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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9ALY0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005215 | transporter activity | 1 | 4 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 4 |
GO:0022804 | active transmembrane transporter activity | 3 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 4 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 4 |
GO:0140657 | ATP-dependent activity | 1 | 4 |
GO:0140359 | ABC-type transporter activity | 3 | 3 |
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 | 0.464 |
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.417 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 547 | 549 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.273 |
DEG_APCC_DBOX_1 | 469 | 477 | PF00400 | 0.483 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.546 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.668 |
DOC_CDC14_PxL_1 | 637 | 645 | PF14671 | 0.336 |
DOC_CKS1_1 | 354 | 359 | PF01111 | 0.653 |
DOC_CYCLIN_yCln2_LP_2 | 214 | 220 | PF00134 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 360 | 366 | PF00134 | 0.512 |
DOC_CYCLIN_yCln2_LP_2 | 550 | 556 | PF00134 | 0.345 |
DOC_CYCLIN_yCln2_LP_2 | 574 | 580 | PF00134 | 0.292 |
DOC_MAPK_DCC_7 | 638 | 646 | PF00069 | 0.379 |
DOC_MAPK_FxFP_2 | 221 | 224 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 203 | 212 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 546 | 556 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 514 | 521 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 52 | 60 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 536 | 543 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 568 | 576 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 584 | 593 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 638 | 646 | PF00069 | 0.379 |
DOC_PP1_RVXF_1 | 512 | 519 | PF00149 | 0.234 |
DOC_PP1_RVXF_1 | 612 | 619 | PF00149 | 0.526 |
DOC_PP1_SILK_1 | 647 | 652 | PF00149 | 0.285 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.484 |
DOC_PP2B_LxvP_1 | 294 | 297 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 451 | 454 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 574 | 577 | PF13499 | 0.323 |
DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.496 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.643 |
DOC_SPAK_OSR1_1 | 464 | 468 | PF12202 | 0.506 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.438 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 359 | 363 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 382 | 389 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 443 | 453 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 584 | 590 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 613 | 619 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 455 | 472 | PF00022 | 0.518 |
LIG_Actin_WH2_2 | 525 | 542 | PF00022 | 0.439 |
LIG_Actin_WH2_2 | 569 | 586 | PF00022 | 0.394 |
LIG_Actin_WH2_2 | 705 | 722 | PF00022 | 0.389 |
LIG_AP2alpha_2 | 336 | 338 | PF02296 | 0.557 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.665 |
LIG_BRCT_BRCA1_1 | 626 | 630 | PF00533 | 0.472 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.522 |
LIG_EH1_1 | 510 | 518 | PF00400 | 0.308 |
LIG_eIF4E_1 | 511 | 517 | PF01652 | 0.314 |
LIG_eIF4E_1 | 587 | 593 | PF01652 | 0.336 |
LIG_EVH1_1 | 451 | 455 | PF00568 | 0.500 |
LIG_EVH1_2 | 216 | 220 | PF00568 | 0.467 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.583 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.630 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.502 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.399 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.374 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.665 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.604 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.324 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.643 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.607 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.331 |
LIG_LIR_Apic_2 | 324 | 328 | PF02991 | 0.704 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 289 | 297 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 348 | 358 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 569 | 579 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 620 | 629 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 682 | 690 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.766 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 569 | 574 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 617 | 621 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 682 | 687 | PF02991 | 0.270 |
LIG_MYND_1 | 328 | 332 | PF01753 | 0.644 |
LIG_Pex14_1 | 70 | 74 | PF04695 | 0.553 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.535 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.483 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.644 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.566 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.514 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.276 |
LIG_SH2_CRK | 654 | 658 | PF00017 | 0.304 |
LIG_SH2_GRB2like | 290 | 293 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 626 | 630 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 587 | 591 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 626 | 630 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.141 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.259 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.454 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.722 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.762 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.690 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.724 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.758 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.529 |
LIG_SH3_5 | 331 | 335 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 588 | 593 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 153 | 159 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 390 | 400 | PF11976 | 0.691 |
LIG_SUMO_SIM_par_1 | 492 | 497 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 563 | 569 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 712 | 718 | PF11976 | 0.308 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.730 |
LIG_TYR_ITIM | 657 | 662 | PF00017 | 0.370 |
LIG_UBA3_1 | 150 | 158 | PF00899 | 0.464 |
LIG_WRC_WIRS_1 | 322 | 327 | PF05994 | 0.645 |
LIG_WW_3 | 356 | 360 | PF00397 | 0.571 |
LIG_WW_3 | 453 | 457 | PF00397 | 0.494 |
MOD_CDK_SPxK_1 | 353 | 359 | PF00069 | 0.592 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.469 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.596 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.432 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.541 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.665 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.343 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.381 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.339 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.415 |
MOD_CMANNOS | 615 | 618 | PF00535 | 0.333 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.403 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.713 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.473 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.200 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.651 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.584 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.275 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.445 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.591 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.301 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.446 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.421 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.393 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.216 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.303 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.382 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.593 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.614 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.450 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.446 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.540 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.420 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.434 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.259 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.403 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.375 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.260 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.611 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.413 |
MOD_N-GLC_1 | 691 | 696 | PF02516 | 0.390 |
MOD_N-GLC_2 | 234 | 236 | PF02516 | 0.392 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.396 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.447 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.253 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.290 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.422 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.444 |
MOD_NEK2_2 | 146 | 151 | PF00069 | 0.407 |
MOD_NEK2_2 | 153 | 158 | PF00069 | 0.289 |
MOD_NEK2_2 | 290 | 295 | PF00069 | 0.476 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.411 |
MOD_NEK2_2 | 531 | 536 | PF00069 | 0.382 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.396 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.464 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.627 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.511 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.415 |
MOD_PK_1 | 349 | 355 | PF00069 | 0.527 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.542 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.559 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.601 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.419 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.414 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.362 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.404 |
MOD_Plk_1 | 691 | 697 | PF00069 | 0.421 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.399 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.465 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.304 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.212 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.566 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.408 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.418 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.383 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.412 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.446 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.329 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.342 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.391 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.323 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.592 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.659 |
MOD_SUMO_rev_2 | 188 | 196 | PF00179 | 0.219 |
TRG_DiLeu_BaEn_1 | 235 | 240 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.228 |
TRG_DiLeu_BaLyEn_6 | 639 | 644 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.128 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 684 | 687 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.334 |
TRG_NES_CRM1_1 | 54 | 67 | PF08389 | 0.342 |
TRG_NLS_MonoCore_2 | 545 | 550 | PF00514 | 0.401 |
TRG_NLS_MonoExtN_4 | 546 | 551 | PF00514 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I174 | Leptomonas seymouri | 53% | 100% |
A0A0S4JPC7 | Bodo saltans | 30% | 85% |
A0A1X0NZQ7 | Trypanosomatidae | 34% | 100% |
A0A3R7KD05 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H7K9 | Leishmania donovani | 93% | 100% |
A4HHA4 | Leishmania braziliensis | 82% | 100% |
A4I4F0 | Leishmania infantum | 94% | 100% |
E9ADV0 | Leishmania major | 92% | 100% |
Q7TMS5 | Mus musculus | 21% | 100% |
V5BLN9 | Trypanosoma cruzi | 33% | 100% |