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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0016592 | mediator complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AZ98
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:0000086 | G2/M transition of mitotic cell cycle | 5 | 1 |
GO:0000365 | mRNA trans splicing, via spliceosome | 9 | 1 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044839 | cell cycle G2/M phase transition | 4 | 1 |
GO:0045291 | mRNA trans splicing, SL addition | 10 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 1 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 446 | 450 | PF00656 | 0.504 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.647 |
CLV_C14_Caspase3-7 | 904 | 908 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 936 | 940 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 751 | 753 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 925 | 927 | PF00675 | 0.737 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 750 | 752 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 925 | 927 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.385 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.622 |
DEG_SPOP_SBC_1 | 165 | 169 | PF00917 | 0.503 |
DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.516 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.640 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.518 |
DEG_SPOP_SBC_1 | 65 | 69 | PF00917 | 0.695 |
DOC_CDC14_PxL_1 | 621 | 629 | PF14671 | 0.291 |
DOC_CYCLIN_RxL_1 | 651 | 661 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 652 | 658 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 581 | 590 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 493 | 501 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 98 | 105 | PF00069 | 0.512 |
DOC_MAPK_RevD_3 | 638 | 654 | PF00069 | 0.385 |
DOC_PP1_RVXF_1 | 566 | 573 | PF00149 | 0.385 |
DOC_PP2B_LxvP_1 | 673 | 676 | PF13499 | 0.367 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.588 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.806 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 855 | 859 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 868 | 872 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 878 | 882 | PF00917 | 0.694 |
DOC_USP7_UBL2_3 | 334 | 338 | PF12436 | 0.421 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 870 | 875 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 281 | 289 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 292 | 299 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 513 | 519 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 699 | 709 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 829 | 837 | PF00244 | 0.759 |
LIG_Clathr_ClatBox_1 | 373 | 377 | PF01394 | 0.533 |
LIG_deltaCOP1_diTrp_1 | 639 | 647 | PF00928 | 0.367 |
LIG_EVH1_2 | 79 | 83 | PF00568 | 0.682 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.684 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.408 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.687 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.303 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.291 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.367 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.663 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.577 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.460 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.681 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.760 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.571 |
LIG_LIR_Apic_2 | 619 | 625 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 561 | 572 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 592 | 603 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 592 | 598 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 626 | 632 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 678 | 684 | PF02991 | 0.315 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.566 |
LIG_Pex14_2 | 647 | 651 | PF04695 | 0.367 |
LIG_REV1ctd_RIR_1 | 761 | 767 | PF16727 | 0.319 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.419 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.336 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.388 |
LIG_SH2_CRK | 564 | 568 | PF00017 | 0.367 |
LIG_SH2_CRK | 685 | 689 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 276 | 280 | PF00017 | 0.474 |
LIG_SH2_NCK_1 | 515 | 519 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 532 | 536 | PF00017 | 0.431 |
LIG_SH2_PTP2 | 595 | 598 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 515 | 519 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 634 | 638 | PF00017 | 0.291 |
LIG_SH2_STAT3 | 299 | 302 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.357 |
LIG_SH3_2 | 209 | 214 | PF14604 | 0.644 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.619 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.446 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.489 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.681 |
LIG_SH3_3 | 767 | 773 | PF00018 | 0.428 |
LIG_SH3_CIN85_PxpxPR_1 | 378 | 383 | PF14604 | 0.666 |
LIG_SUMO_SIM_anti_2 | 355 | 360 | PF11976 | 0.468 |
LIG_SUMO_SIM_anti_2 | 372 | 377 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 616 | 622 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 735 | 743 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 372 | 377 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 665 | 671 | PF11976 | 0.385 |
LIG_TRAF2_1 | 676 | 679 | PF00917 | 0.363 |
LIG_TYR_ITIM | 537 | 542 | PF00017 | 0.522 |
LIG_TYR_ITIM | 562 | 567 | PF00017 | 0.367 |
LIG_UBA3_1 | 6 | 12 | PF00899 | 0.588 |
LIG_WW_3 | 322 | 326 | PF00397 | 0.433 |
MOD_CDC14_SPxK_1 | 387 | 390 | PF00782 | 0.632 |
MOD_CDK_SPK_2 | 540 | 545 | PF00069 | 0.536 |
MOD_CDK_SPxK_1 | 384 | 390 | PF00069 | 0.627 |
MOD_CDK_SPxxK_3 | 376 | 383 | PF00069 | 0.640 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.649 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.657 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.692 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.693 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.525 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.496 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.691 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.770 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.814 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.556 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.529 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.385 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.619 |
MOD_CK1_1 | 809 | 815 | PF00069 | 0.681 |
MOD_CK1_1 | 831 | 837 | PF00069 | 0.590 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.518 |
MOD_CK1_1 | 873 | 879 | PF00069 | 0.513 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.715 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.607 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.603 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.701 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.665 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.717 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.593 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.563 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.325 |
MOD_CK2_1 | 844 | 850 | PF00069 | 0.622 |
MOD_CK2_1 | 855 | 861 | PF00069 | 0.622 |
MOD_CK2_1 | 935 | 941 | PF00069 | 0.602 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.693 |
MOD_GlcNHglycan | 181 | 185 | PF01048 | 0.618 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.662 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.593 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.373 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.644 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.648 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.588 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.654 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.692 |
MOD_GlcNHglycan | 735 | 738 | PF01048 | 0.340 |
MOD_GlcNHglycan | 753 | 756 | PF01048 | 0.206 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.800 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.740 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.725 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.776 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.680 |
MOD_GlcNHglycan | 870 | 873 | PF01048 | 0.648 |
MOD_GlcNHglycan | 902 | 906 | PF01048 | 0.687 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.625 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.570 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.531 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.768 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.699 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.634 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.510 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.671 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.659 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.679 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.719 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.492 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.635 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.689 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.689 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.693 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.338 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.408 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.797 |
MOD_GSK3_1 | 873 | 880 | PF00069 | 0.695 |
MOD_GSK3_1 | 897 | 904 | PF00069 | 0.625 |
MOD_GSK3_1 | 921 | 928 | PF00069 | 0.696 |
MOD_LATS_1 | 923 | 929 | PF00433 | 0.692 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.541 |
MOD_N-GLC_1 | 700 | 705 | PF02516 | 0.454 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.441 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.514 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.412 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.281 |
MOD_NEK2_1 | 693 | 698 | PF00069 | 0.319 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.367 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.175 |
MOD_OFUCOSY | 102 | 107 | PF10250 | 0.543 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.510 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.503 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.694 |
MOD_PIKK_1 | 809 | 815 | PF00454 | 0.713 |
MOD_PIKK_1 | 951 | 957 | PF00454 | 0.448 |
MOD_PK_1 | 558 | 564 | PF00069 | 0.385 |
MOD_PKA_1 | 751 | 757 | PF00069 | 0.385 |
MOD_PKA_1 | 925 | 931 | PF00069 | 0.693 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.648 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.492 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.757 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.660 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.385 |
MOD_PKA_2 | 751 | 757 | PF00069 | 0.291 |
MOD_PKA_2 | 809 | 815 | PF00069 | 0.664 |
MOD_PKA_2 | 828 | 834 | PF00069 | 0.503 |
MOD_PKA_2 | 924 | 930 | PF00069 | 0.713 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.562 |
MOD_Plk_1 | 677 | 683 | PF00069 | 0.291 |
MOD_Plk_1 | 849 | 855 | PF00069 | 0.623 |
MOD_Plk_2-3 | 414 | 420 | PF00069 | 0.591 |
MOD_Plk_2-3 | 935 | 941 | PF00069 | 0.602 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.483 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.607 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.484 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.399 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.484 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.405 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.300 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.610 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.328 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.341 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.447 |
MOD_Plk_4 | 759 | 765 | PF00069 | 0.172 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.631 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.630 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.705 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.551 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.623 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.534 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.385 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.591 |
MOD_ProDKin_1 | 870 | 876 | PF00069 | 0.645 |
MOD_SUMO_for_1 | 443 | 446 | PF00179 | 0.511 |
MOD_SUMO_for_1 | 764 | 767 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 524 | 531 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 576 | 586 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 355 | 360 | PF01217 | 0.396 |
TRG_DiLeu_BaLyEn_6 | 947 | 952 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.767 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 749 | 752 | PF00400 | 0.385 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.572 |
TRG_NLS_MonoExtN_4 | 9 | 15 | PF00514 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 577 | 582 | PF00026 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 950 | 955 | PF00026 | 0.738 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6G8 | Leptomonas seymouri | 46% | 100% |
A0A3R7KFZ3 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H7I2 | Leishmania donovani | 88% | 100% |
A4HFW9 | Leishmania braziliensis | 76% | 100% |
A4I302 | Leishmania infantum | 88% | 100% |
C9ZJF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ADH4 | Leishmania major | 88% | 100% |