entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
Q7MXI5
|
YIDD_PORGI
|
Putative membrane protein insertion efficiency factor
|
MRLIKAFLVQLLLLPIFFYKRFISPLTPPSCRFTPSCSSYAIEALRKYGPGKGLLLSIKRILRCHPWGGSGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7MXZ3
|
YIDD_PHOLL
|
Putative membrane protein insertion efficiency factor
|
MASSLSFGSRFLIALIRGYQLVISPLLGPRCRFNPTCSQYGIEALRRFGVIKGCWLTVKRVLKCHPLHEGGDDPVPPVKNNDNREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7MY03
|
FDHE_PHOLL
|
Protein FdhE homolog
|
MSIHIVPKEQLSKDRINEKTADYIPPLLFANLRNLYQRRAERLQQLAKESSFVDYLNFSAQVAEAQQKALHDNPLKMEIADILEKSVIEGKPPLDCKTFQRTEHWQKLLHSLIAELLPDASEHVNAALDNLEKASEQELEQMADALLKNEFSQVSPEKALFIWAALSLYWAQMANQIPGKARAEYGEHRQFCPVCNSMPVSSVVQIGTTNGLRYLHCSLCESEWHVVRVKCSNCEQTRDLNYWSLDSEHAAVKAESCGDCGSYLKILYQEKDPKVEAVADDLASLILDAKMEEEGFARSSINPFLFPNE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q7N772
|
NRDI_PHOLL
|
Protein NrdI
|
MNINPLIYFSSSSSNSHRFVQKLEIPAFRIPINQSDSPLNITSPYILLTPSYGGGSTKGAVPPQVIRFLNIAENRAFIRGVIAAGNTNFGEAYGIAGRIISEKCRIPLLYRFELLGTEEDVQRVRQGIQRFWQHDSLENM
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q7N7I1
|
FETP_PHOLL
|
Probable Fe(2+)-trafficking protein
|
MNRTVFCTFLQREAEGLDFQLYPGELGKRIFNEISKEAWRQWMSKQTMLINEKKLSTMNPEDRKLLEQEMTKFLFEGHDIQIDGYTPPEK
|
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}.
|
Q7NJB9
|
YIDD_GLOVI
|
Putative membrane protein insertion efficiency factor
|
MELVRRAATGAIRFYQRFVSPLTPPTCRYVPTCSEYTRQAIERFGVAAGIWLGTKRLCRCHPLHPGGYDPVPERRSVR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7NPT7
|
YIDD_CHRVO
|
Putative membrane protein insertion efficiency factor
|
MSRILILLIRFYQLAISPWLAPRCRFQPTCSGYAIEAVSKHGALKGGCLAARRICRCHPWGGSGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7NSR4
|
FETP_CHRVO
|
Probable Fe(2+)-trafficking protein
|
MSRTVNCIKLGREAEGLDFPPLPGELGKRVYESVSKEAWQGWLRYQTMLINENRLSLADARARQYLASQLDAYFFGQGADAPAGYTPPQN
|
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}.
|
Q7TDB6
|
RDRP_MYRV9
|
RNA-directed RNA polymerase VP1 (EC 2.7.7.48)
|
MSLTSRYTHFVPDSTITEILNDSNTPQILLHYANIVNGSTPVHFTSHHDNQVNWTVATLTRMSQYMIPDFMKLFPPLEPTLSLQPDCHCSFINLPRPEIKIPIEILSPPKPNYAKYHYDATTSRVFVNSKHEMYMDNFDVSQLIRDVAAIKTDSPSGNITKGLLKTFHDSIKLRALSPIMSMFHSLLSYRCPCCTSLNGMKKLNHLCFQYSSIYAFLCDMVRPYMCVPFFVDRLGVQILPGFKVSSQYPLLFFEAIELMHTVGLGNLSDSLSGWCFYTWLDRARIGVFREMFNRRGSITMLKSRVVSTGTIFRFSQREFVIESITEQRSTDISPTFEECSFSDSQYIQDNCYKPIYDITTTLDDVKCRWLDVALNYFYGAVLYVTGPVSLALEQSGMGRPGSLNLQFGGTTDVYVEGRWITIDVEPVSPFVSRIKQLADRELAKTKVNGDSLEHGFFEAQTTNSAGNTKETLAGLRSEIIEQHDSPQEGRLLASMAGIRVIDAMRRFNTTFRDHTEFLNEVRRPTKAGMRYQQQRRPRVIQMTGTEAQLGGWLLLNVYEPTYKRLGYTSSGKNIGDIRDMQAVLEASGQNGINSSVDIIGMDASTQNTHVTLLGSAAIKAYNPERIGFPKMFFQSTHNGGDANSRVLPTRVTRDGQTIPKDDDVKYNLPQLAIIYSLHGMHGPTILYDGYFAPAVLTSQTVFRSGWYNTSSQHTMLGSLVLLSLEEDIRNGYKNPYDGAPERSLIAKHWHSIRIIGRVLGDDILLKAFGPPTLTPDELREVTAEVCAEFEHRMELLGFLCERAFSDVMCEFLKQKGFGGAPHMFPDRLVLYTSERGNQAMTNPTTMYRVCDALIIEFNSRSRNIFNTCVSRRVLQTVCSTFALRMTSSGHLVRRSYASRKPYSRVAKVSDGILSELHNHKTVFRIIDYNVLGDHIAMIFLPMLWATNHILGCPPPAIVSISGANIPAASPLTYPSAAITTFWLTATSRRKIDFDSSATAYKKSMSDISNLTAVPLDIIFSFSNAMELSPLSINLDKDYDIDTLRTFGFIVGIMSDSLFPTPSATRAKIKSPVVDDWSRYADSLLNPTRVRSSHHGSEILAESNVVVPYELRYAHRGTAKVRQSMYELPVTDLEYGENTMTTLTQLSESLKVKPGTSKLLRDAMLAGEVFVIPTTHPVTLPCPSFDAHGYGHIIPPNSLQSLLLTHLGLPVSSASYTSSFAKTILSDGKLPGSAEAYLSLYQETYKKGPSAVAYLKDAIGFSDSSMSALERLASNGLYGISGASFAYNPRGGFFFRFDQDNADRFGTSLSPSPTIRRLDIVHMMFTMLMYPTTMVSQNQWMMVRFGRSFSRLARR
|
RNA-directed RNA polymerase that is involved in transcription and genome replication. Following infection, it catalyzes the synthesis of fully conservative plus strands. After core assembly, which consists in recruitment of one capped plus-strand for each genomic segments and polymerase complexes, the polymerase switches mode and catalyzes the synthesis of complementary minus-strands (By similarity).
|
Q7TF75
|
VP8_FDVS
|
Microtubule-associated protein VP8
|
MTTGTDVRISLRLLFYELWDNNAKLTKNKTTTPTTSKTTSKILFNSKRTTPTHGYDADYIAELSNNFEFAGFTAPTPHNIRKAFTRLKIMFERMNRYPDEIFLSRHRMLGFVIYQPETSGPIPAFHPKCKFYKLSDNHTHDEKIEIVKNHILNGEIVKTVDLKIDQSFESYYYDKSNAQASQKFLASMHTCDFSFLSFPYINDLTATELGLLPEWAAILLSYMKIINVRGIYNDVVECIDPSQQFCVFEIIGSLTGISNGHFWSVLNDRRSMDVIAKEVEKIALDNQPFXKDGNLNHLLFNSINLSDPLNFNIFHYSFKLKIFPTTLNPLDDLVLLRMKDLIKAFNAGNDVQVIGNKCIGKTRLTAELKKKYLNLLIIDSDDYGKFITLLLNNCPNLFLNNDFEINDEVFEEEIFNVTVIEYANVIRDGTIVIETFFERLMFEIMSLNLTNGEYDVDAIFHSFNARFHAIVNSSMIGYRLFFTKFRKLMFDNFNYTQVLHFVHSYSELSFYPHCVAYITLEPSYNPCCLLYKNRVKRFLSITRSDKGVSSELFLHQFYEKFTTKVNPTPVFVFRYYFGLTNGLSISELALDENT
|
Minor inner capsid component. Displays NTPase and RNA 5'-triphosphatase (RTPase) activities. May function as a cofactor of polymerase VP1. 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).
|
Q7TT23
|
DAAF9_MOUSE
|
Dynein axonemal assembly factor 9 (DNAAF9)
|
MDSFDPQQLGLSPARFAGTFGSGAASVSCSRLRQVQSVLTQSSKSQPDGILCILGIDSRYNEGCRELANYLLFGLYSQNATDFEKTGFSEEILDDVILLIKSDSVHLYCNPVNYRYLLPYVAHWRNLHFHCMTENEYEDEEAAEEFKISSFVDMVRDCSRIGIPYSSQGHLQIFDMFVVEKWPIVQAFALEGIGGDGFFTMKYELQDVSLSLWNVYSRMDPASLENMLSEDLAVFEHQWTSFFANFDTEIPFLLELSESQAGEPFRSYFGHGMLSSHITENSPHRQPFVLFGNHSTRDNLSAGSFNFPSEGHLVRNTGPAGSFAKHMVAQCVSPKGPLACSRTYFFGATHVPYLGDNEKLPRTTEQIRLLSQIYAAVIEAVLAGIACYAKTCSLAKAKEVAEHTLESGLVFTELVPFKADLRSKVTFHIHAVNNQGRIVPLNNEDSLSFVKTARMTVYDIPDLLGGGGGGCLGSVVFSESFLTSRILVKEKDGTITPETSYIILTAAIPRFCSWLVEDSEIKLSEKTLQATKGDDCCLGTLLTGGKGAYLYSNSPQSGPEEGSAYFFSGGLLFSHRHHGSIVIAKEHVDAFSFYDGDSTSVVAALLIHFRSSILPHLPVHFHGSSNFLMLALFPKSKIYQAFYSEVFSPWQQQDNSGLSLKVIQEDGLSAEQKRLHSNAQKLFSALSPPAQDWSSPKLLSGKLPELDRFLQHFAIGSIGQEPVMRAHLVGLLQQPEMSPAHEVESDKVVISIVTGLPGCHASKLCAFLITLHKEYGRWMVYRQIMDSSECFHAAHFQKYLSSALEAQQNRSARQSAYIRKKTRLLVVLQGYTDVIDVVQALQTHPDPNVRSYFTIGAVTVCVEPLSCYMEHRFLFPKCLDQCSQGVVSNVVFTSHTAEQKHPLLVQLQTLIRASNPTAAFILAENGIVTRNEDIELILSENSFSSPQMLRSRYLLFPGWYEGKFDAGSVFPLMVQICVWFDCPLEKTRFVSRCRAIQSSIKPSPFSGNIYHILGKVKFSDSEKTMEVCHNTLTNSLTIVPVLEGPTPPPNSRSSPQDNGQPECYLVFIGCSLKEDSLKDWLRQSAKQRPQRKALKTRGMLTQQEIKNIHVKRHLDPLPAGYFYNGTQFVNFFGDKTDFHPLMDQFMNDYVEEANREIERYNRELEQQEYRDLFEQKPKP
|
May act as an effector for ARL3.
|
Q7U3Z7
|
HRCA_PARMW
|
Heat-inducible transcription repressor HrcA
|
MKPLSARQQQVLQATVHHYVDTMEPVGSRTLVQRFGIPASSATVRSAMGALEKRGLLTQPHTSAGRIPSALGYRCYVDDLLPEPGVAVQHLERELTGLSLRWAALDDLLQQLARRLTDFTGLMSLITRPQQPRAQLEAIRLVQSGDRLLVMLVEDSGRASHLNLRLPPGASDELTAIERWTDQQLEDGSINWRSLPPQLQRSGDVLRSALDHPSMSPETPLVVHGLSRLVAEPEFHSTAELRPLLELIDDQPCAVVSATDQPGVWIGEEHPQKALQACSVVQAPYRCGQEGVGQVALVGPMRMAYATAHAAVQRVARHLDLLLN
|
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}.
|
Q7U5L0
|
YIDD_PARMW
|
Putative membrane protein insertion efficiency factor
|
MLAGIGFYRRFISPLIGPRCRFTPTCSAYGLEAIQRHGPWKGGWLTVKRLLRCHPFTPCGCDPVPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7UBJ0
|
GLGS_SHIFL
|
Surface composition regulator
|
MEHSLNSLNNFDFLARSFARMHAEGRPVDILAVTGNMDEEHRTWFCARYAWYCQQMMQARELELEH
|
Major determinant of cell surface composition. Negatively regulates motility, adhesion and synthesis of biofilm exopolysaccharides. {ECO:0000255|HAMAP-Rule:MF_00525}.
|
Q7V2R0
|
YIDD_PROMP
|
Putative membrane protein insertion efficiency factor
|
MFKTINKSITSILLFMISCYQKWFSPFFGPRCRFIPSCSSYGYEAITRHGPWKGGWLTLRRLSRCHPLTPCGCDPVPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7V8U8
|
YIDD_PROMM
|
Putative membrane protein insertion efficiency factor
|
MRESNTLSGGIFALLNRAIGSVLLALIGFYRTWLSPLLGPHCRFIPSCSAYGLEAIQRHGPWRGGWLTLRRLSRCHPFTPCGCDPVPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7VDG6
|
YIDD_PROMA
|
Putative membrane protein insertion efficiency factor
|
MIKKINAVISNLFLTLIRFYRSWISPLLGPSCRFVPTCSEYGVEAIEKHGPWKGGWLTLKRLLRCNPLTPCGYDPVPDK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7VKB6
|
FETP_HAEDU
|
Probable Fe(2+)-trafficking protein
|
MARMVFCEYLKKEAEGLDFQLYPGELGKRIFNSISKQAWAEWIKKQTMLVNEKKLNMMNPEHRQLLEAEMVNFLFEGKDVHIDGYVPVQTNTKA
|
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}.
|
Q7VLK4
|
SSPA_HAEDU
|
Stringent starvation protein A homolog
|
MTISANKRSVMSLFSDKNDIYSHQVRIVLAEKGVPYELENINPNTISEDFLELNPYANIPTLVDRDLVLFNSRIIMEYLDERFPHPPLMPVYPVLRGKSRLTMHRIEQDWYSLIDIVNKNPESKEAKKALSQLREEMLALGSVFAATSYFMSDEFSLVDCYIAPLLWRMHNLGVQFTGAGGKAIKAYMTKVFQRDSFSQSIGGSAPKHLMDDKE
|
Forms an equimolar complex with the RNA polymerase holoenzyme (RNAP) but not with the core enzyme.
|
Q7VM84
|
FDHE_HAEDU
|
Protein FdhE homolog
|
MSIRILPENEIKPSASAFEIPPLLFANPKNLYTRRAKRLRELAKNNPLRDYLEFAAHLVDIQLTLLETAPIGNYAEKLTAYLTENQGQKPLNKQQFARDEKWLELLLALIKQCKPYATGAILTTLEFLEKASYAELNNLADHLLNERYEQVSPDQSVFIWLALSLYWTQLAQQLPRHTQAEIGERHTCPVCGSAPITSVIHLDKTQGLRYLHCALCESEWNMTRAQCSNCDESGDLNYWSFDTVEAPIKAESCGDCHSYLKVLYQEKDPYVEPLADDLASLMLDIEMEQKGFVRSGLNPFLFSIE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q7VPK3
|
SDHE_HAEDU
|
FAD assembly factor SdhE
|
MAELNRFKIEWQCRRGMRELDKMIMPFYQQYFEQLSEAEQRTFVTMLSYTDPELFRWVMHQSPAPTVAISALIERIRASIEA
|
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.
|
Q7VQV2
|
YIDD_BLOFL
|
Putative membrane protein insertion efficiency factor
|
MVSLPKLSAKIIIRLIYIYQIGISPILGHHCRFSITCSQYGINSIRNFGILKGCWKTCIRILKCHPFNKNDNTQ
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7VRG9
|
FETP_BLOFL
|
Probable Fe(2+)-trafficking protein
|
MTKIIYCIYLKKYAEGLKFPCYPGKLGEYIYKNISQEAWNKWQNVQTILINENKLNMLCAKDRSIIEKKMKKFLCLKPL
|
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}.
|
Q7VSD7
|
YIDD_BORPE
|
Putative membrane protein insertion efficiency factor
|
MIRRLLIAPIRFYRYFLSPWVGRQCRFTPTCSAYAIEAIERHGAWRGLWLAARRIGRCHPWSPGGYDPVPPGHGAGAQACCAHRHRTEPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7VWC4
|
FETP_BORPE
|
Probable Fe(2+)-trafficking protein
|
MSRIVNCVKLKREAEGLDFPPYPGELGTRIWQQISKEAWEEWKQIQTRLVNENRLNLADARARKYLQQQMERFLFEDGTVEAQGYVPPSA
|
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}.
|
Q7W2K2
|
YIDD_BORPA
|
Putative membrane protein insertion efficiency factor
|
MIRRLLIAPIRFYRYFLSPWVGRQCRFTPTCSAYAIEAIERHGAWRGLWLAARRIGRCHPWSPGGYDPVPPGHGAGAQACCAHRHRTEPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7W514
|
HRCA_BORPA
|
Heat-inducible transcription repressor HrcA
|
MDDRARALLKALIERYIADGQPVGSRTLSKVFDLSPATIRNVMADLEELGLIHSPHTSAGRVPTPRGYRMFVDSLLAVRAYQFEPAHIGELLPVSEPSRAVNAAAALLSNLTQFAGVVLTPKRTQIFRQIEFIRLSDKRVLLIIVTPEGDVQNRILSAQRDYTEAELLEAGNFFNVHFSGKSFDAVRRTLSTELAQLRDDISRLMQAAVEAGAEAADDGEAVVISGERKLLDVTDIASDMDRLRKMFSLFEKKTDLLQLLDVSSRAQGVQIYIGGDSQLVPMEEVSVITAPYGVDGKVIGTLGVIGPTRMAYERVIPIVDITARLLSNALSHNQ
|
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}.
|
Q7W9Q2
|
FETP_BORPA
|
Probable Fe(2+)-trafficking protein
|
MSRIVNCVKLKREAEGLDFPPYPGELGTRIWQQISKEAWEEWKQIQTRLVNENRLNLADARARKYLQQQMERFLFEDGTVEAQGYVPPSA
|
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}.
|
Q7WDJ6
|
YIDD_BORBR
|
Putative membrane protein insertion efficiency factor
|
MIRRLLIAPIRFYRYFLSPWVGRQCRFTPTCSAYAIEAIERHGAWRGLWLAARRIGRCHPWSPGGYDPVPPGHGAGAQACCAHRHRTEPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q7WH06
|
FETP_BORBR
|
Probable Fe(2+)-trafficking protein
|
MSRIVNCVKLKREAEGLDFPPYPGELGTRIWQQISKEAWEEWKQIQTRLVNENRLNLADARARKYLQQQMERFLFEDGTVEAQGYVPPSA
|
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}.
|
Q7ZWY2
|
PIHD1_XENLA
|
PIH1 domain-containing protein 1
|
MESDKSLLSAELNSEFEQALYEQMLLKAKQEMQNRLPNTPESKQIRPQPGFCIKTQTSEKAKIFINICKTNDIPAPPDLSEAELVNILESDDPSGYRVPMSIGEPHVEVDNSGNGCTVYDIVINSTFFDKMKSNELFREFFITVAMEGLENKYEMELSRDWRMLKNRKFMGSISDQNIRTKSKPIIQELDTSSSQTLQSKPLISEIQSSPKVPEYTIAAEPSEGHPSFLVAEISLPNVTSVRSLVLDLGEDRIVLWGRPDLYHLDIFLPYNIVQEESGAQFNRDTKVLTITMPVQTI
|
Involved in the assembly of C/D box small nucleolar ribonucleoprotein (snoRNP) particles (By similarity). Recruits the SWI/SNF complex to the core promoter of rRNA genes and enhances pre-rRNA transcription (By similarity). Mediates interaction of TELO2 with the R2TP complex which is necessary for the stability of MTOR and SMG1 (By similarity). Positively regulates the assembly and activity of the mTORC1 complex (By similarity).
|
Q805P6
|
TCRM_VACCW
|
Truncated Cytokine response-modifying protein B
|
MWKLICIQLTTTTGLSESISTSELTITMNHKDCNPVFREEYFSVLNKVATSGFFTGERCAL
|
The protein is truncated in this strain and presumably inactive. It has similarities with variola virus CrmB, but the product is inactivated due to several premature stop codon.
|
Q80DT4
|
PROF_CWPXG
|
Profilin
|
MAEWHKIIEDISKNNKFEDAAIVDYKTTKNVLAAIPNRTFAKINPGEVIPLITNHNILKPLIGQKFCIVYTNSLMDENTYAMELLTGYAPVSPIVIARTHTALIFLMGKPTTSRRDVYRTCRDHATRVRATGN
|
More likely to influence phosphoinositide metabolism than actin assembly.
|
Q80LT4
|
LEF11_NPVAH
|
Late expression factor 11
|
MSKKENIIGNKNRTQKYNNACLTRSDVYALVKETINKRKHDGEFCNITAHIFDEGFEQQKEYIREKLSTASIVTDCRQNRKRLALHRKKIESIFNIHTSLQEEFNSCSRRYNGSPNLE
|
Involved in late/very late gene activation.
|
Q812M8
|
YIDD_BACCR
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQKHGALKGFWLTCKRILKCHPFHPGGFDPVPDKKDDKVNS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q819W1
|
Y3844_BACCR
|
UPF0122 protein BC_3844
|
MLEKTTRMNYLFDFYQSLLTQKQRSYMSLYYLDDLSLGEIAEEFDVSRQAVYDNIKRTEAMLEEYEEKLVLLQKFQERQRLVAKLKQLISEEEHVNEEMKQVVEAIEKLD
|
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}.
|
Q81KF2
|
YIDD_BACAN
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQKHGAFKGFWLTCKRILKCHPFHPGGFDPVPDKKDDKVNS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q81ND5
|
LUTA2_BACAN
|
Lactate utilization protein A 2
|
MKVSLFITCLSDVFFPQVGKSVVEIMNQCGVELDFPEGQTCCGQPAYNSGYQEDAKLAAKQMIKAFEHSEYIVTPSGSCASMVHHYYKEMFKGDSEWYEKAVHLADRTYELTDFVVNILGKNDWKSKLVEKAVFHQSCHMSRALGIKEEPLKLLSQVEGLDIKELPYCQDCCGFGGTFAVKMSSISETMVDEKIKHIEATEANLLIGADMGCLMNIGGRLRRENKNIQVLHVAEVLAKGLNK
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
Q81TG0
|
LUTC_BACAN
|
Lactate utilization protein C
|
MTGLIQNRDSFLDNIAKELGRTRKTDGVERPVWKNNVNKETLKDYSQEELLEVFKNQCTNIHTTVVETTNDRLREDIQKVIVENGGGPIMLSADERFDSYGLTSLFKEELPKQNVEVNVWDPEKKEENMRIAERANIGIAFSDYTLAESGTIVVQSHKGQGRSLHFLPTVYFAIIPRETLVPRITQAVQDMNTRVENGEEVASCINFITGPSNSADIEMNLVVGVHGPLKAVYFIV
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
Q81TG2
|
LUTA1_BACAN
|
Lactate utilization protein A 1
|
MKVTLFVTCLVDMFETNVGKATVEVLERLGCEIEFPEAQVCCGQPAYNSGHVEAAKEAMKHMIETFEDAEYIVTPSGSCATMFHEYPHVFKDDPKWAKRAQKVADKTYEFTQFIVDVLKVTDVGASLPGIATIHKSCHMTRMLGVTEAPGILLSNVKGLTVRELPNVQNCCGFGGTFSVKMTPISEQMVDEKVDSAMETGADYLIGADCGCLLNIGGRIERLGKEIKVMHIAEVLNSRS
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
Q81WJ1
|
Y3984_BACAN
|
UPF0122 protein BA_3984/GBAA_3984/BAS3697
|
MLEKTTRMNYLFDFYQSLLTQKQRSYMSLYYLDDLSLGEIAEEFDVSRQAVYDNIKRTEAMLEEYEEKLVLLQKFQERQRLVAKLKQLISEEEHVNEEMKQVVEAIEKLD
|
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}.
|
Q824J6
|
YIDD_CHLCV
|
Putative membrane protein insertion efficiency factor
|
MSFKLFIKNLPTNLCCGLIHIYRWTISPLLGSPCRFFPTCSQYALQALKHHGCIKGLGLTIKRIGKCGPWHPGGVDLVPMTTLEEALDISPAVDDDESCDLHA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q82FE1
|
YIDD_STRAW
|
Putative membrane protein insertion efficiency factor
|
MKYPLLALIKLYQWTISPLLGPVCKYYPSCSHYGYQAIDRHGAIKGTALTAWRILRCNPWSLGGVDHVPPRKRPRWHEMLRNAWRARKGGPSAAEPAIEGHIPSSPAAETPSHVQGA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q82SG6
|
SDHE_NITEU
|
FAD assembly factor SdhE
|
MNHQARMRWRCRRGMLELDIVLQRFIDNHYEQLDEHQLELFEMLLSLSDHDLWNIIIGNTKEPNNQFQPVLKLLQEN
|
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.
|
Q82XA0
|
YIDD_NITEU
|
Putative membrane protein insertion efficiency factor
|
MKQLIIDLIKLYRYSIGLLIPPSCRFYPTCSNYMHEALVKHGLIKGLWLGMKRILRCHPWNQGGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q82XF2
|
FETP_NITEU
|
Probable Fe(2+)-trafficking protein
|
MVRSVKCIRLGCEAEGLDFPPYPGELGKRIFDNVSKEAWSQWIKHQTMLVNEMRLNLADIKARKYLASQMEAYFFGEGADQPAGYIPPDK
|
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}.
|
Q830M0
|
YABA_ENTFA
|
Initiation-control protein YabA
|
MDKRSLYDGLNSLETDLDSSVTQLREIKAALHELVEKNTTLEIENQRLREHLQELNKLAGNTTETEKQELSKSRMNLEKLYEEGFHVCNILYGSRRENDEECAFCLDVIYGERTR
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q83250
|
MVP_CMVM4
|
Movement protein (MP) (Protein 3A)
|
MAFQGTSRTLTQQSSAATSDELQKILFSPDAIKKMAAECDLGRHHWMRADNAISVRPLVPEVTHGRIASFFKSGYDAGELCSKGYMSVPQVLCAVTRTVSTDAEGSLRIYLADLGDKELSPIDKQCVTLHNHDLPALVSFQPTYDCPMETVGNRKRCFAVVVERHGYVGYTGTTASVCSNWQARFSSKNNNYTHIAAGKTLVLPFNRLAEQTKPSAVARLLKSQLNNIESSQYVLTDSKINQNARSESEELNVESPPVAIGSSSASRFESFRPQVVNGL
|
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).
|
Q833N1
|
YIDD_ENTFA
|
Putative membrane protein insertion efficiency factor
|
MKNPLIGGVRFYQRFISPGLPARCRYYPTCSQYMIDAIHTHGSVKGTTMGVARILRCHPFVKGGIDYVPLKFRLTKNPDETYHGPYTYRRNKKTEVEKDG
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q834F4
|
Y1701_ENTFA
|
UPF0122 protein EF_1701
|
MEMEKTNRMNALFEFYSTLLTEKQMNYMELYYADDFSLGEIAEEYEVSRQAVYDNIKRTEKILEEYEKKLHLYSNYVVRKEFLEQLQQYVQETYPKDSEIKKYIEQIQEIEE
|
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}.
|
Q83CJ1
|
CBPM_COXBU
|
Chaperone modulatory protein CbpM
|
MTKQIIKGIIIERSSPLKIDELSQAVHLRREIIIEMVEHRLIEPEGSSPTSWKFDNVCLKRAKIAASFYRDLEINMPGIAIALDLLDKIEHLEQRLRTLERFENQE
|
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}.
|
Q83FE1
|
YIDD_TROWT
|
Putative membrane protein insertion efficiency factor
|
MLRIVPRNIFILFIIAYRKIISPMYGPVCKYYPSCSEYCQNSIANNGVFLGAAYTFMRLVRCNPWSKGGVDMPRVSTKYRVNKFGFASRKNV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q83H58
|
YIDD_TROW8
|
Putative membrane protein insertion efficiency factor
|
MLRIVPRNIFILFIIAYRKIISPMYGPVCKYYPSCSEYCQNSIANNGVFLGAAYTFMRLVRCNPWSKGGVDMPRVSTKYRVNKFGFASRKNV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q83PE8
|
FDHE_SHIFL
|
Protein FdhE homolog
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQKVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q83QD1
|
SYDP_SHIFL
|
Protein Syd
|
MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQPTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTNLASNLAEFLNQLKPLL
|
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}.
|
Q83R06
|
LPHI_SHIFL
|
his operon leader peptide (his operon attenuator peptide)
|
MTRVQFKHHHHPD
|
This protein is involved in the attenuation mechanism for the control of the expression of the his operon structural genes.
|
Q83SQ6
|
FIXX_SHIFL
|
Ferredoxin-like protein FixX
|
MTSPVNVDVKLGVNKFNVDEEHPHIVVKADADKQVLELLVKACPAGLYKKQDDGSVRFDYAGCLECGTCRILGLGSALEQWEYPRGTFGVEFRYG
|
Could be part of an electron transfer system required for anaerobic carnitine reduction. Could be a 3Fe-4S cluster-containing protein (By similarity).
|
Q84709
|
P0_PEMVW
|
Suppressor of silencing P0 (ORF0 protein)
|
MHGIEQPQLPLDYVHRCASTSFLLASLDGLLSEARELSGPLALITSSYYLLVSIALCWAIPGSFWYRPGCWLQPVSGRNLIFCGPTEALQRFRLYAARLGLVLSENCPRHGQSAAITLQSYWALPNNIWMDMAQLDLLTFSMPIANTFAYLADCEARFPPIVEGVGSAYYVPTLLGLTHQDPRLYLALRRRNLDLSGEPHRVRPGVLESMALLCSSVRSTSRSRQIPPLYGSVLHHVLGLAERDCILFDTDSNYSSYTHRVLEQDRNRADQSLFSIDLEYVHDLELIALGYSDEDDEDLDNFF
|
Suppressor of RNA-mediated gene silencing.
|
Q84B70
|
HRCA_NODSP
|
Heat-inducible transcription repressor HrcA
|
MEVQLTNRQQHILWATVRHYIATAEPVGSKALVDEYDLGVSSATIRNVMGVLEKSGLLYQPHTSAGRIPSDSGYRIYVDQLITPGLRDAARTDVLAKEVELALQNRLHWEDWSLEAVLQGAAQILATVSGCISLITMPQTTTAILRHLQLMQIEANKIMLIVVTDDYETHSKLMNLSPTEEEAKLDADGIDHELKIVSNFLNTHLRGRSLLELATLDWSDLDQEFQRYGEFLKGSVTELTRRHLTPTTTQIMVRGVAEVLRQPEFSQLQQVQTIIQLLEEEQDQLWRLIFAEPETEEAGKSKVTVRIGTENPLEPIRTCTLITSTYRRGLLPVGSVGVLGPTRLDYDSAIAVVAAAADYLSDAFS
|
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}.
|
Q85055
|
RDRP_AHV2H
|
RNA-directed RNA polymerase (EC 2.7.7.48)
|
MSTLLIPQDTIAHTFDEAVASESNLRIDEVPENYLERFIHPSEPENFEFYSLRDSDIPSKRIPKNGIQVFENLKYHTNSKDNLYKDQPSSGPSPMRGVANIIREYFPQYLDDLRTWCRPKSSDDSIFNDFNHEQRITQPFTEERERRLLPLIDHFLGIKPYDIVHYCDTRFYPWKLSTRADYFHNHSRDRKAHAAKSHPDFATGPTKKSYFINSHLFFDRSTVHNIKEYGFPFRPTTDSARNETLLDLWFKKVPTELLVRSHISKRDNLKVRPVYNAPMIYIRIECMLFYPLLAQARKRDCCIMYGLETIRGGMNELERISNAFNSFLLIDWSRFDHLAPFTISNFFFKKWLPTKILIDHGYAQISNYHDHVHSFSAQAQSHGIPMISKEYQTPPEATVFAKKVLNLISFLERWYRDMVFVTPDGFAYRRTHAGVPSGILMTQFIDSFVNLTILLDGLIEFGFTDEEIKQLLVFIMGDDNVIFTPWTLLKLIEFFDWFAKYTLDRFGMVINISKSAVTSIRRKIEVLGYTNNYGFPTRSISKLVGQLAYPERHVTDADMCMRAIGFAYASCAQSETFHALCKKVFQYYFAKTSINERLILKGRKAELPGMFFAYPDVSEHIRLDHFPSLSEVRILLSKFQGYLKETPFGTIPTFSTPQTLRDQTQ
|
RNA-dependent RNA polymerase which replicates the viral genome.
|
Q85056
|
CAPSD_AHV2H
|
Capsid protein (CP) (Coat protein)
|
MSSNDSAQTRNLQEERFNERTSTPTVVTAVLPDTNGPTTNSTSGSVGPPHPTPNVPVPTQSSSDPPSASGIFAKEIDLPRNVIQHSGNKFILDVVPDSRFPTFAITEFVQRSFSNFTFEQYSYVSPASLVGYLVYMIHAFVFLVDAFERSPMSAYASEIDASHAYLRIIDAFSDAYIPDFLFEILDTYLSHRLDIRSKLEMNVSYGSVLYKYDAPRIVAPSIFLLAHNQLISQSRESTAYEKWLDSIVIHYSRAVIRVGNLVGGLYQSSHGSTTTHFTYRNWFARSLSRLADSATHRTHLRRPMISEFDYNIPSVNNNTYNPYVHLLMLEPNNRNITLDFIRSLSSFCSTELKATRTLRDHISRRSAAISRCVIKGPEAPTWHSSPLDDLKEKSKQGNFSQFCEVAKFGLPRKENSESYTFKFPKDASTIDTAFYLIQENGRSSVLDPTTADEELHTEGMNLLFDPYDDESSAHYATVLSGKLIQNSNIDGETLLLPDPTTGLARTNSRYLQGSVLIRNVLPEFDQHEIRLFPRYPQISRLSASLTLLFNMRQVWIPRFKQKVDEQPKLSNFSWNEGCDGTVPSLNVVTAESSTNGPAAEQQVILWSSYRHVSNSDRPTVDTVYYYSTLELLFGTRSSMMQTYNLHQLLSLH
|
The capsid protein self-assembles to form an icosahedral capsid with a T=2 symmetry made of 120 subunits.
|
Q85447
|
VSR_RDVA
|
Suppressor of RNA-mediated gene silencing (Non-structural protein 10) (Pns10)
|
MEVDTATFVRLHHELLCAHEGPSIISKFDAIKKVKLGTLANQSGGVNNITEAFLAKLRNFERKSEAYLASDLAERELTRDTHKAIVFVTKSVLLGGKSLKDLLPYGVIVCAFIFIPETASVLDNVPVMIGNQKRPLTVALIKYIAKSLNCDLVGDSYDTFYYCNSSAYGKNLISVSDNDFSNPQRALLSVGDLCYQAARSLHVAAANYIRIFDRMPPGFQPSKHLFRIIGVLDMETLKTMVTSNIAREPGMFCHDNVKDVLHRIGVYSPNHHFSAVILWKGWASTYAYMFNQEQLNMLSGTSGLAGDFGKYKLTYGSTFDEGVIHVQYQFVTPEVVRKRNIYPDLSALKGGGS
|
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.
|
Q859K5
|
CAPSD_BP44A
|
Major capsid protein (Gene product 20) (gp20) (Major head protein)
|
MAQQSTKNETALLVAKSAKSALQDFNHDYSKSWTFGDKWDNSNTMFETFVNKYLFPKINETLLIDIALGNRFNWLAKEQDFIGQYSEEYVIMDTVPINMDLSKNEELMLKRNYPRMATKLYGNGIVKKQKFTLNNNDTRFNFQTLADATNYALGVYKKKISDINVLEEKEMRAMLVDYSLNQLSETNVRKATSKEDLASKVFEAILNLQNNSAKYNEVHRASGGAIGQYTTVSKLKDIVILTTDSLKSYLLDTKIANTFQIAGIDFTDHVISFDDLGGVFKVTKEFKLQNQDSIDFLRAYGDYQSQLGDTIPVGAVFTYDVSKLKEFTGNVEEIKPKSDLYAFILDINSIKYKRYTKGMLKPPFHNPEFDEVTHWIHYYSFKAISPFFNKILITDQDVNPKPEEELQE
|
Assembles to form an icosahedral capsid.
|
Q86563
|
MVP_RBDVR
|
Putative movement protein
|
MFSRSSSTRSSLVGSRSGSIFGGGSVKKSSTVRGFSAGLERSRGLPSASAGENQISLPGLRIPVKASSQPGNYYLKERGIDLPIVQQQKFLAADGKEMGECYLLDTSRTDLLDAAKAALNESNLLEFNKFKEFKKYKGKNNEFSLVEASVFDKLIRKDDSPIHLNRLLIAVLPAVGKGTPGTARIKIRDARLDDGYGELFSSENRVDSGYIYCINVGYSVPKSEIDYKINIDFAGVPIKDGKSPIWVKAAFSLAGGPPVFLDGTMSLGAEILPDSHKELLGTSALLLNEANSNRKSFSGDDGELRRDYPYKRFEEISPLDSISQVDTASQDSVNEVNTENVQNGTGEVYLAPPSHSVY
|
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).
|
Q86564
|
CAPSD_RBDVR
|
Capsid protein (CP) (Coat protein)
|
MSKKAVPPIVKAQYELYNRKLNRAIKVSGSQKKLDASFVGFSESSNPETGKPHADMSMSAKVKRVNTWLKNFDREYWDNQFASKPIPRPAKQVLKGSSSKSQQRDEGEVVFTRKDSQKSVRTVSYWVCTPEKSMKPLKYKEDENVVEVTFNDLAAQKAGDKLVSILLEINVVGGAVDDKGRVAVLEKDAAVTVDYLLGSPYEAINLVSGLNKINFRSMTDVVDSIPSLLNERKVCVFQNDDSSSFYIRKWANFLQEVSAVLPVGTGKSSTIVLT
|
Capsid protein self-assembles to form a capsid about 33 nm in diameter. The capsid encapsulates two genomic RNAs as well as a third, subgenomic RNA (RNA3) (Potential).
|
Q87BS6
|
HRCA_XYLFT
|
Heat-inducible transcription repressor HrcA
|
MCASFSPTLDSRSRQLLRTLISCYIQNGEPIGSKTLAQQAGLDISPATIRNILADLEELGLLNSPHTSAGRVPTAHGYRMFVDSLVQMQPPSEDDIRRLRVEMTGGGTQTLLGSASEILSAMTHFVGVVSAPRREQFVFRHIDFVPLDARQIMAILIFADNEVQNRVIEPRRVYEPGELERVSNYLNAHFIGRTLADIRTTVLCELRKAKDEMEQLLAHSLDLASQMLVPNDSEDIVVTGQTRLMALQDLSDMDRLRELFEIFASKREILQLLERTIDAPGVRIFIGEETGMVSMEDISLVTAPYAAHGQVLGVLGVIGPKRMAYDRVIPLVQVVAQVLGTALEPPTMP
|
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}.
|
Q87BY1
|
PARB_XYLFT
|
Probable chromosome-partitioning protein ParB
|
MNKPSLPLKKRGLGRGLEALLGSKGGSSVPPTVAQEQLPGEVLRTLQTTQLQPSKYQPRREMSEAKLAELADSIKAQGVIQPIIVRELDVDMFEIVAGERRWRASQLAGLTEVPVIVRELDDRTVVAMALIENIQREDLNPLEEAQALQRLIDEFSLTHAEAAEAVGRSRAAVSNLLRLLELPLGIRTLLESHQLEMGHARALLTLTPELAAKLAKEAADQGWSVREVEHRAQQFAAGKVPDIRDKKSKSLASAPAQPDIASLETELSERLGTKVAINHGRTGKGKLVIHYTDLDVLDGVLERLRARAVG
|
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).
|
Q87D06
|
FETP_XYLFT
|
Probable Fe(2+)-trafficking protein
|
MQRIIFCEYEKRDTEGLDFVPYPGELGQKIFACIGKVGWAAWLAHQTMLINENRLSPRNPSHRAFLEEELNKFLFERSAAKPEGYIEPDA
|
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}.
|
Q87EF7
|
SDHE_XYLFT
|
FAD assembly factor SdhE
|
MRYCRCQRATAEEPTMDKPAELNKLRWRSRRGMRELDHLFDRYLSHCWAQASEAERGVFLRFLDCEDDKLWRWLMGYEVCQDASFAALIVTMRALPA
|
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.
|
Q87L41
|
TUSC_VIBPA
|
Protein TusC homolog
|
MSQLTYLFRSAPHGSAAGREGVDALLAASAYCEDITVIFIGDGVYQLLLGQEPSGILSKDYAPMLKLFDLYDIEQVFVCSESLAQRGLAQADLVIDAQALSLEQVKEKLQQAGKLLSF
|
Could be part of a sulfur-relay system.
|
Q87LI5
|
FETP_VIBPA
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCARLKKEGEGLDFQLYPGELGKRIFDNISKEAWAQWQHKQTMLINEKKLNMMDPEHRKLLETEMVNFLFEGKDVHIEGYTPPSE
|
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}.
|
Q87LM9
|
SDHE_VIBPA
|
FAD assembly factor SdhE
|
MYTPEEKARIKWACRRGMLELDVVIMPFFEECFDALNEQEQRDFVSLLECDDPDLFTWVMGHGRSENLGHAAMVDKIVAHNLSKVR
|
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.
|
Q87RS5
|
SYDP_VIBPA
|
Protein Syd
|
MTQTVTQALQDFSLRYQQAWQNKHNELPRNEELADLVSPCVEEKCDGAVLWKAFPREEMADFTNVENAIELTLHEDIKAFYGSQYSADMDATWQTNPLTLLQVWSDDDFVRLQENILGHLVTQRRLKLKPTVFIAATDAELDVISICNLTGNVILERLGTDKREVLAENVVEFLAKIEAAV
|
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}.
|
Q87TS0
|
YIDD_PSESM
|
Putative membrane protein insertion efficiency factor
|
MRKLALVPIQFYRYAISPLMASHCRFYPSCSCYAYEAIDNHGLLRGGWLSIRRLGRCHPWNPGGYDPVPAVPTSRSSSMAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q87UF5
|
FETP_PSESM
|
Probable Fe(2+)-trafficking protein
|
MTRTVMCRKYKEELPGLERAPYPGAKGEDIFNHVSQKAWADWQKHQTLLINERRLNMMNAEDRKFLQTEMDKFLSGEEYAQAEGYVPPEK
|
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}.
|
Q87XF1
|
SDHE_PSESM
|
FAD assembly factor SdhE
|
MVEDVELNRLYWHSRRGMLELDVLLVPFVREVYPHLNDVDRDLYRRLLTCEDQDMFGWFMQRAESEDAELQRMVRMILDRVQPK
|
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.
|
Q88887
|
MP_TPCTV
|
Putative movement protein (MP)
|
MATTNCRICGSSFACPINERFSVCESRGATLSDFLLYFRRKYIETSPGLISYLNALQAEINELFSAIKEVSRSEIRHGSCEDKCQPSSIQKGKAEA
|
May be involved in the viral transport within, and between cells.
|
Q88899
|
P32_TRVPP
|
32 kDa protein
|
MVIVTKGAYVHEFPRTAEWNAFAQILSREHGYIVSDTALEGAAKPYYVVNSSGFYGPPGLDGLISTLDRELQYYSKLLYEIKGLGVMSDENVFGTQYDGNLTARVSRLERRLNPMSNIGSSSRPWSEHKSAVKKADLERYVYANFADWSNHLGPAGKSTREVVKYLMYRMGYYSDTSGIGHDLNYKHFRDHLDIYNLTCSPPFLVSSAVVDGHYARDKFVSFQGVCGFNPMFPDVNGLKSSWSLGRQLDDIRSQKKEVSGTNQEPNYYYDGDTLKPIGSGASVVGERRPGWR
|
May be involved in transmission by vector nematode species.
|
Q88DH8
|
CBPM_PSEPK
|
Chaperone modulatory protein CbpM
|
MSSTLIVQLDMRTLCQEADVTAECVIEIVEHGIVEPSGRTPEDWLFDDQAPLVTKRAVKLHQELELEWEGVALALELLQEVQQLRSENSMLKQRLGRFIQL
|
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}.
|
Q88MZ4
|
SDHE_PSEPK
|
FAD assembly factor SdhE
|
MVEQTELNRLFWHSRRGMLELDVLLVPFTQEVYPTLNETDRELYVRLLSCEDQDMFGWFMERTESEDPELQRMVRIILDRVQPK
|
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.
|
Q88QJ9
|
FDHE_PSEPK
|
Protein FdhE homolog
|
MITDEKKDERLSIILEPGQIEASAVTPPFLHLPAANLFELRAARLEQLAEGNALGDYLRLIARLCRIQQQLVDNPPGGMPVAEARQRLCMDHGLPPLAADSLVREGPWLVWLQALLEHLSGETRGPMGEALQVLRGSDDNQRKGWGIALLAGQYDGVPAALVPFLGAALQAAWSSWLLALPAHQLKPAGSLAQCPACGSPAMAGVVRNRGKHNGLRYLACSLCACEWHVVRVKCVYCESSKDLRYTSLEDDRHAPGKAPLRAECCPGCDSYLKQNYLENDAAAEPLADDLASLALDIRLDGEGFHRLAPNLMLAPGGG
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Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
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Q88R49
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FETP_PSEPK
|
Probable Fe(2+)-trafficking protein
|
MTRTVMCRKYQEELPGLERPPYPGAKGQDIFEHISQKAWADWQKHQTMLINEKRLNMMNAEDRKFLQAEMDKFFAGEEYAQAEGYVPPAE
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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}.
|
Q88WJ7
|
Y1634_LACPL
|
UPF0122 protein lp_1634
|
MEIEKNYRINSLFEFYEPLLTNKQKAYIQLYYADDYSLGEIAAEFSVSRQAVYDNIKRTEKILEGYEAKLHLYHDFVERNHEVDAISDYIKQNYHGDTQLIKMIQQLVNLEADSE
|
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}.
|
Q88YP3
|
YABA_LACPL
|
Initiation-control protein YabA
|
MDKRDLYDSFGEMEQQMQQMLDKMAKLRADMTTVLEKNAELVIENEHLREHMVEIENELPKKAASTTTLSKSRQNLEKLYDEGFHVCNQFYGKRRDDDESCVFCLEVIYGERERA
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q892Q8
|
HRCA_CLOTE
|
Heat-inducible transcription repressor HrcA
|
MLINGVIIMEMDKRKIKILQAIIHDYIQTAEPVGSRTIAKKYDLGVSSATIRNEMSDLEDMGYLEQLHSSSGRKPSDKGYRLYVDKLMNIQKLSSMEECAIKTHIINSALYEIEKVVREASAILADLTKLTTVVMSPSSIESYIKSIQLIGLDANTVLLVLVIDTGIIKNNVIKLHAKMTIDELVKINRILNIKLNKIRVESINLDFLKVVLEEFKDYEKWLKDILPVLYETLLSGIDSNEIYLEGATNIFNYPEYNDIQRAKDFLSLIDDKDKVKNLIKSDDNITIKIGKENFIEDAKDCTIITAVYKLKDRPLGTIGVIGPTRMPYSRVVSILSTLVDELDKLLKDDNI
|
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}.
|
Q89554
|
3002R_ASFB7
|
Protein MGF 300-2R
|
MITLYEAAIKTLITHRKQILKHPDSREILLALGLYWDKTHILVKCRECGKMSLTGKHSTKCININCLLILAIKKKNKRMVDTLIRMGADVTYIHLLKNKIKLSYNQLSMLKSNSQISLKELHAICYLLYGRLPKKIKQGMQLCKTMAGLCGELL
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q895M5
|
Y1247_CLOTE
|
UPF0122 protein CTC_01247
|
MEEKIEMSMLLDFYGILLTDKQKSIMNLYCNEDFSLAEISEHTKTSRQAVHDIIKRCGKLLKSYEEKLKLMGKHIEKIKAKKNMLNKLDYLKENCKEEELQKLIEELKNELNNSLGG
|
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}.
|
Q89A16
|
HSCA_BUCBP
|
Chaperone protein HscA
|
MITLKTIKKKYNIEQKNTKLSIGIDFGTTYSLVASALEDNIYIILDQNNRALLPSIINYTSKKPIVGWEAQKQAINDPKNTIISIKRLIGHSYDEINKLYPNLPYHLTYDKNGILSFIVQDNLINTINVSSEIFKTLKNRVNTIFNQKILGAVITVPAHFNDLQRQEIKKSAELANLNIIRLLNEPTSAAIAYGLHLNKNKIVAIYDLGGGTFDISILKLNQGIFEVLATSGNTNLGGDDFDQLLVNYIQKKTHFSYSKLDFIFQRKLLYLAKSIKIKLTSHNSVQFQFNNSKMHTITRFEFEKMIEPLILKTLNICQHVLHDSNTNLTHIEEIILVGGSTNIPIVQRKVSDFFKQLPLCTINPEQVVVAGAAIQANMLTNGSKYNNFILLDVVPLSLGIEVIGNIVEKIILKNTPLPISKTKTFTTFKDKQTTMLIHVLQGEHKLVNKCQSLCRFVLKEIPKKPAGKIIVLVNFQIDVNGLLSVTAEIKSTKIRKNITVNASIPIKKYRN
|
Chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB. Involved in the maturation of IscU (By similarity).
|
Q89A44
|
FETP_BUCBP
|
Probable Fe(2+)-trafficking protein
|
MNKKNDINRKIFCNFFKKYEEGLTYIPYPGLLGHKIYNEISKLAWNKWILQQTIIINEKKMNMLNKNDQKKIENYMIKFLFKNKQQL
|
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}.
|
Q89AZ5
|
FLIK_BUCBP
|
Flagellar hook-length control protein
|
MFKIEYNVSRNSTSVRRGQFYLNAFQLKKECNNYVVSKNKNTFFRDMILKMQQTIKFKDNMKSINDDYIYLKNNYCHSYGIKNKNFCSFDYFIFSKLFIIKKTSSFSNLFVLPKISEFFVQKKCLFIGLNKSKYTNFSLGHNISSWFYDDKLCCLFSILNFLADTSLNSIFSLNRKRYYSIIYSLDRDKIFKFGKIYKLFDIFKKKFILSCDYKFWKKFVFKKMLVFLNNKTKCITFILNSKHLGSVFIYFKIINNKSIILDLVTCRNEIKKIFQSHIIYLKNVLKDCGIEVSSINVSSREEFLNAVRTNYDRKFDSKILNHYNTVISKTKSHALRFYELDKNDYQYNYNNINMYV
|
Controls the length of the flagellar hook.
|
Q89B46
|
REPA1_BUCBP
|
Probable replication-associated protein repA1
|
MLKRKNYVNNISPLFTPPKGDKRRPAFINYALEQAKKIDVARSELNYILKLRDPKTGSIIPRHRQLNEHRAAAMRVIVPAMIYHFNITSDLVQASIEQLADECGLSTVSKSGNKSITRASRLISQFMEPMGFIKCKKKWDKILGCYMPKIIMLTPLFFELIGISKEKLNNAKKQQLGWLNTKLIERGLKPLSFSDAKLVSREKQINKILELRNNFHLLQRKKRYAKKLFKLDEKDIRQKIIKYLVSKYSSSELAQISLQEFKKQVNIEYFYLRNLANEPYLISRR
|
This protein is essential for plasmid replication it is involved in copy control functions.
|
Q89B47
|
REPA2_BUCBP
|
Probable replication-associated protein repA2
|
MLNIKTKKKNKKRIYVFNKNPEFKFKHLVFQKNKFILKIINEIDKIDLMRSEIFNSTLPIDPQTGNILVRFRKLNRNRLLAIKAIIQAMLYHFNIKTKKVTASVEQLADECGLSTVSKSGNKSITRASRLISQFMEPMGFIKCKKIKTTNNKFSKEIILTPLFFMILVKNSSLSEGDTHLKQEFKILKNKNVHINSSETFAKQEILKKIINKYSLNKLKKLGPKKIKEKINTEYKNIKK
|
This protein is essential for plasmid replication it is involved in copy control functions.
|
Q89IV9
|
YIDD_BRADU
|
Putative membrane protein insertion efficiency factor
|
MKHSACEHCSTPVEGALRLPRRFGRALIWLYRHTLSPLVGYNCRHLPTCSVYGDEAIERFGLWAGGWMTLARLLRCNPFGTSGIDNVPLAAPQDARWYLPWRYGRWRGVNAP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8A2S7
|
YIDD_BACTN
|
Putative membrane protein insertion efficiency factor
|
MSLKSLVRKVFSFLLLIPIYFYRVCISPLTPPSCRFTPTCSAYAVEAIKKHGPVKGLYLAVRRILRCHPWGGSGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8B9L3
|
LEF11_NPVR1
|
Late expression factor 11
|
MLPKNCTHLGECNSDCLTRSEIQALFREVINTLKHTMNTENVCAHMLDIVSFERIKEYIRANLGHYTVITDKCSKRKVCLHHKRIARLLGIKKIYHQEYKRVVSKVYKKQTW
|
Involved in late/very late gene activation.
|
Q8CQ89
|
CTSR_STAES
|
Transcriptional regulator CtsR
|
MHNMSDIIEQYIKRLFEEADEDVVEIQRAHIAQRFDCVPSQLNYVIKTRFTNEHGYEIESKRGGGGYIRITKIENKDATGYINHLLQLIGPSISQQQGYYVIDGLLDKGLINEREAKMIQTIIDRETLKMDVVARDIIRANILKRLLPVINYY
|
Negative regulator of clpC, clpB and clpP transcription by binding directly and specifically to their promoter region.
|
Q8CS22
|
YIDD_STAES
|
Putative membrane protein insertion efficiency factor
|
MLKKILLSLVVFYQRFISPLTPPTCRFYPTCSQYTREAIEYHGALKGLYLGVRRILKCHPLHKGGFDPVPLKKDKNSKTTHHH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8CSV1
|
Y911_STAES
|
UPF0122 protein SE_0911
|
MGQNDLVKTLRMNYLFDFYQSLLTNKQKNYLEFFYLQDYSLSEIADTFEVSRQAVYDNIRRTGDLVEDYESKLRLYQRFEKRRELYNLMKQSLNQPELLKQYITQLEELE
|
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}.
|
Q8D079
|
LPHI_YERPE
|
his operon leader peptide (his operon attenuator peptide)
|
MNRVQFNHHHHHHPD
|
This protein is involved in the attenuation mechanism for the control of the expression of the his operon structural genes.
|
Q8D1U5
|
NRDI_WIGBR
|
Protein NrdI
|
MSVLVYFSSSSENTHRFVKKLCIPAKRIPLIDKKEFQIKSPYILVIPSYNNGILDTAVPHQVTNFLNTLHNKFFLKGVIGSGNKNFGVNFCIAGNIISKKYKVPLLYKFELLGTNKDVINVKNGINKFWKKLNLEKKNQNA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
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