entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
Q0K981
|
FETP_CUPNH
|
Probable Fe(2+)-trafficking protein
|
MARMVQCIKLNKEAEGLDFPPLPGELGKKIWQSVSKEAWAGWLKHQTMLINENRLNMADARARQYLLKQTEKYFFGEGADQAQGYVPPQS
|
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}.
|
Q0SAH0
|
YIDD_RHOJR
|
Putative membrane protein insertion efficiency factor
|
MKSALHESRADTAEATSSASSAWKSVRALPARTLIFFIELYRTYVSPLRMPTCRFMPTCSEYAVESLRTHGVIKGLFLTVVRLAKCAPWHPGGWDPVPARRDRHAGGRRCCPANVDEQRST
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0SP20
|
YIDD_BORAP
|
Putative membrane protein insertion efficiency factor
|
MNIFKIFFILNYTIIFLIKIYQNTFSKLFGQQCIYKPTCSKYSIECLKKYNFLTALVLMTLRTIRCNALFKGGNDFIPKYNPISTSLKEFQKRLIK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0SPQ0
|
YIDD_CLOPS
|
Putative membrane protein insertion efficiency factor
|
MKKLFIVMIKFYRKYISPLKRPCCRFYPTCSQYALEAIQKYGAFKGGFMSIGRILRCNPFCKGGYDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0SQ60
|
SP5G_CLOPS
|
Putative septation protein SpoVG
|
MNITDVRIRKISAEGKMKAIVSVTFENQFVVHDIKVIEGQNGLFIAMPSRKTPDGEFKDIAHPIDTQTREQIQKAILDEYEKVKNLDMQE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q0SRE1
|
HRCA_CLOPS
|
Heat-inducible transcription repressor HrcA
|
MIDDRKLQILRAIIQDYISTGEPVGSRTIAKKYNLGVSSATIRNEMADLEDMGFLEQPHTSAGRIPSSRGYRLYVDRMIEFERLSSEEEGLIRNSIIDGTLYEVDKIIKQTSALLSELTKMTCIVKAPSVHKSFVKSIQLLKVDDVSILCVLVTDNGVIRNTVIKVKSVPISEELIKISKIITERLKNLTIEQINLEVISNLNRALNGYEDIVNAVLPALYESLKGDETSEVFLEGTINIFNYPEYNNIHKAKEILELLHDKKSISELISDSDDMTVKIGDEIFVPEAKECSIISAGYHVGDRSLGTIALIGPRRINYSKVLSIMTEVMKELNETLKNK
|
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}.
|
Q0SSA6
|
Y1686_CLOPS
|
UPF0122 protein CPR_1686
|
MENRFEISMLIDYYGTLLTEKQFNVMTLYYNEDLSLAEIAEINKTSRQAIYDLIKRCSKQLHSYDEKLKLSKKVDKRYRIKEELMAELNKNSNLDEDIKKYIDEKLEEIINA
|
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}.
|
Q0SZ81
|
FDHE_SHIF8
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQKVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q0T1A7
|
NRDI_SHIF8
|
Protein NrdI
|
MSQLVYFSSSSENTQRFIERLGLPAVRIPLNERERIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIARKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q0T1Q9
|
SYDP_SHIF8
|
Protein Syd
|
MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQSTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLASNLAEFLNQLKPLL
|
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}.
|
Q0T635
|
CBPM_SHIF8
|
Chaperone modulatory protein CbpM
|
MANVTVTFTITEFCLHTGISEEELNEIVGLGVVEPREIQETTWVFDDHAAIVVQRAVRLRHELALDWPGIAVALTLMDDIAHLKQENRLLRQRLSRFVAHP
|
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}.
|
Q0TAG8
|
FDHE_ECOL5
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTTRIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q0TD58
|
GLGS_ECOL5
|
Surface composition regulator
|
MDHSLNSLNNFDFLARSFARMHAEGRPVDILAVTGNMDEEHRTWFCARYAWYCQQMMQTRELELEH
|
Major determinant of cell surface composition. Negatively regulates motility, adhesion and synthesis of biofilm exopolysaccharides. {ECO:0000255|HAMAP-Rule:MF_00525}.
|
Q0TE65
|
SYDP_ECOL5
|
Protein Syd
|
MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQPTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLASNLAEFLNQLKPLL
|
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}.
|
Q0TEK1
|
NRDI_ECOL5
|
Protein NrdI
|
MSQLVYFSSSSENTQRFIERLGLPAVRIPLNERERIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIARKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q0TJ67
|
CBPM_ECOL5
|
Chaperone modulatory protein CbpM
|
MANVTVTFTITEFCLHTGISEEELNEIVGLGVVEPSEIQETTWVFDDHAAIVVQRAVRLRHELALDWPGIAVALTLMDDIAHLKQENRLLRQRLSRFVAHP
|
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}.
|
Q0TLZ1
|
YIDD_CLOP1
|
Putative membrane protein insertion efficiency factor
|
MKKLFIVMIKFYRKYISPLKRPCCRFYPTCSQYALEAIQKYGAFKGGFMSIGRILRCNPFCKGGYDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0TMG2
|
SP5G_CLOP1
|
Putative septation protein SpoVG
|
MNITDVRIRKISAEGKMKAIVSVTFENQFVVHDIKVIEGQNGLFIAMPSRKTPDGEFKDIAHPINTETREQIQKAILDEYEKVKNLDVQE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q0TNS5
|
HRCA_CLOP1
|
Heat-inducible transcription repressor HrcA
|
MIDDRKLQILRAIIQDYISTGEPVGSRTIAKKYNLGVSSATIRNEMADLEDMGFLEQPHTSAGRIPSSRGYRLYVDRMIEFERLSSEEEGLIRSSIIDGTLYEVDKIIKQTSALLSELTKMTCIVKAPSVHKSFVKSIQLLKVDDVSILCVLVTDNGVIRNTVIKVKSVPISEELIKISKIITERLKNLTIEQINLEVISNLNRALSGYEDIVNAVLPALYESLKGDETSEVFLEGTINIFNYPEYNNIHKAKEILELLHDKKSISELISDSDDMTVKIGDEIFVPEAKECSIISAGYHVGDRSLGTIALIGPRRINYSKVLSIMTEVMKELNETLKNK
|
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}.
|
Q0TPN9
|
Y1968_CLOP1
|
UPF0122 protein CPF_1968
|
MENRFEISMLIDYYGTLLTEKQFNVMTLYYNEDLSLAEIAEINKTSRQAIYDLIKRCCKQLHSYDEKLKLSKKIDKRYRIKEELMAELNKNSNLDEDIKKYIDEKLEEIINA
|
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}.
|
Q0UAF6
|
LCL2_PHANO
|
Long chronological lifespan protein 2
|
MARFTSIVLVLSACFVSSRAQFGFFDQMFGNQGHQQHQEPQNVRSDSSWYQAQYEGAQCTHYLCPGTLSCVHFPHHCPCAWESVEDKAELGDGIAICGSKGGWKEGEFAKKVELARKGVL
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
Q0UI01
|
ELCX_PHANO
|
Elsinochrome C biosynthesis cluster protein SNOG_08613
|
MALMIEKLAPPSKRSMTKFTQHCTGNCGQFWPKTWFWSRSSFIHWRLVSRHWPLAPFQLPKTTMAYALVNTKLSALRDIGN
|
Part of the gene cluster that mediates the biosynthesis of elsinochrome C, a perelyenequinone phytotoxin structurally similar to cercosporin. The first step of elsinochrome C biosynthesis is performed by the polyketide synthase elcA which catalyzes the formation of nor-toralactone. The starter unit acyltransferase (SAT) domain of elcA initiates polyketide extension by the selective utilization of acetyl-CoA, which is elongated to the heptaketide in the beta-ketoacyl synthase (KS) domain by successive condensations with six malonyl units introduced by the malonyl acyltransferase (MAT) domain (By similarity). The product template (PT) domain catalyzes C4-C9 and C2-C11 aldol cyclizations and dehydrations to a trihydroxynaphthalene, which is thought to be delivered to the thioesterase (TE) domain for product release (By similarity). The bifunctional enzyme elcB then methylates nor-toralactone to toralactone before conducting an unusual oxidative aromatic ring opening. The next step in perylenequinone biosynthesis is an O-methylation at the nascent OH-6 of the elcB product performed by the O-methyltransferase elcD. The oxidative coupling of the two monomeric naphthol units in perylenequinone biosynthesis is catalyzed by the FAD-dependent monooxygenase elcE and the multicopper oxidase elcG. ElcG might catalyze the first intermolecular coupling in a regio- and stereo-selective manner via a phenol radical coupling mechanism and the elcE could forge the second C-C bond intramolecularly via a hydride transfer mechanism. The fasciclin domain-containing protein elcF might also play a role duting this step (Probable). The last piece of the puzzle in the biosynthesis of elsinochrome C is the additional annulation by enolate coupling to afford the dihydrobenzo(ghi)perylenequinone system, catalyzed by the FAD-dependent monooxygenase elcH.
|
Q0V9U8
|
PHIPL_XENTR
|
Phytanoyl-CoA hydroxylase-interacting protein-like
|
MEVPRLSQHISTPNSPCEEMIKNLSLENIQLCERDGNKSQDSGIAEMEELPVPHNIKISNITCDSFKISWDMDPKSKDRITHYFIDLNKKENKNSNKFKHKDVPTKLVAKAVPLPMTVRGHWFLSPRTEYTVAVQTASKQVDGDYVVSEWSEIIEFCTADYSKVHLTQLMEKAEAIAGRMLKFSVFYRNQHKEYFDYIREHHGNVMQPSLKDNSGSHGSPISTKLEGIFFSCNTEFNTGKPPQDSPYGRYRVEVPAEKLFNPNTNLYFGDFYCMYTAYHYVILVIAPMGSPGDEFCKQRLPQLSLSDNKFLTCTQEHGGLVFHQAQDVILEVIYTDPVDLSWGTVAEIIGHQLMSLSTANAKKDPSCKTCNISVGR
|
May play a role in the development of the central system.
|
Q0VCL9
|
CC038_BOVIN
|
Uncharacterized protein C3orf38 homolog
|
MTGLSYTEMEGCRNLLSLLDNDEIMALCDTITNRLVQPEDRQDAIRAILVYSQSVEELLRRRKVHREIIFKYLATQGVIIPPATEKHNLIQHAKDYWKKQLQPKLKETPEPVKTEDIRLSEQQEKEEKNAEKVDFRRLGEEFCQWFFELLNSQNPLLGPPQDEWGPQHFWHDVKLRFYYNTSEQNVIDYHGAEIVSLRLLSLVKEEYLFLSPNLDSHGQKYAASPHGLVMVGVAGTVHRGNTCLGIFEQIFGLIRCPFVENTWKIKFINLRIIGESSLAPGRLMKPAITFEPSDLEAFYNVNTLCGPVKYNSM
|
May be involved in apoptosis regulation.
|
Q0VM64
|
FETP_ALCBS
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCRKYQSDMEGLPRPPFPGPKGQDIFDHVSQQAWKEWLHEQTMLINEKHLNVMDPEAKRFLDEQRDRFLNNENYEKAEGYVPPAHDANK
|
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}.
|
Q0Z8B5
|
HJMI_ENTHR
|
Hiracin-JM79 immunity factor
|
MDFTKEEKLLNAISKVYNEATIDDYPDLKEKLFLYSKEISEGKSVGEVSMKLSSFLGRYILKHKFGLPKSLIELQEIVSKESQVYRGWASIGIWS
|
Imparts immunity to bacteriocin hiracin-JM79 to naturally sensitive host strains.
|
Q10757
|
ANGT_THETS
|
Angiotensin
|
DRVYIHPFHLLXWG
|
In leeches, the angiotensins are involved in diuresis.
|
Q10VR4
|
YIDD_TRIEI
|
Putative membrane protein insertion efficiency factor
|
MKVLLVRLIKGYKIFISPILPPSCRFQPTCSEYAMEAIERFGIFKGTAMAVMRILRCHPFHPGGYDPVPPKK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q11B41
|
HRCA_CHESB
|
Heat-inducible transcription repressor HrcA
|
MTKPVADQSLQSLDARSRDIFRLIVESYLQRGEPVGSRNLSRLLPTQLSPATIRNVMSDLEHLGLIYAPHVSAGRLPTQQGLRFFVDAFMEVGDLSEEERRVIEAQIKASGRGQSLDHMLTEASQMLSGLSRGAGLVLAAKTEAPLKHIEFIQLEPRKALAILVSQNGDVENRVIELPAGVTASQLVEASNFLNAHIRGRTLAEAKSEMARLKEETREALDSLSQSLVEQGLAIWAGAESDTPARIIIRGRANLLENVTAQADLELLRHLFDDLETKEALIQLLGLAEEGPGVRIFIGSENKLFSLSGSSLIVAPYRDQDSRVIGALGIIGPTRLNYARIVPMVDYTAQLVGRLLR
|
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}.
|
Q11JM2
|
YIDD_CHESB
|
Putative membrane protein insertion efficiency factor
|
MALPAGYSRNWSGPWPKTPGRVLGTAFVRLYQLTLSGFIGNSCRHFPTCSEYAYEAIARHGLWAGGWMGLFRVMHCGPGGTHGIDPVPEILQPRHAWWAPWRLWKLKP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q11SD8
|
YIDD_CYTH3
|
Putative membrane protein insertion efficiency factor
|
MNKKEFFTGAVKQVFIIPVKIYQYSISPLLPGACRYTPTCSEYCVQAIEKYGPLKGIWLGTKRICSCNPWGGSGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q12B25
|
FETP_POLSJ
|
Probable Fe(2+)-trafficking protein
|
MARMVKCIKLGREAEGLDFPPYPGPLGKRLWEEVSKEAWADWMKQQTMLVNENRLNLADARARQYLARQMEKHFFGDGADAVQGYVPPSA
|
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}.
|
Q12HM7
|
YIDD_SHEDO
|
Putative membrane protein insertion efficiency factor
|
MAQAQSPLQWLATTVIRGYQLFISPLMGPRCRFNPTCSHYAIEAIKLHGTAKGSWFALKRILRCHPLHPGGSDPVPPKNDRCNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q12KP8
|
FETP_SHEDO
|
Probable Fe(2+)-trafficking protein
|
MARNVNCVYLNKEAPGLDFQLYPGDLGKRIFDNISKEAWGLWQQKQTMLINEKKLNMMNLEDRQFLEQQMINFLFEGKQVEIEGYVPPVED
|
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}.
|
Q12P27
|
SYDP_SHEDO
|
Protein Syd
|
MSCSSALEKFINSYLNSYQNALSELPRYYPMGVASPCIAQTFDEQSEDAVFWQPVKREPAGDFDNVASALAITLHQDINHFYASFFSAPLQFNSPWGEGELLLAWSLEDFEYLQQNIIGHLLMKQKLKQAPTWFIGVLSDGDTMITVENDTGAVWIEVPGEVPKQQLAPSIAEFITQLSPRITPAIKPVQEVDPQWQHPGIWQRMKLMWRDLTHRSRK
|
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}.
|
Q12ZB3
|
BRIX_METBU
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MLITSSRKPSANTRTMCKYLASFFNCKYMTRGKMGLIDIVSLCENGLLMVVGDYHGSPGSIMFYDSHGVELLSIHLSVFYPDGYKYTPLKALEPSINGDGELFNLLSYYLDIPEGECYYDSKCLIASDDHLEFVYLDNMLFRLNIKNYRKMVMSE
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
Q138N7
|
COWN_RHOPS
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MSGSFDRYVSFKNCDWKVRSERVMARLQRHIDAAENPFWAYFAQKRTELREKQGLDDLRVLHNYLPTLRELLEDNGDLETLAMLEELEVNLM
|
Is required to sustain N(2)-dependent growth in the presence of low levels of carbon monoxide (CO). Probably acts by protecting the N(2) fixation ability of the nitrogenase complex, which is inactivated in the presence of CO. {ECO:0000255|HAMAP-Rule:MF_02117}.
|
Q13SH3
|
YIDD_PARXL
|
Putative membrane protein insertion efficiency factor
|
MQTVLIALLRFYKVAVSPMLGNRCRFYPSCSDYAREAIQYHGAARGTYLAARRICRCHPFSAGGIDLVPPPTSEKR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q13WU6
|
FETP_PARXL
|
Probable Fe(2+)-trafficking protein
|
MTRMVQCAKLGKEAEGLDFPPLPGELGKRIYESISKEAWQAWLKQQTMLINENRLNMADPRARQYLMKQTEKFFFGEGADTAQGYVPPSA
|
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}.
|
Q145F6
|
HRCA_PARXL
|
Heat-inducible transcription repressor HrcA
|
MLDPRAQTLLKTLIERYIAEGQPVGSRTLSRYSGLELSPATIRNVMSDLEDLGLVISPHTSAGRIPTPRGYRLFVDTMLTVESAADEEAVMRTVKTTLQAGEPQKIVAAAASVLSNLSQFAGVVLTPRRSHVFKQIEFMRLSDKRILLIIVTPEGDVQNRIMATQRDFSPSQLVEASNYINAHFAGLSFDDVRRRLREEIDELRGDMTTLMHAAVTASTDEADTGETVLISGERNLLEVADLSSDMARLRKLFDVFDQKTSLLQLLDVSSHAAGVQIFIGGESNLVPIEEMSVVTAPYEVNGKIVGTLGVIGPTRMAYNRVIPIVDITARLLSLTLSQQ
|
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}.
|
Q148I0
|
L10K_BOVIN
|
Leydig cell tumor 10 kDa protein homolog
|
MAQGQRKFQAQKPAKSKAAAAAASARNRGPRKGGRVIAPKKARIVQQQQLKKNLEVGIRKKIEHDVVMKASTSLPKKLALLKASTKKKEASSSTKMPA
|
May have a potential role in hypercalcemia of malignancy.
|
Q15QZ0
|
SYDP_PSEA6
|
Protein Syd
|
MTSTVNQSLDDFMGRFAAFVKEHAEAGAIEYDEDWPSPCYATDVTPESGTSIPWKPVLREQTSEFKDLSEALELTLHPDVAQFYSRYWSDNIVAQHPSGKLQILQAWNEEDFERLQQNIVGHILMKRRLRQPETIFIALTDEDDFVLSVDNQTGAVMLEQVGLQPKEQISPDLATFLDEIEPTTTD
|
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}.
|
Q15ZT1
|
FETP_PSEA6
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCQHLNKEADGLDFQLYPGELGKKIFDNISKEAWTEWQKKQTMLINEKKLNMMEPTARNFLETQMQAYLFEGKEPDIEGYVPPKS
|
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}.
|
Q16A98
|
YIDD_ROSDO
|
Putative membrane protein insertion efficiency factor
|
MSPLAHLLALPVRAYRLIFSPWVGYNCRYQPTCSAYALEALQKHGGLIGAWLTLRRILRCHPWGKCGYDPVPERTRKP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q16MY0
|
WDR48_AEDAE
|
WD repeat-containing protein 48 homolog
|
MLTHKNNQGGRKKMQVSFVIRDAEEKRHRNGVNALQLDTINGRLYSAGRDAIIRVWNSMQNNSQEPYIQSMEHHNDWVNDIVLCCGGRNLISASCDTTVKVWNAHKGFCMSTLRTHRDYVQALAYAKDREQVASAGLDKAIFLWDINTLTALTASNNTVTTSSITGSKDSIYSLAMNPSGTVIVCGSTENTLRIWDPRTCNKIAKLKGHAENVKALVVSEDGQHVISGSSDGKIKQWSIGQQRCVQTISVHSEGVWALLMTDNFSHVISGSRDKKIIMTDLRNPTNSVLICEERAPVLSLCYNYDQTGVWATTWNSDIRCWKLNPSEKLSFEVACIKGGAAIKKYHVLNDKRFMLTKDSEMNVAIYDVLKVKKVEDLGKVDYEEEIKKRSQKVYVPNWFTVDLKTGMPTIVLGQDEVDCFAAWVSAEAGLPEHAESGTDPKVNYGSLLLQALLEYWKPPPPHHHLQGVGSDLDSNGCDGDIRGNEYFSVPKHTPIIFSEVGGRNVCRLLVKDAVGETESALLSETVPSWVTNVVIERTIPKFIKLPFYLLAHPSMLKQDRSKKERLIANEFIQCRKVCEHVLEKVLGADLPASTGNSNSSQNNSQSDANSEGSQVPAEERIELLCNDVICDPNMDLRTVRHFIWKQSSDLTFHYRTKSN
|
Regulator of deubiquitinating complexes. Activates deubiquitination by increasing the catalytic turnover without increasing the affinity of deubiquitinating enzymes for the substrate (By similarity).
|
Q196Y1
|
VF282_IIV3
|
Putative transcription factor 079L
|
MSKKQTTAAATAPIDILELHTQIQQFIETESKNVVVLEAKLVKINQLLECDYLRPRIIYRLKMEKEMCEKLIIEHHNLDFFNIDVAHLIEEYHMLNRTEIVLPFFSPTKDQLTQQLEHKRKKMDLEKQFLNKLKNYTHLKNFEFMMKHCEFIPKSSPPPCVCGNKTEFIKDDDRAVCAICCTEQSLISNTSSFSDVGRVNMASKYTYNRKVHFRDCITQYQGKQKTHIPEEIYTILETKLLEKNLLNTEPGLTVEKRYEKVTRAMVLDILKELGSKDVKKFYDDIVLIHHTLTKQPCDNIEYLEDSLLDDFDKLTETYDNLYVNQDSPDDERGGTKRKNFINAQFVLYQLLRKHNHPCNSMDFLTLKKSERKRFHHTICKKLFSILEWKYSYSIC
|
Transcription activation.
|
Q1AR60
|
YIDD_RUBXD
|
Putative membrane protein insertion efficiency factor
|
MAGRLVILVLRAYQRFVSPLFPPSCRFTPSCSQYAVEAVERYGPLKGGAMAAWRVLRCHPFSRGGVDPVR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1B6B7
|
HRCA_MYCSS
|
Heat-inducible transcription repressor HrcA
|
MGSADDRRFEVLRAIVADFVATKEPIGSKTLVERHNLGVSSATVRNDMAVLEAEGYITQPHTSSGRVPTEKGYREFVDRLDDVKPLSSAERRAILKFLETGVDLDDVLRRAVRLLAQLTRQVAIVQYPTLSTSSVRHLEVVALTPARLLLVVITDTGRVDQRIVELGDAIDEHELATLRDLLGQALEGKRLSAASVAVSDLATHLSGSPGMSHRLADAVGRSATVLVETLVEHTEERLLLGGTANLTRNTADFGGSLRSVLEALEEQVVVLRLLAAQQEAGKVTVRIGHETEAEQMAGTSVVTTAYGSSGKVYGGMGVVGPTRMDYPGTIANVAAVALYIGEVLGTR
|
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}.
|
Q1BB09
|
NRDI_MYCSS
|
Protein NrdI
|
MGNIVYFSSVSENTHRFVEKLELPATRIPILGRIQDPDFVREPYVLVLPTYGGGHANGPDPDAGGYVPKQVIAFLNNEHNRSLIRGVIAAGNTNFGAEFGYAGDVVSRKCGVPYLYRFELMGTTDDVLAVRAGLENFWKEQTCHPPSQLQSL
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q1BHX0
|
FETP_BURO1
|
Probable Fe(2+)-trafficking protein
|
MARMIQCAKLGKEAEGLDFPPLPGELGKRIYESVSKEAWQGWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGDGADQASGYVPPTEG
|
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}.
|
Q1BSF6
|
YIDD_BURO1
|
Putative membrane protein insertion efficiency factor
|
MKTVLIALLRFYKVAVSPMLGNRCRFYPSCSDYAREAIQYHGAARGTYLAVRRVCRCHPFSAGGVDLVPPPNSDTRARGEADARSHRL
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1BYY0
|
HRCA_BURO1
|
Heat-inducible transcription repressor HrcA
|
MLDPRARTLLKTLIERYIADGQPVGSRTLSRYSGLELSPATIRNVMSDLEELGLVSSPHTSAGRVPTPRGYRLFVDTMLTVEAPIDAEAVARQVQNTLQAGEPQQRVVAAAASVLSNLSQFAGVVLTPRRSHVFKQIEFMRLSDKRILLIIVTPEGDVQNRMLATPRDYSPSQLTEASNYINAHFAGLSFDEVRRRLRDEIDQLRGDMTTLMHAAVTASTEVPDTEDTVLISGERNLLEVADLSSDMARLRKLFDVFDQKTGLLQLLDVSSHAQGVQIFIGGESTLVPIEEMSVVTAPYEVNGQIVGTLGVIGPTRMAYNRVIPIVDITARLLSLTLSQQ
|
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}.
|
Q1C0B5
|
YIDD_YERPA
|
Putative membrane protein insertion efficiency factor
|
MASPLSPGSRILIGLIRGYQLVISPLLGPRCRFHPTCSHYGIEALRRFGMIKGSWLTLKRVLKCHPLNSGGDDPVPPKLDDNREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1C3I0
|
FDHE_YERPA
|
Protein FdhE homolog
|
MSIRIVPKDQLGKQREKGTTAGNIPPLLFANLKSLYTRRTERLQQLALDNPLADYLDFAAKITEAQQKALHDHPLVLDMQAELVQSAASGKPPLDGSVFPRTEHWRKLLSALIAELRHDAPDHILAVLDNLDKASVHELELYADALLNRDFSQVGSEKAPFIWAALSLYWAQMASQIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTHNGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLASLILDAKMEGEGFARSSINPFLFPGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q1CAP5
|
SYDP_YERPA
|
Protein Syd
|
MDLNISTALRSFTQRYIDLWQQQTGHLPASKELYGVPSPCIVETGEDQVFWQPQAFLPEATLTNIERALEIQLHPDIHDFYTQQYAGDMMADLGNHRFTLLQVWSEDDFIRLQENLIGHLVTQKRLKLSPTLFLATTSSEMTMASLCNVSGNVVLEQFGSDKRTLLASTLSHFLDALRPVLPE
|
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}.
|
Q1CB93
|
FETP_YERPA
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLKKDAERQDFQLYPGEIGKRIYNEISKEAWSQWITKQTMLINEKKLSMMNIEDRKLLEQEMVNFLFEGQDVHIAGYTPPSK
|
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}.
|
Q1CCJ5
|
YIDD_YERPN
|
Putative membrane protein insertion efficiency factor
|
MASPLSPGSRILIGLIRGYQLVISPLLGPRCRFHPTCSHYGIEALRRFGMIKGSWLTLKRVLKCHPLNSGGDDPVPPKLDDNREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1CDA1
|
FDHE_YERPN
|
Protein FdhE homolog
|
MSIRIVPKDQLGKQREKGTTAGNIPPLLFANLKSLYTRRTERLQQLALDNPLADYLDFAAKITEAQQKALHDHPLVLDMQAELVQSAASGKPPLDGSVFPRTEHWRKLLSALIAELRHDAPDHILAVLDNLDKASVHELELYADALLNRDFSQVGSEKAPFIWAALSLYWAQMASQIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTHNGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLASLILDAKMEGEGFARSSINPFLFPGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q1CEV2
|
FETP_YERPN
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLKKDAERQDFQLYPGEIGKRIYNEISKEAWSQWITKQTMLINEKKLSMMNIEDRKLLEQEMVNFLFEGQDVHIAGYTPPSK
|
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}.
|
Q1CFD6
|
SYDP_YERPN
|
Protein Syd
|
MDLNISTALRSFTQRYIDLWQQQTGHLPASKELYGVPSPCIVETGEDQVFWQPQAFLPEATLTNIERALEIQLHPDIHDFYTQQYAGDMMADLGNHRFTLLQVWSEDDFIRLQENLIGHLVTQKRLKLSPTLFLATTSSEMTMASLCNVSGNVVLEQFGSDKRTLLASTLSHFLDALRPVLPE
|
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}.
|
Q1CRI0
|
YIDD_HELPH
|
Putative membrane protein insertion efficiency factor
|
MRNNKTPFLSAIFTASIRGYQRFFSAFTPSSCRFYPTCSNYALWLLCFENPLSAMGKIAIRILSCNPFCSGGIAYPTTRLKRPSLLQSHKDFNRNFKTITFWLVPTTKSRTTYYIIKV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1CVG0
|
YIDD_MYXXD
|
Putative membrane protein insertion efficiency factor
|
MSPLAFVISLPIRFYRKFLGPLLPKVCRFHPSCSTYAMEALEKHGGLKGSWLTLWRLVRCQPFHPGGIDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1D295
|
SP5G_MYXXD
|
Putative septation protein SpoVG
|
MNITDVRVFPVEEDKLKAYVTITLDHCFVIRDLKVIHGSTGLFIAMPAKKRKDGTYKDIAHPLNADTRSQMERVILMEYERHLHQAQAGMLVAAPADLD
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q1E2I3
|
DML1_COCIM
|
Protein DML1
|
MREIITLQLGQRSNYLATHFWNVQESYFTYSENEASPVDHDISFRPGIGADGSETFTPRTIIYDLKGGFGSLRQYNALYEVEENVGMPKGLWDGNEVIQRQPNIPQSEYQKALELGLPLPRLTPETVRYWSDFNRLFYHPKSIVQLNEYEMNSQLMPFEDWTVGEAFFNSLDREHDLLDRDFRPFAEECDQLRGIQLFTGTDDAWGGFAARYIDRLRDEFGKKIIWTFALESGLKTEREKQFLRAKNSAKSISEISRQSTAYVPISMPPSKLPHYVNLNIASEWYISALTSVAVESVTLPGRLRWYEGIEPWFLDNAGPQRIFALRATIRSENSELPFASHLRPNDSTQMDTDEVDHDEIEQSEQRFDLGFSPIGSATRTNNTHIFSQVQVVRDSKCNSERPERAEVGQGLTSHRLSLMTGYVPSTLSNFRSTLEFPILDSFPSDLIHEQGPAGSTLRVDAALSATSGIGRDLKNLQQTIGRRIALEEREDLINGLHELSHAYQAGWENDSDSGDD
|
Involved in the partitioning of the mitochondrial organelle and mitochondrial DNA (mtDNA) inheritance.
|
Q1GAW1
|
YIDD_LACDA
|
Putative membrane protein insertion efficiency factor
|
MRQIMILLVRFYQRAISPILPDSCCFYPTCSSYMITALEKQGPLLGLLMGLARILRCNPFNRGGVDPVPDKFTLLRNPHPEEYEDEIIARKFHSH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1GJX2
|
YIDD_RUEST
|
Putative membrane protein insertion efficiency factor
|
MRLLARLIALPVRGYRLLFSPWVGFNCRYQPTCSAYALDALERHGPFKGTYLMLRRIGRCHPFGGSGYDPVPGADPKHDRCCGRTP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1GN72
|
YIDD_SPHAL
|
Putative membrane protein insertion efficiency factor
|
MIARLLILIARAWQLGPSRVLPPTCRYAPSCSEYAIVALRRHGAIKGGWIATKRLLRCHPWGGHGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1GXL5
|
YIDD_METFK
|
Putative membrane protein insertion efficiency factor
|
MLARLLVGLIKLYQWTLSPLLGQRCRFYPTCSQYAVEAIQKHGAWRGAFFTICRLSKCHPWHDGGHDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1I0U9
|
CAPSD_MPRVN
|
Major inner capsid protein VP3
|
MSNTMPEGYIPRPGKDQTLEAYISEELSKHNLTFNDVLNNEEMMAELSKDDAFMKLKAEFENKDKPEVVEASSNKKEEKVSEPKVEEKKDPEPEKDAPALVVEEVVMDDDDADEVEKPTMEAPKSTVAKLTETQFRIDSSNLMSKIDFTIAYDKLMTVDSFGVEDLVTKSPFYATRLDKPRHMRMDEFCNEFIEPAIPSALGHPNSEGYTDMVGFDWEKNQYLNLYEELGRRSVEAIELDDDANAGDVIIGGVTSLSMIKQVNAIVHDAILPKGRLAYIMAQMRAARCLQFTRVANGQEATPEDKLQAYMDAYMNPTYTRALRIRTPEPRVVTYNKAIDYVMYRLTLNADNDFISPMVQISDSIDVGRGVRSRSYQAATTVMSVIASSHRNLERPMTSARAPAKVITAFTDLVAPPAAEAMQKLGSYCLGGRRAELTVDMTDPILQSTDSVLAPIAAAANLILLDTNRLGNDIKRTLVYRMLSPFYGTGTRAEVDRINFNNIPRIVLTPIPDRRGLHGRLANFIRRQLTKPAYGRMDRNDSRIWRADIQTTPMLPFVPAGGMTPLSMHIGDERLENQAYAPQANELKVSLMDFVKMFDLMHARQGKETYLSSQFSAILTNESSYLYNSISMVMRTMIRGWESLDLLPPLDGAVPGALEMDRTEAFVLPFTGAVSFICYGIEDDGLEYVPWEQRKEIPMPSSFPMLLDMEIRVANELLLEAADPAGRFTRSDMLINQDEFINMAEFIMKKYLTSIDGGEFGTRYRLHWYLFEGIRIHNRTLQTPGIEDLKVARRILDGVKYPEDIATAVYIKIYESVNPIDLVNPDPQRSDYQVYMEEIPADDEILEIKDIVTYRREDGGEDFNFTPYLHSGETFNLDLIRKLAKSIPGDHRYVKVPTKVTVKPVELLDNVDVIAEDFTVALKFKKGVNEMRFEASDIPLYYRWDKFNGRSQLTLDVRVFPDTNVLLDHVMESDPRMGYAPQVLNDGTVGWVSTLSGNVYLEERKVCRREEEVLKSGIDLLIDPYGV
|
Self-assembles to form an icosahedral capsid with a pseudo T=2 symmetry, about 60 nm in diameter, and consisting of 120 VP3 subunits. The capsid encapsulates the genomic RNA (By similarity).
|
Q1I2H3
|
YIDD_PSEE4
|
Putative membrane protein insertion efficiency factor
|
MRKLALVPIQFYRYAISPLMASHCRFYPSCSCYAYEAIENHGLLRGGWLAVRRLGRCHPWNDGGFDPVPPAPSSRTSSIAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1I3G0
|
FETP_PSEE4
|
Probable Fe(2+)-trafficking protein
|
MTRTVKCRKYNEELPGLDRPPYPGAKGQDIFEHISQKAWKEWQDHQTMLINEKRLNMMNAEDRKFIQAEMDKFFAGEDYAQAEGYVPPSN
|
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}.
|
Q1I491
|
CBPM_PSEE4
|
Chaperone modulatory protein CbpM
|
MSSTLIVQLDMRTLCQEADVSADWVIEIVEHGIVEPSGRTPEEWVFDDRAPVTLKRAVKLHQELELEWEGVALALELLEEVQQLRSENSMLKQRLGRFTQM
|
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}.
|
Q1IJI6
|
FETP_KORVE
|
Probable Fe(2+)-trafficking protein
|
MAHMVKCVKLGREAEGLEEPPFDSELGQKIYNNVSAEAWRGWTEHQKMLLNEYRLQPWKKEHQEFLVQQMEAYFFGEGSEAPKEFVPPSH
|
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}.
|
Q1IV77
|
YIDD_KORVE
|
Putative membrane protein insertion efficiency factor
|
MKAVLVQMLKGYKRWISPLLPVSCRYVPTCSEYAMEAISIHGAVRGSVLALGRLLRCHPFVRGGYDPVPRSHSCCDDKISTTAHDAVR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1IY23
|
YIDD_DEIGD
|
Putative membrane protein insertion efficiency factor
|
MSAAARGLVRLVKSYQRHLSPRKPAPTCRFTPTCSQYAVEAIERHGALKGAWLAAWRVLRCNPLVPGGCDPVPEHFPSWRGPHPKTPSRKTPE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1J576
|
HRCA_STRPF
|
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}.
|
Q1J6G8
|
Y1065_STRPF
|
UPF0122 protein MGAS10750_Spy1065
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q1J861
|
NRDI_STRPF
|
Protein NrdI
|
MAELIIVYFSSKSNNTHRFVQKLGLPAQRIPVDNRPLEVSTHYLLIVPTYAAGGSDAKGAVPKQVIRFLNNPNNRKHCKGVISSGNTNFGDTFALAGPIISQKLQVPLLHQFELLGTATDVKKVQAIFARLKHHTHDKQNKPTT
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q1J881
|
YABA_STRPF
|
Initiation-control protein YabA
|
MNKKELFDAFDGFSQNLMVTLAEIEAMKKQVQSLVEENTILRLENTKLRERLSHLEHETVAKNPSKQRKDHLEGIYDEGFHICNFFYGQRRENDEECMFCRELLDRK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q1J8A6
|
YIDD_STRPF
|
Putative membrane protein insertion efficiency factor
|
MMKKLLIVSVKAYQKYISPLSPPSCRYKPTCSAYMLTAIEKHGTKGILMGIARILRCHPFVAGGVDPVPEDFSLMRNKNTSKNAEKA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1JA81
|
HRCA_STRPB
|
Heat-inducible transcription repressor HrcA
|
MITQRQNDILNLIVELFTQTHEPVGSKALQRTIDSSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYHVIKAFDFEAFKLEDMLQKASHILAEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDNSVIDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQSLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLAAKLGDYYRYLNSNHYEVH
|
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}.
|
Q1JBN1
|
Y975_STRPB
|
UPF0122 protein MGAS2096_Spy0975
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q1JD89
|
NRDI_STRPB
|
Protein NrdI
|
MAELIIVYFSSKSNNTHRFVQKLGLPAQRIPVDNRPLEVSTHYLLIVPTYAAGGSDAKGAVPKQVIRFLNNPNNRKHCKGVISSGNTNFGDTFALAGPIISQKLQVPLLHQFELLGTATDVKKVQAIFARLKHHTHDKQKQTNNLITERTHPCHKPMRHTSH
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q1JDA2
|
YABA_STRPB
|
Initiation-control protein YabA
|
MNKKELFDAFDGFSQNLMVTLAEIEAMKKQVQSLVEENTILRLENTKLRERLSHLEHETVAKNPSKQRKDHLEGIYDEGFHICNFFYGQRRENDEECMFCRELLDRK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q1JDC8
|
YIDD_STRPB
|
Putative membrane protein insertion efficiency factor
|
MMKKLLIVSVKAYQKYISPLSPPSCRYKPTCSAYMLTAIEKHGTKGILMGIARILRCHPFVAGGVDPVPEDFSLMRNKNTSKNAEKA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q1JFC6
|
HRCA_STRPD
|
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}.
|
Q1JGP9
|
Y1030_STRPD
|
UPF0122 protein MGAS10270_Spy1030
|
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. {ECO:0000255|HAMAP-Rule:MF_00245}.
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Q1JIB1
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NRDI_STRPD
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Protein NrdI
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MAELIIVYFSSKSNNTHRFVQKLGLPAQRIPVDNRPLEVSTHYLLIVPTYAAGGSDAKGAVPKQVIRFLNNPNNRKHCKGVISSGNTNFGDTFALAGPIISRKLQVPLLHQFELLGTATDVKKVQAIFARLKHHTHDKQKQTNNLITERTHPCHKPMRHTSH
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Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
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Q1JIC7
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YABA_STRPD
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Initiation-control protein YabA
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MNKKELFDAFDGFSQNLMVTLAEIEAMKKQVQSLVEENTILRLENTKLRERLSHLEHETVAKNPSKQRKDHLEGIYDEGFHICNFFYGQRRENDEECMFCRELLDRK
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Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
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Q1JIF2
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YIDD_STRPD
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Putative membrane protein insertion efficiency factor
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MMKKLLIVSVKAYQKYISPLSPPSCRYKPTCSAYMLTAIEKHGTKGILMGIARILRCHPFVAGGVDPVPEDFSLMRNKNTSKNAEKA
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Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
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Q1JKD4
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HRCA_STRPC
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Heat-inducible transcription repressor HrcA
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MITQRQNDILNLIVELFTQTHEPVGSKALQRTIDSSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYHVIKAFDFEAFKLEDMLQKASHILAEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDNSVIDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQSLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLAAKLGDYYRYLNSNHYEVH
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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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Q1JLL4
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Y1018_STRPC
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UPF0122 protein MGAS9429_Spy1018
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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. {ECO:0000255|HAMAP-Rule:MF_00245}.
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Q1JN60
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NRDI_STRPC
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Protein NrdI
|
MAELIIVYFSSKSNNTHRFVQKLGLPAQRIPVDNRPLEVSTHYLLIVPTYAAGGSDAKGAVPKQVIRFLNNPNNRKHCKGVISSGNTNFGDTFALAGPIISQKLQVPLLHQFELLGTATDVKKVQAIFARLKHHTHDKQKQTNNLITERTHPCHKPMRHTSH
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Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
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Q1JN74
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YABA_STRPC
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Initiation-control protein YabA
|
MNKKELFDAFDGFSQNLMVTLAEIEAMKKQVQSLVEENTILRLENTKLRERLSHLEHETVAKNPSKQRKDHLEGIYDEGFHICNFFYGQRRENDEECMFCRELLDRK
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Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
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Q1JNA1
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YIDD_STRPC
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Putative membrane protein insertion efficiency factor
|
MMKKLLIVSVKAYQKYISPLSPPSCRYKPTCSAYMLTAIEKHGTKGILMGIARILRCHPFVAGGVDPVPEDFSLMRNKNTSKNAEKA
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Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
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Q1LLM6
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FETP_CUPMC
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Probable Fe(2+)-trafficking protein
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MARMVHCIKLNKEAEGLDFPPLPGDLGKKIWQNVSKEAWAGWLKHQTMLINENRLNMADPRARQYLIKQTEKYFFGDGADQAAGYVPPPAA
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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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Q1LSZ8
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FETP_BAUCH
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Probable Fe(2+)-trafficking protein
|
MSKNIYCVFLRKQAEGQDFQSYPGELGKHIFNNISKEAWAKWQQKQTMLINENKLNLISNTDRNFLEKEMIKFLFKS
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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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Q1LTW0
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YIDD_BAUCH
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Putative membrane protein insertion efficiency factor
|
MASLLSPIIKLLSYVIRCYQLIISPLIKPHCRFLPTCSQYSITAIHRFGIFKGIWLTLIRILRCNPWSQGGEDQVPLNIFDKREY
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Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
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Q1LYL8
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ASTE1_DANRE
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Protein asteroid homolog 1
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MGVQGLKTYIESSSRNDLKTWAFRDKQLIIDGCNLFYSLCFDSNLDQIHGGDYDTFEKVVRQFFENLSACDVHPYVVIDGGDDHTDKKWDTLLTRKQKKIKDAYDLSVGKRRQVLPLLTEKVFKQVLKKLKVPVVQTLEEADWEIAALAEEWNCPVLSNDSDFYIFNLRAGLLPITHFHWRKVRVNRKTNQKFILSKHFIARKFCKSFKMNVSLLPVFASILGNDYVKLPNIKNRHWERYSNPGSENPQIEGLLNWLSQFSGPDEAISALLRPTSNKTKAQEELSHGIQDYKLVPGSLAQIFRSTKVPQKISKGPLHVLPRWTLRPILDGKMSSYIINVLLHNRASLNAQVEDFQLPSANETSLHIRQVFYGLLLLGEQQTAGKRESVKGTTKRYVVEYSRQQIKRSSENVEAIQTKAMEGLRLETLYQEPHAVRLQVILDTLGVSCEMLKGTPDALQLQMFVTRYWLVNAEPQPCRVHLWGLLLGMVYGKLSSSPNAQKDMLSRLRVKASRKGGSVDIDVAHAYSQWQSCLKYSLNLNYLLSFPLTEPDCASLYRGSLVHQAVGELRRGISLEALLVKGSSAERIFKQLKDIIVSLMGDDFIKKMKSGLEHRDAGKTQRASKGQKDELDIYFEQMMIESIDSEDEELLDVRKSKAKNHLMELPVCPIRARHKAKARNARHPCKKYERRCFE
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Possible role in EGF receptor signaling.
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Q1MBD4
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NRDI_RHIL3
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Protein NrdI
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MGLIVYYSSRSENTHRFVAKLGLRAARIPPSGAAGAFHIREPFVLIVPTYSGDGGKGAVPKQVIRFLNDAENRGHIRGVIAAGNSNFGETYGLAGDVVSQKCQVPYLYRFELLGTEADVANVKHGMERFWTREHL
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Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
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