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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALJ8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.469 |
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.510 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.569 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.424 |
DEG_APCC_DBOX_1 | 529 | 537 | PF00400 | 0.427 |
DOC_CYCLIN_RxL_1 | 265 | 275 | PF00134 | 0.511 |
DOC_MAPK_gen_1 | 25 | 31 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 253 | 260 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 300 | 307 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 313 | 320 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 272 | 281 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 300 | 307 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.544 |
DOC_MAPK_NFAT4_5 | 367 | 375 | PF00069 | 0.548 |
DOC_PP2B_PxIxI_1 | 592 | 598 | PF00149 | 0.467 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.404 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.643 |
LIG_14-3-3_CanoR_1 | 127 | 135 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 290 | 294 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 302 | 306 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 629 | 635 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 245 | 263 | PF00022 | 0.464 |
LIG_APCC_ABBA_1 | 303 | 308 | PF00400 | 0.477 |
LIG_APCC_ABBAyCdc20_2 | 302 | 308 | PF00400 | 0.518 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.589 |
LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.331 |
LIG_EH1_1 | 204 | 212 | PF00400 | 0.537 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.610 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.646 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.761 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.584 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.614 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.556 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.724 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.551 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.497 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.781 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.508 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.544 |
LIG_GBD_Chelix_1 | 277 | 285 | PF00786 | 0.566 |
LIG_KLC1_Yacidic_2 | 640 | 644 | PF13176 | 0.360 |
LIG_LIR_Gen_1 | 485 | 495 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 615 | 624 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 633 | 643 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 485 | 490 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 615 | 620 | PF02991 | 0.644 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.531 |
LIG_NRBOX | 485 | 491 | PF00104 | 0.603 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.462 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 617 | 621 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.529 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.746 |
LIG_SUMO_SIM_anti_2 | 275 | 281 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 682 | 689 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 27 | 32 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 370 | 376 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 618 | 625 | PF11976 | 0.665 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.614 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.571 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.700 |
LIG_TRAF2_1 | 546 | 549 | PF00917 | 0.634 |
LIG_TRAF2_1 | 616 | 619 | PF00917 | 0.487 |
LIG_WRC_WIRS_1 | 139 | 144 | PF05994 | 0.450 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.696 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.680 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.493 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.553 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.414 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.773 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.588 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.626 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.551 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.662 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.656 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.594 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.572 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.497 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.482 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.746 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.598 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.767 |
MOD_CK2_1 | 613 | 619 | PF00069 | 0.504 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.524 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.613 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.745 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.551 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.555 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.656 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.741 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.473 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.568 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.632 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.479 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.484 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.668 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.627 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.711 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.748 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.547 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.700 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.644 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.597 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.566 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.534 |
MOD_N-GLC_1 | 550 | 555 | PF02516 | 0.700 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.385 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.596 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.680 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.727 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.494 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.739 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.655 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.517 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.681 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.591 |
MOD_NEK2_2 | 256 | 261 | PF00069 | 0.405 |
MOD_NEK2_2 | 263 | 268 | PF00069 | 0.559 |
MOD_NEK2_2 | 499 | 504 | PF00069 | 0.490 |
MOD_NEK2_2 | 604 | 609 | PF00069 | 0.466 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.544 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.714 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.614 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.511 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.485 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.484 |
MOD_PK_1 | 272 | 278 | PF00069 | 0.502 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.588 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.569 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.644 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.586 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.374 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.525 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.493 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.580 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.628 |
MOD_Plk_2-3 | 289 | 295 | PF00069 | 0.660 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.563 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.527 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.366 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.424 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.444 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.496 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.585 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.573 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.605 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.611 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.735 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.644 |
MOD_SUMO_rev_2 | 13 | 22 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 669 | 676 | PF00179 | 0.624 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.436 |
TRG_DiLeu_BaEn_1 | 361 | 366 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_2 | 410 | 416 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 124 | 129 | PF01217 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 368 | 373 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.645 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 591 | 594 | PF00400 | 0.682 |
TRG_NES_CRM1_1 | 295 | 308 | PF08389 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 196 | 200 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYM6 | Leptomonas seymouri | 51% | 94% |
A0A1X0P953 | Trypanosomatidae | 31% | 100% |
A0A3R7K9I4 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X2P1 | Leishmania donovani | 89% | 100% |
A4HHM5 | Leishmania braziliensis | 76% | 100% |
A4I4T4 | Leishmania infantum | 89% | 100% |
C9ZLI5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AE87 | Leishmania major | 87% | 100% |
V5BC22 | Trypanosoma cruzi | 31% | 100% |