Related to other Eukaryotic ABC transporters.. Expanded on the Trypanosoma rangeli and theileri lineages
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9ADV0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0005215 | transporter activity | 1 | 6 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0022804 | active transmembrane transporter activity | 3 | 6 |
GO:0022857 | transmembrane transporter activity | 2 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 6 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0140359 | ABC-type transporter activity | 3 | 4 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.413 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 547 | 549 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.306 |
DEG_APCC_DBOX_1 | 469 | 477 | PF00400 | 0.568 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.592 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.734 |
DOC_CDC14_PxL_1 | 637 | 645 | PF14671 | 0.439 |
DOC_CKS1_1 | 354 | 359 | PF01111 | 0.747 |
DOC_CYCLIN_yCln2_LP_2 | 214 | 220 | PF00134 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 574 | 580 | PF00134 | 0.453 |
DOC_MAPK_DCC_7 | 638 | 646 | PF00069 | 0.424 |
DOC_MAPK_FxFP_2 | 221 | 224 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 203 | 212 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 546 | 556 | PF00069 | 0.626 |
DOC_MAPK_gen_1 | 613 | 619 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 93 | 99 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 514 | 521 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 52 | 60 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 536 | 543 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 568 | 576 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 584 | 593 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 638 | 646 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 512 | 519 | PF00149 | 0.304 |
DOC_PP1_RVXF_1 | 612 | 619 | PF00149 | 0.577 |
DOC_PP1_SILK_1 | 647 | 652 | PF00149 | 0.350 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.596 |
DOC_PP2B_LxvP_1 | 294 | 297 | PF13499 | 0.635 |
DOC_PP2B_LxvP_1 | 574 | 577 | PF13499 | 0.484 |
DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.597 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.733 |
DOC_SPAK_OSR1_1 | 464 | 468 | PF12202 | 0.608 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.497 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 359 | 367 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 386 | 395 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 584 | 590 | PF00244 | 0.366 |
LIG_Actin_WH2_2 | 455 | 472 | PF00022 | 0.627 |
LIG_Actin_WH2_2 | 525 | 542 | PF00022 | 0.500 |
LIG_Actin_WH2_2 | 569 | 586 | PF00022 | 0.485 |
LIG_Actin_WH2_2 | 705 | 722 | PF00022 | 0.450 |
LIG_BIR_III_4 | 226 | 230 | PF00653 | 0.552 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.581 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.809 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.765 |
LIG_BRCT_BRCA1_1 | 552 | 556 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 626 | 630 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.576 |
LIG_CtBP_PxDLS_1 | 188 | 193 | PF00389 | 0.458 |
LIG_EH1_1 | 510 | 518 | PF00400 | 0.358 |
LIG_eIF4E_1 | 511 | 517 | PF01652 | 0.362 |
LIG_eIF4E_1 | 587 | 593 | PF01652 | 0.396 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.616 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.564 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.463 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.414 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.688 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.656 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.386 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.602 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.370 |
LIG_Integrin_isoDGR_2 | 77 | 79 | PF01839 | 0.433 |
LIG_LIR_Apic_2 | 324 | 328 | PF02991 | 0.769 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 289 | 297 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 348 | 358 | PF02991 | 0.772 |
LIG_LIR_Gen_1 | 569 | 579 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 620 | 629 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 682 | 690 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.759 |
LIG_LIR_Nem_3 | 569 | 574 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 620 | 626 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 682 | 687 | PF02991 | 0.324 |
LIG_MYND_1 | 328 | 332 | PF01753 | 0.724 |
LIG_Pex14_1 | 70 | 74 | PF04695 | 0.659 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.581 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.775 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.617 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.573 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.370 |
LIG_SH2_CRK | 654 | 658 | PF00017 | 0.365 |
LIG_SH2_GRB2like | 290 | 293 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 626 | 630 | PF00017 | 0.418 |
LIG_SH2_SRC | 605 | 608 | PF00017 | 0.238 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 587 | 591 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 626 | 630 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.747 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.163 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.297 |
LIG_SH3_2 | 451 | 456 | PF14604 | 0.625 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.773 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.748 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.774 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.759 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.644 |
LIG_SH3_CIN85_PxpxPR_1 | 451 | 456 | PF14604 | 0.569 |
LIG_Sin3_3 | 480 | 487 | PF02671 | 0.494 |
LIG_SUMO_SIM_anti_2 | 588 | 593 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 153 | 159 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 390 | 400 | PF11976 | 0.694 |
LIG_SUMO_SIM_par_1 | 492 | 497 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 563 | 569 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 700 | 705 | PF11976 | 0.345 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.783 |
LIG_TYR_ITIM | 657 | 662 | PF00017 | 0.509 |
LIG_UBA3_1 | 150 | 158 | PF00899 | 0.510 |
LIG_WRC_WIRS_1 | 322 | 327 | PF05994 | 0.740 |
LIG_WW_1 | 377 | 380 | PF00397 | 0.738 |
LIG_WW_3 | 356 | 360 | PF00397 | 0.703 |
LIG_WW_3 | 453 | 457 | PF00397 | 0.594 |
MOD_CDK_SPxK_1 | 353 | 359 | PF00069 | 0.711 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.509 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.648 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.450 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.706 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.623 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.733 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.400 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.462 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.366 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.427 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.560 |
MOD_CMANNOS | 615 | 618 | PF00535 | 0.472 |
MOD_Cter_Amidation | 191 | 194 | PF01082 | 0.429 |
MOD_Cter_Amidation | 77 | 80 | PF01082 | 0.552 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.454 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.708 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.519 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.239 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.715 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.683 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.541 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.576 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.391 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.469 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.422 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.455 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.464 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.283 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.346 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.450 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.684 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.721 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.649 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.490 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.648 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.461 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.451 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.350 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.494 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.431 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.695 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.493 |
MOD_N-GLC_1 | 691 | 696 | PF02516 | 0.460 |
MOD_N-GLC_2 | 234 | 236 | PF02516 | 0.525 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.463 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.500 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.435 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.286 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.362 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.426 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.462 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.438 |
MOD_NEK2_1 | 715 | 720 | PF00069 | 0.460 |
MOD_NEK2_2 | 146 | 151 | PF00069 | 0.572 |
MOD_NEK2_2 | 153 | 158 | PF00069 | 0.471 |
MOD_NEK2_2 | 290 | 295 | PF00069 | 0.533 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.495 |
MOD_NEK2_2 | 531 | 536 | PF00069 | 0.518 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.558 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.535 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.508 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.762 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.553 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.510 |
MOD_PK_1 | 349 | 355 | PF00069 | 0.675 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.573 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.681 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.613 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.466 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.558 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.577 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.446 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.496 |
MOD_Plk_1 | 691 | 697 | PF00069 | 0.493 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.421 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.508 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.400 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.272 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.733 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.478 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.494 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.421 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.408 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.391 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.325 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.395 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.431 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.589 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.755 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.657 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.713 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.618 |
TRG_DiLeu_BaEn_1 | 235 | 240 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.272 |
TRG_DiLeu_BaLyEn_6 | 639 | 644 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.721 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.141 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 684 | 687 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.543 |
TRG_NES_CRM1_1 | 54 | 68 | PF08389 | 0.461 |
TRG_NLS_MonoCore_2 | 545 | 550 | PF00514 | 0.544 |
TRG_NLS_MonoExtN_4 | 546 | 551 | PF00514 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.652 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I174 | Leptomonas seymouri | 52% | 100% |
A0A0S4JPC7 | Bodo saltans | 29% | 85% |
A0A1X0NXY3 | Trypanosomatidae | 22% | 100% |
A0A1X0NZQ7 | Trypanosomatidae | 33% | 100% |
A0A3R7KD05 | Trypanosoma rangeli | 34% | 100% |
A0A3S5H7K9 | Leishmania donovani | 94% | 100% |
A4HHA4 | Leishmania braziliensis | 81% | 100% |
A4I4F0 | Leishmania infantum | 95% | 100% |
E9ALY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BIB9 | Trypanosoma cruzi | 21% | 100% |
V5BLN9 | Trypanosoma cruzi | 33% | 100% |