entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
O30169
|
CAS5_ARCFU
|
CRISPR-associated protein Cas5
|
MQWVKLTLHFPSFFSYRIPDYSSQYALSVPLPSPSAIKLSLVATAIRTTGNVAEGERVFYAVRDADIRILPPEQIAINSVLIKRLKKKKNPTELETFEKTFGVREYVFFPDDVNLFIGCDDIDIAIKYFGMLRYLGSSDSMLYVKCIEKINEPPKSAIKAIADKEFAEAISKEPYIVYPVKDISKKAKFEQINPYSGKSGRNVFERKYYLIKARIKKGKKWKLLEIQC
|
CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA) (By similarity).
|
O30498
|
PITX_RHIME
|
Putative pit accessory protein
|
MLGLFRKLLPREDRFFDLFADHSRTVMGAAEALNALLAGGPDIESHCDRIVALENEADEITREVLLAVRRSFITPFDRGDIKDLIQSMDDAIDMMHKTVKTIRLYEQKSFDPGMQAMGAAVVEAAHLVAEAIPLLSRIGANAHRLSAIAEEVTHVEDRSDQLHEQGLKDLFQRHGASNPMAYIIGSEIYGELEKVVDRFEDVANEISGIVIENV
|
Could be involved in orthophosphate transport.
|
O32276
|
USD_BACSU
|
Protein usd
|
MGIFHKLTFKTIQRRSGIMNDSLQNTDLISHFSHPF
|
Required for translation of SpoIIID.
|
O34055
|
ARPU_BPO12
|
Putative autolysin regulatory protein ArpU
|
MLLPEIDEKATVKRCKRKLREYPRWREIAHDSAEQKITQEFTFMPRGGSGVNKPVENIAVRRVDALSELEAIEQAVNGLYRPDYRRILIEKYLAYPPQPNWKIAQAIGFERTAFQELLKHSILAFAELYRNGQLVVER
|
May be involved in the regulation of muramidase export.
|
O34601
|
YIDD_BACSU
|
Putative membrane protein insertion efficiency factor
|
MKTLFIALIRGYQKFISPLTPPTCRFYPTCSQYGIEAIKTHGALKGGWLTIKRILKCHPFHPGGVDPVPEKKQKH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
O35003
|
T1214_ARCFU
|
Probable transposase for insertion sequence element ISA1214
|
MNLGFRVTGKFVRELLDVLDEIAEEIRQEEKEKYPYTEWERKREVVKERLRKLPEYVREAISVITVQKRVGRPKKVDLEKRVMLFLFARLMDKSNRDIEELLELFEPLFGIKVSYKTIERLYSDEEVRMALHNLFILLLREEGVSGDFSGDGTGYSLTITKHYRSNPKRKGKDFRYVFRIIDIDTGMYVGFGYSDRSEKDAFEKALGMLKSMGVKVNSISLDKYYSSRKTLRLFDAETAVYVIPKRNLARIGFDWLRVIERIVEAPYRFLKRYFKRNLSEAGFSADKRRFGWLIRQRREDRREMALFAVGLWHNVFAVRVVR
|
Involved in the transposition of the insertion sequence ISA1214.
|
O36639
|
MVP_CMVAS
|
Movement protein (MP) (Protein 3A)
|
MAFQGTSRTLTQQSSAATSDELQKILFSPEAIKKMAAECDLGRHHWMRADNAISVRPLVPEVTHGRIASFFKSGYDAGELCSKGCVSVPQVLCAVTRTVSTDAEGSLRIYLPDLGDKELSPIDKQCVTLHNHHLPALVSFQPTYDCPMETVGNRKRCFAVVIERHGYIGYTGTTASVCSNWQARFSSKNNNYTHIAAGKTLVLPFNRLAEQTKPSAVARLLKSQLNNMGSSQYVLTDSKINQNARSESEELNVESPPAAIGSSVASRFESFRPQVVNGL
|
Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier. Acts by forming a tubular structure at the host plasmodesmata, enlarging it enough to allow free passage of virion capsids (By similarity).
|
O40979
|
MVP_CMVNT
|
Movement protein (MP) (Protein 3A)
|
MAFQGTSRTLTQQSSAATSDELQKILFSPEAIKKMATECDLGRHHWMRADNAISVRPLVPEVTHGRIASFFKSGYDAGELSSKGYMSVPQVLCAVTRTVSTDAEGSLRIYLADLGDKELSPIDGQCVTLHNHDLPALVSFQPTYDCPMETVGNRKRCFAVVIERHGYIGYTGTTASVCSNWQARFSSKNNNYTHIAAGKTLVLPFNRLAEQTKPSAVARLLKSQLNNIESSQYVLTNAKINQNARSESEELNVESPPIAIGSSSASRSETFRPQVVNGTLVFS
|
Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier. Acts by forming a tubular structure at the host plasmodesmata, enlarging it enough to allow free passage of virion capsids (By similarity).
|
O40982
|
MVP_CMVC7
|
Movement protein (MP) (Protein 3A)
|
MAFQGTSRTLTQQSSAATSDELQKILFSPDAIKKMATECDLGRHHWMRADNAISVRPLVPEVTHGSIASFFKSGYDAGELRSKGYMSVPQVLCAVTRTVSTDAEGSLRIYLADLGDKELSPIDGQCVSLHNHDLPALVSFQPTYDCPMETIGNRKRCFAVVIERHGYIGYTGTTASVCSNWQARFSSKNNNYTHIAAGKTLVLPFNRLAEQTKPSAVARLLKSQLNNIESSQYVLSKAKINQNARSESEELNVESPSFAIGSSSASRSEAFRPQVVNGL
|
Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier. Acts by forming a tubular structure at the host plasmodesmata, enlarging it enough to allow free passage of virion capsids (By similarity).
|
O41253
|
VP7_RRSVT
|
Microtubule-associated protein VP7
|
MDELTLSIGGSPGKLAGTQLLYKQKIDKEIRLSPTDLLFSSNTVDHKLRNKRTTIALLSREVQARLGKWMISFADQKGTAADFGLQLAKWVQASTQLHYYVHPADMSALRAADQSLIRQLPRVTVEVCKTKKVSQTDPIEHKYQSRPGMIEGGVTITPRQAVTLEEIYPLASRPEKGVIMFMLSQAHLEHLIHPVIKQVSNYFTCVKVGTSGFSLNYNHPYIRAMFLEPITACDVVELPLQALHARFSAGKGHLYLCGDGHAPRTLTCAQMFDIPHVHDFTMPSVTVVSFYAPEQHIAIARYASWYEKDTICRLLQSTLPDVEKLVWLCAMSYPIFPSLRPTLTGSIFSRCKVVVSVSAERSRLLSDGLPKWAEWVDNVLSDRIAKPACLILIGPKASSKSFVTRQLVAKLNASSLSVEGDNFGRVDSDAFGKWVTMMVSNSTLPTSWAQFDLMQNDKEIASYVDIRFNDICVKHGFCELDDLRTKNAGVLQGEFARSFIEIIKDPSCGLRAFFSWLFSLYGLPRGLMLESHTNVEIAEYPPTTCILQLLPNYDVMSVLLERDARKGISKLAEMQMEEYYNGLRIGTYRSVLACELLRVAEVGPPVEG
|
Minor inner capsid component. Displays NTPase and RNA 5'-triphosphatase (RTPase) activities. May function as a cofactor of polymerase. Associates with microtubules and plays a role in the formation, structural organization and morphology of viral inclusions, where the assembly of cores and the replication of viral RNA occur (By similarity).
|
O41518
|
CAPSD_GLRV3
|
Capsid protein (CP) (Coat protein)
|
MAFELKLGQIYEVVPENNLRVRVGDAAQGKFSKASFLKYVKDGTQAELTGIAVVPEKYVFATAALATAAQEPPRQPPAQVAEPQETDIGVVPESETLTPNKLVFEKDPDKFLKTMGKGIALDLAGVTHKPKVINEPGKVSVEVAMKINAALMELCKKVMGADDAATKTEFFLYVMQIACTFFTSSSTEFKEFDYIETDDGKKIYAVWVYDCIKQAAASTGYENPVRQYLAYFTPTFITATLNGKLVMNEKVMAQHGVPPKFFPYTIDCVRPTYDLFNNDAILAWNLARQQAFRNKTVTADNTLHNVFQLLQKK
|
Capsid protein self-assembles to form filamentous capsids, about 1400-2200 nm in length.
|
O41519
|
CPM_GLRV3
|
Minor capsid protein (CPm)
|
MGAYTHVDFHESRLLKDKQDYLSFKSADEAPPDPPGYVRPDSYVRAYLIQRADFPNTQSLSVTLSIASNKLASGLMGSDAVSSSFMLMNDVGDYFECGVCHNKPYLGREVIFCRKYIGGRGVEITTGKNYTSNNWNEASYVIQVNVVDGLAQTTVNSTYTQTDVSGLPKNWTRIYKITKIVSVDQNLYPGCFSDSKLGVMRIRSLLVSPVRIFFRDILLKPLKKSFNARIEDVLNIDDTSLLVPSPVVPESTGGVGPSEQLDVVALTSDVTELINTRGQGKICFPDSVLSINEADIYDERYLPITEALQINARLRRLVLSKGGSQTPRDMGNMIVAMIQLFVLYSTVKNISVKDGYRVETELGQKRVYLSYSEVREAILGGKYGASPTNTVRSFMRYFAHTTITLLIEKKIQPACTALAKHGVPKRFTPYCFDFALLDNRYYPADVLKANAMACAIAIKSANLRRKGSETYNILESI
|
Minor capsid protein that encapsidates the 5'-terminal portion of the viral genome.
|
O42047
|
M22_HRSVB
|
Protein M2-2
|
MTKPKIMILPDKYPCSISSILISSESMIATFNHKNILQFNHNHLDNHQRLLNNIFDEIHWTPKNLLDATQQFLQHLNIPEDIYTIYILVS
|
Mediates the regulatory switch from transcription to RNA replication. Acts late in infection by inhibiting viral transcription and up-regulating RNA replication. Inhibition of transcription by protein M2-2 requires phosphorylation of the phosphoprotein.
|
O48429
|
REGQ_BPH19
|
Antitermination protein Q
|
MRDIRQVLERWGAWAANNHEDVTWSPIAAGFKGLIPEKVKSRPQCCDDDAMIICGCMARLNRNNSDLHDLLVDYYVLGETFMALARKHGCSDTCIGKRLHKAEGIVEGMLMMLGVRLEMDRYVERELPGGRTSVFYQRKNSLRS
|
Positively regulates expression of some phage genes. Bacterial host RNA polymerase modified by antitermination proteins transcribes through termination sites that otherwise prevent expression of the regulated genes (By similarity).
|
O50638
|
YIDD_LEPIN
|
Putative membrane protein insertion efficiency factor
|
MNRFVIQLIQLYKRLLSPLLPPACRFTPTCSEYAAQAFQEYGFFRALQLSIWRILRCNPLSRGFDDPLPPNTKG
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
O51168
|
YIDD_BORBU
|
Putative membrane protein insertion efficiency factor
|
MNIFKILFILNYALIFLIKIYQNTLSKIFGLQCIYKPTCSKYSIECLKKYNFLTALILMTLRIIRCNALFKGGNDFTPKYKPILESLKEFKKRLIK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
O52163
|
HRCA_STRAL
|
Heat-inducible transcription repressor HrcA
|
MLSERRLEVLRAIVQDYVGTEEPVGSKALTERHRLGVSPATVRNDMAALEDEGYIAQPHTSAGPIPTDKGYRLFVDRLADVKPMTAPERRAIHHFLDQAVDLDDVVARTVRLLAHVTRQVAVVQYPSLTRSTVRHVELLSMAPARLMLVLITDTGRVEQRMIDCPAPFGESSVADLRARLNSQVAGRRFADVPQLVQDLPESFESEDRPTVSTVLSTLLETLVEETEERLMIGGTANLTRFGHDFPLTIRPVLEALEEQVVLLKLLGEAKDSAMTVRIGHENAHEGLSSTSVVSVGYGSGREAVAKLGVVGPTRMDYPGTMGAVRAVARYVGQILAES
|
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}.
|
O53334
|
Y3188_MYCTU
|
Probable mycobacterial cidal antitoxin Rv3188
|
MAVTLDRAVEASEIVDALKPFGVTQVDVAAVIQVSDRAVRGWRTGDIRPERYDRLAQLRDLVLLLSDSLTPRGVGQWLHAKNRLLDGQRPVDLLAKDRYEDVRSAAESFIDGAYV
|
Probable antitoxin component of a type II toxin-antitoxin (TA) system. Neutralizes the activity of cognate toxin Rv3189 by blocking access to the toxin active site.
|
O53464
|
VPB45_MYCTU
|
Putative antitoxin VapB45
|
MAGDQELELRFDVPLYTLAEASRYLVVPRATLATWADGYERRPANAPAVQGQPIITALPHPTGSHARLPFVGIAEAYVLNAFRRAGVPMQRIRPSLDWLIKNVGPHALASQDLCTDGAEVLWRFAERSGEGSPDDLVVRGLIVPRSGQYVFKEIVEHYLQQISFADDNLASMIRLPQYGDANVVLDPRRGYGQPVFDGSGVRVADVLGPLRAGATFQAVADDYGVTPDQLRDALDAIAA
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC45.
|
O53465
|
VPC45_MYCTU
|
Putative ribonuclease VapC45 (RNase VapC45) (EC 3.1.-.-) (Toxin VapC45)
|
MQPDRNLLADLDHIFVDRSLGAVQVPQLLRDAGFRLTTMREHYGETQAQSVSDHKWIAMTAECGWIGFHKDANIRRNAVERRTVLDTGARLFCVPRADILAEQVAARYIASLAAIARAARFPGPFIYTVHPSKIVRVL
|
Toxic component of a type II toxin-antitoxin (TA) system. An RNase. The cognate antitoxin is VapB45.
|
O53468
|
HIGB2_MYCTU
|
Putative toxin HigB2
|
MNVPWENAHGGALYCLIRGDEFSAWHRLLFQRPGCAESVLACRHFLDGSPVARCSYPEEYHPCVISRIALLCDSVGWTADVERISAWLNGLDRETYELVFAAIEVLEEEGPALGCPLVDTVRGSRHKNMKELRPGSQGRSEVRILFAFDPARQAIMLAAGNKAGRWTQWYDEKIKAADEMFAEHLAQFEDTKPKRRKRKKG
|
Putative toxic component of a type II toxin-antitoxin (TA) system. Its cognate antitoxin would be HigA2.
|
O57243
|
PROF_VACCA
|
Profilin
|
MAEWHKIIEDISKNNKFEDAAIVDYKTTKNVLAAIPNRTFAKINPLITNRNILKPLIGQKYCIVYTNSLMDENTYAMELLTGYAPVSPIVIARTHTALIFLMGKPTTSRRDVYRTCRDHATRVRATGN
|
More likely to influence phosphoinositide metabolism than actin assembly.
|
O59961
|
PT494_SACBA
|
COX3 mRNA-specific translational activator PET494
|
MHLKKGKRSIGTVWRLLWKRLYSVHYKTNTYSTRSRKKLVTNFTRVNGLLLSCNGDTFPYMRTLWRYFNAPGNLMFVTTNIITFTGIVAYNTMVTVSNERVFEEQMIAAQMSLAKQKEELETRALDFPANHEQIKEADDANCEQPAIERSGEDRSVKQQNEQLDSPIRHYSLTDLVLNKEARVADYDSQRVKASLFHMLYAYMLYRDTIQPNSDSPNHNSEEWRHEVELLTRDKWLQGAHQRIDVFYDLWNNQLDKIVTSPEKVQNFHLPNWSKYPTLLKFICTELHNNELTTLDEFKQFYGKVRSNEVKKLLGLWLYDHSFLFPRNIYDNKNQEVFYDTLISDSMQDNKIFQKYSSIVMNPDNERTQLFFPNIYAQPVNKPIPSISLETYTRLLRGYITLQETNCKYDYNDNIFKLISILKMNCFLQHDKKIRTGASVRILLPRDEDRSPVLNTIPQAEKKTCYQILSKNRDILALLKRISDIQIDSS
|
Required for the expression of the mitochondrial gene for cytochrome c oxidase subunit III (COX3).
|
O64039
|
BHLA_BPSPB
|
Protein bhlA
|
MEMDITQYLSTQGPFAVLFCWLLFYVMKTSKERESKLYNQIDSQNEVLGKFSEKYDVVIEKLDKIEQNFK
|
May be involved in the secretion of the autolysin blyA.
|
O64228
|
VG341_BPMD2
|
Gene 34.1 protein (Gp34.1)
|
MKILSRDKVALKVATAGTVAVGGLAFSLSFTALSELSAANGVAQSWMVPLVIDGGILVATMATVALSRHGWYAWALLILSSLMSVAGNVAHAQPHGLIAMVIAAIPPLWLLASTHLTVLLYREAQESGSESISEPLLTRGFAEAA
|
Putative excisionase.
|
O64321
|
DECO7_BPN15
|
Putative decoration protein (Gene product 7) (gp7)
|
MAITEVFTHKQPLGNSDPAHTAYGPGELTASTPAMTPLMLDATSGKLTVWDGAHAGAATGILAVTADQNSAELAFYKSGSFRIEDVLWPSAVTDENIKRNAFAGTAISIV
|
Putative decoration protein.
|
O66562
|
YIDD_AQUAE
|
Putative membrane protein insertion efficiency factor
|
MKSIVLIFLKFWQKFISPLYPSSCRYYPTCSTYAIMAVEKYGVLKGLIKAFFRVLRCNPFFKGGVDYP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
O66631
|
PLPHP_AQUAE
|
Pyridoxal phosphate homeostasis protein (PLP homeostasis protein)
|
MNACERLSRVLERIQKACERAGRGENCAKLLGASKTVPPEVIREFYNCGLKVYGENRVQEFLKKYEALKDLDLEWHFIGRLQTNKVKYLMGKVVLIHSLDRKNLADEIQKRAFKNNIVQDVLIEVNVGGEETKGGVEPENLKELFEYTLELPNVKVLGLMTIPPYLENPEDVRPYFRKLRELRDELQREYNVALPHLSMGMSHDFEVAIEEGATIVRIGTLLFGERKY
|
Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis. {ECO:0000255|HAMAP-Rule:MF_02087}.
|
O69266
|
HRCA_LYSSH
|
Heat-inducible transcription repressor HrcA
|
MLTNRQLQILQVIIDDFILSAQPVGSRQISKKQGITFSPATIRNEMADLEELGYLEKTHTSSGRVPSEKGYRFYVDHLLSPQGINSRDIQQIQSIFNDRLVEVEHIIRKSANILSELTSYTSILLGPDVQRHRVKRFSIVPLSSDTAVAIIVTNNGHVENRLFNLPPDFTASDLEKMVNILNDRLIGVSLEELHKSLEAEVLAVLQQHVQSADDFYPRTRNSDNAIIQKAKIFYGGKTNMFNQPEFHDLNKVRMILDLMETTSQVQSLFHPNESGIHIRIGSENKQLEMENCSVITTTYSIGDDQQGAIAIIGPTRMDYKRVVALLDVIRLDLTQAFTKNRSE
|
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}.
|
O69272
|
NRDI_CORAM
|
Protein NrdI
|
MLVVYSSSVTDNTHRFVQKLDLPNVRIPLRLKDEPLIVNEPYVLVCPTYGGGVSLTGENSRPVPRQVIRFLNNEHNRSFIRAVVAGGNSNFGADFGKAGEVISAKCKVPYVYRFEMMGNEDDVRICRGGLVQNAAKLGLEKQAS
|
Probably involved in ribonucleotide reductase function.
|
O69717
|
VPB50_MYCTU
|
Putative antitoxin VapB50
|
MTSLLEVLGAPEVSVCGNAGQPMTLPEPVRDALYNVVLALSQGKGISLVPRHLKLTTQEAADLLNISRPTLVRLLEDGRIPFEKPGRHRRVSLDALLEYQQETRSNRRAALGELSRDALGELQAALAEKK
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC50.
|
O73571
|
MVP_SBMVA
|
Movement protein P1 (Cell-to-cell transport protein)
|
MSYRFLTVRAFGFTGFHCDATRLLSETEVIDVPSSLDFVGETELRLETAWPQCEENCYTILPRFNVQVDFEYYPVRVEIVCRVCAASLSVIFSKWDFYCSRRGHFVPVDQNGDLFRIGTLQETGEKYFYFCDKSICRQCIIQAAHHHS
|
Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier (Potential). Likely acts as a suppressor of RNA-mediated gene silencing, also known as post-transcriptional gene silencing (PTGS), a mechanism of plant viral defense that performs sequence-specific inhibition of viral mRNAs expression (By similarity). {ECO:0000250, ECO:0000305}.
|
O74000
|
Y106A_PYRHO
|
Putative antitoxin PH1062.1
|
MSKTITIADDVYYELVKMKGKRSFSEVLRELIGKKKEGNLDVLMIAFGTMDEEEAKELEEKIKEVGKWLNSWTPV
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. {ECO:0000255|HAMAP-Rule:MF_00794}.
|
O74104
|
BRIX_PYRHO
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MMLITTSHRPTRRTRSFGHDLERVIPNSLYLTRGKKTIQELLMEAYDRGYERLLIINVWKGNPLKMTFIKVHPEDWGYLGYLYLHGVKLQREMGFKGLNPIREDMPLVITTAKRVGLDHLAFAQVFSELTTGKFVPRGDKSLLSIADRYNTDVLAVIERHPRGIVINFYRLDITKDRPVGPLINVKIWIMEDGRRWDYKEAFGIKVPPRRREFEGKRGEGKNSD
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
O74703
|
TDF1_TUBDR
|
11.9 kDa wall protein
|
MSFKTRAVAESTYYIKSGAYYLAVTPERQIITQNTVYAWEVSIEGEYNYLKDPGTTHYLTDNGGQNLLNPRSDVDGKWGGGSEDQATQLINAETEKPLSVPYGQPFQTWLFVKV
|
May play a role in the structure of the hypha-forming fruit bodies.
|
O80644
|
ACR9_ARATH
|
ACT domain-containing protein ACR9 (Protein ACT DOMAIN REPEATS 9)
|
MGILNDDAVLIEPGKISGDPTVVTVNCPDESGLGSTLCRIILEFGLSITRADFSTDGRWCYIVFWVTPDISSPKIDWDSLKNRLLSACPSCLGSFYFCLQSNVSKPPSLYLLKFFCRDRKGLLHDVTKVLTELEFTIQRVKVMTTPDGRVLDMFFITDAMDLLHTKQRQTKTCDHLTAVLGEHGVSCELELAGPELESVQRFSSLPPLAADELFGPDGFDISGSSSNKAVLTVDNQLSPAHTLLQIRCVDQKGLFYDILRTSKDCDVHIAYGRFSSKVKGYRNLELFVRGTDGNKIMDPKHQANFCARLKEEMVCPLRVIIVNRGPDTELLVANPVELSGKGRPRVFYDVTLALKSLGICIFSAEIGRHSTLDRQWEVYRFLLDESREFPLASLRARNQVVDRVTKTLMGW
|
May bind amino acids.
|
O84479
|
YIDD_CHLTR
|
Putative membrane protein insertion efficiency factor
|
MQTSRISSFFRGLVHLYRWAISPFLGAPCRFFPTCSEYALVALKKHPLRKSLFLIAKRLLKCGPWCIGGIDLVPRTSVEEYLSSPTPLAESPDDRTVPHTQETS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
O85060
|
REPA1_BUCAP
|
Probable replication-associated protein repA1
|
MSSRENYVYNRNPVFTAPKNNKRRPSFICYAMKKASEIDVARCELNYVIQPKNIKTGLPLKRFRRLNEHRACALRAMVSAMLYHFNISSELVQASVEQLSDECGLSTLSKVGNKSITRASRLITNFMEPMGFVTCKKIWDRVLGNYMPKMITLTPLFFMLLDISEKQLINAKKQQLGWINKNLITKGLKPITVIEAKRRAKDIQMRNLFKYRISKHNFYKKRKNAQRLIALDEKEARQKILRALVAKYSISELTTLGPSGLKKQVNISYYYLKKIATNRYPDN
|
This protein is essential for plasmid replication it is involved in copy control functions.
|
O85062
|
REPA2_BUCAP
|
Probable replication-associated protein repA2
|
MPRKNYICNLKPVFNPPKNEKKRSNFIDYAMKKASEIDVARSKLNYTLLAIDPKTGNILPRFRRLNEHRACAMRAIVLAMLYYWNTNSNLVEASIEKLSDECGLSTFSNSGNKSITRASRLITDFMEPMGFIKCKRKKTQSSSNYIPKKIFLTSNFFMLFHISQSTINQYLSEQKQSIKNLKKEKKIFISFSDIRVISKLDEKAARNKILNALIKYYSASELTKIGPQGLKKKIDIEYSNLCKLYKKNNK
|
This protein is essential for plasmid replication it is involved in copy control functions.
|
O87775
|
HRCA_LATSK
|
Heat-inducible transcription repressor HrcA
|
MLTERQLMILKEIIRLFTESGQPVGSKKLMSELPMHVSSATIRNDMADLENVGLIEKTHSSSGRVPSMKGYRYYLDHLIQPAVLNPMDVATVQQSFGRHYHKIDEIVSQSANILSNLTSYTAITLGPEMAEIRLTGFRLVPLGNHQVMAIIVTSAGTVDNQVFTIPNAISGDELEKAIRVVNDHLIGLPLTVVSQKLKTEVPALLMQYMGSPGGFLNIFDDVLKQASQERLYVGGQSNLLNFSELTDVSQLKSIYNIINQSDDLAKLLELSPGEANSQVQVRLGDEMTNDLLKNYSLMTVNYDVGEHGQGLIALLGPTSMPHSRMIGLLDLFREELAKKLIDYYADFDDNQS
|
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}.
|
O92404
|
LEF11_NPVBM
|
Late expression factor 11
|
MPPKNCTHLGGCNSDCLTRSEIQALFREAINTLKHTMNTEDVCAHMLDIVSFERIKEYIRANLGHFTVITDKCSKRKVCLHHKRIARLLGIKKIYHQEYKRVVSKVYKNQTW
|
Involved in late/very late gene activation.
|
O96566
|
A37C_DROSI
|
Protein anon-37Cs
|
FKLASRRRLYNARVLQADNIGDKQRNPDVDAARQNTQIVVVGAGLPGLSAAQHLLYNGFRRTVILEATDRYGGRINTQRFGDTYCELGAKWVKIDGSQDSMYELLRNTEGLDKQIKQPDRATYLQDGSHINPAMVELIDTLFRQLCRGFKVSERVKTGGDLHSLDNVMNYFRTESDRIIGTSFQQPKDQLAAREIFQSLFKEFGSILGCCLEYVNIEHITKCPVQQELRPLYVPTGLDNVVDDLIQNMDKAQLQTGKPVGQIQWTPAPMKSVGCLDGSLYNADHIICTLPLGVLKSFAGVLFRPTLPLDKMLAIRNLGFGNPLKIYLSYKKPIGRWLKGSLRPLGTLLNPSAEQQPERNWTQQVVEISQVPSSQHVLEVHVGGGYYEEIEKLPDDELLEQITGLLRRCVSNNLVPYPQELLRSNWSTSACYLGGRPYFSTINSARDVQRLAAPLGEKSPGLLFAGDATSLNGFGTIDAARSSGIREAQRIIDFYLKRAHFG
|
Has a non-vital function.
|
O96570
|
A37C_DROLE
|
Protein anon-37Cs
|
MVHPQLKRSIESLSFSGYKLTRRNLYNAPALKVMGRSVNNSSSNNNDQQQYNLESAKQNTQIVVIGAGLAGLSAAQHLLRHGFRSTIVLEATDRYGGRVNSKRFGDTYCELGAKWVNMNIDGAHNTIYELLRNAEGLRKQLKQRECANYVHTQGREVPPNMVELIDMQFRQLCRGFKVSEKVKSGGDLHVLDNVMAYFKTESEKLVGHSYPDPEKRALAREIFQSLFKEFSSILGCCLEYVNIEHITSCPVQQELRPLYVPTGLDNVLDTLTQHISKEQLQTGKPVGSIQWQTLSDFGAPTSPLPQERKCVACLDGTLYSADHIICTLPLGVLKNFSAILFKPALPLEKLQAIRNLGYGNPVKIYLAYKRPISRWLKSNLRPLGAQLGKDEPAITVNGRQERLWTQQVVEISQLPSSQHVLEIRVGGGYYDEIEKLPDVTLLEQITALLRQCLRNRLVPYPQALLRSNWSTSACYLGGRPYFSTTSSARDVQRLAEPLGDIAPTLLFAGDATALKGFGTIDGARTSGIREAQRIIDYYYLKQYM
|
Has a non-vital function.
|
P01158
|
DSIP_RABIT
|
Delta sleep-inducing peptide (DSIP)
|
WAGGDASGE
|
When infused into the mesodiencephalic ventricle of recipient rabbits induces spindle and delta EEG activity and reduced motor activities.
|
P01547
|
FULC_MYXFU
|
Bacteriocin fulvocin-C
|
ANCSCSTASDYCPILTFCTTGTACSYTPTGCGTGWVYCACNGNFY
|
Bacteriocin.
|
P03037
|
RANT_BPP22
|
Antirepressor protein ant
|
MNSIAILEAVNTSYVPFNGQHVLTAMVAGVAYVAMKPVVDNIGLSWSSQVQKLLKMKDKFNYVDIDMVAGDMKKRLMGCIPLKKLNGWLFSINPEKVRADIRDKLIKYQEECFTVLYDYWTKGKAENPRKKTSVDERTPLRDAVNMLVSKKHLMYPEAYAMIHQRFNVESIEELEASQIPLAVEYIHRVVLEGEFIGKQEKKTNDLSAKEANSLVWLWDYANRSQALFRELYPAMRQIQSNYSGKCYDYGHEFSYIIGIARDVLINHTRDVDINEPDGPTNLSAWMRLKDKELPPSLHRY
|
This protein prevents the prophage P22 c2 repressor protein from binding to its operators and also inhibits the action of other prophage repressor proteins, including those of phages lambda and 434. The synthesis of antirepressor is negatively regulated by the protein products of the two other immI genes, mnt and arc.
|
P03596
|
MVP_AMVST
|
Movement protein (MP) (Protein 3A)
|
MENTKTNASSSGMFSSSSFSVSYAEEMLLADEVSKINSMSILGPNQLKLCTQLVLSNGAAPVVLSLVSKEKKSISNRMLPKIGQRMYVHHSAIYLLYMPNILKSSSGSITLKLFNEATEELVDVDTDHDATQACIFAGRYPRSILAKDAAKGHDLKLVVHAVASTKANSAVGVLYPIWEDELSRKQILERGADFLKFPIAETEPVRDLLNAGKLTNFVLDRTRLGVGSKSDPSPVLLEPRAKITGKAKTFFIPEGPSVPNTTISGIAPSVRIDAGSPKGLGVPKGFTYESFIKDEILPDH
|
Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier. Acts by forming a tubular structure at the host plasmodesmata, enlarging it enough to allow free passage of virion capsids (By similarity).
|
P03597
|
MVP_TOBSV
|
Movement protein (MP) (Protein 3A)
|
MALAPTMKALTFSADDETSLEKAVTEALSGSVDLNMGLRRCAAFPAENTGAFLCELTTKETKSFIGKFSDKVRGRVFIDHAVIHMMYIPVILNTTHAIAELKLKNLATGDELYGGTKVNLNKAFILTMTWPRSLFAEAVHNHKGLYLGGTVSCASSVPAHAKIGMWYPIWSEKVSIKQLYQNTIDIHKTEAIETFTPTMISSDKEMRSLLRSRASIDVAAKTREKPVICSERVSLLDQHTQGVDFTVTEIEPEKDDDAGTSILGPKMVPIEQVPSVKLSSEAGRNLLTA
|
Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier. Acts by forming a tubular structure at the host plasmodesmata, enlarging it enough to allow free passage of virion capsids (By similarity).
|
P03636
|
VGC_BPG4
|
C protein
|
MRKFNLNLKNSRSSYFATFRHHLNVLAKTDALDEEKYLNMLGALLKDWFRYEEHFVHGKQSMLDILKERGLLSTSSTDTNHKGN
|
C protein is one of the proteins involved in the production and packaging of viral single-stranded DNA.
|
P03654
|
VGK_BPG4
|
K protein
|
MKPKTTLLLQELLLLTYELNRSGLLVENEEIQSQLKKLEVVLLCNLSPSSQRAGKN
|
No function has yet been ascribed to K protein.
|
P03723
|
GP13_BPT7
|
Probable scaffold protein gp13 (Gene product 13) (Gp13)
|
MMTIRPTKSTDFEVFTPAHHDILEAKAAGIEPSFPDASECVTLSLYGFPLAIGGNCGDQCWFVTSDQVWRLSGKAKRKFRKLIMEYRDKMLEKYDTLWNYVWVGNTSHIRFLKTIGAVFHEEYTRDGQFQLFTITKGG
|
May act as an organizer for the correct association of several proteins in the surrounding of the head-tail connector protein gp8.
|
P03839
|
YT93_ECOLX
|
Uncharacterized 12.7 kDa protein in transposon Tn903
|
MCFTVNGEMQLTPDTAAFLAMLFDFPFAFTKDLQPGGINHQMRDFTPGERFETDINRLCPPADTAVIRAAQRNIHQCKNGINKALRSAQGQPEYAFNDQHSRDGKVRIALRSAS
|
May be associated with transposition functions of transposon Tn903.
|
P03865
|
RLX2_STAAU
|
Protein rlx
|
MATTKLGNTKSASRAINYAEKRAEEKSGLNCDVDYAKSAFKQTRALYGKEDGIQAHTVIQSFKPGEVTPEQCNQLGLELAEKIAPNHQVAVYTHTDKDHYHNHIVINSVDLETGKKYQSNKKQRDLVKKENDNICREHGLSVTERGIAKMRYTQAEKGIVFDRDEYSWKDELRDLIENAKTHTSNLETFSEHLEEKGVGVKLRGETISYKPENENKWVRGRTLGSEYEKGAIDHEHERHQKQQREPEYADEFKINWDAVEQHTEQLKQRRVERAQETKQAHSKISSRDTRESENQRERAKGNNIRIERGDEGLSR
|
This protein is probably required for relaxation complex formation and plasmid mobilization by conjugative plasmids.
|
P05137
|
NS3A_IBVM
|
Non-structural protein 3a (ns3a) (Accessory protein 3a)
|
MIQSPTSFLIVLILLWCKLVLSCFREFIIALQQLIQVLLQIINSNLQPRLTLCHSLD
|
Involved in resistance to IFN.
|
P05463
|
VEPS_BPP4
|
Derepression protein
|
MRNKKAPQTVSARHDAREHLSIEAYHKLNRASAVSRFVGGDLIHRELSGLHQLYIPHIFSYLNEDIDFVLNELKAKGLCRDFLAQQKDRGDRTHV
|
Required for derepression (induction) of the P2 prophage helper by P4.
|
P05467
|
YKP1_KLULA
|
Uncharacterized killer plasmid pGKl-2 protein 1
|
MSYIDYLAYTGNTTFYDRFDGDLTSEHRIKCIINGCLINIMFSIRTIKEFPEEIKICQAAVSKFLTCGYVNDYLIEKYPPFYLWHKRFCDYDIYKMLMEKHPKLNYTVAKAAIMQRYNDLYFSFDFQPEEELIMTAALTENTEIYEDQINKAKKLGYCYSYLDYDNYCIKEEPGIEEIPDIEPKFNPFYVYVESGSKMEDVEYAVVNLVEEFKYLQMVYDMSKI
|
The presence of the two linear plasmids, termed pGKL1 and pGKL2, in strains of Kluyveromyces lactis confers the killer phenotype to the host cell, by promoting the secretion of a toxin able to inhibit the growth of sensitive strains.
|
P05469
|
YKP3_KLULA
|
Uncharacterized killer plasmid pGKl-2 protein 3
|
MSGSFRSNFSIASIHLRLYETIKSQSRIILLFCRGMFKRFAKYKSNLESAMVDVELEARIQIPKPTNIIFEDETVITYYRSTMYPSLIFRRINNGKLNSKETVEKIKYGEVTICLSIEQTYSNMDIKFPIIPANKRTISRKRICENPIVDITKCGDQYTLEIEFDYSNYMHIEKILKEWKNPYWPPVKPMEISSSNLAKKLANNEQWCISPKADGIHVLVYSDGENQFIVHTNGYTEGDTNIKVNRIFEGELMSNGEILYFDCLMWENKNITKLDYIARYKYLENMNKKEIILFNNIYAIKKYLDKKHDFETDGYIITNIKNRKKVYKSKFKNTVDLRYKNGYLLLENEEFSERSPKNVNEQLEEDKIYEFDMEMNLIRERKDKTIANYKMPYDDNPIYKIAHSIGVPTLRYYHNKIKRELLSMLPKTTLLDIGSAKGGDITKWTNLKFEKVYAVDPNLELRQRSKKVVEIRENIEDVYKMFDYESVSLFFVPWNDKFMDVINKAKYFVLICMDKPVTVKEDCFECKIENEKVILKIPDTQTSEYVEENLIKYTDVFKKLKNWKHMKINRTMNTGSAQEIELSRMYSYHFFSKK
|
The presence of the two linear plasmids, termed pGKL1 and pGKL2, in strains of Kluyveromyces lactis confers the killer phenotype to the host cell, by promoting the secretion of a toxin able to inhibit the growth of sensitive strains.
|
P05471
|
YKP5_KLULA
|
Uncharacterized killer plasmid pGKl-2 protein 5
|
MIYDKIDTKLIKLGKTNKFSGEEEKSITSLYYEDESFEFSFKNKYVKITKIETNAYGKKFVTIKSKLYADIVEKVAKELDAVSPILSDGSFRATINDATSFSKDVGEYSFYACVSLYFPSIYKDTEKTTLQVYLKEVVVTKIIKNNLEVEFDKLSLAI
|
The presence of the two linear plasmids, termed pGKL1 and pGKL2, in strains of Kluyveromyces lactis confers the killer phenotype to the host cell, by promoting the secretion of a toxin able to inhibit the growth of sensitive strains.
|
P05473
|
YKP7_KLULA
|
Uncharacterized killer plasmid pGKl-2 protein 7
|
MNENIISNLNYFSEITQRTLSAFHFSGTDSTLEDEVEELKRFVSKNRFKKLIKIDILDDNRYCRHFSDGSKDIVDEEDINTKVAYDKNELFEVIDRALSKDISPIMSIKLSRNIQLVENKKIENPSEKIFFL
|
The presence of the two linear plasmids, termed pGKL1 and pGKL2, in strains of Kluyveromyces lactis confers the killer phenotype to the host cell, by promoting the secretion of a toxin able to inhibit the growth of sensitive strains.
|
P05474
|
YKP8_KLULA
|
Uncharacterized killer plasmid pGKl-2 protein 8
|
MLLYLNSTLCSIISIMYKITNVSFVEYYSNNVSKDVIYSYLMNSTCSNKGTIKLNLESGKRLKQEGPYILPPIRWLDSFEKNAEFTILCEVDDIK
|
The presence of the two linear plasmids, termed pGKL1 and pGKL2, in strains of Kluyveromyces lactis confers the killer phenotype to the host cell, by promoting the secretion of a toxin able to inhibit the growth of sensitive strains.
|
P05475
|
YKP9_KLULA
|
Uncharacterized killer plasmid pGKl-2 protein 9
|
MEIIEHKVEFKYKSIDEYQWTDNFKLDKQWEILRFKKNKIVQKSYMNRFPYSEPKKDYSIALYSKNKWYCLKDGVGSYISIQKEKPQIKDLTITEIKYEPYLVIYKLDFEYHIMMTILHCDERVKLLEYKRPFLKEGIILFNEMKIYVYNGLFSYKGNKIEDFELFVNEFNSQYKENYDRLFKIFGKSNHTHKSIDYKTWCKAKRENQQEWPLFTNIKIKDSIEFPNNSGIYYYYPDKYVGLARRNDDNLIPLIPKIYRKNHYENKNSLLYKYVNGLPIDEEENIPYSFIKEKYKNIKYHEDEKIIEVDYNNNVVKQKDMAEYYCYNNKLIQKIEEPVKLPKIEAQILNKRNERVEVLIDNEWKNLAGNRIDGIPTLPWNYKHIIHDYNKLGRLKKGKIMDLTHIGIVNENGTDIITWPYTDDLYIGRSIETKRLITFKYQKNVEIYDKLIDM
|
The presence of the two linear plasmids, termed pGKL1 and pGKL2, in strains of Kluyveromyces lactis confers the killer phenotype to the host cell, by promoting the secretion of a toxin able to inhibit the growth of sensitive strains.
|
P05624
|
LPW_THET8
|
trp operon leader peptide
|
MALPSALWWPG
|
This protein is involved in control of the biosynthesis of tryptophan.
|
P05672
|
MVP_AMVMA
|
Movement protein (MP) (Protein 3A)
|
MENTKTNASSSGMSSSSSFSVSYAEEMLLADEVSKINSMSILGPNQLKLCTQLVLSNGAAPVVLSLVSKEKKSILNRMLPKIGQRMYVHHSAIYLLYMPNILKSSSGSITLKLFNEATGELVDVDTDHDATQACIFAGRYPRSILAKDAAKGHDLKLVVHAVASTNANSAVGVLYPIWEDELSRKQILERGADFLKFPIAETEPVRDLLNAGKLTDFVLDRTRLGVGSKNDPSPVLLEPRAKITGKAKTVFIPEGPSVPNTTINGMAPTVRIDAGSPKGLGVPKGFTYESFIKDEILPDH
|
Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier. Acts by forming a tubular structure at the host plasmodesmata, enlarging it enough to allow free passage of virion capsids (By similarity).
|
P05830
|
REPI_ECOLX
|
Regulatory protein RepI
|
MATHKPINILEAFAAAPPPLDYVLPNMVAGTVGALVSPGGAGKSMLALQLAAQIAGGPDLLEVGELPTGPVIYLPAEDPPTAIHHRLHALGAH
|
This protein is involved in regulating the plasmid copy-number. Increasing the level of this protein results in a higher plasmid copy-number.
|
P05831
|
INCB_ECOLX
|
Protein IncB
|
MTFNKISSEKGFTQVPLCLRKSKLSNLREYQNRIADIAKRSKAVLGWASTAQFGTDNQFIKDDAARAASILEAARKDPVFAGISDNATAQIATAWASALADYAAAHKSMPRPEILASCHQTLENCLIESTRNSMDATNKAMLESVAAEMMSVSDGVMRLPLFLAMILPVQLGAATADACTFIPVTRDQSDIYEVFNVAGSSFWFLCCW
|
This protein is thought to be cis acting and to contain the putative attachment site on the DNA for the cellular partition apparatus.
|
P06154
|
REGN_BPPH8
|
Probable regulatory protein N
|
MIDDIKRIDSMINALRNMKQDIKRQQKLSEINSLDLSPKQAQKRNADADWIAMEQIKRRHELHALSVELGFAERRESYAPFELTDGWHRFDHKPREPQ
|
This N protein may have, like the lambda N protein, an antitermination activity.
|
P06294
|
IGAO_GIBZA
|
Galactose oxidase inhibitor
|
AGQNTES
|
Binds one copper ion per molecule but does not bind the galactose oxidase apoenzyme. It may inactivate the enzyme by binding to its prosthetic copper group.
|
P06496
|
E312_ADE05
|
Early E3A 12.5 kDa protein
|
MLSGEAEQLRLKHLVHCRRHKCFARDSGEFCYFELPEDHIEGPAHGVRLTAQGELARSLIREFTQRPLLVERDRGPCVLTVICNCPNLGLHQDLCCHLCAEYNKYRN
|
Not yet known.
|
P06690
|
MERE_PSEAI
|
Broad mercury transporter MerE
|
MNNPERLPSETHKPITGYLWGGLAVLTCPCHLPILAVVLAGTTAGAFLGEHWVIAALGLTGLFLLSLSRALRAFRERE
|
Broad mercury transporter that mediates the transport of both CH(3)Hg(I) and Hg(II) across the membrane.
|
P07235
|
RAL_BPPH3
|
Restriction inhibitor protein ral (Antirestriction protein)
|
MTTTIDKNQWCGQFKRCNGCKLQSECMVKPEEMFPVMEDGKYVDKWAIRTTAMIARELGKQLDEDARLCSLSVFDA
|
Ral interferes with the cleavage of DNA by E.coli EcoK restriction-modification system, by modifying the activity of the host methylase. This modulation allows incoming, unmodified phages to escape the host's restriction system.
|
P07448
|
DFTS_RAT
|
Dentinal fluid transport-stimulating peptide (DFT-stimulating peptide)
|
GVIAWELQHNEPGRKDSTAG
|
This peptide stimulates the transport of dentinal fluid, which is important for the prevention of dental caries.
|
P07543
|
VIRE1_RHIRD
|
Protein virE1
|
MAIIKPHANKNRTTSPIERPESLIEEMSGSNPPIGFTSLDLAMIELEDFVHRCPLPGDNLAGQKE
|
Involved in DNA transformation controls virE2 polymerization and prevents virE2 binding to DNA.
|
P07580
|
P12_BPPH6
|
Morphogenetic protein (Protein P12)
|
MVIGLLKYLTPAVKVQMAARALGLSPAEVAAIDGTLGRVSAMPAVAVVLGGKPLSLATIASVVSDANPSATVGALMPAVQGMVSSDEGASALAKTVVGFMESDPNSDVLVQLLHKVSNLPIVGFGDTQYADPADFLAKGVFPLIRKPEVEVQAAPFTCRQCDHVDHITDVPQTSTFVHKCTSCGFVQMVHRKDVP
|
Assembly factor active in membrane morphogenesis.
|
P07716
|
V12_BPT3
|
Gene 1.2 protein
|
MMMGRIYSGNLNDYKDAVARLQEDHDVTVKMESFSYENPAKMCRSCGEVLSVFTRSGHLVASRTFEHSDSDVQINAQTAWLRKVHSELKHWK
|
This is an inhibitor of the host (E.coli) dGTP triphosphohydrolase (dGTPase). It is implicated in DNA replication.
|
P07719
|
V17_BPT3
|
Gene 1.7 protein
|
MLQHHWNKPDLEARFPVNSVVRYSGGGLKRILGMSGVVTGHSHTGLVKVRFGTQYAEVLPNNLIPLPKADVKTPNVEAPKTEVKSDVTHPNHYMLFDNVEAIEVIARSMTVEAFRGYCLGNILKYRLRAGKKSELATMDKDLKKAAFYQELFDKHRGLCYDAS
|
The function of this late gene protein is unknown.
|
P09137
|
NIFW_KLEPN
|
Nitrogenase-stabilizing/protective protein NifW
|
MMEWFYQIPGVDELRSAESFFQFFAVPYQPELLGRCSLPVLATFHRKLRAEVPLQNRLEDNDRAPWLLARRLLAESYQQQFQESGT
|
May protect the nitrogenase Fe-Mo protein from oxidative damage.
|
P09352
|
SR2A_PHYPO
|
Spherulin-2A
|
MAFQVNAHVGNRTASSHGVVERIMTDSDRRAFGLDGDNLFRAVERFRGRWPTGAWVRSPAIAGGVDLYQAYAHQGWRQVVTRLEPISSTIHHPNTDRTTVVTARLSNNSSFPGEFFANLSNETTNSATTSWSSTHGIEVGQSVSYSIGVVSGETSFGYSYQWGRGGEQTTASSVSFVTGVTVHLQPGQGVIVRLLAEQGWARITTRYRASLTGHVAQNFNPPHQGHHFWAHSVNSILQASGLPTQIFIENTVDVGFFANSHVDMQDLVTGVIVPIGTDKIFRPLALKYDEIKEDDEKFADEKEQQKGEHKKETKH
|
Structural protein.
|
P09677
|
A1_BPSP
|
Minor capsid protein A1
|
MAKLNQVTLSKIGKNGDQTLTLTPRGVNPTNGVASLSEAGAVPALEKRVTVSVAQPSRNRKNFKVQIKLQNPTACTRDACDPSVTRSAFADVTLSFTSYSTDEERALIRTELAALLADPLIVDAIDNLNPAYWAALLVASSGGGDNPSDPDVPVVPDVKPPDGTGRYKCPFACYRLGSIYEVGKEGSPDIYERGDEVSVTFDYALEDFLGNTNWRNWDQRLSDYDIANRRRCRGNGYIDLDATAMQSDDFVLSGRYGVRKVKFPGAFGSIKYLLNIQGDAWLDLSEVTAYRSYGMVIGFWTDSKSPQLPTDFTQFNSANCPVQTVIIIPSL
|
Minor capsid protein.
|
P0A0N0
|
Y749_STAAM
|
DegV domain-containing protein SAV0749
|
MKIAVMTDSTSYLSQDLIDKYNIQIAPLSVTFDDGKNFTESNEIAIEEFYNKMASSQTIPTTSQPAIGEWITKYEMLRDQGYTDIIVICLSSGISGSYQSSYQAGEMVEGVNVHAFDSKLAAMIEGCYVLRAIEMVEEGYEPQQIIDDLTNMREHTGAYLIVDDLKNLQKSGRITGAQAWVGTLLKMKPVLKFEDGKIIPEEKVRTKKRAIQTLEKKVLDIVKDFEEVTLFVINGDHFEDGQALYKKLQEDCPSGYQVAYSEFGPVVAAHLGSGGLGLGYVGRKIRLT
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0A0N1
|
Y704_STAAN
|
DegV domain-containing protein SA0704
|
MKIAVMTDSTSYLSQDLIDKYNIQIAPLSVTFDDGKNFTESNEIAIEEFYNKMASSQTIPTTSQPAIGEWITKYEMLRDQGYTDIIVICLSSGISGSYQSSYQAGEMVEGVNVHAFDSKLAAMIEGCYVLRAIEMVEEGYEPQQIIDDLTNMREHTGAYLIVDDLKNLQKSGRITGAQAWVGTLLKMKPVLKFEDGKIIPEEKVRTKKRAIQTLEKKVLDIVKDFEEVTLFVINGDHFEDGQALYKKLQEDCPSGYQVAYSEFGPVVAAHLGSGGLGLGYVGRKIRLT
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0A0N2
|
YU230_STAAU
|
DegV domain-containing protein
|
MKIAVMTDSTSYLSQDLIDKYNIQIAPLSVTFDDGKNFTESNEIAIEEFYNKMASSQTIPTTSQPAIGEWITKYEMLRDQGYTDIIVICLSSGISGSYQSSYQAGEMVEGVNVHAFDSKLAAMIEGCYVLRAIEMVEEGYEPQQIIDDLTNMREHTGAYLIVDDLKNLQKSGRITGAQAWVGTLLKMKPVLKFEDGKIIPEEKVRTKKRAIQTLEKKVLDIVKDFEEVTLFVINGDHFEDGQALYKKLQEDCPSGYQVAYSEFGPVVAAHLGSGGLGLGYVGRKIRLT
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P0A0V4
|
OHR_XANAC
|
Organic hydroperoxide resistance protein
|
MASPEKVLYTAHATATGGREGRAVSSDKALDAKLSTPRELGGAGGDGTNPEQLFAAGYAACFIGAMKAVAAQDKLKLPGEVSIDSSVGIGQIPGGFGIVVELRIAVPGMDKAELQTLVDKAHQVCPYSNATRGNIDVTLTLA
|
Organic hydroperoxide detoxification protein. Confers increased resistance to tert-butyl hydroperoxide killing (By similarity).
|
P0A145
|
NAHQ_PSEAI
|
Dibenzothiophene metabolism operon protein PahQ
|
MIKRTICLVYPLFCLASPTWAEESPWTYRIGMTNVAFDASAKVYLNGQRVPGGSADASDNNALTFDFGYAINDQWNVRAIVGIPPTTKVTGAGTLPGIQLGKITYAPTVLTLNYNLPALGPVRPHIGAGVNYTRIFESRDANLKSFDADHAWSPALHVGADIDVNRGWFVSIDIRKLYLKTDASGYLGPQEAKARVTLDPLLTSIAIGRQF
|
May be involved in the conversion of 2-hydroxy-4-(2'-oxo-3,5-cyclohexadienyl)-buta-2,4-dienoate to cis-O-hydroxybenzylidenepyruvate.
|
P0A152
|
PARB_PSEPU
|
Probable chromosome-partitioning protein ParB
|
MAVKKRGLGRGLDALLSGPSVSALEEQAVKIDQKELQHLPVELVQRGKYQPRRDMDPEALEELAHSIRNHGVMQPIVVRPIGDNRYEIIAGERRWRATQQAGLDTIPAMVREVPDEAAIAMALIENIQREDLNPLEEAMALQRLQQEFELTQQQVADAVGKSRVTVANLLRLITLPDAIKTMLAHGDLEMGHARALLGLDENRQEEGARHVVARGLTVRQTEALVRQWLSDKPDPVEPSKPDPDIARLEQRLAERLGSAVQIRHGNKGKGQLVIRYNSLDELQGVLAHIR
|
Involved in chromosome partition. Localize to both poles of the predivisional cell following completion of DNA replication. Binds to the DNA origin of replication (By similarity).
|
P0A179
|
YIDD_PSEPK
|
Putative membrane protein insertion efficiency factor
|
MRKLALVPIQFYRYAISPLMANHCRFFPSCSCYAYEAIENHGIWRGGWLAVRRLGRCHPWNDGGYDPVPPAPSSRTSSIAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P0A180
|
YIDD_PSEPU
|
Putative membrane protein insertion efficiency factor
|
MRKLALVPIQFYRYAISPLMANHCRFFPSCSCYAYEAIENHGIWRGGWLAVRRLGRCHPWNDGGYDPVPPAPSSRTSSIAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P0A1G1
|
IMPC_ECOLX
|
Protein ImpC
|
MIRIEILFDRQSTKNLKSGTLQALQNEIEQRLKPHYPEIWLRIDQGSAPSVSVTGARNDKDKERILSLLEEIWQDDSWLPAA
|
The imp operon is involved in UV protection and mutation, however the ImpC protein is not essential for these functions.
|
P0A1G4
|
MSGA_SALTI
|
Virulence protein MsgA
|
MFVELVYDKRNVEGLPGAREIILNELTKRVHQLFPDAQVKVKPMQANALNSDCTKTEKERLHRMLEEMFEEADMWLVAE
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Affects survival in macrophages.
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P0A1N1
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SPAK_SALTI
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Surface presentation of antigens protein SpaK (Invasion protein InvB)
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MQHLDIAELVRSALEVSGCDPSLIGGIDSHSTIVLDLFALPSICISVKDDDVWIWAQLGADSMVVLQQRAYEILMTIMEGCHFARGGQLLLGEQNGELTLKALVHPDFLSDGEKFSTALNGFYNYLEVFSRSLMR
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Involved in a secretory pathway responsible for the surface presentation of determinants needed for the entry of Salmonella species into mammalian cells.
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P0A1N5
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FLHE_SALTI
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Flagellar protein FlhE
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MRKWLALLLFPLTVQAAGEGAWQDSGMGVTLNYRGVSASSSPLSARQPVSGVMTLVAWRYELNGPTPAGLRVRLCSQSRCVELDGQSGTTHGFAHVPAVEPLRFVWEVPGGGRLIPALKVRSNQVIVNYR
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Not essential for flagellar formation and function.
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P0A1T3
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YCED_SALTI
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Large ribosomal RNA subunit accumulation protein YceD (23S rRNA accumulation protein YceD)
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MQKVKLPLTLDPVRTAQKRLDYQGIYTPDQVERVAESVVSVDSDVECSMSFAIDNQRLAVLTGDAVVTVSLECQRCGKPFTHQVHTTYCFSPVRSDEQAEALPEAYEPIEVNEFGEIDLLATVEDEIILALPVVPVHDSEHCEVSEADMVFGELPDEAQKPNPFAVLASLKRK
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Plays a role in synthesis, processing and/or stability of 23S rRNA.
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P0A201
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CSGE_SALTI
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Curli production assembly/transport component CsgE
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MKRYLTWIVAAELLFATGNLHANEVEVEVPGLLTDHTVSSIGHEFYRAFSDKWESEYTGNLTINERPSARWGSWITITVNQDVIFQTFLFPMKRDFEKTVVFALAQTEEALNRRQIDQTLLSTSDLARDEF
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May be involved in the biogenesis of curli organelles.
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P0A203
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CSGF_SALTI
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Curli production assembly/transport component CsgF
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MRVKHAVVLLMLFSPLTWAGNMTFQFRNPNFGGNPNNGSFLLNSAQAQNSYKDPAYDNDFGIETPSALDNFTQAIQSQILGGLLTNINTGKPGRMVTNDFIIDIANRDGQLQLNVTDRKTGRTSTIEVSGLQTQSTDF
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May be involved in the biogenesis of curli organelles.
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P0A226
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MXII_SHISO
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Protein MxiI
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MNYIYPVNQVDIIKASDFQSQEISSLEDVVSAKYSDIKMDTDIQVSQIMEMVSNPESLNPESLAKLQTTLSNYSIGVSLAGTLARKTVSAVETLLKS
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Necessary for the secretion of IPA invasins.
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P0A228
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MXIK_SHISO
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Protein MxiK
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MIRMDGIYKKYLSIIFDPAFYINRNRLNLPSELLENGVIRSEINNLIINKYDLNCDIEPLSGVTAMFVANWNLLPAVAYFIGSQESRLINHSEMVISYYGGKISKQGEAAIRSGFWHLIAWKENISVGIYERINLLFNPIALEGNYTPVERNLSRLNEGMQYAKRHFTGIQTSCL
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Necessary for the secretion of IPA invasins.
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P0A2M0
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SIRB1_SALTI
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Protein SirB1
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MRSLADFEFNNAPLCDGMILASEMIRLDFPTQFVYDELERLVSLAQEEISQLLSQDEQLEKLLALFYGEWGFTDSRGVYRLSDALWLDKVLKKRQGSAVSLGAILLWIANRLDLPLVPVIFPTQLILRIESLEGEMWLINPFNGETLDEHTLEVWLKGNISPVAELFNEDLDEADNAEVIRKLLDTLKSSLMEERQMELALRVSEALLQFNPEDPYEIRDRGLIYAQLECEHVALTDLSYFVEQCPEDPISEMIRAQINTIAHKQIVLH
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Required for maximal expression of sirC, not required to invade host cells (By similarity).
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P0A3I9
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HRCA_RHIRD
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Heat-inducible transcription repressor HrcA
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MGFSAPLSKDQASLLDERSREIFRRIVEGYLDTGEPLGSRSLSRLLPMSLSPASVRNVMSDLEELGLIYSPHISAGRLPTQTGLRFFVDAFMQVGDLPADERANIDRQIGPVAGHEQSLEGLLTEASRMLSGMSRGAGLVLTAKNDVILKHVEFIRLEPTKALAVLVGDHNQVENRIIELPAGISSSQLTEAANFINAHLSGQTLQELRGQFQTQRTELQSELGMLAQDLVERGLAIWAGDNEEGKLGRLIVRGRSNLLEGLAGEEDIDRVRMLFDDLERKENLIEILNLAESGSGVRIFIGSENKLFSLSGSSLIVAPYRDEENRVVGAVGVIGPTRLNYARIVPMVDYTAQIMARLSRKQR
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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}.
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P0A3M8
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LCIA_LACLC
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Lactococcin-A immunity protein
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MKKKQIEFENELRSMLATALEKDISQEERNALNIAEKALDNSEYLPKIILNLRKALTPLAINRTLNHDLSELYKFITSSKASNKNLGGGLIMSWGRLF
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Imparts immunity to lactococcin-A to naturally sensitive host strains.
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P0A3T6
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GERPB_BACCR
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Probable spore germination protein GerPB
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MNFYVNQSIIINSIKIDSITTSSVFQIGTAGSIKALSKFSNTGGFTEPLRPLQAKGQIISIKPSTSSS
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Required for the formation of functionally normal spores. Could be involved in the establishment of normal spore coat structure and/or permeability, which allows the access of germinants to their receptor (By similarity).
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P0A3T8
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GERPD_BACCR
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Probable spore germination protein GerPD
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MNLNVVNRELKVGQIKMNGVSSSALFLIGDANLLILSSILDTPFETVTEGPFVPLVTDVPPTPG
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Required for the formation of functionally normal spores. Could be involved in the establishment of normal spore coat structure and/or permeability, which allows the access of germinants to their receptor (By similarity).
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