entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
Q61QT3
|
SDZ1_CAEBR
|
Skn-1 dependent zygotic transcript 1 protein
|
MQFSIVYFLVFLIPSTQSTGFLSLKLTSDHDCLVHLEIQSMEYSETVRLLAYETKSLEIFTPEITNQLSIHFQILHHFSGVSLSDVSSQLFKLDNNGIWEPRVIDSDQVILSIQSNFHCQKGFYGPICERRSRSTSTIKTTTSIPTATSSPFHLPISEVQINNLIIYAVLSSVVLLLIIANCFLCFCRPKPSKYIDYTFQNVFPMDEFFPMEKTIGSPDTEYFDSSSRYYSTITLQSRV
|
May have a role in mesendoderm development during embryogenesis.
|
Q61SD1
|
MON2_CAEBR
|
Protein MON2 homolog
|
MSINAVDSKKLVEALLGDLRLLSQEAKKKQNHVKESAETGVVRIRNISTASVGDTVLITNLRAACTELLHPLVLACETRHTRLVQIALQGIQRLVQHRILSGNGATIVTNELWALVEAECEELRVLQTVPPLVSSELIVTGNTLAKCVVMCFRLHFAKDPIVINAASAAVRQLVSTVFERVIQEDGIFSSELTVVNPSGGRPSPRAAPPTLRPCAADAYMLFKDLCLLINGEAPTWLVGIQEMTRTLGLELLESLLKGYPSVFIRHTEFGDLLKDDVCPLIIRLFSPNVKAMHINSQHPSSRISNASMSNYPPTVSHDRQSFPISMRLVRIVTLLVQFYQNILHTECEIFISTLLKFVDGDRKGWQRPLALESLHRIISSTDLVKWMTESFDCRPNSTHVLEQVAVELSVVVQQCLVCTTFSSDQDNELDRSQEDGGPGFLVKGLWVPYVEHLTSKKTILLDSLDRMDAVAISEGYVLSRCCVALCDLTQAVYAVIDRLCVLDENCEAGSSEENLRIAKVAYANTQPSILAAIGSLLAASTDEIVSDQLLCCLSTLISAGCRVGADQDLHRSVYVLAIMSLPSPSYLNQFAGIPPPSPVSKREVSISEQVFDLESWPSTAQVTATGPPCPCPVVSTDLWNKQVLLTSKNLQAARTFIASITTHIKELNGLWYLCMATCEHLSWLLAMRPTQIGQFERETRDDHSNGPTVVTNAALGDIGMLSSLMDKVAPAIAALPNEEFLLVVDALIRLSDESLAVAATGRDSSLFPLAVLYRVCSLSLSGINVFWAKVANHFIKVCNHTSVSMRDWAAVALTSLAKHAIKSKTSMDPKSQQEMVIASLLALCSIPHIQVRRRQLDCVMSLMQTDGSSLLSTSWPNVIQIISSIIDNDTGCELSLVRQGYLGLRLVSSDFLQSIPFDCISGLVEAISRYSKQNTDQNISLSALTLLWTISDFIYRKMESVGNDASEAVWMVLYTCLSESCVDTRFAVRKSACQTLLQTVTAHGHALRAPAWHHVIWQIIIPLLDKVRSQTRCASTEKSNGELIMHHSRDTEQKQWTETCIHTLSAISKIFNSQRKSLLALNDFGAVWEAFLGYLDWAACYENAELSLSAIRSYQEVLLGKISSQTLNVNSHEKSNGSESTLDTVAPELPQAQWVESWKVWLRISRGLARQGCAAVANSVNADTKSTSSTPRMNSSTSSLTSLAPGVYVPGPSHLTAILHIFPPLFDKVAKCITVDDLKYESLPAVLESMMNVPIPSEQAPFVLPSSTTHLTPTQEALLEAVKIVYVECTISGTTLRTAIPDQIRLLLKFASMATQRISPNKVAPGGQKSYRDYALTAIVPFSEYSLRIAIEFFTSTSQYPDVSNSLIAINIIKFLGEPLYMKYTCISASTWKLAASSLMSVLRTSIPYARQNPEVFRSLWSTICDTMERWLFTPNKSSRLAADERKRDELMECQAIEIIRNEMLAYASRLPQEDVQRLISLLHRGSISQIDSTDVLDSHTQRNELAKACFDALLMSTDGAQAGAEEDDHRGILGNVAVTSLLQRCTQVMADFCKDWSAAGDLRLPRSRILEIISALQAIDSLIARLARDPRMTELYSQLVSLFPSVVDVMPCCHADGQLEQQLIKTIKSYQTLFLLQNIPQSTV
|
May be required for traffic between late Golgi and early endosomes.
|
Q62IU9
|
FETP_BURMA
|
Probable Fe(2+)-trafficking protein
|
MARMIHCAKLGKEAEGLDFPPLPGELGKRLYESVSKQAWQDWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGEGADQASGYVPPAQG
|
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}.
|
Q62Q36
|
LUTA_BACLD
|
Lactate utilization protein A
|
MKVSLFITCLVDMFQSNVGKATVELLERLGCEVDFPEGQICCGQPAYNSGYVKDSKKAMRRMIETFESAEYVVSPSGSCAFMFKEYPHLFRDEPAWAEKAQRLADKTYELTDFIVNVLKIEDVGATLEKKATYHTSCHMTRLLGVTDAPMKLLRHVKGLEFTPLPRKHDCCGFGGTFSVKMSQISEQMVDEKVACVEETAADVLIGADCGCLMNIGGRIGRKNKPIEVMHIAEVLNSR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
Q632P7
|
YIDD_BACCZ
|
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}.
|
Q634M5
|
HRCA_BACCZ
|
Heat-inducible transcription repressor HrcA
|
MLTERQLLILQTIIDDFIGSAQPVGSRTLAKKDAITFSSATIRNEMADLEELGFIEKTHSSSGRVPSEKGYRFYVDHLLAPQNLPKDEIVQIKDLFAERIFEAEKIAQQSAQILSELTNYTAIVLGPKLSTNKLKNVQIVPLDRQTAVAIIVTDTGHVQSKTITVPESVDLSDLEKMVNILNEKLSGVPMSELHNKIFKEIVTVLRGYVHNYDSAIKMLDGTFQVPLSEKIYFGGKANMLSQPEFHDIHKVRSLLTMIDNEAEFYDILRHKQVGIQVKIGRENSATAMEDCSLISATYSIGEEQLGTIAILGPTRMQYSRVISLLQLFTRQFTDGLKK
|
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}.
|
Q636I0
|
Y3605_BACCZ
|
UPF0122 protein BCE33L3605
|
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}.
|
Q638X2
|
LUTA2_BACCZ
|
Lactate utilization protein A 2
|
MKVSLFITCLSDVFFPQVGRSVVEIMNQCGVELDFPEGQTCCGQPAYNSGYQEDAKLAAKQMIKAFEHSEYIVTPSGSCASMVHHYYKEMFKGDSEWYEKAVHLADRTYELTDFLVNVLGKNDWKSKLVEKAVFHQSCHMSRALGIKEEPLKLLSQVEGLDIKELPYCQDCCGFGGTFAVKMSSISETMVDEKIKHIEATEANLLIGADMGCLMNIGGRLRRKNKNIQVLHVAEVLAKGLNK
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
Q63E65
|
LUTC_BACCZ
|
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}.
|
Q63E67
|
LUTA1_BACCZ
|
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}.
|
Q63SJ4
|
FETP_BURPS
|
Probable Fe(2+)-trafficking protein
|
MARMIHCAKLGKEAEGLDFPPLPGELGKRLYESVSKQAWQDWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGEGADQASGYVPPAQG
|
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}.
|
Q63YW2
|
YIDD_BURPS
|
Putative membrane protein insertion efficiency factor
|
MQTVLIALLRFYKLAVSPLLGSRCRFYPSCSDYAREAIQYHGAARGTYLAARRLCRCHPFSAGGVDLVPPPNSDARNAPHEAEASSHRL
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q64FN9
|
CAPSD_WCCVB
|
Capsid protein (CP) (Coat protein)
|
MNQDTPLANLNGPEVPSGNVPPANPPGRTNVAPPAQGAVQQPPAPAARRARNPHGPVPPAGPSRSAGAPAMLELSAAYPMYTEQRRAPNYYVPDAQLLFHTLGVCDQLMTTTDRFLRSMPSWLPIVSQLYVSVLWNVMILKVYVNTGYGAAYAHDLDVLLNHLQINECMIPGPLVPFFQSLAAVNGPFDWIGDIIPAMPSFTELWTDEFAPHAAYARQIPIPAILLDQLYRFATLAFDAQLQTNYATFEWYSNIFNQDVNTHNARLRLGPQLCGSLFTTQAQCDSARAFWNPAFANGFTRIDAANGPLMAFPQLLGFISQDGALQSNWFMHISLIMHKYAQYFNGSVPLKSISPVGIGASVIYGTPLEDTNVRDWLYPAAAAIAPFRSTRFLPRRELPATLAVRFAHADHEIEEQAEQYSILCHTNMKWYVNNATQNNHTAIEGNYIHQGEYWNFTPFRYSPPVSLKTQFAQVIASRYHQQAANRAE
|
The capsid protein self-assembles to form an icosahedral capsid with a T=2 symmetry made of 120 subunits.
|
Q650K9
|
YIDD_BACFR
|
Putative membrane protein insertion efficiency factor
|
MKRLLSYILLLPIYFYRACISPMTPPSCRFTPTCSQYAIEAIKKHGPFKGLYLAVRRILRCHPWGGSGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q65114
|
50510_ASFM2
|
Protein MGF 505-10R
|
MFSLQELCRKNIYILPYPLGEHVLQQLGLYWKGYGSLQRIGDDHVLLQQDLIFSINEALRMAGEEGNNEVVKLLLLWEGNLHYAIIGALEGDRYDLIHKYYGQIGDCHKILPLIQDPQIFEKCHELSTSCNIRCLLEHAVKHNMLSILQKHKDQIRFHLALTQILFELACHERKNDIIRWIGYSLHIYQLETIFDVAFAHKNLSLYVLGYELLMHKVNTEAANIDLPNLLSYHLRTAAAGGLLHFMFETLKHGGYVDKAVLSAAISYKHRKVVAHFIHQVPRKTVEKLLLHAVQTRAPKKTLNLLLSSLNYSVHPITKQLVRNVVDYRSTLIVKLLLMRRKRKLNLVDAVLARLVRYSTYTDTVKFMGEFSVSPEKVIKMAARESRTFMIEMISKAVWKNHPQTMIHHLKQLADTMKPQSGKDLIIYTIHYIYQSSNLLVAEEEKNIFKLAKFYANHNSVNRFKQICEDYYTLDVDTRFKTLILECFEIAVQKNYPRIATIVDDFIRFLFYKGDITEEEISEAYSLKNAELYVDLKWLQQEEN
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65122
|
36010_ASFM2
|
Protein MGF 360-10L
|
MFPSLQSFAKKVLARHHVSIDYHYILKHCGLWWYKAPISLDCKHMLIKLPSFADGLDLNTALMLATKENNYQLIKLFTEWGADINYGLICANTPPVREFCWELGAKYQVDKNKVMHMFFKLIHHGTTSSNIILCLKLFNNNPFPTYVIIREIKSSIYWKLRRLVEDTDILSNMSDDDMLTIYCFILALQDNLREAISYFYQHFKHLNTWWLICALCFNKLFDLHDLYEKEKIRMDMDEMMCIACTKDNNFLTIYYCFLLGANINQAMLACVQFYNMDNLFFCIDLGADAFEEAKALADQRNYFLMYHRLSIDIYSPDSSLLTLKEADPKKIYHLLKNYKSKNMMVYFDYDGHDTV
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65124
|
5051R_ASFM2
|
Protein MGF 505-1R
|
MFSLQNLCRKTLPDCKLPEFFDEYILQLLGLYWENHGTIQRAGNNCVLIQQHNLIPVNEALRIAASEENYEIVSLLLAWEGNLYYAIIGALEGNRPDLIRKYDDQIKDHHEILPFIDDPIIFHKCHIMRRCFFNCILYQAVKYSKFRVLLYFKHRLGDDLPLTHLLIEKACEDHNYEVIKWIYENLHSYNIMDTFECAIAHKDLRLYCLGYTFIYNRIVPYKYHHLDICILSSLQLLHKVAAKGYLDFILETLKYDHNINNIDIILTQAATYNHRKILTYFIPQLTYAQIEQCLLVAIKTKASKKTLNLLLSHLNLSIKLIKKISQYVVTYNSTNIISILSMRRKKKIYLDIILTEFVKNAIFNKFVVRCMDTFSINPERIVKMAARINRMMLVKNISERVWKNHAVKLKHLKHAVHTMKHQEGKNRLMNFIYDHCYYHMQGEEIFGLARFYAIHHAPKLFDVFYDCCMLDATRFKSLLLDCPHIIGKNAYDAGINLVNKYIGNLFAMGVLSKKEILQDYPSIYSKHDMF
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65125
|
36012_ASFM2
|
Protein MGF 360-12L
|
MLPSLQSLTKKVLAGQCLPTDQYYLLKCYDLWWYDSPITFDHNLGLIKSAGIKDGLDLNTALVKAVRENNYNLIKLFTEWGADINYGLVSVNTEHTRDLCRELGAKETLNEEEILRIFIDLKFYKTSSNIILCHEVFSNNPLLQKVNNLKMRIEIFWELRELIKKTDLLNNEFSLNTLLLKYWYAIAVRYNLKEAIQYFYQKYTHLNTWRLTCALCFNNVFDLHEAYEKDKIYMDLEEMMRVACIKDHNLSTIYYCYVLGANINQAMLASIQYYNIENMFFCMDLGADVFEENMPVGEGYELIRNILSLKIYSPSTAPLPKNTDPEIIDHVLKNYKSKNMMTFLSYDLR
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65126
|
36013_ASFM2
|
Protein MGF 360-13L
|
MSAPLSLQTLVKKTVASTSCLSIDEHILKYCDLWWHDAPLKLYMDRGRIQIKSGFLGEDIDLCVALIIAVKENNYNLIKLFTELGANINYSLLSINTKHVRDLCRQLGAKETLEDYDIFCIFNKIMHNKTSGSVILCHEIFINNPNLENKFAAQLRRLIYKRLCGLIEIKETDELSELLVKYWYAKAVQYDYKDAICFLDEKYTDLNEWRLKCYLYYNKIYELHDIYHKEKIQIDVNEMLSLACIRDNNPLTIYYCYALGGNINQAMLTSVQYYNIGNIYFCIDLGGNAFEEGSAIARQKGYNFLSHSLVLNIYSSDASLPLNLKDPEEISSLLKNYKSKNLSIILDYSHNIL
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65128
|
5052R_ASFM2
|
Protein MGF 505-2R
|
MFSLQDLCRKHLFILPDVFGEHVLQQLGLYWKRHGSLQRIGDDHILIRRDLILSTNEALKMAGEEGNNEVVKLLLLWEGNLHYAIIGALQGDQYDLIHKYENQIEDYHHILPLIQDAKTFEKCHALERFCDVPCLLEHATKHNMLPILQKYQEELSIRVYLRETLFELACLWQRYDVLKWIEQTMHVYDLKIMFNIAISKRDLSMYSLGYVLLFDRGNIEATFLTQHLEKTAAKGLLHFVLETLKYGGNLNIVLSQAVKYNHRKLLDYFLRQLPRKNIEKLLLLAVQEKASKKTLNLLLSHLNYSVKHIKKLLRYVIEYESTLVIKLLLKKRVNLIDAVLEKNVRYFSAIKVRTIMDELSISPERVIKMAIQKMRTDIVIQTSYIWEDDLERLIRLKNMVYTIKYEHGKKMLIKVIHGIYKNLLYGEKEKVMFHLAKLYVAQNAATQFRDICKDCCKLDVARFKPRFKQLILDCLEMVTKKSCFSIIEILENYIISLFVMKVITEEEKNLCLELLYKVISYKTI
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65129
|
5053R_ASFM2
|
Protein MGF 505-3R
|
MSLQELCRKNLPDCELPEFFDDYVLQLLGLHWQDHGSLQRTGKNQVLVQQEPIHINEALKSAASEGNYEIVELLLSWEADPRYAVVGALESNYYDLVHKYYDQVKDCHDMLPLIQNPEMFEKCHELNNTCSLKCLFKHAVIHDMLPILQKYSDYLDGWQYCNQILFELACKRQKYNMVVWIEGVLGVGNFKILFTIAINNRDLQLYSLGYLIILERLYSCGQDPTFLLNHFLRDVSMKGLLPFVLKTIEFGGSKEIAITLAKKYQHKHILKYFETEEC
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65160
|
TFIIB_ASFB7
|
Initiation factor TFIIB homolog (pC315R)
|
MDALLKEIEKLSQPSLQKENNDVCDLCFMQMKKISNYQLLCEECGQLKDWFEPEYNEKFTVYSRLKIVGANSSYHQRDLDKANSSDYSSLQFHHILEELKSLNVKYMDAGQKPFPIQVLKETAHSYNQVQQHRVIRSITKLQILASILRSICLKLNIACTVADAARFTQLNTKGISRGMDLLRSLFVDNKITLNVDLNPIDSFINSTYSALQIKQIHQELQEENVYNLKEIVKSFILYADEKNIGVDLNRRTVVIATMYNVLRRAYYPIEIDTVVYQCKIRKNTITRALKMYEDYYSHFKSLYEQYHLNAAKKLI
|
Putative initation factor.
|
Q65177
|
ETFL_ASFB7
|
Early transcription factor large subunit homolog (pG1340L) (VETFL homolog)
|
MDFQNDFLTNPLRVTLYNPAENEYTKTFIFLGSVPANVLQACRKDLQRTPKDKEILQNFYGKDWEKKLSQYVVGGDSDDLDEFEKLFVEDSGEETNVMMPEIETMYSEYSIFPEDTFKDIREKIYVATGIPPYRQHIFFFQNNALQVTYRLLLSGSGVALDIRDYKKEFQQVGGLNIDASMESQKDELYVEALDSFQLIKNIHHIFVADLNTLVAPMRRQISIAMEDNYQFDLLYYGLIMKYWPLLSPDAFKLLVQSPLQMEKQYPALSPSLTSLKKRLLLEQKLINFTYARAQQVIAKYEGNRLTRGTLAVTSAMIKISPLVNIQINVRNVFDLFPATPDIPQLVVFFYSKTGPTVVSKHHITSTEPEKFSNKTFRVPTIILIRFINKKAFILTIQNNGHYFIESNWSENERHDFNSVVSTLNNFINPIIHTINDMGPAAFPRGGSLPLPSNEDIQISISSMSVSTFWPYTLSSKGFTELKSRWREYEQAGIISVRGLQQTGIYNFLFKKGIYSYDPHEIERMIIISSGPGRKMDINVALLQNTYAYLFDANVAARWETIYGGRNIRIYHRVTDIKIEMFNITQEEFNYLWVYLFVFLDNLITGPDKILVNKLSQLHDKQQGKGASQLRALQEQDPDLYDLRKYDTQATVYSVLCQHPRPPVIYSEAEVKSMPPAKRKELVKYWNFTEGVPAYYSCPHPDYPHLSLLEGRHPLNYCLPCCQKTKALLGTKRFYINNTCLTKHTFVEQDLEDLNTQTSRHTLSYGKKIPVNRIAFLPHQIADELFLNTIKEPDIFCIVGVEQTMLGISNAGLFYSLARILDLAPKALAIEIAKAANTPQYYILGNGAGNMFSSGAELANLILQTFVEQKNQLLQWDTTWQDIFLDLVAICYDLHCVFFKDKQGDIEFEVSPSTIQKILSPSKKIAIIFDTDEGIYPMAITQQKRFLKNSEAQYIFTEDDPVMEVVQSMSEFMCKDNWWDIHDVKNIPGYTVGKKLINRHNFCYALLIDSDTDRPIYFPIRLSSYIHDDIPIDFDLRPTQIASFEETWKFITLFNKQYKQYEIVPSAVLQNIKKEFVGFLSEGKTGLYFYYAPTQTLPATLEKLPIATLTIDPRDIDQAILYPLEEPYPQQNKANKAFYINHLYKFLLIEFFDVLYGLQSNSTRKHIENLFQKTDFQKITSVTEFYTKLSDFVDLNDIHTIKHILETTDAEHALKVLQKNIFNFDYTLLSPLQSYTYDELCQHLKKLLTPRIEFYEDIETIDRGLINIYTSCQYSTLNQPQCKKKRLRIPVNHFENYIHILAADILNPLKHSTLLLTGLGVIDDLQFILRPQEIISVKNKF
|
Putative initation factor.
|
Q651A1
|
LPA1H_ORYSJ
|
P-loop NTPase domain-containing protein LPA1 homolog (Protein LOW PHYTIC ACID 1 homolog)
|
MAAVQGQGQGKLLYIVVVDDDGATFRYTRSLLHSTLQLMGCKPRHAFEISGRVFDEIRGHMGGDMAMGGGGGVQRYELAADAEAASPRQFQFELYKRRTTLLIPRPLFLRLVCHALALYKYVAPDQRSDLHRACRIRERKESVTILLCGTSGCGKSTLSTLLGSRLGITTVVSTDSIRHMMRSFVEEKQNPLLWASTYHAGECLDPVAVADAKARRKAKKRSGISTTSTIDFDKTRPLNDKPDGKPIGKKQMAIEGYKAQSEMVIDSLDRLITAWEDRKESVVVEGVHLSLNFVMGLMRKHPSIIPFMIYISDEGKHTERFAVRAKYMTLDPTKNKYVKYISNIRTIQEYLCSRADKYLVPKVNNTNVDRSVASIHATVFSCLRRRAAGDQLYDPATNTVAVVNEEYKNQCVANSMSSKGMFKLIQRLGSSRKLMAIVNVDGSVSKAWPVESSSGDGKGGSENGSKKYVGDPIYGPLNIGRAESVNLQFGAFGISAWPTDAGCTSQAGSVNESWDNANEGTGSHVPSSSGSPKKLDGHCKEIKESAAASGSDDDEEEEEEAADVPPNSGSEEDLSEEDIRAIHEEMEGSVDEDCNRSDEEYDDLAMRDCMENGFLTDDGVVHTVFDGNGQKHSTLRKRQVNLRTLSKIDLDSPDTARSSSALPISASSKRNGTRRWKRSLSESFRSRPRSAPSLVELTPKHKGSAVPEVAPDK
|
Required for the accumulation of phytic acid in seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds.
|
Q65209
|
1002L_ASFB7
|
Protein MGF 100-2L
|
MGNKESKYLEMCSEEAWLNIPNIFKCIFIRKLFYNKWLKYQEKKLKKSLKLLSFYHPKKDFVGIRDMLHMAPGGSYFITDNITEEFLMLVVKHPEDGSAEFTKLCLKGSCIVIDGYYYDTLHIFLSETPDIYKYPLIRYDR
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65210
|
1003L_ASFB7
|
Protein MGF 100-3L
|
MGNRLIRSYLPNTVMSIEDKQNKYNETIEDSKICNKVYIKQSGKIDKQELTRIKKLGFFYSQKSDHEIERMLFSMPNGTFLLTDDATNENIFIVQKDLENGSLNIAKLEFKGKALYINGKDYYSLENYLKTFEDFYKYPLIYNKNK
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65211
|
36018_ASFB7
|
Protein MGF 360-18R
|
MLERLYDANIYNILSRLRPEKVRNKAIELYWVFRAIHICHAPLVLDIVRYEEPDFAELAFICAAYFGEPQVMYLLYKYMPLTRAVLTDAIQISLESNNQVGICYAYLMGGSLKGLVSAPLRKRLRAKLRSQRKKKDVLSPHDFLLLLQ
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65235
|
CAPSP_ASFM2
|
Penton protein H240R (pH240R)
|
MAANIIATKAATKMASKKEHQYCLLDSQEKRHGQHPFSFELKPYGQTGGNIIGVQGSLTHVIKMIVFPFMIPFPLQKTHIDDFIGGRVYLFFKELDMQAVSDVNGMQYHFEFKVVPVSSNQVELLPVNNKYKFTYAIPEVQYLTPIFYDLSGPLDFPLDTLSVHVDSLTNHIHLPIQNHNLTKGDRVFISGYKHPQTIESYKNNTIFIKCIPPLLSEKINLYIPKNRIRIPLYFKSLKTSK
|
Forms the penton at the fivefold vertices of the icosahedral capsid (By similarity). Together with the minor capsid proteins (p17, p49, and M1249L), forms a complicated network immediately below the outer capsid shell, stabilizing the whole capsid (By similarity).
|
Q65258
|
36016_ASFM2
|
Protein MGF 360-16R
|
MLSLQAMAKMAVATNTYSKYHYPILKVFGLWWKNNTLNGPIKICNHCNNITVGEYPMCYNHGMSMDVALIRAVKDRNISLIQLFTEWGGNIDYGALCANTPSMQRLCESLGAKPPKGRMYMDTLIHLSDTLNDNDLIRGYEIFDDNSVLDYVNLVRLKIMLTLKARIPLMEQLDQIALKQLLQRYWYAMAVQHNLRIAIHYFDNHIPNIKPFSLRCALYFNDPFKIHDACRTVTMDPNEMMNIACQQDLNFQSIYYCYLLGADINQAMLMSLNYGNLSNMWFCIDLGANVFKEARALAGKKNRRVLQYILGLNIFKRELIPPCKDPDPSQIQILLKNYILKNVSTVFTYYCQ
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65259
|
50511_ASFM2
|
Protein MGF 505-11L
|
MFSLQKKALQHIYMTPENASELSKDLLQHLGLYWNGPIIKMDTVVHLHNKIFSNRSVLKYALAKQANITIIETLVLWVEPEYALAQALKHNRKDVLECIFSYHLTTPKYHHIMHLTSSQELFEFFHLFICKSKNYHARMECLLYAATLYNFQNILEKNREYIIRHSIGNPLFAIACKERHINLIAWFVTAGVLDTYDDSTLFNTAFKLGDYSLLEVACDLPITYPDYLIISMMQTAIQKNYFRFFKKLLTHFSIYRPIIITDAAYYDRRKILLLLLNQNIFNNFTILCALSAAIKGHASKKTLNLLINRLDSQMTVIDSVYYSIIKYNNIDCIPLLMHIKTFRMETLISIAVHGDNIDIIAACKAFLPKDTLYHLVLKMAIILRNHKLFKLYTEKEHPMYIFTILKAIISDFINYTVFQALAIEYLCKFHQEKQLPIVPLLMVLAEHNYITKFKKTCYAANMSDQKVKRALIKCLFIATQKNYCQIFKYCFGSLLKVLSKHEQEKFFNSVVFAKKLASYYDHQNMIQLIDSLIERFRYLLKA
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65269
|
36022_ASFM2
|
Protein MGF 360-22R
|
MMPSTLQTLAKKTLATQHISKKYWPSEEYCYILKCCGLWWHDSPITIFTCIKQILIKTANFKHGLDLNLALMKAVQENNYELIMLFTEWGADINLGLITVNTECTRDLCQKLGAKEALSAKEILEIFYKIQYIKSSNNIIISHELISNHPLFLNNDQLKLRIVGELNAISINFILDEISFNEMLTRYWYSMAILYKLPAAIQYFYQSYKYFKDWRLICSLAYNNVFDLHEIYNKEKTDINIDEMMRLACRYDGNYTTIYYCFMLGADINQAMITSVMNLWDGNLFLCIDLGADVFEECMKIAIEDHNGVLESILSFKNYYSPDVSLLSLKTTDPEKINDLLDEDIYKSKNRLIYKSC
|
Plays a role in virus cell tropism, and may be required for efficient virus replication in macrophages.
|
Q65370
|
LEF2_NPVOP
|
Late expression factor 2
|
MERVWNPAAGIDGLKRSETYLVDPHDFVGVLTLSPYTVFERGLFVRMSGMRLLALLAAPKPQEPQPAVRRFPQRSRRNVCLKACADGAQSLAKVLAARVSMPPCMSKTMADLSSAPRGNMYRKRFEFNCYLANVITCTKCKTACLIGALLHFYRMDAKCVGEVTHLLIKAQDVYKPSNCAKMKKVTKLCPQASMCKGLNPICNF
|
Required for late and very late gene expression. Specifically required for expression from the vp39 and polh promoters (By similarity).
|
Q65670
|
P31_BNYVS
|
31 kDa protein (31k protein) (p31)
|
MADGEICRCQVTDPPLIRHEDYDCTARMVQKRIEIGPLGVLLNLNMLFHMSRVRHIDVYPYLNNIMSISVSLDVPVSSGVGVGRVRVLIFTTSRERVGIFHGWQVVPGCFLNAPCYSGVDVLSDELCEANITNTSVSSVAMFNGSYRPEDVWILLLTSSTCYGYHDVVVDIEQCTLPSNIDGCVCCSGVCYFNDNHCFCGRRDSNPFNPPCFQFIKDCNELYGTNETKQFICDLVGDDNLDSVNTLTKEGWRRFCDVLWNTTYGDVESRTFARFLWFVFYHD
|
Involved in efficient vector transmission. Might slightly enhance symptom expression and increase root-specific silencing suppression (Potential).
|
Q65677
|
VSR_BNYVS
|
Probable suppressor of RNA silencing (14kD cysteine rich protein) (P14)
|
MSMGMVDSLCVFVGRVITEGSESVEGVERFSIKFSDWKLFTTAVYVEYRQLGEKECSLKDVGRLHFNMSCVKCCQKLKCKKQNKNHSKHVQNGYLRKVRNFSILGVCGDCCESFTLADEKHHVIVDPEV
|
Suppressor of RNA-mediated gene silencing, also known as post-transcriptional gene silencing (PTGS), a mechanism of plant viral defense that performs sequence-specific inhibition of viral mRNAs expression.
|
Q656A5
|
MFT1_ORYSJ
|
Protein MOTHER of FT and TFL1 homolog 1 (OsMFT1)
|
MASHVDPLVVGRVIGDVVDLFVPTTAMSVRFGTKDLTNGCEIKPSVAAAPPAVQIAGRVNELFALVMTDPDAPSPSEPTMREWLHWLVVNIPGGTDPSQGDVVVPYMGPRPPVGIHRYVMVLFQQKARVAAPPPDEDAARARFSTRAFADRHDLGLPVAALYFNAQKEPANRRRRY
|
May form complexes with phosphorylated ligands by interfering with kinases and their effectors.
|
Q65EM1
|
LUTC_BACLD
|
Lactate utilization protein C
|
MTNGTIHNKDGFLNRIAERLGRNRRSAGVTVPDYIHQPQHRVYQGYTQDELVGVLKDHCRKIHTELIETDVIGLHDALYEQAARFGGGPVMIPKDDRFKEYGLSGLLTDKWPNEGTKVWEWDAAAGDENIQRAEQANIGVTFSEITLAESGTVVLFSSKDKGRSVSLLPTTYIAIVPKSTIVPRMTQASAIIKQKIADGDVIPSCINYVTGPSNSADIEMDLVVGVHGPVKAAYIVVEDR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
Q65FU4
|
YIDD2_BACLD
|
Putative membrane protein insertion efficiency factor 2
|
MKTVFLLLIRFYQKWISPALPPTCRFYPTCSNYGLEAIEKHGAFKGGWLTIKRILKCHPFHPGGIDPVPEKKQKD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q65GZ1
|
YIDD1_BACLD
|
Putative membrane protein insertion efficiency factor 1
|
MKRAAIIFIRFYQKAISPLFPPTCRFYPTCSNYGLEAIQRFGFIKGSYLLIKRLLKCHPLHPGGFDPVPNQTDQKKEGDSD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q65IG4
|
GERT_BACLD
|
Spore germination protein GerT
|
MFDWQRFFPFQQFSKDGLKNADPKDVEQYIHHMMKSVFGPGYAVQFPFRDPLSKETSAADESDPIDIFETTSHVFVKIPLTKEQLNLLKIKHTSQTLIIENYPEKGRQEKVVLPSLVRRKGTKAIFKDGILEVMFLKNEDFNLSEIDITF
|
Involved in spore germination.
|
Q65JQ2
|
Y2321_BACLD
|
UPF0122 protein BLi01817/BL02321
|
MTLEKTTRMNYLFDFYQTLLTSKQKSYMSLYYLDDFSLGEIAEEYHVSRQAVYDNIKRTEAMLEQYEEKLLLFKKFQERKKIFEALRKLTDGQPEAESLIDALEKLD
|
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}.
|
Q65VC1
|
YIDD_MANSM
|
Putative membrane protein insertion efficiency factor
|
MATSHSLGEKILVKLIRFYQLAISPMIGPRCRFTPTCSCYGIEAIKTHGALKGSWLTLKRILKCHPLSKGGYDPVPPKINNNVEKK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q65VT7
|
FETP_MANSM
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCEYLKQEAEGLDFQLYPGELGKRIFDNISKRAWGEWMKKQTMLVNEKKLNMMNADHRKLLEQEMVNFLFEGKDVHIEGYIPQATN
|
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}.
|
Q65YV0
|
VP6_MYRV9
|
Microtubule-associated protein VP6
|
MELPHDKAWAYLLLTPPPLRDYFIQLPKPATLQLALNRFAAYLEKQYLRDSLYMEKIVIGTHYNVRKNRVLQPRIFVSPSNYTRILSTFYDHPDLIAEVLPIQHLSKSQLKRGGLTKNVLTSGLPEMNNEQNPYAVFEVNTIDDLKACFAFPTEWLIDILTGRNSISLHYTIDRTSIPKWYAHLEARFQYSDGVTKSLTDADLRQHYIGVQPIPVTCEELLQKMNDASINGNTMYRVHGYESIVSSRMETVNDLVKASGKPYDVVNVQTMSSYSRSISKAINQAVTKDRHNKHVGSTKLKNSQGPRTTIFVMPPYITVDVVCSPMTIKPGLGPIQTKLLKSIVDQSPRRFRIAYAAKPQIEQDVLNKRIFSTDEGPESYFQGVELLTPEAKSLLTALPQLVGTFHYEKLSYAHFPSYRLTAGGYNVDYFKRGVTVIVARKHGGKGMVAKLIWKLGTPVIDSDDYGRIIKLVEAGLTIDDAVTQLFSMDYDQRNSTVSAFDEHMEMIVSQSKMKQEITYPRASDPRITAFADYYSKWFLKVPYSDYVASVKNFVTKNGLSGPNGIQSTNHYDTLVIQVHTLPEATQFLGVNNIIEVYPIIDSYIGMILRQQTSNTCAELLLARYYESIHLRNFDMLPVGVVASTLEALVG
|
Minor inner capsid component. Displays NTPase and RNA 5'-triphosphatase (RTPase) activities. May function as a cofactor of polymerase VP2. 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).
|
Q65ZY9
|
SP5G_BORGP
|
Putative septation protein SpoVG
|
MDITDIRIKKVESKNSGSKLLAYVAVTFDNCLVLHNIRVIKGQKGVFIAMPNRRTRVGEYKDIVHPISQDFRKTLQTSIFKEYIRENPADLELELDF
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q66011
|
MVP_CFMVN
|
Movement protein P1 (Cell-to-cell transport protein)
|
MCEPPPGFITVQCYTSDDLLTGDSTIVKSIPVRSCFFRQGVEVVLFRCESNKHRWSKIRGPVSLTVHCDICEFRETVVIPSLPKGFKVSSDFSYSVTWNCCYSRGRTE
|
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). Also likely to act as a suppressor of RNA-mediated gene silencing, also known as post-transcriptional gene silencing (PTGS), a mechanism of plant viral defense that performs sequence-specific inhibition of viral mRNAs expression. Silencing activity has been seen in Nicotiana benthamiana and Nicotiana tabacum, two non-host plants.
|
Q66095
|
MP_CRSVL
|
Movement protein (MP)
|
MAVHVDNVKDLAKTNEGVSVILNRYTDWKCKSGVTEAPLLPSNLGTRITDYAKTTLKGDSVALNFSDLVLSLGATVSVGTPGSVLVELINPNMDGPFQLVQGQSLSWSPGSGRPCLMIFSIHHQLTADAEPFRIRISNNGIPTKKTFARCHAYWGFDLSPRMRYYKNEPAKRIDLDVGFYKTHLSNMKQVRDYVQYTFDNSRMDGNPQLVAKSTMNVVPRIADVPKYVGIAPPSRSGNHQEATPDDWLKQYVDKDSETNKLSDVESSSDSSSLLSMRARSRRYTKNYKIPIKRHPQATGEVGTT
|
Cell-to-cell movement and long-distance transport of the viral infection. Also acts as a 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 (By similarity).
|
Q66119
|
MVP_CMVIX
|
Movement protein (MP) (Protein 3A)
|
MAFQGTSRTLTQQSSAATSDELQKLLFSPEAIKKMATECDLGRHHWMRADNAISVRPLVPEVTHGRIASFFKSGYDAGELSSKGYMSVTQVLCAVTRTVSTDAEGSLRIYLADLGDKELSPIDRQCVTLHNHDLPALVSFQPTYDCPMESVGNRKRCFAVVIERHGYIEYTGTTASVCSNWQARFSSKNNNYTHIAAGKTLVLPFNRLAEQTKPSAVARLLKSQLNNIESSQYVLTDAKINQNARSESEEIIVESPPIVIGSSSASRSEAFRPQVVNGL
|
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).
|
Q663S8
|
YIDD_YERPS
|
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}.
|
Q663U4
|
FDHE_YERPS
|
Protein FdhE homolog
|
MSIRIVPKDQLGKQREKGTTAGNIPPLLFANLKSLYTRRTERLQQLALDNPLADYLDFAAKITEAQQKALHDHPLVLDMQAELVQSAASGKPPLDGSVFPRTEHWRKLLSALIAELRHDAPDHILAVLDNLDKASVHELELYADALLNRDFSQVGSEKAPFIWAALSLYWAQMASQIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTHNGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLASLILDAKMEGEGFARSSINPFLFPGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q666M3
|
FETP_YERPS
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLKKDAEGQDFQLYPGEIGKRIYNEISKEAWSQWITKQTMLINEKKLSMMNIEDRKLLEQEMVNFLFEGQDVHIAGYTPPSK
|
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}.
|
Q667I1
|
SYDP_YERPS
|
Protein Syd
|
MDLNISTALRSFTQRYIDLWQQQTGHLPASKELYGVPSPCIVETGEDQVFWQPQAFLPEATLTNIERALEIQLHPDIHDFYTQQYAGDMMADLGNHRFTLLQVWSEDDFIRLQENLIGHLVTQKRLKLSPTLFLATTSSEMTMASLCNVSGNVVLEQFGSDKRTLLASTLSHFLDALRPVLPE
|
Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}.
|
Q667N6
|
NRDI_YERPS
|
Protein NrdI
|
MNPLVYFSSSSENSHRFVEKLQLPAIRIPIAGAREKLRVEQPYILLVPSYGGGSPVGAVPIQVIRFLNDVHNRSLIRGVIAAGNTNFGDAYCLAGDIISHKCQVPYLYRFELLGTAEDVANVRKGVTEFWQRQN
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q66H33
|
CC038_RAT
|
Uncharacterized protein C3orf38 homolog
|
MSGLSHLESEGCRNLLGMLDNDEIMALCDTVTNRLVQPVDRQDAIRAILVYSQNVEELLRRKKVHREVIFKYLATQGVVVPPTTEKHGLIQYAKSYWEEQSPKLKETAEPVKKTEDIQLFEQQAKEDKEAEKVDFRRLGEEFCHWFFELLNSQNPFLGPPQDEWGPQHFWHDVKLRFYYNTSEQNMTDYEGAEMVSLRLLSLVKEEFLFLSPNLDSQGLKCASSPHGLVMVGVAGTVHRGNSCLGIFEQIFGLIRSPFVENTWKIKFINLRIVGGSSLAPGSSLKPSVTFEQSDFEAFYNVITLCNTPEVRPNVRQILDSGTGDQVLCSGDEALLNKKEMNLPTPLKH
|
May be involved in apoptosis regulation.
|
Q67J30
|
YIDD_SYMTH
|
Putative membrane protein insertion efficiency factor
|
MTRLLMLLVRFYQRYLSPLKGGPTCRFTPSCSQYAYEALAKYGAIKGTWLAVRRVLRCHPFHPGGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q67PE4
|
Y1464_SYMTH
|
UPF0122 protein STH1464
|
MKDVQRIALLFDFYGPLLTERQQELIRAYYLEDHSLAEIADADGVSRQAVHELIRRSEAALQEYEQRLGFVAEHQRRLRLLDELQEALDRADLSAARRALAALRAEA
|
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}.
|
Q68FA2
|
ADSSP_XENTR
|
Adipose-secreted signaling protein
|
MAAAKKGAKPKVAGVRFAAGFPEEGAHNHVHFDEQLHDSVVMVSQQEDGNFLVKVGFLKILHKYEISFSLPPVQRLGKSICAVPLPTLNLKVLSITSQAEGHSIKCEYTAHKEGVLKEEMILASETNDKAFVKVVVQARVLDRHHGTPMLLEGVRCTGTELEYDSEQSDWHGFD
|
May be involved in thermogenesis and glucose homeostasis.
|
Q68X21
|
YIDD_RICTY
|
Putative membrane protein insertion efficiency factor
|
MTKILLLTITFYKYFISPLLGNNCIFSPTCSEYAQEAIITHGIIKGLWLTFRRIIKCQPFCIGGYDNVPTSIKNSKQPTKKI
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q68XW4
|
Y041_RICTY
|
Probable ABC transporter permease protein RT0041
|
MLLNIANLVGKHTIKFAQSVGIFALFSFIAISSIIKPPLYLSLIMRQLLFIGFHSLPVVAMTTFFSGAVLALQSYTGFSRFSAENSIATVVVLSLTRELGPVLAGLIVAGRVGASIAAEIATMKVTEQVDALYTLSTDPIKYLVCPRVIAAIITMPCLVLIGDVIGVMGGYLVGIYKLNFNSTAYLTSTFQYLELIDVISGLVKATVFGFIISIISCYSGYYSGKGAKGVGRATTSAVVNSSILILISNYLITELLFKV
|
Could be part of an ABC transporter complex.
|
Q6ABV4
|
YIDD_LEIXX
|
Putative membrane protein insertion efficiency factor
|
MLRGYRAVFSPFYGDVCRYYPSCSAYTLQAVQEHGVIFGGYLGVCRILRCHPWAAGGVDDVPLRGKRRYRMTAFGFVVATSQGKA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q6AEB9
|
HRCA_LEIXX
|
Heat-inducible transcription repressor HrcA
|
MVSERSLDVLRAIVQDYVSSCEPVGSKSIVERHSFGVSAATIRNDMALLEEEELIAAPHTSSGRIPTDKGYRLFVDHLAEARPLSPAQRTAIEILLGQSVDLDDVLSRTVRLLSQLTNQTAIVQYPSLSRSRIRHIELVSLAPRRLLSVLITDSGAVEQRVIELTDELAEADIAEIRGAINGAAAGLSLADAAVRLSELPDALADRARALVAPVASALLDQIAANRQDRLMMAGAANLVRTGDDFPSSITPVLEAIEEQVVLLRLFDEMAHDQHSVAVSIGRENDGFGLTEASVMSSGYSSAGADIARVGLIGPLRMDYSGNMAAVRAVARYLSRLLGD
|
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}.
|
Q6AX58
|
PHIPL_XENLA
|
Phytanoyl-CoA hydroxylase-interacting protein-like
|
MEVPRLSQHMSTPNSPCEEMIKNLSLENIQLCERDGNKSQDSGIAEMEELPVPHNIKISNITCDSFKISWDMDPKSKDRITHYFVDLNKKENKNSNKFKHKDVPTKLVAKAVPLPMTVRGHWFLSPRTEYTVAVQTASKQVDGDYAVSEWSEIIEFCTADYSKVHLTQLMEKAEAIAGRMLKFSVFYRNQHKEYFDYIREHHGNVMQPSPKDNSGSHGSPISAKLEGIFFSCNTEFNTGKPQQDSPYGRYRVEIPAEKLFNPNTNLYFGDFYCMYTAYHYVILVIAPMGSPGDEFCKQRLPQLSLSDNKFLTCTQEHDGLVFHQAQDVILEVIYTDPVDLSWGNVAEIIGHQLMSLSTADAKKDPSCKTCNISVGR
|
May play a role in the development of the central system.
|
Q6AXB2
|
RABEK_XENLA
|
Rab9 effector protein with kelch motifs
|
MGLLEVLDPEDLPKMSTWYALVPRGEGPSARVGHTCMYVSSSEDSSKGKILILGGADPSGCYSDTHIIDLDNHEWDNPDSEGLLPRYEHASFISASNPGNIWVFAGAEQAENRNCVQVLNPGAASWKSPKVMGTPPSPRTFHTSSAAIEDKLYVFGGGEKGAEPVADTNLYIYDAATMTWTQPVTSGDPPQARHGHVLTALGTKLFVHGGMAGSTFFKDMFCIDTDTMKWERLKTKGDLPPACAAHSSVAWKSYIYIFGGMTSTGATNSMYRYNTETLLWKQLKFDSACPPARLDHSMCLLPWKTRTNTDNAEKLPCKAKEESNLKECSSATSKTLEQGIVHLCFIFGGMDTDGELHSDCCVTILQ
|
Rab9 effector required for endosome to trans-Golgi network (TGN) transport.
|
Q6BNN2
|
LCL2_DEBHA
|
Long chronological lifespan protein 2
|
MIGNIAYILFTLTVVSANLFDFIQNQFQGNNQQAQRQTPGEYENANLNSGCSKYLCPDTSICVDEPKFCPCPYPSSQLRCFLPNGRYVCISKPAGEVSLNYADPKTNWKIDAKDDNIRDCGWVGRAWKGLV
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
Q6BYJ1
|
RRT14_DEBHA
|
Regulator of rDNA transcription 14
|
MSFTSKTSKSHAEATVNKLFSSLLPGTQGTTSKQSSSLSSAELLSIEIENKNKLSKEELKKIHKQNKFKQHKKIKKALEDEKRFNKLAKYHLIKHHKTGGELSEEEAKYLKKLVKKNVNSLNRVSEIDDMEIKSELDQVRQDILKINKEKHDKKAKRIQNKKTKDFNSKVAKGMISYPGLTPGLAPVGLDDSDDE
|
Involved in ribosome biogenesis, probably through modulation of rDNA transcription.
|
Q6CFG3
|
LCL2_YARLI
|
Long chronological lifespan protein 2
|
MRPTVILTCAAAAHAQIFGNFFNQMLKKEFAVEESWHNQEYHKVSCDNGHVCPDTLTCVNSPLECPCQFPASEIKCVYPDKSGYVCISKPGDGYDGSDASSKAEDGKRDCAWVNKAFRGEL
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
Q6CIF3
|
AEP3_KLULA
|
ATPase expression protein 3
|
MDKLRLLGSYLRKSPLTSTVSEPGIKISPKQFTFSVRVRDKDRPSKISTTKINEPASKLENTSTVVHNEYLNSLQLPYLARTSLRVSKYDYKRAAQFSNTLKRTLKTQDAHERIFSISSEDVAKLISSLFQVSEDNVSLVAKKRFFERECFTEIPKITEEVLSDIQEFEDYIGLLTHTKFHHKGSSLQDGIIPKLLKNLLHPSNLRIAPLKTASVFNDVIYYYGNKNNFATCRELYAQMKSEGIAPNVQTYNLMLRNLLRNSRLIKQQLPYREAIFYLERMKKENISADVITWNTCYFLLKDNISRAIFLEKMVERGVPLTYHLLYGILEEEDIPFNVIIDFLRENDIPVDTKIIKICHRSLIKRDKFQASWKLMEYARHLNFRVKDPFFLEEYLRQFSEKGRMDMCIMTVNTFKATFEVEPTLHCYDLLFKCLVRQGYSSEFSRVYQMLLINLKEHTGGHVVMNYWIAKCRAIMNSNIKTIPTHDSITRLDALAKRCIWDKRGIKWNCWLEYSEYRNVFRRLGSVPYQSNSRDQLDKHEVAKSSKKKVKYLKKLKETAIRNKQSHDAAYRNDYYSALKNDLINRGIIEEQAK
|
Required for respiration.
|
Q6CJB8
|
LCL2_KLULA
|
Long chronological lifespan protein 2
|
MKLLGTIIGSAFFLQAVSGFFFDSGHQNRQQQQQQQQQRDVGSYQQMFLDNDCPHYLCPQTLDCVRQKSDCACPFPNSQLKCNLPNGQVICISKPATHDPTLVEIYDDPVMGPAQRTEGFRDCGWILDVYDGKI
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
Q6CJH4
|
TSC3_KLULA
|
Serine palmitoyltransferase-regulating protein TSC3
|
MAAEKIYEPYKKSRGTMIYTPTNQQMSRGGIGEKLADFVKNLYWVYYIHLPFYLMTSLDAFCLHTIFLVVVSLSLFGLLKYIFL
|
Stimulates the activity of serine palmitoyltransferase (SPT).
|
Q6CK52
|
MTC2_KLULA
|
Maintenance of telomere capping protein 2
|
MSLVSISEGVRAGLVLKRHVVCFTGTSNDQGLKSISDLLSHMDNPAVPSPQSCSIDSLPDTETQNGISCYLVPYSGTAEIDYELQNRFALWLHKSTVPVILVLQDNPLMIPYLRHQFWFACGEDMGQWQDSVVAESIVDSVYMHHSIRRYILDLIVHLRMHRLSKPSQGGGAHSRSLSDMTLLCKWIALTSGSSFITPDMVQTACERYFPWHLQLIESSKEDPSVMYGSQEELVDELINRFDTFAIKMAQEYKNPLFKQLCIVQSVMKDIIPAT
|
May be involved in telomere capping.
|
Q6CK85
|
RRG1_KLULA
|
Required for respiratory growth protein 1, mitochondrial
|
MVRPFGEIGSHRKHVLEWYRYSLRNIRANVPTDNLQIELWNTLRQAVRRNRNHKAGWYVRGLLEDLSHLNKYIVGDDIIKLVALKNKYTEQIEPAPEPLQQANKPISGVVVTENMGDESRREKKKRLAPIPGDGDLYRYLLRYYKIYGPTKTIPRKHIDELLRPLAIHERYCKILYRIEYRIAKGPPKVSINYTNAGQSRIWFIRSPFNRKARQSKKLTGIIIKARLRAQDNLDRFRECESKLFYAFQEAQWEYTLIHKQPCSRKFNDVVTQIKSGKSNDIPAVFIDWIKPILEDMDILNRINANTQRKFTESRDHLIDGKQYEYYKQLNQRLYKKRLERFLGLKAELPTTNPFTEEKNLGALLVKWRFLRPDQLVKVKS
|
Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).
|
Q6CM46
|
CS111_KLULA
|
F-box protein COS111
|
MGKTNKNRIKTGISYRSLHLLISANETVKEKREAEQLPALDNDTQCLMSTGKVHILNADYSRYGVSVYDKLYGYSSSAASTIEEEDKGSGDGFKKRYMSLMQGSSQWKSRKLKQKKNAPKASAKAKAFLVRLHSEKRRHEVDFADINCLPEEIICRIIANLNDADSQRNCLLVSQEWSECAKRIIYKDVKFTSTYRVGQFVTTLRENPQYGKYVESLDLSQLKNGFINDESSTLENDVSQSSYGFEPPDIAYAGWRDWRYRKNSLYGSEMLSSIHRSRTRRSSDASSMNSSVFSHNYNRTRSSSVTSLVSRSTQTAAGSKNVVKRIRKLFSNSFRGKGQQKTHLHQNNGSGLSTLELKDEQFAAGTDSCSLRRSHLPFTNKFFLKYAHLRDLPLGYIIHLLTLCVNLKSINLSNLSLSPDFEIEELEYKRNGYVSFFPEETEEENLNGLNTFNGDRELTPKFFSDSDKPYHYYKDTQYESIIWKLDSSRDNNMFTNRRRSRKKFQLKILTNDDLCEAILSLKHMKHLNVGNVVWLMQRDMKRLIVHSMESCIIEDRCLDKIYMNFEGSGLQTNLPLAGQGLLKAMVLLQVITDMTNNCSDDQILEWFELRWIPTFRRVSQPADLVYLARACDQLHYVIQSEESPTYTRVGEVLITESHTGHYKYEISRNVNNVYLTIQIENGKPDTITDVKLKECSDRLLERVSNLRKNQLLQHTGENFFSTAGLA
|
F-box protein probably involved in ubiquitin conjugation pathway.
|
Q6CPQ2
|
SIA1_KLULA
|
Protein SIA1
|
MFRNRRILLYARRFFLVWICFLFITSWSLIQRHLKNWLVQAPDLKLSGSLQDTGIKVRDVRISKCYSWFSNCDAIWDYSLQDDLVTWYRIDMGKMQDTSIGQGFGWTSYVYWQPLYPNERGSAVVDLALSRNGLPLGLANERYNKIKNNDIDGYHVHSNTDNEFYVKDDSSNRFNPDMKWSAKFGNHLEDWFWRGDGIWCKYGRRSNGIKEIKAFIGEDFIESRPMWKEMVHCLHREGYSKPISISFQKSRLDDFTYGKEKDLSQISEPSLVMKRADFKILQISDLHFGRHIVSDSRKEKPDSIFRYDWPNVQFIHSVIRNERPDLAVITGHIFKDFNKNLDYESQILKMVSPIISNGIPFLFTWGEPQVTTEFKVNILNFIKSLPFCLNKFDLKNSTYLMLPLLLPAKTPGSQKQIGTIFAFDSNVTESYNFLDKFPRSPQSVYNLAFQHLPLHEYRPQGSFALIGNYEQKGSLDYIPHTKAFRNLLGEKDIKAISCGHEHGNDCCVLSDGKQQNLKNNMWLCYGGVTGYDQAYESKVRIFKIDTEKNDITSWKRSIKDTSKVSDYQYIWSRTLNTQ
|
May be involved in the activation of the plasma membrane proton-ATPase by glucose.
|
Q6CQ02
|
IRC19_KLULA
|
Increased recombination centers protein 19
|
MVLIKSRKSIVTATNVCINSSSKFYLTEEQVQSLGDKEFLTASYRRFLRMRQFISKRQMVKESYTTYLRYKFKIEDFELKRSKLLSVSGMSAMDFRSSVQKSLCFLIKAFSISDAYSKDMIDDSHKCKKIIKNLLTVDYHRNRIINRSSNMYQYYRKDFTFFTDGQNIGLKQFEENLMRLNECLGTRL
|
Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).
|
Q6CQ91
|
PP4R3_KLULA
|
Serine/threonine-protein phosphatase 4 regulatory subunit 3 (PP4R3)
|
MSESNNMHVSGDGAKQSVYTEKKRVKVYVLENNEWKDTGTGFCQGTVEERTIDDTQTAEKMAYLLVVDEDSDDQVLLKSRLEQNIEYQRQEETLIVWKDLNGQDIALSFEESIGCDSLCEYICFVQKNIESRISLVAVRSTDDGIGSVHEIITGPVNLPSNVPNQTEESLLEALKILNENTSFDYLRNETIQFVINDHYLATLIRSFYQSEESKLYRNLLLLSNIVKTLILFNSKEILEEMINDENFLCVCGILEYDTEFPNSKLNHRQYLKDKEPNFKEMIPISDPTIKLMITQNFRLQFLKDVVLVRFLDDQSFTFISDLMLSYQNSIIDFLQEDSNNFINQVISMYKVEEDSTVTPDKRRDGIKLLHECIQLSQNLNSIEKTLFYKFLIKKGLFQVIQFAFNMETNNDIRILATDIVVGLIEHDIQLIQSVQSDEVTLLNDENSDIDSTDMSLLLILTKILLTDKSPGLKEQSFQALVSLLDPEDYIVDDYQNHDDNIDTRIDNMLQIQNGKNHDGLDGERNHEKFQLAEYLQCFYRQVAPSLFHCFIDGSVNLYECDQQLLIKLVKLLNLMIQGHEASISRRFILENGILIRLISLASSDYILQLRLAAVRCFKNIVFLNDDFYLRYLIGKNLFDPIFEVFKENLNEDNMANSTILDFLKSLNTQLKVVEQEDIPLSGSKSSRNFMLLNKYICGRYGDILLKADYVSFTREMMAIYHEETQKLASLSTTETSFDENDNTTLEVEV
|
Core regulatory subunit of the histone H2A phosphatase complex, which dephosphorylates H2AS128ph (gamma-H2A) that has been displaced from sites of DNA lesions in the double-stranded DNA break repair process. Dephosphorylation is necessary for efficient recovery from the DNA damage checkpoint (By similarity).
|
Q6CVZ8
|
NMD4_KLULA
|
Nonsense-mediated decay protein 4
|
MILNFIIDSSSFEKGLGNIAIWSKLNDPKLTINAYLPLFTIQELDFQRFKRKSVVAKRALHFIDLLQDSTSFKLHLEYPELNEAISWNETVKLCQQNSHTSLSQHQISVIPIRFKKLLKSCYYKCHYKSHDLDEDIDHTNEKSDPDDKGWVLVTEDDTVRSLATQFQIPFISVVEADAIINACIKDKSYVVNEKFSKTVIKKANKVKEQEDGKKVFVTDFKNDFLAPRAKSGELWTPTSAKNKS
|
Involved in nonsense-mediated decay of mRNAs containing premature stop codons.
|
Q6CYE2
|
IRC6_KLULA
|
Increased recombination centers protein 6
|
MDNHKVLILLPESLEIQEHIAFISTIFQKQYDETESIARDVQWKTKYYETTLDLYIDTYDVLQEWVNDFVSDECKELRDVISGIIFVFKDEDHKPPVECLKNLIDERIEDFTAKFFIGCYFNENVIEEDELYELNSDLLVQNFEIVNWFDKPDPSMDKVGSERIKEIIDVHPWLSHPETLKKNQGQINISPIDLDSFMTKLEQAKERYQTFDDSKEAELFIEKIIDELSDMIV
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
Q6D2U2
|
FDHE_PECAS
|
Protein FdhE homolog
|
MSIRIVPQEQLEQNEQSTREGHIPPLLFANLKSLYSSRAERLRQLAEDHPLGDYLTFAAGVVEAQQKVLHDHPLHLDLSDVLKQSGERPPLDIAVFPRDAHWHTLLRALIEELKPDASGQVLSTLENLEKASEQELEEQATALLQHEFRAENNDKAPFIWAALSLFWAQMAGLLPGKARAVPGEHRQFCPVCGSIPVSGVVQLGTSSGLRYLHCNLCESEWHMVRVKCSNCEESSELNYWSLDSENSAIKAESCGHCGTYVKLLYQEKDHRVEAVADDLASLVLDVKMEEEGFSRSSINPFLFPESSIE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q6D8F3
|
SYDP_PECAS
|
Protein Syd
|
MEHEVVSALAAFTQRYVACWQQEKGHLPASEALYGIPSPCIVENHEDTVYWSPQPFAPSVALDGVERALEISLHPDVHAFYTAQYAGDMAAQFDSLSCQLLQVWSEEDFTRMQENLIGHLLTQKRLKLTPTLFLATTDSEMTMVSLCNVSGEIVLEAFGTKKRQHLAPTLAAFLSGLNPLAV
|
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}.
|
Q6D8J9
|
FETP_PECAS
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTVLQRDAEGQDFQLYPGDLGKRIYNEISKEAWAQWQTKQTMLINEKKLSMMNVDDRKLLEQEMIKFLFEGKDVHIEGYTPPSH
|
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}.
|
Q6F0N9
|
RIBV_MESFL
|
Putative riboflavin transporter RibV
|
MDKKYKLWNYKYDFSEINLKNWKEVLKDTFKLNTRKIALLSMLFAIEILMTIISKVIMGLAIPMIVGVYTIEISFFVILIIYLCSNYIYASILSITAIWFRLLLGSEPVGLLSMMISDTAFLTIFAVLFFILKKFIFLKFKFKNQIKILIALICFAGLISMIGSGFISMLCNDKFIFEMYYLSDDGSGYWKMLLWVGFGVTLAKYSINILLFASTLKVLLILIKQSRV
|
Probably transports riboflavin.
|
Q6F6K9
|
YIDD_ACIAD
|
Putative membrane protein insertion efficiency factor
|
MVRILHWLIRFYQIAISPMLGPRCRYIPTCSQYSLEAIHTHGAMKGTWLAIHRVCRCHPWGGSGYDPVPPKAIRFISFQQIDSQMLHVTVPFRERLLNLNHSNHLG
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q6F7U1
|
SDHE_ACIAD
|
FAD assembly factor SdhE
|
MSEELTLEERKVIYRARRGLKEIDVYFDPYVKNYYLTAPASEKALFAELVAQEDPDLLDWFMEVSEPPQVELKQLIQKLKHYVHG
|
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.
|
Q6FFB3
|
FETP_ACIAD
|
Probable Fe(2+)-trafficking protein
|
MTRLVFCRKYQQEMEGLDFAPFPGAKGQEFFDNVSKQAWQEWLQHQTTLINEKRLNVFEPEAKKFLEEQREKFFNNDASVEKAEGWKPEA
|
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}.
|
Q6FIV0
|
LCL2_CANGA
|
Long chronological lifespan protein 2
|
MNLLMVLFVAQAHAFFFGQQQQQQQQQASYEDRVLDSGCAKYLCSDTLECVDSWKDCPCPFPKSQLKCMLPKGSNRPYVCISKPATHDEKLNLIYDDPVQGPKAAIKGMRDCGWVQQNL
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
Q6FKK0
|
PALA_CANGA
|
pH-response regulator protein palA/RIM20
|
MTELIDIPFLLTKDCSADLEDRLRFCIETGSLYQTHESFKKDIGEIVNTRQALVNLKFGDSKLLTKYYGYLECLLKKIDPEALAFSWSYTNYTIFEGNVFRDENLLGERRNILFNLGIAYYQSAKHIDDYKNNLPLVCDYLKRSAGCFEILSQRTKERNSEKAIISETMLKALKSMCMGLAQETVWFKSLAAKKDLLTSKLAYKCFEYFQESLNSFQLVGQSTEYIKLILVFVESKMLYFKAVCVYRLAQSIESIADNVGVVIRCLSIAVAALTNSKLESTVVFKNKCLEMLRQLEKDNDFIYLKHVPSHLQFSDFVKLYKLDSMKDLIVLPDLTEIAPSMLDQILFRNLLPIEIMDYGTSYNEKQDIYVLQHFVEPINLLNIQLDEELASFFEIDPQHIVNAHNKTKSFVTRKELDVIGQSFGDLESNAINIETQLANITSYLDLEIKTYEEDKQQYGDVWTIVDARDVTKEFYEKVEKLRQYLEIGRNINLETQELFASIDKSLVTSRTSKAHLTAQYNDPFLNKIEALKKRRERFISEIEKKSYENRIISKLIMYYKETDDIPGTISEREEIFDNIYSKHMKVFAVDMKYIEDCKNENYGLIKEIEEYKSRTNFNNEDRSSDPRTQYIQDVRQSLASLDDVKTQLKKGTAYYQQLIEKVNELVQVIVGFLEARRNDRERLLNEISTAA
|
Required for the proteolytic cleavage of the transcription factor RIM101 in response to alkaline ambient pH. May act as a scaffold protein that recruits the calpain-like protease RIM13 via VPS32 to its substrate RIM101 (By similarity).
|
Q6FT66
|
NMD4_CANGA
|
Nonsense-mediated decay protein 4
|
MNQYNFILDASAFEKGLGNVKRWCQSNGNVDGKKNVYLRFYVPTFTLQELNFLQYRHKSFSAKEALKFIDKLETATSEGQRNHVVIGRKKEEDLRSDLELFIEFPDILDAVTWPTVLSYCTEGQATIDSLNKLPKRFKILLKSCVYKCHLEDDDRIRWILVTEDPQVRKIASQCHIPWCSIVDADSIISKDMNDRSFRDSEKFNSMMLKRGVAKSENMDGKEVIKTNFDQTVYATRGSGKLWTP
|
Involved in nonsense-mediated decay of mRNAs containing premature stop codons.
|
Q6FTE0
|
YKR18_CANGA
|
IML2-like protein CAGL0G03245g
|
MFSFFGGNKAPELTQEEKTKLILQQAYDFEVALRAMDYVLDDNPERGLNLLKESDDSANEDERTINVLARGVIEFLEATLSFEAEEMKKASATLAKAETLSQKSKANAEKLNLSNSSKYPPGTVFAVTYTESLLLHALLMIFSESMMEVAKALLKLRKAYYTLQEVLEQIKAANEASITNAENNGEESKSSSASFISEGDIFNSIDIPYKLTEEEAKDKELLEFADKVHKMRAKRLSGAHIDNPPAINRLRNDLGLQAMNSLPKEEIKEHLPLSDDVDRSQATIDEFIHSGVNLCFGILQVVLSLLPPAIGAVLSAVGFRGSREEGLRLVWKATKHRNVHGCIGLLGLMFYYDGPFQFTDDDFDVPASVKEYLNSTEDKKGQEENNDDTSTMTKDMESLKLKDDDLHMDSNTILHPGKILEDALLKSRALFPNSALWLLNEARMLSGKGRLEDAVALMDSIDVNSIQMRQVKTLMIFDRAITLIHLHEYDRAADDILSLLDISDWSHAFYSYFAGCCYLENWRMIQMGDLKSDKEEFYKEKATTLIFKSVDYLGKKTWRSKNLPLDRFVARKVDQFKAMQVKLNLTNPLDAIATGPVYEIAYFYNGFNRMSQKHLDISKKMLTEYKNPAVEANDPDQNLIRDLLVSLCLRRSDKIKEGCDLLDQKVLPTFFKELPDGKVEYVKKNEDPWLYPSALYERALFCWKLNGVQGLSECKEWLLRAQNYADDYELSSRVGMKIKAAIDRVDSALNN
|
May be involved in mitochondrial DNA stability.
|
Q6FTZ5
|
MTC2_CANGA
|
Maintenance of telomere capping protein 2
|
MTEMDFDLEQIQKYELPDFETALLFSIVAKKNFLVLFDAEQRKLNDEISNEELIQKSVGDVMQKRTDFKINFKYQCINHVTDEMISEIQKCELDDYKNLETMEHVDEKGDRSANIAGVDQNVTIEFYLVEDIDRQSLADYYQLGRLMREGYIFNVQHNGIANNKKYWKLFIGTVAWKRDEYIIPDDILQLGAADKKYSHKHGQSFKLKSFSTGFEDWIRHKFWLVTTLAMPNIKPTIEVQAADDTASFSSVVITKDEAKEEEAITGSSDGAEKIISGDYKNYDNIHIQASLRRYILDIMVHIRTHRLTFNARGGGIHKNCYSNMITLSKIICIKDHKSFVVPQHVRLAAMWFLPLQLSVIDDSLKDNSILYGSKPELVRELMKRVVYVRNKQIIDMDNPLFMEALIVKSALKKIVPPV
|
May be involved in telomere capping.
|
Q6FWU4
|
DSE3_CANGA
|
Protein DSE3
|
MPRKFLGEKIDRNTDFLRPSSLTLTADDLKVIPDFKCDDDDAVLSGNKTGKRLSRKFGGTMRLKQRLESVPELFLHDFRKRRGQKLQERNNDEQISRAKLPPHLSGLRRPNGLPARKPLRTITEVLPPVTSYNNSIEQNEDDLYYVEKKDPKEHVVETNHKEMRPLDKPLIEKVENVYLEPLIFPVQVSEPVNQMSIPMEELQKYGKSDSEILFDEIISAYEPHMETTGDVSNVLNSEILSVLDRVSNAPKKNWNLMAPKVISAEAIEENKRLSINSIASSGRTPESTRNSRFCENLSSPEYSTAASVSDRWSSGDEFSDVASSNPNSHAISHDGSYTTALGSIPSLAGSVDNLDILDQKDILSPTVSNEIITVKPVPQNTVETMHVTKIVIKPQLFLDWESEEEDDPIDALSRQVDNIEIASVYSGSSSVYSDHFAT
|
May be involved in the establishment of the daughter fate.
|
Q6FWX8
|
IRC6_CANGA
|
Increased recombination centers protein 6
|
MLDESSSSDESRATELPVSSEDECEEVTDAKVLPNKVLVVFEGESTLFRDQLLDTVFGVQDQGNIVKQLSWDTKYYAVEYDLYVDECVDIHGWLNEVNSDDYEELRDLLTMIIIVRSFDSTQDTKEYNSVLYDFIQGNSVSVISVNTNSARQVKDTYDEFLELDASSIEFINYHDDRVEKETNECKGMARLKEIIDTHPWTDCKVVLKNKESTSDKVNKPDLEYLIDTLKKAKIHYQKLSNGSDGFSEEAEQFALQMATDIANNL
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
Q6FZZ6
|
YIDD_BARQU
|
Putative membrane protein insertion efficiency factor
|
MFKLHPQKKKTQTRNYTGPWRKTPGRLLGLLLIRFYQITLSSFIGNQCRHAPTCSEYIYEAIARHGLWAGAWMGLFRIMRCGPFGTHGFDPVPTSLGNSYYFYKPWCYWKISARHNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q6G3K0
|
YIDD_BARHE
|
Putative membrane protein insertion efficiency factor
|
MFNPYPQKKKRQTRNYTGPWRKTPGRLLGLLLIRFYQITLSGFIGNQCRHLPTCSEYTYEAIARHGLWAGAWMGFFRIIRCGPFGTHGFEPVPTSLGNSYCFYKPWCYWKISTKHNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q6G7P0
|
MAZE_STAAS
|
Antitoxin MazE
|
MLSFSQNRSHSLEQSLKEGYSQMADLNLSLANEAFPIECEACDCNETYLSSNSTNE
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Labile antitoxin that binds to cognate MazF toxin and counteracts its endoribonuclease activity.
|
Q6G8D8
|
YIDD_STAAS
|
Putative membrane protein insertion efficiency factor
|
MKKIFLAMIHFYQRFISPLTPPTCRFYPTCSEYTREAIQYHGAFKGLYLGIRRILKCHPLHKGGFDPVPLKKDKSASKHSHKHNH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q6G8Y5
|
HRCA_STAAS
|
Heat-inducible transcription repressor HrcA
|
MITDRQLSILNAIVEDYVDFGQPVGSKTLIERHNLNVSPATIRNEMKQLEDLNYIEKTHSSSGRSPSQLGFRYYVNRLLEQTSHQKTNKLRRLNQLLVENQYDVSSALTYFADELSNISQYTTLVVHPNHKQDIINNVHLIRANPNLVIMVIVFSSGHVEHVHLASDIPFNNDKLNTISNFVTNKLTEFNQNLQDDIVSFVQSEQEEIFINKLLNTMNNHISNQSNSIYMGGKVKLIDALNESNVSSIQPILQYIESNRIAELLQDISSPNINVKIGNEIDDSLSDISIVTSQYHFDETLKGQIAVIGPTAMHYQNVIQLLNRIW
|
Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}.
|
Q6G9D2
|
CVFC_STAAS
|
Conserved virulence factor C
|
MEILRIEPTPSPNTMKVVLSYTREDKLSNTYKKVEETQPRFINQLLSIDGITSIFHVMNFLAVDKAPKADWEVILPDIKAAFSDANKVLESVNEPQIDNHFGEIKAELLTFKGIPYQIKLTSADQELREQLPQTYVDHMTQAQTAHDNIVFMRKWLDLGNRYGNIEEVMDGVLEEVLATYPESQLPVLVKHALEENHATNNYHFYRHVSLDEYHATDNWKTRLRMLNHFPKPTFEDIPLLDLALSDEKVPVRRQAIVLLGMIESKEILPYLYKGLRDKSPAVRRTAGDCISDLGYPEALPEMVLLLDDPQKIVRWRAAMFIFDEGNAEQLPALKAHINDNAFEVKLQIEMAISRIENGDEALGSVWKQMANRTI
|
Required for hemolysin production.
|
Q6G9D6
|
Y1368_STAAS
|
DegV domain-containing protein SAS1368
|
MTKQIIVTDSTSDLSKEYLEANNIHVIPLSLTIEGASYVDQVDITSEEFINHIENDEDVKTSQPAIGEFISAYEELGKDGSEIISIHLSSGLSGTYNTAYQASQMVDANVTVIDSKSISFGLGYQIQHLVELVKEGVSTSEIVKKLNHLRENIKLFVVIGQLNQLIKGGRISKTKGLIGNLMKIKPIGTLDDGRLELVHNARTQNSSIQYLKKEIAEFIGDHEIKSIGVAHANVIEYVDKLKKVFNEAFHVNNYDINVTTPVISAHTGQGAIGLVVLKK
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q6G9G0
|
MSA_STAAS
|
Protein msa (Modulator of SarA)
|
MKYLILSLVANLLVFGVLSAIGLNINILAAMMIVLVIPIMISGILFFKTNIDKTYIFFNIIFIDFYYYIYNVHLMTLPKFNNYIKAEMMELEDIDVLITSKDFGFDEILFYTLYLLLILIVLYYLKKQVKHKI
|
Accessory element involved in the expression of sarA and several virulence factors. Modulates SarA production and/or function in a strain-dependent manner. Affects the transcription of the accessory gene regulator (agr) and genes encoding virulence factors including alpha toxin (hla) and protein A (spa) (By similarity).
|
Q6G9H0
|
CVFB_STAAS
|
Conserved virulence factor B
|
MALDKDIVGSIEFLEVVGLQGSTYLLKGPNGENVKLNQSEMNDDDELEVGEEYSFFIYPNRSGELFATQNMPDITKDKYDFAKVLKTDRDGARIDVGLPREVLVPWEDLPKVKSLWPQPGDHLLVTLRIDRENHMYGRLASESVVENMFTPVHDDNLKNEVIEAKPYRVLRIGSFLLSESGYKIFVHESERKAEPRLGESVQVRIIGHNDKGELNGSFLPLAHERLDDDGQVIFDLLVEYDGELPFWDKSSPEAIKEVFNMSKGSFKRAIGHLYKQKIINIETGKITLTKKGWSRMDSKE
|
Contributes to the expression of virulence factors and to pathogenicity. Involved in the production of hemolysin, DNase, protease and protein A (By similarity).
|
Q6G9X7
|
Y1170_STAAS
|
UPF0122 protein SAS1170
|
MGQNDLVKTLRMNYLFDFYQSLLTNKQRNYLELFYLEDYSLSEIADTFNVSRQAVYDNIRRTGDLVEDYEKKLELYQKFEQRREIYDEMKQHLSNPEQIQRYIQQLEDLE
|
Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.