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:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005657 | replication fork | 2 | 1 |
Related structures:
AlphaFold database: A4H6E9
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006310 | DNA recombination | 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 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0032200 | telomere organization | 6 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 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 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
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: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:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.823 |
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.715 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.650 |
CLV_C14_Caspase3-7 | 770 | 774 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 1004 | 1006 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 1009 | 1011 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.531 |
CLV_PCSK_FUR_1 | 1007 | 1011 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 1004 | 1006 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 1009 | 1011 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 1025 | 1027 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 1025 | 1027 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.735 |
CLV_PCSK_PC7_1 | 1005 | 1011 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 1012 | 1016 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 1049 | 1053 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 817 | 821 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.746 |
DEG_COP1_1 | 128 | 136 | PF00400 | 0.531 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.479 |
DEG_SPOP_SBC_1 | 200 | 204 | PF00917 | 0.441 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.539 |
DOC_CKS1_1 | 133 | 138 | PF01111 | 0.531 |
DOC_CKS1_1 | 584 | 589 | PF01111 | 0.745 |
DOC_CKS1_1 | 802 | 807 | PF01111 | 0.591 |
DOC_CYCLIN_RxL_1 | 426 | 436 | PF00134 | 0.231 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 231 | 237 | PF00134 | 0.587 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 819 | 828 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 636 | 639 | PF00134 | 0.556 |
DOC_MAPK_DCC_7 | 728 | 737 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 1007 | 1015 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 440 | 447 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 478 | 486 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 506 | 514 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 93 | 104 | PF00069 | 0.664 |
DOC_MAPK_gen_1 | 956 | 965 | PF00069 | 0.428 |
DOC_MAPK_HePTP_8 | 437 | 449 | PF00069 | 0.385 |
DOC_MAPK_JIP1_4 | 808 | 814 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 206 | 215 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 440 | 449 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 478 | 486 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 506 | 514 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 743 | 750 | PF00069 | 0.515 |
DOC_MAPK_NFAT4_5 | 479 | 487 | PF00069 | 0.266 |
DOC_MAPK_NFAT4_5 | 743 | 751 | PF00069 | 0.329 |
DOC_MAPK_RevD_3 | 500 | 516 | PF00069 | 0.307 |
DOC_PP1_RVXF_1 | 492 | 499 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 514 | 521 | PF00149 | 0.583 |
DOC_PP1_SILK_1 | 859 | 864 | PF00149 | 0.291 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.210 |
DOC_PP2B_LxvP_1 | 636 | 639 | PF13499 | 0.533 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.768 |
DOC_PP4_FxxP_1 | 874 | 877 | PF00568 | 0.526 |
DOC_USP7_MATH_1 | 1055 | 1059 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.686 |
DOC_USP7_MATH_2 | 60 | 66 | PF00917 | 0.489 |
DOC_USP7_UBL2_3 | 1025 | 1029 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 658 | 662 | PF12436 | 0.573 |
DOC_WW_Pin1_4 | 1074 | 1079 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 801 | 806 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 115 | 122 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 259 | 266 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 515 | 519 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 575 | 584 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 681 | 690 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 745 | 751 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 901 | 909 | PF00244 | 0.291 |
LIG_Actin_WH2_2 | 424 | 442 | PF00022 | 0.328 |
LIG_Actin_WH2_2 | 482 | 499 | PF00022 | 0.505 |
LIG_Actin_WH2_2 | 502 | 517 | PF00022 | 0.243 |
LIG_APCC_ABBA_1 | 781 | 786 | PF00400 | 0.629 |
LIG_BIR_III_4 | 298 | 302 | PF00653 | 0.696 |
LIG_BRCT_BRCA1_1 | 456 | 460 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_1 | 473 | 477 | PF00533 | 0.300 |
LIG_BRCT_BRCA1_1 | 516 | 520 | PF00533 | 0.585 |
LIG_BRCT_BRCA1_1 | 710 | 714 | PF00533 | 0.729 |
LIG_CtBP_PxDLS_1 | 511 | 515 | PF00389 | 0.460 |
LIG_CtBP_PxDLS_1 | 638 | 642 | PF00389 | 0.586 |
LIG_CtBP_PxDLS_1 | 915 | 919 | PF00389 | 0.421 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.477 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.550 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.328 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.523 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.504 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.796 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.598 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.445 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.388 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.333 |
LIG_FHA_1 | 893 | 899 | PF00498 | 0.446 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.731 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.541 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.616 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.577 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.503 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.498 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.479 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.466 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.476 |
LIG_FHA_2 | 788 | 794 | PF00498 | 0.475 |
LIG_FHA_2 | 973 | 979 | PF00498 | 0.329 |
LIG_GBD_Chelix_1 | 318 | 326 | PF00786 | 0.480 |
LIG_Integrin_isoDGR_2 | 885 | 887 | PF01839 | 0.591 |
LIG_Integrin_RGD_1 | 174 | 176 | PF01839 | 0.697 |
LIG_IRF3_LxIS_1 | 395 | 402 | PF10401 | 0.473 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.775 |
LIG_LIR_Apic_2 | 871 | 877 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 414 | 424 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 457 | 468 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 793 | 801 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 243 | 247 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 73 | 78 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 793 | 798 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 866 | 870 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 904 | 909 | PF02991 | 0.267 |
LIG_LYPXL_S_1 | 732 | 736 | PF13949 | 0.544 |
LIG_MYND_1 | 634 | 638 | PF01753 | 0.546 |
LIG_PCNA_yPIPBox_3 | 478 | 490 | PF02747 | 0.323 |
LIG_PCNA_yPIPBox_3 | 537 | 548 | PF02747 | 0.635 |
LIG_PCNA_yPIPBox_3 | 830 | 841 | PF02747 | 0.490 |
LIG_Pex14_1 | 645 | 649 | PF04695 | 0.397 |
LIG_Pex14_2 | 477 | 481 | PF04695 | 0.392 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.400 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.637 |
LIG_SH2_STAP1 | 37 | 41 | PF00017 | 0.713 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 864 | 868 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 920 | 924 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 632 | 635 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 649 | 652 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 676 | 679 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 761 | 764 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 850 | 853 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 951 | 954 | PF00017 | 0.381 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.719 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.748 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.576 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.611 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.602 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.787 |
LIG_SH3_3 | 728 | 734 | PF00018 | 0.499 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.327 |
LIG_SH3_3 | 803 | 809 | PF00018 | 0.456 |
LIG_SH3_3 | 874 | 880 | PF00018 | 0.449 |
LIG_SH3_3 | 887 | 893 | PF00018 | 0.341 |
LIG_SH3_3 | 909 | 915 | PF00018 | 0.261 |
LIG_SH3_3 | 954 | 960 | PF00018 | 0.411 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.683 |
LIG_SUMO_SIM_anti_2 | 2 | 8 | PF11976 | 0.454 |
LIG_SUMO_SIM_anti_2 | 207 | 212 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 417 | 423 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 323 | 331 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 417 | 423 | PF11976 | 0.328 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.690 |
LIG_UBA3_1 | 1015 | 1024 | PF00899 | 0.419 |
LIG_UBA3_1 | 362 | 367 | PF00899 | 0.362 |
LIG_WRC_WIRS_1 | 661 | 666 | PF05994 | 0.584 |
LIG_WRC_WIRS_1 | 965 | 970 | PF05994 | 0.490 |
MOD_CDK_SPxxK_3 | 157 | 164 | PF00069 | 0.693 |
MOD_CDK_SPxxK_3 | 471 | 478 | PF00069 | 0.396 |
MOD_CDK_SPxxK_3 | 801 | 808 | PF00069 | 0.585 |
MOD_CK1_1 | 1032 | 1038 | PF00069 | 0.698 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.602 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.620 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.466 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.566 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.356 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.781 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.670 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.596 |
MOD_CK1_1 | 715 | 721 | PF00069 | 0.571 |
MOD_CK1_1 | 832 | 838 | PF00069 | 0.489 |
MOD_CK1_1 | 964 | 970 | PF00069 | 0.553 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.546 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.624 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.580 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.540 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.649 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.669 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.751 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.745 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.454 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.461 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.717 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.666 |
MOD_GlcNHglycan | 1057 | 1060 | PF01048 | 0.691 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.769 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.757 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.370 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.789 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.734 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.497 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.401 |
MOD_GlcNHglycan | 773 | 776 | PF01048 | 0.312 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.685 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.669 |
MOD_GSK3_1 | 1055 | 1062 | PF00069 | 0.434 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.536 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.374 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.721 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.288 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.641 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.705 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.592 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.495 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.460 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.547 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.554 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.684 |
MOD_GSK3_1 | 901 | 908 | PF00069 | 0.489 |
MOD_GSK3_1 | 964 | 971 | PF00069 | 0.500 |
MOD_GSK3_1 | 999 | 1006 | PF00069 | 0.477 |
MOD_LATS_1 | 162 | 168 | PF00433 | 0.529 |
MOD_N-GLC_1 | 1065 | 1070 | PF02516 | 0.528 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.551 |
MOD_N-GLC_1 | 712 | 717 | PF02516 | 0.686 |
MOD_N-GLC_1 | 829 | 834 | PF02516 | 0.439 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.702 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.327 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.558 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.604 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.414 |
MOD_NEK2_1 | 938 | 943 | PF00069 | 0.412 |
MOD_NEK2_1 | 963 | 968 | PF00069 | 0.428 |
MOD_NEK2_1 | 972 | 977 | PF00069 | 0.413 |
MOD_NEK2_1 | 982 | 987 | PF00069 | 0.410 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.413 |
MOD_NEK2_2 | 570 | 575 | PF00069 | 0.778 |
MOD_NEK2_2 | 920 | 925 | PF00069 | 0.393 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.448 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.737 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.644 |
MOD_PIKK_1 | 987 | 993 | PF00454 | 0.574 |
MOD_PK_1 | 693 | 699 | PF00069 | 0.478 |
MOD_PK_1 | 857 | 863 | PF00069 | 0.566 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.386 |
MOD_PKA_2 | 1003 | 1009 | PF00069 | 0.654 |
MOD_PKA_2 | 1055 | 1061 | PF00069 | 0.674 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.785 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.519 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.503 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.716 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.680 |
MOD_PKA_2 | 698 | 704 | PF00069 | 0.451 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.682 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.580 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.578 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.613 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.379 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.268 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.777 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.748 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.569 |
MOD_Plk_1 | 793 | 799 | PF00069 | 0.471 |
MOD_Plk_1 | 857 | 863 | PF00069 | 0.554 |
MOD_Plk_1 | 938 | 944 | PF00069 | 0.437 |
MOD_Plk_1 | 982 | 988 | PF00069 | 0.411 |
MOD_Plk_2-3 | 39 | 45 | PF00069 | 0.489 |
MOD_Plk_2-3 | 412 | 418 | PF00069 | 0.448 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.745 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.698 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.337 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.299 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.328 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.414 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.482 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.373 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.608 |
MOD_Plk_4 | 832 | 838 | PF00069 | 0.486 |
MOD_Plk_4 | 857 | 863 | PF00069 | 0.552 |
MOD_Plk_4 | 928 | 934 | PF00069 | 0.440 |
MOD_Plk_4 | 968 | 974 | PF00069 | 0.508 |
MOD_ProDKin_1 | 1074 | 1080 | PF00069 | 0.668 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.736 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.586 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.679 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.473 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.342 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.793 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.436 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.465 |
MOD_ProDKin_1 | 801 | 807 | PF00069 | 0.561 |
MOD_SUMO_for_1 | 1030 | 1033 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 1042 | 1051 | PF00179 | 0.659 |
MOD_SUMO_rev_2 | 317 | 327 | PF00179 | 0.716 |
TRG_DiLeu_BaEn_3 | 753 | 759 | PF01217 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 467 | 472 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 733 | 736 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 951 | 954 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 1003 | 1005 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 439 | 441 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 536 | 539 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 742 | 745 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 776 | 779 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.662 |
TRG_NES_CRM1_1 | 324 | 335 | PF08389 | 0.357 |
TRG_NES_CRM1_1 | 928 | 939 | PF08389 | 0.438 |
TRG_NLS_Bipartite_1 | 1009 | 1028 | PF00514 | 0.615 |
TRG_NLS_Bipartite_1 | 83 | 100 | PF00514 | 0.778 |
TRG_NLS_MonoExtC_3 | 92 | 97 | PF00514 | 0.782 |
TRG_NLS_MonoExtN_4 | 1007 | 1014 | PF00514 | 0.621 |
TRG_NLS_MonoExtN_4 | 90 | 97 | PF00514 | 0.778 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 429 | 433 | PF00026 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIS5 | Leptomonas seymouri | 63% | 79% |
A0A0S4IUA9 | Bodo saltans | 38% | 100% |
A0A1X0NVS9 | Trypanosomatidae | 44% | 100% |
A0A3R7MZY3 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WRJ2 | Leishmania donovani | 79% | 88% |
A4HUU3 | Leishmania infantum | 80% | 71% |
D0A7L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9ANH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 88% |
Q384Y0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 45% | 100% |
Q4QH48 | Leishmania major | 79% | 100% |
V5DSX3 | Trypanosoma cruzi | 40% | 100% |