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. | no | 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:0005874 | microtubule | 6 | 12 |
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 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: E9ARX7
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007018 | microtubule-based movement | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0006810 | transport | 3 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
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: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:0017076 | purine nucleotide binding | 4 | 12 |
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 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.812 |
CLV_C14_Caspase3-7 | 572 | 576 | PF00656 | 0.378 |
CLV_MEL_PAP_1 | 252 | 258 | PF00089 | 0.500 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.394 |
CLV_PCSK_FUR_1 | 302 | 306 | PF00082 | 0.807 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.599 |
CLV_PCSK_PC7_1 | 300 | 306 | PF00082 | 0.780 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 834 | 838 | PF00082 | 0.712 |
DEG_APCC_DBOX_1 | 338 | 346 | PF00400 | 0.636 |
DEG_APCC_DBOX_1 | 422 | 430 | PF00400 | 0.575 |
DOC_CDC14_PxL_1 | 391 | 399 | PF14671 | 0.770 |
DOC_CYCLIN_RxL_1 | 794 | 805 | PF00134 | 0.394 |
DOC_MAPK_gen_1 | 749 | 756 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 705 | 714 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 797 | 804 | PF00069 | 0.413 |
DOC_MAPK_NFAT4_5 | 705 | 713 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 473 | 480 | PF00149 | 0.587 |
DOC_PP1_RVXF_1 | 795 | 802 | PF00149 | 0.378 |
DOC_PP1_RVXF_1 | 823 | 830 | PF00149 | 0.524 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.446 |
DOC_USP7_UBL2_3 | 360 | 364 | PF12436 | 0.649 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.516 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 802 | 807 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 131 | 140 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 244 | 253 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 255 | 263 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 430 | 434 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 780 | 785 | PF00244 | 0.394 |
LIG_Actin_WH2_2 | 418 | 436 | PF00022 | 0.524 |
LIG_APCC_ABBA_1 | 560 | 565 | PF00400 | 0.234 |
LIG_APCC_ABBA_1 | 633 | 638 | PF00400 | 0.378 |
LIG_BIR_III_4 | 539 | 543 | PF00653 | 0.446 |
LIG_BRCT_BRCA1_1 | 816 | 820 | PF00533 | 0.378 |
LIG_CaM_IQ_9 | 477 | 493 | PF13499 | 0.583 |
LIG_Clathr_ClatBox_1 | 546 | 550 | PF01394 | 0.435 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.537 |
LIG_deltaCOP1_diTrp_1 | 99 | 106 | PF00928 | 0.529 |
LIG_eIF4E_1 | 726 | 732 | PF01652 | 0.435 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.537 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.691 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.531 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.537 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.632 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.608 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.595 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.378 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.403 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.195 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.450 |
LIG_FHA_1 | 783 | 789 | PF00498 | 0.378 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.553 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.843 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.552 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.492 |
LIG_FHA_2 | 644 | 650 | PF00498 | 0.454 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.495 |
LIG_LIR_Gen_1 | 152 | 162 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 177 | 183 | PF02991 | 0.721 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 520 | 530 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 548 | 557 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 611 | 619 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 548 | 552 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 611 | 617 | PF02991 | 0.394 |
LIG_NRBOX | 783 | 789 | PF00104 | 0.378 |
LIG_PCNA_yPIPBox_3 | 67 | 81 | PF02747 | 0.595 |
LIG_PDZ_Class_3 | 836 | 841 | PF00595 | 0.488 |
LIG_Pex14_1 | 128 | 132 | PF04695 | 0.483 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.602 |
LIG_PTAP_UEV_1 | 554 | 559 | PF05743 | 0.525 |
LIG_SH2_CRK | 495 | 499 | PF00017 | 0.511 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.378 |
LIG_SH2_CRK | 68 | 72 | PF00017 | 0.639 |
LIG_SH2_CRK | 726 | 730 | PF00017 | 0.435 |
LIG_SH2_GRB2like | 494 | 497 | PF00017 | 0.525 |
LIG_SH2_NCK_1 | 495 | 499 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 68 | 72 | PF00017 | 0.639 |
LIG_SH2_PTP2 | 711 | 714 | PF00017 | 0.378 |
LIG_SH2_SRC | 711 | 714 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.632 |
LIG_SH2_STAP1 | 451 | 455 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 451 | 454 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 529 | 532 | PF00017 | 0.525 |
LIG_SH2_STAT3 | 636 | 639 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 666 | 669 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.378 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.390 |
LIG_SUMO_SIM_anti_2 | 629 | 634 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 191 | 199 | PF11976 | 0.617 |
LIG_SUMO_SIM_par_1 | 626 | 634 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 76 | 82 | PF11976 | 0.493 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.733 |
LIG_TRAF2_1 | 497 | 500 | PF00917 | 0.547 |
LIG_TYR_ITIM | 709 | 714 | PF00017 | 0.378 |
LIG_UBA3_1 | 157 | 163 | PF00899 | 0.663 |
MOD_CDC14_SPxK_1 | 5 | 8 | PF00782 | 0.641 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.646 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.643 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.632 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.467 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.499 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.378 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.393 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.390 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.390 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.385 |
MOD_CK1_1 | 812 | 818 | PF00069 | 0.373 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.717 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.670 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.491 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.513 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.561 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.550 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.411 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.448 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.378 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.378 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.394 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.561 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.644 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.618 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.753 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.583 |
MOD_GlcNHglycan | 539 | 543 | PF01048 | 0.442 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.459 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.378 |
MOD_GlcNHglycan | 741 | 745 | PF01048 | 0.394 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.256 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.352 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.604 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.723 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.722 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.651 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.512 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.530 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.677 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.504 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.579 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.426 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.492 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.355 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.376 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.384 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.394 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.516 |
MOD_LATS_1 | 242 | 248 | PF00433 | 0.630 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.498 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.623 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.642 |
MOD_N-GLC_1 | 595 | 600 | PF02516 | 0.448 |
MOD_N-GLC_1 | 756 | 761 | PF02516 | 0.378 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.234 |
MOD_N-GLC_1 | 809 | 814 | PF02516 | 0.380 |
MOD_N-GLC_1 | 834 | 839 | PF02516 | 0.725 |
MOD_N-GLC_2 | 224 | 226 | PF02516 | 0.585 |
MOD_N-GLC_2 | 578 | 580 | PF02516 | 0.378 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.552 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.487 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.598 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.746 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.607 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.468 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.378 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.378 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.439 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.235 |
MOD_NEK2_1 | 779 | 784 | PF00069 | 0.394 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.409 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.499 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.588 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.586 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.615 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.525 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.604 |
MOD_PKA_1 | 620 | 626 | PF00069 | 0.394 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.751 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.521 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.575 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.566 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.348 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.523 |
MOD_PKA_2 | 714 | 720 | PF00069 | 0.394 |
MOD_PKA_2 | 779 | 785 | PF00069 | 0.365 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.806 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.520 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.373 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.786 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.666 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.396 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.378 |
MOD_Plk_1 | 756 | 762 | PF00069 | 0.378 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.234 |
MOD_Plk_2-3 | 203 | 209 | PF00069 | 0.524 |
MOD_Plk_2-3 | 248 | 254 | PF00069 | 0.672 |
MOD_Plk_2-3 | 258 | 264 | PF00069 | 0.491 |
MOD_Plk_2-3 | 289 | 295 | PF00069 | 0.813 |
MOD_Plk_2-3 | 365 | 371 | PF00069 | 0.513 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.474 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.540 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.679 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.491 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.664 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.378 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.396 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.387 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.365 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.475 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.392 |
MOD_Plk_4 | 814 | 820 | PF00069 | 0.495 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.756 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.714 |
MOD_ProDKin_1 | 802 | 808 | PF00069 | 0.394 |
MOD_SUMO_rev_2 | 225 | 232 | PF00179 | 0.590 |
MOD_SUMO_rev_2 | 432 | 439 | PF00179 | 0.642 |
MOD_SUMO_rev_2 | 467 | 477 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 482 | 490 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 528 | 538 | PF00179 | 0.327 |
MOD_SUMO_rev_2 | 599 | 605 | PF00179 | 0.429 |
TRG_DiLeu_BaEn_1 | 193 | 198 | PF01217 | 0.662 |
TRG_DiLeu_BaEn_1 | 22 | 27 | PF01217 | 0.627 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.554 |
TRG_DiLeu_BaEn_1 | 323 | 328 | PF01217 | 0.738 |
TRG_DiLeu_BaLyEn_6 | 565 | 570 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 726 | 729 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 510 | 513 | PF00400 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.787 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 431 | 435 | PF00026 | 0.543 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8X9 | Leptomonas seymouri | 76% | 100% |
A0A0S4KHP9 | Bodo saltans | 51% | 93% |
A0A1X0P6D6 | Trypanosomatidae | 61% | 100% |
A0A3S5H751 | Leishmania donovani | 92% | 100% |
A0A422P3A3 | Trypanosoma rangeli | 59% | 100% |
A4H9Y3 | Leishmania braziliensis | 79% | 100% |
A4HY48 | Leishmania infantum | 92% | 100% |
D0A0E6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
Q4QDJ5 | Leishmania major | 92% | 100% |
V5BWY3 | Trypanosoma cruzi | 61% | 100% |