFPSPPSPSSDVQLTTLAHRVKEVLPHVPLNVIQRDLARTGCVDLTITNLLEGAVAFMPEDVTEGSQSPPAPSAPKFPSSGLATPQPTALTFAKSSWARQESLQERKQALYEYARRRFRERQAQEAE
Aup1 Lipid droplet-regulating VLDL assembly factor AUP1 1 20 MEPPPAPGPERLFDSHRLPS
Aup1 Lipid droplet-regulating VLDL assembly factor AUP1 42 410 RLFLGLHVFLVSCALPDSVLRRFVVRTMCAVLGLVARQEDSGLRDHRVRVLISNHVTPFDHNIVNLLTTCSTPLLNSPPSFVCWSRGFMEMDRRVELVESLKKFCASTRLPPTPLLLFPEEEATNGREGLLRFSSWPFSIQDVVQPLTLQVQRPLVSVTVSDASWVSELLWSLFVPFTVYQVRWLHPIRRQLGEENEEFALRVQQLVAKELGQIGTRLTPADKAEHMKRQRHPRLRPQSVQSSFPSPPSPSSDVQLTILAQRVKEVLPHVPLNVIQRDLARTGCVDLTITNLLEGAVAFMPEDVTEGSQSLPTASAPKFPSSGLVTPQPTALTFAKSSWARQESLQERKQALYEYARRRFRERQAQEAE
Avpr1a Vasopressin V1a receptor 77 88 HRTPRKTSRMHL
Avpr1a Vasopressin V1a receptor 148 168 DRYIAVCHPLKTLQQPARRSR
Avpr1a Vasopressin V1a receptor 358 424 SGHLLQDCVQSFPCCHSMAQKFAKDDSDSMSRRQTSYSNNRSPTNSTGMWKDSPKSSKSIRFIPVST
Avpr1a Vasopressin V1a receptor 357 423 SGHLLQDCVQSFPCCQSIAQKFAKDDSDSMSRRQTSYSNNRSPTNSTGTWKDSPKSSKSIRFIPVST
AVPR1A Vasopressin V1a receptor 77 88 HRTPRKTSRMHL
AVPR1A Vasopressin V1a receptor 148 168 DRYIAVCHPLKTLQQPARRSR
AVPR1A Vasopressin V1a receptor 240 293 CYNIWCNVRGKTASRQSKGAEQAGVAFQKGFLLAPCVSSVKSISRAKIRTVKMT
AVPR1A Vasopressin V1a receptor 352 418 SGHLLQDCVQSFPCCQNMKEKFNKEDTDSMSRRQTFYSNNRSPTNSTGMWKDSPKSSKSIKFIPVST
Avpr1a Vasopressin V1a receptor 77 88 HRTPRKTSRMHL
Avpr1a Vasopressin V1a receptor 242 299 CYHIWRNIRGKTASSRHSKGDKGSGEAVGPFHKGLLVTPCVSSVKSISRAKIRTVKMT
Avpr1a Vasopressin V1a receptor 148 168 DRYIAVCHPLKTLQQPARRSR
Avpr1a Vasopressin V1a receptor 242 298 CYHIWRNVRGKTASRQSKGGKGSGEAAGPFHKGLLVTPCVSSVKSISRAKIRTVKMT
Avpr1b Vasopressin V1b receptor 339 421 NSHLLPRSLSHRACCRGSKPRVHRQLSNSSLASRRTTLLTHTCGPSTLRLSLNLSLHAKPKPAGSLKDLEQVDGEATMETSIS
Avpr1b Vasopressin V1b receptor 224 284 HEIYKNLKVKTQAGREERRGWRTWDKSSSSAVATAATRGLPSRVSSISTISRAKIRTVKMT
Avpr1b Vasopressin V1b receptor 131 151 DRYLAVCHPLRSLRQPSQSTY
Avpr1b Vasopressin V1b receptor 131 151 DRYLAVCHPLRSLQQPSQSTY
Avpr1b Vasopressin V1b receptor 60 71 GRHGHKRSRMHL
Avpr1b Vasopressin V1b receptor 60 71 GLQGHKRSRMHL
AVPR1B Vasopressin V1b receptor 60 71 GQLGRKRSRMHL
AVPR1B Vasopressin V1b receptor 131 151 DRYLAVCHPLRSLQQPGQSTY
AVPR1B Vasopressin V1b receptor 223 283 CHEICKNLKVKTQAWRVGGGGWRTWDRPSPSTLAATTRGLPSRVSSINTISRAKIRTVKMT
AVPR1B Vasopressin V1b receptor 342 424 NSHLLPRPLRHLACCGGPQPRMRRRLSDGSLSSRHTTLLTRSSCPATLSLSLSLTLSGRPRPEESPRDLELADGEGTAETIIF
Avpr1b Vasopressin V1b receptor 343 425 NSRLLPRSLSHHACCTGSKPQVHRQLSTSSLTSRRTTLLTHACGSPTLRLSLNLSLRAKPRPAGSLKDLEQVDGEATMETSIF
Avpr1b Vasopressin V1b receptor 224 280 HEIYKNLKVKTQAGREERRGWPKSSSSAAAAATRGLPSRVSSISTISRAKIRTVKMT
Avpr2 Vasopressin V2 receptor 221 271 IAACQVLIFREIHASLVPGPSERAGRRRRGRRTGSPSEGAHVSAAMAKTVR
Avpr2 Vasopressin V2 receptor 136 159 DRHRAICRPMLAYRHGGGARWNRP
Avpr2 Vasopressin V2 receptor 136 159 DRHRAICRPMLAYRHGGGARWNRP
Avpr2 Vasopressin V2 receptor 329 371 SSSVSSELRSLLCCAQRHTTHSLGPQDESCATASSSLMKDTPS
Avpr2 Vasopressin V2 receptor 329 371 SSSVSSELRSLLCCAQRHTTHSLGPQDESCATASSSLMKDTPS
AVPR2 Vasopressin V2 receptor 61 77 ALARRGRRGHWAPIHVF
AVPR2 Vasopressin V2 receptor 136 158 DRHRAICRPMLAYRHGSGAHWNR
AVPR2 Vasopressin V2 receptor 227 271 LIFREIHASLVPGPSERPGGRRRGRRTGSPGEGAHVSAAVAKTVR
AVPR2 Vasopressin V2 receptor 326 371 ASFSSSVSSELRSLLCCARGRTPPSLGPQDESCTTASSSLAKDTSS
Avpr2 Vasopressin V2 receptor 64 77 RRGRRGRWAPMHVF
Avpr2 Vasopressin V2 receptor 221 271 IAACQVLIFREIHASLVPGPSERAGRRRRGHRTGSPSEGAHVSAAMAKTVR
Avpr2 Vasopressin V2 receptor 64 77 RRGRRGRWAPMHVF
Axl Tyrosine-protein kinase receptor UFO 467 888 HRRKKETRYGEVFEPTVERGELVVRYRVRKSYSRRTTEATLNSLGISEELKEKLRDVMVDRHKVALGKTLGEGEFGAVMEGQLNQDDSILKVAVKTMKIAICTRSELEDFLSEAVCMKEFDHPNVMRLIGVCFQGSDREGFPEPVVILPFMKHGDLHSFLLYSRLGDQPVFLPTQMLVKFMADIASGMEYLSTKRFIHRDLAARNCMLNENMSVCVADFGLSKKIYNGDYYRQGRIAKMPVKWIAIESLADRVYTSKSDVWSFGVTMWEIATRGQTPYPGVENSEIYDYLRQGNRLKQPVDCLDGLYALMSRCWELNPRDRPSFAELREDLENTLKALPPAQEPDEILYVNMDEGGSHLEPRGAAGGADPPTQPDPKDSCSCLTAADVHSAGRYVLCPSTAPGPTLSADRGCPAPPGQEDGA
AXL Tyrosine-protein kinase receptor UFO 473 894 HRRKKETRYGEVFEPTVERGELVVRYRVRKSYSRRTTEATLNSLGISEELKEKLRDVMVDRHKVALGKTLGEGEFGAVMEGQLNQDDSILKVAVKTMKIAICTRSELEDFLSEAVCMKEFDHPNVMRLIGVCFQGSERESFPAPVVILPFMKHGDLHSFLLYSRLGDQPVYLPTQMLVKFMADIASGMEYLSTKRFIHRDLAARNCMLNENMSVCVADFGLSKKIYNGDYYRQGRIAKMPVKWIAIESLADRVYTSKSDVWSFGVTMWEIATRGQTPYPGVENSEIYDYLRQGNRLKQPADCLDGLYALMSRCWELNPQDRPSFTELREDLENTLKALPPAQEPDEILYVNMDEGGGYPEPPGAAGGADPPTQPDPKDSCSCLTAAEVHPAGRYVLCPSTTPSPAQPADRGSPAAPGQEDGA
B1 Light-harvesting protein B-800/850 beta 1 chain 2 19 AERSLSGLTEEEAIAVHD
B2 Light-harvesting protein B-800/850 beta 2 chain 2 25 AERSLSGLTEEEAVAVHAQFQTTF
B3GALNT1 UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1 1 20 MASALWTVLPSRMSLRSLKW
B3galnt1 UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1 1 20 MAPAVLTAIPNRMSLRSLKW
B3galnt1 UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1 1 20 MAPAVLTALPNRMSLRSLKW
B3galnt1 UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1 1 20 MAPAVLTALPNRMSLRSLKW
B3GALNT2 UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2 1 6 MRNWLV
B3galnt2 UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2 1 3 MRN
B3galt1 Beta-1,3-galactosyltransferase 1 1 6 MASKVS
B3GALT1 Beta-1,3-galactosyltransferase 1 1 6 MASKVS
B3GALT2 Beta-1,3-galactosyltransferase 2 1 24 MLQWRRRHCCFAKMTWNAKRSLFR
B3galt2 Beta-1,3-galactosyltransferase 2 1 20 MLQWRRRHCCFAKMTWSPKR
B3GALT4 Beta-1,3-galactosyltransferase 4 1 8 MQLRLFRR
B3galt4 Beta-1,3-galactosyltransferase 4 1 4 MPLS
B3galt4 Beta-1,3-galactosyltransferase 4 1 4 MPLS
B3GALT5 Beta-1,3-galactosyltransferase 5 1 7 MAFPKMR
B3galt5 Beta-1,3-galactosyltransferase 5 1 7 MAHMKTR
B3galt6 Beta-1,3-galactosyltransferase 6 1 11 MKVFRRAWRHR
B3GALT6 Beta-1,3-galactosyltransferase 6 1 11 MKLLRRAWRRR
B3GALT9 Beta-1,3-galactosyltransferase 9 1 12 MQVTFCRLRTHQ
B3GAT1 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 1 6 MPKRRD
B3gat1 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 1 6 MPKRRD
B3gat1 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 1 6 MPKRRD
B3GAT2 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 1 2 MK
B3gat2 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 1 2 MK
B3gat2 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 1 2 MK
B3GAT3 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 1 7 MKLKLKN
B3gat3 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 1 7 MKLKLKN
B3glct Beta-1,3-glucosyltransferase 1 1 M
B3GLCT Beta-1,3-glucosyltransferase 1 6 MRPPAC
B3GNT2 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 1 7 MSVGRRR
B3GNT2 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 1 7 MSVGRRR
B3GNT3 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 3 1 10 MKYLRHRRPN
B3gnt3 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 3 1 10 MRLPRQSPYE
B3GNT4 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4 1 28 MLPPQPSAAHQGRGGRSGLLPKGPAMLC
B3gnt4 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4 1 4 MLPR
B3gnt5 Lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase 1 14 MRVFVSSRRVKRWQ
B3gnt5 Lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase 1 13 MRLFVSRRVKRWK
B3GNT5 Lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase 1 14 MRMLVSGRRVKKWQ
B3GNT6 Acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase 1 12 MAFPCRRSLTAK
B3gnt6 Acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase 1 11 MALPSSRRFKS
B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 1 6 MSLWKK
B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 1 6 MSLWKK
B3GNT7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 1 6 MSLWKK
B3GNT8 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 8 1 6 MRCPKC
B3gnt8 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 8 1 7 MRCRKCQ
B3gnt9 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9 1 12 MRRRRRPRLCPD
B3GNT9 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9 1 10 MRRRLRLRRD
B3KV58_HUMAN cDNA FLJ16153 fis, clone BRAMY3000210, highly similar to Nesprin-1 1 1354 MEELKGQMLKFSSMAPDLDRLNELGYRLPLNDKEIKRMQNLNRHWSLISSQTTERFSKLQSFLLQHQTFLEKCETWMEFLVQTEQKLAVEISGNYQHLLEQQRAHELFQAEMFSRQQILHSIIIDGQRLLEQGQVDDRDEFNLKLTLLSNQWQGVIRRAQQRRGIIDSQIRQWQRYREMAGKLRKWLVEVSYLPMSGLGSVPIPLQQARTLFDEVQFKEKVFLRQQGSYILTVEAGKQLLLSADSGAEAALQAELAEIQEKWKSASMRLEEQKKKLAFLLKDWEKCEKGIADSLEKLRTFKKKLSQSLPDHHEELHAEQMRCKELENAVGSWTDDLTQLSLLKDTLSAYISADDISILNERVELLQRQWEELCHQLSLRRQQIGERLNEWAVFSEKNKELCEWLTQMESKVSQNGDILIEEMIEKLKKDYQEEIAIAQENKIQLQQMGERLAKASHESKASEIEYKLGKVNDRWQHLLDLIAARVKKLKETLVAVQQLDKNMSSLRTWLAHIESELAKPIVYDSCNSEEIQRKLNEQQELQRDIEKHSTGVASVLNLCEVLLHDCDACATDAECDSIQQATRNLDRRWRNICAMSMERRLKIEETWRLWQKFLDDYSRFEDWLKSSERTAAFPSSSGVIYTVAKEELKKFEAFQRQVHECLTQLELINKQYRRLARENRTDSACSLKQMVHEGNQRWDNLQKRVTSILRRLKHFIGQREEFETARDSILVWLTEMDLQLTNIEHFSECDVQAKIKQLKAFQQEISLNHNKIEQIIAQGEQLIEKSEPLDAAIIEEELDELRRYCQEVFGRVERYHKKLIRLPLPDDEHDLSDRELELEDSAALSDLHWHDRSADSLLSPQPSSNLSLSLAQPLRSERSGRDTPASVDSIPLEWDHDYDLSRDLESAMSRALPSEDEEGQDDKDFYLRGAVGLSGDHSALESQIRQLGKALDDSRFQIQQTENIIRSKTPTGPELDTSYKGYMKLLGECSSSIDSVKRLEHKLKEEEESLPGFVNLHSTETQTAGVIDRWELLQAQALSKELRMKQNLQKWQQFNSDLNSIWAWLGDTEEELEQLQRLELSTDIQTIELQIKKLKELQKAVDHRKAIILSINLCSPEFTQADSKESRDLQDRLSQMNGRWDRVCSLLEEWRGLLQDALMQCQGFHEMSHGLLLMLENIDRRKNEIVPIDSNLDAEILQDHHKQLMQIKHELLESQLRVASLQDMSCQLLVNAEGTDCLEAKEEVHVIGNRLKLLLKEVSRHIKELEKLLDVSSSQQDLSSWSSADELDTSGSVSPTSGRSTPNRQKTPRGKCSLSQPGPSVSSPHSRSTKGGSDSSLSEPGPGQSGRGFLFRVLR
B4galnt1 Beta-1,4 N-acetylgalactosaminyltransferase 1 1 7 MRLDRRA
B4galnt1 Beta-1,4 N-acetylgalactosaminyltransferase 1 1 7 MRLDRRA
B4GALNT1 Beta-1,4 N-acetylgalactosaminyltransferase 1 1 7 MWLGRRA
B4GALNT2 Beta-1,4 N-acetylgalactosaminyltransferase 2 1 67 MGSAGFSVGKFHVEVASRGRECVSGTPECGNRLGSAGFGALCLELRGADPAWGPFAAHGRSRRQGSR
B4galnt2 Beta-1,4 N-acetylgalactosaminyltransferase 2 1 15 MTSSVSFASFRFPWL
B4galnt3 Beta-1,4-N-acetylgalactosaminyltransferase 3 1 24 MGSPRAALLMLLLRPIKLLRRRFR
B4GALNT3 Beta-1,4-N-acetylgalactosaminyltransferase 3 1 24 MGSPRAARPPLLLRPVKLLRRRFR
B4galnt4 N-acetyl-beta-glucosaminyl-glycoprotein 4-beta-N-acetylgalactosaminyltransferase 1 1 12 MPWFPVKKVRKQ
B4GALNT4 N-acetyl-beta-glucosaminyl-glycoprotein 4-beta-N-acetylgalactosaminyltransferase 1 1 15 MPRLPVKKIRKQMKL
B4GALT1 Beta-1,4-galactosyltransferase 1 1 24 MRLREPLLSGSAAMPGASLQRACR
B4galt1 Beta-1,4-galactosyltransferase 1 1 24 MRFREQFLGGSAAMPGATLQRACR
B4GALT2 Beta-1,4-galactosyltransferase 2 1 15 MSRLLGGTLERVCKA
B4galt2 Beta-1,4-galactosyltransferase 2 1 15 MSRLLGGTLERVCKA
B4GALT3 Beta-1,4-galactosyltransferase 3 1 10 MLRRLLERPC
B4galt3 Beta-1,4-galactosyltransferase 3 1 10 MLRRLLERPC
B4galt3 Beta-1,4-galactosyltransferase 3 1 10 MLRRLLERPC
B4GALT4 Beta-1,4-galactosyltransferase 4 1 12 MGFNLTFHLSYK
B4galt4 Beta-1,4-galactosyltransferase 4 1 12 MGCNPPYHLSYR
B4galt4 Beta-1,4-galactosyltransferase 4 1 12 MGCNPPYLLSYR
B4GALT5 Beta-1,4-galactosyltransferase 5 1 14 MRARRGLLRLPRRS
B4galt5 Beta-1,4-galactosyltransferase 5 1 14 MRARRGLLRLPRRS
B4galt6 Beta-1,4-galactosyltransferase 6 1 15 MSALKRMMRVSNRSL
B4galt6 Beta-1,4-galactosyltransferase 6 1 15 MSALKRMMRVSNRSL
B4GALT6 Beta-1,4-galactosyltransferase 6 1 14 MSVLRRMMRVSNRS
B4galt7 Beta-1,4-galactosyltransferase 7 1 30 MLPSRRKAAQLPWEDGRARLLPGGLRRKCS
B4GALT7 Beta-1,4-galactosyltransferase 7 1 30 MFPSRRKAAQLPWEDGRSGLLSGGLPRKCS
B4GAT1 Beta-1,4-glucuronyltransferase 1 1 8 MQMSYAIR
B4gat1 Beta-1,4-glucuronyltransferase 1 1 8 MQMSYAIR
B8AAS8_ORYSI Protein ROOT HAIR DEFECTIVE 3 homolog 1 676 MDACFSTQLIDGDGVFNVSGLENFMKEVKMGECGLSYAVVSIMGPQSSGKSTLLNHLFRTNFREMDAFKGRHVTTKGIWMAKAHNIEPCTLVMDLEGTDGRERGEDDTAFEKQSALFALAVSDIVLINMWCHDIGREQAANKPLLKTVFQVMMRLFSPRKTTLLFVIRDKSKTPLENLEPILREDIQKIWDGVPKPHAHKETPLSEFFNVEVVALSSYEEKEELFKEQVASLRDRFQQSIAPGGLAGDRRGVVPASGFSFSSQQFWKVIKENKDLDLPAHKVMVATVRCEEIGNEKIASFTADEEWQQFEEAVQHDYVPGFGKKISNLLDRCLSEYDMEAIYFDEGVRTSKRHQLESKLLQLVNPAYQNLLDHLRTRTLEAFKESFDKSLEKEGFAVAARDCTKVFLEKFDKGSEDAAIQQVKWDPSKIKDKLKRDIEAHVASVRAKKLSELCSKYEGQLTKALAEPVEALLDSASEETWPAIRKLLQRETKSAVSGFESAMASFELDEVTQKELLSKLESHGKSVVESKAKEEAARVLIRMKDRFSTLFSRDADSMPRVWTGKEDIKAITKTARSASMKLLSTMAAIRLDEDGDNIENTLSLALVDTARPGTTDRSIQSFDPLASSSWERVPEEKTLITPVQCKSLWRQFKAETEYTVTQAIAAQEANKRNNNWL
B8AAS8_ORYSI Protein ROOT HAIR DEFECTIVE 3 homolog 722 806 IAKEFQNGFLPAVLSLSTKFVPTIMNILKRLADEGQRPAAPERQREMELQPKSTRNGSHSNVTSAGSSSITSSESGPEYSSPIAH
B8BL90_ORYSI Protein ROOT HAIR DEFECTIVE 3 homolog 734 823 ITAYFRHGTLSGLLTITSGFLPTIMDIITAVINMSHNQKSSSHPPRHRPPLHPQSFRNQAQQQSQAQVQYQAPSSLSSSSSVGSNSDDES
B8BL90_ORYSI Protein ROOT HAIR DEFECTIVE 3 homolog 1 688 MEVPISGGGGGERFCHAAQVVGADGEMDGEAMARFAAGAGLLGRGLSYAVVSIVGPQGSGKSTLLNQLFGTSFTEMDALKGRSQTTKGIWIAKAVGIEPFTVVMDLEGTDGRERGEDDTAFEKQSALFALAVSDIVMINLWCHDIGREHAANRPLLKTIFEVLMRLFSPRKTTLLLVIRDKTKTPLEYLTQALKEDIQKIWNAVLKPEVYKEAALSEFFNVEVTALSSYEEKENLFKEQVGQLRQRFIHSIAPGGLAADRRGVIPASGFCLSALQIWKVIRENKDLNLPAHKIMVATVRCEEIADEKLKSFISDKGWLELETAANSGLVPGFGKKLNAILDFYLSEYDTEAMYFDEDVRTAKRQQLESEILKHTYDAFKKMLEHLHHVVLNKFKSDLEQSLRSGEGFAASARYCVQSSMAEFDAGLRDALVKHAEWDTTKVRSKLEQHIEAHATSVRGTKLAELKANYEKKLLDTLAGPVQSILETGEKDSWACIRRLYRHATESAILAFSASLSEFELDQTTIHKMVMELREHARSIVEEKAREEAGNVLMRMKERFSTVLSRDKDSMPRTWKGNEDIRAITREARLAALRLMSVMAAVRLDDKPDKIDRALTTALLDGGPLSQKRSIEFTSDPLASSTWEEVSEKNTLITPVQCKSIWRQFNAETEYAVAQAISMQEAHRRSNNWL
B8BMV9_ORYSI Protein ROOT HAIR DEFECTIVE 3 homolog 1 680 MDEAAAAEAVQLIDGEGEFAADSAERFMAAAGVAGCGLSYAVVSIMGPQSSGKSTLLNQLFGTNFREMDAFRGRSQTTKGIWIARCVGVEPCTVVMDLEGTDGRERGEDDTAFEKQSSLFALAISDIVLINMWCHDIGREQAANKPLLKTVFQVMMRLFSPRKTTLLFVIRDKTRTPLEHLEPVLREDIQKIWNSVAKPEAHKDTPISEFFNVQVTALPSFEEKEEQFREQVQQLRQRFSNSIAPGGLAGDRRGVVPASGFLFSSQQIWKVIRENKDLDLPAHKVMVATVRCDEIAHEKFSCLTSDAEWMELESDVQSGPVPGFGKKLGYIVDVHMQEYDKEAIYFDEAVRTAKRQLLKSRVLNLVQPAFQKMLAHLRTRALEKYKTELNLTLESGKGFAAAVRDTTESNLNEFDQGCADAVIEQADWDYSKILEKVRRDVEDHTLSIREGKLSELTNHAKEKLRKALVEPVESLFDAAGPSTWASIRNLFKRETEAILPEFQKNLAGFEMESATSEGMVSKLRDYARSIVENKAKEEAGKVLIHMKERFTTVFSHDKDSIPRVWTGKEDVRAIAKDARSAALKLLSVLAAIRWDEKPDKIEKILTSTLLDGSVTPKSKGASASSDPLASTTWEEVSPKYTLITPSQCKSLWKQFKAETEFAITQAVSTQQAHKRGNGRL
B8BMV9_ORYSI Protein ROOT HAIR DEFECTIVE 3 homolog 726 867 INREFQNGVVPGIISVTAKLIPTLQNILNKVATEQQQQQGHHQDAAAEAPQQQQQPQPQPPPLLLSPRSPMSELRRPLHMPFSPVRKAVSPSPSSSSSTVTSPRNAGEDQKPRQMVPHDYKGSKILQDLQLNLQFYYYNSCC
B9EXN4_ORYSJ Protein ROOT HAIR DEFECTIVE 3 homolog 722 806 IAKEFQNGFLPAVLSLSTKFVPTIMNILKRLADEGQRPAAPERQREMELQPKSTRNGSHSNVTSAGSSSITSSESGPEYSSPIAH
B9EXN4_ORYSJ Protein ROOT HAIR DEFECTIVE 3 homolog 1 676 MDACFSTQLIDGDGVFNVSGLENFMKEVKMGECGLSYAVVSIMGPQSSGKSTLLNHLFRTNFREMDAFKGRHVTTKGIWMAKAHNIEPCTLVMDLEGTDGRERGEDDTAFEKQSALFALAVSDIVLINMWCHDIGREQAANKPLLKTVFQVMMRLFSPRKTTLLFVIRDKSKTPLENLEPILREDIQKIWDGVPKPHAHKETPLSEFFNVEVVALSSYEEKEELFKEQVASLRDRFQQSIAPGGLAGDRRGVVPASGFSFSSQQFWKVIKENKDLDLPAHKVMVATVRCEEIGNEKIASFTADEEWQQFEEAVQHDYVPGFGKKISNLLDRCLSEYDMEAIYFDEGVRTSKRHQLESKLLQLVNPAYQNILDHLRTRTLEVFKESFDKSLEKEGFAVAARDCTKVFLEKFDKGSEDAAIQQVKWDPSKIKDKLKRDIEAHVASVRAKKLSELCSKYEGQLTKALAEPVEALLDSASEETWPAIRKLLQRETKSAVSGFESAMASFELDEVTQKELLSKLESHGKSVVESKAKEEAARVLIRMKDRFSTLFSRDADSMPRVWTGKEDIKAITKTARSASMKLLSTMAAIRLDEDGDNIENTLSLALVDTARPGTTDRSIQSFDPLASSSWERVPEEKTLITPVQCKSLWRQFKAETEYTVTQAIAAQEANKRNNNWL
B9GE56_ORYSJ Protein ROOT HAIR DEFECTIVE 3 homolog 726 867 INREFQNGVVPGIISVTAKLIPTLQNILNKVATEQQQQQGHHQDAAAEAPQQQQQPQPQPPPLLLSPRSPMSELRRPLHMPFSPVRKAVSPSPSSSSSTVTSPRNAGEDQKPRQMVPHDYKGSKILQDLQLNLQFYYYNSCC
B9GE56_ORYSJ Protein ROOT HAIR DEFECTIVE 3 homolog 1 680 MDEAAAAEAVQLIDGEGEFAADSAERFMAAAGVAGCGLSYAVVSIMGPQSSGKSTLLNQLFGTNFREMDAFRGRSQTTKGIWIARCVGVEPCTVVMDLEGTDGRERGEDDTAFEKQSSLFALAISDIVLINMWCHDIGREQAANKPLLKTVFQVMMRLFSPRKTTLLFVIRDKTRTPLEHLEPVLREDIQKIWNSVAKPEAHKDTPISEFFNVQVTALPSFEEKEEQFREQVQQLRQRFSNSIAPGGLAGDRRGVVPASGFLFSSQQIWKVIRENKDLDLPAHKVMVATVRCDEIAHEKFSCLTSDAEWMELESDVQSGPVPGFGKKLGYIVDVHMQEYDKEAIYFDEAVRTAKRQLLKSRVLNLVQPAFQKMLAHLRTRALEKYKTELNLTLESGKGFAAAVRDTTESNLNEFDQGCADAVIEQADWDYSKILEKVRRDVEDHTLSIREGKLSELTNHAKEKLRKALVEPVESLFDAAGPSTWASIRNLFKRETEAILPEFQKNLAGFEMESATSEGMVSKLRDYARSIVENKAKEEAGKVLIHMKERFTTVFSHDKDSIPRVWTGKEDVRAIAKDARSAALKLLSVLAAIRWDEKPDKIEKILTSTLLDGSVTPKSKGASASSDPLASTTWEEVSPKYTLITPSQCKSLWKQFKAETEFAITQAVSTQQAHKRGNGRL
Bace1 Beta-secretase 1 479 501 QWRCLRCLRHQHDDFADDISLLK
Bace1 Beta-secretase 1 479 501 QWRCLRCLRHQHDDFADDISLLK
BACE1 Beta-secretase 1 479 501 QWRCLRCLRQQHDDFADDISLLK
Bace2 Beta-secretase 2 491 514 HCRHAPRDPEVVNDESSLVRHRWK
Bace2 Beta-secretase 2 491 514 HCRHAPRDPEVVNDESSLVRHRWK
BACE2 Beta-secretase 2 495 518 RCQRRPRDPEVVNDESSLVRHRWK
baeS Signal transduction histidine-protein kinase BaeS 187 467 RGLLAPVKRLVDGTHKLAAGDFTTRVTPTSEDELGKLAQDFNQLASTLEKNQQMRRDFMADISHELRTPLAVLRGELEAIQDGVRKFTPETVASLQAEVGTLTKLVDDLHQLSMSDEGALAYQKAPVDLIPLLEVAGGAFRERFASRGLKLQFSLPDSITVFGDRDRLMQLFNNLLENSLRYTDSGGSLQISAGQRDKTVRLTFADSAPGVSDDQLQKLFERFYRTEGSRNRASGGSGLGLAICLNIVEAHNGRIIAAHSPFGGVSITVELPLERDLQREV
baeS Signal transduction histidine-protein kinase BaeS 1 11 MKFWRPGITGK
BAK1 LRR receptor kinase BAK1 259 624 AWYRRRKPQEHFFDVPAEEDPEVHLGQLKRFSLRELQVATDTFSNKNILGRGGFGKVYKGRLADGSLVAVKRLKEERTPGGELQFQTEVEMISMAVHRNLLRLRGFCMTPTERLLVYPYMANGSVASRLRERPPSEPPLDWRTRRRIALGSARGLSYLHDHCDPKIIHRDVKAANILLDEDFEAVVGDFGLAKLMDYKDTHVTTAVRGTIGHIAPEYLSTGKSSEKTDVFGYGIMLLELITGQRAFDLARLANDDDVMLLDWVKGLLKEKRLEMLVDPDLQSNYIDVEVESLIQVALLCTQGSPTERPKMAEVVRMLEGDGLAERWEEWQKIEVVRQEVELGPHRNSEWIVDSTDNLHAVELSGPR
BAK1 LRR receptor kinase BAK1 259 624 AWYRRRKPQEHFFDVPAEEDPEVHLGQLKRFSLRELQVATDTFSNKNILGRGGFGKVYKGRLADGSLVAVKRLKEERTPGGELQFQTEVEMISMAVHRNLLRLRGFCMTPTERLLVYPYMANGSVASRLRERPPSEPPLDWRTRRRIALGSARGLSYLHDHCDPKIIHRDVKAANILLDEDFEAVVGDFGLAKLMDYKDTHVTTAVRGTIGHIAPEYLSTGKSSEKTDVFGYGIMLLELITGQRAFDLARLANDDDVMLLDWVKGLLKEKRLEMLVDPDLQSNYIDVEVESLIQVALLCTQGSPTERPKMAEVVRMLEGDGLAERWEEWQKIEVVRQEVELGPHRNSEWIVDSTDNLHAVELSGPR
Bambi BMP and activin membrane-bound inhibitor homolog 174 260 RMLRSENKRLQDQRQQMLSRLHYSFHGHHSKKGQVAKLDLECMVPVSGQENCCLTCDKMRQADLSNEKILSLVHWGMYSGHGKLEFV
Bambi BMP and activin membrane-bound inhibitor homolog 174 260 RMLRSENKRLQDERQQMLSRLHYSFHGHHSKKGQVAKLDLECMVPVSGQENCCLTCDKMRQAELSNEKILSLVHWGMYSGHGKLEFI
BAMBI BMP and activin membrane-bound inhibitor homolog 174 260 RMLRSENKRLQDQRQQMLSRLHYSFHGHHSKKGQVAKLDLECMVPVSGHENCCLTCDKMRQADLSNDKILSLVHWGMYSGHGKLEFV
barA Signal transduction histidine-protein kinase BarA 197 918 RLMRDVTGPIRNMVNTVDRIRRGQLDSRVEGFMLGELDMLKNGINSMAMSLAAYHEEMQHNIDQATSDLRETLEQMEIQNVELDLAKKRAQEAARIKSEFLANMSHELRTPLNGVIGFTRLTLKTELTPTQRDHLNTIERSANNLLAIINDVLDFSKLEAGKLILESIPFPLRSTLDEVVTLLAHSSHDKGLELTLNIKSDVPDNVIGDPLRLQQIITNLVGNAIKFTENGNIDILVEKRALSNTKVQIEVQIRDTGIGIPERDQSRLFQAFRQADASISRRHGGTGLGLVITQKLVNEMGGDISFHSQPNRGSTFWFHINLDLNPNIIIEGPSIQCLAGKRLAYVEPNSAAAQCTLDILSETPLEVVYSPTFSALPPAHYDMMLLGIAVTFREPLTMQHERLAKAVSMTDFLMLALPCHAQVNAEKLKQDGIGACLLKPLTPTRLLPALTEFCHHKQNTLLPVTDESKLAMTVMAVDDNPANLKLIGALLEDMVQHVELCDSGHQAVERAKQMPFDLILMDIQMPDMDGIRACELIHQLPHQRQTPVIAVTAHAMAGQKEKLLGAGMSDYLAKPIEEERLHNLLLRYKPGSGISSRVVTPEVNEIVVNPNATLDWQLALRQAAGKTDLARDMLQMLLDFLPEVRNKVEEQLAGENPEGLVDLIHKLHGSCGYSGVPRMKNLCQLIEQQLRSGTKEEDLEPELLELLDEMDNVAREASKILG
barA Signal transduction histidine-protein kinase BarA 197 918 RLMRDVTGPIRNMVNTVDRIRRGQLDSRVEGFMLGELDMLKNGINSMAMSLAAYHEEMQHNIDQATSDLRETLEQMEIQNVELDLAKKRAQEAARIKSEFLANMSHELRTPLNGVIGFTRLTLKTELTPTQRDHLNTIERSANNLLAIINDVLDFSKLEAGKLILESIPFPLRSTLDEVVTLLAHSSHDKGLELTLNIKSDVPDNVIGDPLRLQQIITNLVGNAIKFTENGNIDILVEKRALSNTKVQIEVQIRDTGIGIPERDQSRLFQAFRQADASISRRHGGTGLGLVITQKLVNEMGGDISFHSQPNRGSTFWFHINLDLNPNIIIEGPSTQCLAGKRLAYVEPNSAAAQCTLDILSETPLEVVYSPTFSALPPAHYDMMLLGIAVTFREPLTMQHERLAKAVSMTDFLMLALPCHAQVNAEKLKQDGIGACLLKPLTPTRLLPALTEFCHHKQNTLLPVTDESKLAMTVMAVDDNPANLKLIGALLEDMVQHVELCDSGHQAVERAKQMPFDLILMDIQMPDMDGIRACELIHQLPHQQQTPVIAVTAHAMAGQKEKLLGAGMSDYLAKPIEEERLHNLLLRYKPGSGISSRVVTPEVNEIVVNPNATLDWQLALRQAAGKTDLARDMLQMLLDFLPEVRNKVEEQLVGENPEGLVDLIHKLHGSCGYSGVPRMKNLCQLIEQQLRSGTKEEDLEPELLELLDEMDNVAREASKILG
barA Signal transduction histidine-protein kinase BarA 197 918 RLMRDVTGPIRNMVNTVDRIRRGQLDSRVEGFMLGELDMLKNGINSMAMSLAAYHEEMQHNIDQATSDLRETLEQMEIQNVELDLAKKRAQEAARIKSEFLANMSHELRTPLNGVIGFTRLTLKTELTPTQRDHLNTIERSANNLLAIINDVLDFSKLEAGKLILESIPFPLRSTLDEVVTLLAHSSHDKGLELTLNIKSDVPDNVIGDPLRLQQIITNLVGNAIKFTENGNIDILVEKRALSNTKVQIEVQIRDTGIGIPERDQSRLFQAFRQADASISRRHGGTGLGLVITQKLVNEMGGDISFHSQPNRGSTFWFHINLDLNPNIIIEGPSTQCLAGKRLAYVEPNSAAAQCTLDILSETPLEVVYSPTFSALPPAHYDMMLLGIAVTFREPLTMQHERLAKAVSMTDFLMLALPCHAQVNAEKLKQDGIGACLLKPLTPTRLLPALTEFCHHKQNTLLPVTDESKLAMTVMAVDDNPANLKLIGALLEDMVQHVELCDSGHQAVERAKQMPFDLILMDIQMPDMDGIRACELIHQLPHQQQTPVIAVTAHAMAGQKEKLLGAGMSDYLAKPIEEERLHNLLLRYKPGSGISSRVVTPEVNEIVVNPNATLDWQLALRQAAGKTDLARDMLQMLLDFLPEVRNKVEEQLVGENPEGLVDLIHKLHGSCGYSGVPRMKNLCQLIEQQLRSGTKEEDLEPELLELLDEMDNVAREASKILG
barA Signal transduction histidine-protein kinase BarA 1 9 MTNYSLRAR
barA Signal transduction histidine-protein kinase BarA 197 918 RLMRDVTGPIRNMVNTVDRIRRGQLDSRVEGFMLGELDMLKNGINSMAMSLAAYHEEMQHNIDQATSDLRETLEQMEIQNVELDLAKKRAQEAARIKSEFLANMSHELRTPLNGVIGFTRLTLKTELTPTQRDHLNTIERSANNLLAIINDVLDFSKLEAGKLILESIPFPLRSTLDEVVTLLAHSSHDKGLELTLNIKSDVPDNVIGDPLRLQQIITNLVGNAIKFTENGNIDILVEKRALSNTKVQIEVQIRDTGIGIPERDQSRLFQAFRQADASISRRHGGTGLGLVITQKLVNEMGGDISFHSQPNRGSTFWFHINLDLNPNIIIEGPSTQCLAGKRLAYVEPNSAAAQCTLDILSETPLEVVYSPTFSALPPAHYDMMLLGIAVTFREPLTMQHERLAKAVSMTDFLMLALPCHAQVNAEKLKQDGIGACLLKPLTPTRLLPALTEFCHHKQNTLLPVTDESKLAMTVMAVDDNPANLKLIGALLEDMVQHVELCDSGHQAVERAKQMPFDLILMDIQMPDMDGIRACELIHQLPHQQQTPVIAVTAHAMAGQKEKLLGAGMSDYLAKPIEEERLHNLLLRYKPGSGISSRVVTPEVNEIVVNPNATLDWQLALRQAAGKTDLARDMLQMLLDFLPEVRNKVEEQLVGENPEGLVDLIHKLHGSCGYSGVPRMKNLCQLIEQQLRSGTKEEDLEPELLELLDEMDNVAREASKILG
barA Signal transduction histidine-protein kinase BarA 1 9 MTNYSLRAR
barA Signal transduction histidine-protein kinase BarA 1 9 MTNYSLRAR
barA Signal transduction histidine-protein kinase BarA 1 10 MTNYSLRARM
basS Sensor protein BasS 89 363 RRITRPLAELQKELEARTADNLTPIAIHSATLEIEAVVSALNDLVSRLTSTLDNERLFTADVAHELRTPLAGVRLHLELLAKTHHIDVAPLVARLDQMMESVSQLLQLARAGQSFSSGNYQHVKLLEDVILPSYDELSTMLDQRQQTLLLPESAADITVQGDATLLRMLLRNLVENAHRYSPQGSNIMIKLQEDDGAVMAVEDEGPGIDESKCGELSKAFVRMDSRYGGIGLGLSIVSRITQLHHGQFFLQNRQETSGTRAWVRLKKDQYVANQI
basS Sensor protein BasS 89 356 RRITRPLAELQKELEARTADNLAPIAIHSSTLEIESVVSAINQLVTRLTTTLDNERLFTADVAHELRTPLSGVRLHLELLSKTHNVDVAPLIARLDQMMDSVSQLLQLARVGQSFSSGNYQEVKLLEDVILPSYDELNTMLETRQQTLLLPESAADVVVRGDATLLRMLLRNLVENAHRYSPEGTHITIHISADPDAIMAVEDEGPGIDESKCGKLSEAFVRMDSRYGGIGLGLSIVSRITQLHQGQFFLQNRTERTGTRAWVLLKKA
basS Sensor protein BasS 1 13 MHFLRRPISLRQR
basS Sensor protein BasS 1 13 MRFQRRAMTLRQR
BB3702 putative conserved inner membrane protein 1 3 MRL
BC10 Glycosyltransferase BC10 1 17 MKPPRRWMYGRGGGKGK
Bcam Basal cell adhesion molecule 563 622 YCMRRKGRPGCCRRAEKGAPPAREPELSHSGSERPEHTGLLMGGPSGGGRGGSGGFGDEC
BCAM Basal cell adhesion molecule 569 628 YCVRRKGGPCCRQRREKGAPPPGEPGLSHSGSEQPEQTGLLMGGASGGARGGSGGFGDEC
Bcam Basal cell adhesion molecule 565 624 YCMRRKGRPGCCQRAEKGAPPAREPELSHSGSERPEHTGLLMGGPSGGGRGGNGGFGDEC
BCAP29 B-cell receptor-associated protein 29 28 43 PPQRWQKIFSFNVWGK
BCAP29 B-cell receptor-associated protein 29 125 241 TQLAKELSNKGVLKTQAENTNKAAKKFMEENEKLKRILKSHGKDEECVLEAENKKLVEDQEKLKTELRKTSDALSKAQNDVMEMKMQSERLSKEYDQLLKEHSELQDRLERGNKKRL
Bcap29 B-cell receptor-associated protein 29 28 43 PPQRWQKIFSFSVWGK
Bcap29 B-cell receptor-associated protein 29 125 240 TQLAKEIANKGVLKIQAENTNKAAKKFMEENEKLKLGLRNDNAEEHLLEAENKKLIESKENLKTELKKASDALLKAQNDVMTMKIQSERLSKEYDRLLKEHSELQNRLEKEKKKGL
Bcap31 B-cell receptor-associated protein 31 124 245 SQQATLLASNEAFKKQAESASEAAKKYMEENDQLKKGAAEDGDKLDIGNTEMKLEENKSLKNDLRKLKDELASTKKKLEKAENEALAMQKQSEGLTKEYDRLLEEHAKLQASVRGPSVKKEE
Bcap31 B-cell receptor-associated protein 31 28 43 SPKRWQKVFKSRLVEL
BCAP31 B-cell receptor-associated protein 31 28 43 SPKRWQKIFKSRLVEL
BCAP31 B-cell receptor-associated protein 31 124 246 SQQATLLASNEAFKKQAESASEAAKKYMEENDQLKKGAAVDGGKLDVGNAEVKLEEENRSLKADLQKLKDELASTKQKLEKAENQVLAMRKQSEGLTKEYDRLLEEHAKLQAAVDGPMDKKEE
bceS Sensor protein BceS 56 334 RYRKETAFYKSLKTWENNLDVTAINEPETPFEAMVERSIAGQTEHLKQTAARHRLALENEKDELMAWIHEVKTPLTAMHLIIDRMEEKALKSQLSYEWLRIHLLLDQQLHQKRISFIENDLSVEFIQLQPLIFKEIKDLQSWCIQKGIGFDIQLEAKEVLSDAKWLAFIIRQLLTNAVKYSEASEIEIKSFQKGEQTQLQVKDCGRGIDPKDVPRIFDKGFTSTTDHHDQASTGMGLYLAKKAAAPLLIHIDVESEFGAGTVFTLTFPIRNQFEHVISV
bceS Sensor protein BceS 1 12 MIKAFLIERRSW
bcr Bicyclomycin resistance protein 66 76 GPMADSFGRKP
bcr Bicyclomycin resistance protein 269 285 NSRFVRRIGALNMFRSG
bcr Bicyclomycin resistance protein 186 214 KETLPPERRQPFHIRTTIGNFAALFRHKR
bcr Bicyclomycin resistance protein 391 396 SRPKKR
bcr Bicyclomycin resistance protein 333 344 DEFPHMAGTASS
bcr Bicyclomycin resistance protein 123 137 MRDIYPKEEFSRMMS
bcr Bicyclomycin resistance protein 1 8 MTTRQHSS
bcrR HTH-type transcriptional activator BcrR 203 204 MK
bcrR HTH-type transcriptional activator BcrR 1 81 MEFNEKLQQLRTGKNLTQEQLAEQLYVSRTAISKWESGKGYPNMESLKCISKFFSVTIDELLSGEELITLAETENRSNLKK
bcrR HTH-type transcriptional activator BcrR 148 154 THLDKEK
bcsB Cyclic di-GMP-binding protein 764 779 RLLRIISRRRLNPDNE
bcsB Cyclic di-GMP-binding protein 774 788 LRRRTAERLNDGGGA
bcsB Cyclic di-GMP-binding protein 751 766 RLLRILSRRRLDPDHE
bcsB Cyclic di-GMP-binding protein 786 802 KHALRRRRELQEERQRT
bcsB Cyclic di-GMP-binding protein 751 766 RLLRILSRRRLDPDHE
bcsB Cyclic di-GMP-binding protein 766 785 WVLWRLLRIISRRRLNPDNE
bcsB Cyclic di-GMP-binding protein 786 802 KHALRRRRELQEERQRT
bcsBI Cyclic di-GMP-binding protein 788 804 RHAMFRRRQLQEERQKS
BC_3793 Cell division protein ftsK 178 793 CITNKHIGEVLAPVGRILRSQFQVMQGDYKDWRAKRTAEQTEKKKTTRSTRSKRAAEQEEIIEPMEEISIDPPIISNFTENYPVNEEEDKRIEVEQEELITSPFIEETPPIEEPKKKRGEKIVESLESEAQAPPMQFSNVENKDYKLPSLDILKFPKNKQVTNENAEIYENARKLERTFQSFGVKAKVTKVHRGPAVTKYEVYPDMGVKVSKIVSLSDDLALALAAKDIRIEAPIPGKSAVGIEVPNSEVSMVTLREVLDSKANNHPEEKLLIGLGRDITGEAVLARLNKMPHLLVAGATGSGKSVCINGIIVSILMRAKPHEVKLMMIDPKMVELNVYNGVPHLLTPVVTDPKKASQALKKVVSEMERRYELFAHSGTRNIEGYNDYIKEHNSQSEAKQPELPYIVVIVDELADLMMVASSDVEDAIMRLAQMARAAGIHLIIATQRPSVDVITGVIKANIPSRIAFAVSSQTDSRTILDGGGAEKLLGRGDMLFIPIGASKPVRVQGAFLSDDEVERVVEYVIGQQKAQYQEDMIPQDVLDTKQEVEDELYDEAVQLVVEMQTASVSMLQRRFRVGYTRAARLIDAMEMNGVVGPYEGSKPREVLINDVQEKSS
BC_3908 Cell division protein ftsQ 1 30 MNNSKVIKLQDRVPKLKNQKKKNKKNVNHR
BC_3917 Cell division protein ftsL 1 36 MTNLAVKYKQQAQEEVQIQTPPQQMAKPKVKAKITR
BC_3946 Heme O monooxygenase 293 311 GTRSKVNAKEAELTSKQTK
BC_3946 Heme O monooxygenase 233 243 RHYKQQPVVYW
BC_3946 Heme O monooxygenase 1 6 MQRFIK
BC_3946 Heme O monooxygenase 84 91 KHVRETKT
BC_3946 Heme O monooxygenase 143 159 EIDQKFDARSLIMDKKM
BC_4649 Septation ring formation regulator 26 570 RNRSYKDIEALEQWKQEIKDKPVADELKRVKDLNMTGQTEELFGKWREEWDEIVSTTLPKADKDLAQARKFASQFSFRKAKHAMNESISGLDDADNRITDILNELQQLLESHEKNSSEIEGLRDTYRSMKKSVLAHRHMYGAAEQKIEEMLDAESEKFKTFEEATNNGDYLKAREIVISLEEGLADLEIIIHQIPDLLVECQATLPVQLEDLLHGHNDMVRQGYVLDYLEVPKEVRDMTKQLQTCLMDIQELHITEAAEKVENLKTRLDGFYDQLEQEVHARHYVEQKTLSVYDDLEEMRIETIETKTETQLVKQSYQLQDKDIESQKVIEKQMHILTKRFEMLQLRVAEQDIAFSIIREELEEVYEQCETLKVLHAEYKEMLQAMRKEEFEAREKLQEMRNTIFETKRFMQKSNLPGLPESIMEDLKRGQMAMQAVYEQLEVKPLNMNAVNSSLEEAYTTVNGVAEMTEELIGQAYLVEKLIQYGNRYRSHDENLAESLNYAEKLFREYQYDAALEQAASVLEQLEPGVVQKIAEYVDNDQTLS
BC_5265 Transcriptional regulator, LytR family 1 4 MKKK
Bdkrb1 B1 bradykinin receptor 239 261 LRGQKEASRTRCGGPKGSKTTGL
Bdkrb1 B1 bradykinin receptor 236 258 LRGQKEASRTRCGGPKDSKTMGL
Bdkrb1 B1 bradykinin receptor 63 83 LPWRQWWWQQRQRQQRLTIAE
Bdkrb1 B1 bradykinin receptor 324 334 RLFKTRVLGTL
BDKRB1 B1 bradykinin receptor 65 73 PRRQLNVAE
BDKRB1 B1 bradykinin receptor 134 155 DRYRVLVHPMASRRQQRRRQAR
BDKRB1 B1 bradykinin receptor 227 247 ASLRTREEVSRTRCGGRKDSK
BDKRB1 B1 bradykinin receptor 315 353 VGRLFRTKVWELYKQCTPKSLAPISSSHRKEIFQLFWRN
Bdkrb1 B1 bradykinin receptor 143 164 QDRYRLLVYPMTSWGYRRRRQA
Bdkrb1 B1 bradykinin receptor 327 337 RLLKTRVLGTL
Bdkrb1 B1 bradykinin receptor 63 80 LPWRRWWQQRRQRLTIAE
Bdkrb1 B1 bradykinin receptor 140 161 QDRYRLLVYPMTSWGNRRRRQA
Bdkrb2 B2 bradykinin receptor 254 272 QVLRNNEMKKFKEVQTEKK
Bdkrb2 B2 bradykinin receptor 90 98 HKTNCTVAE
Bdkrb2 B2 bradykinin receptor 341 396 GKRFRKKSREVYQAICRKGGCMGESVQMENSMGTLRTSISVDRQIHKLQDWAGNKQ
Bdkrb2 B2 bradykinin receptor 159 180 DRYLALVKTMSMGRMRGVRWAK
BDKRB2 B2 bradykinin receptor 85 93 HKSSCTVAE
BDKRB2 B2 bradykinin receptor 154 175 DRYLALVKTMSMGRMRGVRWAK
BDKRB2 B2 bradykinin receptor 249 267 QVLRNNEMQKFKEIQTERR
BDKRB2 B2 bradykinin receptor 336 391 GKRFRKKSWEVYQGVCQKGGCRSEPIQMENSMGTLRTSISVERQIHKLQDWAGSRQ
Bdkrb2 B2 bradykinin receptor 250 268 QVLRNNEMKKFKEVQTERK
Bdkrb2 B2 bradykinin receptor 86 94 HKNSCTVAE
Bdkrb2 B2 bradykinin receptor 337 392 GKRFRKKSREVYRVLCQKGGCMGEPVQMENSMGTLRTSISVERQIHKLQDWAGKKQ
Bdkrb2 B2 bradykinin receptor 155 176 DRYLALVKTMSMGRMRGVRWAK
BDLP_NOSP7 Bacterial dynamin-like protein 575 693 ALLGLGVGFLQADQARRELVKTAKKELVKHLPQVAHEQSQVVYNAVKECFDSYEREVSKRINDDIVSRKSELDNLVKQKQTREINRESEFNRLKNLQEDVIAQLQKIEAAYSNLLAYYS
BDLP_NOSP7 Bacterial dynamin-like protein 1 521 MVNQVATDRFIQDLERVAQVRSEMSVCLNKLAETINKAELAGDSSSGKLSLERDIEDITIASKNLQQGVFRLLVLGDMKRGKSTFLNALIGENLLPSDVNPCTAVLTVLRYGPEKKVTIHFNDGKSPQQLDFQNFKYKYTIDPAEAKKLEQEKKQAFPDVDYAVVEYPLTLLQKGIEIVDSPGLNDTEARNELSLGYVNNCHAILFVMRASQPCTLGERRYLENYIKGRGLTVFFLVNAWDQVRESLIDPDDVEELQASENRLRQVFNANLAEYCTVEGQNIYDERVFELSSIQALRRRLKNPQADLDGTGFPKFMDSLNTFLTRERAIAELRQVRTLARLACNHTREAVARRIPLLEQDVNELKKRIDSVEPEFNKLTGIRDEFQKEIINTRDTQARTISESFRSYVLNLGNTFENDFLRYQPELNLFDFLSSGKREAFNAALQKAFEQYITDKSAAWTLTAEKDINAAFKELSRSASQYGASYNQITDQITEKLTGKDVKVHTTTTAEEDNSPGWAKWA
benK Benzoate transport protein 319 325 ADRYNVK
benK Benzoate transport protein 141 150 SEYAPKKFKS
benK Benzoate transport protein 82 93 DKLEHLGVSRKK
benK Benzoate transport protein 1 22 MSREINVNQMIDDSKLTPFHWR
benK Benzoate transport protein 436 466 NDRRMYQPEPISPIANQNDTTTVKVNEAVSH
benK Benzoate transport protein 203 258 ESIDYLVRKKKDETVRFIMTKMVPSYQYQPDHVFVLNSSNQNQAQAPVKMIFQEQR
benK Benzoate transport protein 370 387 LAYMAKFYAPNVRSTGIG
Best1 Bestrophin-1 1 31 MTITYTNKVANARLGSFSSLLLCWRGSIYKL
BEST1 Bestrophin-1 1 31 MTITYTSQVANARLGSFSRLLLCWRGSIYKL
BEST1 Bestrophin-1 83 237 GFYVTLVVTRWWNQYENLPWPDRLMSLVSGFVEGKDEQGRLLRRTLIRYANLGNVLILRSVSTAVYKRFPSAQHLVQAGFMTPAEHKQLEKLSLPHNMFWVPWVWFANLSMKAWLGGRIRDPILLQSLLNEMNTLRTQCGHLYAYDWISIPLVYT
BEST1 Bestrophin-1 289 585 KVAEQLINPFGEDDDDFETNWIVDRNLQVSLLAVDEMHQDLPRMEPDMYWNKPEPQPPYTAASAQFRRASFMGSTFNISLNKEEMEFQPNQEDEEDAHAGIIGRFLGLQSHDHHPPRANSRTKLLWPKRESLLHEGLPKNHKAAKQNVRGQEDNKAWKLKAVDAFKSAPLYQRPGYYSAPQTPLSPTPMFFPLEPSAPSKLHSVTGIDTKDKSLKTVSSGAKKSFELLSESDGALMEHPEVSQVRRKTVEFNLTDMPEIPENHLKEPLEQSPTNIHTTLKDHMDPYWALENRDEAHS
Best1 Bestrophin-1 289 551 KVAEQLINPFGEDDDDFETNWIIDRNLQVSLLSVDGMHQNLPPMERDMYWNEAAPQPPYTAASARSRRHSFMGSTFNISLKKEDLELWSKEEADTDKKESGYSSTIGCFLGLQPKNYHLPLKDLKTKLLCSKNPLLEGQCKDANQKNQKDVWKFKGLDFLKCVPRFKRRGSHCGPQAPSSHPTEQSAPSSSDTGDGPSTDYQEICHMKKKTVEFNLNIPESPTEHLQQRRLDQMSTNIQALMKEHAESYPYRDEAGTKPVLYE
Best1 Bestrophin-1 83 237 GFYVTLVVSRWWSQYENLPWPDRLMIQVSSFVEGKDEEGRLLRRTLIRYAILGQVLILRSISTSVYKRFPTLHHLVLAGFMTHGEHKQLQKLGLPHNTFWVPWVWFANLSMKAYLGGRIRDTVLLQSLMNEVCTLRTQCGQLYAYDWISIPLVYT
Best2 Bestrophin-2 1 31 MTVTYTARVANARFGGFSQLLLLWRGSIYKL
Best2 Bestrophin-2 289 508 KVAEQLINPFGEDDDDFETNFLIDRNFQVSMLAVDEMYDDLAMLEKDLYWDAAEARAPYTAATAFLLQQPSFQGSTFDIALAKEDMQFQRLDGVDGPLGEVHGDFLQRLLPAGAGSVGPLGRRLSLLRRKNSCVSEASTAASCGCAGAADGGGVECGCGDPLLDPSLREPELEPPACPEPPAPIPGPTPEPFTTVSIPGPRAPAPPWLPSPIGEEEESPA
Best2 Bestrophin-2 83 238 GFYVTLVVHRWWNQYLCMPLPDALMCIVAGTVHGRDDRGRLYRRTLMRYAGLSAVLILRSVSTAVFKRFPTIDHVVEAGFMTREERKKFENLNSSYNKYWVPCVWFSSLAAQARREGRIRDNSALKLLLEELNVFRSKCGMLFHYDWISIPLVYTQ
BEST2 Bestrophin-2a 289 509 KVAEQLINPFGEDDDDFETNFLIDRNFQVSMLAVDEMYDDLAVLEKDLYWDAAEARAPYTAATVFQLRQPSFQGSTFDITLAKEDMQFQRLDGLDGPMGEAPGDFLQRLLPAGAGMVAGGPLGRRLSFLLRKNSCVSEASTGASCSCAVVPEGAAPECSCGDPLLDPGLPEPEAPPPAGPEPLTLIPGPVEPFSIVTMPGPRGPAPPWLPSPIGEEEENLA
BEST2 Bestrophin-2a 83 238 GFYVTLVVNRWWSQYLCMPLPDALMCVVAGTVHGRDDRGRLYRRTLMRYAGLSAVLILRSVSTAVFKRFPTIDHVVEAGFMTREERKKFENLNSSYNKYWVPCVWFSNLAAQARREGRIRDNSALKLLLEELNVFRGKCGMLFHYDWISVPLVYTQ
BEST2 Bestrophin-2a 1 31 MTVTYTARVANARFGGFSQLLLLWRGSIYKL
Best3 Bestrophin-3 289 669 KVAEQLINPFGEDDDDFETNWCIDRNLQVSLLAVDEMHMSLPKMKKDIYWDDSAARPPYTLAAADYCIPSFLGSTIQMGLSGSNFPAEDWLWNYEKHGNRHSVMRRVKRFLSTHEHPGSPRRRRSFGRQASDSSMFLPPSPARDLLDVPSRNPHRGSPTRKQSRSQEGSPKLHSSMGELSTIRETSRTSTLQSLSPQSSVRSSPTKMPQVPEVLITAAEAPAFSADSHQHDSTTSILSLEFTGVQPSGTEQQVEPSGTPPGDPNPQTTSASTERDLFKFEEDLEDDRFPKRWSLPEFLESRHTSLGNLGPDPVSPRDALLLPDTETPSETNGIHPGAGSALAPDILYLMESLDKETDILEFNNEHTGESPKGTPQRPRTWF
Best3 Bestrophin-3 1 31 MTVTYSSKVANATFFGFHRLLLKWRGSIYKL
Best3 Bestrophin-3 83 237 GFYVTLVVNRWWNQFVNLPWPDRLMLLISSSVHGSDQHGRLLRRTLMRYVNLTSLLIFRSVSTAVYKRFPTMDHVVEAGFMTADERKLFDHLKSPHLKYWVPFIWFGNLATKARNEGRIRDSVDLQSLMTEMNRYRSWCSLLFGYDWVGIPLVYT
BEST3 Bestrophin-3 289 668 KVAEQLINPFGEDDDDFETNWCIDRNLQVSLLAVDEMHMSLPKMKKDIYWDDSAARPPYTLAAADYCIPSFLGSTVQMGLSGSDFPDEEWLWDYEKHGHRHSMIRRVKRFLSAHEHPSSPRRRSYRRQTSDSSMFLPRDDLSPARDLLDVPSRNPPRASPTWKKSCFPEGSPTLHFSMGELSTIRETSQTSTLQSLTPQSSVRTSPIKMPLVPEVLITAAEAPVPTSGGYHHDSATSILSSEFTGVQPSKTEQQQGPMGSILSPSEKETPPGGPSPQTVSASAEENIFNCEEDPGDTFLKRWSLPGFLGSSHTSLGNLSPDPMSSQPALLIDTETSSEISGINIVAGSRVSSDMLYLMENLDTKETDIIELNKETEESPK
BEST3 Bestrophin-3 83 237 GFYVTLVVNRWWNQFVNLPWPDRLMFLISSSVHGSDEHGRLLRRTLMRYVNLTSLLIFRSVSTAVYKRFPTMDHVVEAGFMTTDERKLFNHLKSPHLKYWVPFIWFGNLATKARNEGRIRDSVDLQSLMTEMNRYRSWCSLLFGYDWVGIPLVYT
BEST3 Bestrophin-3 1 31 MTVTYSSKVANATFFGFHRLLLKWRGSIYKL
BEST4 Bestrophin-4 1 31 MTVSYTLKVAEARFGGFSGLLLRWRGSIYKL
BEST4 Bestrophin-4 304 473 KVAEQIINPFGEDDDDFETNQLIDRNLQVSLLSVDEMYQNLPPAEKDQYWDEDQPQPPYTVATAAESLRPSFLGSTFNLRMSDDPEQSLQVEASPGSGRPAPAAQTPLLGRFLGVGAPSPAISLRNFGRVRGTPRPPHLLRFRAEEGGDPEAAARIEEESAESGDEALEP
BEST4 Bestrophin-4 83 237 GFYVTLVVNRWWSQYTSIPLPDQLMCVISASVHGVDQRGRLLRRTLIRYANLASVLVLRSVSTRVLKRFPTMEHVVDAGFMSQEERKKFESLKSDFNKYWVPCVWFTNLAAQARRDGRIRDDIALCLLLEELNKYRAKCSMLFHYDWISIPLVYT
BET1 BET1 homolog 1 94 MRRAGLGEGVPPGNYGNYGYANSGYSACEEENERLTESLRSKVTAIKSLSIEIGHEVKTQNKLLAEMDSQFDSTTGFLGKTMGKLKILSRGSQT
Bet1 BET1 homolog 1 94 MRRAGLGDGAPPGSYGNYGYANTGYNACEEENDRLTESLRSKVTAIKSLSIEIGHEVKNQNKLLAEMDSQFDSTTGFLGKTMGRLKILSRGSQT
Bet1 BET1 homolog 1 94 MRRAGLGDGAPPGGYGNYGYANSGYNACEEENDRLTESLRSKVTAIKSLSIEIGHEVKNQNKLLAEMDSQFDSTTGFLGKTMGRLKILSRGSQT