entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
P39534
|
MBB1_YEAST
|
Uncharacterized protein MBB1
|
MYKVSACGVRIMSGISEIWIGELRDYKYALRLDREEYPAVLVYEYDSSSTRNYLFTIKYSDQRPNWQLITRDAALTAYDLLNRGGEFTTLSFPGATIHRSVSELSRLH
|
May be involved in metabolic processes.
|
P40076
|
YEV1_YEAST
|
Uncharacterized protein YER121W
|
MGLSRWHDKNSRPAEEKSEEMQQDAHYYALAASDSLNASVSNEYGNQVMNSFWKVGIDSPYVDDEAIRNRDVENNLPSLKQSVYNANEPNATSSAFSTASYAHETFDFRNLKLR
|
May be involved in phosphatase regulation and/or generation of precursor metabolites and energy.
|
P40428
|
HYPC_RHOCA
|
Hydrogenase maturation factor HypC
|
MCLGIPGQIVAITDAGRMMALADVSGVKRAVNVACVAEGPLEDLLGHWALIHVGFAMSLIDEAEAARTLEALRDLGEAQETLAQMAEGAAALEGRG
|
Involved in the maturation of [NiFe] hydrogenases. Involved in the biosynthesis of the Fe(CN)(2)CO cofactor.
|
P41421
|
AC11_NPVAC
|
Protein AC11
|
MSLAAKLIIYNYYAKYNEVHDVYGESYHHYRIVQEYLSESYVNGMSCIERDVTAMRRLKSGSCTFDEAVKMIDAGDSIKSLSHWFSTSETMGIDDNVREVLEQIDAVVPVSVRVQNGWQIFSLNNFEREISQDMLDCLQIILGRFEYFMRNGKLLRIANVFNPNNDVVGWWYNKFCVVTYVHRIMYRSVPAELVPRLSEAVKKFIRLRKSDYDDRLHVDESYNCPRVIAEMYGRFCGIGKEHFSKHKLSCMHILFQYLRGKTTQEEKSFPCYRVIKDFGRQCKDVYKNLKDVFDLLHAHSMSDKDKNSLMDLLCVMDCEEIDVDCFYYIFESFLNNKHLQ
|
Plays an essential role in nucleocapsid egress from the host nucleus to form the budded virion (BV). Does not participate in nucleocapsid formation.
|
P41446
|
AC41_NPVAC
|
Protein AC41
|
MTMENNAEFNRRLEYVGTIATMMKRTLNVLRQQGYCTQQDADSLCVSDDTAAWLCGRLPTCNFVSFRVHIDQFEHPNPALEYFKFEESLAQRQHVGPRYTYMNYTLFKNVVALKLVVYTRTLQANMYADGLPYFVQNFSETSYKHVRVYVRKLGAIQVATLSVYEQIIEDTINELVVNHVD
|
Plays a role in late gene expression.
|
P41448
|
AC43_NPVAC
|
Protein AC43
|
MNTRYATCYVCDELVYLFKKTFSNMSPSAAAFYQRRMAIVKNGIVLCPRCSSELKIGNGVSIPIYPHRAQQHARRSR
|
Plays a role in the production of occlusion bodies as well as expression of the polyhedrin gene.
|
P41450
|
ORF45_NPVAC
|
Protein ORF45
|
MLPYEMVIAVLVYLSPAQILNLNLPFAYQKSVLFASNSAKVNERIRRRARDDNDDDPYFYYKQFIKINFLTKKIINVYNKTEKCIRATFDGRYVVTRDVLMCFVNKSYMKQLLREVDTRITLQQLVKMYSPEFGFYVNSKIMFVLTESVLASICLKHSFGKCEWLDKNIKTVCLQLRKICINNKQHSTCLSY
|
Plays a role in the expression of ORF41, which itself is required for late gene expression.
|
P41663
|
AC110_NPVAC
|
Per os infectivity factor AC110
|
MKYFLSATFLIIVFMYLMYFCISIVVNNARVQQDLFYHYNYVPDTLLNTVRVHKLK
|
Plays an essential role in the process of oral infection. May participate in the crossing of occlusion-derived virions through the host peritrophic membrane during oral infection.
|
P41674
|
AC121_NPVAC
|
Transactivator protein ORF121
|
MMSSSQIIVCNKINIFVCKYNLLQINFTLNQSVFVFVVRSSNLVFQPLGMVKMRRSNC
|
Stimulates the expression of 39k gene most probably by increasing IE1 expression.
|
P41708
|
AC152_NPVAC
|
Protein AC152
|
MNFFAMQKSSLLPDTPYTVQSLQIVDYFIRIVYTVRYAPNILLHYQLFCITKKFIFAWQVPPPLLSYQSCSTDKQYKYSCRSTRKHSSSLTA
|
Acts as a transactivator of AC102 and HE65 genes. Therefore, participates in the global recruitment of G-actin to the host nucleus.
|
P41727
|
LEF5_GVCL
|
Late expression factor 5 homolog
|
MSFSERPRVTQNGPSMIHLFNVFSKFRKENDYDGLVNYLITNYSQNVKNRTFNFHNTGHIFHMLYAYVPSPSSKERKQIRLDCIENLLESTKNDFKLYEDLIKLMNGDDKCPCELITARLNDNIAYNESLKNKNFDSKPCKLKKEPIDSILFKYSINWKNSLNKKRSLPKSTTTKKSEEKENMDEIEVDASKISSQSSLSNLNGYTIASCVHDYVIEEHQLRAGDEMVSFIKFCKKCGHK
|
Required for late and very late gene expression.
|
P42107
|
YXAH_BACSU
|
Uncharacterized protein YxaH
|
MSSLQPTLTNERIGVLDVLRGMAIFGILFVNLAHFSYPDMYLSMLGKENFFMDKWSEADFAAADILKFFIQTKCILLFSFLFGFGMVVMMERAENKGKRFVPLYVRRLMALLLFGTIHAFLIWDGDILTEYALLGFVLLLFRKAKPKTLLIWAVSLYLLFSIPFMLTSFDQSNGQEWVQAVTQQAKQAIHVYGSGSLKDIAEQRIHDRLVYMSSNGMLTYNPLNYFFASIPYFSMFLLGAAAAKSRYLHEPEKHRKGLKRLWMAGLVIGIGAQVLYSVTDKEICLLIGAPFLMFFYVTTVVYLYHKTRVRTVLQSFSAVGRMAFTNYLMQSIVCTWIFYHYGLGLYGKVYPAAGVLITIAVCAVQMVFSHLWLRVFRMGPFEWLWRSATYLSWQPIAKKTKV
|
Involved in transport.
|
P42265
|
NDD_BPT6
|
Nucleoid disruption protein (Nuclear disruption protein)
|
MKYMTVTDLNNAGATVIGTIKGGEWFLGTPHKDILSKPGFYFLVSKLGGPFSSPCVSARFYVGNQRSKQGFSAVLSHIRQRRSQLARTIANNNVPYTVFYLPASKMKPLTTGFGKGQLALAFTRNHHSEYQTLEEMNRMLADNFKFVLQAY
|
Disorganizes the host nucleoid and inhibits replication, but without host DNA cleavage or degradation. Only the architecture of the nucleoid is affected. May act on the host chromosomal sequences that determine the structure of the nucleoid. Binds to dsDNA but not to ssDNA.
|
P42267
|
NDD_BPR69
|
Nucleoid disruption protein (Nuclear disruption protein)
|
MKYMTVTDLNNAGATVIGTIKGGEWFLGTPHKDILSKPGFYFLVSKLDGRPFSNPCVSARFYVGNQRSKQGFSAVLSHIRQRRSQLARTIANNNMVYTVFYLPASKMKPLTTGFGKGQLALAFTRNHHSEYQTLEEMNRMLADNFKFVLQAY
|
Disorganizes the host nucleoid and inhibits replication, but without host DNA cleavage or degradation. Only the architecture of the nucleoid is affected. May act on the host chromosomal sequences that determine the structure of the nucleoid. Binds to dsDNA but not to ssDNA.
|
P42268
|
NDD_BPR70
|
Nucleoid disruption protein (Nuclear disruption protein)
|
MKYMTVTDLNNAGATVIGTIKGGEWFLGTPHKDILSKPGFYFLVSEFDGSCVSARFYVGNQRSKQGFSAVLSHIRQRRSQLARTIANNNMAYTVFYLPASKMKPLTTGFGKGQLALAFTRNHHSEYQTLEEMNRMLADNFKFVLQAY
|
Disorganizes the host nucleoid and inhibits replication, but without host DNA cleavage or degradation. Only the architecture of the nucleoid is affected. May act on the host chromosomal sequences that determine the structure of the nucleoid. Binds to dsDNA but not to ssDNA.
|
P42333
|
BCRB_BACLI
|
Bacitracin transport permease protein BCRB
|
MAKKAKYPDVPIRFSETFSDTNLYIVLLIGVPLYGVITSYLFNREYAESTLKNLLTIPVSRISLIVSKLVLLLIWIMMLTLIAWVLTLLFGLIGQFEGLSSAVLIEGFKQFMIGGALLFFLVSPIIFVTLLFKNYVPTIIFTIIISMVSIMVYGTEYSALFPWSAVWVIASGTFFPEYPPEYSFISVAATTVLGLAATIVYFKKIDIH
|
Part of the binding-protein-dependent transport system for bacitracin that confer resistance to this antibiotic probably responsible for the translocation of the substrate across the membrane.
|
P42547
|
YO12_BPL2
|
Uncharacterized 17.2 kDa protein (ORF12)
|
MARSKKGKNLIYVLLGLVGLLAFFVLFVPTLTISASTPVWLENTITYATSFRDAFNVSGMVYMVILLGVLIAYLLLKYSKTRQNKDALKVVLAVVIAFAVYLLFTPALAAAFSDQVWLVDFSKLATDITSFIDTNNGFLTIIAGLGALTFFIVKKSK
|
May be a DNA-binding protein involved in virion nucleoprotein condensation.
|
P42648
|
14331_ENTH1
|
14-3-3 protein 1 (14-3-3-1) (EhP1)
|
MASREDCVYTAKLAEQSERYDEMVQCMKQVAEMEAELSIEERNLLSVAYKNVIGAKRASWRIISSLEQKEQAKGNDKHVEIIKGYRAKIEKELSTCCDDVLKVIQENLLPKASTSESKVFFKKMEGDYYRYFAEFTVDEKRKEVADKSLAAYTEATEISNAELAPTHPIRLGLALNFSVFYFEIMNDADKACQLAKQAFDDAIAKLDEVPENMYKDSTLIMQLLRDNLTLWTSDACDEE
|
Probable adapter protein.
|
P42649
|
14332_ENTH1
|
14-3-3 protein 2 (14-3-3-2) (EhP2)
|
MTSREDLVYLSKLAEQSERYEEMVQYMKQVAEMGTELSVEERNLISVAYKNVVGSRRASWRIISSLEQKEQAKGNTQRVELIKTYRAKIEQELSQKCDDVLKIITEFLLKNSTSIESKVFFKKMEGDYYRYYAEFTVDEKRKEVADKSLAAYQEATDTAASLVPTHPIRLGLALNFSVFYYEIMNDADKACQLAKEAFDEAIQKLDEVPEESYKDSTLIMQLLRDNLTLWTSDMGDDE
|
Probable adapter protein.
|
P42728
|
TFXF_RHILT
|
Trifolitoxin-processing protein TfxF
|
MRASKTPILINGSPWLLDFRRRSSREFDWEIAEHLEVPEAYFQAYDPLTTWFEWFSRIGYRDYTDAEAEIERDAEENVRQHQVSVQPDLTLTQRLSSEGSIQLPVPFLKTADQFCILSSLLYAGFGVVETRKFHGDTIFLKNVPSVGARHGIEAYVSLDDGRYYYDCEQHRLFSAGYRGDLRSGQIDIVFRPEVYMWRYQTAACLADVYLDLGHILGTLSMVASLYDTSITSRSAEAAPVDLINAVHLQRIAVDGFNP
|
The actions of the proteins TfxB, TfxD and TfxF are implicated in the processing of the inactive trifolitoxin (TfxA) precursor into the active peptide.
|
P42729
|
TFXG_RHILT
|
Trifolitoxin immunity protein
|
MNDEICLTGGGRTTVTRRGGVVYREGGPWSSTVISLLRHLEASGFAEAPSVVGTGFDERGRETLSFIEGEFVHPGPWSEEAFPQFGMMLRRLHDATASFKPPENSMWRDWFGRNLGEGQHVIGHCDTGPWNIVCRSGLPVGLIDWEVAGPVRADIELAQACWLNAQLYDDDIAERVGLGSVTMRAHQVRLLLDGYGLSRKQRGGFVDKLITFAVHDAAEQAKEAAVTPESNDAEPLWAIAWRTRSASWMLHHRQTLEAALA
|
Required for TFX resistance.
|
P43486
|
MCRB_STRLA
|
Mitomycin resistance protein McrB
|
MTSSDGSDLTTLVNVGRSVARYFERIGITEIAQLRDRDPVELYERMSAAFGQRLDPCLLDTVMSAVDQAEGLPARPWWHYTPERKRLLAGEGHDRAGGTAGEGTA
|
Involved in mitomycin resistance. May operate with McrA or may be a type of transcriptional activator protein.
|
P43520
|
YFMT_THETH
|
Nucleotide-binding protein in fmt 3'region
|
MRFLVLTGLSGAGKTTARGFLEDLGYFMVDNLPPRLWPPLLQEAAARGLARVGVVVDARALAFFQDLEEVLEALRPTVVYLEARPEVLLRRYNLTRRVHPLGAGNLMREI
|
Displays ATPase and GTPase activities.
|
P43684
|
ORFC_HERAU
|
Control protein C.HgiCIP (Controlling protein C) (ORFC) (Transcriptional activator for HgiCI restriction system)
|
MTFGTFKLKPKPEHLEGVLNVLAQKIFASPHIIAKESGLSLTAVKCALAQLEQEDQLIIKHQLTSPKLQVALKDKSSDVNISATSDPE
|
May control expression of its associated restriction-modification system HgiCI.
|
P44226
|
VPF_HAEIN
|
Mu-like prophage FluMu F protein
|
MNITWNWYEQLESAHARAFTVAKATKAEVLDTIRWATEQAIANGTGEREYIKKLEPMLKELGWWGKAKDENGNEVQLGSPRRLRTILRTNKITAYHAARYAQQMENVDEQPYWRYVAVNDSRTRASHLALHGKIYRADDPIWQTMYPPNDWGCRCRVEALSEYAVQSRGLKISSSDGEMEMEEAVVGIDKDTGEEIRTTVSKIKTDQGEMKVGAGWNYNVGSAAFGTDVAVLRKLQQVKNRELRQQTIQAINNSEARHKAFADWVLANLGKRGASARYMSAGLVTTEIAEAVTEITQGGKNAELVLVMSEKRLAHANSDKHHEGGVGLTAEEYASISRIVANPSLVLWDTLEGHNNLIYINQERTIQVIVDVPNKHSIKPKEKVDAIINAYKVDMNNVKRQLSGGNYVLLKGKL
|
Involved in virion morphogenesis.
|
P44233
|
VPL_HAEIN
|
Mu-like prophage FluMu tail sheath protein
|
MSISFNNIPSALRVPLTYIEFDNTKAVSGPPTALHKVLMLGTKLATGSAKAGEAVRVSAYAQAKTLFGRGSQLAEMVKTFKAHNSTLDLWVLPLDEAPSGAKATGSVQITGTATQAGTFSLMIAGNNYKTAVTSGDTADVVAGKLQKLIAADQDVPVVATVAGNTITLTCRFKGETGNEIDLRCNYYSGEAFPEGLKATITDMKNGAVNPDMSVAITGLGAEWWNYIINPFTDTESLNLLRADLVKRWGPLKQIDGICFMAKRGTHAEVTTFAEQRNDYLFSLLATHKAPQPAYLWASAYAAVVAGSLAIDPARPVQTLVMDLLPPSMSDRWDLPERNTLLYSGVSTYTVNAGSQPQVEAAITMYRKNAFGDNDESYLYVETIATLSYLRYAIRSRITQKFPRHKLANDGTRIGPGQAIVTPKIIRNELLALFTELEFAGLVEDFEQFNQTLFVERDSNNPCRVNVLSNENLVNQFRIYAHAIQFIL
|
Major component of the tail.
|
P44506
|
PLPHP_HAEIN
|
Pyridoxal phosphate homeostasis protein (PLP homeostasis protein)
|
MNIQHNLNLIQQKIETACKEENRNQNTVKLLAVSKTKPISAILSAYQAGQTAFGENYVQEGVEKIQYFESQGINLEWHFIGPLQSNKTRLVAEHFDWMQTLDRAKIADRLNEQRPTNKAPLNVLIQINISDEESKSGIQPEEMLTLAKHIENLPHLCLRGLMAIPAPTDNIAEQENAFRKMLELFEQLKQVLPNQQIDTLSMGMTDDMPSAIKCGSTMVRIGTAIFGARNYSTSQNK
|
Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis. {ECO:0000255|HAMAP-Rule:MF_02087}.
|
P44972
|
YIDD_HAEIN
|
Putative membrane protein insertion efficiency factor
|
MAETHSLGTKILIKIIRLYQIMISPFIGARCRFVPTCSCYGIEALKTHGLLKGGWLTLKRVLKCHPLNAGGFDPVPPKTNNNDEKK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P45183
|
MOP_HAEIN
|
Probable molybdenum-pterin-binding protein
|
MKISARNQLKGKVVSIENGSVNAIVHIDIGGGNVLSSTVSLAAVKELNLEVGKEAYAIIKATSVMVGVE
|
Binds one mole of molybdenum per mole of protein and contains a pterin.
|
P45312
|
Y1677_HAEIN
|
Probable iron-sulfur cluster repair protein HI_1677
|
MSFAQQKLSELAVSIPGATKIFREYDLDFCCGGSVLLEVAAQQKNLNLAEIEKRLTDLQQSKAENNDKDWTSASYAEMIDHIITRFHNRHREQLPELITLAEKVENIHGDRDDCPIGVVAQLEKIYAELSQHLMKEEQILFPMIKMGNYAMASMPIRVMEMEHDEAGQDVEVIKSLTNNCTPPADACFSWKALYSGINEFIDDLMHHIHLENNILFPRVLNEK
|
Di-iron-containing protein involved in the repair of iron-sulfur clusters.
|
P45649
|
YIDD_COXBU
|
Putative membrane protein insertion efficiency factor
|
MYKQIVHAIGKAIQTLLLGLIKSYRYLISPVLMSSCRFYPSCSCYAETALKRFGVIKGSGLTVWRLLRCHPFHPGGVDFVPEKSNEMV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P45921
|
YQBE_BACSU
|
Putative prophage capsid protein YqbE
|
MRNQEVINKAEMTLSTLESGGIMNPTQASTFIRMVQDTPTILRDARVIQMDHDTQKIEKIGFGQRILRAAQEGVALTKDQKSVPSTSTVNLSTKEVIAEVNITYDTLENNIEKDGLQNTIMQMIAERAAVDIEELLVNGDTSSSDSYLAQLDGIRKQATSHIVDAAGEELTRQTFKRGYKAVPPKYLRIPQEFRFYTSPGIEVEWKDRVADRQTNLGDAAVQGGLSSAFGVPIKGIANLQPYTIGEGDTAADVSDIILTHPKNIILGFSRNIRIEVDKDIRRRMFIIVLTAKLDSVFEEEDAVAKIVKVKE
|
Possibly a prophage capsid protein.
|
P45999
|
FASC_ECOLX
|
Protein FasC
|
MIMGQLMNMRELFNKKKLHALVFSMWCVNLHASSLSDGIAIEPFEINAKSNRFVEFKVYNNTDEDYIVTQKVVSEENSIKKAKIPFVVNPPIRLLRKRSDAAMGIIYLNEGEVFDKKRKYYLSVSFIPKKKDSDDLGFNIIFTQQIAVKLSALN
|
Could be required for the biogenesis of a putative fimbria.
|
P46043
|
FEOA_LEPBY
|
Putative Fe(2+) transport protein A (ORF3)
|
MTGFTIEGSSLKLLKPQEQGVVSRIDSSRGDFVAQKLRSMNITLGTRVTVEQRSPRFLLRVGADQVALSDPLQDAIYVRLSR
|
Might be involved in Fe(2+) ion uptake (By similarity).
|
P47460
|
HMW2_MYCGE
|
Cytadherence high molecular weight protein 2 (Cytadherence accessory protein 2)
|
MKPFDKKPSLQPIYDIGFDDGYLQSEYEKNRSKTDVDKIENQLLKEIKSLEDELKNLKGLKNQAEDNPELDKKINHLEVDLNRLVNEYKNFQFQKNHMVDKVSELDNLTRFYKNELTRLQQENADFLNSKYANLANFQANYHNKLNDFHRLIENQNQTINRLNQKINGNQNLIDNNVALLQNPNITVEKKNYLLNVIDQLYNELDQLENQKRLLSIEYENTYRELVSADNELQNVYENIDQNQIQFKHQYQTYRDELSQLERKIQLTKQELVDKESALRVKIDDADFYINARLAELDDVAKQLSFQDGITKQNAQHVEDKLVALNKEKDRLNTQKEAFFNLRQSALIDINKLQQENELFAKHLEHQQNEFEQKQSDSLLKLETEYKALQHKINEFKNESATKSEELLNQERELFEKRREIDTLLTQASLEYEHQRESSQLLKDKQNEVKQHFQNLEYAKKELDKERNLLDQQKKVDSEAIFQLKEKVAQERKELEELYLVKKQKQDQKENELLFFEKQLKQHQADFENELEAKQQELFEAKHALERSFIKLEDKEKDLNTKAQQIANEFSQLKTDKSKSADFELMLQNEYENLQQEKQKLFQERTYFERNAAVLSNRLQQKREELLQQKETLDQLTKSFEQERLINQREHKELVASVEKQKEILGKKLQDFSQTSLNASKNLAEREMAIKFKEKEIEATEKQLLNDVNNAEVIQADLAQLNQSLNQERSELQNAKQRIADFHNDSLKKLNEYELSLQKRLQELQTLEANQKQHSYQNQAYFEGELDKLNREKQAFLNLRKKQTMEVDAIKQRLSDKHQALNMQQAELDRKTHELNNAFLNHDADQKSLQDQLATVKETQKLIDLERSALLEKQREFAENVAGFKRHWSNKTSQLQKIYELTKKQESEQTQKETELKIAFSDLQKDYQVFELQKDQEFRQIEAKQRELDKLAEKNNQVKLELDNRFQALQNQKQDTVQAQLELEREQHQLNLEQTAFNQANESLLKQREQLTKKIQAFHYELKKRNQFLALKGKRLFAKEQDQQRKDQEINWRFKQFEKEYTDFDEAKKRELEELEKIRRSLSQSNVELERKREKLATDFTNLNKVQHNTQINRDQLNSQIRQFLLERKNFQRFSNEANAKKAFLIKRLRSFASNLKLQKEALAIQKLEFDKRDEQQKKELQQATLQLEQFKFEKQNFDIEKQRQLVAIKTQCEKLSDEKKALNQKLVELKNLSQTYLANKNKAEYSQQQLQQKYTNLLDLKENLERTKDQLDKKHRSIFARLTKFANDLRFEKKQLLKAQRIVDDKNRLLKENERNLHFLSNETERKRAVLEDQISYFEKQRKQATDAILASHKEVKKKEGELQKLLVELETRKTKLNNDFAKFSRQREEFENQRLKLLELQKTLQTQTNSNNFKTKAIQEIENSYKRGMEELNFQKKEFDKNKSRLYEYFRKMRDEIERKESQVKLVLKETQRKANLLEAQANKLNIEKNTIDFKEKELKAFKDKVDQDIDSTNKQRKELNELLNENKLLQQSLIERERAINSKDSLLNKKIETIKRQLHDKEMRVLRLVDRMKLAEQKYQTEINRLRTQTFDSEKQDIKNFFPPLFKINGNDMAFPYLYPWLYPQQKQDDNTLQIRQLFEQQLQFMQQRYENELNELRRQRNLLEKKLDQIQLESQLNNKQSEFSKVESMMEKLLEKTESRLNDFDQKINYLTKKVNQHNTYQPSSYQPTPSYQDSDKQQLLFRIQELEKQNLFQQQFQPAPAVVQQPTSFAAPNITKQQQIAQLNAEINNIKRLIAQKAASK
|
Component of the cytoskeleton-like structure which stabilizes the shape of the wall-less Mycoplasma. This cytoskeleton-like network of accessory proteins containing HMW proteins 1 to 5 allows the proper anchoring of cytadhesin proteins in the mycoplasmal membrane at the attachment organelle (By similarity).
|
P47568
|
Y326_MYCGE
|
DegV domain-containing protein MG326
|
MKKTAIITDSTASIKPGEINGVYILPLQVIVDGEKSFRDGIEIDYDHVHKLLKENPHGLNISTSLPRQSDLLKIFEEIKTKYDRFIFLPLSKGLSGTYDMLVQLAKELSEQNKDKEFLVFETSDIAISLKWLVEDIKALVDKGCDNQTIKAKVESHKQNILSAVTLKNLVQMRKGGRISGLKKFITTLLRVKPIILFDKGVNTLGAKVFSFSQAVEKIFGFVKTKFGDNYKIKRIGFCYSFCKNYANEIKKIITDFIEHNKINFQNEIENAFITSVIIVHTGIDAFSISLLIDNK
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
P48971
|
OPCA_NOSP7
|
Putative OxPP cycle protein OpcA
|
MTKSKISNPKLPMALQTSTIFSLQAPKDISLNEIDAELNQIWQSYGITGEDGGLPSATRATTFTLVVYEPEETQYLLAALGFYNGPIDGILGPQMAAALREVQKKHKLPETGTATQETLTILREEFAKGQRGGTGGEHAIAGLNSGSPRIADEIALRNPCRIIALFPITGEDEGVKAQVSAYCPIQKQSSSTLICCEYITLSGTAAALERIGGMIPALLIGGLPKFLWWKATPDPNNGLFKRLAAICNNVIVDSCNFNEPESDLLRLEELVEAGVPLADLNWRRLASWQELTAEAYDSPKRRAALREIDRVTIDYEKGNPAQALLFLGWLASRLEWQPVSYQKESGDYDITRIHFISQDQRQVEAELAGVPVADVGDIIGDLIALRLSSTNPQADCGTVICSETGGCMRMETHGGAQSAGLFQQVTSLSEQKAEALLSQQVQRWGRESLFEESLGVTANIFKLAN
|
May be involved in the functional assembly of glucose 6-phosphate dehydrogenase.
|
P50871
|
LPW_AZOBR
|
trp operon leader peptide
|
MIFVATSLSCRWWWPVM
|
This protein is involved in control of the biosynthesis of tryptophan.
|
P51705
|
VCOX_BPHC1
|
Regulatory protein cox
|
MSKQNAICINIHMEQPYMTREEFAKKLDVSTRTIDRLRQQGVLKCIKMKNDEGEETERGLVLVDLVAIAVRNAKNAFQI
|
Accessory protein needed to activate excisive recombination. Appears to serve the additional function of repressing the production of the lysogenic repressor.
|
P51731
|
TMP_BPHC1
|
Probable tape measure protein (TMP) (Gene product 27) (gp27)
|
MSAAQGLEYIISLTDQISAPLKGVMKSIDDLGKRGEAAMKKIGLGVAGIVGAGFALKSALDPAIELNRALGEVHSLGVADDALEKLSKTALNFSSQYGESAVDFVRSSYDIQSAIAGLNGNELAEFTQTSNLLAKGTKASAATITNYMGTMYGIFAEDAAKLGNANWVNKIAGQTALAVKMFKTSGDGMSAAFTSLGAAAKAAKIDVAEQFGVLGNLQATMSGSEAGTKYKAFLAGVSGAQKELGLSFVDTNGDMLDMVTILNKIKGKFGDTLDVAQAAKLKKAFGSDQAVDLIKLLLPKTKELKNNIADIAKVSDTKALAQMARSMVDPWSRLSQIITGVKTAIGGEILKKLDPIMHKVADLGQEFIDWLKTYKNIARWIGYAVGALIGFTGLTAALTLMSGIISAIGVAFSFLASPIMLVTAAIVGLGIFIYKFRDEFMQFISGFIQGFKAASVSLDPLFNAFSLVWGALQKIGATIGRIIGLFGGASDSAYSFQQFGIDLGYALGVVFNTVLDAVELVAQAFNFVADVFSIVVNSIIDGWQAVLTLWDSSAPIDSFLKIGDALGNIFLNAFQGIVNAFVKMLNFIIEKANSLPGINIPLIPEWKDNPTAQALSPALATGVSDGSNFSLSDSLQPQLNSMPQGSVTKTLTQNRTEQRTVNYGGVTINSNNSEEIWQKLRNKEQLAAG
|
Serves as a base for tail tube protein polymerization and acts as a template for tail length determination.
|
P51733
|
BP29_BPHC1
|
Putative baseplate protein gp29 (Gene 29 protein) (Gp29)
|
MSENFKQMLAESGLPTEETQIRQEFERLTAEEGLITNTSRMSPFWRLITAIAVKPVKWLTDHLIAEILPNLFVKTAKDSWLQIQAWAVGLDFKAATKAEGVVHFTKESDVTDLTIKAGTVIQTERINDVIFRLIVTQETIIPKGVLRAPVPVIAEQAGANFNLAAGYYRILPESIAGVSAVENLEDWLTSPGADRETNDELRERYRTQFSSVGQHHIDSVYKGMIAKVAALSVDRIYFKHDAPRGPGTANAYLLLDTGVTSQPFIDKVNRYVRDEGFHGHGDDLICYAMPETKHNLTCAIYFQPSIFVGDVRKQEIVQQVENMIRCAFRENNNYGVTRTYPFTVLVGRNWARKFTTTSAKLHLSYGGKSTFKASYLFHAFSNYPSQSKSKGQK
|
Putative baseplate protein.
|
P51734
|
TAIL1_BPHC1
|
Putative tail protein gp30 (Gene product 30) (gp30)
|
MKIKLPFWMDKGELSKIAVLFGKWWDYVLSAVKFPFNILDEEHCSERILNLIAYQRDVERFEGEPLELFRKRVKYAFLNAKDAGSKAGFIRIFERLGIGYVEIEERFDRENWDVIKIRISDSQLAKKTELLNLIIRKYGRTCRRYTFEVITKETVSIYHGEFNHDHQSFYVKVN
|
Putative tail protein.
|
P51987
|
CCNB_HYDVD
|
G2/mitotic-specific cyclin-B
|
MAGVQRRILISRNEENLLNKGIGTKNVLGGKTTSTRTALSNISNIQRRPQLGGKVKKEDVGALEEKAPTNKSLGRMISQTNLLNEVQMKKNIQNLEDMAEVDLPINSMIDSFTDLEVDDIDLEDLGNPTLCAEYVKDIYKYMNKLEQRLVPGDYMPNQTEINFKMRSILVDWLIQVQSRFNLLQETLYLTIYILDRFLNKQNVKRAELQLVGVTAMLLASKYEEMYAPEIGDFVYITDNAYSKEKIRQMEQKMLKACEYDFSNPLCLHFLRRNSKAGAVDAQKHTLAKYLMELTLVEYEFITKLPSEVAAAALYLSMKLIDDSNWTPTLVHYSGYTEDAILPTVSKLSVLTLSMDNSKYQAVKNKYAASKFLRISRIPQLKGHVLNKFAERI
|
Essential for the control of the cell cycle at the G2/M (mitosis) transition. Interacts with the CDC2 protein kinase to form MPF. G2/M cyclins accumulate steadily during G2 and are abruptly destroyed at mitosis (By similarity).
|
P51988
|
CCNB_HYDVU
|
G2/mitotic-specific cyclin-B
|
SSRTVLSNISNIQRRPQVVGKIKKEDGVALEEKAPLNKGLGRMVSQSNLISDVQLKTTKIIPAYQDIADVEVPINAMINSFTELEVDDIDLEDLGNPTLCAEYLKDIYKYMNKLERRLEPSDYMAHQAEINFKMRSILVDWLIQVQSRFNLLQETLYLTIYIIDRYLSKQNVKRAELQLEGVTAMLIASKYEEMYAPEIGDFVYITDNAYSKEKIRQMEQKMLKTCEYDFSNPLCLHFLRRNSKAGAVDAQKHTLAKYLMELTLVEYEFITKLPSEIAAAALYLALKLIDDSNWTPTLAHYSGYTEDEILSTVSKLSILTLSMDNSKYQAVKNKYSASKFLRISLIPQLKGHILSKFAERN
|
Essential for the control of the cell cycle at the G2/M (mitosis) transition. Interacts with the CDC2 protein kinase to form MPF. G2/M cyclins accumulate steadily during G2 and are abruptly destroyed at mitosis (By similarity).
|
P52055
|
PLPHP_VIBAL
|
Pyridoxal phosphate homeostasis protein (PLP homeostasis protein)
|
MSSIQQNIEHITSQIRYDEQKCGRTPESVQLLAVSKTKPVEAILEAYQAGQTAFGENYVQEGVSKVQHFAEHYPDNRIEWHFIGPIQSNKSRLVAEHFDWVHTIDRTKIAQRLNDQRPSELKPLQVLIQVNTSGEASKSGVTEAEVFELAELISRLPNLTLRGLMSIPANVSDYESQLHEFQKLATLKQTLEAQFPEIDTLSMGMSGDMTAAIEAGSTMVRIGTAIFGARDYS
|
Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis. {ECO:0000255|HAMAP-Rule:MF_02087}.
|
P52056
|
PLPHP_SYNY3
|
Pyridoxal phosphate homeostasis protein (PLP homeostasis protein)
|
MFSPSVYSEIIATLPPSVRLVAVTKTKAIADIEAAYGAGIRDFAESRIQEALPKIEALANYQDINWHFIGRLQSNKARKVVENFTYIHSVDNLAIAVKLDRIAEELNKFPQGLLQIKLLPDENKSGWTREELKLDLPQLELLKNLKICGLMTILPLGLSPGDRQLTFGELKNLATAINQQSSLSLTELSMGMSGDYPEAIAAGATMIRLGTILFGDRL
|
Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis. {ECO:0000255|HAMAP-Rule:MF_02087}.
|
P52531
|
U79_HHV7J
|
Protein U79
|
MIAEDREYGTFESVTQAYQQIISHTLQLRRYEFETGCMIMFSANSGKCEMLSNGWISMISWTSETDTAGSLTLDICTEGGQCKTYSARGHILCSKNITSISQKNEGKEKVLTICHDNGKLHLTYITVLKSGLDCDIKDQKLEKLFEKEHAERKKQDDDYKKKALKQKDKRRSEQKILEDCDKKDEKKRMDDTEKRKLQEDRRNEKQDLKKRVDDTEKRKLEDDRRNEKQDLEG
|
May be involved in DNA replication.
|
P52622
|
FLIV_YEREN
|
Flagellar biosynthetic protein FliV
|
RLHHNQFAIRGGQPLLKEFYLLMVDFFFIRSLISAHILKVGLITEDDVIDIFYSYHAFRQHSAKVEADFRTEIDKVKINDDLSLLQLLV
|
Required for the secretion of flagellin and expression of motility.
|
P52629
|
FLIZ_YEREN
|
Protein FliZ
|
MPGLQLKKRPLSRYLKDYKHGQTHCSHCHKQLDRMALVFRGQIINKEAIAGMDQPIDDQVWSKLQH
|
May regulate sigma factor activity.
|
P54076
|
PAFB_MYCLE
|
Protein PafB
|
MATSKVERLVNLVIALLSTRGYMTAEKIRSSVAGYSDSPTVEAFSRMFERDKNELRDLGIPLEVGKVSALDPSEGYRINRDAYALPPVELTPDEAAAVAVATQLWESQELITATQGALLKLRAAGVDIDPLDTPVVIASSSGVSSLRGSEDFLSILLSAIGSRQAVQFPYRPSRAEPYTMRNVEPWGVITENSCWYLVGHDCDRNATRTFRLSRIGSEVAPIGPAGAVTVPDGVDLRRIVSDAVAEVSTGATARVWVVDGRATALRHAGRPAGVRRLGGRDGQVIELDIGSIDRLARDIAGHGADAVVLEPDALRDDVLIRLRAHAGTGPS
|
Does not seem to be involved in pupylation or substrate degradation.
|
P54442
|
YRKO_BACSU
|
Uncharacterized protein YrkO
|
MIVQKEGRGQPVSLRERVHFLDIVRGFALLGIIIVNYFLIVDSVKGFEMASDDVLHKLVSWFAEGKFVTLFSFLFGVGFMIFMDRAAQKVESPNKLFARRLSILLGFGILHITFVWVGDILAFYAVSGFLLLAFYKRTAKTVLRWIIALIVFQFLTPVFTMLYNVINTAGSKNPNFSEFTLFSHSSLTYMESISTRWTDMVTMAAGSFSMIYSMFLMFLLGVYFVKMEFFKDMEAKKPIWKRIWIISTIAFLITQSSILLDMFNLSENMLWKDISSVLGQNGGLTGSMFYMSTFAMLFLYLPQLRGPMMIFTKVGRMSLTCYLLHSIIGTVLFLRYGFGLADHIQSAGTFMFSLAVYFVLMSFSTLWLKRFRYGPMELVWRKLTYGKVNGSPKATPLHSEKSIQK
|
Involved in transport.
|
P55470
|
Y4GN_SINFN
|
Uncharacterized protein y4gN
|
MDQTLSRRLFLWHNPQTDNQCRNERHMIHTSKIYREINRIGVQIKGLPDYWMGQARRISYDRVGSAGNTITEGRKPVSADMAILLIYQPRGLLESLFLQLEHLLSKGLGVVIVSNRKVLEHDRNRLSEYCHLIIERKNIGYDFGGYRDGILALHKRSIHPKSLFVMNDSVWFPIRKDCDLIDRCRESRSDIVGVFYNNKSKFPKNHHLQSYFYRFGEKVVSDSRFLAYWRKIPMYNDKRNVIRNLEIKLTKNFQLMGFGISSLYAPEDILKAFKNIEVRNIRPVLDYYISALGYDQNTFWSAYKNESPKGGDTHALPIDVPNSRVFFHFLDAHPEILIRKLNSPIIKKNRDKRFVAQRKAIIEGGFLKEIDAVIQKELINWDR
|
Could have an enzymatic function.
|
P55510
|
Y4JJ_SINFN
|
Putative plasmid stability protein y4jJ
|
MANVTVRNLPDEVHRALRVRAAMHGRSTEAEIRDILETTVRPPERVKLGSLLASIAHEAGGLTDAEAEHFNQLRDKTPAEPMSFE
|
Involved in plasmid stability.
|
P55528
|
Y4KH_SINFN
|
Probable toxin y4kH (EC 2.4.2.-)
|
MRERAVGSKGSFPIGIAELQEVSCASVEINQPLLLADLRSDGMLRMRIPTDAARAASHELGKQWSRALWLHDEKPDGIIYDSRLNGEANTALFDRALPKLNVKSSGPLLDFRDEVAQILDDFSLEIV
|
Probable toxic component of a type II toxin-antitoxin (TA) system. It is not known which gene encodes its antitoxin.
|
P55534
|
Y4KP_SINFN
|
Putative toxin Y4kP
|
MSRKRIRWTLRALRRLDEIGAYIEKDDPDAAARVVARIGTAVDALAEYPASGRPGRIKSTRELVLADIPYIIPYRISRDVEILTVMHAHQQWPQVL
|
Toxic component of a type II toxin-antitoxin (TA) system.
|
P55620
|
Y4PO_SINFN
|
Probable transposase for insertion sequence element ISRM3-like
|
MAIEKELLDQLLAGRDPSEVFGKDGLLDDLKKALSERILNAELDEHLDVERSEGTAANRRNGSSKKTVLTGTSKMTLTIPRDRAGTFDPKLIARYQRRFPDFDDKIISMYARGMTVREIQGHLEDIYGIDVSPDLISAVTDQVLEAVGEWQNRPLELCYPLVFFDAIRVKIRDEGFVRNKAVYVALAVLADGTKEILGLWIEQTEGAKFWLRVMNELKSRGCQDILIAVVDGLKGFPDAITAVFPQTIVQTCIVHLIRHSLEFVSYKDRKPVVPALRAIYRARDAEAGLKALEAFEEGYWGQKYPAISQSWRRNWEHVVPFFAFPEGVRRIIYTTNAIEALNSKLRRAVRSRGHFPGDEAAMKLLYLVLNNAAEQWKRAPREWVEAKTQFAVIFGERFFN
|
Required for the transposition of the insertion element.
|
P55758
|
PSIB_RHILP
|
Protein PsiB
|
MRSFRAAELPDRNSIASISGLIGSDLIQMIRFDDMHSLFVGEEALRVGLTAFTIFDGYPIPLAGQIALLGGDGSKPYRSPSITMTEAARRFECCRPVLDPVFAPMDRVANKGLIVAGALESLQVRIDRRSPVLL
|
Could be involved directly or indirectly in exopolysaccharide synthesis.
|
P55767
|
YLXQ_GEOSE
|
RNA-binding protein YlxQ
|
EKKVTDKCAFYGVPLCKVPDRYVLGGAIGKDARVVVAVTDEGFARQLQTMLDRSLWG
|
RNA-binding protein that recognizes the K-turn motif present in ribosomal RNA, but also in box C/D and box C'/D' sRNAs.
|
P55768
|
YLXQ_ENTFC
|
RNA-binding protein YlxQ
|
MNEGNRQKAMNLIGLAMRAGKLITGEELTIADIRNEKAKIVFVANDASENTKKKVKDKSSYYEVPCFELFSEAEITQMIGKPRKVFGIVDNGFAKKTKELIEG
|
RNA-binding protein that recognizes the K-turn motif present in ribosomal RNA, but also in box C/D and box C'/D' sRNAs.
|
P55959
|
NO40_PEA
|
Early nodulin-40
|
MKFLCWQKSIHGS
|
Modulates the action of auxin, and may function as plant growth regulator that alters phytohormone responses.
|
P55960
|
NO40_SOYBN
|
Early nodulin-40
|
MELCWLTTIHGS
|
Modulates the action of auxin, and may function as plant growth regulator that alters phytohormone responses.
|
P55961
|
NO40_VICSA
|
Early nodulin-40
|
MKLLCWQKSIHGS
|
Modulates the action of auxin, and may function as plant growth regulator that alters phytohormone responses.
|
P56583
|
AMIS_MYCSM
|
Putative amidate substrates transporter protein
|
MGGVGLFYVGAVLIIDGLMLLGRISPRGATPLNFFVGGLQVVTPTVLILQSGGDAAVIFAASGLYLFGFTYLWVAINNVTDWDGEGLGWFSLFVAIAALGYSWHAFTAEADPAFGVIWLLWAVLWFMLFLLLGLGHDALGPAVGFVAVAEGVITAAVPAFLIVSGNWETGPLPAAVIAVIGFAAVVLAYPIGRRLAAPSVTNPPPAALAATTR
|
Possible transporter that might be responsible for the adsorption of amidase substrates or release of their hydrolysis products.
|
P56936
|
REPA1_BUCAI
|
Probable replication-associated protein repA1
|
MIIRKCYINNPNPFFTPPKNNKRRPSFICYAMKRASEIDVARCELNYILQIKNIKIGFPVKRFRRLNEHRACAMRAMVLAMLYHFNISSDLVQASVEQLSDECGLSTLSKAGNKSITRASRLITNFMEPMGFVTCKKTWDKILGNYMPKMITLTPLFFMLFGVSEKKLMDAKKQQLGWINKNLISKGFKPITMIDAKRRSKDTQIKNIFQYRISKHAFYKKKRNAQRLISLDEKEARQTILRALVAKYSITELTKLGPNGLKKQVNISYYYLRKIATNTYPDN
|
This protein is essential for plasmid replication it is involved in copy control functions.
|
P57181
|
FLIK_BUCAI
|
Flagellar hook-length control protein homolog
|
MHESSNIKKKNDFDFKNLKNKTLQKKINVFDTIKNHIKIINNEEKIILPLNIKKNKKIVFDSKNINKINPMISKRHSCKILSNKKEFIKSYIEPFMSSDTKNSIEWKKLISHKILLSISNKYNQAKIHLKPESLGSIYVSISMKNNIATLKFISEHNEVKTFLDSYMPFLYNSLKKNGIKLKEFKISISSKKNQLKNYKNLFYKNIYYTDHIKKTLNWNEKKIDYIKDKTIDVYV
|
Controls the length of the flagellar hook.
|
P57421
|
FLGD_BUCAI
|
Basal-body rod modification protein FlgD
|
MSTININSSDINLPNIQPPIINNEAVKKNDNNLPNDINPPDLQKNFLSLLIAQIKNQDPTDPIKNSDLTSQLAQINTASGMQKLNNTVDQFSNQISKNQNIQLSTLIGRHVMVPNKKIIHTKDTKTQFGIELFEKATSVEIKITDDNNKTLYLKQLKETEAGRHNFFWDGQDLNKNSVMSGQYNISVIAKKNNQNIPVNSLSVGVVNSIIMSSGNAIIDLGESGQITPLSIREILK
|
Required for flagellar hook formation. May act as a scaffolding protein (By similarity).
|
P57798
|
FEOA_HELPY
|
Putative Fe(2+) transport protein A
|
MTLNEAIKDKVYEIVEIANCDEALKKRFLSFGIHEGVQCILLHYSMKKATLSVKINRIQVALRSHEAQYLVIKESV
|
Might be involved in Fe(2+) ion uptake (By similarity).
|
P58092
|
PARD_ECO57
|
Antitoxin ParD
|
MRKITSVSVGEQLDSFITRMVQSGRYGSASEVMRSALRLLEQQESRDEAVRNAVIEGLESGESSMTLRDIAAERKQKHRV
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Neutralizes the effect of toxin ParE (By similarity).
|
P58093
|
PARD_VIBCH
|
Antitoxin ParD
|
MAKNTSITLGEHFDGFITSQIQSGRYGSASEVIRSALRLLENQETKLQSLRQLLIEGEQSGDADYDLDSFINELDSENIR
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Neutralizes the effect of toxin ParE (By similarity).
|
P58235
|
YEFM_SYNY3
|
Antitoxin YefM
|
MKAITTTQAKDHLDELINAVISDLEPTIVSNNQGQQAVLISLDEFNSWQETLYLLSNPTNAEHLMASIKQAETGQIIKQKLPDLLEL
|
Antitoxin component of a type II toxin-antitoxin (TA) system. A probable antitoxin for the putative mRNA interferase YeoB (By similarity).
|
P58615
|
GLGS_SALTI
|
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}.
|
P59106
|
YPEB_OCEIH
|
Sporulation protein YpeB
|
MFRWIAIGVLSVAVIGTAVWGYNEYSEKNEIKIQAENEYQRSFHELTYYMDLLNDEIGTALAMNSKERLSPQFVDIWRLTSQAHSNVGQLPLGLLPFHKTEQFLSDIGEFTYQTAVRNLDDNPLTEEETQKLKDYYDQSGQIKDELRQVQHVALEEGLNWMDVELALSDENAQQDNTIVNGFQTVEKSVEGFGQADPENSTISTNTQDHSYKNLTGSEVTENEALQRAMEIFEIKDKDLLSISKSGEGADTPLYSISYNKDEEHGYMDMAIKGGHPLNLLVSREMKEKKVSLNEGSEKAKDYLASFGLEDMTLFQSSEYDHIGVYSYLYNDNGVRVYSDAVEVKVGLDNGDLLGLTTNSYFMNHTDREIPEPKISEDEARDNVNSTVDIQESHLAIIDNNAGEEVLTYEFLGIMDDETYRIFINAENGQEELVEKLDGKEVNYNSVL
|
Required for spore cortex hydrolysis during germination. Appears to be required for either expression, localization, activation or function of SleB (By similarity).
|
P59203
|
MALA_STRPN
|
Maltodextrose utilization protein MalA
|
MLPYPFSYFSSIWGVRKPLSKRFELNWFQLLFTSIFLISLSMVPIAIQNSSQETYPLETFIDNVYEPLTDKVVQDLSEHATIVDGTLTYTGTASQAPSVVIGPSQIKELPKDLQLHFDTNELVISKESKELTRISYRAIQTESFKSKDSLTQAISKDWYQQNRVYISLFLVLGASFLFGLNFFIVSLGASFLLYITKRSRLFSFNTFKECYHFILNCLGLPTLITLILGLFGQNMTTLITVQNILFVLYLVTIFYKTHFRDPNYHK
|
Has a role in maltotetraose utilization.
|
P59471
|
YIDD_BUCBP
|
Putative membrane protein insertion efficiency factor
|
MVLLLSMISRCLILIILCYQRYISVFLSPRCRFYPTCSHYAVDALYTFGLLKGLLLIAKRILKCHPFHSGGLNSISIKTKSKREY
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P59787
|
TRA6_ENTFA
|
Transposase for insertion sequence element IS256 in transposon Tn4001
|
MTQVHFTLKSEEIQSIIEYSVKDDVSKNILTTVFNQLMENQRTEYIQAKEYERTENRQSQRNGYYERSFTTRVGTLELKVPRTRDGHFSPTVFERYQRNEKALMASMLEMYVSGVSTRKVSKIVEELCGKSVSKSFVSSLTEQLEPMVNEWQNRLLSEKNYPYLMTDVLYIKVREENRVLSKSCHIAIGITKDGDREIIGFMIQSGESEETWTTFFEYLKERGLQGTELVISDAHKGLVSAIRKSFTNVSWQRCQVHFLRNIFTTIPKKNSKSFREAVKGIFKFTDINLAREAKNRLIHDYIDQPKYSKACASLDDGFEDAFQYTVQGNSHNRLKSTNLIERLNQEVRRREKIIRIFPNQTSANRLIGAVLMDLHDEWIYSSRKYINFDK
|
Required for the transposition of the insertion element.
|
P59834
|
NIFW_KLEOX
|
Nitrogenase-stabilizing/protective protein NifW
|
CSLPVLATFHRKLRAEVPLQNRLEDNDRAPWLLARRLLAESYQQQFQESGT
|
May protect the nitrogenase Fe-Mo protein from oxidative damage.
|
P59842
|
INSA_HAEDU
|
Insertion element IS1 protein InsA
|
MASVSISCPSCSATDGVVRNGKSTAGHQRYLCSHCRKTWQLQFTYTASQPGTHQKIIDMAMNGVGCRATARIMGVGLNTILRHLKNSGRSR
|
Absolutely required for transposition of IS1.
|
P59965
|
MBTH_MYCBO
|
Protein MbtH
|
MSTNPFDDDNGAFFVLVNDEDQHSLWPVFADIPAGWRVVHGEASRAACLDYVEKNWTDLRPKSLRDAMAED
|
Could be involved in mycobactin synthesis.
|
P60005
|
USPE_PHOLL
|
Universal stress protein E
|
MANYQNLLVVIDPSQDDQPALRRAVYIVQRNGGRIKAFLPIYDLSYEMTTLLSPEEGSTMRKGVTSQRTAWLKQQAYYYLEAGIDIEIKVVWHNRPYEAIIQEVITGNHDLLLKMTHKHDKLGSLIFTPLDWQLLRKCPCPVWMVKDQIWPDQGSVVVAVNLSNEESYHHELNLKLVKETQELANQVMKNPEIHLVSAYPVAPLNIAIELPDFNPSVYNHALRGQHLIAMKELRQTFCIDEKYTHIHEGLPESVIPQMCDEMNAGIIVLGILGRTGLSAAFLGNTAEHVIDHLKCDILTIKPDGFECPIKAAKE
|
Required for resistance to DNA-damaging agents.
|
P60084
|
SYDP_SALTY
|
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}.
|
P60085
|
SYDP_SALTI
|
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}.
|
P60155
|
SYDP_PHOLL
|
Protein Syd
|
MISNVTEALSNFTRCYVDLWQKETGAPPASRELYGVPSPCITQTGDNIVYWLPQPFPLEEKLNSVEVALDIQLQPAIHDFYTSQLAGDMTVTFEGQRLSLIQVWSEDDFIRLQENLIGHLVTQKRLKLSPTAFIATMESDDMGIISLCNLTGEVILEQFGSHKRERLFTDLVGFLGAIEPVFMR
|
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}.
|
P60156
|
SYDP_VIBVY
|
Protein Syd
|
MSSPVSLALADFSQRFQAAWQAQHNALPSSEELADLPSPCVVESKGDEVLWRSVSLSAPVDFANVEQAIELTLHDDIKAFYGSQLSADMTATWEGNELTLLQVWNDDDFTRLQENILGHLVTQRRLKLKPTVFIAATDAELDVLSICNITGNVVLERLGTSQRDVLAENVTEFLTKLQPMV
|
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}.
|
P60996
|
LPHI_ECOL6
|
his operon leader peptide (his operon attenuator peptide)
|
MTRVQFKHHHHHHHPD
|
This protein is involved in the attenuation mechanism for the control of the expression of the his operon structural genes.
|
P60997
|
LPHI_SALTY
|
his operon leader peptide (his operon attenuator peptide)
|
MTRVQFKHHHHHHHPD
|
This protein is involved in the attenuation mechanism for the control of the expression of the his operon structural genes.
|
P61446
|
HRCA_LEPIC
|
Heat-inducible transcription repressor HrcA
|
MDLTERHKRILKALVDEFIQENRPVGSKTLFDKHDIGLSPASIRTVLKDLEDFGYLASKHTSGGRIPTERGYRFYVDSLVILYELTLKEKQRIQQEYLKMQFKLDQILKATASVLSSLSNAAGIVIGPAKNLDTLKHIELIHVRGDEILMILVMRSGTVLHRNIFVDQNYSQEALYQVSKYLNDNLKGYDIYEIQNVIIPKLMIRKDGPEDFIRIADLISSAMTPDNSEVTLYIDGFKNLYANFRDEEQQLSQVLSLLDDQGFLKAFFSEYIDQDGVFTIIGKDGDRSMSGVSIITSNYKMGEKKIGALGIIGPQRMDYNRALPLVDFTSKLVSEMVTRISK
|
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}.
|
P61464
|
YIDD_BACC1
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQKHGALKGFWLTCKRILKCHPFHPGGFDPVPDKKDDKVHS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61465
|
YIDD_CORGL
|
Putative membrane protein insertion efficiency factor
|
MCAPTSDDPFDIPEPKSIPAKTAASAVRFYQKYLSGLKMGSTCRFDPVCSTYALKAVSVHGAFKGTILSAARLSKCGPWHPGGFDPVPNHGFWSTETVT
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61466
|
YIDD_DESVH
|
Putative membrane protein insertion efficiency factor
|
MSVMLRRLVVLPVRFYQYCISPLFPPACRYVPTCSAYTAEAVMRHGVMRGLWLAARRILRCHPWCAGGHDPVPPVPPQRYPSAQEH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61467
|
YIDD_ECOL6
|
Putative membrane protein insertion efficiency factor
|
MAPPLSPGSRALIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFDTREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61468
|
YIDD_ECO57
|
Putative membrane protein insertion efficiency factor
|
MAPPLSPGSRVLIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFNTREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61469
|
YIDD_GEOSL
|
Putative membrane protein insertion efficiency factor
|
MLKGILYIIGIYQRYLSPLKGPTCRFYPSCSRYAHESLTRYGLVKGLWLTTIRILKCHPFHPGGVDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61470
|
YIDD_LACJO
|
Putative membrane protein insertion efficiency factor
|
MNKLLIGLVNVYKKFISPILPPTCRYYPTCSSYMIDALKKHGAILGLIMGLARILRCNPFIKGGVDPVPDYFTLRRNPHPERYEDEIIAQAFHSNKK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61471
|
YIDD_RHOPA
|
Putative membrane protein insertion efficiency factor
|
MQLPSRGTDWIAQVLRLPRNAGRGLIWLYRHTLSPLVGYNCRHYPTCSMYGDEAIRKFGLWAGGWMTLARLLRCQPWGTSGIDLVPQTAPSRARWYLPWRYARWRGVNAPPPDVAEPCGCGSHSQLTPH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61472
|
YIDD_SALTI
|
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}.
|
P61473
|
YIDD_SHIFL
|
Putative membrane protein insertion efficiency factor
|
MAPPLSPGSRVLIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGHPPVPPGPFDTREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61474
|
YIDD_TREDE
|
Putative membrane protein insertion efficiency factor
|
MRKLLVSFLCACIIFYQKAISPHFPPSCRYEPTCSQYAIESIKKYGPFKGAGMALLRILRCNPLCKGGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
P61475
|
YIDD_YERPE
|
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}.
|
P62187
|
LPER_BACAN
|
Erythromycin resistance leader peptide (23S rRNA methylase leader peptide)
|
MTHSMRLRFPTLNQ
|
This peptide is involved in the control mechanism of the synthesis of the macrolide-lincosamide-streptogramin B resistance protein. It acts as a transcriptional attenuator.
|
P62188
|
LPER_BACLI
|
Erythromycin resistance leader peptide (23S rRNA methylase leader peptide)
|
MTHSMRLRFPTLNQ
|
This peptide is involved in the control mechanism of the synthesis of the macrolide-lincosamide-streptogramin B resistance protein. It acts as a transcriptional attenuator.
|
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