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: A4H9Y3
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 | 186 | 190 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 570 | 574 | PF00656 | 0.345 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.362 |
CLV_PCSK_FUR_1 | 300 | 304 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.739 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.562 |
CLV_PCSK_PC7_1 | 303 | 309 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 832 | 836 | PF00082 | 0.656 |
CLV_Separin_Metazoa | 313 | 317 | PF03568 | 0.494 |
DEG_APCC_DBOX_1 | 336 | 344 | PF00400 | 0.608 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.556 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.552 |
DOC_CDC14_PxL_1 | 389 | 397 | PF14671 | 0.723 |
DOC_CYCLIN_RxL_1 | 792 | 803 | PF00134 | 0.361 |
DOC_MAPK_gen_1 | 468 | 475 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 703 | 712 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 795 | 802 | PF00069 | 0.380 |
DOC_MAPK_NFAT4_5 | 703 | 711 | PF00069 | 0.345 |
DOC_PP1_RVXF_1 | 793 | 800 | PF00149 | 0.345 |
DOC_PP1_RVXF_1 | 821 | 828 | PF00149 | 0.486 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 809 | 813 | PF00917 | 0.359 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.600 |
DOC_USP7_UBL2_3 | 483 | 487 | PF12436 | 0.480 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 672 | 677 | PF00397 | 0.245 |
DOC_WW_Pin1_4 | 800 | 805 | PF00397 | 0.361 |
LIG_14-3-3_CanoR_1 | 253 | 261 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 277 | 281 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 28 | 35 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 489 | 493 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 778 | 786 | PF00244 | 0.361 |
LIG_APCC_ABBA_1 | 631 | 636 | PF00400 | 0.345 |
LIG_BRCT_BRCA1_1 | 557 | 561 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 814 | 818 | PF00533 | 0.345 |
LIG_CaM_IQ_9 | 475 | 491 | PF13499 | 0.543 |
LIG_Clathr_ClatBox_1 | 544 | 548 | PF01394 | 0.403 |
LIG_deltaCOP1_diTrp_1 | 98 | 105 | PF00928 | 0.500 |
LIG_eIF4E_1 | 724 | 730 | PF01652 | 0.403 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.617 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.411 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.615 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.592 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.593 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.552 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.345 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.370 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.223 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.417 |
LIG_FHA_1 | 781 | 787 | PF00498 | 0.345 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.509 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.548 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.796 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.519 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.421 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.467 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 259 | 269 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 491 | 499 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 546 | 555 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 609 | 617 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 546 | 550 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 723 | 727 | PF02991 | 0.245 |
LIG_NRBOX | 781 | 787 | PF00104 | 0.345 |
LIG_PCNA_yPIPBox_3 | 428 | 438 | PF02747 | 0.385 |
LIG_PCNA_yPIPBox_3 | 66 | 80 | PF02747 | 0.565 |
LIG_Pex14_1 | 127 | 131 | PF04695 | 0.455 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.575 |
LIG_PTAP_UEV_1 | 552 | 557 | PF05743 | 0.492 |
LIG_SH2_CRK | 493 | 497 | PF00017 | 0.478 |
LIG_SH2_CRK | 506 | 510 | PF00017 | 0.345 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.607 |
LIG_SH2_CRK | 724 | 728 | PF00017 | 0.403 |
LIG_SH2_GRB2like | 492 | 495 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 493 | 497 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.607 |
LIG_SH2_PTP2 | 709 | 712 | PF00017 | 0.345 |
LIG_SH2_SRC | 709 | 712 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.716 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 527 | 530 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 664 | 667 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 709 | 712 | PF00017 | 0.345 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.357 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.245 |
LIG_SUMO_SIM_anti_2 | 373 | 379 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 620 | 629 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.464 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.717 |
LIG_TRAF2_1 | 495 | 498 | PF00917 | 0.513 |
LIG_TYR_ITIM | 707 | 712 | PF00017 | 0.345 |
LIG_UBA3_1 | 156 | 164 | PF00899 | 0.662 |
LIG_UBA3_1 | 611 | 619 | PF00899 | 0.370 |
MOD_CDK_SPK_2 | 672 | 677 | PF00069 | 0.315 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.418 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.616 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.452 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.466 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.345 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.370 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.357 |
MOD_CK1_1 | 780 | 786 | PF00069 | 0.357 |
MOD_CK1_1 | 803 | 809 | PF00069 | 0.352 |
MOD_CK1_1 | 810 | 816 | PF00069 | 0.340 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.596 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.670 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.438 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.667 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.515 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.462 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.517 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.378 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.345 |
MOD_CK2_1 | 641 | 647 | PF00069 | 0.345 |
MOD_CK2_1 | 738 | 744 | PF00069 | 0.361 |
MOD_Cter_Amidation | 305 | 308 | PF01082 | 0.629 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.375 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.598 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.600 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.742 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.538 |
MOD_GlcNHglycan | 537 | 541 | PF01048 | 0.409 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.431 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.345 |
MOD_GlcNHglycan | 739 | 743 | PF01048 | 0.361 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.223 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.442 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.566 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.522 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.707 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.713 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.540 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.432 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.704 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.733 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.537 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.396 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.290 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.356 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.343 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.351 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.361 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.520 |
MOD_N-GLC_1 | 754 | 759 | PF02516 | 0.345 |
MOD_N-GLC_1 | 807 | 812 | PF02516 | 0.347 |
MOD_N-GLC_1 | 832 | 837 | PF02516 | 0.663 |
MOD_N-GLC_2 | 576 | 578 | PF02516 | 0.345 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.490 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.456 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.632 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.692 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.551 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.379 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.345 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.345 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.406 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.361 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.376 |
MOD_NEK2_1 | 817 | 822 | PF00069 | 0.466 |
MOD_NEK2_2 | 152 | 157 | PF00069 | 0.503 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.555 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.572 |
MOD_PIKK_1 | 526 | 532 | PF00454 | 0.492 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.573 |
MOD_PIKK_1 | 766 | 772 | PF00454 | 0.375 |
MOD_PKA_1 | 276 | 282 | PF00069 | 0.532 |
MOD_PKA_1 | 618 | 624 | PF00069 | 0.361 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.533 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.532 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.396 |
MOD_PKA_2 | 712 | 718 | PF00069 | 0.361 |
MOD_PKA_2 | 777 | 783 | PF00069 | 0.332 |
MOD_PKB_1 | 328 | 336 | PF00069 | 0.611 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.451 |
MOD_Plk_1 | 621 | 627 | PF00069 | 0.345 |
MOD_Plk_1 | 754 | 760 | PF00069 | 0.345 |
MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.529 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.669 |
MOD_Plk_2-3 | 256 | 262 | PF00069 | 0.515 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.768 |
MOD_Plk_2-3 | 363 | 369 | PF00069 | 0.462 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.451 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.350 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.418 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.677 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.515 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.613 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.396 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.345 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.359 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.354 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.233 |
MOD_Plk_4 | 725 | 731 | PF00069 | 0.332 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.359 |
MOD_Plk_4 | 812 | 818 | PF00069 | 0.462 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.585 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.643 |
MOD_ProDKin_1 | 672 | 678 | PF00069 | 0.245 |
MOD_ProDKin_1 | 800 | 806 | PF00069 | 0.361 |
MOD_SUMO_rev_2 | 464 | 470 | PF00179 | 0.555 |
MOD_SUMO_rev_2 | 480 | 488 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 526 | 536 | PF00179 | 0.294 |
MOD_SUMO_rev_2 | 597 | 603 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 613 | 621 | PF00179 | 0.285 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.679 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.596 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 321 | 326 | PF01217 | 0.723 |
TRG_DiLeu_BaEn_1 | 373 | 378 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_4 | 191 | 197 | PF01217 | 0.665 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 563 | 568 | PF01217 | 0.345 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 709 | 712 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 724 | 727 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 278 | 282 | PF00026 | 0.713 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8X9 | Leptomonas seymouri | 74% | 99% |
A0A0S4KHP9 | Bodo saltans | 52% | 92% |
A0A1X0P6D6 | Trypanosomatidae | 60% | 100% |
A0A3S5H751 | Leishmania donovani | 80% | 100% |
A0A422P3A3 | Trypanosoma rangeli | 58% | 100% |
A4HY48 | Leishmania infantum | 80% | 100% |
D0A0E6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9ARX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
P28739 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 33% | 100% |
Q4QDJ5 | Leishmania major | 79% | 100% |
V5BWY3 | Trypanosoma cruzi | 59% | 100% |