| A0A1Y3NX94_9PSED |
N-acetylmuramoyl-L-alanine amidase |
24 |
163 |
TSHPSVNYDNRVQFVVVHYTSATLERSLELLTHGEVSAHYLIGDTPPTIYKLVDESARAWHAGESEWDGRTWLNSASIGIEIVNPGYRDTPTGRLWYPYTEGQIQALIVLLKDIVKRNHIDPRHIIGHSDIAPARKLDPG |
| A0A1Y3P1P4_9PSED |
N-acetylmuramoyl-L-alanine amidase |
7 |
158 |
NSYRATKSFNHRTRFLVMHYTACNFRQSVAALTGPSVSTHYLVPDPSDKTYTDAGFTDMRIFNLVDEGERAWHAGVSGWAKRYNLNDTAIGVEIVYVATEDKGVFTFPPYNPTQIEAVKELAKNILQRYPDITPVNVVGHSDIAIGRKSDPG |
| A0A1Y3PAB5_9PSED |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
18 |
168 |
SPNFNARPAGEVSLLVIHNISLPPAQFKTGKVQAFFQNQLDVTEHPYFEGIADLRVSAHFLIERDGEVTQFVSCLDRAWHAGVSNFEGRETCNDFSIGIELEGTDEQPFTDAQYSALIDLTRQLQSAYPAISSARICGHSDIAPGRKTDPG |
| A0A4U0S513_9ACTN |
Tat pathway signal protein |
169 |
333 |
DGTENSPTKYYPAQTITVHHTDTQNDDPDPAATVRAIYEYHAVTLDWGDIGYHFLIDEAGRVYEGRYSGDDGIPAHDKDGNVVTAFHVGGYNSGNLGIALLGTLVDQGPTHAAQASLTALIRVLDRYHGFDPQAKVTYTNPVNAVTKDVTTVSGHRDWLQTDCPG |
| A0A4U0SGT1_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
285 |
422 |
HDLADRPNDEKIDYIVIHDTEGSWDTTLKLVQDPTYLAWHYTIRSADGHVDQHVQTKDVGWHAGNWYVNAKSIGIEHEGFLAEPGTWYTESMYRSSARLVAYLAQKYRIPLDRQHILGHDTVPGPTTSYIPGMHTDPG |
| A0A4U0SJW4_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
51 |
201 |
AREPKGEVQMLEWRPEKIIVHHTATANTDDYSLDRAYTLARAMQKNQMDVRGWLDTGQHFTISRGAYVMEGRHESLTALRRGSRMVEGAHCSGQNSVAIGIENEGTYVEEEPPVEQYAALVGLCVHICRQYEVAAQEIYGHRDFNTTQCPG |
| A0A4U0SKA9_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
308 |
469 |
LRHGHKIYTGGIKAVFVHHTATGNSYTCAQAPSIIRGIYRYHARSRGWRDLGYNFLVDKCGNIYEGRAGGVSRAVYGAHTLGFNSHTMGIAVLGNYRKAEPSEEALEAVAELAAWKLGLYGADPAGTTYLKSGGGNRYKKGKKVRFNVISGHRDGYATSCPG |
| A0A4Z0ADU0_9PSED |
N-acetylmuramoyl-L-alanine amidase |
11 |
160 |
QGFNERNGEAVRQVILHYTAAPFASSLHTLTREGVSAHYLLPDSREPSYCAAGYDELRVFRLVDEGKRAWHAGVSQWGGRDNLNSRSIGIEIVNLARDDAGVFTFPAYGEAQIQVLIMLLRDILGRHPQIGPTDILGHCDVAYWRKSDPG |
| A0A4Z0AHC2_9PSED |
N-acetylmuramoyl-L-alanine amidase |
24 |
164 |
TSHPSVNHDNRVQFVVVHYTSTNLERSLALLTHGQVSSHYLIGDDASGTIYKLVDESQRAWHAGESEWMGRTWLNSSSIGIEIVNPGYRDTPTGRVWYPYTEPQVQSLVVLLKDISKRNGIDPKNIIGHSDIAPLRKLDPG |
| A0A4Z0ARM8_9PSED |
N-acetylmuramoyl-L-alanine amidase |
11 |
160 |
KGFNERNGEAAQQVIVHYTAAPFAASLRTLTEDGVSAHYLLPDPEESSYRAAGYDELRVFRLVDEDKRAWHAGVSQWGGRDNLNSRAIGIEIVNLARDEAGMFTFPAYEEEQIQVLVALLRDILGRFAQIGPTDILGHSDVAYWRKSDPG |
| A0A4Z0B277_9PSED |
N-acetylmuramoyl-L-alanine amidase |
24 |
164 |
TSHPSVNHDNRVQFVIVHYTSTNLERSLALLTHGQVSSHYLIGDDASATIYKLVDESQRAWHAGESEWMGRTWLNSSSIGIEIVNPGYRDTPTGRVWYPYSESQVQSLVVLLKDISKRNGIDPKNIIGHSDIAPLRKLDPG |
| A0A543I359_9MICO |
N-acetylmuramoyl-L-alanine amidase |
259 |
396 |
HDLASRPSSPKITNIVIHNTEASYDTTLKLVTDPTYLSWQYSLRSSDGHIAQHLEPQDVGWHAGNWYVNSHSIGLEHEGFAATGAQWFSESMYRSSARLVKYLARKYDIPLDMQHIFGHDQIPGVTPANVAGMHWDPG |
| A0A6B9FQK1_9HYPH |
N-acetylmuramoyl-L-alanine amidase |
16 |
152 |
SPNHGARRAGPLDMLILHYTGMESGAAALARLRDPLSEVSAHYLVFEDGGIVQLVPEGRRAWHAGAGAWKGETDINSRSIGIEIVNPGHAGGLPPYPEAQIDAVTALSRDILGRWPIPPERVLGHSDIAPERKEDPG |
| A0A6N9TXA1_STRHA |
N-acetylmuramoyl-L-alanine amidase |
48 |
178 |
YTVSSRPSAYPVDFVVIHVTQETFTQTLNIFKNPAKQVSAHYVVRSGDGYIAQCVREKDIAWHAGNWDYNTRSIGIEHEGWVDQPAYFTHSLYEQSARLTADICDRYGVPKDRAHIIGHHEVPGSDHTDPG |
| A0AAE5VUW3_PSESY |
N-acetylmuramoyl-L-alanine amidase |
24 |
164 |
TSHPSVNFDGRAQYVVMHYTSTSLERSLQLLTHGEVSAHYLIGDDSKATIYKLVDESARAWHAGESEWEGRTWLNSSSIGIEIVNPGFKETPTGRLWYPYTEAQTQSIIVLLKDIVKRNRIDPKHIIGHSDIAPLRKQDPG |
| A0AAE8HNJ6_9HYPH |
N-acetylmuramoyl-L-alanine amidase |
16 |
152 |
SPNHGARRAGPLDMLVLHYTGMDSGAAALARLRDPLSEVSAHYLVFEDGGIVQMVPEARRAWHAGAGAWKGETDINTRSIGIEIVHPGHAGGLPSYPDAQIEAVIALARDIIGRWPIPPERVLGHSDIAPERKEDPG |
| A0ABD5CBD8_9BURK |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
21 |
170 |
SPNFEARPQGAVPTLIVVHNISLPPNEFGGTAIAELFLNTLDCDAHPYYDAHLRGVRVSAHFVIHRDGALEQFVSCNERAWHAGPSNFFGRERCNDFSIGIELEGSDTTAFEAAQYRTLSALVRALAARYPIEALAGHSDIAPGRKTDPG |
| A0ABR4S2H4_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
288 |
449 |
LREKNFAYTGKVKAAFVHHSATGNNYTCAQAPSVIRGIYRYHTQSSGWRDLGYNFMVDKCGTVYEGRAGGVDKAVLGAHTLGFNSNSTGIAVLGSYSSVKPPKAAVDAVAKLTAWKLGLSGANPKGKVTLTSGGSNLYAKGKKVSLHVISGHRDGYSTECPG |
| A0ABR4S6J8_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
83 |
212 |
WRRADRPDDFTVDRVIIHVVQGSYAVALKVFQDPAHRAATHYVVGKDGRVAQLIRELDVAYQAGNREYNERAVGIEHEGFVDRPQDFTGAMYESSARLTADICLRHGIPVDRTHVIGHVEVPGTDHTDPG |
| A0ABR4SDR3_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
55 |
185 |
YTVANRPRQYPVDFVVIHVTQETYADTLGIFQNPAKKVSAHYVVRSADGRVAQCVREADVAWHAGNWDYNTRSVGIEHEGWVDKPEYFTDAMYSASAALTAAICDSYAVPKTRAHIIGHHEVPGATHTDPG |
| A0ABR4SEA6_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
268 |
405 |
HDKADRPRSARIDSIVIHDTEATWDTTLALVQDPEYVSWHYSLRSTDGHIAQHLRTKDVGWHAGNWYTNAKSIGLEHEGFLADPDAWYTEAMYRTSARLVSHLAKKYGIPLDRQHILGHDTVPGTTPATIPGMHTDPG |
| A0ABR4SEC3_9ACTN |
N-acetylmuramoyl-L-alanine amidase |
228 |
355 |
GNFASGRSAAISQVVVHVTQGSYAGSISWFQNPTAQVSAHYVIRSSDGEVTQMVKDADTAYHARSANASSLGIEHEGFVDDPAWFTEAMYRSSAALTAYLCEQYGIPKDRSHIVGHVEVPGNDHTDPG |
| A0ABR4SGD3_9ACTN |
Peptidoglycan-binding protein |
23 |
177 |
WRSHNRNSKGAWGPVNGVMIHHTVTSGSARTVDICRNGYSGLPGPLCHGVITKDGRVHLVGYGRANHAGLGDDDVLAAVIAERASYPPVNEANTDGNARFYGFECENLGDGKDPWTSAQLDAIERVSAAICRVHGWNQQSVIGHLEWQPGKIDPR |
| A0ABS6TS47_STRHA |
N-acetylmuramoyl-L-alanine amidase |
275 |
442 |
LNDESPDYMDRVKAVFVHHTAQTNSYSCADSAAIVRGLHAYHVKSNGWKDLGYNFLVDKCGTVFEGRKGGVDRAVQGAHTYGFNRETAGIAVIGMYTDTAAASAATASVARVAAWKLGQYKGDPAGTTTLTAGAAGNNYAGKVFTAGKTYTFQQVSGHRDGFNTQCPG |
| A0ABS6TS87_STRHA |
N-acetylmuramoyl-L-alanine amidase |
76 |
205 |
WRRADRPDDYAVDRVIIHVTQGSYASAVRVFQDPSHRAASHYIVGKDGRVTQMIRELDVAYHAGNRSFNERSVGIEHEGFVDRPQDFTREMYESSARLTASICARHGIPVDREHVIGHVEVPGTDHTDPG |
| A0ABS6TSV7_STRHA |
N-acetylmuramoyl-L-alanine amidase |
24 |
157 |
PTQFIVHSIIAPWTAKRVYEYWRDSTNLESHFGIGYEAGDVGQYIGTETRADANAGANRRSDGTGAVSAETASNLQGSDPWTDAQVEELIRLGVWLHQRHGIPLRICRTQSDPGFGYHSMFPQWSTSGTACPGP |
| A0ABS6TUM1_STRHA |
N-acetylmuramoyl-L-alanine amidase |
222 |
349 |
ANYATGRTATVDKVVVHVTQGSYAGTISWFQNAASQVSSHYVVRSSDGQITQMVRDKDTAYHAKSANSSSLGIEHEGFVDDPSWFTDPMYRSSAALTAHLCDHYGIPKDRSHIIGHSEAPGNDHTDPG |
| A0ABS6TYU5_STRHA |
N-acetylmuramoyl-L-alanine amidase |
68 |
209 |
YGNYDTADRPRGNAVRFIVLHDTEVDYDTTLKIFQDPANQTSAHYVVRSSDGHVTQMVKNKDIAWQAGNWYLNTHSIGIEQEGVAAEGAKWYTDAMYRSTARLVRHLAATYDIPLDRQHILGHDGVPPTSAAGTPNMHWDPG |
| A0ABS6U0U9_STRHA |
N-acetylmuramoyl-L-alanine amidase |
27 |
186 |
WRTHNRNKVGAWGPVNGSMVHHTVTSGTAATVALCRDGYADLPGPLCHGMIAKNGRVHLVGWGRANHAGGGDPRVLDQVIAESYGTRPSPPTKGNSNGVDGNARFYGWECENLGDGKDPWPAAQYDAIVRVQAAVCRAHGWSAKSVIGHLEWSNDKIDPR |
| A0ABU8IST4_9BURK |
N-acetylmuramoyl-L-alanine amidase |
39 |
185 |
DTSRVAQYQDTRIRFLVMHYTEIDEKESLDVLTKEQVSAHYVVPDHPKEKHGEPIIWQLVPESQRAWHAGISSWQGTTELNAASIGIENVNLGPVDTPQGRTWQPYPPEQVDAMIRLAKDIVTRYNIPPTRVVGHSDIAPQRKIDPG |
| A0ABY2RDG8_9NOCA |
Cold-shock protein |
360 |
524 |
SIRCQEPVYDDSLGGATVHHTAGSNDYSKSESVEIVRAIYAYHASTLGWCDVGYNVLVDKYGQIFEGRSGGLDRNVQGAHAGGFNENTMGIAMMGDFSTVTPPQETVNAVGKFLGWRLAKAGLDPKGRTTMYSEGTEFTPYAQGEAVDLPIIFAHRDVGNTSCPG |
| A6KMR5_RAT |
RCG64212 |
1 |
130 |
MNLPAKFVIIIHTAGESCNESADCLIRVRDTQSFHMDKQDFCDIAYHFLVGQDGVVYEGVGWTIEGSHTYGYNDIALGIAFMGNFVEKPPNEASLEAAQSLIQCAVAMGYLASNYLLMGHSDVSNILSPG |
| ami |
Protein Ami |
118 |
245 |
KPEGIVIHETANNSSTITGEINYMSTNYNNAFVHAFVDKSRIIQIHPTENGVWGAGQYANARFIQVELVRSKTFDEFARSINNYAYYAAYLLDQYNLPVDSAHSDGKGTVWSHDAVTRYLGGTTHTDP |
| amiD |
N-acetylmuramoyl-L-alanine amidase AmiD |
42 |
179 |
PRIKVLVIHYTADDFDSSLATLTDKQVSSHYLVPAVPPRYNGKPRIWQLVPEQELAWHAGISAWRGATRLNDTSIGIELENRGWQKSAGVKYFAPFEPAQIQALIPLAKDIIARYHIKPENVVAHADIAPQRKDDPGP |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
44 |
195 |
SPHWNLRPNDIDISLLVIHCISLPASQFGNSYIDDLFMGVLDTTADNSFADLAGVRVSAHCVIFRNGVVRQYVPFHYRAWHAGVSEFNGRQNCNDFSIGIELEGTEHLPYTDAQYQSLVLLTRQLMQDFPAITTERIVGHQQIAPGRKTDPG |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
25 |
174 |
SPNFEVRPNGARPTLIVVHNISLPPNEFGGPGITDLFLNRLDCDAHPYYDAHLRGVRVSAHFVIRRDGALEQYVSCDERAWHAGASSFFGRERCNDFSIGVELEGSDASPFEAAQYETLAPLVQALAGHYAIDSVAGHADIAPGRKTDPG |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
30 |
167 |
LLVVHNISLPPGEFGGPWIDALFTGTIDPNAHPYFAGIAHLRVSAHCLIRRDGEIVQYVPFDKRAWHAGVSSYQGRERCNDFSIGIELEGTDTLAYTDAQYQQLAAVTNALITRYPAIANNMTGHCNIAPERKTDPGP |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
30 |
167 |
LLVVHNISLPPGEFGGPWIDALFTGTIDPQAHPFFAEIAHLRVSAHCLIRRDGEIVQYVPFDKRAWHAGVSQYQGRERCNDFSIGIELEGTDTLAYTDAQYQQLAAVTRALIDCYPDIAKNMTGHCDIAPDRKTDPGP |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
29 |
167 |
TLLVVHNISLPPGEFGGPWIDALFTGTIDPDAHPFFAEIAHLALSADCLIRRDGEVVQYVPFDKRAWHAGVSMYQGRERCNDFSIGIELEGTDTTPYTDAQYEKLVAVTQTLIGRYPAIADNITGHSDIAPERKTDPGP |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
29 |
167 |
SLLVVHNISLPPGEFGGPWIDALFTGTIDPDAHPFFAEIAHLRVSAHCLIRRDGEIVQYVPFDKRAWHAGVSNYQGRERCNDFSIGIELEGTDTLAYTDAQYQQLAAVTRTLIASYPAIADNMTGHCNIAPDRKTDPGP |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
29 |
167 |
SLLVVHNISLPPGEFGGPWIDALFTGTIDPDAHPFFAEIAHLRVSAHCLIRRDGEIVQYVPFDKRAWHAGVSNYQGRERCNDFSIGIELEGTDTLAYTDAQYQQLAAVTRTLIASYPAIADNMTGHCNITPDRKTDPGP |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
18 |
168 |
SPNFNARPEGEISLLVIHNISLPPAQFKTGKVQAFFQNQLDIDEHPYFVGIADLRVSAHFLIERDGEVVQFVSCLDRAWHAGVSSFQGREGCNDFSVGIELEGTDDQPFTEAQYDALIDLTRQLRQAFEAITPERICGHSDVAPGRKTDPG |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
18 |
168 |
SPNFNERPAGEISLLVVHNISLPPAQFATGKVQEFFQNRLDVTEHPYFEGIADLRVSAHFLIERDGAVTQFVSCRDRAWHAGVSCFEGRETCNDFSVGIELEGTDDLPFTDAQYKSLIDLTGQLLAAYPGITPQRICGHSDIAPGRKTDPG |
| ampD |
1,6-anhydro-N-acetylmuramyl-L-alanine amidase AmpD |
18 |
168 |
SPNFNQRPAGEISLLVVHNISLPPAQFATGKVQEFFQNRLDVTEHPYFEGIADLRVSAHFLIERDGAVTQFVSCIDRAWHAGVSRFEGRETCNDFSLGIELEGTDDLPFTHAQYASLIDLTRQLLAAYPDITPQRICGHSDIAPGRKTDPG |
| blyA |
N-acetylmuramoyl-L-alanine amidase BlyA |
24 |
158 |
VKKCVLHYTANPGAGADNHRRYFSNAQVYASAHIFVDKAEAICIIPLNEVAYHANDIQQRDSAGNPYRGVAALKPNANFLSIGVEMCLEKDGSFHSDTVERTEDVFVELCNKFGLDPIDDIVRHYDITHKNCPAP |
| cwhA |
N-acetylmuramoyl-L-alanine amidase A |
23 |
158 |
QTSAVIMHTMEGSYAGSISWFQNPSAQVSAHYLIRKSDGQITQMVREYHQAWHAKNHNYYTIGIEHDGRAADAGNWSAAMVNASARLTKSICARRGVNCASAWKGPGYDTFHLVPDSVRVKGHGMLSGNENRYDPG |
| cwlA |
N-acetylmuramoyl-L-alanine amidase CwlA |
24 |
142 |
KAEYITIHNTANDASAANEISYMKNNSSSTSFHFAVDDKQVIQGIPTNRNAWHTGDGTNGTGNRKSIGVEICYSKSGGVRYKAAEKLAIKFVAQLLKERGWGIDRVRKHQDWNGKYCPH |
| cwlA |
N-acetylmuramoyl-L-alanine amidase CwlA |
38 |
140 |
INERNNVANNSTGTSFHIAVDDKEAIQLIPFNRNAWHAGDGTNGRGNRHSIGVEICYSQSGGARYRKAELNAVEVIAQLMIQFDIPISKVKTHQERNGKYCPH |
| cwlH |
N-acetylmuramoyl-L-alanine amidase CwlH |
45 |
141 |
KFVKNPNTSESWHFTVDDSVIYQHLPIDENGWHAGDGTNGTGNRKSIGIEICENADGDFEKATSNAQWLIRKLMKENNIPLNRVVPHKKWSGKECPR |
| cwlL |
N-acetylmuramoyl-L-alanine amidase CwlL |
40 |
154 |
LNERDYFNGTCIAIKRKASSAHYFVDRKEAQHIIPENEVAYHAHDKNRCYVSFLKPNANTKSISVEMCVEKDGMIHSETVQNAAELVADLCKRYGLSTNKIVRHYDVTNKICPAP |
| CWLX_BACLI |
Probable N-acetylmuramoyl-L-alanine amidase |
40 |
152 |
LNERNYFNGTCIADKRYASAHYFVDRHEAQHIIPDHEVAYHAHDQNRCYVSFLKPNANTTALGVEMCVEKDGTIHEETIRNAAELVADLCKTYGLSADRIVRHYDVTNKGCPT |
| HI_0300 |
ampD signalling protein (ampD) |
30 |
171 |
QDISLLVIHYISLPPEQFGGGYVDDFFQGKLDPKIHPYFAEIYQMRVSAHCLIERNGRITQYVNFNDRAWHAGVSNFQGREKCNDFAIGIELEGSNEQPFTDAQYFSLQELTNVIMKSYPKITKDRIVGHCDISPKRKIDPG |
| HI_1494 |
N-acetylmuramoyl-L-alanine amidase |
2 |
73 |
DGSVGTGRQVGEIGAHVKGHNQNSVGICLVGGITASGKNHGEYTEAQWQSLYKLLQELEAEHPKALICGHRD |
| LOC103506806 |
N-acetylmuramoyl-L-alanine amidase |
74 |
223 |
NHYDSRDGMSVKYLILHYTVYNFAHIITAFTSNRAHNLHSSHYVISEKEGKYLPGGKVIQIVPDNMRAWHAGIGKWRRDRNLNSMSIGIHLVNGGVVGEKFRSTNYYPFDENQIHTLGLLGKDIVSQFKIKPQYVLGHTDIAPGSKMDPG |
| LOC134485743 |
Peptidoglycan recognition protein 3 |
30 |
165 |
SSLTCRVPLSLPVPYLIIEQVTRMQCQEQTSCSQVLRVLQSHYVHNKGWCDVAFNFLAGNDGKVYEGVGWHVQGLHTQGYNNVSLGIAFFGSKIGSSPSPAALPATEDLIFFAILNGYLSPKYIHPFLLKEETCLV |
| LOC134485743 |
Peptidoglycan recognition protein 3 |
187 |
324 |
ARETHCSQMNLPAKFVIIIHTAGESCNESADCLIRVRDTQSFHMDKQDFCDIAYHFLVGQDGVVYEGVGWTIEGSHTYGYNDIALGIVFMGNFVEKPPNEASLEAAQSLIQCAVAMGYLASNYLLMGHSDVSNILSPG |
| LOC299567 |
LOC299567 protein |
176 |
315 |
YRGHPTPLRLPLGLLYVHHTYVPAPPCTTFQSCAADMRSMQRFHQNVRGWADIGYSFVVGSDGYVYQGRGWHWVGAHTLGYNSRGFGVAFVGNYTGSLPSEAALNTVRDVLPSCAIRAGLLRPDYKLFGHRQLGKTDCPG |
| lytA |
autolysin |
19 |
151 |
PYRQVHAHSTGNPHSTVQNEADYHWRKDPELGFFSHIVGNGCIMQVGPVDNGAWDVGGGWNAETYAAVELIESHSTKEEFMTDYRLYIELLRNLADEAGLPKTLDTGSLAGIKTHEYCTNNQPNNHSDHVDPY |
| lytA |
Autolysin |
198 |
323 |
SNPKGIVIHNDAGSKGATAEAYRNGLVNAPLSRLEAGIAHSYVSGNTVWQALDESQVGWHTANQIGNKYYYGIEVCQSMGADNATFLKNEQATFQECARLLKKWGLPANRNTIRLHNEFTSTSCPH |
| lytO |
Probable autolysin LytO |
198 |
323 |
SNPKGIVIHNDAGSKGATAEAYRNGLVNAPLSRLEAGIAHSYVSGNTVWQALDESQVGWHTANQIGNKYYYGIEVCQSMGADNATFLKNEQATFQECARLLKKWGLPANRNTIRLHNEFTSTSCPH |
| Pglyrp1 |
Peptidoglycan-recognition protein |
41 |
179 |
LPSECSKGLKKPVRYVVISHTAGSFCSSPDSCEQQARNVQLYQMKQLGWCDVAYNFLIGEDGHVYEGRGWTIKGDHTGPIWNPMSIGITFMGDYSHRVPAKRALRAALNLLKCGVSEGFLRSNYEVKGHRDVQSTLSPG |
| Pglyrp1 |
Peptidoglycan-recognition protein |
30 |
168 |
LPSECSKGLKKPVRYVVISHTAGSFCSSPDSCEQQARNVQLYQMKQLGWCDVAYNFLIGEDGHVYEGRGWTIKGDHTGPIWNPMSIGITFMGDYSHRVPAKRALRAALNLLKCGVSEGFLRSNYEVKGHRDVQSTLSPG |
| Pglyrp1 |
Peptidoglycan recognition protein 1 |
1 |
90 |
MAGSSSFLIGEDGHVYEGRGWTIKGDHTGPIWNPMSIGITFMGDYSHRVPAKRALRAALNLLKCGVSEGFLRSNYEVKGHRDVQSTLSPG |
| Pglyrp1 |
Peptidoglycan recognition protein 1 |
40 |
168 |
KPVRYVVISHTAGSFCSSPDSCEQQARNVQLYQMKQLGWCDVAYNFLIGEDGHVYEGRGWTIKGDHTGPIWNPMSIGITFMGDYSHRVPAKRALRAALNLLKCGVSEGFLRSNYEVKGHRDVQSTLSPG |
| Pglyrp1 |
Peptidoglycan-recognition protein |
29 |
167 |
LPSECSSRLGHPVRYVVISHTAGSFCNSPDSCEQQARNVQHYHKNELGWCDVAYNFLIGEDGHVYEGRGWNIKGDHTGPIWNPMSIGITFMGNFMDRVPAKRALRAALNLLECGVSRGFLRSNYEVKGHRDVQSTLSPG |
| Pglyrp1 |
Peptidoglycan recognition protein 1 |
89 |
227 |
LPSECSKGLKKPVRYVVISHTAGSFCSSPDSCEQQARNVQLYQMKQLGWCDVAYNFLIGEDGHVYEGRGWTIKGDHTGPIWNPMSIGITFMGDYSHRVPAKRALRAALNLLKCGVSEGFLRSNYEVKGHRDVQSTLSPG |
| Pglyrp1 |
Peptidoglycan recognition protein 1 |
39 |
167 |
HPVRYVVISHTAGSFCNSPDSCEQQARNVQHYHKNELGWCDVAYNFLIGEDGHVYEGRGWNIKGDHTGPIWNPMSIGITFMGNFMDRVPAKRALRAALNLLECGVSRGFLRSNYEVKGHRDVQSTLSPG |
| PGLYRP1 |
Peptidoglycan recognition protein 1 |
53 |
180 |
PLRYVVVSHTAGSSCNTPASCQQQARNVQHYHMKTLGWCDVGYNFLIGEDGLVYEGRGWNFTGAHSGHLWNPMSIGISFMGNYMDRVPTPQAIRAAQGLLACGVAQGALRSNYVLKGHRDVQRTLSPG |
| PGLYRP2 |
N-acetylmuramoyl-L-alanine amidase |
406 |
532 |
FLYVHHTYVPAPPCTDFTRCAANMRSMQRYHQDTQGWGDIGYSFVVGSDGYVYEGRGWHWVGAHTLGHNSRGFGVAIVGNYTAALPTEAALRTVRDTLPSCAVRAGLLRPDYALLGHRQLVRTDCPG |
| Pglyrp2 |
Peptidoglycan recognition protein 2 |
365 |
504 |
YRGHPTPLRLPLGLLYVHHTYVPAPPCTTFQSCAADMRSMQRFHQNVRGWADIGYSFVVGSDGYVYQGRGWHWVGAHTLGYNSRGFGVAFVGNYTGSLPSEAALNTVRDVLPSCAIRAGLLRPDYKLFGHRQLGKTDCPG |
| Pglyrp2 |
Peptidoglycan recognition protein 2 |
323 |
462 |
YRGHPTPLRLPLGFLYVHHTYVPAPPCTTFQSCAADMRSMQRFHQDVRKWDDIGYSFVVGSDGYLYQGRGWHWVGAHTRGYNSRGFGVAFVGNYTGSLPNEAALNTVRDALPSCAIRAGLLRPDYKLLGHRQLVLTHCPG |
| Pglyrp2 |
Peptidoglycan recognition protein 2 |
373 |
512 |
YRGHPTPLRLPLGFLYVHHTYVPAPPCTTSQSCAADMRSMQRFHQDVRKWDDIGYSFVVGSDGYLYQGRGWHWVGAHTRGYNSRGFGVAFVGNYTGSLPNEAALNTVRDALPSCAIRAGLLRPDYKLLGHRQLVLTHCPG |
| Pglyrp2 |
TagL-alpha |
373 |
511 |
YRGHPTPLRLPLGFLYVHHTYVPAPPCTTFQSCAADMRSMQRFHQDVRKWDDIGYSFVVGSDGYLYQGRGWHWVGAHTRGYNSRGFGVAFVGNYTGSLPNEAALNTVRDALPSAIRAGLLRPDYKLLGHRQLVLTHCPG |
| Pglyrp2 |
N-acetylmuramoyl-L-alanine amidase |
386 |
512 |
FLYVHHTYVPAPPCTTFQSCAADMRSMQRFHQDVRKWDDIGYSFVVGSDGYLYQGRGWHWVGAHTRGYNSRGFGVAFVGNYTGSLPNEAALNTVRDALPSCAIRAGLLRPDYKLLGHRQLVLTHCPG |
| Pglyrp2 |
TagL-beta |
344 |
482 |
YRGHPTPLRLPLGFLYVHHTYVPAPPCTTFQSCAADMRSMQRFHQDVRKWDDIGYSFVVGSDGYLYQGRGWHWVGAHTRGYNSRGFGVAFVGNYTGSLPNEAALNTVRDALPSAIRAGLLRPDYKLLGHRQLVLTHCPG |
| Pglyrp3 |
Peptidoglycan recognition protein 3 |
176 |
313 |
ARETHCSQMNLPAKLVIIIHTVGESCNESVDCLVRVRDTQSFHMDKQDFCNIEHHFLVGQDGVVYDGVGWTIEGSHTYGYNDIALGIAFMGNFVEKPPNEASLEAAQSLIQCAVAMGYLASNYLLMGHSDMSNILSPG |
| Pglyrp3 |
Peptidoglycan recognition protein 3-like |
196 |
333 |
ARETHCSQMNLPAKFVIIIHTAGESCNESADCLIRVRDTQSFHMDKQDFCDIAYHFLVGQDGVVYEGVGWTIEGSHTYGYNDIALGIAFMGNFVEKPPNEASLEAAQSLIQCAVAMGYLASNYLLMGHSDVSNILSPG |
| Pglyrp3 |
Peptidoglycan recognition protein 3-like |
39 |
170 |
SSLTCRVPLSLPVPYLIIEQVTRMQCQDQTSCSQVLRVLHSHYVHNKGWCDVAFNFLVGNDGKVYEGVGWHVQGLHTQGYNNVSLGIAFFGSKIGSSPSPAALSATEDLIFFAILNGYLSPKYIQPFLLKEE |
| Pglyrp4 |
Peptidoglycan recognition protein 4 |
66 |
200 |
EAIGCSSKLSRPVDVLVIHHIPGLECHNKTVCSQKLRELQAYHIHNSWCDVAYNFLVGDDGRVYEGVGWNVQGSHDQGYKNISLGVAFFGTQEGHSPSPVALSAMKGLISYAVKKGHLSSKYIQPLLAKSEDCLV |
| Pglyrp4 |
Peptidoglycan recognition protein 4 |
223 |
360 |
ARDSHCSRMTLPAKYAIILHTAGRTCSQPDECRLLVRDLQSFFMNRLNACDIGYNFLVGQDGGVYEGVGWNNQGSKTDSYNDISLSITFMGTFTGSPPNAAALEAAQDLIRCAVVKGYLTPNYLLMGHSDVSNTLSPG |
| Pglyrp4 |
Peptidoglycan recognition protein 4 |
232 |
369 |
ARESHCFKMTLPAKYAIILHTAGRTCSQPDECRLLIQDLQSFFMDRLNACDIGYNFLVGQDGGVYEGVGWNNQGSKTDGYNDIALSIAFMGIFTGSSPNAAALQAAQDLIQCAVVKGYLTPNYLLMGHSDVSNTLSPG |
| Pglyrp4 |
Peptidoglycan recognition protein 4 |
75 |
219 |
EATGCSSKLGRPVDVLVIHHVPGLECHNQTVCSQKLRELQAYHIRNHWCDVAYNFLVGDDGKVYEGVGWNVQGSHDQGYNNISLGVAFFGTQEGHSPSPVALLAMEALISHAVKKGHLSSKYIQPLLVKSEDCLVPPQKGKQKKA |
| Pglyrp4 |
Peptidoglycan recognition protein 4 |
339 |
476 |
ARESHCFKMTLPAKYAIILHTAGRTCSQPDECRLLIQDLQSFFMDRLNACDIGYNFLVGQDGGVYEGVGWNNQGSKTDGYNDIALSIAFMGIFTGSSPNAAALQAAQDLIQCAVVKGYLTPNYLLMGHSDVSNTLSPG |
| Pglyrp4 |
Peptidoglycan recognition protein 4 |
75 |
219 |
EATGCSSKLGRPVDVLVIHHVPGLECHNQTVCSQKLRELQAYHIRNHWCDVAYNFLVGDDGKVYEGVGWNVQGSHDQGYNNISLGVAFFGTQEGHSPSPVALLAMEALISHAVKKGHLSSKYIQPLLVKSEDCLVPPQKGKQKKA |
| Pglyrp4_predicted |
Peptidoglycan recognition protein 4 (Predicted) |
66 |
208 |
EATGCSSKLGRPVDVLVIHHVPGLECHNQTVCSQKLRELQAYHIRNHWCDVAYNFLVGDDGKVYEGVGWNVQGSHDQGYNNISLGVAFFGTQEGHSPSPVALLAMEALISHAVKKGHLSSKYIQPLLVKSEDCLVPPQKGKQK |
| Q87A14_XYLFT |
N-acetylmuramoyl-L-alanine amidase |
16 |
159 |
VTALQLRPLDTITLAVIHCTELPDLATARTYSERVLYPSGTGDSGHYYIDRNGHIEQYVPPERIAHHVRNQNAHTLGIELVNRGRYPHWLDTRHQTMDEPYPAAQIQALIALLTWLTHTLPALNSIAGHDTLDTEHVPASNDPT |
| S5NFZ2_9HEMI |
N-acetylmuramoyl-L-alanine amidase |
30 |
177 |
NKSFSSITQYERIEFLIFHFTTVNDTYSLQLLTRGNVSAHYLIMTNPKTKNDTFTVFNLVPEYKKARHAGISNWNGKTNLNDVSIGIEIVNEGFTVDKFGNKIWHNFREEQISVLISLSNDIIKRYQISPDNILGHSDIAPLRKYDPG |
| xlyA |
N-acetylmuramoyl-L-alanine amidase XlyA |
45 |
140 |
RYLKNPDTTTSWHFTVDDTEIYQHLPLNENGWHAGDGNGSGNRASIGIEICENADGDFAKATANAQWLIKTLMAEHNISLANVVPHKYWSGKECPR |
| xlyB |
N-acetylmuramoyl-L-alanine amidase XlyB |
40 |
142 |
ANEISYMIGNTSSTSFHFAVDDQEVIQGLPLNRNAWHTGDGTNGPGNRKSIGVEICYSKSGGPKYEAAEALAISFVAQLLKERGWGIDRVRKHQDWSGKYCPH |
| Y497_RICCN |
Putative N-acetylmuramoyl-L-alanine amidase RC0497 |
33 |
141 |
TCVVITYSVSKDIKAVREVLDERGASVHYIIDKDGTQKEYHNDLTDQAFYAGKSSWKGEVGVNKFGIGVMLINDAKSDFPAEQIGKLKEFLKDVTERYPNLDLKHDLVG |