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: 0 |
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: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 17 |
GO:0099080 | supramolecular complex | 2 | 17 |
GO:0099081 | supramolecular polymer | 3 | 17 |
GO:0099512 | supramolecular fiber | 4 | 17 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
Related structures:
AlphaFold database: E9AVN8
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 22 |
GO:0007018 | microtubule-based movement | 3 | 22 |
GO:0009987 | cellular process | 1 | 22 |
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 | 22 |
GO:0003774 | cytoskeletal motor activity | 1 | 22 |
GO:0003777 | microtubule motor activity | 2 | 22 |
GO:0005488 | binding | 1 | 22 |
GO:0005515 | protein binding | 2 | 22 |
GO:0005524 | ATP binding | 5 | 22 |
GO:0008017 | microtubule binding | 5 | 22 |
GO:0008092 | cytoskeletal protein binding | 3 | 22 |
GO:0015631 | tubulin binding | 4 | 22 |
GO:0017076 | purine nucleotide binding | 4 | 22 |
GO:0030554 | adenyl nucleotide binding | 5 | 22 |
GO:0032553 | ribonucleotide binding | 3 | 22 |
GO:0032555 | purine ribonucleotide binding | 4 | 22 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 22 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 22 |
GO:0036094 | small molecule binding | 2 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043168 | anion binding | 3 | 22 |
GO:0097159 | organic cyclic compound binding | 2 | 22 |
GO:0097367 | carbohydrate derivative binding | 2 | 22 |
GO:0140657 | ATP-dependent activity | 1 | 22 |
GO:1901265 | nucleoside phosphate binding | 3 | 22 |
GO:1901363 | heterocyclic compound binding | 2 | 22 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 1 |
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 | 260 | 264 | PF00656 | 0.634 |
CLV_C14_Caspase3-7 | 752 | 756 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 774 | 776 | PF00675 | 0.779 |
CLV_PCSK_FUR_1 | 427 | 431 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 816 | 818 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 816 | 818 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 763 | 767 | PF00082 | 0.469 |
CLV_Separin_Metazoa | 625 | 629 | PF03568 | 0.561 |
DEG_SCF_FBW7_2 | 408 | 413 | PF00400 | 0.389 |
DOC_CYCLIN_RxL_1 | 455 | 465 | PF00134 | 0.477 |
DOC_MAPK_gen_1 | 427 | 437 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 531 | 539 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 579 | 587 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 688 | 696 | PF00069 | 0.345 |
DOC_MAPK_gen_1 | 814 | 823 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 824 | 832 | PF00069 | 0.436 |
DOC_MAPK_HePTP_8 | 813 | 825 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.265 |
DOC_MAPK_MEF2A_6 | 807 | 815 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 816 | 825 | PF00069 | 0.426 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.527 |
DOC_USP7_UBL2_3 | 855 | 859 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 218 | 228 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 364 | 372 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 419 | 423 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 568 | 572 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 618 | 627 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 702 | 710 | PF00244 | 0.557 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.333 |
LIG_APCC_ABBA_1 | 380 | 385 | PF00400 | 0.273 |
LIG_APCC_ABBAyCdc20_2 | 127 | 133 | PF00400 | 0.389 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.254 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.336 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.333 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.334 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.505 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.456 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.266 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.572 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.601 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.499 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.646 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.666 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.406 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.523 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.407 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.668 |
LIG_FHA_2 | 750 | 756 | PF00498 | 0.740 |
LIG_Integrin_RGD_1 | 660 | 662 | PF01839 | 0.461 |
LIG_LIR_Gen_1 | 115 | 122 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 400 | 408 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 48 | 57 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 681 | 689 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 681 | 685 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 726 | 732 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.260 |
LIG_NRBOX | 145 | 151 | PF00104 | 0.334 |
LIG_NRBOX | 387 | 393 | PF00104 | 0.319 |
LIG_NRBOX | 727 | 733 | PF00104 | 0.459 |
LIG_PCNA_yPIPBox_3 | 143 | 151 | PF02747 | 0.384 |
LIG_SH2_CRK | 682 | 686 | PF00017 | 0.567 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 53 | 57 | PF00017 | 0.233 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.296 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.240 |
LIG_SH2_STAT3 | 478 | 481 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 664 | 667 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.285 |
LIG_SH3_3 | 880 | 886 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 692 | 698 | PF11976 | 0.474 |
LIG_SUMO_SIM_anti_2 | 766 | 772 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 582 | 588 | PF11976 | 0.471 |
LIG_SxIP_EBH_1 | 374 | 384 | PF03271 | 0.233 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.331 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.672 |
LIG_TRAF2_1 | 525 | 528 | PF00917 | 0.491 |
LIG_TRAF2_1 | 629 | 632 | PF00917 | 0.514 |
LIG_TRAF2_2 | 743 | 748 | PF00917 | 0.479 |
LIG_UBA3_1 | 845 | 852 | PF00899 | 0.487 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.501 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.426 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.311 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.371 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.681 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.470 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.329 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.282 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.352 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.325 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.704 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.603 |
MOD_CK1_1 | 706 | 712 | PF00069 | 0.435 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.326 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.306 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.260 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.272 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.681 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.262 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.335 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.423 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.610 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.356 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.508 |
MOD_CK2_1 | 618 | 624 | PF00069 | 0.491 |
MOD_Cter_Amidation | 298 | 301 | PF01082 | 0.537 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.410 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.480 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.326 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.444 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.338 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.459 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.452 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.689 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.586 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.562 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.326 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.490 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.306 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.379 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.666 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.295 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.338 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.367 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.698 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.597 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.690 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.439 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.576 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.618 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.356 |
MOD_LATS_1 | 317 | 323 | PF00433 | 0.176 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.176 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.333 |
MOD_N-GLC_1 | 706 | 711 | PF02516 | 0.453 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.292 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.207 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.286 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.500 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.621 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.563 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.440 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.603 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.421 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.434 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.562 |
MOD_NEK2_1 | 851 | 856 | PF00069 | 0.563 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.323 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.424 |
MOD_NEK2_2 | 749 | 754 | PF00069 | 0.508 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.349 |
MOD_NEK2_2 | 863 | 868 | PF00069 | 0.418 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.717 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.556 |
MOD_PIKK_1 | 585 | 591 | PF00454 | 0.450 |
MOD_PIKK_1 | 643 | 649 | PF00454 | 0.503 |
MOD_PIKK_1 | 680 | 686 | PF00454 | 0.390 |
MOD_PIKK_1 | 736 | 742 | PF00454 | 0.625 |
MOD_PIKK_1 | 753 | 759 | PF00454 | 0.442 |
MOD_PIKK_1 | 853 | 859 | PF00454 | 0.656 |
MOD_PKA_1 | 618 | 624 | PF00069 | 0.386 |
MOD_PKA_1 | 774 | 780 | PF00069 | 0.514 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.332 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.321 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.715 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.694 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.333 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.286 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.582 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.600 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.413 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.558 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.566 |
MOD_PKA_2 | 753 | 759 | PF00069 | 0.624 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.652 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.327 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.426 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.324 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.543 |
MOD_Plk_1 | 666 | 672 | PF00069 | 0.405 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.595 |
MOD_Plk_2-3 | 257 | 263 | PF00069 | 0.599 |
MOD_Plk_2-3 | 33 | 39 | PF00069 | 0.389 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.375 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.291 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.317 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.471 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.666 |
MOD_Plk_4 | 719 | 725 | PF00069 | 0.486 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.331 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.316 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.398 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.402 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.362 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.690 |
MOD_SUMO_rev_2 | 528 | 535 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 601 | 608 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 808 | 815 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 622 | 627 | PF01217 | 0.473 |
TRG_DiLeu_BaEn_1 | 692 | 697 | PF01217 | 0.514 |
TRG_DiLeu_BaEn_4 | 528 | 534 | PF01217 | 0.607 |
TRG_DiLeu_BaEn_4 | 632 | 638 | PF01217 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 651 | 656 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 727 | 732 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 682 | 685 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.257 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 789 | 792 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 876 | 879 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 663 | 676 | PF08389 | 0.413 |
TRG_NLS_MonoExtN_4 | 427 | 433 | PF00514 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 600 | 605 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 794 | 798 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVM1 | Leptomonas seymouri | 65% | 96% |
A0A0S4INA4 | Bodo saltans | 41% | 100% |
A0A0S4JAQ8 | Bodo saltans | 27% | 73% |
A0A1X0NUN6 | Trypanosomatidae | 42% | 95% |
A0A3R7NW09 | Trypanosoma rangeli | 30% | 85% |
A0A3S5H5N6 | Leishmania donovani | 26% | 100% |
A0A3S7WX05 | Leishmania donovani | 91% | 100% |
A0A422N2N4 | Trypanosoma rangeli | 42% | 100% |
A4H4I4 | Leishmania braziliensis | 24% | 100% |
A4HCA1 | Leishmania braziliensis | 77% | 100% |
A4HMM9 | Leishmania braziliensis | 30% | 100% |
A4HSQ9 | Leishmania infantum | 26% | 100% |
A4HZT3 | Leishmania infantum | 91% | 100% |
E9AKP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AXS9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 83% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q7S4 | Leishmania major | 26% | 100% |
Q4QBU1 | Leishmania major | 90% | 100% |
Q4QJ61 | Leishmania major | 26% | 100% |
V5BLH7 | Trypanosoma cruzi | 43% | 100% |