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: 35 |
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 3 |
GO:0005875 | microtubule associated complex | 2 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0051286 | cell tip | 3 | 2 |
GO:0060187 | cell pole | 2 | 2 |
GO:0099080 | supramolecular complex | 2 | 3 |
GO:0099081 | supramolecular polymer | 3 | 3 |
GO:0099512 | supramolecular fiber | 4 | 3 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0035869 | ciliary transition zone | 2 | 1 |
Related structures:
AlphaFold database: A4HSZ5
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 17 |
GO:0007018 | microtubule-based movement | 3 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0051231 | spindle elongation | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003774 | cytoskeletal motor activity | 1 | 17 |
GO:0003777 | microtubule motor activity | 2 | 17 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 17 |
GO:0005515 | protein binding | 2 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0008017 | microtubule binding | 5 | 17 |
GO:0008092 | cytoskeletal protein binding | 3 | 17 |
GO:0015631 | tubulin binding | 4 | 17 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 193 | 197 | PF00656 | 0.263 |
CLV_C14_Caspase3-7 | 557 | 561 | PF00656 | 0.676 |
CLV_C14_Caspase3-7 | 567 | 571 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 629 | 633 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 794 | 796 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 825 | 827 | PF00675 | 0.599 |
CLV_PCSK_FUR_1 | 388 | 392 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 794 | 796 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 825 | 827 | PF00082 | 0.599 |
CLV_PCSK_PC7_1 | 227 | 233 | PF00082 | 0.301 |
CLV_PCSK_PC7_1 | 507 | 513 | PF00082 | 0.456 |
CLV_PCSK_PC7_1 | 821 | 827 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 845 | 849 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 886 | 890 | PF00082 | 0.456 |
CLV_Separin_Metazoa | 846 | 850 | PF03568 | 0.454 |
DEG_APCC_DBOX_1 | 509 | 517 | PF00400 | 0.461 |
DEG_APCC_DBOX_1 | 878 | 886 | PF00400 | 0.438 |
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.263 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.540 |
DOC_CYCLIN_RxL_1 | 437 | 448 | PF00134 | 0.442 |
DOC_CYCLIN_RxL_1 | 570 | 580 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.288 |
DOC_MAPK_gen_1 | 271 | 280 | PF00069 | 0.301 |
DOC_MAPK_gen_1 | 871 | 880 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 273 | 282 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 4 | 11 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 586 | 593 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 873 | 882 | PF00069 | 0.467 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 740 | 744 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.564 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.285 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 664 | 669 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 783 | 788 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 166 | 173 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 586 | 592 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 602 | 608 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 616 | 624 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 71 | 80 | PF00244 | 0.231 |
LIG_14-3-3_CanoR_1 | 749 | 756 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 798 | 804 | PF00244 | 0.578 |
LIG_Actin_WH2_2 | 95 | 111 | PF00022 | 0.291 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.416 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.488 |
LIG_BIR_III_4 | 582 | 586 | PF00653 | 0.588 |
LIG_BRCT_BRCA1_1 | 795 | 799 | PF00533 | 0.529 |
LIG_Clathr_ClatBox_1 | 877 | 881 | PF01394 | 0.445 |
LIG_CtBP_PxDLS_1 | 410 | 414 | PF00389 | 0.577 |
LIG_EH1_1 | 88 | 96 | PF00400 | 0.327 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.504 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.301 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.322 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.420 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.420 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.508 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.306 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.659 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.571 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.323 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.465 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.299 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.543 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.686 |
LIG_FHA_2 | 693 | 699 | PF00498 | 0.556 |
LIG_FHA_2 | 851 | 857 | PF00498 | 0.456 |
LIG_LIR_Gen_1 | 368 | 379 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 448 | 457 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 448 | 453 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 638 | 643 | PF02991 | 0.799 |
LIG_LIR_Nem_3 | 702 | 706 | PF02991 | 0.561 |
LIG_NRBOX | 334 | 340 | PF00104 | 0.414 |
LIG_Pex14_2 | 69 | 73 | PF04695 | 0.327 |
LIG_Pex14_2 | 799 | 803 | PF04695 | 0.523 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.327 |
LIG_SH2_CRK | 450 | 454 | PF00017 | 0.438 |
LIG_SH2_PTP2 | 135 | 138 | PF00017 | 0.344 |
LIG_SH2_PTP2 | 640 | 643 | PF00017 | 0.563 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.327 |
LIG_SH2_SRC | 58 | 61 | PF00017 | 0.270 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.327 |
LIG_SH2_STAP1 | 418 | 422 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 457 | 461 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.295 |
LIG_SH2_STAT3 | 457 | 460 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 706 | 709 | PF00017 | 0.571 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.435 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.466 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.635 |
LIG_SH3_3 | 693 | 699 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 836 | 844 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 25 | 30 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.301 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.444 |
LIG_TRAF2_1 | 642 | 645 | PF00917 | 0.599 |
LIG_TRAF2_1 | 779 | 782 | PF00917 | 0.561 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.344 |
LIG_TYR_ITIM | 369 | 374 | PF00017 | 0.327 |
LIG_UBA3_1 | 98 | 106 | PF00899 | 0.276 |
MOD_CDC14_SPxK_1 | 623 | 626 | PF00782 | 0.657 |
MOD_CDK_SPxK_1 | 620 | 626 | PF00069 | 0.654 |
MOD_CDK_SPxxK_3 | 391 | 398 | PF00069 | 0.525 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.286 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.244 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.414 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.420 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.572 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.428 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.622 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.681 |
MOD_CK1_1 | 743 | 749 | PF00069 | 0.573 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.600 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.552 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.552 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.231 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.348 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.591 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.453 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.585 |
MOD_CK2_1 | 692 | 698 | PF00069 | 0.568 |
MOD_CK2_1 | 809 | 815 | PF00069 | 0.591 |
MOD_CK2_1 | 850 | 856 | PF00069 | 0.428 |
MOD_DYRK1A_RPxSP_1 | 176 | 180 | PF00069 | 0.318 |
MOD_DYRK1A_RPxSP_1 | 391 | 395 | PF00069 | 0.510 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.357 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.297 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.327 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.586 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.466 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.769 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.668 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.534 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.526 |
MOD_GlcNHglycan | 836 | 840 | PF01048 | 0.442 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.238 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.298 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.383 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.400 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.570 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.653 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.466 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.576 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.739 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.595 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.593 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.566 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.535 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.535 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.327 |
MOD_N-GLC_2 | 466 | 468 | PF02516 | 0.372 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.313 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.327 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.387 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.433 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.613 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.341 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.535 |
MOD_NEK2_1 | 799 | 804 | PF00069 | 0.568 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.433 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.299 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.341 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.460 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.474 |
MOD_PIKK_1 | 595 | 601 | PF00454 | 0.636 |
MOD_PIKK_1 | 624 | 630 | PF00454 | 0.587 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.576 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.327 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.279 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.412 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.420 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.556 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.551 |
MOD_PKA_2 | 793 | 799 | PF00069 | 0.571 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.356 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.327 |
MOD_Plk_1 | 814 | 820 | PF00069 | 0.530 |
MOD_Plk_1 | 835 | 841 | PF00069 | 0.433 |
MOD_Plk_2-3 | 815 | 821 | PF00069 | 0.530 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.276 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.487 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.342 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.415 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.541 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.351 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.400 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.281 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.452 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.285 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.519 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.768 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.641 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.689 |
MOD_ProDKin_1 | 664 | 670 | PF00069 | 0.643 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.534 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.638 |
MOD_ProDKin_1 | 783 | 789 | PF00069 | 0.582 |
MOD_SUMO_rev_2 | 269 | 275 | PF00179 | 0.294 |
MOD_SUMO_rev_2 | 429 | 439 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 881 | 888 | PF00179 | 0.466 |
TRG_DiLeu_BaEn_1 | 23 | 28 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.327 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.748 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 509 | 512 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.458 |
TRG_NES_CRM1_1 | 567 | 580 | PF08389 | 0.510 |
TRG_NLS_MonoExtC_3 | 506 | 511 | PF00514 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 483 | 488 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IEL2 | Leishmania donovani | 29% | 100% |
A0A3Q8IHG6 | Leishmania donovani | 29% | 100% |
A0A3S7WPL3 | Leishmania donovani | 99% | 100% |
A4H4R6 | Leishmania braziliensis | 75% | 99% |
A4H7S0 | Leishmania braziliensis | 27% | 83% |
A4HHY2 | Leishmania braziliensis | 26% | 100% |
A4I4V2 | Leishmania infantum | 29% | 100% |
A4I4V3 | Leishmania infantum | 29% | 100% |
E9AEA0 | Leishmania major | 29% | 100% |
E9AEA1 | Leishmania major | 29% | 100% |
E9AKY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4QIX3 | Leishmania major | 92% | 99% |