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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QAQ7
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 2 |
GO:0000725 | recombinational repair | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0007131 | reciprocal meiotic recombination | 3 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0035825 | homologous recombination | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0045003 | double-strand break repair via synthesis-dependent strand annealing | 8 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0140527 | reciprocal homologous recombination | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0015616 | DNA translocase activity | 3 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0051213 | dioxygenase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1058 | 1062 | PF00656 | 0.445 |
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 1006 | 1008 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.205 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.205 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.205 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.205 |
CLV_NRD_NRD_1 | 759 | 761 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.645 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.205 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 848 | 850 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 848 | 850 | PF00082 | 0.239 |
CLV_PCSK_PC7_1 | 410 | 416 | PF00082 | 0.407 |
CLV_PCSK_PC7_1 | 667 | 673 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 1078 | 1082 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 627 | 631 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 667 | 671 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 884 | 888 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 911 | 915 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 959 | 963 | PF00082 | 0.342 |
DEG_MDM2_SWIB_1 | 48 | 55 | PF02201 | 0.601 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.631 |
DOC_ANK_TNKS_1 | 538 | 545 | PF00023 | 0.405 |
DOC_CKS1_1 | 498 | 503 | PF01111 | 0.405 |
DOC_MAPK_gen_1 | 340 | 348 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 402 | 409 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 420 | 427 | PF00069 | 0.310 |
DOC_MAPK_gen_1 | 434 | 443 | PF00069 | 0.271 |
DOC_MAPK_gen_1 | 655 | 663 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 723 | 731 | PF00069 | 0.405 |
DOC_MAPK_JIP1_4 | 782 | 788 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 241 | 249 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 420 | 427 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 436 | 445 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 684 | 693 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 793 | 801 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 871 | 879 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 227 | 233 | PF00149 | 0.491 |
DOC_PP1_RVXF_1 | 882 | 889 | PF00149 | 0.405 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.589 |
DOC_PP4_FxxP_1 | 374 | 377 | PF00568 | 0.610 |
DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.656 |
DOC_PP4_FxxP_1 | 618 | 621 | PF00568 | 0.405 |
DOC_PP4_FxxP_1 | 634 | 637 | PF00568 | 0.405 |
DOC_PP4_FxxP_1 | 856 | 859 | PF00568 | 0.427 |
DOC_USP7_MATH_1 | 1031 | 1035 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 1068 | 1072 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 746 | 750 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 766 | 770 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 983 | 987 | PF00917 | 0.583 |
DOC_USP7_UBL2_3 | 292 | 296 | PF12436 | 0.377 |
DOC_USP7_UBL2_3 | 959 | 963 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 711 | 716 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 841 | 846 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 1027 | 1035 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 659 | 664 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 917 | 924 | PF00244 | 0.289 |
LIG_Actin_WH2_2 | 469 | 486 | PF00022 | 0.418 |
LIG_Actin_WH2_2 | 551 | 567 | PF00022 | 0.405 |
LIG_APCC_ABBA_1 | 729 | 734 | PF00400 | 0.454 |
LIG_BIR_III_2 | 211 | 215 | PF00653 | 0.650 |
LIG_BRCT_BRCA1_1 | 1052 | 1056 | PF00533 | 0.321 |
LIG_BRCT_BRCA1_1 | 310 | 314 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.569 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.589 |
LIG_Clathr_ClatBox_1 | 168 | 172 | PF01394 | 0.659 |
LIG_Clathr_ClatBox_1 | 885 | 889 | PF01394 | 0.405 |
LIG_CtBP_PxDLS_1 | 637 | 641 | PF00389 | 0.499 |
LIG_FHA_1 | 1039 | 1045 | PF00498 | 0.424 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.706 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.662 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.408 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.379 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.579 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.516 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.405 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.405 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.405 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.452 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.626 |
LIG_FHA_1 | 818 | 824 | PF00498 | 0.405 |
LIG_FHA_1 | 919 | 925 | PF00498 | 0.292 |
LIG_FHA_1 | 970 | 976 | PF00498 | 0.319 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.530 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.661 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.618 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.510 |
LIG_FHA_2 | 921 | 927 | PF00498 | 0.417 |
LIG_FHA_2 | 952 | 958 | PF00498 | 0.406 |
LIG_FHA_2 | 966 | 972 | PF00498 | 0.328 |
LIG_FHA_2 | 977 | 983 | PF00498 | 0.397 |
LIG_LIR_Apic_2 | 125 | 129 | PF02991 | 0.553 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.633 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.535 |
LIG_LIR_Apic_2 | 59 | 63 | PF02991 | 0.664 |
LIG_LIR_Apic_2 | 678 | 683 | PF02991 | 0.405 |
LIG_LIR_Apic_2 | 854 | 859 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 355 | 363 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 550 | 558 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 610 | 619 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 628 | 638 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 688 | 695 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 698 | 708 | PF02991 | 0.405 |
LIG_LIR_LC3C_4 | 566 | 571 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 550 | 554 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 628 | 633 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 688 | 693 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 854 | 858 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.638 |
LIG_LYPXL_S_1 | 96 | 100 | PF13949 | 0.641 |
LIG_LYPXL_yS_3 | 97 | 100 | PF13949 | 0.642 |
LIG_Pex14_1 | 508 | 512 | PF04695 | 0.405 |
LIG_Pex14_2 | 48 | 52 | PF04695 | 0.598 |
LIG_Pex14_2 | 630 | 634 | PF04695 | 0.405 |
LIG_Pex14_2 | 888 | 892 | PF04695 | 0.405 |
LIG_PTB_Apo_2 | 54 | 61 | PF02174 | 0.491 |
LIG_PTB_Apo_2 | 9 | 16 | PF02174 | 0.640 |
LIG_Rb_pABgroove_1 | 441 | 449 | PF01858 | 0.283 |
LIG_REV1ctd_RIR_1 | 312 | 321 | PF16727 | 0.381 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.493 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.508 |
LIG_SH2_CRK | 480 | 484 | PF00017 | 0.405 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.405 |
LIG_SH2_CRK | 701 | 705 | PF00017 | 0.459 |
LIG_SH2_CRK | 916 | 920 | PF00017 | 0.270 |
LIG_SH2_GRB2like | 855 | 858 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 260 | 264 | PF00017 | 0.376 |
LIG_SH2_SRC | 680 | 683 | PF00017 | 0.405 |
LIG_SH2_STAT3 | 929 | 932 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 837 | 840 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 855 | 858 | PF00017 | 0.519 |
LIG_SH3_1 | 179 | 185 | PF00018 | 0.604 |
LIG_SH3_1 | 270 | 276 | PF00018 | 0.444 |
LIG_SH3_1 | 32 | 38 | PF00018 | 0.552 |
LIG_SH3_2 | 273 | 278 | PF14604 | 0.436 |
LIG_SH3_3 | 1006 | 1012 | PF00018 | 0.669 |
LIG_SH3_3 | 1062 | 1068 | PF00018 | 0.432 |
LIG_SH3_3 | 1073 | 1079 | PF00018 | 0.590 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.686 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.466 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.444 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.681 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.317 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.418 |
LIG_SH3_3 | 641 | 647 | PF00018 | 0.405 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.667 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 1104 | 1114 | PF11976 | 0.696 |
LIG_SUMO_SIM_anti_2 | 297 | 302 | PF11976 | 0.313 |
LIG_SUMO_SIM_anti_2 | 545 | 550 | PF11976 | 0.405 |
LIG_SUMO_SIM_anti_2 | 566 | 571 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 714 | 720 | PF11976 | 0.428 |
LIG_SUMO_SIM_anti_2 | 811 | 817 | PF11976 | 0.405 |
LIG_SUMO_SIM_anti_2 | 822 | 827 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 246 | 253 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 297 | 302 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 545 | 550 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 714 | 720 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 811 | 817 | PF11976 | 0.405 |
LIG_TRAF2_1 | 1080 | 1083 | PF00917 | 0.685 |
LIG_TRAF2_1 | 1121 | 1124 | PF00917 | 0.716 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.520 |
LIG_TRAF2_1 | 923 | 926 | PF00917 | 0.298 |
LIG_TRAF2_1 | 954 | 957 | PF00917 | 0.401 |
LIG_TYR_ITIM | 258 | 263 | PF00017 | 0.289 |
LIG_TYR_ITIM | 549 | 554 | PF00017 | 0.242 |
LIG_TYR_ITIM | 699 | 704 | PF00017 | 0.298 |
LIG_TYR_ITIM | 835 | 840 | PF00017 | 0.401 |
LIG_TYR_ITIM | 853 | 858 | PF00017 | 0.374 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.639 |
LIG_UBA3_1 | 718 | 724 | PF00899 | 0.242 |
LIG_UBA3_1 | 825 | 833 | PF00899 | 0.374 |
LIG_WRC_WIRS_1 | 1032 | 1037 | PF05994 | 0.599 |
LIG_WRC_WIRS_1 | 1051 | 1056 | PF05994 | 0.203 |
MOD_CDK_SPK_2 | 527 | 532 | PF00069 | 0.242 |
MOD_CDK_SPxK_1 | 841 | 847 | PF00069 | 0.374 |
MOD_CDK_SPxxK_3 | 22 | 29 | PF00069 | 0.508 |
MOD_CDK_SPxxK_3 | 222 | 229 | PF00069 | 0.543 |
MOD_CDK_SPxxK_3 | 841 | 848 | PF00069 | 0.374 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.579 |
MOD_CK1_1 | 1050 | 1056 | PF00069 | 0.435 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.709 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.624 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.522 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.242 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.690 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.251 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.705 |
MOD_CK1_1 | 817 | 823 | PF00069 | 0.242 |
MOD_CK1_1 | 920 | 926 | PF00069 | 0.296 |
MOD_CK1_1 | 986 | 992 | PF00069 | 0.501 |
MOD_CK2_1 | 1098 | 1104 | PF00069 | 0.575 |
MOD_CK2_1 | 1118 | 1124 | PF00069 | 0.449 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.615 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.552 |
MOD_CK2_1 | 672 | 678 | PF00069 | 0.242 |
MOD_CK2_1 | 920 | 926 | PF00069 | 0.296 |
MOD_CK2_1 | 951 | 957 | PF00069 | 0.420 |
MOD_CK2_1 | 976 | 982 | PF00069 | 0.412 |
MOD_Cter_Amidation | 418 | 421 | PF01082 | 0.526 |
MOD_Cter_Amidation | 756 | 759 | PF01082 | 0.692 |
MOD_GlcNHglycan | 1015 | 1018 | PF01048 | 0.489 |
MOD_GlcNHglycan | 1029 | 1032 | PF01048 | 0.388 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.634 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.674 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.709 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.443 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.584 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.346 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.541 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.355 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.242 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.711 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.585 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.293 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.202 |
MOD_GlcNHglycan | 744 | 747 | PF01048 | 0.577 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.634 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.622 |
MOD_GlcNHglycan | 938 | 941 | PF01048 | 0.439 |
MOD_GlcNHglycan | 989 | 992 | PF01048 | 0.500 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.691 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.485 |
MOD_GSK3_1 | 1027 | 1034 | PF00069 | 0.563 |
MOD_GSK3_1 | 1119 | 1126 | PF00069 | 0.650 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.704 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.707 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.466 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.560 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.540 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.226 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.668 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.242 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.311 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.596 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.611 |
MOD_GSK3_1 | 965 | 972 | PF00069 | 0.332 |
MOD_GSK3_1 | 983 | 990 | PF00069 | 0.480 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.644 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.623 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.494 |
MOD_N-GLC_1 | 676 | 681 | PF02516 | 0.289 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.513 |
MOD_N-GLC_1 | 817 | 822 | PF02516 | 0.242 |
MOD_N-GLC_2 | 507 | 509 | PF02516 | 0.242 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.597 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.349 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.537 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.242 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.242 |
MOD_NEK2_1 | 829 | 834 | PF00069 | 0.287 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.274 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.242 |
MOD_NEK2_1 | 918 | 923 | PF00069 | 0.290 |
MOD_NEK2_1 | 976 | 981 | PF00069 | 0.382 |
MOD_NEK2_1 | 987 | 992 | PF00069 | 0.483 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.697 |
MOD_PIKK_1 | 1089 | 1095 | PF00454 | 0.522 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.671 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.591 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.242 |
MOD_PIKK_1 | 670 | 676 | PF00454 | 0.242 |
MOD_PIKK_1 | 766 | 772 | PF00454 | 0.663 |
MOD_PIKK_1 | 817 | 823 | PF00454 | 0.242 |
MOD_PIKK_1 | 858 | 864 | PF00454 | 0.242 |
MOD_PK_1 | 241 | 247 | PF00069 | 0.492 |
MOD_PK_1 | 286 | 292 | PF00069 | 0.413 |
MOD_PK_1 | 421 | 427 | PF00069 | 0.460 |
MOD_PK_1 | 659 | 665 | PF00069 | 0.279 |
MOD_PK_1 | 672 | 678 | PF00069 | 0.225 |
MOD_PKA_1 | 1013 | 1019 | PF00069 | 0.536 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.571 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.708 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.242 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.242 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.614 |
MOD_PKA_2 | 991 | 997 | PF00069 | 0.579 |
MOD_PKB_1 | 657 | 665 | PF00069 | 0.173 |
MOD_PKB_1 | 758 | 766 | PF00069 | 0.628 |
MOD_Plk_1 | 1084 | 1090 | PF00069 | 0.713 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.619 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.242 |
MOD_Plk_1 | 685 | 691 | PF00069 | 0.242 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.756 |
MOD_Plk_2-3 | 152 | 158 | PF00069 | 0.693 |
MOD_Plk_4 | 1047 | 1053 | PF00069 | 0.371 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.405 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.301 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.569 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.344 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.242 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.242 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.391 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.141 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.242 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.361 |
MOD_Plk_4 | 795 | 801 | PF00069 | 0.295 |
MOD_Plk_4 | 957 | 963 | PF00069 | 0.481 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.630 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.439 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.242 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.242 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.242 |
MOD_ProDKin_1 | 711 | 717 | PF00069 | 0.314 |
MOD_ProDKin_1 | 841 | 847 | PF00069 | 0.374 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.632 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.648 |
MOD_SUMO_for_1 | 277 | 280 | PF00179 | 0.435 |
MOD_SUMO_for_1 | 329 | 332 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 1016 | 1025 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 22 | 31 | PF00179 | 0.641 |
MOD_SUMO_rev_2 | 321 | 329 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 332 | 341 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 920 | 928 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 956 | 961 | PF00179 | 0.488 |
TRG_DiLeu_BaEn_1 | 809 | 814 | PF01217 | 0.318 |
TRG_DiLeu_BaEn_1 | 863 | 868 | PF01217 | 0.242 |
TRG_DiLeu_BaEn_4 | 1114 | 1120 | PF01217 | 0.593 |
TRG_DiLeu_BaEn_4 | 635 | 641 | PF01217 | 0.321 |
TRG_DiLeu_BaLyEn_6 | 32 | 37 | PF01217 | 0.684 |
TRG_DiLeu_BaLyEn_6 | 881 | 886 | PF01217 | 0.242 |
TRG_DiLeu_BaLyEn_6 | 914 | 919 | PF01217 | 0.294 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 660 | 663 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 837 | 840 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 916 | 919 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.642 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.242 |
TRG_ER_diArg_1 | 657 | 660 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.225 |
TRG_ER_diArg_1 | 758 | 760 | PF00400 | 0.726 |
TRG_NES_CRM1_1 | 559 | 573 | PF08389 | 0.318 |
TRG_NLS_MonoExtN_4 | 1012 | 1017 | PF00514 | 0.634 |
TRG_NLS_MonoExtN_4 | 845 | 851 | PF00514 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 514 | 518 | PF00026 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G3 | Leptomonas seymouri | 80% | 99% |
A0A1X0NIN9 | Trypanosomatidae | 65% | 100% |
A0A3S7WY74 | Leishmania donovani | 95% | 100% |
A0A422MV13 | Trypanosoma rangeli | 66% | 100% |
A4HDD3 | Leishmania braziliensis | 89% | 100% |
A4HRE5 | Leishmania infantum | 26% | 100% |
A4I0R4 | Leishmania infantum | 95% | 100% |
D0A743 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
E9AWR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q6PFE3 | Mus musculus | 39% | 100% |
Q9DG67 | Gallus gallus | 37% | 100% |
V5BVU6 | Trypanosoma cruzi | 73% | 100% |