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. | yes | yes: 20 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B466
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 1 |
GO:0003777 | microtubule motor activity | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.575 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 776 | 778 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 773 | 779 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.560 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.549 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.582 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.465 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.529 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.531 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.546 |
DEG_SPOP_SBC_1 | 336 | 340 | PF00917 | 0.503 |
DEG_SPOP_SBC_1 | 375 | 379 | PF00917 | 0.552 |
DEG_SPOP_SBC_1 | 414 | 418 | PF00917 | 0.541 |
DEG_SPOP_SBC_1 | 44 | 48 | PF00917 | 0.668 |
DEG_SPOP_SBC_1 | 453 | 457 | PF00917 | 0.545 |
DEG_SPOP_SBC_1 | 492 | 496 | PF00917 | 0.538 |
DEG_SPOP_SBC_1 | 531 | 535 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 570 | 574 | PF00917 | 0.531 |
DEG_SPOP_SBC_1 | 609 | 613 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 648 | 652 | PF00917 | 0.499 |
DOC_CYCLIN_RxL_1 | 114 | 124 | PF00134 | 0.539 |
DOC_MAPK_MEF2A_6 | 8 | 16 | PF00069 | 0.620 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 781 | 785 | PF00917 | 0.544 |
DOC_USP7_UBL2_3 | 710 | 714 | PF12436 | 0.595 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 38 | 45 | PF00244 | 0.673 |
LIG_BRCT_BRCA1_1 | 701 | 705 | PF00533 | 0.526 |
LIG_Clathr_ClatBox_1 | 120 | 124 | PF01394 | 0.489 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.546 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.474 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.551 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.601 |
LIG_GBD_Chelix_1 | 721 | 729 | PF00786 | 0.530 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 95 | 106 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.437 |
LIG_RPA_C_Fungi | 161 | 173 | PF08784 | 0.478 |
LIG_RPA_C_Fungi | 200 | 212 | PF08784 | 0.518 |
LIG_RPA_C_Fungi | 239 | 251 | PF08784 | 0.543 |
LIG_RPA_C_Fungi | 278 | 290 | PF08784 | 0.497 |
LIG_RPA_C_Fungi | 317 | 329 | PF08784 | 0.543 |
LIG_RPA_C_Fungi | 356 | 368 | PF08784 | 0.543 |
LIG_RPA_C_Fungi | 395 | 407 | PF08784 | 0.534 |
LIG_RPA_C_Fungi | 434 | 446 | PF08784 | 0.539 |
LIG_RPA_C_Fungi | 473 | 485 | PF08784 | 0.539 |
LIG_RPA_C_Fungi | 512 | 524 | PF08784 | 0.530 |
LIG_RPA_C_Fungi | 551 | 563 | PF08784 | 0.539 |
LIG_RPA_C_Fungi | 590 | 602 | PF08784 | 0.518 |
LIG_RPA_C_Fungi | 629 | 641 | PF08784 | 0.508 |
LIG_RPA_C_Fungi | 668 | 680 | PF08784 | 0.484 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.568 |
LIG_SH2_GRB2like | 57 | 60 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.679 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.707 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.575 |
LIG_SUMO_SIM_par_1 | 118 | 124 | PF11976 | 0.487 |
LIG_TRAF2_1 | 789 | 792 | PF00917 | 0.613 |
MOD_CAAXbox | 808 | 811 | PF01239 | 0.594 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.675 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.819 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.687 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.567 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.547 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.698 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.615 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.547 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.566 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.520 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.620 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.610 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.630 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.610 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.559 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.565 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.550 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.607 |
MOD_CK2_1 | 647 | 653 | PF00069 | 0.584 |
MOD_CK2_1 | 786 | 792 | PF00069 | 0.547 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.693 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.634 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.579 |
MOD_GlcNHglycan | 783 | 787 | PF01048 | 0.663 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.716 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.467 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.524 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.671 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.537 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.535 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.621 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.552 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.556 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.675 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.554 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.546 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.583 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.551 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.543 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.557 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.535 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.525 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.501 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.580 |
MOD_LATS_1 | 36 | 42 | PF00433 | 0.645 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.788 |
MOD_N-GLC_1 | 699 | 704 | PF02516 | 0.517 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.587 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.671 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.643 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.711 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.738 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.672 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.650 |
MOD_SUMO_for_1 | 60 | 63 | PF00179 | 0.527 |
TRG_AP2beta_CARGO_1 | 95 | 105 | PF09066 | 0.447 |
TRG_DiLeu_BaEn_1 | 735 | 740 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_1 | 783 | 788 | PF01217 | 0.614 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.713 |
TRG_ER_diArg_1 | 775 | 778 | PF00400 | 0.550 |
TRG_NES_CRM1_1 | 681 | 697 | PF08389 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 119 | 124 | PF00026 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X6W4 | Leishmania donovani | 80% | 77% |
A4HLU0 | Leishmania braziliensis | 62% | 100% |
C9ZSW5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 98% |
E9AHP6 | Leishmania infantum | 76% | 100% |
Q4Q3W0 | Leishmania major | 77% | 100% |