CPLM 1.0 - Compendium of Protein Lysine ModificationTag | Content |
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CPLM ID | CPLM-037139 | UniProt Accession | | Genbank Protein ID | | Genbank Nucleotide ID | | Protein Name | DNA-dependent protein kinase catalytic subunit | Protein Synonyms/Alias | | Gene Name | PRKDC | Gene Synonyms/Alias | | Created Date | July 27, 2013 | Organism | Homo sapiens (Human) | NCBI Taxa ID | 9606 | Lysine Modification | Position | Peptide | Type | References |
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71 | GLLVFVRKSLNSIEF | ubiquitination | [1] | 99 | FLEKMGQKIAPYSVE | ubiquitination | [1, 2] | 108 | APYSVEIKNTCTSVY | ubiquitination | [1, 3, 4, 5] | 117 | TCTSVYTKDRAAKCK | ubiquitination | [1, 2, 4, 5, 6] | 122 | YTKDRAAKCKIPALD | ubiquitination | [1] | 124 | KDRAAKCKIPALDLL | ubiquitination | [1] | 148 | SRLMDEFKIGELFSK | ubiquitination | [1, 2, 4, 5, 7] | 155 | KIGELFSKFYGELAL | ubiquitination | [1, 2, 4, 7] | 163 | FYGELALKKKIPDTV | ubiquitination | [1, 2, 4, 7] | 164 | YGELALKKKIPDTVL | ubiquitination | [1] | 205 | RAFLGELKTQMTSAV | ubiquitination | [1, 2, 3, 4, 7] | 216 | TSAVREPKLPVLAGC | ubiquitination | [1, 5] | 225 | PVLAGCLKGLSSLLC | ubiquitination | [2] | 236 | SLLCNFTKSMEEDPQ | ubiquitination | [1, 4, 5, 6] | 254 | EIFNFVLKAIRPQID | acetylation | [8] | 254 | EIFNFVLKAIRPQID | ubiquitination | [1, 2, 3, 4, 5] | 263 | IRPQIDLKRYAVPSA | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 310 | HTNVELKKAALSALE | ubiquitination | [1, 2, 3] | 329 | QVSNMVAKNAEMHKN | ubiquitination | [2] | 357 | RNVDSNNKELSIAIR | acetylation | [8] | 357 | RNVDSNNKELSIAIR | ubiquitination | [1, 2, 3, 4] | 374 | GLFAGPCKVINAKDV | ubiquitination | [1, 4, 5] | 379 | PCKVINAKDVDFMYV | ubiquitination | [1, 2, 4] | 393 | VELIQRCKQMFLTQT | ubiquitination | [1, 4, 5] | 471 | VFLALAAKGPVLRNC | ubiquitination | [1, 3, 4, 5] | 493 | GLIRICSKPVVLPKG | ubiquitination | [1, 4, 5, 6] | 499 | SKPVVLPKGPESESE | ubiquitination | [1, 5] | 520 | EVRTGKWKVPTYKDY | ubiquitination | [1, 5] | 525 | KWKVPTYKDYVDLFR | ubiquitination | [1, 2, 3, 4, 5, 7] | 574 | EFVKSVLKIVEKLDL | ubiquitination | [1, 2] | 679 | ITVRNAKKIKYFEGV | ubiquitination | [1] | 681 | VRNAKKIKYFEGVSP | acetylation | [9] | 681 | VRNAKKIKYFEGVSP | ubiquitination | [1, 2, 3, 5] | 689 | YFEGVSPKSLKHSPE | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 692 | GVSPKSLKHSPEDPE | ubiquitination | [1, 2, 4, 5] | 700 | HSPEDPEKYSCFALF | ubiquitination | [1] | 712 | ALFVKFGKEVAVKMK | ubiquitination | [1, 2, 5] | 717 | FGKEVAVKMKQYKDE | ubiquitination | [1] | 790 | HVMQPYYKDILPCLD | ubiquitination | [1, 4] | 801 | PCLDGYLKTSALSDE | ubiquitination | [1, 3, 4, 5] | 810 | SALSDETKNNWEVSA | acetylation | [8] | 810 | SALSDETKNNWEVSA | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 824 | ALSRAAQKGFNKVVL | ubiquitination | [1] | 828 | AAQKGFNKVVLKHLK | acetylation | [8] | 828 | AAQKGFNKVVLKHLK | ubiquitination | [1, 5, 6] | 832 | GFNKVVLKHLKKTKN | ubiquitination | [1, 3, 5] | 836 | VVLKHLKKTKNLSSN | ubiquitination | [1] | 838 | LKHLKKTKNLSSNEA | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 868 | SLGGQINKNLLTVTS | ubiquitination | [1, 2, 4, 5, 6, 7] | 881 | TSSDEMMKSYVAWDR | ubiquitination | [1, 2, 4, 5, 7] | 890 | YVAWDREKRLSFAVP | ubiquitination | [1] | 902 | AVPFREMKPVIFLDV | ubiquitination | [1, 2] | 963 | PPMYQLYKRTFPVLL | ubiquitination | [1, 2, 3, 4, 6, 7] | 1038 | RCIREFLKWSIKQIT | ubiquitination | [1, 3] | 1042 | EFLKWSIKQITPQQQ | ubiquitination | [1, 3, 4, 5, 6] | 1051 | ITPQQQEKSPVNTKS | ubiquitination | [1, 2, 5, 6] | 1057 | EKSPVNTKSLFKRLY | acetylation | [8, 9] | 1057 | EKSPVNTKSLFKRLY | ubiquitination | [1, 2, 4, 5, 6, 7] | 1074 | ALHPNAFKRLGASLA | ubiquitination | [1, 3, 4, 5] | 1147 | KKHVSLNKAKKRRLP | ubiquitination | [4, 6] | 1186 | PQTECRHKSIELFYK | ubiquitination | [1, 2, 4, 5] | 1193 | KSIELFYKFVPLLPG | ubiquitination | [1, 2, 4, 7] | 1209 | RSPNLWLKDVLKEEG | acetylation | [9] | 1209 | RSPNLWLKDVLKEEG | ubiquitination | [1, 2, 3, 4, 7] | 1310 | HDIIAAEKCFGTGAA | ubiquitination | [2] | 1333 | GERYNYSKCTVVVRI | ubiquitination | [1, 2, 4, 5, 6] | 1356 | NTSPEGWKLLKKDLC | ubiquitination | [1, 2, 4] | 1359 | PEGWKLLKKDLCNTH | ubiquitination | [1] | 1360 | EGWKLLKKDLCNTHL | ubiquitination | [1] | 1406 | VNLMKALKMSPYKDI | ubiquitination | [1, 2, 7] | 1411 | ALKMSPYKDILETHL | ubiquitination | [1, 2, 3, 4, 5] | 1421 | LETHLREKITAQSIE | ubiquitination | [1, 4, 5, 6] | 1455 | AAVVSACKQLHRAGL | ubiquitination | [1, 2, 4, 5, 6] | 1488 | ELLSLVYKGIAPGDE | ubiquitination | [1, 2, 4, 5] | 1611 | FRERANQKHQGLKLA | ubiquitination | [2] | 1616 | NQKHQGLKLATTILQ | ubiquitination | [1, 4] | 1626 | TTILQHWKKCDSWWA | ubiquitination | [1, 2, 3] | 1627 | TILQHWKKCDSWWAK | ubiquitination | [1, 5] | 1634 | KCDSWWAKDSPLETK | ubiquitination | [1] | 1641 | KDSPLETKMAVLALL | ubiquitination | [1, 2, 4, 7] | 1743 | NNYVDCMKKFLDALE | ubiquitination | [1, 4, 5, 6] | 1744 | NYVDCMKKFLDALEL | ubiquitination | [5] | 1806 | SVYEMFRKDDPRLSF | ubiquitination | [1] | 1856 | VLKSRFTKLNESTFD | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 1868 | TFDTQITKKMGYYKI | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 1869 | FDTQITKKMGYYKIL | ubiquitination | [1, 5] | 1874 | TKKMGYYKILDVMYS | ubiquitination | [1, 2, 3, 4] | 1885 | VMYSRLPKDDVHAKE | ubiquitination | [1] | 1891 | PKDDVHAKESKINQV | ubiquitination | [1, 2, 4] | 1894 | DVHAKESKINQVFHG | ubiquitination | [1, 4, 5, 6] | 1912 | TEGNELTKTLIKLCY | ubiquitination | [1, 3, 4, 5, 6] | 1916 | ELTKTLIKLCYDAFT | ubiquitination | [4, 5] | 1969 | QGFLFSEKPEKNLLI | acetylation | [8, 9] | 1969 | QGFLFSEKPEKNLLI | ubiquitination | [1, 2, 3, 5, 6, 7] | 1972 | LFSEKPEKNLLIFEN | ubiquitination | [3] | 1984 | FENLIDLKRRYNFPV | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 2001 | EVPMERKKKYIEIRK | ubiquitination | [1] | 2002 | VPMERKKKYIEIRKE | ubiquitination | [1] | 2101 | APLTALVKHMHRSLG | ubiquitination | [1, 4, 5] | 2126 | RDLPSWMKFLHGKLG | ubiquitination | [1, 3, 4, 5] | 2131 | WMKFLHGKLGNPIVP | ubiquitination | [1, 3, 4, 5] | 2226 | MKHVFHPKRAVFRHN | ubiquitination | [4] | 2238 | RHNLEIIKTLVECWK | ubiquitination | [1] | 2245 | KTLVECWKDCLSIPY | ubiquitination | [1, 4] | 2258 | PYRLIFEKFSGKDPN | ubiquitination | [1, 2, 3, 5] | 2262 | IFEKFSGKDPNSKDN | ubiquitination | [1, 2] | 2312 | NMSFVRYKEVYAAAA | ubiquitination | [1] | 2333 | LRYVMERKNILEESL | ubiquitination | [1, 5, 6] | 2346 | SLCELVAKQLKQHQN | ubiquitination | [1, 2, 4, 5] | 2349 | ELVAKQLKQHQNTME | ubiquitination | [1, 2, 5] | 2358 | HQNTMEDKFIVCLNK | ubiquitination | [1, 5] | 2365 | KFIVCLNKVTKSFPP | ubiquitination | [1, 5] | 2368 | VCLNKVTKSFPPLAD | ubiquitination | [2, 3, 5] | 2417 | LYFQLKSKDFVQVMR | ubiquitination | [1, 2, 4, 5] | 2432 | HRDDERQKVCLDIIY | ubiquitination | [1, 4, 5] | 2440 | VCLDIIYKMMPKLKP | ubiquitination | [1, 4, 5, 6] | 2444 | IIYKMMPKLKPVELR | ubiquitination | [1, 3, 5] | 2446 | YKMMPKLKPVELREL | ubiquitination | [1, 2, 4, 5] | 2502 | QEIFKLAKDVLIQGL | ubiquitination | [1, 2, 7] | 2682 | DSLLFAHKRSERLQR | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 2693 | RLQRAPLKSVGPDFG | ubiquitination | [1, 2, 3, 5, 6] | 2701 | SVGPDFGKKRLGLPG | ubiquitination | [1, 2, 5] | 2702 | VGPDFGKKRLGLPGD | ubiquitination | [1, 5] | 2714 | PGDEVDNKVKGAAGR | ubiquitination | [1, 2, 4, 5, 6, 7] | 2716 | DEVDNKVKGAAGRTD | ubiquitination | [1, 5, 6] | 2737 | RFMRDQEKLSLMYAR | acetylation | [8] | 2737 | RFMRDQEKLSLMYAR | ubiquitination | [1, 3, 5, 6] | 2754 | VAEQKREKEIKSELK | ubiquitination | [1] | 2757 | QKREKEIKSELKMKQ | ubiquitination | [1, 5] | 2763 | IKSELKMKQDAQVVL | ubiquitination | [1, 2, 4, 5, 6, 7] | 2785 | DLPDIQIKHSSLITP | ubiquitination | [1, 2, 3, 4, 5, 7] | 2805 | QRDPIIAKQLFSSLF | ubiquitination | [2, 3, 4, 7] | 2817 | SLFSGILKEMDKFKT | ubiquitination | [1] | 2823 | LKEMDKFKTLSEKNN | ubiquitination | [5] | 2828 | KFKTLSEKNNITQKL | ubiquitination | [1, 2, 5] | 2834 | EKNNITQKLLQDFNR | ubiquitination | [1, 2, 3, 4, 7] | 2907 | LPAELPAKRVRGKAR | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 2927 | LRWVELAKLYRSIGE | ubiquitination | [1, 2, 3, 4, 6, 7] | 2949 | FTSEIGTKQITQSAL | ubiquitination | [1, 2, 3, 4, 5, 6, 7, 10] | 2969 | SDYSEAAKQYDEALN | acetylation | [8] | 2969 | SDYSEAAKQYDEALN | ubiquitination | [1, 2, 4, 5, 7] | 2977 | QYDEALNKQDWVDGE | ubiquitination | [2, 7] | 3049 | YMIRSKLKLLLQGEA | ubiquitination | [2] | 3066 | SLLTFIDKAMHGELQ | ubiquitination | [1, 2, 7] | 3157 | LSSQVPLKRLLNTWT | ubiquitination | [1, 2, 4, 5, 6, 7] | 3171 | TNRYPDAKMDPMNIW | ubiquitination | [1, 2, 4, 5, 7] | 3191 | NRCFFLSKIEEKLTP | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 3195 | FLSKIEEKLTPLPED | ubiquitination | [1, 2, 4, 5, 7] | 3234 | SSLIRSCKFSMKMKM | ubiquitination | [1, 5] | 3238 | RSCKFSMKMKMIDSA | ubiquitination | [1] | 3240 | CKFSMKMKMIDSARK | acetylation | [5, 9] | 3240 | CKFSMKMKMIDSARK | ubiquitination | [1, 5] | 3247 | KMIDSARKQNNFSLA | ubiquitination | [1, 2, 5, 6] | 3256 | NNFSLAMKLLKELHK | ubiquitination | [1, 3, 4] | 3259 | SLAMKLLKELHKESK | acetylation | [5, 9] | 3259 | SLAMKLLKELHKESK | ubiquitination | [1, 5] | 3263 | KLLKELHKESKTRDD | ubiquitination | [1, 2] | 3301 | EQVLTVLKTVSLLDE | ubiquitination | [1] | 3317 | NVSSYLSKNILAFRD | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 3354 | LAEIEEDKARRILEL | acetylation | [5, 8] | 3354 | LAEIEEDKARRILEL | ubiquitination | [1, 4, 5, 6] | 3371 | SSSEDSEKVIAGLYQ | ubiquitination | [1, 2, 4, 5, 7] | 3425 | FCDQQLRKEEENASV | ubiquitination | [1, 2, 5] | 3448 | YPALVVEKMLKALKL | ubiquitination | [1, 2, 4, 5, 7] | 3451 | LVVEKMLKALKLNSN | ubiquitination | [1] | 3454 | EKMLKALKLNSNEAR | ubiquitination | [1, 2, 5, 6, 7] | 3549 | KDTSTGHKNKEFVAR | ubiquitination | [1] | 3551 | TSTGHKNKEFVARIK | acetylation | [5] | 3551 | TSTGHKNKEFVARIK | ubiquitination | [1, 2, 3, 5] | 3597 | DVRAELAKTPVNKKN | ubiquitination | [1, 5] | 3607 | VNKKNIEKMYERMYA | acetylation | [9] | 3607 | VNKKNIEKMYERMYA | ubiquitination | [1] | 3620 | YAALGDPKAPGLGAF | ubiquitination | [1, 2, 3, 5] | 3630 | GLGAFRRKFIQTFGK | ubiquitination | [1, 5, 6] | 3637 | KFIQTFGKEFDKHFG | acetylation | [8] | 3637 | KFIQTFGKEFDKHFG | ubiquitination | [1, 3] | 3641 | TFGKEFDKHFGKGGS | ubiquitination | [1, 5] | 3645 | EFDKHFGKGGSKLLR | ubiquitination | [1] | 3649 | HFGKGGSKLLRMKLS | ubiquitination | [1] | 3654 | GSKLLRMKLSDFNDI | ubiquitination | [1, 5, 6] | 3668 | ITNMLLLKMNKDSKP | acetylation | [8] | 3668 | ITNMLLLKMNKDSKP | ubiquitination | [1, 2, 3, 4, 7] | 3671 | MLLLKMNKDSKPPGN | ubiquitination | [1] | 3690 | SPWMSDFKVEFLRNE | acetylation | [8] | 3690 | SPWMSDFKVEFLRNE | ubiquitination | [1, 4, 5] | 3709 | GQYDGRGKPLPEYHV | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 3752 | REHPFLVKGGEDLRQ | ubiquitination | [1, 2, 3, 4, 5, 6, 7] | 3808 | RAPPCEYKDWLTKMS | ubiquitination | [1, 3, 4, 5] | 3813 | EYKDWLTKMSGKHDV | ubiquitination | [1, 2, 3, 5, 6, 7] | 3817 | WLTKMSGKHDVGAYM | ubiquitination | [1, 6] | 3828 | GAYMLMYKGANRTET | ubiquitination | [1, 2, 3, 4, 7] | 3845 | SFRKRESKVPADLLK | ubiquitination | [1, 5] | 3852 | KVPADLLKRAFVRMS | ubiquitination | [1, 2, 4, 5, 6, 7] | 3975 | NTMDVFVKEPSFDWK | ubiquitination | [1, 2, 4, 5, 7] | 3982 | KEPSFDWKNFEQKML | ubiquitination | [1, 4] | 3987 | DWKNFEQKMLKKGGS | ubiquitination | [1, 2] | 3991 | FEQKMLKKGGSWIQE | ubiquitination | [1, 2, 6, 7] | 4004 | QEINVAEKNWYPRQK | ubiquitination | [1, 2, 3, 5, 7] | 4011 | KNWYPRQKICYAKRK | ubiquitination | [1] | 4016 | RQKICYAKRKLAGAN | ubiquitination | [1] | 4018 | KICYAKRKLAGANPA | ubiquitination | [1, 5, 6] | 4038 | ELLLGHEKAPAFRDY | ubiquitination | [1, 4, 5, 6] | 4073 | LSEETQVKCLMDQAT | ubiquitination | [1, 4, 6] |
| 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] 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] [4] 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] [5] 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] [6] Methods for quantification of in vivo changes in protein ubiquitination following proteasome and deubiquitinase inhibition. Udeshi ND, Mani DR, Eisenhaure T, Mertins P, Jaffe JD, Clauser KR, Hacohen N, Carr SA. Mol Cell Proteomics. 2012 May;11(5):148-59. [ PMID: 22505724] [7] 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] [8] 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] [9] Proteomic investigations reveal a role for RNA processing factor THRAP3 in the DNA damage response. Beli P, Lukashchuk N, Wagner SA, Weinert BT, Olsen JV, Baskcomb L, Mann M, Jackson SP, Choudhary C. Mol Cell. 2012 Apr 27;46(2):212-25. [ PMID: 22424773] [10] Proteome-wide identification of ubiquitylation sites by conjugation of engineered lysine-less ubiquitin. Oshikawa K, Matsumoto M, Oyamada K, Nakayama KI. J Proteome Res. 2012 Feb 3;11(2):796-807. [ PMID: 22053931] | Functional Description | | Sequence Annotation | | Keyword | ATP-binding; Complete proteome; Kinase; Nucleotide-binding; Reference proteome; Transferase. | Sequence Source | UniProt (SWISSPROT/TrEMBL); GenBank; EMBL | Protein Length | 4096 AA | Protein Sequence | MAGSGAGVRC SLLRLQETLS AADRCGAALA GHQLIRGLGQ ECVLSSSPAV LALQTSLVFS 60 RDFGLLVFVR KSLNSIEFRE CREEILKFLC IFLEKMGQKI APYSVEIKNT CTSVYTKDRA 120 AKCKIPALDL LIKLLQTFRS SRLMDEFKIG ELFSKFYGEL ALKKKIPDTV LEKVYELLGL 180 LGEVHPSEMI NNAENLFRAF LGELKTQMTS AVREPKLPVL AGCLKGLSSL LCNFTKSMEE 240 DPQTSREIFN FVLKAIRPQI DLKRYAVPSA GLRLFALHAS QFSTCLLDNY VSLFEVLLKW 300 CAHTNVELKK AALSALESFL KQVSNMVAKN AEMHKNKLQY FMEQFYGIIR NVDSNNKELS 360 IAIRGYGLFA GPCKVINAKD VDFMYVELIQ RCKQMFLTQT DTGDDRVYQM PSFLQSVASV 420 LLYLDTVPEV YTPVLEHLVV MQIDSFPQYS PKMQLVCCRA IVKVFLALAA KGPVLRNCIS 480 TVVHQGLIRI CSKPVVLPKG PESESEDHRA SGEVRTGKWK VPTYKDYVDL FRHLLSSDQM 540 MDSILADEAF FSVNSSSESL NHLLYDEFVK SVLKIVEKLD LTLEIQTVGE QENGDEAPGV 600 WMIPTSDPAA NLHPAKPKDF SAFINLVEFC REILPEKQAE FFEPWVYSFS YELILQSTRL 660 PLISGFYKLL SITVRNAKKI KYFEGVSPKS LKHSPEDPEK YSCFALFVKF GKEVAVKMKQ 720 YKDELLASCL TFLLSLPHNI IELDVRAYVP ALQMAFKLGL SYTPLAEVGL NALEEWSIYI 780 DRHVMQPYYK DILPCLDGYL KTSALSDETK NNWEVSALSR AAQKGFNKVV LKHLKKTKNL 840 SSNEAISLEE IRIRVVQMLG SLGGQINKNL LTVTSSDEMM KSYVAWDREK RLSFAVPFRE 900 MKPVIFLDVF LPRVTELALT ASDRQTKVAA CELLHSMVMF MLGKATQMPE GGQGAPPMYQ 960 LYKRTFPVLL RLACDVDQVT RQLYEPLVMQ LIHWFTNNKK FESQDTVALL EAILDGIVDP 1020 VDSTLRDFCG RCIREFLKWS IKQITPQQQE KSPVNTKSLF KRLYSLALHP NAFKRLGASL 1080 AFNNIYREFR EEESLVEQFV FEALVIYMES LALAHADEKS LGTIQQCCDA IDHLCRIIEK 1140 KHVSLNKAKK RRLPRGFPPS ASLCLLDLVK WLLAHCGRPQ TECRHKSIEL FYKFVPLLPG 1200 NRSPNLWLKD VLKEEGVSFL INTFEGGGCG QPSGILAQPT LLYRGPFSLQ ATLCWLDLLL 1260 AALECYNTFI GERTVGALQV LGTEAQSSLL KAVAFFLESI AMHDIIAAEK CFGTGAAGNR 1320 TSPQEGERYN YSKCTVVVRI MEFTTTLLNT SPEGWKLLKK DLCNTHLMRV LVQTLCEPAS 1380 IGFNIGDVQV MAHLPDVCVN LMKALKMSPY KDILETHLRE KITAQSIEEL CAVNLYGPDA 1440 QVDRSRLAAV VSACKQLHRA GLLHNILPSQ STDLHHSVGT ELLSLVYKGI APGDERQCLP 1500 SLDLSCKQLA SGLLELAFAF GGLCERLVSL LLNPAVLSTA SLGSSQGSVI HFSHGEYFYS 1560 LFSETINTEL LKNLDLAVLE LMQSSVDNTK MVSAVLNGML DQSFRERANQ KHQGLKLATT 1620 ILQHWKKCDS WWAKDSPLET KMAVLALLAK ILQIDSSVSF NTSHGSFPEV FTTYISLLAD 1680 TKLDLHLKGQ AVTLLPFFTS LTGGSLEELR RVLEQLIVAH FPMQSREFPP GTPRFNNYVD 1740 CMKKFLDALE LSQSPMLLEL MTEVLCREQQ HVMEELFQSS FRRIARRGSC VTQVGLLESV 1800 YEMFRKDDPR LSFTRQSFVD RSLLTLLWHC SLDALREFFS TIVVDAIDVL KSRFTKLNES 1860 TFDTQITKKM GYYKILDVMY SRLPKDDVHA KESKINQVFH GSCITEGNEL TKTLIKLCYD 1920 AFTENMAGEN QLLERRRLYH CAAYNCAISV ICCVFNELKF YQGFLFSEKP EKNLLIFENL 1980 IDLKRRYNFP VEVEVPMERK KKYIEIRKEA REAANGDSDG PSYMSSLSYL ADSTLSEEMS 2040 QFDFSTGVQS YSYSSQDPRP ATGRFRRREQ RDPTVHDDVL ELEMDELNRH ECMAPLTALV 2100 KHMHRSLGPP QGEEDSVPRD LPSWMKFLHG KLGNPIVPLN IRLFLAKLVI NTEEVFRPYA 2160 KHWLSPLLQL AASENNGGEG IHYMVVEIVA TILSWTGLAT PTGVPKDEVL ANRLLNFLMK 2220 HVFHPKRAVF RHNLEIIKTL VECWKDCLSI PYRLIFEKFS GKDPNSKDNS VGIQLLGIVM 2280 ANDLPPYDPQ CGIQSSEYFQ ALVNNMSFVR YKEVYAAAAE VLGLILRYVM ERKNILEESL 2340 CELVAKQLKQ HQNTMEDKFI VCLNKVTKSF PPLADRFMNA VFFLLPKFHG VLKTLCLEVV 2400 LCRVEGMTEL YFQLKSKDFV QVMRHRDDER QKVCLDIIYK MMPKLKPVEL RELLNPVVEF 2460 VSHPSTTCRE QMYNILMWIH DNYRDPESET DNDSQEIFKL AKDVLIQGLI DENPGLQLII 2520 RNFWSHETRL PSNTLDRLLA LNSLYSPKIE VHFLSLATNF LLEMTSMSPD YPNPMFEHPL 2580 SECEFQEYTI DSDWRFRSTV LTPMFVETQA SQGTLQTRTQ EGSLSARWPV AGQIRATQQQ 2640 HDFTLTQTAD GRSSFDWLTG SSTDPLVDHT SPSSDSLLFA HKRSERLQRA PLKSVGPDFG 2700 KKRLGLPGDE VDNKVKGAAG RTDLLRLRRR FMRDQEKLSL MYARKGVAEQ KREKEIKSEL 2760 KMKQDAQVVL YRSYRHGDLP DIQIKHSSLI TPLQAVAQRD PIIAKQLFSS LFSGILKEMD 2820 KFKTLSEKNN ITQKLLQDFN RFLNTTFSFF PPFVSCIQDI SCQHAALLSL DPAAVSAGCL 2880 ASLQQPVGIR LLEEALLRLL PAELPAKRVR GKARLPPDVL RWVELAKLYR SIGEYDVLRG 2940 IFTSEIGTKQ ITQSALLAEA RSDYSEAAKQ YDEALNKQDW VDGEPTEAEK DFWELASLDC 3000 YNHLAEWKSL EYCSTASIDS ENPPDLNKIW SEPFYQETYL PYMIRSKLKL LLQGEADQSL 3060 LTFIDKAMHG ELQKAILELH YSQELSLLYL LQDDVDRAKY YIQNGIQSFM QNYSSIDVLL 3120 HQSRLTKLQS VQALTEIQEF ISFISKQGNL SSQVPLKRLL NTWTNRYPDA KMDPMNIWDD 3180 IITNRCFFLS KIEEKLTPLP EDNSMNVDQD GDPSDRMEVQ EQEEDISSLI RSCKFSMKMK 3240 MIDSARKQNN FSLAMKLLKE LHKESKTRDD WLVSWVQSYC RLSHCRSRSQ GCSEQVLTVL 3300 KTVSLLDENN VSSYLSKNIL AFRDQNILLG TTYRIIANAL SSEPACLAEI EEDKARRILE 3360 LSGSSSEDSE KVIAGLYQRA FQHLSEAVQA AEEEAQPPSW SCGPAAGVID AYMTLADFCD 3420 QQLRKEEENA SVIDSAELQA YPALVVEKML KALKLNSNEA RLKFPRLLQI IERYPEETLS 3480 LMTKEISSVP CWQFISWISH MVALLDKDQA VAVQHSVEEI TDNYPQAIVY PFIISSESYS 3540 FKDTSTGHKN KEFVARIKSK LDQGGVIQDF INALDQLSNP ELLFKDWSND VRAELAKTPV 3600 NKKNIEKMYE RMYAALGDPK APGLGAFRRK FIQTFGKEFD KHFGKGGSKL LRMKLSDFND 3660 ITNMLLLKMN KDSKPPGNLK ECSPWMSDFK VEFLRNELEI PGQYDGRGKP LPEYHVRIAG 3720 FDERVTVMAS LRRPKRIIIR GHDEREHPFL VKGGEDLRQD QRVEQLFQVM NGILAQDSAC 3780 SQRALQLRTY SVVPMTSSDP RAPPCEYKDW LTKMSGKHDV GAYMLMYKGA NRTETVTSFR 3840 KRESKVPADL LKRAFVRMST SPEAFLALRS HFASSHALIC ISHWILGIGD RHLNNFMVAM 3900 ETGGVIGIDF GHAFGSATQF LPVPELMPFR LTRQFINLML PMKETGLMYS IMVHALRAFR 3960 SDPGLLTNTM DVFVKEPSFD WKNFEQKMLK KGGSWIQEIN VAEKNWYPRQ KICYAKRKLA 4020 GANPAVITCD ELLLGHEKAP AFRDYVAVAR GSKDHNIRAQ EPESGLSEET QVKCLMDQAT 4080 DPNILGRTWE GWEPWM 4096 | Gene Ontology | GO:0005634; C:nucleus; IEA:InterPro. GO:0005524; F:ATP binding; IEA:UniProtKB-KW. GO:0003677; F:DNA binding; IEA:InterPro. GO:0004677; F:DNA-dependent protein kinase activity; IEA:InterPro. GO:0006303; P:double-strand break repair via nonhomologous end joining; IEA:InterPro. | Interpro | | Pfam | | SMART | | PROSITE | | PRINTS | |
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