CPLM 1.0 - Compendium of Protein Lysine ModificationTag | Content |
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CPLM ID | CPLM-022146 | UniProt Accession | | Genbank Protein ID | | Genbank Nucleotide ID | | Protein Name | Midasin | Protein Synonyms/Alias | MIDAS-containing protein | Gene Name | MDN1 | Gene Synonyms/Alias | KIAA0301 | Created Date | July 27, 2013 | Organism | Homo sapiens (Human) | NCBI Taxa ID | 9606 | Lysine Modification | Position | Peptide | Type | References |
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22 | LIAAKNEKSRSELGR | ubiquitination | [1] | 33 | ELGRFLAKQVWTPQD | ubiquitination | [1, 2, 3] | 81 | ERNAEAIKAGGQINH | ubiquitination | [1, 2, 3] | 100 | RLCVSMSKLIGNHPD | ubiquitination | [1] | 117 | PFALRYFKDTSPVFQ | ubiquitination | [1, 2, 3, 4, 5] | 208 | HKLSFLKKIFNSDEL | ubiquitination | [1] | 247 | PEVSLWRKQKELQYL | ubiquitination | [1] | 249 | VSLWRKQKELQYLQG | ubiquitination | [1, 2] | 350 | AAVTGRTKPPQLLKV | ubiquitination | [1, 2] | 356 | TKPPQLLKVQLGDQT | ubiquitination | [1, 2] | 366 | LGDQTDSKMLLGMYR | ubiquitination | [1, 2, 3] | 433 | PGRGDCLKVAPGFQF | ubiquitination | [1, 6, 7] | 466 | SHATLLDKYWTKIHL | ubiquitination | [1] | 478 | IHLDNLDKRELNEVL | ubiquitination | [1, 2, 7] | 592 | SEHTSKLKMAEVIGS | ubiquitination | [1, 2] | 600 | MAEVIGSKLNISRKK | ubiquitination | [1, 2, 3] | 636 | GRVRLLRKQSEAVHL | ubiquitination | [1] | 683 | VGETGTGKTSTIQYL | ubiquitination | [1] | 717 | ADLLGGYKPVDHKLI | ubiquitination | [1, 2] | 722 | GYKPVDHKLIWLPLR | ubiquitination | [1] | 742 | LFAQTFSKKQNFTFL | ubiquitination | [1] | 743 | FAQTFSKKQNFTFLG | ubiquitination | [1] | 778 | VHKSAVNKDGKDSET | ubiquitination | [1, 2] | 781 | SAVNKDGKDSETGLL | ubiquitination | [1, 2] | 790 | SETGLLIKEKWEAFG | ubiquitination | [2] | 792 | TGLLIKEKWEAFGLR | ubiquitination | [1] | 891 | NPATDVGKRNLPPGI | ubiquitination | [1] | 931 | LKGLSVNKNTVQGII | ubiquitination | [1] | 1008 | ASHPIVQKLICQHIV | ubiquitination | [1] | 1020 | HIVPGNVKSLLKQPI | ubiquitination | [1] | 1024 | GNVKSLLKQPIPEPK | ubiquitination | [1, 2, 3] | 1031 | KQPIPEPKGGRLIQV | ubiquitination | [1] | 1184 | TETQEVVKAHPRFML | ubiquitination | [1, 2, 3] | 1234 | ELETILHKRCSLPPS | ubiquitination | [1, 2] | 1248 | SYCSKLVKVMLDLQS | ubiquitination | [2] | 1266 | SSSVFAGKQGFITLR | ubiquitination | [1, 2] | 1312 | LLAGRVRKQEEIDVI | ubiquitination | [1] | 1344 | FSKENVLKLLGKLST | ubiquitination | [1] | 1435 | GLRPVRQKPNDKEEI | ubiquitination | [1] | 1439 | VRQKPNDKEEIDTSR | ubiquitination | [2] | 1489 | NSVLEVEKSLVLAEK | ubiquitination | [1, 2, 6] | 1502 | EKGSPEDKDSEIELL | ubiquitination | [1, 2] | 1513 | IELLTAGKKFRILAT | ubiquitination | [2, 3] | 1514 | ELLTAGKKFRILATM | ubiquitination | [1] | 1529 | NPGGDFGKKELSPAL | ubiquitination | [2] | 1530 | PGGDFGKKELSPALR | ubiquitination | [1] | 1597 | THQEFGRKCVVSIRD | ubiquitination | [1] | 1683 | VRLTEYQKNELKIYD | acetylation | [8] | 1683 | VRLTEYQKNELKIYD | ubiquitination | [2] | 1687 | EYQKNELKIYDRMKA | ubiquitination | [1, 2] | 1695 | IYDRMKAKEFTGIDN | ubiquitination | [1, 6] | 1746 | LLRATKLKKPILLEG | ubiquitination | [1] | 1747 | LRATKLKKPILLEGS | ubiquitination | [1] | 1768 | SLVGALAKASGNTLV | ubiquitination | [1, 2] | 1799 | DLPVEGGKGGEFAWR | ubiquitination | [2] | 1863 | QVQHEKTKIFGCQNP | ubiquitination | [1] | 1940 | VEKKWGQKGGPWEFN | ubiquitination | [1, 2, 4, 5] | 1989 | RTEEDKKKVIAVFKD | ubiquitination | [1] | 1995 | KKVIAVFKDVFGSNS | ubiquitination | [1] | 2120 | PWRRLLEKVEGTVRA | ubiquitination | [2] | 2198 | YCKAEFAKLVEEFRS | ubiquitination | [2] | 2406 | QHSPANRKLVQALLE | ubiquitination | [1, 7] | 2414 | LVQALLEKHVSSLRA | ubiquitination | [1, 2] | 2471 | CLNRMSMKTSSWTRS | ubiquitination | [1] | 2488 | FTLQDLEKIMQSPSP | ubiquitination | [2] | 2656 | NLVSVGSKKLRESVL | ubiquitination | [1, 2] | 2657 | LVSVGSKKLRESVLR | ubiquitination | [1] | 2825 | SQLKVLNKVLAIREQ | ubiquitination | [1] | 2858 | VASQWTLKKSLLQAW | ubiquitination | [2] | 2896 | QCLELKAKGLSLGFL | ubiquitination | [1, 2, 7] | 2905 | LSLGFLEKKHDEASS | ubiquitination | [2, 4, 5] | 2906 | SLGFLEKKHDEASSL | ubiquitination | [1, 7] | 3056 | SVLDSTLKGPGNLNR | ubiquitination | [1, 2, 4, 5, 7] | 3211 | FVGEGESKRSLPEPA | ubiquitination | [1] | 3246 | ARFDPAVKREYKLNY | ubiquitination | [1, 2] | 3250 | PAVKREYKLNYVKEE | ubiquitination | [1] | 3255 | EYKLNYVKEELHQLQ | ubiquitination | [1, 7] | 3312 | NLTCHLLKKQAFRPQ | acetylation | [7] | 3312 | NLTCHLLKKQAFRPQ | ubiquitination | [1] | 3313 | LTCHLLKKQAFRPQL | ubiquitination | [1] | 3370 | QVAQSLLKEEASWQQ | ubiquitination | [1, 2, 7] | 3473 | EVLRGLGKLILKRSG | ubiquitination | [1, 7] | 3482 | ILKRSGGKELEGKGQ | acetylation | [7] | 3513 | LRSHVLCKGELDQRA | ubiquitination | [1, 7] | 3545 | QERIAQEKAEQESGL | ubiquitination | [1, 2, 7] | 3950 | KEFVKISKWNDVSFW | ubiquitination | [1] | 3960 | DVSFWSIKQSVEKTH | ubiquitination | [1] | 3972 | KTHRTLFKFMKKFEA | ubiquitination | [1] | 3976 | TLFKFMKKFEAVLSE | ubiquitination | [1] | 4066 | KLRKRMRKMCLTFMK | ubiquitination | [1] | 4132 | RALSDLFKHLAKIGL | ubiquitination | [1, 4, 5] | 4143 | KIGLSYRKGLAWARS | ubiquitination | [1] | 4194 | SSWDGCQKYFYRSLA | ubiquitination | [1] | 4215 | AALATPAKEMGMGNV | ubiquitination | [1, 2, 4, 5] | 4375 | PSGCRMRKQDHLWQQ | ubiquitination | [1] | 4392 | TRLTEMLKTIKTVKA | ubiquitination | [1] | 4705 | QVEDTFQKGQEKDKE | acetylation | [9] | 4736 | MSEDFDGKMHDGELE | ubiquitination | [6] | 5168 | QTYDVASKEQQQSAK | acetylation | [9] | 5253 | HKETENEKPERSRES | ubiquitination | [2] | 5342 | LEPTQAAKLKGDYRT | ubiquitination | [1, 2] | 5344 | PTQAAKLKGDYRTGK | ubiquitination | [1] | 5357 | GKRLNIRKVIPYIAS | ubiquitination | [1] | 5506 | RGLFLEGKERVLAAV | ubiquitination | [1, 2] | 5541 | RDSILDIKVPIFKGP | ubiquitination | [1, 2, 3, 4, 5] | 5546 | DIKVPIFKGPGEMPE | ubiquitination | [1, 2, 3] |
| Reference | [1] Refined preparation and use of anti-diglycine remnant (K-ε-GG) antibody enables routine quantification of 10,000s of ubiquitination sites in single proteomics experiments. Udeshi ND, Svinkina T, Mertins P, Kuhn E, Mani DR, Qiao JW, Carr SA. Mol Cell Proteomics. 2013 Mar;12(3):825-31. [ PMID: 23266961] [2] Systematic and quantitative assessment of the ubiquitin-modified proteome. Kim W, Bennett EJ, Huttlin EL, Guo A, Li J, Possemato A, Sowa ME, Rad R, Rush J, Comb MJ, Harper JW, Gygi SP. Mol Cell. 2011 Oct 21;44(2):325-40. [ PMID: 21906983] [3] Landscape of the PARKIN-dependent ubiquitylome in response to mitochondrial depolarization. Sarraf SA, Raman M, Guarani-Pereira V, Sowa ME, Huttlin EL, Gygi SP, Harper JW. Nature. 2013 Apr 18;496(7445):372-6. [ PMID: 23503661] [4] A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles. Wagner SA, Beli P, Weinert BT, Nielsen ML, Cox J, Mann M, Choudhary C. Mol Cell Proteomics. 2011 Oct;10(10):M111.013284. [ PMID: 21890473] [5] hCKSAAP_UbSite: improved prediction of human ubiquitination sites by exploiting amino acid pattern and properties. Chen Z, Zhou Y, Song J, Zhang Z. Biochim Biophys Acta. 2013 Aug;1834(8):1461-7. [ PMID: 23603789] [6] Global identification of modular cullin-RING ligase substrates. Emanuele MJ, Elia AE, Xu Q, Thoma CR, Izhar L, Leng Y, Guo A, Chen YN, Rush J, Hsu PW, Yen HC, Elledge SJ. Cell. 2011 Oct 14;147(2):459-74. [ PMID: 21963094] [7] Integrated proteomic analysis of post-translational modifications by serial enrichment. Mertins P, Qiao JW, Patel J, Udeshi ND, Clauser KR, Mani DR, Burgess MW, Gillette MA, Jaffe JD, Carr SA. Nat Methods. 2013 Jul;10(7):634-7. [ PMID: 23749302] [8] Lysine acetylation targets protein complexes and co-regulates major cellular functions. Choudhary C, Kumar C, Gnad F, Nielsen ML, Rehman M, Walther TC, Olsen JV, Mann M. Science. 2009 Aug 14;325(5942):834-40. [ PMID: 19608861] [9] Proteomic investigations of lysine acetylation identify diverse substrates of mitochondrial deacetylase sirt3. Sol EM, Wagner SA, Weinert BT, Kumar A, Kim HS, Deng CX, Choudhary C. PLoS One. 2012;7(12):e50545. [ PMID: 23236377] | Functional Description | Nuclear chaperone required for maturation and nuclear export of pre-60S ribosome subunits (By similarity). | Sequence Annotation | DOMAIN 5384 5583 VWFA. NP_BIND 329 336 ATP (Potential). NP_BIND 677 684 ATP (Potential). NP_BIND 1084 1091 ATP (Potential). NP_BIND 1390 1397 ATP (Potential). NP_BIND 1753 1760 ATP (Potential). NP_BIND 2066 2073 ATP (Potential). MOD_RES 1 1 N-acetylmethionine. MOD_RES 1177 1177 Phosphothreonine. MOD_RES 1683 1683 N6-acetyllysine. MOD_RES 4538 4538 Phosphoserine. MOD_RES 4752 4752 Phosphoserine. MOD_RES 4754 4754 Phosphoserine. MOD_RES 4889 4889 Phosphoserine. MOD_RES 4898 4898 Phosphothreonine. MOD_RES 4937 4937 Phosphoserine. MOD_RES 4946 4946 Phosphoserine. MOD_RES 5015 5015 Phosphoserine. | Keyword | Acetylation; ATP-binding; Chaperone; Complete proteome; Nucleotide-binding; Nucleus; Phosphoprotein; Polymorphism; Reference proteome; Repeat. | Sequence Source | UniProt (SWISSPROT/TrEMBL); GenBank; EMBL | Protein Length | 5596 AA | Protein Sequence | MEHFLLEVAA APLRLIAAKN EKSRSELGRF LAKQVWTPQD RQCVLSTLAQ LLLDKDCTVL 60 VGRQLRPLLL DLLERNAEAI KAGGQINHDL HERLCVSMSK LIGNHPDVLP FALRYFKDTS 120 PVFQRLFLES SDANPVRYGR RRMKLRDLME AAFKFLQQEQ SVFRELWDWS VCVPLLRSHD 180 TLVRWYTANC LALVTCMNEE HKLSFLKKIF NSDELIHFRL RLLEEAQLQD LEKALVLANP 240 EVSLWRKQKE LQYLQGHLVS SDLSPRVTAV CGVVLPGQLP APGELGGNRS SSREQELALR 300 SYVLVESVCK SLQTLAMAVA SQNAVLLEGP IGCGKTSLVE YLAAVTGRTK PPQLLKVQLG 360 DQTDSKMLLG MYRCTDVPGE FVWQPGTLTQ AATMGHWILL EDIDYAPLDV VSVLIPLLEN 420 GELLIPGRGD CLKVAPGFQF FATRRLLSCG GNWYRPLNSH ATLLDKYWTK IHLDNLDKRE 480 LNEVLQSRYP SLLAVVDHLL DIYIQLTGEK HHSWSDSSVG CEQAPEEVSE ARRENKRPTL 540 EGRELSLRDL LNWCNRIAHS FDSSSLSASL NIFQEALDCF TAMLSEHTSK LKMAEVIGSK 600 LNISRKKAEF FCQLYKPEIV INELDLQVGR VRLLRKQSEA VHLQREKFTF AATRPSSVLI 660 EQLAVCVSKG EPVLLVGETG TGKTSTIQYL AHITGHRLRV VNMNQQSDTA DLLGGYKPVD 720 HKLIWLPLRE AFEELFAQTF SKKQNFTFLG HIQTCYRQKR WHDLLRLMQH VHKSAVNKDG 780 KDSETGLLIK EKWEAFGLRL NHAQQQMKMT ENTLLFAFVE GTLAQAVKKG EWILLDEINL 840 AAPEILECLS GLLEGSSGSL VLLDRGDTEP LVRHPDFRLF ACMNPATDVG KRNLPPGIRN 900 RFTELYVEEL ESKEDLQVLI VDYLKGLSVN KNTVQGIINF YTALRKESGT KLVDGTGHRP 960 HYSLRTLCRA LRFAASNPCG NIQRSLYEGF CLGFLTQLDR ASHPIVQKLI CQHIVPGNVK 1020 SLLKQPIPEP KGGRLIQVEG YWIAVGDKEP TIDETYILTS SVKLNLRDIV RVVSAGTYPV 1080 LIQGETSVGK TSLIQWLAAA TGNHCVRINN HEHTDIQEYI GCYTSDSSGK LVFKEGVLID 1140 AMRKGYWIIL DELNLAPTDV LEALNRLLDD NRELLVTETQ EVVKAHPRFM LFATQNPPGL 1200 YGGRKVLSRA FRNRFVELHF DELPSSELET ILHKRCSLPP SYCSKLVKVM LDLQSYRRSS 1260 SVFAGKQGFI TLRDLFRWAE RYRLAEPTEK EYDWLQHLAN DGYMLLAGRV RKQEEIDVIQ 1320 EVLEKHFKKK LCPQSLFSKE NVLKLLGKLS TQISTLECNF GHIVWTEGMR RLAMLVGRAL 1380 EFGEPVLLVG DTGCGKTTIC QVFAALANQK LYSVSCHLHM ETSDFLGGLR PVRQKPNDKE 1440 EIDTSRLFEW HDGPLVQAMK EDGFFLLDEI SLADDSVLER LNSVLEVEKS LVLAEKGSPE 1500 DKDSEIELLT AGKKFRILAT MNPGGDFGKK ELSPALRNRF TEIWCPQSTS REDLIQIISH 1560 NLRPGLCLGR IDPKGSDIPE VMLDFIDWLT HQEFGRKCVV SIRDILSWVN FMNKMGEEAA 1620 LKRPEIISTV TSFVHAACLV YIDGIGSGVT SSGFGTALLA RKECLKFLIK RLAKIVRLTE 1680 YQKNELKIYD RMKAKEFTGI DNLWGIHPFF IPRGPVLHRN NIADYALSAG TTAMNAQRLL 1740 RATKLKKPIL LEGSPGVGKT SLVGALAKAS GNTLVRINLS EQTDITDLFG ADLPVEGGKG 1800 GEFAWRDGPL LAALKAGHWV VLDELNLASQ SVLEGLNACF DHRGEIYVPE LGMSFQVQHE 1860 KTKIFGCQNP FRQGGGRKGL PRSFLNRFTQ VFVDPLTVID MEFIASTLFP AIEKNIVKKM 1920 VAFNNQIDHE VTVEKKWGQK GGPWEFNLRD LFRWCQLMLV DQSPGCYDPG QHVFLVYGER 1980 MRTEEDKKKV IAVFKDVFGS NSNPYMGTRL FRITPYDVQL GYSVLSRGSC VPHPSRHPLL 2040 LLHQSFQPLE SIMKCVQMSW MVILVGPASV GKTSLVQLLA HLTGHTLKIM AMNSAMDTTE 2100 LLGGFEQVDL IRPWRRLLEK VEGTVRALLR DSLLISADDA EVVLRAWSHF LLTYKPKCLG 2160 EGGKAITMEI VNKLEAVLLL MQRLNNKINS YCKAEFAKLV EEFRSFGVKL TQLASGHSHG 2220 TFEWVDSMLV QALKSGDWLL MDNVNFCNPS VLDRLNALLE PGGVLTISER GMIDGSTPTI 2280 TPNPNFRLFL SMDPVHGDIS RAMRNRGLEI YISGEGDAST PDNLDLKVLL HSLGLVGNSV 2340 CDILLALHTE TRSTVVGSPT SSVSTLIQTA ILIVQYLQRG LSLDRAFSEA CWEVYVCSQH 2400 SPANRKLVQA LLEKHVSSLR AHETWGDSIL GMGLWPDSVP SALFATEDSH LSTVRRDGQI 2460 LVYCLNRMSM KTSSWTRSQP FTLQDLEKIM QSPSPENLKF NAVEVNTYWI DEPDVLVMAV 2520 KLLIERATNQ DWMLRVKWLY HLAKNIPQGL ESIQIHLEAS AASLRNFYSH SLSGAVSNVF 2580 KILQPNTTDE FVIPLDPRWN MQALDMIRNL MDFDPQTDQP DQLFALLESA ANKTIIYLDR 2640 EKRVFTEANL VSVGSKKLRE SVLRMSFEFH QDPESYHTLP HEIVVNLAAF FELCDALVLL 2700 WVQSSQGMVS DASANEILGS LRWRDRFWTV ADTVKVDAPG LALLALHWHW VLKHLVHQIP 2760 RLLMNYEDKY YKEVQTVSEH IQNCLGSQTG GFAGIKKLQK FLGRPFPFKD KLVVECFSQL 2820 KVLNKVLAIR EQMSALGESG WQEDINRLQV VASQWTLKKS LLQAWGLILR ANILEDVSLD 2880 ELKNFVHAQC LELKAKGLSL GFLEKKHDEA SSLSHPDLTS VIHLTRSVQL WPAMEYLAML 2940 WRYKVTADFM AQACLRRCSK NQQPQINEEI SHLISFCLYH TPVTPQELRD LWSLLHHQKV 3000 SPEEITSLWS ELFNSMFMSF WSSTVTTNPE YWLMWNPLPG MQQREAPKSV LDSTLKGPGN 3060 LNRPIFSKCC FEVLTSSWRA SPWDVSGLPI LSSSHVTLGE WVERTQQLQD ISSMLWTNMA 3120 ISSVAEFRRT DSQLQGQVLF RHLAGLAELL PESRRQEYMQ NCEQLLLGSS QAFQHVGQTL 3180 GDMAGQEVLP KELLCQLLTS LHHFVGEGES KRSLPEPAQR GSLWVSLGLL QIQTWLPQAR 3240 FDPAVKREYK LNYVKEELHQ LQCEWKTRNL SSQLQTGRDL EDEVVVSYSH PHVRLLRQRM 3300 DRLDNLTCHL LKKQAFRPQL PAYESLVQEI HHYVTSIAKA PAVQDLLTRL LQALHIDGPR 3360 SAQVAQSLLK EEASWQQSHH QFRKRLSEEY TFYPDAVSPL QASILQLQHG MRLVASELHT 3420 SLHSSMVGAD RLGTLATALL AFPSVGPTFP TYYAHADTLC SVKSEEVLRG LGKLILKRSG 3480 GKELEGKGQK ACPTREQLLM NALLYLRSHV LCKGELDQRA LQLFRHVCQE IISEWDEQER 3540 IAQEKAEQES GLYRYRSRNS RTALSEEEEE EREFRKQFPL HEKDFADILV QPTLEENKGT 3600 SDGQEEEAGT NPALLSQNSM QAVMLIHQQL CLNFARSLWY QQTLPPHEAK HYLSLFLSCY 3660 QTGASLVTHF YPLMGVELND RLLGSQLLAC TLSHNTLFGE APSDLMVKPD GPYDFYQHPN 3720 VPEARQCQPV LQGFSEAVSH LLQDWPEHPA LEQLLVVMDR IRSFPLSSPI SKFLNGLEIL 3780 LAKAQDWEEN ASRALSLRKH LDLISQMIIR WRKLELNCWS MSLDNTMKRH TEKSTKHWFS 3840 IYQMLEKHMQ EQTEEQEDDK QMTLMLLVST LQAFIEGSSL GEFHVRLQML LVFHCHVLLM 3900 PQVEGKDSLC SVLWNLYHYY KQFFDRVQAK IVELRSPLEK ELKEFVKISK WNDVSFWSIK 3960 QSVEKTHRTL FKFMKKFEAV LSEPCRSSLV ESDKEEQPDF LPRPTDGAAS ELSSIQNLNR 4020 ALRETLLAQP AAGQATIPEW CQGAAPSGLE GELLRRLPKL RKRMRKMCLT FMKESPLPRL 4080 VEGLDQFTGE VISSVSELQS LKVEPSAEKE KQRSEAKHIL MQKQRALSDL FKHLAKIGLS 4140 YRKGLAWARS KNPQEMLHLH PLDLQSALSI VSSTQEADSR LLTEISSSWD GCQKYFYRSL 4200 ARHARLNAAL ATPAKEMGMG NVERCRGFSA HLMKMLVRQR RSLTTLSEQW IILRNLLSCV 4260 QEIHSRLMGP QAYPVAFPPQ DGVQQWTERL QHLAMQCQIL LEQLSWLLQC CPSVGPAPGH 4320 GNVQVLGQPP GPCLEGPELS KGQLCGVVLD LIPSNLSYPS PIPGSQLPSG CRMRKQDHLW 4380 QQSTTRLTEM LKTIKTVKAD VDKIRQQSCE TLFHSWKDFE VCSSALSCLS QVSVHLQGLE 4440 SLFILPGMEV EQRDSQMALV ESLEYVRGEI SKAMADFTTW KTHLLTSDSQ GGNQMLDEGF 4500 VEDFSEQMEI AIRAILCAIQ NLEERKNEKA EENTDQASPQ EDYAGFERLQ SGHLTKLLED 4560 DFWADVSTLH VQKIISAISE LLERLKSYGE DGTAAKHLFF SQSCSLLVRL VPVLSSYSDL 4620 VLFFLTMSLA THRSTAKLLS VLAQVFTELA QKGFCLPKEF MEDSAGEGAT EFHDYEGGGI 4680 GEGEGMKDVS DQIGNEEQVE DTFQKGQEKD KEDPDSKSDI KGEDNAIEMS EDFDGKMHDG 4740 ELEEQEEDDE KSDSEGGDLD KHMGDLNGEE ADKLDERLWG DDDEEEDEEE EDNKTEETGP 4800 GMDEEDSELV AKDDNLDSGN SNKDKSQQDK KEEKEEAEAD DGGQGEDKIN EQIDERDYDE 4860 NEVDPYHGNQ EKVPEPEALD LPDDLNLDSE DKNGGEDTDN EEGEEENPLE IKEKPEEAGH 4920 EAEERGETET DQNESQSPQE PEEGPSEDDK AEGEEEMDTG ADDQDGDAAQ HPEEHSEEQQ 4980 QSVEEKDKEA DEEGGENGPA DQGFQPQEEE EREDSDTEEQ VPEALERKEH ASCGQTGVEN 5040 MQNTQAMELA GAAPEKEQGK EEHGSGAADA NQAEGHESNF IAQLASQKHT RKNTQSFKRK 5100 PGQADNERSM GDHNERVHKR LRTVDTDSHA EQGPAQQPQA QVEDADAFEH IKQGSDAYDA 5160 QTYDVASKEQ QQSAKDSGKD QEEEEIEDTL MDTEEQEEFK AADVEQLKPE EIKSGTTAPL 5220 GFDEMEVEIQ TVKTEEDQDP RTDKAHKETE NEKPERSRES TIHTAHQFLM DTIFQPFLKD 5280 VNELRQELER QLEMWQPRES GNPEEEKVAA EMWQSYLILT APLSQRLCEE LRLILEPTQA 5340 AKLKGDYRTG KRLNIRKVIP YIASQFRKDK IWLRRTKPSK RQYQICLAID DSSSMVDNHT 5400 KQLAFESLAV IGNALTLLEV GQIAVCSFGE SVKLLHPFHE QFSDYSGSQI LRLCKFQQKK 5460 TKIAQFLESV ANMFAAAQQL SQNISSETAQ LLLVVSDGRG LFLEGKERVL AAVQAARNAN 5520 IFVIFVVLDN PSSRDSILDI KVPIFKGPGE MPEIRSYMEE FPFPYYIILR DVNALPETLS 5580 DALRQWFELV TASDHP 5596 | Gene Ontology | | Interpro | | Pfam | | SMART | | PROSITE | | 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