entry
stringlengths 6
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| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
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|---|---|---|---|---|
Q5F553
|
FETP_NEIG1
|
Probable Fe(2+)-trafficking protein
|
MARMVFCVKLNKEAEGMKFPPLPNELGKRIFENVSQEAWAAWTRHQTMLINENRLSLADPRAREYLAQQMEQYFFGDGADAVQGYVPQ
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
Q5FRF2
|
HRCA_GLUOX
|
Heat-inducible transcription repressor HrcA
|
MMRPQPPLFRPSIPMPHGLGDREAAILREIVEEYVETGEPIGSQTLAQRLQPSLSPATIRNVMAELARAGLLFSPHVSAGRLPTEKGVRLFVDGLLQFSSLTEEDRASIDSRLDIHGRSYQDILSEASSLLSGLSSAAGLVLAPKSDATLKHIEFVALGPGRVLVILVGSDGQVENRIIETPPGVPPSALVEAGNYLNSRLGDLTLGNLRERVRAEMDASRHELDALTASVIESGLATWDADGGTLFVKGQGKLLADITEIERLTTIRMLFDHLETQETMLQLLQLADASEGVRIYIGRESGMFGMSGVSMIVAPARNEAQKIVGAIGVIGPTRLNYGRIVPVVDYTARMVGRLLG
|
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}.
|
Q5GY22
|
FETP_XANOR
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCHYQQSDAEGLDFVPYPGELGQRIFAHIGKTAWQAWLAHQTMLINENRLSPRDPKHRAFLETELQKFLFERNADKPDGYVAPLGEE
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
Q5H0G1
|
SDHE_XANOR
|
FAD assembly factor SdhE
|
MQRHRPLGQVPLSFSARHTARWRDEMDEQTRLKKLRWRCRRGMRELDQLFGRYLDQRWAQAPDAERAVFLQLLDCEDDKLWRWFMGYEACPDVANAALIADIRALPA
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q5H188
|
HRCA_XANOR
|
Heat-inducible transcription repressor HrcA
|
MRASQSPMLDPRTRQLLRTLIARYIRDGEPVGSKTLAQHAGLDVSPATIRNILADLEDVGLLSSPHTSAGRVPTAHGYRVFVDSLVQMQPPGEEEVRRLRAELASGNGTQSLLGSASQMLSAMSHFVGVVSAPRREQFAFRHIDFVALDARRVLAILVFADNEVQNRVIEPRRAYEPAELERVANYLNAQFAGRALADIRACLLRELRMAKNEMEQLLAHSVDLASEALVPADADDMVMAGQTRLMGVQDLSDLDRLRELFEVFASKREILQLLERTIQAPGVRIFIGEETGMVSLEDVSLVTAPYTAHGQVLGVLGVIGPKRMAYDRLIPLVQTAADVLGAAMESPGTR
|
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}.
|
Q5HEI2
|
OMP7_STAAC
|
77 kDa membrane protein
|
MKFKSLITTTLALGVLASTGANFNNNEASAAAKPLDKSSSSLHHGYSKVHVPYAITVNGTSQNILSSLTFNKNQNISYKDLEDRVKSVLKSDRGISDIDLRLSKQAKYTVYFKNGTKKVIDLKAGIYTADLINTSEIKAININVDTKKQVEDKKKDKANYQVPYTITVNGTSQNILSNLTFNKNQNISYKDLEDKVKSVLESNRGITDVDLRLSKQAKYTVNFKNGTKKVIDLKSGIYTANLINSSDIKSININVDTKKHIENKAKRNYQVPYSINLNGTSTNILSNLSFSNKPWTNYKNLTSQIKSVLKHDRGISEQDLKYAKKAYYTVYFKNGGKRILQLNSKNYTANLVHAKDVKRIEITVKTGTKAKADRYVPYTIAVNGTSTPILSDLKFTGDPRVGYKDISKKVKSVLKHDRGIGERELKYAKKATYTVHFKNGTKKVININSNISQLNLLYVQDIKKIDIDVKTGTKAKADSYVPYTIAVNGTSTPILSKLKISNKQLISYKYLNDKVKSVLKSERGISDLDLKFAKQAKYTVYFKNGKKQVVNLKSDIFTPNLFSAKDIKKIDIDVKQYTKSKKNNKSNNVKFPVTINKFENIVSNEFVFYNASKITINDLSIKLKSAMANDQGITKHDIGLAERAVYKVYFKNGSSKYVDLKTEYKDERVFKATDIKKVDIELKF
|
Binds various plasma and ECM-proteins.
|
Q5HEY4
|
YIDD_STAAC
|
Putative membrane protein insertion efficiency factor
|
MKKIFLAMIHFYQRFISPLTPPTCRFYPTCSEYTREAIQYHGAFKGLYLGIRRILKCHPLHKGGFDPVPLKKDKSASKHSHKHNH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5HFH8
|
HRCA_STAAC
|
Heat-inducible transcription repressor HrcA
|
MITDRQLSILNAIVEDYVDFGQPVGSKTLIERHNLNVSPATIRNEMKQLEDLNYIEKTHSSSGRSPSQLGFRYYVNRLLEQTSHQKTNKLRRLNQLLVENQYDVSSALTYFADELSNISQYTTLVVHPNHKQDIINNVHLIRANPNLVIMVIVFSSGHVEHVHLASDIPFNNDKLNTISNFVTNKLTEFNQNLQDDIVSFVQSEQEEIFINKLLNTMNNHISNQSNSIYMGGKVKLIDALNESNVSSIQPILQYIESNRIAELLQDISSPNINVKIGNEIDDSLSDISIVTSQYHFDETLKGQIAVIGPTAMHYQNVIQLLNRIW
|
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}.
|
Q5HFZ4
|
CVFC_STAAC
|
Conserved virulence factor C
|
MEILRIEPTPSPNTMKVVLSYTREDKLSNTYKKVEETQPRFINQLLSIDGITSIFHVMNFLAVDKAPKADWEVILPDIKAAFSDANKVLESVNEPQIDNHFGEIKAELLTFKGIPYQIKLTSADQELREQLPQTYVDHMTQAQTAHDNIVFMRKWLDLGNRYGNIQEVMDGVLEEVLATYPESQLPVLVKHALEENHATNNYHFYRHVSLDEYHATDNWKTRLRMLNHFPKPTFEDIPLLDLALSDEKVPVRRQAIVLLGMIESKEILPYLYKGLRDKSPAVRRTAGDCISDLGYPEALPEMVLLLDDPQKIVRWRAAMFIFDEGNAEQLPALKAHINDNAFEVKLQIEMAISRIENGDEALGSVWKQMANRTI
|
Required for hemolysin production.
|
Q5HFZ8
|
Y1460_STAAC
|
DegV domain-containing protein SACOL1460
|
MTKQIIVTDSTSDLSKEYLEANNIHVIPLSLTIEGASYVDQVDITSEEFINHIENDEDVKTSQPAIGEFISAYEELGKDGSEIISIHLSSGLSGTYNTAYQASQMVDANVTVIDSKSISFGLGYQIQHLVELVKEGVSTSEIVKKLNHLRENIKLFVVIGQLNQLIKGGRISKTKGLIGNLMKIKPIGTLDDGRLELVHNARTQNSSIQYLKKEIAEFIGDHEIKSIGVAHANVIEYVDKLKKVFNEAFHVNNYDINVTTPVISAHTGQGAIGLVVLKK
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q5HG29
|
CVFB_STAAC
|
Conserved virulence factor B
|
MALDKDIVGSIEFLEVVGLQGSTYLLKGPNGENVKLNQSEMNDDDELEVGEEYSFFIYPNRSGELFATQNMPDITKDKYDFAKVLKTDRDGARIDVGLPREVLVPWEDLPKVKSLWPQPGDYLLVTLRIDRENHMYGRLASESVVENMFTPVHDDNLKNEVIEAKPYRVLRIGSFLLSESGYKIFVHESERKAEPRLGESVQVRIIGHNDKGELNGSFLPLAHERLDDDGQVIFDLLVEYDGELPFWDKSSPEAIKEVFNMSKGSFKRAIGHLYKQKIINIETGKIALTKKGWSRMDSKE
|
Contributes to the expression of virulence factors and to pathogenicity. Involved in the production of hemolysin, DNase, protease and protein A (By similarity).
|
Q5HGJ6
|
Y1252_STAAC
|
UPF0122 protein SACOL1252
|
MGQNDLVKTLRMNYLFDFYQSLLTNKQRNYLELFYLEDYSLSEIADTFNVSRQAVYDNIRRTGDLVEDYEKKLELYQKFEQRREIYDEMKQHLSNPEQIQRYIQQLEDLE
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q5HHM6
|
EMP_STAAC
|
Extracellular matrix protein-binding protein emp
|
MKKKLLVLTMSTLFATQIMNSNHAKASVTESVDKKFVVPESGINKIIPAYDEFKNSPKVNVSNLTDNKNFVASEDKLNKIADSSAASKIVDKNFVVPESKLGNIVPEYKEINNRVNVATNNPASQQVDKHFVAKGPEVNRFITQNKVNHHFITTQTHYKKVITSYKSTHVHKHVNHAKDSINKHFIVKPSESPRYTHPSQSLIIKHHFAVPGYHAHKFVTPGHASIKINHFCVVPQINSFKVIPPYGHNSHRMHVPSFQNNTTATHQNAKVNKAYDYKYFYSYKVVKGVKKYFSFSQSNGYKIGKPSLNIKNVNYQYAVPSYSPTHYVPEFKGSLPAPRV
|
Adhesin that binds to the host cell extracellular matrix proteins fibronectin, fibrinogen, collagen, and vitronectin.
|
Q5HHS1
|
Y812_STAAC
|
DegV domain-containing protein SACOL0812
|
MKIAVMTDSTSYLSQDLIDKYNIQIAPLSVTFDDGKNFTESNEIAIEEFYNKMASSQTIPTTSQPAIGEWITKYEMLRDQGYTDIIVICLSSGISGSYQSSYQAGEMVEGVNVHAFDSKLAAMIEGCYVLRAIEMVEEGYEPQQIIDDLTNMREHTGAYLIVDDLKNLQKSGRITGAQAWVGTLLKMKPVLKFEDGKIIPEEKVRTKKRAIQTLEKKVLDIVKDFEEVTLFVINGDHFEDGQALYKKLQDDCPSAYQVAYSEFGPVVAAHLGSGGLGLGYVGRKIRLT
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q5HHU1
|
NRDI_STAAC
|
Protein NrdI
|
MKIIYFSFTGNVRRFIKRTELENTLEITAENCMEPVHEPFIIVTGTIGFGEVPEPVQSFLEVNHQYIRGVAASGNRNWGLNFAKAGRTISEEYNVPLLMKFELHGKNKDVIEFKNKVGNFNENHGREKVQSY
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q5HIF2
|
CTSR_STAAC
|
Transcriptional regulator CtsR
|
MHNMSDIIEQYIKRLFEESNEDVVEIQRANIAQRFDCVPSQLNYVIKTRFTNEHGYEIESKRGGGGYIRITKIENKDATGYINHLLQLIGPSISQQQAYYIIDGLLDKMLINEREAKMIQAVIDRETLSMDMVSRDIIRANILKRLLPVINYY
|
Negative regulator of clpC, clpB and clpP transcription by binding directly and specifically to their promoter region.
|
Q5HIH8
|
SP5G_STAAC
|
Putative septation protein SpoVG
|
MKVTDVRLRKIQTDGRMKALVSITLDEAFVIHDLRVIEGNSGLFVAMPSKRTPDGEFRDIAHPINSDMRQEIQDAVMKVYDETDEVVPDKNATSEDSEEA
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q5HIJ1
|
YABA_STAAC
|
Initiation-control protein YabA
|
MDRNEIFEKIMRLEMNVNQLSKETSELKALAVELVEENVALQLENDNLKKVLGNDEPTTIDTANSKPAKAVKKPLPSKDNLAILYGEGFHICKGELFGKHRHGEDCLFCLEVLSD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q5HJ88
|
ESAB_STAAC
|
Type VII secretion system accessory factor EsaB
|
MNQHVKVTFDFTNYNYGTYDLAVPAYLPIKNLIALVLDSLDISIFDVNTQIKVMTKGQLLVENDRLIDYQIADGDILKLL
|
Seems to regulate secreted factors that contribute to the establishment of persistent infections in the host.
|
Q5HNB4
|
YIDD_STAEQ
|
Putative membrane protein insertion efficiency factor
|
MKKILLSLVVFYQRFISPLTPPTCRFYPTCSQYTREAIEYHGALKGLYLGVRRILKCHPLHKGGFDPVPLKKDKNSKTTHHH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5HPV5
|
Y802_STAEQ
|
UPF0122 protein SERP0802
|
MGQNDLVKTLRMNYLFDFYQSLLTNKQKNYLELFYLQDYSLSEIADTFEVSRQAVYDNIRRTGDLVEDYESKLRLYQRFEKRRELYNLMKQSLNQPELLKQYITQLEELE
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q5HRN1
|
CTSR_STAEQ
|
Transcriptional regulator CtsR
|
MHNMSDIIEQYIKRLFEEADEDVVEIQRAHIAQRFDCVPSQLNYVIKTRFTNEHGYEIESKRGGGGYIRITKIENKDATGYINHLLQLIGPSISQQQGYYVIDGLLDKGLINEREAKMIQTIIDRETLKMDVVARDIIRANILKRLLPVINYY
|
Negative regulator of clpC, clpB and clpP transcription by binding directly and specifically to their promoter region.
|
Q5HRR9
|
YABA_STAEQ
|
Initiation-control protein YabA
|
MNRNELFERLMKLEHHVEQLTTDMSELKDLTVELVEENVALQVENENLKRLMNKTEESVETHLDKDNYKHVKTPSPSKDNLAMLYREGFHICKGELFGKHRHGEDCLLCLNVLSD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q5HUK0
|
YIDD_CAMJR
|
Putative membrane protein insertion efficiency factor
|
MICLKILRFYQKFLSPLKPAACRYYPSCSEYALWQFQKKNFFLAFFSTFFRVLRCNPFFKGGFDYPRVSKNFYPINLCFKPIFLAKKQLCFLYIPYKNKSFYLIKIIFKRTNQ
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5JDM5
|
BRIX_THEKO
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MMLITTSHRPTRRTRSFGHDLEKVFPNSLYLTRGKKTIQDLLMEAYDRGYERLLIINVWKGNPLKMTFIKVDPEDWGYIGYLYLHGIKLQREIGFRNIPPIREEMPFVVTTAKRVGIDHTAFAQVFAELTGGKFVPRGNKSLQTIADKNNTDVIGVIENYPRGMAVNFYRFDITRERPVGPLILVKIWIMEDGRRWDYKEALGIKPKE
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
Q5JDU6
|
Y1752_THEKO
|
Putative antitoxin TK1752
|
MGKTITIADDVYYELVKMKGKKSFSELLRELIGKKKKGNLDVLMIAFGTRTPEEVEELKKELKEVEEWMDSWTPASL
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. {ECO:0000255|HAMAP-Rule:MF_00794}.
|
Q5KVY7
|
YIDD_GEOKA
|
Putative membrane protein insertion efficiency factor
|
MGQWLIWCIRFYQRFLSPLKPPTCRFYPTCSNYGIEAIRRFGAIKGGWLTAKRILKCHPFHPGGFDPVPESSEHAKRNKIT
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5L0Q0
|
Y1195_GEOKA
|
UPF0122 protein GK1195
|
MLEKTMRMNYLYDFYQALLTPKQRNYMALYYLDDYSLGEIAEQYEVSRQAVYDNIRRTEAMLEQYEEKLGLLRKYERRRQIIERLKDYISRRYGADAELAALVRELDELD
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q5L300
|
LUTA_GEOKA
|
Lactate utilization protein A
|
MKVSLFVTCLIDLFYTEVGKATVELLERLGCKVDFPEAQTCCGQPAYNSGYVKEAKEAMKQMMRAFADADYVVTPSGSCAAMLKEYPHIFHGDPEWEAEAKRLAAKTYELTQFLVDVLKVEDVGASLHGRATYHTSCHMTRLLGVKDAPLRLLEHVKGLELVPLPNAHQCCGFGGTFSVKMGPISEQMVDEKIGHIEEAEADYLIGADCGCLLNIGGRIARLGKPIRVMHIAEVLNARN
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
Q5L302
|
LUTC_GEOKA
|
Lactate utilization protein C
|
MTRGAIHNRDAFLEHIAHRLGRAPRLSGVSRPQWSNQPQWKVLAGYSQDDLLNVLQKQCGLIHTDYIETTSAELAGALRRQVAAYGGGPVIVPDDPRFAEYGLSALLRDEWPAEQTTVHIWNPALGRQNIDAAEQANVGIAFSDITLAESGTVVLFSRNEQGRAIHFLPKTYIAIVPKSTVVPRMTQAAAVIHEQIEKGGLVPSCINFITGPSNSADIEMNLVVGVHGPMKAAYIVVTDR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
Q5L3V1
|
SP5G_GEOKA
|
Putative septation protein SpoVG
|
MEVTDVRLRRVNTEGRMKAIASITLDNEFVVHDIRVIDGNNGLFVAMPSKRTPDGEFRDIAHPINSATRGKIQEAILAEYHRLGKLEEELEEAGAS
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q5L6W5
|
YIDD_CHLAB
|
Putative membrane protein insertion efficiency factor
|
MSFKQLLYNLPTHLCCGLIHLYRWTISPLLGSPCRFFPSCSQYALQALKHHKCIRGLWLTIKRIGKCGPWHPGGIDLVPMTTLEEALDVSQVTNDDDSGDSHA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5LJ21
|
YIDD_BACFN
|
Putative membrane protein insertion efficiency factor
|
MKRLLSYILLLPIYFYRACISPMTPPSCRFTPTCSQYAIEAIKKHGPFKGLYLAVRRILRCHPWGGSGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5M027
|
Y888_STRT1
|
UPF0122 protein str0888
|
MEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFGVSRQAVYDNIKRTEKILEDYEMKLHMYSDYIVRSQIFDDIMEKYADDSYLQEQIAILSSIDNRD
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q5M1H7
|
YIDD_STRT1
|
Putative membrane protein insertion efficiency factor
|
MMKKFLIALVKAYQRWISPLFPLSCRFCPTCSVYMIQAIEKHGLKGVLMGIARILRCHPLSETGDDPVPDYFSLKRKKTPLDN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5M1U0
|
HRCA_STRT1
|
Heat-inducible transcription repressor HrcA
|
MITQRQNAILNLIVEMFTRTHEPVCSKALQDSIDSSSATIRNDMAKLEKMGYLEKAHISSGRMPSRAGFQYFVANSLNLDTIDEQDVYQVVKAFDFEAFKLEDILDAAAKLLAEMTGCTAVIQDVEPTKQRLTGFEIVQLSNHDALAVLTLDESKPVTVQFAIPKNFLSSDLEIFHKLVQGRFLGNTVLDIHYRLRTETPQIVQKYFKITDNVLDLFDYIFSHLFKELIFIEGKVASLAYADLKTYQFLDNPQHVALALRSAISDDEVTKISVAESTEEALENVTVMSHKFLIPYRGTALMHVIGPIEMDYRRMVSLVNVISRVLVMKLTDYYRYLNSNHYEVFLSRNVLKNIERGECLD
|
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}.
|
Q5M4P2
|
Y888_STRT2
|
UPF0122 protein stu0888
|
MEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFGVSRQAVYDNIKRTEKILEDYEMKLHMYSDYIVRSQIFDDIMEKYADDSYLQEQIAILSSIDNRD
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q5M619
|
YIDD_STRT2
|
Putative membrane protein insertion efficiency factor
|
MMKKFLIALVKAYQRWISPLFPLSCRFCPTCSVYMIQAIEKHGLKGVLMGIARILRCHPLSETGDDPVPDYFSLKRKKTPLDN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5MGP9
|
DFP2_LONON
|
Defense protein 2 (DFP-2)
|
TGSGKYNILHNDNHNLDLTGKFLECSRSNPNLSDYNKYSAILDYLYKDKLSASLGVAHSGLLDRTDLSALGKVNLLNDKNTRLDLFGGLTKSMSPKFDSGLKPNFGLQLESSF
|
Has antibacterial activity against both Gram-positive and Gram-negative bacteria.
|
Q5MZ58
|
YIDD_SYNP6
|
Putative membrane protein insertion efficiency factor
|
MKLLLLALIQFYRRWISPLTPASCRFYPTCSQYGLEAIDRFGPLKGSWLTLCRILRCHPFHPGGYDPVPPLPSCSCGKSPCD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5N3M2
|
HRCA_SYNP6
|
Heat-inducible transcription repressor HrcA
|
MLVSRLTARQQTILSATVRHYVRTAEPVGSKALAEQYGLSVSAATIRNAMGVLERAGLLYQPHTSAGRVPSEGGYRLYVDQLMEPDRALQRQTEQQLSQQLPDRRQSLEALLRGAAQILASLSGYLSLITFPLGLEFQVRHLQLVAIAPHQVLLIVVNDSYETQSALLTLPELDRDLEADQLDRQLLLLSNFLNQELQGRSLQALANLDWPVLGSELQSLAGILQQGLQDLEKRWQPTPATSLLVCGLADLLRQPEFNELQQVQALLELLEGEQTQLLPLMLADPAADQVRVRIGSELPLAPIRSCSLVSAFYCREQQPVGSVSLIGPTRMLYENAVAAVEATASYLSEAIAS
|
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}.
|
Q5NDN1
|
VSR_PNLV
|
Putative suppressor of silencing
|
MQNVNIPVGICNNRIVFRSLGFALSENNLTIEVLSRPIESLGRVLLFLYLYPSFAADYAQRYYGATWNQAYDISVRSLAFLLPFLFSPAVEWAVGPVFKSFVPLTELLKWSLAVGYYPTFPGSRQQLPSVPYDVNYGVQSTKAATVKLLRRAMLDDCIQSKTRLEAMLERGPDTFRNVLKAHISRIDRFTSSSGWHVADDYHMDLVLDISSGISRPSVHDNISFIQRSMRRISDILYDLCVPAHFLDLWRFTGLQCFWIDPNLGKF
|
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.
|
Q5NFS4
|
SDHE_FRATT
|
FAD assembly factor SdhE
|
MLIKNNDLIFSSVDKIKYSARRGMLELDIILAPYLNNCYMHEDLANKKLFVEFLTSEDSDMFDWLFKGVTPPQRYQQLIDKIIKEKKKFNQTKLK
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q5NHJ8
|
FETP_FRATT
|
Probable Fe(2+)-trafficking protein
|
MTKVFCKKYHQELDAIPFQPLPGELGKKIHNEISNKAWQAWLAHQTILINEYRLNLIEPKAKEFLKEEMHKFLFEGKEEKPEQFSEI
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
Q5NI55
|
YIDD_FRATT
|
Putative membrane protein insertion efficiency factor
|
MLINLYRYCISPFIPARCRYYPTCSEYALEALKTHGILKGLYLTTRRLLRCHPLSKRDYYDLVPCKNKKG
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5NVD7
|
ELMD1_PONAB
|
ELMO domain-containing protein 1
|
MKHFLRMLIQVCLYFYCKFLWRCLKFVMRKLTGRCELQRICYNTKPGASRTMKIETSLRDSKSKLLQTSVSVHPDAIEKTIEDIMELKKINPDVNPQLGISLQACLLQIVGYRNLIADVEKLRREPYDSDNPQHEEMLLKLWKFLKPNTPLESRISKQWCEIGFQGDDPKTDFRGMGLLGLYNLQYFAERDATAAQQVLSDSLHPKCSKFSKAEWEKKRMDKAIGYSFAIVGINITDLAYNLLVSGALKTHFYNIAPEAPTLSHFQQTFCYLMHEFHKFWIEEDPMDIMEFNRVREKFRKRIIKQLQNPDMALCPHFAASEGLINM
|
Acts as a GTPase-activating protein (GAP) toward guanine nucleotide exchange factors like ARL2, ARL3, ARF1 and ARF6, but not for GTPases outside the Arf family.
|
Q5P4P3
|
YIDD_AROAE
|
Putative membrane protein insertion efficiency factor
|
MKALVLGLLRVYRYAISPMLGRNCRFHPCCSEYAQEAVERHGAMRGGWLALKRVGRCHPFHPGGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5PC89
|
GLGS_SALPA
|
Surface composition regulator
|
MNNNNVYSLNNFDFLARSFARMQAEGRPVDIQAVTGNMDEEHRDWFCKRYALYCQQATQAKKLELEH
|
Major determinant of cell surface composition. Negatively regulates motility, adhesion and synthesis of biofilm exopolysaccharides. {ECO:0000255|HAMAP-Rule:MF_00525}.
|
Q5PEK1
|
SYDP_SALPA
|
Protein Syd
|
MDELTAQALKAFTTRYCDAWQEKHGSWPLSEELYGVPSPCIISSTRDAVYWQPQPFEGEENVNAVERAFDIMVQPALHAFYTTQFAGDMPAQFADEKLTLLQTWSQDDFRRVQENLIGHLVTQKRLKLPPTLFIATQENELEVISVCNLSGEVIKETLGTRNRTVLAATLAEFLTQLNPLL
|
Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}.
|
Q5PF04
|
NRDI_SALPA
|
Protein NrdI
|
MSALVYFSSSSENTHRFMQRLGLPATRIPLNERERIRVDEPYILVVPSYGGGGMAGAVPRQVIRFLNDEHNRARIRGVIASGNRNFGDAWGCAGDVIAQKYGVPWLYRFELMGTQRDIDNVRRGVNEFWQQLPRSA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q5PGA1
|
CBPM_SALPA
|
Chaperone modulatory protein CbpM
|
MANITVTFTITEFCLHTGVTEEELNEIVGLGVIEPYEDDNTDWQFDDRAASVVQRALRLREELALDWPGIAVALTLLEENSRLREENRLLLQRLSRFISHP
|
Interacts with CbpA and inhibits both the DnaJ-like co-chaperone activity and the DNA binding activity of CbpA. Together with CbpA, modulates the activity of the DnaK chaperone system. Does not inhibit the co-chaperone activity of DnaJ. {ECO:0000255|HAMAP-Rule:MF_01155}.
|
Q5PKF1
|
FDHE_SALPA
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNVYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEANDQGKPPLDIHVLPRDKHWQKLLHSLIAELKPEMNGPALAVIENLEKASEQELEQMASALFASDFASVSSDKAPFIWAALSLYWAQMASLIPGKARAEYGEARQYCPVCGSMPVSSMVQIDTTQGLRYLHCNLCETEWHVVRVKCSNCEQSRDLHYWSLENEQAAVKAESCGDCGTYLKILYQEKDPKVEAVADDLASLVLDARMEQEGFARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q5PKU3
|
YIDD_SALPA
|
Putative membrane protein insertion efficiency factor
|
MAPPLSPGSRVLIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFDTREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5PPV3
|
MORN3_XENLA
|
MORN repeat-containing protein 3
|
MPLVKAPKKAEPIWKEWDAKAQKAGLRHSVYSVNGDEYTGEWLNNLRHGKGTYMWKRRKSIYEGDWKCGERSGFGTYSVQDSNTGEYIKVYSGYWDNDKKHGYGTHFYSAKEYYEGEWKCGKRCGWGRMYFANGDIYEGEWLEDKHSGQGMLCLANENRYEGSWKDGKKHGPGKFYYLNKGQLYEGVWVEDIPKCGTMVDFGRTEAPYPTKYPLPEVKVADPEGVLKEAQQPLFGEHE
|
Assembles a suppression complex (suppresome) by tethering SIRT1 and MDM2 to regulate composite modifications of p53/TP53. Confers both deacetylation-mediated functional inactivation, by SIRT1, and ubiquitination-dependent degradation, by MDM2, of p53/TP53, promoting a proliferative and cell survival behaviors (By similarity). May play a role in the regulation of spermatogenesis (By similarity).
|
Q5PQ44
|
CF299_XENLA
|
Cilia- and flagella-associated protein 299
|
MEQSEAGSAADSIITQFNTYEDFLDSQITALDLHYLEDEELARQLVELGYRGSGEVLKRDEFEARKAAAEASRLSQRTQQKTLSSAGKDPKDNFLKALAMREEANRNGKMTSVIFIRDKNAHGQEVSGYIDFAHRLKTEDFEVYFSGKKKLLPRPTDLSFYNWESHVSTSNPSPNYQVIAETSSGLLFKNKRDRKILNVDPKASPGDNSTRTSIQTDIYIQAVIYDHITRRKS
|
May be involved in spermatogenesis.
|
Q5QW09
|
SYDP_IDILO
|
Protein Syd
|
MKTLEESIDALMTRYKENVPVRYTEYVEEWNSPIYGTVIDENTVEWTPCRQPEALNFDDLESALEMSFHQSIKTLFGRWYAGDLALDYQGHTISLLQTQSAEDGERLLENITGHILMKRRLKQPETVFIGLGSEDDGLLVTIDNQSGAVGLEWVGKEQHDVLSDSLAAWLDNCQPQVETDKNS
|
Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}.
|
Q5QY58
|
FETP_IDILO
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCEHFQKEAEGLDFQLYPGELGERIFNHISKDAWAEWQKKQTMLINEKRLNMMDPTDREFLEKQMTAFLFEGKAPEIEGYTPPES
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
Q5R0Z7
|
SDHE_IDILO
|
FAD assembly factor SdhE
|
MLPLKQSEEALKDKRRLRWACRRGMLELDVLFEPFVDQAYDELSEEQKAVFRRLITCDDPDLFAWFMGHQKCEDEELAEMIRFMLSRVKV
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q5R796
|
FBX36_PONAB
|
F-box only protein 36
|
MASWLPETLFETVGQGPPPSKDYYQLLVTRSQVIYRWWKISLRSEYRSTKPGEAKETHEDFLENSHLQGQTALIFGARILDYVINLCKGKFDFLERLSDDLLLNIISYLDLEDIARLCQTSHRFAKLCMSDKLWEQIVQSTCDTITPDVRALAEDTGWRQLFFTNKLQLQRQLRKRKQKYGNLREKQP
|
Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex.
|
Q5R8D4
|
AVPI1_PONAB
|
Arginine vasopressin-induced protein 1 (AVP-induced protein 1)
|
MGTPASVVSEPPPWQAPTEARGRKQASANIFQDAELLQIQGLFQRSGDQLAEERAQIIWECAGDHHVAEALKRLRRKRPPRQKPLGHSLHHCSRLRILEPHSPLADPQSATETASTEQYLHSRRKSARIRRNWKKPGPTSYLHQIRH
|
May be involved in MAP kinase activation, epithelial sodium channel (ENaC) down-regulation and cell cycling.
|
Q5RBE4
|
DEPP_PONAB
|
Protein DEPP
|
MRSRLLLSVAHLPTIRETTEEMLLGGPGQEPPPSPSLDDYVRSISRLAQPTSVLDKATAQGQPRPPHRPAQACRKGRPAVSLRDITARFSGQQPTLPMADTVDPLDWLFGESQEKQPSQRDLPRRTGPSAGLWGPHRQMDSSKPMGAPRGRLCEARMPGHSLARPPQDGQQSSDLRSWTFGQSAQAMASRHRPRPSSVLRTLYSHLPVIHEL
|
May play a role in autophagy.
|
Q5RCY5
|
ASTE1_PONAB
|
Protein asteroid homolog 1
|
MGIRGLMSFVEDHSNEFFTDLKLRDTKIVIDGYALFHRLCFSSNLDLRYGGDYDSFADVVQKFFESLFACNICPYVVLDGGCDISDKKLTTLKDRAREKIQMAHSLSVGGSGYVCPLLIREVFIQVLIKLRVCFVQCFSEADRDIMTLANHWNCPVLSSDSDFCIFDLKTGFCPLNSFQWRNMDTIKGTQNYIPAKCFSLDAFCHHFSNMNKALLPLFAVLCGNDHVNLPIMETFLSKARLPLGATSSKGRRHHRILGLLNWLSHFANPTEALDNVLKYLPKKDRENVKELLCCSMEEYQQSQVKLQDFFQCGTYVCPDALNLGLPEWVLVALAKGQLSPFISDALVLRRTILPTQVENMQQPNAHRISQPIRQIIYGLLLNASPHLDKTSWNALPPQPLAFSEVERINKNIRTSIIDAVELAKDHSDLSRLTELSLRRRQMLLLETLKVKQTILEPIPTSLKLPIAVSCYWLQHTETKAKLHHLQSLLLTMLVGPLIAIINSPGKEELQEDGAKMLYAEFQRVKAQTRLGTRLDLDTAHIFCQWQSCLQMGMYLNQLLPTPLPEPDLTRLYSGSLVHGLCQQLLASTSVESLLSICPEAKQLYEYLFNATRSYAPAEIFLPKGRSNSKKKRQKKQNTSCSKNRGRTTAHTKCWYEGNNRFGLLMVENLEEHSEASNIE
|
Possible role in EGF receptor signaling.
|
Q5RD58
|
CL004_PONAB
|
Protein C12orf4 homolog
|
MKKNRERFCNREREFVYKFKVGSQCLELRVPLRFPVQENASHLHGRLMLLHSLPCFIEKDLKEALTQFIEEESLSDYDRDAEASLEAVKSGEVDLHQLASTWAKAYAETTLEHARPEEPSWDEDFADVYHDLIHSPASETLLNLEHNYFVSISELIGERDVELKKLRERQGIEMEKVMQELGKSLTDQDVNSLAAQHFESQQDLENKWSNELKQSTAIQKQEYQEWVIKLHQDLKNPNNSSLSEEIKVQPSQFRESVEAIGRIYEEQRKLEESFTIHLGAQLKTMHNLRLLRADMLDFCKHKRNHRSGVKLHRLQTALSLYSTSLCGLVLLVDNRINSYSGIKRDFATVCQECTDFHFPRIEEQLEVVQQVVLYARTQRRSKLKESLDSGNQNGGNDDKTKNAERNYLNVLPGEFYITRHSNLSEIHVAFHLCVDDHVKSGNITARDPAIMGLRNILKVCCTHDITTISIPLLLVHDMSEEMTIPWCLRRAELVFKCVKGFMMEMASWDGGISRTVQFLVPQSISEEMFYQLSNMLPQIFRVSSTLTLTSKH
|
Plays a role in mast cell degranulation.
|
Q5REM2
|
L10K_PONAB
|
Leydig cell tumor 10 kDa protein homolog
|
MAQGQRKFQARKPAKSKTAATASEKNRGPRKGGRVIAPKKARVVQQQKLKKNLEVGIRKKIEHDVVMKASSSLPKRLALLKAPAKKKGAAAATSSKTPS
|
May have a potential role in hypercalcemia of malignancy.
|
Q5RFN8
|
TM101_PONAB
|
Transmembrane protein 101
|
MASKIGSRRWMLQLIMQLGSVLLTRCPFWGCFSQLMLYAERAEARRKPDIPVPYLYFDMGAAVLCASFMSFGVKRRWFALGAALQLAISTYAAYIGGYVHYGDWLKVRMYSRTVAIIGGFLVLASGAGELYRRKPRSRSLQSTGQVFLGIYLICVAYSLQHSKEDRLAYLNHLPGGELMIQLFFVLYGVLALAFLSGYYVTLAAQILAVLLPPVMLLIDGNVAYWHNTRRVEFWNQMKLLGESVGIFGTAVILATDG
|
May activate NF-kappa-B signaling pathways.
|
Q5SL49
|
YIDD_THET8
|
Putative membrane protein insertion efficiency factor
|
MREVLILLIRFYRRFLSPLKPRTCRFHPTCSAYALEALERHGAFWGSYLAVRRVLRCHPWNPGGLDPVPVLFPPGKVRGGAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5UQD7
|
SUI1_MIMIV
|
Protein translation factor SUI1 homolog
|
MLNRIIYDPFNDGLDTEQHFEKIHIKTKQRTKTKSITIIENIPEKIDLKLFLKKLKYTFHCSGSIQQNYDDDSKFIQLSGDHRELVKNFLIKNSIVKESNIVMHGY
|
Additional factor that functions in concert with eIF-2 and the initiator tRNA in directing the ribosome to the proper start site of translation.
|
Q5WF19
|
YIDD_ALKCK
|
Putative membrane protein insertion efficiency factor
|
MRKLLIQIIRLYQRFISPLTPPSCRFYPTCSAYGIEAIETHGAIKGSYLAIKRILKCHPFHPGGVDPVPECQHTKHKKTP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5WFN0
|
Y2295_ALKCK
|
UPF0122 protein ABC2295
|
MLDKTLRMNYLFDFYHSLLTEKQRNYMSYYYLDDLSLGEIADEYDVSRQAVYDNIRRTEAMLEEYEQKLRLLEKFETRRSLLAELRKAIASDQAVEACNSLIDRIEKLD
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q5WJD9
|
LUTC_ALKCK
|
Lactate utilization protein C
|
MIKNRDSFLDHVANQLGRPRQTEGVLRPNYRVSPQFEVLKDASKDELVTVLKEQCVAIHTDFKQVESGQLETALDETIDMYGAKSVIAWDDRRFHEFGLGSFLTRPSVSLWDNRDSKRSIEQAEIADVGITFSDITLAESGTVTLFSSNGKGRSVSLLPRYYIAIIPKSTLVARMTQAARHIRQLTGEGRLPSCINFISGPSNSADIEMSLVVGVHGPLKACYIVVDDK
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
Q5WJE1
|
LUTA_ALKCK
|
Lactate utilization protein A
|
MNVSLFVTCLADIFYPGVGKDTVEVLERHGCNVKFPENQICCGQPAFNSGYHEDTKKAAKHTIETFADADYVVLPSGSCAAMLLEYKELFADDPEWEKRAEELASKTYELTQFLVRVLKVEDIGAVCHKKATYHTSCHMSRLLRETEAPFSLLEQVKGLELAPLANKESCCGFGGTFSVKMPAISEQMVEEKVGHIEATGADLLIGADCGCLMNIGGRIERNGKTIEVKHIAQVLNSKE
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
Q5WQ00
|
REPA1_BUCCC
|
Probable replication-associated protein repA1
|
MFKRKKYVDNPYPKFVQPKNHKKRPAFIRYAMRCAAQTDVARNELYYTNPLKNPITGCVLHRKRRLNEHRARALRAVVQAMLYYFNIASMLVMASVEKLSDVCGLSTYSSAGNKSITRASRLITQFMEPMGLISCEKIWDKILGMYIPKIIYLKPLFFMLFDISKIRLKRVRIKQLEWINSQLKKKGEYPITLLEIEKQAKEKHIHSALLFRKSKYIIKKQKNKAKKFLELDEKYAKSYILNNLVKKYSTKELCKLGLTKLKRKVNCEYFRLKKLAQLPVV
|
This protein is essential for plasmid replication it is involved in copy control functions.
|
Q5WSE8
|
YIDD_LEGPL
|
Putative membrane protein insertion efficiency factor
|
MGKINLMLRQIVCLPIKMYQYFISPLITPCCRYYPSCSEYADSAIKHYGVIKGLLMALNRLSRCHPWSKGGYDPLFPNDKN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5WVC4
|
FETP_LEGPL
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCCKLKQEAEGLEKQPFPGELGKKVFNEVSKQAWNMWLSHQTMLINEYRLNLIEARAREFLKEEMQKYFFGEGSDKPSGYKEIK
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
Q5WWK6
|
SDHE_LEGPL
|
FAD assembly factor SdhE
|
MDNREKSRLLWKCRRGMLELDLVLQKFIANEIDRLTENQLKAFDNLLTHNDPNLYAWLMGHEEPEKELLEIVSFIRNCD
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q5X0M1
|
YIDD_LEGPA
|
Putative membrane protein insertion efficiency factor
|
MGKISLMLRQIVCLPIKMYQYFISPLITPCCRYYPSCSEYADSAIKHYGVIKGLLMALNRLSRCHPWSKGGYDPLFPNDKN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5X3X9
|
FETP_LEGPA
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCCKLKQEAEGLEKQPFPGELGKKVFNEVSKQAWNMWLSHQTMLINEYRLNLIEARAREFLKEEMQKYFFGEGSEKPSGYKEIK
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
Q5X4Y4
|
SDHE_LEGPA
|
FAD assembly factor SdhE
|
MDNREKSRLLWKCRRGMLELDLLLQKFIANEIDRLTENQLKAFDNLLTHNDPSLYAWLMGHEEPEKELLEIVSFIRNCD
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q5X9X0
|
Y1658_STRP6
|
DegV domain-containing protein M6_Spy1658
|
MTFTIMTDSTADLNQTWAEDHDIVLIGLTILCDGEVYETVGPNRISSDYLLKKMKAGSHPQTSQINVGEFEKVFREHARNNKALLYLAFSSVLSGTYQSALMARDLVREDYPDAVIEIVDTLAAAGGEGYLTILAAEARDSGKNLLETKDIVEAVIPRLRTYFLVDDLFHLMRGGRLSKGSAFLGSLASIKPLLWIDEEGKLVPIAKIRGRQKAIKEMVAQVEKDIADSTVIVSYTSDQGSAEKLREELLAHENISDVLMMPLGPVISAHVGPNTLAVFVIGQNSR
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q5XAD4
|
HRCA_STRP6
|
Heat-inducible transcription repressor HrcA
|
MITQRQNDILNLIVELFTQTHEPVGSKALQRTIDSSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYHVIKTFDFEAFKLEDMLQKASHILAEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDSSVIDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQSLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLAAKLGDYYRYLNSNHYEVH
|
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}.
|
Q5XAI8
|
Y1140_STRP6
|
DegV domain-containing protein M6_Spy1440
|
MTWKIVTDSGCDLRSLTRQSKELRFERVPLTLQIGTEIFRDDDGLDIDNMMTTMYQSSKATTSSCPSPEAFLQAYRGADNVIVMTITGTLSGSHNSARLAKNELLEENPNVNIHLIDSLSAGGEMDLLVLELERLINLGLSFEEVVKQITAYQQKTRLIFVLAKVDNLVKNGRLSKLVGKVIGLLNIRMVGKASNKGTLELLQKARGQKKAVSALIEEIQKEGYVGGKVYIAHAQNPKICEQISEKIKSLYPDAVIQTGRTSGLCSFYAEDGGLLMGYEI
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q5XC23
|
Y905_STRP6
|
UPF0122 protein M6_Spy0905
|
MNTMEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIADEFGVSRQAVYDNIKRTEKILETYEMKLHMYSDYVVRSEIFDDMIAHYPHDEYLQEKISILTSIDNRE
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q5XCN8
|
Y690_STRP6
|
DegV domain-containing protein M6_Spy0690
|
MKLAVITDSTATLPIDLKQDKAIFSLDIPVIIDDETYFEGRNLSIDDFYQKMADSQNLPKTSQPSLSELDNLLGLLSSKGYTHVIGLFLAGGISGFWQNIQFLAEEHPEIEMAFPDSKITSAPLGSMVKNVLDWSRQGMTFQAILNKLQEQIDRTTAFIMVDDLNHLVKGGRLSNGSALLGNLLSIKPILRFDEEGKIVVYEKVRTEKKAMKRLVEILNDLIADGQYNVSIIHSKAQDKADYLKRLLQDSGYQYDIEEVHFGAVIATHLGEGAIAFGVTPRL
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q5XDK5
|
NRDI_STRP6
|
Protein NrdI
|
MAELIIVYFSSKSNNTHRFVQKLGLPAQRIPVDNRPLEVSTHYLLIVPTYAAGGSDAKGAVPKQVIRFLNNPNNRKHCKGVISSGNTNFGDTFALAGPIISQKLQVPLLHQFELLGTATDVKKVQAIFARLKHHTHDKQKQTNNLITERTHPCHKPMRHTSH
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q5XDL8
|
YABA_STRP6
|
Initiation-control protein YabA
|
MNKKELFDAFDGFSQNLMVTLAEIEAMKKQVQSLVEENTILRLENTKLRERLSHLEHETVAKNPSKQRKDHLEGIYDEGFHICNFFYGQRRENDEECMFCRELLDRK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q5XDP1
|
YIDD_STRP6
|
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}.
|
Q5YMR8
|
YIDD_NOCFA
|
Putative membrane protein insertion efficiency factor
|
MRSAAAALHRLPARALIFLIELYRTYVSPTRMPVCRFTPTCSEYAVTALRTRGLVVGLGLTAVRLAKCAPWHPGGWDPVPQRRPRRRDAAAADAAMSAPHACKGSPHAVVGDTNDGST
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5YZX1
|
HRCA_NOCFA
|
Heat-inducible transcription repressor HrcA
|
MGPMSSSTEDRRFEVLRAIVADYVATKEPIGSKTLVERHNLGVSSATVRNDMAVLEAEGYITQPHTSSGRIPTDKGYRQFVDRISEVKPLSAAERRAILQFLESGVDLDDVLRRGVRLLAQLTRQVAVVQYPTVSASTVRHIEVVALNPARLLLVVITDTGRVDQRIVELGAVVDDDDLSALRALLGAAMDGKRLAAASAAVAELPESAPQQLRDVLIRVSTVLVETLVEHPEERLVLGGTANLTRNAADFGLPGSLRQVLEALEEQVVVLKLLAAAQQPGTVTVRIGEETQVEEMRSASVVTTGYGVSGSVLGGMGVLGPTRMDYPGTIASVATVARYIGEVLAER
|
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}.
|
Q5ZJ37
|
RABEK_CHICK
|
Rab9 effector protein with kelch motifs
|
MGPRVLPLLEPGCRPQAGKWYRMAPRGEWPRGRVGHGCLFVPGGSGRVLLLGGADPAGAFADAHFVELGAHLWAPAAWSGLRPRYEHATFLSACRPPRLWVFGGAHRAGNRSCVQVLDPEIGTWESPEVTGIPPLPRTFHTSSAAIGDCLYVFGGGDKGAEPVKDQQLHVFDTVALAWTQPDTHGDPPSPRHGHVVVAVGTKLFIHGGLAGDIFYNDLFCIDTTDMKWVKIAATGDVPGGRASHSSAVFKDHLYIFGGIGPDGTLDTTYKYHIEEQQWTLLQFDSPLPAGRLDHAMCVIPWRVGKNGDAAAVSKEDKAEPTASAGDRAGHLCRGQDKKACTEDTMMHLLLIFGGMDTQAEIYRDCIVSLIE
|
Rab9 effector required for endosome to trans-Golgi network (TGN) transport.
|
Q5ZL79
|
NOL11_CHICK
|
Nucleolar protein 11
|
MAALCEAFTLCGLGPAGGVGLGSGLLALEPGADPDHVLLTDRGRTTTLFKVSDQKPLGCWSVKHGQIITCPVVCNFETHEYIAVHDNKVLRIWKDEDVNLDKVFKATLSAEVYRIHSLPHAEPLVLFKGGGVRTLDVLLEAPQQEIENVISDEVIKWSEAFLESRQPVLIFVTEKDGDFFVYVQKPKMRSLHKYKLEQQELCNPLSFTAYIKKQIITLLCLYSSDSVYKVLIPLQQSSEEEEQTSSKSLLLNLSISGSVLKGTSFVVLDKDHVAVLGSLAASGEESKECLTIWNTKFQTLQASKELPLGTSGQLWCYGEKFFFTHGKVLTVVIYKCETSSLAAAVGKLKDSQTSDLSSFVNWNTLGDEELLVSLQSQQSVALKSESKMTLRSKKSAVANIQPDTSTVGQFLLSIKDASTAAVEDQLRQLLSKAQMPDFQATIGCIISALINRCKTDPKFYPRNFLVQMIQKGELSYSLCPDLMAVALEKKDVHLLQICLQRFPDIPEEITYACLKVFLSISDDYLERTDVNLESVISYIDIEPNNKEVKTEVVENGFNTELEEDGCDVTGMKETHMMDSVEFCPVGPQKAALLNAVLHSAYSETFLLPHLKDLPAQQAVLFLRYLHYLYVKCSEKINTTLPGILSPTISQIMDWMCLLLDAHFTVMVMLPEAKGLLSSMHRFVRAQVRLYSELNKIEGSLQELQRIKCQKHSQAYSIEVLELI
|
Ribosome biogenesis factor. May be required for both optimal rDNA transcription and pre-rRNA processing (By similarity).
|
Q5ZR80
|
YIDD_LEGPH
|
Putative membrane protein insertion efficiency factor
|
MGKISLMLRQIVCLPIKMYQYFISPLITPCCRYYPSCSEYADSAIKHYGVIKGLLMALNRLSRCHPWSKGGYDPLFPNDKN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q5ZU80
|
FETP_LEGPH
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCCKLKQEAEGLEKQPFPGELGKKVFNEVSKQAWNMWLSHQTMLINEYRLNLIEARAREFLKEEMQKYFFGEGSEKPSGYKEIK
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
Q60228
|
RELX_ECOLX
|
Putative RelE-like toxin protein
|
MRYQVKFREDALKEWQKLDKAIQQQFAKKLKKCCDNPHIPSAKLRGIKDCYKIKLRASGFRLVYQVIDEQLIIAVVAVGKRERSDVYNLASERMR
|
Toxic component of a type II toxin-antitoxin (TA) system.
|
Q60265
|
Y3531_METJA
|
Putative antitoxin MJECL31
|
MSEIIEVIYEDGVLKPLKPLKIKGKKRLKIKIVNDDVEEFLKSMIIKKCKDIDYKKLKEAYYESF
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
|
Q602M7
|
YIDD_METCA
|
Putative membrane protein insertion efficiency factor
|
MQRLLITLIRLYQYLLSPWLGHHCRFFPTCSNYAMDAIGRFGAMRGAYLTIRRLMRCHPWHPGGIDPVPEKLGKQ
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q60373
|
RELB1_METJA
|
Putative antitoxin RelB1
|
MLNINKEIAQIETELNELKKLRDEISERIEKLEIKLLKLKALAIPEEEFEEDYEEIIEDVKKSLDKKETVPAEEALKELGLL
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is RelE1 (Potential).
|
Q60374
|
RELE1_METJA
|
Putative toxin RelE1
|
MKFNVEIHKRVLKDLKDLPPSNLKKFKELIETLKTNPIPKEKFDIKRLKGSDEVYRVRIGKFRVQYVVLWDDRIIIIRKISRREGAYKNP
|
Toxic component of a type II toxin-antitoxin (TA) system. Its cognate antitoxin is RelB1 (Potential).
|
Q607A3
|
HRCA_METCA
|
Heat-inducible transcription repressor HrcA
|
MASFPELSERAQQLLKALVERYIGEGQPVGSRVLARDAGLSPATIRNVMADLEELGLITSPHTSAGRLPTVSGYRLFVDSLLTVKPLHQAIVDQLWLDLESRENPRDLLETASKLLSELTHMACIISMPRRETLVFQHIEFLPLSDNRVLAILVTSDQEIHNKIIHTPHKFSAAELQTAANFFNAVCGGKDMVSAREHLRAELAKERDRLSEQLLQAGEIAEQALAEGGRSRKPFLVRGETNLMDFVELADVDRLRGLFEAFRQKESIVGLLDRCLESPGVKIIIGEESGFRPLEPCSLVTASYSVDNRVMGVLGVIGPTRMKYERVIPLVDVTAKLVGAALNQRTLAPT
|
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}.
|
Q608F1
|
SDHE_METCA
|
FAD assembly factor SdhE
|
MSQRGRLLWSCRRGMAELDRVLALYVHGAYQEADVSERQAFERLLDLQDADLWRCLTGLARPEDPALAALAAKLRALVGQAAC
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q60AJ7
|
FETP_METCA
|
Probable Fe(2+)-trafficking protein
|
MARRIICAKLGIEADGLDAPPFPGPQGQRIFEHVSKEAWQDWLKLQTMLINEHRLTPFEASARKFLEQEREKFLFGGGTSTPQGYVPPRS
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
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