Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 12 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0099080 | supramolecular complex | 2 | 12 |
GO:0099081 | supramolecular polymer | 3 | 12 |
GO:0099512 | supramolecular fiber | 4 | 12 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QDJ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007018 | microtubule-based movement | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003774 | cytoskeletal motor activity | 1 | 12 |
GO:0003777 | microtubule motor activity | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0005543 | phospholipid binding | 3 | 12 |
GO:0008017 | microtubule binding | 5 | 12 |
GO:0008092 | cytoskeletal protein binding | 3 | 12 |
GO:0008289 | lipid binding | 2 | 12 |
GO:0015631 | tubulin binding | 4 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 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:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032182 | ubiquitin-like protein binding | 3 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035091 | phosphatidylinositol binding | 4 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043130 | ubiquitin binding | 4 | 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: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 | 285 | 289 | PF00656 | 0.793 |
CLV_C14_Caspase3-7 | 569 | 573 | PF00656 | 0.358 |
CLV_MEL_PAP_1 | 249 | 255 | PF00089 | 0.465 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.374 |
CLV_PCSK_FUR_1 | 299 | 303 | PF00082 | 0.803 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.783 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 297 | 303 | PF00082 | 0.776 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 831 | 835 | PF00082 | 0.699 |
DEG_APCC_DBOX_1 | 335 | 343 | PF00400 | 0.588 |
DEG_APCC_DBOX_1 | 419 | 427 | PF00400 | 0.548 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.557 |
DOC_CDC14_PxL_1 | 388 | 396 | PF14671 | 0.735 |
DOC_CYCLIN_RxL_1 | 791 | 802 | PF00134 | 0.374 |
DOC_CYCLIN_yCln2_LP_2 | 149 | 155 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 327 | 335 | PF00069 | 0.608 |
DOC_MAPK_gen_1 | 746 | 753 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 702 | 711 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 794 | 801 | PF00069 | 0.393 |
DOC_MAPK_NFAT4_5 | 702 | 710 | PF00069 | 0.358 |
DOC_PP1_RVXF_1 | 470 | 477 | PF00149 | 0.542 |
DOC_PP1_RVXF_1 | 792 | 799 | PF00149 | 0.358 |
DOC_PP1_RVXF_1 | 820 | 827 | PF00149 | 0.503 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.602 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.482 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 799 | 804 | PF00397 | 0.374 |
LIG_14-3-3_CanoR_1 | 130 | 139 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 241 | 250 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 777 | 785 | PF00244 | 0.393 |
LIG_Actin_WH2_2 | 416 | 433 | PF00022 | 0.512 |
LIG_APCC_ABBA_1 | 630 | 635 | PF00400 | 0.358 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.704 |
LIG_BIR_III_4 | 536 | 540 | PF00653 | 0.426 |
LIG_BRCT_BRCA1_1 | 813 | 817 | PF00533 | 0.358 |
LIG_CaM_IQ_9 | 474 | 490 | PF13499 | 0.543 |
LIG_Clathr_ClatBox_1 | 543 | 547 | PF01394 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 98 | 105 | PF00928 | 0.493 |
LIG_eIF4E_1 | 723 | 729 | PF01652 | 0.415 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.684 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.497 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.603 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.590 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.561 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.358 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.383 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.175 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.443 |
LIG_FHA_1 | 780 | 786 | PF00498 | 0.358 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.483 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.549 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.514 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.825 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.524 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.509 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.472 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.434 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.485 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.711 |
LIG_LIR_Gen_1 | 258 | 268 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 545 | 554 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 545 | 549 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.374 |
LIG_NRBOX | 780 | 786 | PF00104 | 0.358 |
LIG_PCNA_yPIPBox_3 | 66 | 80 | PF02747 | 0.580 |
LIG_Pex14_1 | 127 | 131 | PF04695 | 0.460 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.588 |
LIG_PTAP_UEV_1 | 551 | 556 | PF05743 | 0.505 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.512 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.482 |
LIG_SH2_CRK | 505 | 509 | PF00017 | 0.358 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.619 |
LIG_SH2_CRK | 723 | 727 | PF00017 | 0.415 |
LIG_SH2_GRB2like | 491 | 494 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 492 | 496 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.619 |
LIG_SH2_PTP2 | 708 | 711 | PF00017 | 0.358 |
LIG_SH2_SRC | 708 | 711 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 448 | 451 | PF00017 | 0.519 |
LIG_SH2_STAT3 | 526 | 529 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 633 | 636 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.358 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.370 |
LIG_SUMO_SIM_anti_2 | 626 | 631 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 188 | 196 | PF11976 | 0.594 |
LIG_SUMO_SIM_par_1 | 623 | 631 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.482 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.719 |
LIG_TRAF2_1 | 494 | 497 | PF00917 | 0.520 |
LIG_TYR_ITIM | 120 | 125 | PF00017 | 0.471 |
LIG_TYR_ITIM | 706 | 711 | PF00017 | 0.358 |
LIG_UBA3_1 | 156 | 161 | PF00899 | 0.649 |
LIG_UBA3_1 | 610 | 618 | PF00899 | 0.383 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.556 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.749 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.479 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.358 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.373 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.352 |
MOD_CK1_1 | 700 | 706 | PF00069 | 0.369 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.370 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.365 |
MOD_CK1_1 | 809 | 815 | PF00069 | 0.353 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.598 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.709 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.638 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.556 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.533 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.520 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.391 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.428 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.358 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.358 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.374 |
MOD_Cter_Amidation | 304 | 307 | PF01082 | 0.648 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.527 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.638 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.583 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.726 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.538 |
MOD_GlcNHglycan | 536 | 540 | PF01048 | 0.422 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.358 |
MOD_GlcNHglycan | 646 | 650 | PF01048 | 0.272 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.389 |
MOD_GlcNHglycan | 738 | 742 | PF01048 | 0.374 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.269 |
MOD_GlcNHglycan | 778 | 781 | PF01048 | 0.465 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.587 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.687 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.496 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.626 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.491 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.651 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.537 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.406 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.472 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.335 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.370 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.364 |
MOD_GSK3_1 | 802 | 809 | PF00069 | 0.374 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.666 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.479 |
MOD_LATS_1 | 239 | 245 | PF00433 | 0.604 |
MOD_N-GLC_1 | 592 | 597 | PF02516 | 0.428 |
MOD_N-GLC_1 | 753 | 758 | PF02516 | 0.358 |
MOD_N-GLC_1 | 806 | 811 | PF02516 | 0.360 |
MOD_N-GLC_1 | 831 | 836 | PF02516 | 0.710 |
MOD_N-GLC_2 | 221 | 223 | PF02516 | 0.549 |
MOD_N-GLC_2 | 575 | 577 | PF02516 | 0.358 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.472 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.566 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.713 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.582 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.358 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.358 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.443 |
MOD_NEK2_1 | 776 | 781 | PF00069 | 0.374 |
MOD_NEK2_1 | 785 | 790 | PF00069 | 0.389 |
MOD_NEK2_1 | 816 | 821 | PF00069 | 0.479 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.570 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.551 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.581 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.505 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.583 |
MOD_PKA_1 | 617 | 623 | PF00069 | 0.374 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.483 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.547 |
MOD_PKA_2 | 711 | 717 | PF00069 | 0.374 |
MOD_PKA_2 | 776 | 782 | PF00069 | 0.358 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.782 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.435 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.786 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.649 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.358 |
MOD_Plk_1 | 753 | 759 | PF00069 | 0.358 |
MOD_Plk_2-3 | 200 | 206 | PF00069 | 0.469 |
MOD_Plk_2-3 | 245 | 251 | PF00069 | 0.645 |
MOD_Plk_2-3 | 255 | 261 | PF00069 | 0.453 |
MOD_Plk_2-3 | 286 | 292 | PF00069 | 0.795 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.441 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.510 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.629 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.556 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.358 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.376 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.383 |
MOD_Plk_4 | 724 | 730 | PF00069 | 0.358 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.464 |
MOD_Plk_4 | 779 | 785 | PF00069 | 0.372 |
MOD_Plk_4 | 811 | 817 | PF00069 | 0.475 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.690 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.689 |
MOD_ProDKin_1 | 799 | 805 | PF00069 | 0.374 |
MOD_SUMO_rev_2 | 222 | 229 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 429 | 436 | PF00179 | 0.616 |
MOD_SUMO_rev_2 | 464 | 474 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 479 | 487 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 596 | 602 | PF00179 | 0.409 |
MOD_SUMO_rev_2 | 615 | 620 | PF00179 | 0.224 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.642 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.611 |
TRG_DiLeu_BaEn_1 | 245 | 250 | PF01217 | 0.527 |
TRG_DiLeu_BaEn_1 | 320 | 325 | PF01217 | 0.708 |
TRG_DiLeu_BaEn_4 | 190 | 196 | PF01217 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 530 | 535 | PF01217 | 0.272 |
TRG_DiLeu_BaLyEn_6 | 562 | 567 | PF01217 | 0.358 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 708 | 711 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 723 | 726 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 507 | 510 | PF00400 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 282 | 286 | PF00026 | 0.772 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.730 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8X9 | Leptomonas seymouri | 76% | 99% |
A0A0S4KHP9 | Bodo saltans | 51% | 92% |
A0A1X0P6D6 | Trypanosomatidae | 61% | 100% |
A0A3S5H751 | Leishmania donovani | 96% | 100% |
A0A422P3A3 | Trypanosoma rangeli | 60% | 100% |
A4H9Y3 | Leishmania braziliensis | 79% | 100% |
A4HY48 | Leishmania infantum | 96% | 100% |
B3H6Z8 | Arabidopsis thaliana | 37% | 78% |
D0A0E6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9ARX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BWY3 | Trypanosoma cruzi | 62% | 100% |