Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QFY1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006283 | transcription-coupled nucleotide-excision repair | 7 | 2 |
GO:0006289 | nucleotide-excision repair | 6 | 2 |
GO:0006304 | DNA modification | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0070580 | base J metabolic process | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 4 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 5 |
GO:0005488 | binding | 1 | 12 |
GO:0005506 | iron ion binding | 6 | 2 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0008198 | ferrous iron binding | 7 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 4 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 12 |
GO:0016706 | 2-oxoglutarate-dependent dioxygenase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 4 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 4 |
GO:0016887 | ATP hydrolysis activity | 7 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 2 |
GO:0050341 | thymine dioxygenase activity | 5 | 12 |
GO:0051213 | dioxygenase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.589 |
CLV_C14_Caspase3-7 | 883 | 887 | PF00656 | 0.425 |
CLV_NRD_NRD_1 | 1004 | 1006 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 1007 | 1009 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 1030 | 1032 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 1065 | 1067 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 668 | 670 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 907 | 909 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 949 | 951 | PF00675 | 0.233 |
CLV_PCSK_FUR_1 | 669 | 673 | PF00082 | 0.278 |
CLV_PCSK_FUR_1 | 947 | 951 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 1004 | 1006 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 1065 | 1067 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 947 | 949 | PF00082 | 0.235 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 671 | 673 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 738 | 740 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 1009 | 1013 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 1023 | 1027 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 1032 | 1036 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 1037 | 1041 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 1046 | 1050 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 1082 | 1086 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 927 | 931 | PF00082 | 0.242 |
DEG_APCC_DBOX_1 | 421 | 429 | PF00400 | 0.442 |
DEG_APCC_DBOX_1 | 499 | 507 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 700 | 708 | PF00400 | 0.552 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.615 |
DEG_ODPH_VHL_1 | 378 | 390 | PF01847 | 0.478 |
DEG_ODPH_VHL_1 | 543 | 555 | PF01847 | 0.467 |
DEG_SPOP_SBC_1 | 8 | 12 | PF00917 | 0.434 |
DOC_CKS1_1 | 596 | 601 | PF01111 | 0.522 |
DOC_CYCLIN_RxL_1 | 109 | 119 | PF00134 | 0.606 |
DOC_CYCLIN_RxL_1 | 120 | 129 | PF00134 | 0.250 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 701 | 708 | PF00134 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.384 |
DOC_MAPK_DCC_7 | 538 | 548 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 1004 | 1013 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 443 | 453 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 499 | 508 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 649 | 657 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 668 | 679 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 699 | 708 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 894 | 903 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 908 | 915 | PF00069 | 0.404 |
DOC_MAPK_HePTP_8 | 891 | 903 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 574 | 583 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 671 | 679 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 699 | 708 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 894 | 903 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 959 | 966 | PF00069 | 0.487 |
DOC_MAPK_NFAT4_5 | 959 | 967 | PF00069 | 0.522 |
DOC_MAPK_RevD_3 | 895 | 909 | PF00069 | 0.474 |
DOC_PP1_RVXF_1 | 121 | 128 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 720 | 727 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 909 | 916 | PF00149 | 0.431 |
DOC_PP2B_LxvP_1 | 319 | 322 | PF13499 | 0.519 |
DOC_PP2B_LxvP_1 | 533 | 536 | PF13499 | 0.350 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.398 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.492 |
DOC_USP7_UBL2_3 | 369 | 373 | PF12436 | 0.478 |
DOC_USP7_UBL2_3 | 443 | 447 | PF12436 | 0.442 |
DOC_USP7_UBL2_3 | 645 | 649 | PF12436 | 0.431 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 1008 | 1014 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 1015 | 1024 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 479 | 483 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 517 | 522 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 538 | 546 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 7 | 17 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 80 | 87 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 859 | 868 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 927 | 934 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 93 | 97 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 438 | 454 | PF00022 | 0.510 |
LIG_Actin_WH2_2 | 690 | 707 | PF00022 | 0.478 |
LIG_APCC_ABBA_1 | 183 | 188 | PF00400 | 0.548 |
LIG_APCC_ABBA_1 | 67 | 72 | PF00400 | 0.336 |
LIG_APCC_ABBAyCdc20_2 | 275 | 281 | PF00400 | 0.466 |
LIG_APCC_ABBAyCdc20_2 | 411 | 417 | PF00400 | 0.442 |
LIG_APCC_ABBAyCdc20_2 | 773 | 779 | PF00400 | 0.535 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.689 |
LIG_BRCT_BRCA1_1 | 630 | 634 | PF00533 | 0.442 |
LIG_BRCT_BRCA1_2 | 225 | 231 | PF00533 | 0.580 |
LIG_deltaCOP1_diTrp_1 | 770 | 777 | PF00928 | 0.431 |
LIG_eIF4E_1 | 485 | 491 | PF01652 | 0.328 |
LIG_EVH1_2 | 736 | 740 | PF00568 | 0.474 |
LIG_FHA_1 | 1028 | 1034 | PF00498 | 0.381 |
LIG_FHA_1 | 1079 | 1085 | PF00498 | 0.435 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.549 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.432 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.431 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.552 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.371 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.515 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.442 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.478 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.531 |
LIG_FHA_1 | 868 | 874 | PF00498 | 0.486 |
LIG_FHA_1 | 934 | 940 | PF00498 | 0.478 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.632 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.393 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.595 |
LIG_GBD_Chelix_1 | 482 | 490 | PF00786 | 0.325 |
LIG_Integrin_RGD_1 | 418 | 420 | PF01839 | 0.225 |
LIG_IRF3_LxIS_1 | 147 | 152 | PF10401 | 0.508 |
LIG_LIR_Apic_2 | 584 | 590 | PF02991 | 0.384 |
LIG_LIR_Apic_2 | 987 | 992 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 263 | 272 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 372 | 381 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 399 | 406 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 580 | 590 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 839 | 846 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 874 | 880 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 886 | 895 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 1012 | 1017 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 718 | 724 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 789 | 793 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 874 | 879 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 886 | 891 | PF02991 | 0.267 |
LIG_NRBOX | 507 | 513 | PF00104 | 0.481 |
LIG_PCNA_yPIPBox_3 | 443 | 457 | PF02747 | 0.511 |
LIG_PCNA_yPIPBox_3 | 722 | 735 | PF02747 | 0.474 |
LIG_PCNA_yPIPBox_3 | 882 | 896 | PF02747 | 0.464 |
LIG_Pex14_1 | 771 | 775 | PF04695 | 0.431 |
LIG_Pex14_2 | 666 | 670 | PF04695 | 0.478 |
LIG_Pex14_2 | 986 | 990 | PF04695 | 0.498 |
LIG_PTB_Apo_2 | 429 | 436 | PF02174 | 0.535 |
LIG_PTB_Apo_2 | 656 | 663 | PF02174 | 0.442 |
LIG_PTB_Apo_2 | 91 | 98 | PF02174 | 0.454 |
LIG_PTB_Phospho_1 | 656 | 662 | PF10480 | 0.442 |
LIG_PTB_Phospho_1 | 91 | 97 | PF10480 | 0.434 |
LIG_SH2_CRK | 1014 | 1018 | PF00017 | 0.442 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.463 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.542 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.427 |
LIG_SH2_CRK | 721 | 725 | PF00017 | 0.442 |
LIG_SH2_CRK | 759 | 763 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 876 | 879 | PF00017 | 0.365 |
LIG_SH2_SRC | 1090 | 1093 | PF00017 | 0.523 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 803 | 807 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 1088 | 1091 | PF00017 | 0.508 |
LIG_SH2_STAT3 | 130 | 133 | PF00017 | 0.466 |
LIG_SH2_STAT3 | 641 | 644 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 790 | 793 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 834 | 837 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 876 | 879 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 918 | 921 | PF00017 | 0.451 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.481 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.478 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.507 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.500 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.467 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.290 |
LIG_SH3_3 | 731 | 737 | PF00018 | 0.477 |
LIG_SH3_5 | 786 | 790 | PF00018 | 0.442 |
LIG_Sin3_3 | 306 | 313 | PF02671 | 0.505 |
LIG_SUMO_SIM_anti_2 | 15 | 24 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 26 | 33 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 593 | 598 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 960 | 968 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 138 | 144 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 575 | 580 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 593 | 598 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 674 | 682 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 960 | 968 | PF11976 | 0.542 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.633 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.547 |
LIG_TRAF2_1 | 951 | 954 | PF00917 | 0.522 |
LIG_TYR_ITSM | 1010 | 1017 | PF00017 | 0.463 |
LIG_UBA3_1 | 367 | 373 | PF00899 | 0.362 |
LIG_UBA3_1 | 594 | 600 | PF00899 | 0.360 |
LIG_UBA3_1 | 961 | 969 | PF00899 | 0.287 |
LIG_WRC_WIRS_1 | 257 | 262 | PF05994 | 0.562 |
LIG_WRC_WIRS_1 | 934 | 939 | PF05994 | 0.350 |
MOD_CDC14_SPxK_1 | 152 | 155 | PF00782 | 0.505 |
MOD_CDK_SPK_2 | 595 | 600 | PF00069 | 0.360 |
MOD_CDK_SPxK_1 | 149 | 155 | PF00069 | 0.500 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.525 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.266 |
MOD_CK1_1 | 841 | 847 | PF00069 | 0.579 |
MOD_CK1_1 | 855 | 861 | PF00069 | 0.643 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.476 |
MOD_CK2_1 | 1015 | 1021 | PF00069 | 0.345 |
MOD_CK2_1 | 1090 | 1096 | PF00069 | 0.449 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.509 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.666 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.285 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.773 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.573 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.354 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.589 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.536 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.558 |
MOD_GlcNHglycan | 1017 | 1020 | PF01048 | 0.397 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.620 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.627 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.529 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.431 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.284 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.427 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.297 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.285 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.557 |
MOD_GlcNHglycan | 890 | 894 | PF01048 | 0.313 |
MOD_GSK3_1 | 1090 | 1097 | PF00069 | 0.545 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.634 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.681 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.661 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.650 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.529 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.279 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.278 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.432 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.435 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.309 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.360 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.554 |
MOD_N-GLC_1 | 855 | 860 | PF02516 | 0.556 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.553 |
MOD_NEK2_1 | 1072 | 1077 | PF00069 | 0.347 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.266 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.321 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.442 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.275 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.283 |
MOD_NEK2_1 | 809 | 814 | PF00069 | 0.582 |
MOD_NEK2_1 | 854 | 859 | PF00069 | 0.529 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.461 |
MOD_NEK2_1 | 964 | 969 | PF00069 | 0.266 |
MOD_NEK2_1 | 975 | 980 | PF00069 | 0.266 |
MOD_NEK2_1 | 985 | 990 | PF00069 | 0.254 |
MOD_NEK2_2 | 1090 | 1095 | PF00069 | 0.525 |
MOD_NEK2_2 | 299 | 304 | PF00069 | 0.432 |
MOD_NEK2_2 | 935 | 940 | PF00069 | 0.411 |
MOD_PIKK_1 | 1025 | 1031 | PF00454 | 0.361 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.496 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.287 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.398 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.411 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.374 |
MOD_PIKK_1 | 581 | 587 | PF00454 | 0.287 |
MOD_PIKK_1 | 860 | 866 | PF00454 | 0.591 |
MOD_PIKK_1 | 918 | 924 | PF00454 | 0.285 |
MOD_PIKK_1 | 941 | 947 | PF00454 | 0.411 |
MOD_PKA_2 | 1042 | 1048 | PF00069 | 0.510 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.509 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.266 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.299 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.485 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.417 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.550 |
MOD_PKA_2 | 860 | 866 | PF00069 | 0.577 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.440 |
MOD_PKA_2 | 941 | 947 | PF00069 | 0.301 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.725 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.623 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.348 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.440 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.424 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.352 |
MOD_Plk_2-3 | 138 | 144 | PF00069 | 0.385 |
MOD_Plk_2-3 | 263 | 269 | PF00069 | 0.367 |
MOD_Plk_4 | 1009 | 1015 | PF00069 | 0.376 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.361 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.383 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.711 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.462 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.281 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.421 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.333 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.308 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.444 |
MOD_Plk_4 | 841 | 847 | PF00069 | 0.501 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.414 |
MOD_Plk_4 | 985 | 991 | PF00069 | 0.266 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.551 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.696 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.543 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.376 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.393 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.331 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.266 |
MOD_SUMO_rev_2 | 1018 | 1025 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 798 | 807 | PF00179 | 0.322 |
MOD_SUMO_rev_2 | 954 | 961 | PF00179 | 0.364 |
TRG_DiLeu_BaEn_1 | 719 | 724 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_1 | 957 | 962 | PF01217 | 0.287 |
TRG_DiLeu_BaEn_4 | 804 | 810 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 1012 | 1017 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 159 | 164 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 502 | 507 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 1014 | 1017 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 721 | 724 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 759 | 762 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 790 | 793 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 834 | 837 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 842 | 845 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 876 | 879 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 1003 | 1005 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 667 | 669 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 859 | 862 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 939 | 942 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 947 | 950 | PF00400 | 0.258 |
TRG_NES_CRM1_1 | 864 | 874 | PF08389 | 0.463 |
TRG_NLS_MonoExtC_3 | 442 | 447 | PF00514 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 505 | 509 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 896 | 900 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5A7 | Leptomonas seymouri | 68% | 100% |
A0A0S4IUR7 | Bodo saltans | 39% | 100% |
A0A1X0NNS9 | Trypanosomatidae | 48% | 100% |
A0A3R7NZA3 | Trypanosoma rangeli | 47% | 100% |
A0A3S7WSQ7 | Leishmania donovani | 97% | 100% |
A4H7G5 | Leishmania braziliensis | 90% | 100% |
A4HVU6 | Leishmania infantum | 97% | 100% |
B6EU02 | Leishmania tarentolae | 94% | 100% |
C9ZT80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9APJ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4DCH3 | Trypanosoma cruzi (strain CL Brener) | 48% | 100% |
Q4QFY1 | Leishmania major | 100% | 100% |
Q57X81 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 44% | 100% |
V5BHQ6 | Trypanosoma cruzi | 48% | 100% |