entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
P9WJ55
|
VAPB9_MYCTU
|
Putative antitoxin VapB9
|
MKTLYLRNVPDDVVERLERLAELAKTSVSAVAVRELTEASRRADNPALLGDLPDIGIDTTELIGGIDAERAGR
|
Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC9.
|
P9WJ56
|
VAPB6_MYCTO
|
Putative antitoxin VapB6
|
MSVTQIDLDDEALADVMRIAAVHTKKEAVNLAMRDYVERFRRIEALARSRE
|
Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC6 (By similarity).
|
P9WJ57
|
VAPB6_MYCTU
|
Putative antitoxin VapB6
|
MSVTQIDLDDEALADVMRIAAVHTKKEAVNLAMRDYVERFRRIEALARSRE
|
Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC6.
|
P9WJ58
|
VAPB3_MYCTO
|
Antitoxin VapB3
|
MLSRRTKTIVVCTLVCMARLNVYVPDELAERARARGLNVSALTQAAISAELENSATDAWLEGLEPRSTGARHDDVLGAIDAARDEFEA
|
Antitoxin component of a type II toxin-antitoxin (TA) system.
|
P9WJ74
|
PARD2_MYCTO
|
Antitoxin ParD2
|
MVVNRALLASVDALSRDEQIELVEHINGNLAEGMHISEANQALIEARANDTDDAHWSTIDDFDKRIRARLG
|
Antitoxin component of a type II toxin-antitoxin (TA) system.
|
P9WJ86
|
MAZE6_MYCTO
|
Antitoxin MazE6
|
MKTAISLPDETFDRVSRRASELGMSRSEFFTKAAQRYLHELDAQLLTGQIDRALESIHGTDEAEALAVANAYRVLETMDDEW
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Labile antitoxin that binds to cognate MazF6 toxin and counteracts its endoribonuclease activity.
|
P9WJ88
|
MAZE5_MYCTO
|
Antitoxin MazE5
|
MKTARLQVTLRCAVDLINSSSDQCFARIEHVASDQADPRPGVWHSSGMNRIRLSTTVDAALLTSARDMRAGITDAALIDEALAALLARHRSAEVDASYAAYDKHPVDEPDEWGDLASWRRAAGDS
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Labile antitoxin that binds to its cognate MazF5 endoribonuclease toxin and neutralizes its activity.
|
P9WJ90
|
MAZE4_MYCTO
|
Probable antitoxin MazE4
|
MPFLVALSGIISGVHDHSMTVRLDQQTRQRLQDIVKGGYRSANAAIVDAINKRWEALHDEQLDAAYAAAIHDNPAYPYESEAERSAARARRNARQQRSAQ
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Labile antitoxin that binds to cognate MazF4 toxin and counteracts its endoribonuclease activity.
|
P9WJD4
|
ESPD_MYCTO
|
ESX-1 secretion-associated protein EspD
|
MDLPGNDFDSNDFDAVDLWGADGAEGWTADPIIGVGSAATPDTGPDLDNAHGQAETDTEQEIALFTVTNPPRTVSVSTLMDGRIDHVELSARVAWMSESQLASEILVIADLARQKAQSAQYAFILDRMSQQVDADEHRVALLRKTVGETWGLPSPEEAAAAEAEVFATRYSDDCPAPDDESDPW
|
Required for ESX-1 function. Required for the maintenance of adequate cellular levels of both EspA and EspC. Facilitates EsxA secretion.
|
P9WJG2
|
CARD_MYCTO
|
RNA polymerase-binding transcription factor CarD
|
MIFKVGDTVVYPHHGAALVEAIETRTIKGEQKEYLVLKVAQGDLTVRVPAENAEYVGVRDVVGQEGLDKVFQVLRAPHTEEPTNWSRRYKANLEKLASGDVNKVAEVVRDLWRRDQERGLSAGEKRMLAKARQILVGELALAESTDDAKAETILDEVLAAAS
|
Controls rRNA transcription by binding to the RNA polymerase (RNAP). Required for replication and persistence during infection of mice (By similarity).
|
P9WL28
|
DPRA_MYCTO
|
Putative DNA processing protein DprA
|
MIDPTARAWAYLSRVAEPPCAQLAALVRCVGPVEAADRVRRGQVGNELAQHTGARREIDRAADDLELLMRRGGRLITPDDDEWPVLAFAAFSGAGARARPCGHSPLVLWALGPARLDEVAPRAAAVVGTRAATAYGEHVAADLAAGLAERDVAVVSGGAYGIDGAAHRAALDSEGITVAVLAGGFDIPYPAGHSALLHRIAQHGVLFTEYPPGVRPARHRFLTRNRLVAAVARAAVVVEAGLRSGAANTAAWARALGRVVAAVPGPVTSSASAGCHTLLRHGAELVTRADDIVEFVGHIGELAGDEPRPGAALDVLSEAERQVYEALPGRGAATIDEIAVGSGLLPAQVLGPLAILEVAGLAECRDGRWRILRAGAGQAAAKGAAARLV
|
May help load RecA onto ssDNA (By similarity).
|
P9WL40
|
VPB43_MYCTO
|
Antitoxin VapB43
|
MRTTIRIDDELYREVKAKAARSGRTVAAVLEDAVRRGLNPPKPQAAGRYRVQPSGKGGLRPGVDLSSNAALAEAMNDGVSVDAVR
|
Antitoxin component of a type II toxin-antitoxin (TA) system.
|
P9WL88
|
ARYLT_MYCTO
|
Putative arylamide transporter
|
MSASLLVRTACGGRAVAQRLRTVLWPITQTSVVAGLAWYLTHDVFNHPQAFFAPISAVVCMSATNVLRARRAQQMIVGVALGIVLGAGVHALLGSGPIAMGVVVFIALSVAVLCARGLVAQGLMFINQAAVSAVLVLVFASNGSVVFERLFDALVGGGLAIVFSILLFPPDPVVMLCSARADVLAAVRDILAELVNTVSDPTSAPPDWPMAAADRLHQQLNGLIEVRANAAMVARRAPRRWGVRSTVRDLDQQAVYLALLVSSVLHLARTIAGPGGDKLPTPVHAVLTDLAAGTGLADADPTAANEHAAAARATASTLQSAACGSNEVVRADIVQACVTDLQRVIERPGPSGMSA
|
May be involved in the import of arylamide compounds.
|
P9WLF8
|
Y2269_MYCTO
|
Uncharacterized protein MT2330.2
|
MANDARPLARLANCRVGDQSSATHAYTVGPVLGVPPTGGVDLRYGGRAGIGRSETVTDHGAVGRRYHQPCAGQIRLSELRVTILLRCETLCETAQLLRCPPLPCDCSTPL
|
May play a regulatory role in sulfomenaquinone (SMK) biosynthesis.
|
P9WLU2
|
VPB11_MYCTO
|
Antitoxin VapB11
|
MYRWCMSRTNIDIDDELAAEVMRRFGLTTKRAAVDLALRRLVGSPLSREFLLGLEGVGWEGDLDDLRSDRPD
|
Antitoxin component of a type II toxin-antitoxin (TA) system.
|
P9WLZ0
|
VPB10_MYCTO
|
Putative antitoxin VapB10
|
MKRTNIYLDEEQTASLDKLAAQEGVSRAELIRLLLNRALTTAGDDLASDLQAINDSFGTLRHLDPPVRRSGGREQHLAQVWRATS
|
Putative antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC10 (By similarity).
|
P9WM78
|
Y0574_MYCTO
|
Probable polyglutamine synthesis accessory protein MT0602
|
MAGNPDVVTVLLGGDVMLGRGVDQILPHPGKPQLRERYMRDATGYVRLAERVNGRIPLPVDWRWPWGEALAVLENTATDVCLINLETTITADGEFADRKPVCYRMHPDNVPALTALRPHVCALANNHILDFGYQGLTDTVAALAGAGIQSVGAGADLLAARRSALVTVGHERRVIVGSVAAESSGVPESWAARRDRPGVWLIRDPAQRDVADDVAAQVLADKRPGDIAIVSMHWGSNWGYATAPGDVAFAHRLIDAGIDMVHGHSSHHPRPIEIYRGKPILYGCGDVVDDYEGIGGHESFRSELRLLYLTVTDPASGNLISLQMLPLRVSRMRLQRASQTDTEWLRNTIERISRRFGIRVVTRPDNLLEVVPAANLTSKE
|
Could be involved in the biosynthesis, transport or localization of poly-alpha-L-glutamine (PLG), a cell wall component. Contributes to stress tolerance and virulence.
|
P9WMA8
|
DATIN_MYCTO
|
Dormancy associated translation inhibitor (DATIN)
|
MEPKRSRLVVCAPEPSHAREFPDVAVFSGGRANASQAERLARAVGRVLADRGVTGGARVRLTMANCADGPTLVQINLQVGDTPLRAQAATAGIDDLRPALIRLDRQIVRASAQWCPRPWPDRPRRRLTTPAEALVTRRKPVVLRRATPLQAIAAMDAMDYDVHLFTDAETGEDAVVYRAGPSGLRLARQHHVFPPGWSRCRAPAGPPVPLIVNSRPTPVLTEAAAVDRAREHGLPFLFFTDQATGRGQLLYSRYDGNLGLITPTGDGVADGLA
|
Involved in translation regulation. Can also stimulate macrophages and peripheral blood mononuclear cells (PBMC) to secrete important cytokines that may be significant in granuloma formation and its maintenance. Increases secretion of IFN-gamma, TNF-alpha, IL-1 beta and IL-8 through human Toll-like receptor 2 (TLR2) signaling pathway.
|
P9WMK2
|
HRCA_MYCTO
|
Heat-inducible transcription repressor HrcA
|
MGSADERRFEVLRAIVADFVATQEPIGSKSLVERHNLGVSSATVRNDMAVLEAEGYITQPHTSSGRVPTEKGYREFVDRLEDVKPLSSAERRAIQSFLESGVDLDDVLRRAVRLLAQLTRQVAVVQYPTLSTSTVRHLEVIALTPARLLMVVITDSGRVDQRIVELGDVIDDHQLAQLREILGQALEGKKLSAASVAVADLASQLGGAGGLGDAVGRAATVLLESLVEHTEERLLLGGTANLTRNAADFGGSLRSILEALEEQVVVLRLLAAQQEAGKVTVRIGHETASEQMVGTSMVSTAYGTAHTVYGGMGVVGPTRMDYPGTIASVAAVALYIGDVLGAR
|
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}.
|
P9WMX6
|
GLTR1_MYCTO
|
PGL/p-HBAD biosynthesis glycosyltransferase MT3031 (EC 2.4.1.-)
|
MAAPMFSIIIPTLNVAAVLPACLDSIARQTCGDFELVLVDGGSTDETLDIANIFAPNLGERLIIHRDTDQGVYDAMNRGVDLATGTWLLFLGADDSLYEADTLARVAAFIGEHEPSDLVYGDVIMRSTNFRWGGAFDLDRLLFKRNICHQAIFYRRGLFGTIGPYNLRYRVLADWDFNIRCFSNPALVTRYMHVVVASYNEFGGLSNTIVDKEFLKRLPMSTRLGIRLVIVLVRRWPKVISRAMVMRTVISWRRRR
|
Involved in glycosylation steps downstream of mono-O-methyl-glycosyl-p-hydroxybenzoic acid derivative (p-HBAD I) and 2-O-methyl-rhamnosyl-phenolphthiocerol dimycocerosate (mycoside B) during the p-hydroxybenzoic acid derivatives (p-HBAD) and glycosylated phenolphthiocerol dimycocerosates (PGL) biosynthesis.
|
P9WP04
|
Y2417_MYCTO
|
DegV domain-containing protein MT2490
|
MTVVVVTDTSCRLPADLREQWSIRQVPLHILLDGLDLRDGVDEIPDDIHKRHATTAGATPVELSAAYQRALADSGGDGVVAVHISSALSGTFRAAELTAAELGPAVRVIDSRSAAMGVGFAALAAGRAAAAGDELDTVARAAAAAVSRIHAFVAVARLDNLRRSGRISGAKAWLGTALALKPLLSVDDGKLVLVQRVRTVSNATAVMIDRVCQLVGDRPAALAVHHVADPAAANDVAAALAERLPACEPAMVTAMGPVLALHVGAGAVGVCVDVGASPPA
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q00189
|
TRAH5_ECOLX
|
Protein TraH
|
MSEPKDQSIEDELDAALAALDSGPLPTSTLPEPQPSPEQATAGQPPAEATAPTPAFTPPPSTGSPTLDALEENRRPKASTVCEHCPNSVWFASPAEVKCYCRVMFLVTWSSKEPNQITHCDGEFLGQEQE
|
The initiation process of transfer DNA synthesis requires the interaction of at least three plasmid-specific components (TraH, TraI, and TraJ) at the transfer origin resulting in the assembly of a specialized nucleoprotein complex - the relaxosome.
|
Q00272
|
MVP_CMVM
|
Movement protein (MP) (Protein 3A)
|
MAFQGTSRTLTQQSSAATSDDLQKILFSPEAIKKMATECDLGRHHWMRADNAISVRPLVPEVTHGRIASFFKSGYDVGELCSKGYMSVPQVLCAVTRTVSTDAEGSLRIYLADLGDKELSPIDGQCVSLHNHDLPALVSFQPTYDCPMETVGNRKRCFAVVIERHGYIGYTGTTASVCSNWQARFSSKNNNYTHIAAGKTLVLPFNRLAEQTKPSAVARLLKSQLNNIESSQYLLTNVKINQNARSESEDLNVESPPAAIGRFSASRSEAFRPQVVNGL
|
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).
|
Q01182
|
NIFW_CERSP
|
Nitrogenase-stabilizing/protective protein NifW
|
MTPGTAVLEELKRLSSAEEIFDALDHPYRPEVVQVARLHIMKRLGQYLAAVDFATLDPADARAAARDALSRAYTDFVDSSPLEQKVFKVFAKPSRAFVPLSGLSVVED
|
May protect the nitrogenase Fe-Mo protein from oxidative damage.
|
Q01438
|
COMCA_BPT4
|
Protein comC-alpha
|
MAIKFEVNKWYQFKNKQAQENFIKDHTDNGIYARRLGMEPFKILDADYLGRPTKIMTSIGVLKRCAGGDILDENFIWLSTNEAGFFDEVENPYQAVEEQEQEEKEQEQIEDFTEFPVMKVTIENNDQAWSLYQMLKAYFKE
|
Plays a role in the expression of some T4 genes involved in DNA synthesis including the helicase/primase gp41. May act as a transcriptional antitermination factor.
|
Q01457
|
ABIC_LACLL
|
Abortive phage resistance protein AbiC
|
MSEKKNTKGSPIYMKKSFWIPTIIFVVFVFVFVMLLKLPSFGLWYGANVKDKVSPNSINISRVELLKILISLIAPILTFLVFMNTLSIQKKNQEESKKLNNSDSANREFYSLLDLFKKEQNKSETIKAISFLYKRAINDKHGNSFINDYNIDIGNGLDFRFNLFESNQWFSITYNSSKYKGKNLTKEQKVELVISRQFDDVYNKMSSYFKIFHRILKSLNKRFDEKKLDESDYKNYIGILRTQLSSEELVVILINSLYVKRGLGLGIELIGTNLFGDEKDFKIDQHFVIPKPEIIQDDLSIFINDNEGKNIKKRKDYEKKLKSIDNIAEFEDIMNFKSFVSADS
|
Provides resistance to bacteriophage by abortive infection.
|
Q01904
|
Y2439_SYNY3
|
Uncharacterized protein ssr2439
|
MQAQTFSHLHSQSSQRTTEVTLYLTIPESYRQEPIVTQLVSRYQLQVNILAATLGTNGGQGQFKLTLIGHAQAINNALAYLEQLQVTIVLDQESDGW
|
May have a regulatory function.
|
Q02174
|
CPEY_SYNPY
|
Bilin biosynthesis protein CpeY
|
MKSATEQDSESDFYTAAAHLINCPGIETEQTLIEFLQYRESSCQSIKITKRKIVEVLARLGCIDAVPAIGKCLWSDDVYLVENSVWALQILQCQDQIFIDQMIDILRVDTTNQRISIQCLATLNISRSVDVIRPFQESSVPGIKGAAISGIAKLTRNFTRVPEISLNLLLPNQMDRHFAIQDLIDVDAIDQLNEIFAAPVSPVLKMRAVREMYGENSASVVDLNLLSSLDSLFSCDLSAINCVHEYDESPSSEFLVRDLYNTDFSRCYLALKYLSSRSASEIFPMLKESWVEEAHNDYGAHYCFICLFGSIFDWSAESKRWIFEVLLSSISNLRPQFQKSRAASILALAKLNPSMLCELIPEILSSRDSMPWDMRYSLIQSIDNYAELEIALKNKMIFQLSDNDIDQFVQARARMALAS
|
Involved in the biosynthesis of bilin.
|
Q02175
|
CPEZ_SYNPY
|
Bilin biosynthesis protein CpeZ
|
MDACVSMSENYFDEALPRLLALLNDPDPTIYRTAVKGLGVFGHGVLFPLLDLYDKTDNGTVKACCIKAFVQVAVNFPDAVFPEQAIQALKLALDDINPVVSQSALMTLGYFSKQEHEKERVIPILIQVCNSTNIAHVQSAVMSLAEIDSTEVDQCFERMINHDSTDVLIKEILEASMSRRQSLFGN
|
Involved in the biosynthesis of bilin.
|
Q02EL6
|
FETP_PSEAB
|
Probable Fe(2+)-trafficking protein
|
MSRTVMCRKYHEELPGLDRPPYPGAKGEDIYNNVSRKAWDEWQKHQTMLINERRLNMMNAEDRKFLQQEMDKFLSGEDYAKADGYVPPSA
|
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}.
|
Q02LJ2
|
YIDD_PSEAB
|
Putative membrane protein insertion efficiency factor
|
MKFLLIGLIRFYQYAISPLIGPRCRFYPSCSHYTLEAIRVHGALRGGYLGARRLLRCHPWHPGGYDPVPERQEQACACHRTAKPGE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q02XJ3
|
YIDD_LACLS
|
Putative membrane protein insertion efficiency factor
|
MKKVLVKAVHGYQRWISPVFPPACRYYPTCSNYMIQAIEKHGPAKGLAMGTARILRCHPFCQPGYDLVPKHFSLRRNWAEPEKKEEEDSK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q02YE3
|
Y1522_LACLS
|
UPF0122 protein LACR_1522
|
MEIEKTNRMNTLFEFYATLLTDKQMNYIELYYADDYSLAEIAEEFNISRQAVYDNIKRTEKVLESYEEKLHLFSNYVVRNQLLEELMKKYPSDQYLISKLQEIQQIDEEEF
|
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}.
|
Q02ZM3
|
NRDI_LACLS
|
Protein NrdI
|
MKLAYFSVTGQTRRFVSKTDLPNVEITPDDDLEMDEPFLLITPSYAEESPTVSKSIDVMDPVFDFMAYNDNYKHCRGIIGTGNRNFAGIYIFTAKEVSAKYQIPLLYDFEFNGTPADVAAVEKLAAQLDQGAKVTFKNPL
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q02ZQ9
|
HRCA_LACLS
|
Heat-inducible transcription repressor HrcA
|
MITERQRQILNLIVSLYAKDHTPIGSKSLLDSIQASSATIRNDMKALERLGLIQKEHTSSGRIPSVSGYKYFVENVIQLEEFSQNDLFKVMKAFDGDFYRLSDLFKTAAKSLSELTGLTSFVLNAPQRDQQLVSFEMVILDNHSVLSVITLGTGEVRTNQFILPKSMTEADLAVFSNLVKERLVGKKVIDIHYTLRTEIPQIVQRYFKVTSEVLQLFESIFDDLFKEHLTVAGRKNIFDYATDNLAELYKLFSDDERMLHEIREITNNDEMRAVKFDNDEKFMKNLTIISQKFVIPYRGFGTLTVVGPVEMDYQRTLSVLDLVAKVLTMKLSDYYRYLDGNHYEISK
|
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}.
|
Q03182
|
RINA_BPPHA
|
Transcriptional activator rinA
|
MTKKKYGLKLSTVRKLEDELCDYPNYHKQLEDLRSEIMTPWIPTDTNIGGEFVPSNTSKTEMAVTNYLCSIRRGKILEFKSAIERIINSSSRKEREFIQEYYFNKKELVKVCVDIHISDRTAHRIKRKIISRLAEELGED
|
Activates int gene expression, probably by direct DNA-binding. Int activation requires both rinA and rinB.
|
Q03183
|
RINB_BPPHA
|
Transcriptional activator rinB
|
MGCLVVVKEILRLLFLLAMYELGKYVTEQVYIMMTANDDVEAPSDFAKLSDQSDLMRAEVSE
|
Activates int gene expression, probably by providing stability to rinA. Int activation requires both rinA and rinB.
|
Q031S0
|
YABA_LACLS
|
Initiation-control protein YabA
|
MADKYDVFDQLGELENTLNTTLTQISGIRQVLEASMTENATLRMELEKLRDRLAEFEKKEVKKETPKDQPNPNLIQIFNEGFHVCHLHYAERLAEGESCLDCLELLYR
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q03313
|
RHIA_RHILV
|
Protein RhiA
|
MSLHVSYVDKEMTDHARASQPGSAALAQGTQYSLLLKNQSAQPWTFYVYQKMPQPVANVFSLAWFCSPYQIRVGNQIKFTWELAYNFVWSDTGQLIPGVDFFASGVEDCSPSGRNTTTFSLSDGPGLTAPIKGDPAGSLVINDAGNVPNNRFSVGIGMSGTGTYVAQAGTNLLHTFTPTPSYWIAAGTNVTIGSVLSIDTITQTREAKFPSAVFNLVGVLQEDNTWDINPA
|
May be involved in plant-microbe interaction.
|
Q03381
|
REGB_PSEAE
|
Protein RegB
|
MRLPAVTPGWPAIPPGATLGGFDGQGRRSWATISRAPSGASCSRNRSATRTYGWGATATTPATITGIPSTTAPAT
|
Required for optimal exotoxin A production.
|
Q03552
|
E3145_ADEB3
|
Early E3 14.5 kDa protein
|
MEPDGVHAEQQFILNQISCANTALQRQREELASLVMLHACKRGLFCPVKTYKLSLNASASEHSLHFEKSPSRFTLVNTHAGASVRVALHHQGASGSIRCSCSHAECLPVLLKTLCAFNFLD
|
Protects virus-infected cells from TNF-induced cytolysis.
|
Q035X2
|
YABA_LACP3
|
Initiation-control protein YabA
|
MEKKELYDGFLTLEKHAQQMLREIAAMKDDMAETLERNAELEIENKHLRQHLAELEKDDNKTSDGGVELSKSKQNLESLYNEGFHVCPMFYGQRRVNDEPCAFCTEIIYGEN
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q038J5
|
Y1603_LACP3
|
UPF0122 protein LSEI_1603
|
MEIEKNYRMNSLFEFYGPLLTDKQHAYLALYYGDDYSLGEIATEFNVSRQAVYDNIRRTEASLEEYEKKLHLFANYQAQNEAVDTLVSYARTHYPDDKALSTLLERVADQTAK
|
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}.
|
Q038N1
|
HRCA_LACP3
|
Heat-inducible transcription repressor HrcA
|
MLTKRQLLVLKEIIRLFTESGQPVGSKTLMQELPVHVSSATIRNDMAALEDAGLITKTHSSSGRVPSTQGYRYYLDHLVEPVRVSRHDLATIKQELGQRYSKMDEIVAQSAQILSNLTSYTAISLGPEVNNIKLTGFRLVPLGNHQVMAILVTNNGNVENQVFTVPPSISFDELEKAIRIVNDQLVGLPLVQVAQRLRTDVPSMLMQYLTSPDGFLDIFGNVLKSAASERFYVGGRLNLMDYLGDSDIHELKKIMSLIDADHGDLTELLGGPIRQTPVQVRLGPELKPIDLANLSLITASYDVGGHGTGMIALLGPTQMPYSKMIGLLDVFREELAKRLTDYYANFDQ
|
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}.
|
Q03A13
|
YIDD_LACP3
|
Putative membrane protein insertion efficiency factor
|
MKQVLTWLVRGYQRFISPLLPPSCRYYPTCSTYMIQALQKHGAIKGSLMGIARILRCNPFVKGGLDPVPAFFTLRRNPHPENDLDLSDIQNLNHKLGGRHG
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q03E63
|
YABA_PEDPA
|
Initiation-control protein YabA
|
MDKKDLFDQITEVTRNTEDLLNKLHETQSAMVEIMEENAELQIENQHLRERLKQATAAENEGTKNTKYGLSKSLQNLEKLYASGYHVCNEFYGKHRQDEEECAFCLTVIYGDR
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q03EL7
|
YIDD_PEDPA
|
Putative membrane protein insertion efficiency factor
|
MKQILLLIIRGYQKFISPMFPPSCRYYPTCSNYSLQAIKRFGAIKGGLMGVARILRCHPFVRGGYDPVPDNFSLKRNQKNSKPRN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q03FW7
|
Y845_PEDPA
|
UPF0122 protein PEPE_0845
|
MEIEKNNRINSLLEFYEQLLTPKQKEYITLYYADDYSLGEISEEFQVSRQAVYDNIKRTVNILEKYEQQLHLLSNFEVRNAKFDQIRAYINQKYPEDTELKHFLDDLEKSEEE
|
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}.
|
Q03KY3
|
Y914_STRTD
|
UPF0122 protein STER_0914
|
MEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFGVSRQAVYDNIKRTEKILEDYEMKLHMYSDYIVRSQIFDDIMEKYADDSYLQEQIAILSSIDNRD
|
Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Q03MF3
|
YIDD_STRTD
|
Putative membrane protein insertion efficiency factor
|
MKKFLIALVKAYQRWISPLFPLSCRFCPTCSVYMIQAIEKHGLKGVLMGIARILRCHPLSETGDDPVPDYFSLKRKKTPLDN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q03MR8
|
HRCA_STRTD
|
Heat-inducible transcription repressor HrcA
|
MITQRQNAILNLIVEMFTRTHEPVCSKALQDSIDSSSATIRNDMAKLEKMGYLEKAHISSGRMPSRAGFQYFVANSLNLDTIDEQDVYQVVKAFDFEAFKLEDILDAAAKLLAEMTGCTAVIQDVEPTKQRLTGFEIVQLSNHDALAVLTLDESKPVTVQFAIPKNFLSSDLEIFHKLVQGRFLGNTVLDIHYRLRTETPQIVQKYFKITDNVLDLFDYIFSHLFKELIFIEGKVASLAYADLKTYQFLDNPQHVALALRSAISDDEVTKISVAESTEEALENVTVMSHKFLIPYRGTALMHVIGPIEMDYRRMVSLVNVISRVLVMKLTDYYRYLNSNHYEVFLSRNVLKNIERGECLD
|
Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}.
|
Q03QZ3
|
YIDD_LEVBA
|
Putative membrane protein insertion efficiency factor
|
MRHILIWFVRGYQRFISPLFPPTCRYYPTCSTYMVQALSKHGALKGSLMGLARILRCQPFVRGGIDPVPDHFTLKRNTAAEAAYRQAMQLDEIERHPHK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q03RT9
|
Y949_LEVBA
|
UPF0122 protein LVIS_0949
|
MEIEKNYRINSLFAFYQPLLTAKQNNYMQLYYGDDYSLGEIAEEFNVSRQAVYDNLRRTEKILEDYEEKLHLYQEFTARNRQADEIQAYVATTYPHDSRLNRLVAGLENLEEQ
|
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}.
|
Q042L9
|
YIDD_LACGA
|
Putative membrane protein insertion efficiency factor
|
MNKLLIGLVNVYKKFISPVLPPTCRYYPTCSTYMIDALKKHGAILGLIMGISRIIRCNPFIKGGVDPVPDYFTLRRNPHPERYEDEIIAQAFHSNKK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q044B1
|
HRCA_LACGA
|
Heat-inducible transcription repressor HrcA
|
MLTERQELILKTIIMDFTQSHEPVGSKTVMNQLPVKVSSATVRNEMAALEEKGLLEKTHSSSGRIPSTAGYRYYLDHLINPVKIPASVYNRIIYQLDQPFQQVNEIVQEAAKILSDLTNYTAFAAGPETRSVKVTGFRIVPLSSHQVMAILVTDDGNVKNQIYTLPHHTNGEEIEKAVRLINDQLVGKPLSSVNEVLLKRIADHLVAGGSAPEILDLLQDVIKDAASEQMYVDGQINLLSNYESDDLAKVKSLYKLIDQNDAISSLIGFNPKDEIKNDSKSKVQVKLGSELQSDLLEDYSLLTAQYSVGKYGKGTIALLGPTNMPYSQMIGLLEYFRNELAKKLLDYYGRFK
|
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}.
|
Q04597
|
YDR14_YEAST
|
Uncharacterized protein YDR114C
|
MKTFFLIEAGRALQIVAFRPAITTVLFQRFSVSFSCSYFTCCTSQLLRENWLFKFLTAFDHVIRASNDLSTMRFMIMYIYVYIYIYTVLRKRLSCYMLIL
|
May be involved in growth at elevated pH and presence of calcium.
|
Q045U2
|
YABA_LACGA
|
Initiation-control protein YabA
|
MDPFSQLSQLQQNLQAMTKTVAGLENDMLEVLKENTELKVENQLLREKISKLDANKEPAENKSQAGLKSLRNIYDSGYHICNMYYGSHRESGEDCMFCLDILDNFVNHGQKNRG
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q049W4
|
HRCA_LACDB
|
Heat-inducible transcription repressor HrcA
|
MLTKRQELILKTIIQDFTKTHEPVGSKTVMNQLSIKVSSATIRNEMAVLEEHGLIEKTHSSSGRVPSTEGYRYYLDNLVQPLQLPEEMYNQIGYQFDQPFNQVDEIVKEAARILSDLTDYTAFAEGPEDKNVSITGFRIVPLAPRQVMAILVISDGSVKNQLYTLPRHISGDEVEQAARLINDQLVGKNLSEINKQTFEQLYSSQIVGKNAPEFLELLESVIKDAASEQMYVDGQLNLLNNIENSDLKAIKSLYELINSSSLAGELIDLSDSPSHYPVHVRLGAELENDLLKDFSLVMAEYSVGRYGRGTIALLGPRHMPYSEMIGLMEYFRQELARKLLDYYGRFK
|
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}.
|
Q04IT5
|
YIDD_STRP2
|
Putative membrane protein insertion efficiency factor
|
MKRILIALVRFYQRFISPVFPPSCRFELTCSNYMIQAIEKHGFKGVLMGLARILRCHPWSKTGKDPVPDHFSLKRNQEGE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q04K36
|
Y1143_STRP2
|
UPF0122 protein SPD_1143
|
MEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFGVSRQAVYDNIKRTEKILEDYEMKLHMYSDYIVRSQIFDQILERYPKDNFLQEQIEILTSIDNRE
|
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}.
|
Q04VD0
|
HRCA_LEPBJ
|
Heat-inducible transcription repressor HrcA
|
MDLTERHKRILKALVDEFIQENRPVGSKTLFDKHDIGLSPASIRTVLKDLEDYGYLASKHTSGGRIPTERGYRFYVDSLVILYELTLKEKQRIQQEYLKMQFKLDQILKATASVLSSLSNAAGIVIGPAKNLDTLKHLELIHVRGDEILMILVMRSGTVLHRNIFVDRNYSQEALYQVSKYLNDNLKGYDIYEIQNVVVPNLMVRRDGPEDFTRIAELLSSAMNPDNSEVTLYIDGFKNLYANFRDEEQQLSQVLSLLDDQGFLKEFFSEYIDQDGVYTIIGKDGNRSMSGVSIITSNYKMGEKKIGALGIIGPQRMDYNRALPLVDFTSKLVSEMVTRISK
|
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}.
|
Q04Y45
|
HRCA_LEPBL
|
Heat-inducible transcription repressor HrcA
|
MDLTERHKRILKALVDEFIQENRPVGSKTLFDKHDIGLSPASIRTVLKDLEDYGYLASKHTSGGRIPTERGYRFYVDSLVILYELTLKEKQRIQQEYLKMQFKLDQILKATASVLSSLSNAAGIVIGPAKNLDTLKHLELIHVRGDEILMILVMRSGTVLHRNIFVDRNYSQEALYQVSKYLNDNLKGYDIYEIQNVVVPNLMVRRDGPEDFTRIAELLSSAMNPDNSEVTLYIDGFKNLYANFRDEEQQLSQVLSLLDDQGFLKEFFSEYIDQDGVYTIIGKDGNRSMSGVSIITSNYKMGEKKIGALGIIGPQRMDYNRALPLVDFTSKLVSEMVTRISK
|
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}.
|
Q05124
|
LEF11_NPVOP
|
Late expression factor 11
|
MPWRAQDHSVDCLTRSEVYALWAEAVNTLKRNLQVKNVSAHLLEDDAADVKDYIRANLSRFTVITGKCSRRTVCHHHRRVQRTLEPRQDLVNEYACSVTDVYRSPKWSICPTTCTRSRSPTTTPR
|
Involved in late/very late gene activation.
|
Q05368
|
CYPC_STRHA
|
Putative polyketide cyclase
|
MAGHTENEIVIAAPLDLVWDMTNDVENWPRLFSEYASAEILEREGDRVRFRLTMHPDDEGRVWSWVSERVADRASLTVRAHRVETGPFQFMDIQWVYEQTPEGVLMRWI
|
Involved in developmentally regulated synthesis of a compound biosynthetically related to polyketide antibiotics which is essential for spore color in Streptomyces halstedii.
|
Q05491
|
MUTL_CLOTT
|
Protein MutL
|
MDAYLLLDFGSTYTKLTAVDIENEGILATAKDITTIESDIMVGFNKAYEKLTEQLEGKEVNFVKKLACSSAAGGLKMIAIGLVPELTAEAAKRAALGAGARVLNVYSYDLTNKEVEEIKNSNLDIILLAGGTDGGNKECMIHNAKMLAEHGVKLPIVVAGNKVVSDEVSEIFDKAGIFYRVTENVMPKLNTLNVEPAREEIRQIFMKKIVEAKGMSNAESFINGILMPTPAAVLKAARVLAEGTDKEDGIGDLIVVDIGGATTDVHSLADGEPSKPGVTLRGLEEPFAKRTVEGDLGMRYSAISLWEASGTRKLQKYLCDNTVDVEACCKYRAEHIKMVPETEEEIKFDEAMAKVATDMAMERHVGVIESMYTPMGVIYSQIGKDLLNVKCVIGTGGVLVHSKNPGEILKAGSFDMADATHLKPQHPEYYIDKTYILSAMGLLAEDLPDKAVRIMKKYLVKV
|
May play a role in glutamate fermentation.
|
Q06813
|
YP078_YEAST
|
Uncharacterized protein YPR078C
|
MQTISGVLPTVLSPSELRSDDERTFQFDEEAEITTHLTESEDLRRLINETAQLGVRVDHIHDKTDQEIARLEKVIKEVTESDTFFRSCSGWFKTNKNFSDSESSSNTQLKSLSQLHGRYDRDWRQRLNKWFRKNKSKLALPSDNNLEEVNDDKVYGYGEDLMERGKTPYFSDIDDFMNGLNIISPLTPDDFENDDTLVKIDETCQIHSASEPEKTSISPTFGKNIKKELVTDDTESIISGPPLQENKKTLLKYRYVRTSLDMLGSEKSSSKNNSGGMFRIFHKSANFGDKNQENVPRVWDTLRNNLGREIYLLQGRFKKWTTKHQNLKKGQPCKDEDAVTVPLPSSDPGKETQLETKLCFVPEPGDQPLVQA
|
Induces the SOS system when expressed in E.coli, therefore, it may play a role in DNA metabolism and/or in genome stability.
|
Q06938
|
MVP_CMVKI
|
Movement protein (MP) (Protein 3A)
|
MAFQGTSRTLTQQSSAASSGDLQKILFSPDAIKKMATECDLGRHHWMRADNAISVRPLVPQVTSNNLLSFFKSGYDAGELRSKGYMSVPQVLCAVTRTVSTDAEGSLKIYLADLGDKELSPIDGQCVTLHNHELPALISFQPTYDCPMELVGNRHRCFAVVVERHGYIGYGGTTASVCSNWQAQFSSKNNNYTHAAAGKTLVLPYNRLAEHSKPSAVARLLKSQLNNVSSSRYLLPNVALNQNAAGHESEILNESPPFAIGSPSASRNNSFRSQVVNGL
|
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).
|
Q07180
|
NIFW_RHOCA
|
Nitrogenase-stabilizing/protective protein NifW
|
MTPESPTLAALTKLSSAEEIFAFLGVEPIREVLNSSRLHIMKRFGAYLRETDMTGLTEDGIFERARDALLRAQADFVASTPLKEKVFKVFETEAAKRKARFVGLETLKVIKS
|
May protect the nitrogenase Fe-Mo protein from oxidative damage.
|
Q07415
|
UREI_BACSB
|
Urease accessory protein UreI
|
MGTRKFFLLHHDKIIRSIIMANGIKNYWQDDGRFDRCSEIFFLSQKQGRGLYRFWLGNKKQGNRD
|
Probably facilitates nickel incorporation. May constitute a multicomponent high-affinity nickel transporter. Not essential for the expression of catalytically active urease.
|
Q07559
|
NIFW_AZOBR
|
Nitrogenase-stabilizing/protective protein NifW
|
MSFKDDLEDLETAEDFLRFLGVTYEQRVVNVNRLHILQRFQDYLSADTGMEGLDDEGMAARYSAHLERAYQDFVASNAIAEKTFKVHQEEARKMADRFVPLDALLPT
|
May protect the nitrogenase Fe-Mo protein from oxidative damage.
|
Q07601
|
CEST_CITFR
|
Tir chaperone
|
MSSRSELLLERFAEKIGIGTISFNENRLCSFVIDEIYYISLSDTNDEYMMIYGVCGKFPTDNPNFALEILNANLWFRENGGPYLCYESGAQSLLLALRFPLDDVTPEKLENEIEVVVKSMENLYLVLHNQGITLENEHMKIEEISSNDNKHYYAGR
|
Chaperone for the type III secretion of Tir. Probably stabilizes the protein, prevents inappropriate protein-proteininteractions and aids in secretion (By similarity).
|
Q07P51
|
YIDD_RHOP5
|
Putative membrane protein insertion efficiency factor
|
MKQSNLCPDCARAALRLPRQAGRGAIWLYRHTLSPLVGYHCRHLPTCSVYGDEAIGRFGLWAGGWMTLARLLRCQPWGTSGIDNVPAEPPGGARWYLPWRYGRWRGVND
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q07PD0
|
COWN_RHOP5
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MTAAFDRYVSFKNADWEGKSQRVMERLQIHIDAAQNPFWAYFAQKRTELNQKQGLDDLRVLHNYLPTLREILEDNGDQETLAMLEDLEVTCM
|
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}.
|
Q07VS5
|
YIDD_SHEFN
|
Putative membrane protein insertion efficiency factor
|
MAQTQSPLQWLATTVIRGYQILISPLLGPRCRFNPTCSYYAIEAIKTHGTVKGSWFAMKRILKCHPLHPGGSDPVPPKNDRCNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q07Z51
|
FETP_SHEFN
|
Probable Fe(2+)-trafficking protein
|
MARTVHCQHLNKSADGLDFQLYPGELGKRIFDNIGKEAWGLWQKKQTMLINEKKLNMMNVDDRKFLEEQMTNFLFEGKDVEIEGYVPPAEDE
|
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}.
|
Q08370
|
HRMA_PSESY
|
Protein HrmA
|
MNPIHARFSSVEALRHSNVDIQAIKSEGQLEVNGKRYEIRAAADGSIAVLRPDQQSKADKFFKGAAHLIGGQSQRAQIAQVLNEKAAAVPRLDRMLGRRFDLEKGGSSAVGAAIKAADSRLTSKQTFASFQQWAEKAEALGRYRNRYLHDLQEGHARHNAYECGRVKNITWKRYRLSITRKTLSYAPQIHDDREEEELDLGRYIAEDRNARTGFFRMVPKDQRAPETNSGRLTIGVEPKYGAQLALAMATLMDKHKSVTQGKVVGPAKYGQQTDSAILYINGDLAKAVKLGEKLKKLSGIPPEGFVEHTPLSMQSTGLGLSYAESVEGQPSSHGQARTHVIMDALKGQGPMENRLKMALAERGYDPENPALRARN
|
Unknown. May serve a regulatory function.
|
Q085G3
|
SYDP_SHEFN
|
Protein Syd
|
MSCSSALDCFIKNYLKSYQDTLSEFPRYYPLGEDSICIQGTFNADTDDTVFWQPVKRDNVADFSNVEHALNIQLHQDIHAFYGQYFSAPLPFTASFGDGELLQAWNQDDFENLQQNVIGHLIMKKKLKQPATWFIGVLGEGDEMLTVNNDDGSVWIEIPGEKQRTKLAESLTEFLESLSPMIKPPSKPVEELPHTVDHPGIWQRIKTMWDYLLRKK
|
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}.
|
Q0A551
|
FETP_ALKEH
|
Probable Fe(2+)-trafficking protein
|
MTRMVQCVRLGREAEGLPRPPYPGELGKRIYENVSKEAWQEWLRHQTMLINEYRLTPVEPRARQFLEKEMENFFFGDGSSAPPDYQPE
|
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}.
|
Q0AE57
|
YIDD_NITEC
|
Putative membrane protein insertion efficiency factor
|
MKQLIIGLIKLYQYSIGLLIPPSCRFYPTCSNYMREALTKHGLIKGLWLGTRRILRCHPWNPGGYDPIP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0AJ41
|
FETP_NITEC
|
Probable Fe(2+)-trafficking protein
|
MARNVQCIKLGCEAEGLDFPPYPGELGKRIFENVSREAWGQWIKHQTMLVNEMRLSMADIKARKYLATQMEAYFFGEGAEQPVGYVPPEK
|
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}.
|
Q0ATU3
|
YIDD_SYNWW
|
Putative membrane protein insertion efficiency factor
|
MQEMLIKLIKIYQKATFFKPASCRFYPSCSNYSIEALRKYGIVKGGWLTVKRLARCHPYNPGGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0BAQ1
|
YIDD_BURCM
|
Putative membrane protein insertion efficiency factor
|
METVLIALLRFYKVAVSPMLGNRCRFYPSCSDYAREAIQYHGAARGTYLAVRRVCRCHPFSAGGIDLVPPPNSDTRARGEADARSHRL
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0BDM3
|
FETP_BURCM
|
Probable Fe(2+)-trafficking protein
|
MARMIQCAKLGKEAEALDFPPLPGELGKRIYESVSKEAWQGWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGDGADQASGFVPPTEG
|
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}.
|
Q0CE76
|
LCL2_ASPTN
|
Long chronological lifespan protein 2
|
MISWIRTLGALLLLASVAQAQFQFFEHMFGNGGHQQQRSQNVPSDSARYQSMWDSAQCDKYLCPGTLACVHFPHHCPCPHPDVEEKVELGEGSAVCVSRGGYRQGEASRKIELARKGLL
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
Q0HD63
|
YIDD_SHESM
|
Putative membrane protein insertion efficiency factor
|
MAQTQSPLQWLATTFIRGYQIFISPLLGPRCRFNPTCSHYAIEAIKVHGTAKGCWFALKRILKCHPLHPGGSDPVPPKNDRCNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0HGT6
|
SYDP_SHESM
|
Protein Syd
|
MSCLPALDKFLQNYHQSYLSTLGELPRYYPQGEPSLCIQGEFDESSDEAVSWLPVKREQLGSFANVEHALELTLWRDINHFYGEYFAAPVLFDSPWGTGELLQVWNEADFDALQQNIIGHLMMKQKLKQPATWFIGLLDEGDKMLTVDNANGSVWVEIPGELPSAQLAPSVAEFIESLSPRIAPPVKHEELPMPALEHPGIFASFKRMWHNLIGKR
|
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}.
|
Q0HL08
|
FETP_SHESM
|
Probable Fe(2+)-trafficking protein
|
MARTVNCVYLNKEADGLDFQLYPGDLGKRIFDNVSKEAWGLWQKKQTMLINEKKLNMMNVDDRKFLEEQMTSFLFEGKDVEIEGFVPEKGQE
|
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}.
|
Q0HP31
|
FDHE_SHESM
|
Protein FdhE homolog
|
MSHTAEIPMVPGSESPLELKPLKAVDPKTVYHRRAQRLLSLAKDSPLADYFELCRRVVAIQARLAAEADFGQLLAWGKDEAIPLSHLGSEADSYWQGLLQQLLSDLLPQVDEDMARVLRLLMQQSPEQLTSWGSALRQGHMSEVPARFSLFIWAAMGVYWSHWAPMVIKRIDQRKVVQQNLCPICGCHPVASVIVDQPRAGLRYLHCSLCESEWHYIRAHCTSCGQDKGTTLWSFDDAKAQVRIESCDECHGYTKMLFVEKSPLMDVAADDLATLMLDSELNAKGFGATTVNPLLLAHETEQ
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q0HPE5
|
YIDD_SHESR
|
Putative membrane protein insertion efficiency factor
|
MAQTQSPLQWLATTFIRGYQIFISPLLGPRCRFNPTCSHYAIEAIKVHGTAKGCWFALKRILKCHPLHPGGSDPVPPKNDRCNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0HT43
|
SYDP_SHESR
|
Protein Syd
|
MSCLPALDKFLQNYHQSYLSTLGELPRYYPQGEPSLCIQGEFDESSDEAVSWLPVKREQLGSFANVEHALELTLWPDINHFYGEYFAAPVLFDSPWGTGELLQVWNEADFDALQQNIIGHLMMKQKLKQPATWFIGLLDEGDKMLTVDNADGSVWVEIPGELPSTQLAPSLAEFIEALSPRIAPPVKHEELPMPALEHPGIFASFKRMWHNLIGKR
|
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}.
|
Q0HXA6
|
FETP_SHESR
|
Probable Fe(2+)-trafficking protein
|
MARTVNCVYLNKEADGLDFQLYPGDLGKRIFDNVSKEAWGLWQKKQTMLINEKKLNMMNVDDRKFLEEQMTSFLFEGKDVEIEGFVPEKGQE
|
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}.
|
Q0I0J9
|
FDHE_SHESR
|
Protein FdhE homolog
|
MSHTAEIPMVPGSESPLELKPLKAVDPKTVYHRRAQRLLSLAKDSPLADYFELCRRVVAIQARLAAEADFGQLLAWGKDEAIPLSHLGSEADSYWQGLLQQLLSDLLPQVDEDMARVLRLLMQQSPEQLTSWGSALRQGHMSEVPARFSLFIWAAMGVYWSHWAPMVIKRIDQRKVVQQNLCPICGCHPVASVIVDQPRAGLRYLHCSLCESEWHYIRAHCTSCGQDKGTTLWSFDDAKAQVRIESCDECHGYTKMLFVEKSPLMDVAADDLATLMLDSELNAKGFGATTVNPLLLAHETEQ
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q0I0Z0
|
YIDD_HISS1
|
Putative membrane protein insertion efficiency factor
|
METSHSFGAKVLIGAIRIYQLMISPLIGPRCRFVPTCSCYGIQAVKTHGVVKGSWLTVKRILKCHPFNVGGYDPVPPKINNNKENE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q0I514
|
FETP_HISS1
|
Probable Fe(2+)-trafficking protein
|
MARNVFCTYLNQEAEGLDFQLYPGELGKRIFDNISKQAWAEWMKKQTMLVNEKKLNMMNSEHRQLLEQEMTNFLFEGKDVHIEGYVPPTEK
|
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}.
|
Q0ICH4
|
YIDD_SYNS3
|
Putative membrane protein insertion efficiency factor
|
MHESTILSAGSTNPFNRIVSAVMLALIELYRRWISPLIGPRCRFIPTCSAYGIEAIQRHGPWRGGWLTLRRLLRCHPFTPCGCDPVPD
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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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Q0IEK6
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EPG5_AEDAE
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Ectopic P granules protein 5 homolog
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MVPLSGEQLAQFYRVDGEMALAEAFEKEFLTRELQENDQCMNHPLYQLLQRYAKARAEFSLNVLEFEALRRKCKALANELWTVREQTFAGTGTCGDGKVVHASHISSVAALQESALADFSSNLQDLMKQSFFQCSQSTYEVDATRIKIEQKIYETLNLHPVLSNLPADSPVVLNPPIDAMQLTAAIGELRLCISILFAFLRKGITDKRFLADVRGWTVKLVATQLRIATVHDHLFVLFHVLRSPSGIANWATSLVQLPTEQDLRWGSSEFQHILVVMACILLPIKKRNEFLEKLKLDMNRSIDVVQEEMWAIVDSDGEDCSGSDSISELKEGDLVALIDQIPFGMVFRALTLVDRKLDGTWRLGEDQVRGTHVMKAIAFGTIFVELLGNGLMTYNADRYRQFAKRVARLIKHTVYYVSDLYRILLERTRSVQVVLDDYETTRINLELDVFVVRAAQYIYRSRKIGTWQYLSGFPFDQLSVGALWKLYYFLHLDEFNEELITAVGTDFRDLCIGPNQREKFRNGLVGMPSEDLYYLLQVFSNMALAREIDDFEFIETVALNLFDIGYLNEYTKDFCYKAVKDLLFNIVYKHPSLVSSLLQYMKQDVAQADHSALYVFKSLPLDRWRPQWDDFELLANWILNYGFDAVQSSTARVILIHLNYNFDSNNELFLPHDIHVRIACLITEIYSKHVPELLGNPQGLVASVSSLVKNKTAQDQFLAWCWNMVSLLRLHCMDQSPTVINGMMKNPALILRYVLELERAQQIYQGVTENRPLAIYLAILISTWGHSVPQICHQGFEQIRLLLNDHRYVVVVRCLQLITPLFLECPDSLSHCESFKSILISLMAADKYYARFTKDQFKPESNSPCLTELPNWTKDPAIIGLLDAMAGVAYQFPDAWHSMKEFFRPYFSVSSIILHSPSSATVFLSIFTLELEYELTEIQSGIWHEVIRGIGLPSSPKLTIETAIKKSTSILGYPSFPPSSLAVFKLANLVANCTIKNFMYPIVCQLFFTIYLSRLPLSTEEQRFANCFGVSDQIYECNVGLMKRIKKQLYDAECFYNSASVSESDERQRSFYNHCTRLFKTFQLWLEDTQLNKISTNAVNLPPQFDRYRLAAIFRGNRDHWTDFIDFRGIRSDHRDLADAWQKLCYRYKPEVSTVATNSPARSLASSHSVTDLQDFKQSIFKRLETYDAPAPAPLVFKPTPLIPPAKFTTQSSNSFLVMYNEHLLLDSFYLEQVPKLYIVEDKVLYKDASCSNGCTESRKVLVRYKVSKLDKNLSAVLRENRSAHEALLQRESKLPDRIVMASVRIDAFLRQIVEAYREFKLSGETNVCAKLNKVGSTLFYEFVGKMNDYNQLCPLTKDVCSLGISQLGFFMRENQNDEGIKLLNITLGRPEMISLLSELLVPASCPPQFFLRMYEFVIDSHIKRHDTQVLFVMLSKFDIIAWMNRYRPKLVDVRRLVELILRGLEGWTQKNAVLIQDLLQRHLMHLFEFDFPEYYGDILQMVLAACSLKKIMAQVLLELLNSMRRRVECQPLTFGLGLVSIKEDFRSFATKQKILSYKDLIDTTVLLTQHFQQERLNHGLHGLYPVHSDYCEVLSLLLGSVGHATVVAAVHAYPGVLADELINWLWPPLCDMFSPWLTPYFPQNMKGQQQVANWIQQVASDSSILPPWSELHSETAFRMVKVFEHCIQYLMDTFPSSSALLGHLFSWYELNFAHPALPRHVAVPIHTNLMNLAWDRFRPAPVHITGFSRILQQFIPEAHKFVGHIFIRIAWTPWLQQNIQSWDYQLRYQMLSALLMIFIKISYEPNAREGLKIVTLLQEACNYPWHMLEYQGVEAVLDWFVLSAEPSVVLKMPSESEVVDSAVLDLLQVASSMKFNSGNPLESTALQSQVQAKRILYVRTTVRLLNSCGAKYQKLLGTKQGVQAFHNAVLGLFNIVETVLLQIRSTKDREFEARNLIGEVIVSLQSQGEYTSKLFTEAIVLWTENCRTSDSYIVPSVLDAVGMCKSFSLNLYLLLEEMLFHYFGKSWHGQVNDGGDPVLDASWVKALHKVGLQTVKGFDEEMLVKHRCLLVLHLLTVQKLRTAGSSGERIVVLQKLFQLLENVKVSDQTESKLILLWSLMAVVGVEIMKASSNGQNHLLTLARYLQTCSKDAEGWGEGLLGAIGIRKDGISIRRKVVAKCLSCIVFLLFGEDSGEALEASESGPPSIDCANRCKEYDQAMGDLKQTLTNKRYGDMHIKTRAAINLVENTAMIANIGENVCKIVRLFCDEHFFHSVEEVWRC
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Involved in autophagy.
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Q0IIE6
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ELMD1_BOVIN
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ELMO domain-containing protein 1
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MKHFLRMLIQVCLFFYCKFLWRCLKFVMRKLTGRCELQRICYNTKPGASRTMKIETSLRDSKSKLLQTSVSVHPDAIEKTIDDIMELKKINPDINPQLGISLQACLLQIVGYRNLIADVEKLRRESYDSDNPQHEEMLLKLWKFLKPNTPLESRISKQWCEIGFQGDDPKTDFRGMGLLGLYNLQYFAERDAAAAQQVLSDSLHPKCSKFSKAEWEKKRMDKAIGYSFAIVGINITDLAYNLLVSGALKTHFYNIAPEAPTLSHFQQTFCYLMHEFHKFWIEEDPMDIMEFNRVREKFRKRIIKQLQNPDMALCPHFAASEGLINM
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Acts as a GTPase-activating protein (GAP) toward guanine nucleotide exchange factors like ARL2, ARL3, ARF1 and ARF6, but not for GTPases outside the Arf family.
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Q0IWM5
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NDX1_ORYSJ
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Protein NEOXANTHIN-DEFICIENT 1
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MAAGSGREEAAAAAGYGRGPPWVFRGRALYQLHLVKAATARAFVPRELRLVEAFGYTLGGMFLARYDDSPAGKFDELVVIAGIVWNPPTSCAWAARVLVNSAEACRHGRKEVGLPSHVATFSQTEADALRNKPLVKSNSFLSLLGMRSTVSNQGNDREIEISETKGSCTRHLCNISVPLTGSHKHKWMGPAIRMSLPSFSGQIEDHPDLLKYSCQVECRVRPVRPAKIWRPRITEPQECPDGKISSKGSEVLAEPDAQKHTVMVLLSKPILALEFNSLEMHVDAPKIVIPHSKKKEVRYSST
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Required for neoxanthin biosynthesis. Probably not involved directly in the enzymatic conversion of violaxanthin to neoxanthin. Is necessary but not sufficient for neoxanthin synthesis.
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Q0K181
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FDHE_CUPNH
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Protein FdhE homolog
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MNQHQATPGTLPSDEASRHFTPLIQPDLAGLYSRRAARLRALAEGHDLADYLRLAARVAEVQASLVAEADVSGPADARAIPQEGHWGALLDRLIERLAHDVPAPVAPHLAALRALPADARLGAAQALTEGRFDAVPAAIAPFLWAALSLQCASAARAAPVPDSGPAEHASCPVCGTAPVASLILIGDRQGMRYLHCALCESQWHMVRAKCTNCGEASELDYLSFDTAEATVRAESCGVCHGYLKVISLERDPPAEAVADDLASLALDDAVTAEGYQRTGFNPFALPG
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Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
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Q0K5C0
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YIDD_CUPNH
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Putative membrane protein insertion efficiency factor
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MKPILLALLRIYKIALSPYLGSRCRFLPTCSDYARDAVIHHGAARGSWMAACRLCRCHPFAQGGYDPVPGTEADDTARPDTHAGRSVHAAAGHAPVAIRLPRP
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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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