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: 40 |
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 2 |
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 | 2 |
GO:0099081 | supramolecular polymer | 3 | 2 |
GO:0099512 | supramolecular fiber | 4 | 2 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0035869 | ciliary transition zone | 2 | 1 |
Related structures:
AlphaFold database: E9AKY2
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 16 |
GO:0007018 | microtubule-based movement | 3 | 16 |
GO:0009987 | cellular process | 1 | 16 |
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 | 16 |
GO:0003774 | cytoskeletal motor activity | 1 | 16 |
GO:0003777 | microtubule motor activity | 2 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005515 | protein binding | 2 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0008017 | microtubule binding | 5 | 16 |
GO:0008092 | cytoskeletal protein binding | 3 | 16 |
GO:0015631 | tubulin binding | 4 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 11 |
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 | 155 | 159 | PF00656 | 0.204 |
CLV_C14_Caspase3-7 | 569 | 573 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 631 | 635 | PF00656 | 0.624 |
CLV_C14_Caspase3-7 | 726 | 730 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 771 | 775 | PF00656 | 0.591 |
CLV_C14_Caspase3-7 | 777 | 781 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 792 | 794 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.587 |
CLV_PCSK_FUR_1 | 388 | 392 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.211 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.820 |
CLV_PCSK_KEX2_1 | 792 | 794 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 823 | 825 | PF00082 | 0.587 |
CLV_PCSK_PC7_1 | 227 | 233 | PF00082 | 0.289 |
CLV_PCSK_PC7_1 | 506 | 512 | PF00082 | 0.404 |
CLV_PCSK_PC7_1 | 819 | 825 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 884 | 888 | PF00082 | 0.440 |
CLV_Separin_Metazoa | 844 | 848 | PF03568 | 0.429 |
DEG_APCC_DBOX_1 | 876 | 884 | PF00400 | 0.403 |
DOC_ANK_TNKS_1 | 143 | 150 | PF00023 | 0.182 |
DOC_CYCLIN_RxL_1 | 436 | 447 | PF00134 | 0.428 |
DOC_MAPK_gen_1 | 271 | 280 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 869 | 878 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 273 | 282 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 4 | 11 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 588 | 595 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 871 | 880 | PF00069 | 0.429 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.223 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 742 | 746 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 769 | 773 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 604 | 610 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 618 | 626 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 747 | 755 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 796 | 802 | PF00244 | 0.540 |
LIG_Actin_WH2_2 | 95 | 111 | PF00022 | 0.278 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.394 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.182 |
LIG_BRCT_BRCA1_1 | 793 | 797 | PF00533 | 0.507 |
LIG_Clathr_ClatBox_1 | 189 | 193 | PF01394 | 0.218 |
LIG_Clathr_ClatBox_1 | 875 | 879 | PF01394 | 0.408 |
LIG_CtBP_PxDLS_1 | 409 | 413 | PF00389 | 0.569 |
LIG_EH1_1 | 88 | 96 | PF00400 | 0.311 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.454 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.507 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.292 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.210 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.394 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.394 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.450 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.300 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.607 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.587 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.489 |
LIG_FHA_1 | 796 | 802 | PF00498 | 0.521 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.488 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.283 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.428 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.681 |
LIG_FHA_2 | 695 | 701 | PF00498 | 0.559 |
LIG_FHA_2 | 765 | 771 | PF00498 | 0.755 |
LIG_FHA_2 | 775 | 781 | PF00498 | 0.545 |
LIG_FHA_2 | 849 | 855 | PF00498 | 0.447 |
LIG_Integrin_RGD_1 | 227 | 229 | PF01839 | 0.246 |
LIG_LIR_Gen_1 | 368 | 379 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 447 | 456 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 640 | 645 | PF02991 | 0.772 |
LIG_LIR_Nem_3 | 704 | 708 | PF02991 | 0.693 |
LIG_NRBOX | 334 | 340 | PF00104 | 0.394 |
LIG_Pex14_2 | 69 | 73 | PF04695 | 0.311 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.311 |
LIG_SH2_CRK | 449 | 453 | PF00017 | 0.415 |
LIG_SH2_PTP2 | 135 | 138 | PF00017 | 0.311 |
LIG_SH2_PTP2 | 642 | 645 | PF00017 | 0.559 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.311 |
LIG_SH2_SRC | 58 | 61 | PF00017 | 0.253 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.253 |
LIG_SH2_STAT3 | 456 | 459 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.608 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.227 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.409 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.574 |
LIG_SH3_3 | 667 | 673 | PF00018 | 0.708 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.559 |
LIG_SUMO_SIM_anti_2 | 834 | 842 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 25 | 30 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 408 | 414 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 441 | 447 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 805 | 811 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.289 |
LIG_TRAF2_1 | 497 | 500 | PF00917 | 0.411 |
LIG_TRAF2_1 | 644 | 647 | PF00917 | 0.594 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.311 |
LIG_TYR_ITIM | 369 | 374 | PF00017 | 0.311 |
LIG_UBA3_1 | 98 | 106 | PF00899 | 0.261 |
MOD_CDC14_SPxK_1 | 181 | 184 | PF00782 | 0.218 |
MOD_CDC14_SPxK_1 | 625 | 628 | PF00782 | 0.645 |
MOD_CDK_SPxK_1 | 178 | 184 | PF00069 | 0.218 |
MOD_CDK_SPxK_1 | 622 | 628 | PF00069 | 0.648 |
MOD_CDK_SPxxK_3 | 391 | 398 | PF00069 | 0.521 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.204 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.386 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.394 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.374 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.419 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.648 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.588 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.625 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.622 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.544 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.532 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.376 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.583 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.484 |
MOD_CK2_1 | 694 | 700 | PF00069 | 0.571 |
MOD_CK2_1 | 764 | 770 | PF00069 | 0.520 |
MOD_CK2_1 | 807 | 813 | PF00069 | 0.563 |
MOD_CK2_1 | 848 | 854 | PF00069 | 0.415 |
MOD_Cter_Amidation | 662 | 665 | PF01082 | 0.546 |
MOD_DYRK1A_RPxSP_1 | 176 | 180 | PF00069 | 0.302 |
MOD_DYRK1A_RPxSP_1 | 391 | 395 | PF00069 | 0.509 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.342 |
MOD_GlcNHglycan | 119 | 123 | PF01048 | 0.274 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.182 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.274 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.580 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.416 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.791 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.572 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.670 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.577 |
MOD_GlcNHglycan | 834 | 838 | PF01048 | 0.422 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.292 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.208 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.369 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.275 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.386 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.482 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.394 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.648 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.560 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.650 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.603 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.523 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.489 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.311 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.311 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.311 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.334 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.426 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.582 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.311 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.546 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.327 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.311 |
MOD_NEK2_2 | 742 | 747 | PF00069 | 0.495 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.424 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.579 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.624 |
MOD_PIKK_1 | 637 | 643 | PF00454 | 0.555 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.271 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.261 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.182 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.394 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.394 |
MOD_PKA_2 | 746 | 752 | PF00069 | 0.577 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.532 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.311 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.513 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.311 |
MOD_Plk_1 | 812 | 818 | PF00069 | 0.493 |
MOD_Plk_1 | 833 | 839 | PF00069 | 0.408 |
MOD_Plk_2-3 | 813 | 819 | PF00069 | 0.492 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.261 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.476 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.311 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.379 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.551 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.324 |
MOD_Plk_4 | 750 | 756 | PF00069 | 0.489 |
MOD_Plk_4 | 802 | 808 | PF00069 | 0.481 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.386 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.414 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.313 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.286 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.628 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.549 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.661 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.641 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.618 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.705 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.556 |
MOD_SUMO_rev_2 | 269 | 275 | PF00179 | 0.353 |
MOD_SUMO_rev_2 | 428 | 438 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 879 | 886 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_1 | 23 | 28 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.311 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.636 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.431 |
TRG_NES_CRM1_1 | 569 | 582 | PF08389 | 0.467 |
TRG_NLS_MonoExtC_3 | 505 | 510 | PF00514 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 482 | 487 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 43% | 100% |
A0A3Q8IEL2 | Leishmania donovani | 29% | 100% |
A0A3Q8IHG6 | Leishmania donovani | 28% | 100% |
A0A3S7WPL3 | Leishmania donovani | 88% | 100% |
A4H4R6 | Leishmania braziliensis | 75% | 99% |
A4HHN8 | Leishmania braziliensis | 28% | 100% |
A4HHY2 | Leishmania braziliensis | 25% | 100% |
A4HSZ5 | Leishmania infantum | 89% | 100% |
A4I4V2 | Leishmania infantum | 28% | 100% |
A4I4V3 | Leishmania infantum | 29% | 100% |
E9AEA0 | Leishmania major | 29% | 100% |
E9AEA1 | Leishmania major | 29% | 100% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
O23826 | Nicotiana tabacum | 26% | 88% |
Q4QIX3 | Leishmania major | 88% | 99% |
Q8NI77 | Homo sapiens | 25% | 99% |