entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
P0CA42
|
EFTL_ASFP4
|
Early transcription factor large subunit homolog (pG1340L) (VETFL homolog)
|
MDFQNDFLTNPLRVTLYNPAENEYTKTFIFLGSVPANVLQACRKDLQRTPKDKEILQNFYGEDWEKKLSQYVVGGDGDDLDEFEKLFVEDSGEETNVMMPEIETMYSEYSIFPEDTFKDIREKIYVATGIPPYRQHIFFFQNNTLQVTYRLLLSGSGVALDIRDYKKEFQQVGGLNIDASMESQKDELYVEALDSFQLIKNIHHIFVADLNTLVAPMRRQISIAIEDNYQFDLLYYGLIMKYWPLLSPDAFKLLVQSPLQMEKQYPALSPSLTSLKKRLLLEQKLINFTYARAQQVIAKYEGNRLTRGTLAVTSAMIKISPLVNIQINVRNVFDLFPATPDIPQLVVFFYSKTGPTVVSKHHITSTEPEKFSNKTFRVPTIILIRFINKKAFILTIQNNGHYFIESNWSENERHDFNSVVSTLNNFINPIIHTINDMGPAAFPRGGSLPLPSNEDIQISISSMSVSTFWPYTLSSKGFTELKSRWREYEQAGIISVRGLQQTGVYNFLFKKGIYSYDPHEIERMIIISSGPGRKMDINVALLQNTYAYLFDTNVAARWETIYGGRNIRIYHRVTDIKIEMFNITQEEFNYLWVYLFVFLDNLITGPDKILVNKLSQLHDKQQGKGASQLRALQEQDPDLYDLRKYDTQATVYSVLCQHPRPPVIYSEAEVKSMPPAKRKELVKYWNFTEGVPAYYSCPHPDYPHLSLLEGRHPLNYCLPCCQKTKALLGTKRFYINNTCLTKHTFVEQDLEDLNTQTSRHTLSYGKKIPVNRIAFLPHQIADELFLNTIKEPDIFCIVGVEQTMLGISNAGLFYSLARILDLAPKALAIEIAKAANTPQYYILGNGAGNMFSSGAELASLILQTFVEQKNQLLQWDTTWQDIFLDLVAICYDLHCVFFKDKQGDFEFEVSPNTIQKILSPSKKIAIIFDTDEGIYPMAITQQKRFLKNSEAQYIFTEDDPVMEVIQSMSEFMCKDNWWDIHDVKNIPGYTVGKKLINRHNFCYALLIDSDTDRPIYFPIRLSSYIHDDIPIDFDLRPTQIASFKETWKFITLFNKQYKQYEIIPSAVLQNIKKEFVGFLSEGKTGLYFYYAPTQTLPAALEKLPIATLTIDPRDIDQAILYPLEEPYPQQNKANKAFYINHLYKFLLIEFFDVLYGLQSNTTRKHIENLFQKTDFQKITSVTEFYTKLSDFVDLNDIHTIKHILETTDAEHALKVLQKNIFNFDYTLLSPLQSYTYDELCQHLKKLLTPRIEFYEDIETIDRGLINIYTSCQYSTLNQPQCEKKRLRIPVNHFENYIHILAADILNPLKHSTLLLTGLGVIDDLQFILRPQEIISVKNKF
|
Putative initation factor.
|
P0CAA7
|
CAPSP_ASFK5
|
Penton protein H240R (pH240R)
|
MATRAATKMAGKKEHQYCLLDTQEKRHGHYPFSFELKPYGQTGANIIGVQGSLTHVVKMTVFPFMIPFPLQKTRIGDFIGGRVYLFFKELDMQAFSDVNGMQYHFEFKVVPVSSSQVELLPVNNTYKFTYAIPELQYLTPIFYDLSGPLDFPLDTLSVHVDSLTHHIHLPIQNHNLTMGDRVFVSGYKHLQTIETCKNNIIFIKDIPPLSSEKINLYIPKNRIRIPLYFKSLKASK
|
Forms the penton at the fivefold vertices of the icosahedral capsid (By similarity). Together with the minor capsid proteins (p17, p49, and M1249L), forms a complicated network immediately below the outer capsid shell, stabilizing the whole capsid (By similarity).
|
P0CAA8
|
CAPSP_ASFP4
|
Penton protein H240R (pH240R)
|
MAANIIATRATPKMASKKEHQYCLLDSQEKRDGHYPFSFELKPYGQTGANIIGVQGSLTHVIKMTVFPFMIPFPLQKIHIDDFIGGRVYLFFKELDVQAISDVNGMQYHFEFKVVPVSSNQVELLPVNNKYKFTYAIPEVQYLTPIFYDLSGPLNFPLDTLSVHVDSLTKHIQLPIQNHNLTTGDRVFISGYKHLQTIELCKNNKIFIKCIPPLSSEKIKLYIPKNRIRIPLYFKSLKNV
|
Forms the penton at the fivefold vertices of the icosahedral capsid (By similarity). Together with the minor capsid proteins (p17, p49, and M1249L), forms a complicated network immediately below the outer capsid shell, stabilizing the whole capsid (By similarity).
|
P0CAA9
|
CAPSP_ASFWA
|
Penton protein H240R (pH240R)
|
MAATRAAPKTASKKEHQYCLLDSQEKRHGHYPFSFELKPYGQTGANIIGVQGSLTHVIKMTVFPFMIPFPLQKIHIDDFIGGRVYLFFKELDVQAISDVNGMQYHFEFKVVPVSSNQVELLPVNNKYKFTYAIPEVQYLTPIFYDLSGPLNFPLDTLSVHVDSLTNHIQLPIQNHNLTTGDRVFISGYKHLQTIELCKNNKIFIKCIPPLSSEKIKLYIPKNRIRIPLYFKSLKNV
|
Forms the penton at the fivefold vertices of the icosahedral capsid (By similarity). Together with the minor capsid proteins (p17, p49, and M1249L), forms a complicated network immediately below the outer capsid shell, stabilizing the whole capsid (By similarity).
|
P0CAC1
|
TBP_ASFK5
|
Putative TATA-binding protein pB263R (TBP)
|
MEDETELCFRSNKVTRLEMFVCTYGGKISSLACSHMELIKLLQIAEPVKALNCNFGHQCLPGYESLIKTPKKSKNMLRRPRKTEGDGTCFNSAIEASILFKDKMYKLKCFPSTGEIQVPGVIFPDFEDGKNIIQQWVEFLQHQPIEKKVQIIEFKTIMINFKFQINSVSPRVIIHLKKFAALLEQIPTPYPIREIKPPLEDSKVSAKFMVSPGKKVRINVFLKGKINILGCNTKESAETIYAFLKDLISVHWQEILCVLPVPD
|
Putative TATA-binding protein.
|
P0CAC2
|
TBP_ASFM2
|
Putative TATA-binding protein pB263R (TBP)
|
MEDETELCFRSNKVTRLEMFVCTYGGKISSLACSHMELIKRLQIAEPVKALNCNFGHQCLPGYESLIKTPKKNKNMLRRPRKTEGDGTCFNSAIEASILFKDKMYKLKCFPSTGEIQVPGVIFPDFEDGKNIIQQWVEFLQHQPIEKKVQIIEFKTIMINFKFQINPVSPRVIIHLKKFAALLEQIPTPYPIREIKPPLEDSKVSAKFMVSPGKKVRINVFLKGKINILGCNTKESAETIYTFLKDLISVHWQEILCVLPVPD
|
Putative TATA-binding protein.
|
P0CAC3
|
TBP_ASFP4
|
Putative TATA-binding protein pB263R (TBP)
|
MEDETELCFRSNKVTRLEMFVCTYGGKISSLACSHMELIKILQIAEPVKALNCNFGHQCLPGYESLIKTPKKTKNMLRRPRKTEGDGTCFNSAIEASILFKDKMYKLKCFPSTGEIQVPGVIFPDFEDGKNIIQQWVDFLQHQPIEKKIQIIEFKTIMINFKFQINPVSPRVIIHLKKFAALLEHIPTPYPIREIKPPLEDSKVSAKFMVSPGKKVRINVFLKGKINILGCNTKESAETIYTFLKDLISVHWQEILCVLPMPD
|
Putative TATA-binding protein.
|
P0CAC4
|
TBP_ASFWA
|
Putative TATA-binding protein pB263R (TBP)
|
MEDETELCFRSNKVTRLEMFVCTYGGKISSLACSHMELIKILQIAEPVKALNCNFGHQCLPGYESLIKTPKKTKNMLRRPRKTEGDGTCFNSAIEASILFKDKMYKLKCFPSTGEIQVPGVIFPDFEDGKNIIQQWVDFLQHQPIEKKIQIIEFKTIMINFKFQINPVSPRVIIHLKKFAALLEHIPTPYPIREIKPPLEDSKVSAKFMVSPGKKVRINVFLKGKINILGCNTKESAETIYTFLKDLISVHWQEILCVLPVPD
|
Putative TATA-binding protein.
|
P0CAC8
|
VF301_ASFK5
|
Uncharacterized protein E301R
|
MSEDIRRGPGRPPKKRVVPNFERKGILEKPVRPQSRLEFSYDNPLIFKNLFIYFKNLKSKNILVRCTPTEITFFSRDQSQASFVIATIDGKNVNHYYASDVFWLGINRELVEKMFNSIDRSFLKITIVHRYDKPETLFFIFTDFDIDKECTYQITVSEPELDMDLIEMEKSISEERLKNYPLRWEFTSKQLKKTFSDLSNYTELVTIEKLGGDTPLHLYFQKFNSISYHEMYKSSNKINLTSTIPKSQVFQINVKIAHIKSLASAMVTDKIRILCEENGNLIFQSEMDALLLNTITLNNMI
|
Plays a role in the inhibition of host innate immune system by acting as a negatively regulator of type I interferon production. Mechanistically, interacts with and prevents host IRF3 nuclear localization to inhibit its transcriptional activity.
|
P0CAC9
|
VF301_ASFP4
|
Uncharacterized protein E301R
|
MSEDIRRGPGRPPKKRVVPNFERKGILEKPVRPQSRLEFSYDNPLIFKNLFIYFKNLKSKNILVRCTPTEITFFSRDQSQASFVIATIDGKNVNHYYASDVFWLGINRELVEKMFNSIDRSFLKITIVHRYDKPETLFFIFTDFDIDKECTYHITVSEPELDMDLIEMEKSISEERLKNYPLRWEFTSKQLKKTFSDLSNYTELVTIEKLGGDTPLHLYFQKFNSISYHEMYKSSNKINLTSTIPKSQVFQINVKIAHIKSLASAMVTDKIRILCEENGNLIFQSEMDALMLNTITLNNMI
|
Plays a role in the inhibition of host innate immune system by acting as a negatively regulator of type I interferon production. Mechanistically, interacts with and prevents host IRF3 nuclear localization to inhibit its transcriptional activity.
|
P0CAD0
|
VF301_ASFWA
|
Uncharacterized protein E301R
|
MSEDIRRGPGRPPKKRVVPNFERKGILEKPVRPQSRLEFSYDNPLIFKNLFIYFKNLKSKNILVRCTPTEITFFSRDQSQASFVIATIDGKNVNHYYASDVFWLGINRELVEKMFNSIDRSFLKITIVHRYDKPETLFFIFTDFDIDKECTYQITVSEPELDMDLIEMEKSISEERLKNYPLRWEFTSKQLKKTFSDLSNYTELVTIEKLGGDTPLHLYFQKFNSISYHEMYKSSNKINLTSTIPKSQVFQINVKIAHIKSLASAMVTDKIRILCEENGNLIFQSEMDALMLNTITLNNMI
|
Plays a role in the inhibition of host innate immune system by acting as a negatively regulator of type I interferon production. Mechanistically, interacts with and prevents host IRF3 nuclear localization to inhibit its transcriptional activity.
|
P0CAD5
|
TFIIB_ASFK5
|
Initiation factor TFIIB homolog (pC315R)
|
MDALLKEIEKLSQPSSLQKENNDVCDLCFMQMKKISNYQLLCEECGQLKDWFEPDYNEKFTVYSRLKIVGANSSYHQRDLDKANSSDYSSLQFHHILEELKSLNVKYMDAGQKPFPIQVLKETAHSYNQVQQHRVIRSITKLQILASILRSICLKLNIACTVADAARFTQLNTKGISRGMDLLRSLFEDNKITLNVDLNPIDSFINSTYSALQIKQIHQELQEENVYNLKEIVKSFIVYADEKNIGVDLNRRTVVIATMYNVLRRAYYPIEIDTVVYQCKIRKNTITRALKMYEDYYSHFKSLYEQYQLNAAKKLI
|
Putative initation factor.
|
P0CAD6
|
TFIIB_ASFM2
|
Initiation factor TFIIB homolog (pC315R)
|
MDALLKEIEKLSQPSLQKENNDVCDLCFMQMKKISNYQLLCEECGQLKDWFEPEYNEKFTVYSRLKIVGANSSYHQRDLDKANSSDYSSLQFHHILEELKSLNVKYMDAGQKPFPIQVLKETAHSYNQVQQHRVIRSITKLQILASILRSICLKLNIACTVADAARFTQLNTKGISKGMDLLRSLFVDNKITLNVDLNPIDSFINSTYSALQIKQIHQELQEENVYNLKEIVKSFILYADEKNIGVDLNRRTVVIATMYNVLRRAYYPIEIDTVVYQCKIRKNTITRALKMYEDYYSHFKSLYEQYHLNAAKKLI
|
Putative initation factor.
|
P0CAD7
|
TFIIB_ASFP4
|
Initiation factor TFIIB homolog (pC315R)
|
MDALLKEIEKLSQPSLQKENNDVCDLCFMQMKKISNYQLLCEECGQLKDWFEPEYNEKFTVYSRLKIVGANSSYHQRDLDKANSSDYSSLQFHHILEELKSLNVKYMDAGQKPFPIQVLKETAHSYNQVQQHRVIRSITKLQILASILRSICLKLNIACTVADAARFTQLNTKGISRGMDLLRSLFVDNKITLNVDLNPIDSFINSTYNALQIKQIHQELQEENVYNLKEIVKSFILYADEKNIGVDLNRRTVVIATMYNVLRRAYYPIEIDTVVYQCKIRKNTITRALKMYEDYYSHFKSLYEQYHLNAAKKLI
|
Putative initation factor.
|
P0CI68
|
LPMG_SALTY
|
mgtA leader peptide (Regulatory leader peptide for mgtA)
|
MDPEPTPLPRWRIFLFR
|
Makes mgtA transcription sensitive to intracellular proline levels. Under low levels of proline this protein cannot be fully translated, and a stem loop forms which permits transcription of the downstream mgtA gene (By similarity).
|
P0CK57
|
UL92_EBVA8
|
Late gene expression regulator BDLF4
|
MSDQGRLSLPRGEGGTDEPNPRHLCSYSKLEFHLPLPESMASVFACWGCGEYHVCDGSSECTLIETHEGVVCALTGNYMGPHFQPALRPWTEIRQDTQDQRDKWEPEQVQGLVKTVVNHLYHYFLNENVISGVSEALFDQEGALRPHIPALVSFVFPCCLMLFRGASSEKVVDVVLSLYIHVIISIYSQKTVYGALLFKSTRNKRYDAVAKRMRELWMSTLTTKC
|
Part of the viral pre-initiation complex (vPIC) that is responsible for the expression of vPIC-dependent late genes (By similarity). vPIC is composed of at least BcRF1 that binds the viral TATT box, BDLF3.5, BDLF4, BFRF2, BGLF3, BGLF4 and BVLF1 (By similarity).
|
P0CK59
|
BALF1_EBVG
|
Apoptosis regulator BALF1
|
MNLAIALDSPHPGLASYTILPRPFYHISLKPVSWPDETMRPAKSTDSVFVRTPVEAWVAPSPPDDKVAESSYLMFRAMYAVFTRDEKDLPLPALVLCRLIKASLRKDRKLYAELACRTADIGGKDTHVRLIISVLRAVYNDHYDYWSRLRVVLCYTVVFAVRNYLDDHKSAAFVLGAIAHYLALYRRLWFARLGGMPRSLRRQFPVTWALASLTDFLKSL
|
May play a role in host B-cell survival by preventing host apoptosis. The survival of infected B-cells is a key step to induce host cell differentiation into memory cells, thereby assuring long term infection of the organism. May also play an active part in oncogenesis in Burkitt's lymphomy and nasopharyngeal carcinoma (By similarity).
|
P0CL44
|
ORGA_SALTY
|
Oxygen-regulated invasion protein OrgA
|
MIRRNRQMNRQPLPIIWQRIIFDPLSYIHPQRLQIAPEMIVRPAARAAANELILAAWRLKNGEKECIQNSLTQLWLRQWRRLPQVAYLLGCHKLRADLARQGALLGLPDWAQAFLAMHQGTSLSVCNKAPNHRFLLSVGYAQLNALNEFLPESLAQRFPLLFPPFIEEALKQDAVEMSILLLALQYAQKYPNTVPAFAC
|
Oxygen-regulated protein required for bacterial internalization.
|
P0CL57
|
MAZE1_MYCTU
|
Probable antitoxin MazE1
|
MTTYYYVLLSVTTWVGLRHEAKRELVYRGRRSIGRMPREWACRRSRRFAANGVDAAR
|
Antitoxin component of a type II toxin-antitoxin (TA) system.
|
P0CL58
|
MAZE2_MYCBO
|
Antitoxin MazE2
|
MKTAISLPDETFDRVSRRASELGMSRSEFFTKAAQRYLHELDAQLLTGQIDRALESIHGTDEAEALAVANAYRVLETMDDEW
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Labile antitoxin that binds to cognate MazF2 toxin and counteracts its endoribonuclease activity.
|
P0CL68
|
DBPB_BORBU
|
Decorin-binding protein B
|
MKIGKLNSIVIALFFKLLVACSIGLVERTNAALESSSKDLKNKILKIKKEATGKGVLFEAFTGLKTGSKVTSGGLALREAKVQAIVETGKFLKIIEEEALKLKETGNSGQFLAMFDLMLEVVESLEDVGIIGLKARVLEESKNNPINTAERLLAAKAQIENQLKVVKEKQNIENGGEKKNNKSKKKK
|
Binds to decorin which may mediate the adherence of B.burgdorferi to collagen fibers in skin and other tissues.
|
P0CN07
|
DCN1_CRYNB
|
Defective in cullin neddylation protein 1
|
MASIVSPLSTKDSLLVTQFRAITGTSSAEAAKYIKRYKHIEAAVDAFYNNEPAPRADPAQERKLGEIWEKFKDPSDPKLIKIDGTMELCEELDIDPGTDAVLFCLAADLGSKATGEWEKAPFVAGIASYPGNIDSLPKLKAYLPTLRKKLVSDPEYFKKVYNHAFQLARGGPQSLTRSLPLDTAIDLWTLFFPPAFNHSPSALSHLPDNSPPQFTQPEFDLWIEFMQQKNKAVSKDTWALLVDFARGIDKDFKEYDEDGAWPSMIDDFVEYVREQKRGQ
|
May contribute to neddylation of cullin components of SCF-type E3 ubiquitin ligase complexes. Neddylation of cullins play an essential role in the regulation of SCF-type complexes activity (By similarity).
|
P0CP19
|
CLMP1_CRYNB
|
Clampless protein 1 (CLP1)
|
MATYLAPPVSSNKENSPAPNIALSDIDAISLSLRTSLSGVTLPAKKKVAALGLGRAPKFTYRRHSNKPYNRSTSITRAKKAAVQTKSVRSKAAVKKSNTRPLPLKLVQRLDVESARLERLRKAVWNPPAPVPGQVRVPLKLPYPRFPSIEYIDNEYLKEIPVQYIFDRMVPLLPSIATITLAYQPYASIPHPDSKILRDTTLAFAIPEVIDGRKPHWAAKARGREPDLALAVAYKSGEGSNGNTVVAVNSLAFATQCAYWPRLLTTSIPIPTPKRPTPSASAVSTSLPAIVETEENVSDASFSSSSSWSDSDSEVEFIDLPRLPRPVKDDKGFLHLPLVELPIPSPSTFPIIHRHLHHPSRALLPDLLGLPEHYTTRSQVLDAISGLSVQQLMDKLTTLQGVWQNLCSLGIGRLGTWRQLGEAWACVVGVIAGQGLLIAGQEEAEVQRTGRKTAAEDVAWEWVRREKAKEQQ
|
Required for developmental progression after cells of opposite mating types fuse with one another, essential for processes common to both dikaryotic filament formation and monokaryotic fruiting. A direct target for transcription factors Sxi1-alpha and Sxi2-a.
|
P0CW29
|
VAPB1_MYCTU
|
Putative antitoxin VapB1
|
MATIQVRDLPEDVAETYRRRATAAGQSLQTYMRTKLIEGVRGRDKAEAIEILEQALASTASPGISRETIEASRRELRGG
|
Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC1.
|
P0CW31
|
VPB16_MYCTU
|
Putative antitoxin VapB16
|
MALWYQAMIAKFGEQVVDAKVWAPAKRVGVHEAKTRLSELLRLVYGGQRLRLPAAASR
|
Putative antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC16.
|
P0CW32
|
VPB23_MYCTU
|
Putative antitoxin VapB23
|
MLSDEEREAFRQQAAAQQMSLSNWLRQAGLRQLEAQRQRPLRTAQELREFFASRPDETGAEPDWQAHLQVMAESRRRGLPAP
|
Putative antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC23.
|
P0CW37
|
VAPB1_METJA
|
Putative antitoxin VapB1
|
MISAKSKTKRITITFEIPEDIDAKKFKDDVKRYVRYKLLANKLYELLEGENIEEIEEEIRKRRE
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC1 (Potential).
|
P0CW38
|
VAPB4_METJA
|
Putative antitoxin VapB4
|
MQLLYDLTKMNYSALYGEGRYLRIPAPIHYADKFVKALGKNWKIDEELLKHGFLYFI
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC4 (Potential).
|
P0CW39
|
VAPB5_METJA
|
Putative antitoxin VapB5
|
MQGPVIIPLISTLGLSFLAILLAYKISFSVIGFINSTLPTTLFPSKPYMLFVKISTISPLTCPSLIILTPALTWSLTALSMAYLYSSYKPNTFFTLSKNVSSFLTTG
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC5 (Potential).
|
P0CW76
|
RELB2_METJA
|
Putative antitoxin RelB2
|
MSIVQSYITDEKGNIKGVILDYKTFKKIEELLLDYGLLKAMEEVENEEEIDLETAKKLLEQ
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is RelE2 (Potential).
|
P0DA52
|
Y586_STRP3
|
DegV domain-containing protein SpyM3_0586
|
MKLAVITDSTATLPIDLKQDKAIFSLDIPVIIDDETYFEGRNLSIDDFYQKMADSKNLPKTSQPSLSELDNLLGLLSSKGYTHVIGLFLAGGISGFWQNIQFLAEEHPEIEMAFPDSKITSAPLGSMVKNVLDWSRQGMTFQAILNKLQEQIDGTTAFIMVDDLNHLVKGGRLSNGSALLGNLLSIKPILRFDEEGKIVVYEKVRTEKKAMKRLVEILNDLIADGQYNVSIIHSKAQDKADYLKRLLQDSGYQYDIEEVHFGAVIATHLGEGAIAFGVTPRL
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DA53
|
Y586_STRPQ
|
DegV domain-containing protein SPs1267
|
MKLAVITDSTATLPIDLKQDKAIFSLDIPVIIDDETYFEGRNLSIDDFYQKMADSKNLPKTSQPSLSELDNLLGLLSSKGYTHVIGLFLAGGISGFWQNIQFLAEEHPEIEMAFPDSKITSAPLGSMVKNVLDWSRQGMTFQAILNKLQEQIDGTTAFIMVDDLNHLVKGGRLSNGSALLGNLLSIKPILRFDEEGKIVVYEKVRTEKKAMKRLVEILNDLIADGQYNVSIIHSKAQDKADYLKRLLQDSGYQYDIEEVHFGAVIATHLGEGAIAFGVTPRL
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DA54
|
Y1149_STRP3
|
DegV domain-containing protein SpyM3_1149
|
MGTIKIVTDSSITIEPELIKALDITVVPLSVMIDSKLYSDNDLKEEGHFLSLMKASKSLPKTSQPPVGLFAETYENLVKKGVTDIVAIHLSPALSGTIEASRQGAEIAETPVTVLDSGFTDQAMKFQVVEAAKMAKAGASLNEILAAVQAIKSKTELYIGVSTLENLVKGGRIGRVTGVLSSLLNVKVVMALKNDELKTLVKGRGNKTFTKWLDSYLAKNSHRPIAEIAISYAGEASLALTLKERIAAYYNHSISVLETGSIIQTHTGEGAFAVMVRYE
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DA55
|
Y1149_STRPQ
|
DegV domain-containing protein SPs0713
|
MGTIKIVTDSSITIEPELIKALDITVVPLSVMIDSKLYSDNDLKEEGHFLSLMKASKSLPKTSQPPVGLFAETYENLVKKGVTDIVAIHLSPALSGTIEASRQGAEIAETPVTVLDSGFTDQAMKFQVVEAAKMAKAGASLNEILAAVQAIKSKTELYIGVSTLENLVKGGRIGRVTGVLSSLLNVKVVMALKNDELKTLVKGRGNKTFTKWLDSYLAKNSHRPIAEIAISYAGEASLALTLKERIAAYYNHSISVLETGSIIQTHTGEGAFAVMVRYE
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DA56
|
Y1478_STRP3
|
DegV domain-containing protein SpyM3_1478
|
MTWKIVTDSGCDLRSLTRQSKELRFERVPLTLQIGTEIFRDDDGLDIDNMMTTMYQSSKATTSSCPSPEAFLQAYRGADNVIVMTITGTLSGSHNSARLAKNELLEENPNVNIHLIDSLSAGGEMDLLVLELERLINLGLSFEEVVKQITAYQQKTRLIFVLAKVDNLVKNGRLSKLVGKVIGLLNIRMVGKASNKGTLELLQKARGQKKAVSALIEEIQKEGYVGGKVYIAHAQNPKICEQISEKIKSLYPDAVIQTGRTSGLCSFYAEDGGLLMGYEI
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DA57
|
Y1478_STRPQ
|
DegV domain-containing protein SPs0389
|
MTWKIVTDSGCDLRSLTRQSKELRFERVPLTLQIGTEIFRDDDGLDIDNMMTTMYQSSKATTSSCPSPEAFLQAYRGADNVIVMTITGTLSGSHNSARLAKNELLEENPNVNIHLIDSLSAGGEMDLLVLELERLINLGLSFEEVVKQITAYQQKTRLIFVLAKVDNLVKNGRLSKLVGKVIGLLNIRMVGKASNKGTLELLQKARGQKKAVSALIEEIQKEGYVGGKVYIAHAQNPKICEQISEKIKSLYPDAVIQTGRTSGLCSFYAEDGGLLMGYEI
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DA58
|
Y1667_STRP3
|
DegV domain-containing protein SpyM3_1667
|
MTFTIMTDSTADLNQTWAEDHDIVLIGLTILCDGEVYETVGPNRISSDYLLKKMKAGSHPQTSQINVGEFEKVFREHARNNKALLYLAFSSVLSGTYQSALMACDLVREDYPDAVIEIVDTLAAAGGEGYLTILAAEARDSGKNLLETKDIVEAVIPRLRTYFLVDDLFHLMRGGRLSKGSAFLGSLASIKPLLWIDEEGKLVPIAKIRGRQKAIKEMVAQVEKDIADSTVIVSYTSDQGSAEKLREELLAHENISDVLMMPLGPVISAHVGPNTLAVFVIGQNSR
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DA59
|
Y1667_STRPQ
|
DegV domain-containing protein SPs1668
|
MTFTIMTDSTADLNQTWAEDHDIVLIGLTILCDGEVYETVGPNRISSDYLLKKMKAGSHPQTSQINVGEFEKVFREHARNNKALLYLAFSSVLSGTYQSALMACDLVREDYPDAVIEIVDTLAAAGGEGYLTILAAEARDSGKNLLETKDIVEAVIPRLRTYFLVDDLFHLMRGGRLSKGSAFLGSLASIKPLLWIDEEGKLVPIAKIRGRQKAIKEMVAQVEKDIADSTVIVSYTSDQGSAEKLREELLAHENISDVLMMPLGPVISAHVGPNTLAVFVIGQNSR
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0DB66
|
HRCA_STRP3
|
Heat-inducible transcription repressor hrcA
|
MITQRQNDILNLIVELFTQTHEPVGSKALQRTIDSSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYHVIKAFDFEAFKLEDMLQKASHILSEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDSSVIDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQSLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLAAKLGDYYRYLNSNHYEVH
|
Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}.
|
P0DC70
|
NRDI_STRP3
|
Protein NrdI
|
MAELIIVYFSSKSNNTHRFVQKLGLPAQRIPVDNRPLEVSTHYLLIVPTYAAGGSDAKGAVPKQVIRFLNNPNNRKHCKGVISSGNTNFGDTFALAGPIISQKLQVPLLHQFELLGTATDVKKVQAIFARLKHHTHDKQKQTNNLITERTHPCHKPMRHTSH
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
P0DC71
|
NRDI_STRPQ
|
Protein NrdI
|
MAELIIVYFSSKSNNTHRFVQKLGLPAQRIPVDNRPLEVSTHYLLIVPTYAAGGSDAKGAVPKQVIRFLNNPNNRKHCKGVISSGNTNFGDTFALAGPIISQKLQVPLLHQFELLGTATDVKKVQAIFARLKHHTHDKQKQTNNLITERTHPCHKPMRHTSH
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
P0DG80
|
Y842_STRP3
|
UPF0122 protein SpyM3_0842
|
MNIMEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIADEFGVSRQAVYDNIKRTEKILETYEMKLHMYSDYVVRSEIFDDMIAHYPHDEYLQEKISILTSIDNRE
|
Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein (By similarity).
|
P0DG81
|
Y842_STRPQ
|
UPF0122 protein SPs1042
|
MNIMEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIADEFGVSRQAVYDNIKRTEKILETYEMKLHMYSDYVVRSEIFDDMIAHYPHDEYLQEKISILTSIDNRE
|
Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein (By similarity).
|
P0DG88
|
YIDD_STRP3
|
Putative membrane protein insertion efficiency factor
|
MKKLLIVSVKAYQKYISPLSPPSCRYKPTCSAYMLTAIEKHGTKGILMGIARILRCHPFVAGGVDPVPEDFSLMRNKNTSKNAEKA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P0DG89
|
YIDD_STRPQ
|
Putative membrane protein insertion efficiency factor
|
MKKLLIVSVKAYQKYISPLSPPSCRYKPTCSAYMLTAIEKHGTKGILMGIARILRCHPFVAGGVDPVPEDFSLMRNKNTSKNAEKA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P0DH54
|
YABA_STRP3
|
Initiation-control protein YabA
|
MNKKELFDAFDGFSQNLMVTLAEIEAMKKQVQSLVEENTILRLENTKLRERLSHLEHETAAKNPSKQRKDHLEGIYDEGFHICNFFYGQRRENDEECMFCRELLDRK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
P0DH72
|
Y4053_ENTFA
|
Putative regulatory protein PrgT
|
MTKKEQSIWRKEMLALMNEDADWYRNEDTERFKRIQELAKKIETASTRQFSSHISKERFEAYQRMGLQFKEIAEEFHITTTALQQWRKDNGYPIYNKNNRK
|
Might be involved in the expression of prgA, but is not required for activation of the expression of prgB.
|
P0DJH1
|
VIRA_VIBAN
|
Virulence protein VirA
|
MKYPRSLSWEKISSSTISIREFNRFENKKKVAIFCGYVRDKYEFNYHDRTYQWLRNNDYYVILVMPKSGILLESDLCKACDVFIERENFGYDFGSYACGLQYVNLIEGSERIDRLLFVNDSFIGPFGYCNLIEDSSEFWGNTDSNQVKYHYQSYLFGFNLEKVNLDIINNFFFSRGDIYTDDKSLVIENFELSLYEYFNGKGLRCSVLHPISVLKSDFIKQTFHFISYPYLTSKIFFYIMVIARDVNPTHQLWLQLFKRGFPFIKKELLRDNPTGYPELYKKVEEVMGSNDFNGEYKQIFKNHL
|
Could be involved in the biosynthesis of a major surface antigen important for virulence.
|
P0DJX3
|
AC4_BGYMJ
|
Protein AC4 (Protein AL4)
|
MRLFSSKVNSSAQIKDCSTWYPQPGQHISIRTFRELNQVPTSKNTSTKMESQSNGDNSKSTADLQEEVSSLPTTHTQRH
|
Pathogenicity determinant. May act as a suppressor of RNA-mediated gene silencing, also known as post-transcriptional gene silencing (PTGS), a mechanism of plant viral defense that limits the accumulation of viral RNAs.
|
P0DJX4
|
SMALL_TMEVD
|
Protein L*
|
MDTQMCALFAQPLTLLPDLNICSWQTVNGSQRTFFVWTWTMTSSGLRTRAINLKQWNGLTYRSYAILSWNPRETPLHLTRVTPSPQVTKGSLSTTSIPINTKIQLICLPAVAMLATPPKTTDNCRTSWAALQMLLLLWHLSSWIKTQRRWRISLTE
|
May be required for viral persistance in the host.
|
P0DOP5
|
PG055_VAR67
|
Protein OPG055 (Protein F11)
|
MGFCIPLRLKMLKRGSRKFSSMLARRHTPKKMNIVTDLENRLKKNSYIENTNQGNILMDSIFVSTMSVETLFGSYITDDSDDYELKDLLNVTYNIKPVIVPDIKLDAVLDRDGNFRPADCFLVKLKHRDGFTKGALYLGHSAGFTATICLKNEGVSGLYIPGTSVIRTNICQGDTIVSRSSRGVQFLLQIGGEAIFLIVSLCPTKKLVETGFVIPNISSNDNAKIAARILSEKRKDTITHIDTLIQYGQQLELAYYNSCMLTEFLHYCNLYANTIKESLLKETIQKDINITHTNITTLLNETAKVIKLVKSLVDKEDTDIVNNFITKEIKNCGGVKNRDTIVNSLSLSNLDFYL
|
Stimulates increases in peripheral microtubule dynamics and may increase the motility of the infected cells, contributing to cell-to-cell spread of the virus. Seems to inhibit the signaling via the GTPase RHOA and DIAPH1/mDia.
|
P0DOP6
|
PG055_VARV
|
Protein OPG055 (Protein F11)
|
MGFCIPLRLKMLKRGSRKFSSMLARRHTPKKMNIVTDLENRLKKNSYIENTNQGNILMDSIFVSTMSVETLFGSYITDDSDDYELKDLLNVTYNIKPVIVPDIKLDAVLDRDGNFRPADCFLVKLKHRDGFTKGALYLGHSAGFTATICLKNEGVSGLYIPGTSVIRTNICQGDTIVSRSSRGVQFLLQIGGEAIFLIVSLCPTKKLVETGFVIPNISSNDNAKIAARILSEKRKDTITHIDTLIQYGQQLELAYYNSCMLTEFLHYCNLYANTIKESLLKETIQKDINITHTNITTLLNETAKVIKLVKSLVDKEDTDIVNNFITKEIKNCGGVKNRDTIVNSLSLSNLDFYL
|
Stimulates increases in peripheral microtubule dynamics and may increase the motility of the infected cells, contributing to cell-to-cell spread of the virus. Seems to inhibit the signaling via the GTPase RHOA and DIAPH1/mDia.
|
P0DSL5
|
TX2A_NEOAP
|
U1-poneritoxin-Na2a (U1-PONTX-Na2a) (Poneratoxin) (Ponericin Pa IV1)
|
GKEKDVFMDKLRDAGAAGIDYLKHFTHHIVKKKN
|
May have antimicrobial properties, like most ant linear peptides.
|
P0DSS9
|
PG189_VAR67
|
Ankyrin repeat protein OPG189
|
MDFFKKEILDWSIYLSLHYIAHACSNSSTSHIIQEYNLIRTYKKVDKTIVDFLSRWPNLFHILEYGENILHIYSMDDANTNIIIFFLDNVLNINKNGSFIHNLGLSSSINIKEYVYQLVNNDHLDNGIRLMLENGRRTRHFLSYILDTVNIYICILINHGFYIDAVDSYGCTLLHRCIYHYKKSESESYNELIKILLNNGSDVDKKDTHGNTPFILLCKHDIDNVELFEICLENANIDSVDFNGYTPLHYVSCRNKYDFVKSLISKGANVNTRNRFGTTPFYCGIIHGISLIKLYLESDTELEIDNEHIVRHLIIFDAVESLDYLLFRGVIDINYRTIYNETSIYDAVSYNAYNMLVYLLNRNGDFETITTSGCTCISKAVANNNKIIMEVLLSKQPSLKIMILSIIAITKHKQHNTNLLKMCIKYTACMTDYDTLIDVQSLQQYKWYILKCFDEIDIMKRCYIKNKTVFQLVFCTKDINTLMRYGRHPSFVKYTSLDVYGSRVRNIIASIRYRQRLISLLSKKLDVGDKWACFPNEIKYKILENFNDNELSTYLKIL
|
Contributes to viral release without involving rearrangement of host actin.
|
P0DST0
|
PG189_VARV
|
Ankyrin repeat protein OPG189
|
MDFFKKEILDWSIYLSLHYIAHACSNSSTSHIIQEYNLIRTYKKVDKTIVDFLSRWPNLFHILEYGENILHIYSMDDANTNIIIFFLDNVLNINKNGSFIHNLGLSSSINIKEYVYQLVNNDHLDNGIRLMLENGRRTRHFLSYILDTVNIYICILINHGFYIDAVDSYGCTLLHRCIYHYKKSESESYNELIKILLNNGSDVDKKDTHGNTPFILLCKHDIDNVELFEICLENANIDSVDFNGYTPLHYVSCRNKYDFVKSLISKGANVNTRNRFGTTPFYCGIIHGISLIKLYLESDTELEIDNEHIVRHLIIFDAVESLDYLLFRGVIDINYRTIYNETSIYDAVSYNAYNMLVYLLNRNGDFETITTSGCTCISKAVANNNKIIMEVLLSKQPSLKIMILSIIAITKHKQHNTNLLKMCIKYTACMTDYDTLIDVQSLQQYKWYILKCFDEIDIMKRCYIKNKTVFQLVFCTKDINTLMRYGRHPSFVKYTSLDVYGSRVRNIIASIRYRQRLISLLSKKLDVGDKWACFPNEIKYKILENFNDNELSTYLKIL
|
Contributes to viral release without involving rearrangement of host actin.
|
P0DTA9
|
D3_FOWPN
|
27 kDa core protein
|
MEIHRLNSYTSVDYLCNSSNNVYILLGDTDEFINKRIILLMNNIELYYVYEISVNDEDELYHSFITSNVVCPIKQRINLMLYKEYKKVIGSCVINNEGNIKMYSQPDKLHVYVLCYRCNGDIKTITMIKCHQLLKPEKEIVIDGYQVNDSSFFYTSPNLIKQINMDKSDLFYKNILLRKEINCLIRKQESSNLYCILNKHIVSLSDTDIWKVIISDELFDSSDIEKLVKFDYDRDKFHAFVRAWYSGQLSNCKEENETIKTVYEMIEKRI
|
Late protein which is part of a large complex required for early virion morphogenesis. This complex participates in the formation of virosomes and the incorporation of virosomal contents into nascent immature virions (By similarity).
|
P0DTB0
|
D3_FOWPV
|
27 kDa core protein
|
MEIHRLNSYTSVDYLCNSSNNVYILLGDTDEFINKRIILLMNNIELYYVYEISVNDEDELYHSFITSNVVCPIKQRINLMLYKEYKKVIGSCVINNEGNIKMYSQPDKLHVYVLCYRCNGDIKTITMIKCHQLLKPEKEIVIDGYQVNDSSFFYTSPNLIKQINMDKSDLFYKNILLRKEINCLIRKQESSNLYCILNKHIVSLSDTDIWKVIISDELFDSSDIEKLVKFDYDRDKFHAFVRAWYSGQLSNCKEENETIKTVYEMIEKRI
|
Late protein which is part of a large complex required for early virion morphogenesis. This complex participates in the formation of virosomes and the incorporation of virosomal contents into nascent immature virions (By similarity).
|
P0DTG1
|
ORF3C_SARS2
|
ORF3c protein (ORF3c) (ORF3h protein) (ORF3h)
|
MLLLQILFALLQRYRYKPHSLSDGLLLALHFLLFFRALPKS
|
May play a role in host modulation.
|
P0DV60
|
LCE7A_HUMAN
|
Late cornified envelope protein 7A
|
MSYQKHQQKWQLPAKCLPKYPSKWTPQAPASCPAPCPPPAPSCCVSSCCISGFGGHCSLVSLRFPRFYLRQPQHSDCCEHESSRCSTCYSSGDCS
|
Precursors of the cornified envelope of the stratum corneum.
|
P10022
|
YGI1_BACTU
|
Uncharacterized 23.6 kDa protein (ORF 1)
|
MTNTIDFKHVEKNARIRDFENEKEKFKQDHNGINQEEVNQAMQVLSKATGGKEIFIGTKRSPQSKVKFAQFIQDNWDYALENAFFTDEEMLFLLRIQRFLQFKSNCIVNDIHSRNALPMSQKQIADRLKTDKSKISRIVNSLVQKGVIVKANGHKPEGVKARTYALFINPNIIYSGERDNVETTLKALFMNSKSLFKKFPIALF
|
Possibly involved in pGI2 replication mechanism.
|
P10023
|
YGI2_BACTU
|
Uncharacterized 30.3 kDa protein (ORF 2)
|
MKKLLISFIAILFFICGFNLKAFAAEEIIDYQSLYNQAIQEGVLDQNSVSYNEWLKQNKEEFMPIYQDGLKQGVFLEPLSYNEWLKLNNYGQAPTGDIELFDDVTPRGSWGGFTLKAGDIFITNATSSAGIVGHAAIANGDNYILHMPGAGQGNQQLSTSNWMQKYTASGKWIKVYRLKDQTLARDVARYADRNFYSTTGSATKNVYLDYGIDTHLYQKNPTYCSKLVFQALYFGSGSRNVMQAVSGIVTPYGLIDTFTSAYRPSLVKTY
|
Possibly involved in pGI2 replication mechanism.
|
P10024
|
YGI3_BACTU
|
Uncharacterized 13.4 kDa protein (ORF 3)
|
MMAIFISIVLVVSFVLFNRVQAKKSIYNYIARQGIQESQLKYIDFHKDFKMGGYWLAVYVEGENPDIYYEYSYQDKKVNFQAYFNSEKAIKKKMWGGSGLTEIEMKKLKYPPLQ
|
Possibly involved in pGI2 replication mechanism.
|
P10031
|
PSIB1_ECOLI
|
Protein PsiB
|
MKTELTLNVLQTMNAQEYEDIRAAGSDERRELTHAVMRELDAPDNWTMNGEYGSEFGGFFPVQVRFTPAHERFHLALCSPGDVSQVWVLVLVNAGGEPFAVVQVQRRFASEAVSHSLALAASLDTQGYSVNDIIHISMAEGGQV
|
In contrast to PsiB protein of plasmid R6-5, this protein is unable to prevent SOS induction for potentially two reasons: less activity and/or insufficient expression.
|
P10032
|
PSIB2_ECOLX
|
Protein PsiB
|
MKTELTLNVLQTMSAQEYEDIRAAGSDERRELTHAVMRELDAPDNWTMNGEYGSEFGGFFPVQVRFTPAHERFHLALCSPGDVSQVWVLVLVNAGGEPFAVVQVQRRFAPEAVSHSLALAASLDAQGYSVSDIIHILMAEGGQA
|
Inhibition of the induction of the SOS pathway.
|
P11189
|
RPC4_BPP1
|
Repressor protein C4
|
MLVRTTADFRYCGIFVSVNRVTPELWWGVMGRLRPAGFTNASLSTLSRPATCLTAGSRLLNLLVRP
|
Repressor of the ant/reb gene.
|
P11190
|
ABC1_BPP22
|
Anti-RecBCD protein 1 (Protein abc1)
|
MRRLNITTAEMESVCGRMVACRAAEHLGLNINQFYYIAKKLSLKTAFIKPRWSDDEDKRMQTLISSGYTQRNVAKILGRSEESVKSRLSRLRKK
|
Modulates the activity of the host recBCD nuclease. And thus protects linear double-stranded DNA from exonuclease degradation.
|
P11191
|
ABC2_BPP22
|
Anti-RecBCD protein 2 (Protein abc2)
|
MPAPLYGADDPRRCSGNSVSEVLDKFRKNYDLIMSLPQETKEEKEFRHCIWLAEKEERERIYQTAIRPFRKATYTKFIEIDPRLRDYRSRYGAISNN
|
Modulates the activity of the host recBCD nuclease. And thus protects linear double-stranded DNA from exonuclease degradation.
|
P11320
|
E316_ADE03
|
Early E3 16 kDa glycoprotein
|
MKAFAVLFVLSLIKTELRPSYGLPLLQSGLYNTNQIFQKTQTLPPFIQDSNSTLPAPSTTNLPETNKLASHLQHRLSRSLLSANTTTPKTGGELRGLPTDDPWVVAGFVTLGVVAGGLVLILCYLYTPCCAYLVILCCWFKKWGPY
|
E3 proteins seem to be dispensable for virus growth in tissue culture cells. They are potentially important for virus growth under special conditions E3 region may help adenoviruses to evade the immune surveillance of the host.
|
P11335
|
B_SPV4
|
Internal scaffolding protein ORF3
|
MKIYTQRNNKVEFSDSGSSEYSEYQRVIDADTKENTYEIVATYNRYDEIQEAGEGTDLRSMLDKYGDDYLELLPPARLGGDDTILPKSVLELENIRLQNTEYLSLLENINSKLDKQGLGDLDNFIKNWQESQKKIENEKGKKEDEKENE
|
Participates in the assembly of the viral procapsid in the cytoplasm. Released from the procapsid upon genome packaging, possibly through affinity displacement by the protein ORF8, or by proteolysis (By similarity).
|
P11337
|
C_SPV4
|
Protein ORF5
|
MDKLISLKDVMRFIFKFGLPGLCIAVGLIVMVANKWLGIPWPCYVIVGSVSLSFGLILFIVQTIKEIIIYRKEKKDENIYSKK
|
Plays a central role in the packaging of viral DNA into phage procapsid, which occurs in the late stage of infection. Can interact with the replicative complex after the completion of one round of DNA synthesis. When protein ORF5 is bound to the replicative form, the complex becomes accessible to procapsid and serves as a DNA packaging apparatus (By similarity).
|
P11735
|
CU30_LOCMI
|
Cuticle protein 30 (LM-ACP 30) (LM-30)
|
GLLGLGYGGY
|
Component of the cuticle of migratory locust which contains more than 100 different structural proteins.
|
P11737
|
CU36_LOCMI
|
Cuticle protein 36 (LM-ACP 36) (LM-36)
|
GGPAAYSXYXNGADFGAVGEXLGSXSKGL
|
Component of the cuticle of migratory locust which contains more than 100 different structural proteins.
|
P12054
|
RLX1_STAAU
|
Protein rlx
|
MATTKLGNTKSASRAINYAEERAEEKSGLNCDVDYAKSYFKQTRALYGKENGVQAHTVIQSFKPGEVTAKECNEIGLELAKKIAPDYQVAVYTHTDKDHYHNHIIINSVNLETGNKYQSNKEQRDFIKKANDQLCEERGLSVPEKSSEIRYTLAEQNMIDKDKRSWKNDIRMAVEETKDNAVAFEEFNTLLKEKGVEITRVTKNNVTYRHIEEDKKVRGNKLGDSYDKGVIENGFAIEKFRREREEEREYDEYADTFEVDWDAFAENSEDLRKRRIARTEETKQASNKIYIRDERTTGLERKGIAGNQVEFEKDDGGLSR
|
This protein is probably required for relaxation complex formation and plasmid mobilization by conjugative plasmids.
|
P12551
|
VDEL_BPP4
|
Transactivation protein
|
MIYCPSCGHVAHTRRAHFMDDGTKIMIAQCRNIYCSATFEASESFFSDSKDSGMEYISGKQRYRDSLTSASCGMKRPKRMLVTGYCCRRCKGLALSRTSRRLSQEVTERFYVCTDPGCGLVFKTLQTINRFIVRPVTPDELAERLHEKQELPPVRLKTQSYSLRLE
|
Positively regulates late transcription from 2 promoters in P4 and 4 promoters in P2.
|
P13057
|
VBET_BPP4
|
Protein beta
|
MKVYFENYSYYPALRTRSAEMTGLNNLSYENKKKILPLISLGKWPRSEEIQVSLDKSLEVMSNLPFILDVTKDNSHHCASSFELLSPENGFKNWIEFCSRNDNIIPVVQMPDSAKLRDISIQARVLEELKGSIAFRIRNLNTDINKTLTSLVSMNSPENAIVFIDLGYIRGNVSAITAAAINSINQIRTEIPEAIISVLATSFPSSVTNFCRENGQSGYIDVIERELHQNIGGSDVAIYGDHGSIHSVVYDNIIGRYVPRIDIALNDSWYFERRPGMNKEGFIEAAKSILAEYPHYQREDSWGAAMIRNAAIGDIAGMGSPAKWIAVRVNLHLNKQIELSEALQYGFDHDEEDLI
|
The presence of this protein prevents gop protein from killing E.coli.
|
P13058
|
GOP_BPP4
|
Protein gop
|
MLNHVYGLIGVVGTIITIATSFIRNQDISQWLLVCSGWLAALLIGWFTHRTIKAISNNHTNVIKSNMEVINSHNESNQNLMAENKELIKELARTSEQKEKMESIAAYLATQNPQINAMPRTASRPENIDSEAN
|
This protein kills E.coli when the beta protein is absent.
|
P13059
|
RCII_BPP4
|
Protein cII
|
MAELLREQEVKIALIEWLYKKGMLSDATIINEMVVANWSRRADLAIANGSLQAFEIKSDFDSLKRLDGQLKIFKSSFEKVTIVCAPKFTSEVSKRVSSDVGVVEFQSNNSSVRFKIIQKGRVCSRLNKFVYLGFLLKSELKDLLNQYGITFSNELHRDCLEVLASKLSLNKIREFVITSIKNRYHATSNDFLSRLHGNQEISINDLALLSKAKRRNNSLVKFEFKACSEKSLNEYHKVDVDSIVRKYGDDVSYIPEKVLKRVVG
|
Mutations in this gene cause a clear-plaque phenotype as a result of efficient killing of infected cells by P4. How this comes about is not understood.
|
P13094
|
VSR_WTV
|
Suppressor of RNA-mediated gene silencing (Non-structural protein 10) (Pns10)
|
MDASVDRITNLHFEILAKAGGHEIHQKYEAIRKLNLTGDSSKSNISVSARSAILKWADAKQGYIASQLDDRDYGDLIAKAVIFVPMSVITGGKNPKDLIPYGVVAAVLIFVPETLTLLDEIVINLMHDKKPLSSILLTKILRDMKIDVCGSNFDSFYYCPISRYNRHIIKLAGALPQMPTSVRLSVNDLARVAISEVHNQLISDKQMFFKLPTGFSPKVHCLKVLCTTEMEIFQKWVRTFMSDRPNEFIYSDQFNILSRTTYFSSDDPFSFFTLWRGWSTYKEILSQDQASSFLEAIGSGKPLRSSIATFPSMFDEGAIYIRYEWITPKDSANSKKAGSSAPSAPKM
|
Suppressor of RNA-mediated gene silencing, also known as post-transcriptional gene silencing (PTGS), a mechanism of plant viral defense that limits the accumulation of viral RNAs.
|
P13268
|
CAD1_ENTFL
|
Sex pheromone CAD1
|
LFSLVLAG
|
Involved in the conjugative transfer of the hemolysin plasmid pAD1.
|
P13269
|
CPD1_ENTFL
|
Sex pheromone cPD1
|
FLVMFLSG
|
cPD1 is involved in the conjugative transfer of the bacteriocin plasmid pPD1.
|
P13660
|
MBED_ECOLX
|
Mobilization protein MbeD
|
MTELETHLLNALEQLQQDYMQRLSEWESAFVELQKMFSLTQRDNAMLNERVMQLSQQVQHLSEQTERLSQLYSENWR
|
This protein is essential to promote the specific transfer of the plasmid in the presence of conjugative plasmids.
|
P13977
|
YP15_STAAU
|
DegV domain-containing 15.5 kDa protein
|
MAKQIIVTDSTSDLSHEYLKQHNIHVIPLSLTIDGKSYTDQADISSSEYIDHIENDADVKTSQPPIGRFIETYEQLAQDDVEIISIHLSSGLSGTYNTAVQASHMVDGNITVIDSKSISFGLGYQIKQIVELVLLQSKKI
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P14109
|
VG17_BPP22
|
Superinfection exclusion protein (Protein gp17)
|
MKLRVWHIPQVPMKPFIVEVGSVEEGVRMMDALADYDAFQYDNNIKPDYCNANGLQMFDESLTDQDLEDMELDDRWIDWYSECQCYDDPREYLESLKEETTAA
|
In the absence of gp17, P22 is sensitive to a superinfection exclusion system of the fel-2 prophage.
|
P14111
|
VKIL_BPP22
|
Protein kil
|
MTIVPVNGTILVQQGNREFNKLYEASFPDTKEGNSAAYAWASSIAMGWEDCQDEDWNRNHAA
|
P22 kil is essential for lytic growth in the absence of abc. Expression of P22 kil causes filamentation and cell death.
|
P14112
|
VARF_BPP22
|
Accessory recombination function protein
|
MQHEFSDEEFIALISPEIEEEVEQQINLAAERQNPIIGWDEFAGYYS
|
Arf may be recombination-related.
|
P14307
|
YSMA_SERMA
|
Control protein C.SmaI
|
MPDADICFMDIKEILAENVRSYRNINNLSQEQLAEISGLHRTYIGSVERKERNVTLSTLIILAKALNTSVPKLLTRQGLKNEQG
|
May control expression of its associated restriction-modification system SmaI.
|
P14491
|
RLX3_STAAU
|
Protein rlx
|
MATTKISSTKSTSRAINYAEKRAEEKSALNCDIDYAKSSFKATREMYGKTDGNEGHVVIQSFKPNEVTPEQCNQLGLELAEKIAPNHQVAVYTHNDTDHVHNHIVINSIDLETGKKFNNNKKALHDIRQANDEICVSHNLSIPEEKAKLRYTQAEYSVLNKGKTSWKDEIRHAIDQSQAASYEELGNDLQQNGIKIERITDKTITYRHLEEDKKVRGKKLGEDYDKGGLEIGFNRQNEQREEQARQRELEQARREKIKRDKEREKEWARFNRSTQAIRQNRERSEREERERERKARELEEQNRRAREERARQERENKHTHEKTRGFDLEL
|
This protein is probably required for relaxation complex formation and plasmid mobilization by conjugative plasmids.
|
P14493
|
RLX2_SALTM
|
22 kDa relaxation protein
|
MSDEIKQIAALIGHHQALEKRVTSLTEQFQAASSQLQQQSETLSRVIRELDSASGNMTDTVRKSVSSALTQVEKELKQAGLAQQKPATEALNQAADTAKAMIHEMRREMSRYTWKSAIYLVLTIFFVLASCVTAFTWFMNDGYSQIAEMQRMEAVWQKKAPLADISRCDGKPCVKVDTRTTYGDKENTWMIIKK
|
This protein is probably required for relaxation complex formation.
|
P14498
|
TRAS2_ECOLX
|
Protein TraS
|
MKRSDLEKDAAYILDKFKQLDYEIPSNRQILKVIFYKLVVVYVFQLLFIIFDIFINSNVRDYHYFDTFVITLGSNAFFSLVFLMSTYNLVSLKISLGSEITEQSVLLKLVERKINSYGQFLMVVNAIVGCVLLSSGERFVAGLGFSWFVTYLISMITLQTSLSRYMTPAVVSSLSKVKELLSASPK
|
Involved in surface exclusion.
|
P14820
|
RPC2_BPPH8
|
Regulatory protein CII
|
MSALIINEYREQGGTAISFPEDISRARQKLFRFLDNRFDSDQYRENVRELTPAIMAVLPVEFRTRLAPQNDTMSLIASAMKECSEAKQAVLLNAPEHQKMKEVSEGIASLFRLMPEQVGPLMTMVTSMLGVI
|
May be involved in activation of synthesis of the CI protein.
|
P15236
|
VFIL_BP186
|
Protein fil
|
MLKSEPSFASLLVKQSPGMHYGHGWIAGKDGKRWHPCRSQSELLKGLKTKSPKSSGFLIIRIVHFVIKGVKHVTR
|
This protein causes filamentation.
|
P15249
|
HMC1A_METSH
|
Chromosomal protein MC1a
|
AETRNFALRDKKGNEIGVFTGKQPRQAALKAANRGHKDIRLRERGTKKVHIFAGERVKVKKPKGAPAWMPNEIWKPKVKKIGVEKLDEI
|
Protects DNA against thermal denaturation and modulates transcription.
|
P15250
|
HMC1B_METSH
|
Chromosomal protein MC1b
|
AEMRNFALRDAQGNEIGVFTGKSPRQAALKAANRGYTEIKLRERGTKKVHIFSGERVQVDKPAGAPAWMPDKIWKPKVKKEGIEKLD
|
Protects DNA against thermal denaturation and modulates transcription.
|
P15251
|
HMC1C_METSH
|
Chromosomal protein MC1c
|
MIEKRNFALRDKEGNEIGVFSGKQPRQAALKAANRGFTDIRLRERGTKKVHIFQGERIQVPKPSNAPKWMPANIWKPNVKKLGVEKLEDI
|
Protects DNA against thermal denaturation and modulates transcription.
|
P15534
|
SCR3_NOTGO
|
S-crystallin 3 (Crystallin SIII)
|
PAPNYTLYYFNGRGRAEILRMLFAAAGQKFNDKXXEFN
|
S-crystallins are structural components of squids and octopi eye lens. Contains relatively little if any GST activity (By similarity).
|
P16007
|
MRH_BPT4
|
RpoH-modulating protein
|
MEAILFEMSINSISMAFVKDVPITVAVMIDKRYDNNMYLVEDFISMPIPEDVEIKLKKIGIIETVQNSPFMAIQAFTKSNYIDVAEAYYNNKPLSFYSYDSIYDWKIDKGNKFIITDESALSYFITSLWNNLNPNLLKIHKFDDAPTIVLGKTNESSEEDA
|
Plays a role in transcriptional regulation of late T4 genes. Modulates the phosphorylation status of host heat shock sigma factor rpoH which is an initiation factor that promotes the attachment of host RNA polymerase to specific initiation sites.
|
P16464
|
F802_SCHMA
|
Female-specific protein 800 (FS800)
|
MIIIIKIRINIHIIILTIIIIKGTINLRMSIVNQNKIHITKKQGIIMMMMMMMKILKEIKNLFDLDIMVIHIGMIKFNLVEIVQKVAVIQKVHISHYILEQIDMVDEMIIHDFKHVDDPMVIVKICFLTFLM
|
FS800 is likely to have some function in the production or maintenance of the schistosome egg. It may have a function unrelated to eggshell formation.
|
P16594
|
VSR_RDVO
|
Suppressor of RNA-mediated gene silencing (Non-structural protein 10) (Pns10)
|
MEVDTATFVRLHHELLCAHEGPSIISKFDAIKKVKLGTLANQSGGANNITEAFLAKLRNFERKSEAYLASDLAERELTRDTHKAIVFVTKSVLLGGKSLKDLLPYGVIVCAFIFIPETASVLDNVPVMIGNQKRPLTVALIKYIAKSLNCDLVGDSYDTFYYCNSSAYGKNLISVSDNDFSNPQRALLSVGDLCYQAARSLHVAAANYIRIFDRMPPGFQPSKHLFRIIGVLDMETLKTMVTSNIAREPGMFCHDNVKDVLHRIGVYSPNHHFSAVILWRGWASTYAYMFNQEQLNMLSGTSGLAGDFGKYKLTYGSTFDEGVIHVQYQFVTPEVVRKRNIYPDLSALKGGSS
|
Suppressor of RNA-mediated gene silencing, also known as post-transcriptional gene silencing (PTGS), a mechanism of plant viral defense that limits the accumulation of viral RNAs.
|
P17369
|
V14_VACCW
|
Ankyrin repeat protein 14
|
MSYACPILSTINICLPYLKDINMIDKRGETLLHKAVRYNKQSLVSLLLESGSDVNIRSNNGYTCIAIAINESRNIELLKMLLCHKPTLDCVIDSLREISNIVDNYYAIKQCIKYAMIIDDCTSSKIPESISQRYNDYIDLCNQELNEMKKIMVGGNTMFSLIFTDHGAKIIHRYANNPELREYYELKQNKIYVEAYDIISDAIVKHDRIHKTIESVDDNTYISNLPYTIKYKIFEQQ
|
May be involved in virus-host protein interaction through the ankyrin repeats.
|
P17565
|
Y35K_HALSI
|
Uncharacterized 36 kDa protein
|
MAKRDGMKLRDELTFDTSRAVKAVSWGEAIDRFQSWYDDQRGTQIVVENELGETVGFDMPNRFTPEYREMLYAKAQSLERGLRERWGSLLHTGMVTLTASSTDDEGRLRPPLEHFEDLLESWEAVRRALARVLEGREWEYLAILEPHESGYVHIHLGVFVRGPVVAEQFEPVLDAHLRNCPTAGEDAHQVFDENGDEDAVRVRRSSHPSRSGGVENLGAYLAAYMAGEYGSEPSEMPENVRAFYATMWASGRQWFRPSNGAQELMQPEEDDEGDSIEEWEMVGIAPEGDLGDIIEVDPSEPRSDPYRRLRTPPPGG
|
Possibly necessary for replication.
|
Subsets and Splits
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