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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9ANI3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 414 | 418 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.712 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 589 | 593 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.362 |
DEG_APCC_DBOX_1 | 22 | 30 | PF00400 | 0.599 |
DEG_APCC_DBOX_1 | 55 | 63 | PF00400 | 0.551 |
DEG_APCC_DBOX_1 | 591 | 599 | PF00400 | 0.362 |
DEG_APCC_DBOX_1 | 87 | 95 | PF00400 | 0.637 |
DEG_SCF_TRCP1_1 | 511 | 516 | PF00400 | 0.633 |
DOC_CYCLIN_RxL_1 | 250 | 263 | PF00134 | 0.625 |
DOC_CYCLIN_RxL_1 | 560 | 570 | PF00134 | 0.646 |
DOC_CYCLIN_yCln2_LP_2 | 551 | 557 | PF00134 | 0.499 |
DOC_MAPK_gen_1 | 112 | 119 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 17 | 28 | PF00069 | 0.657 |
DOC_MAPK_gen_1 | 362 | 368 | PF00069 | 0.633 |
DOC_MAPK_gen_1 | 588 | 598 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 88 | 97 | PF00069 | 0.642 |
DOC_MAPK_MEF2A_6 | 90 | 99 | PF00069 | 0.637 |
DOC_MAPK_NFAT4_5 | 92 | 100 | PF00069 | 0.630 |
DOC_PP2B_LxvP_1 | 565 | 568 | PF13499 | 0.679 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.827 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.738 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.674 |
LIG_14-3-3_CanoR_1 | 313 | 322 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 363 | 367 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 474 | 478 | PF00244 | 0.647 |
LIG_Actin_WH2_2 | 250 | 267 | PF00022 | 0.623 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.619 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.585 |
LIG_BRCT_BRCA1_1 | 511 | 515 | PF00533 | 0.774 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.757 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.587 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.602 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.447 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.679 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.650 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.630 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.687 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.733 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.626 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.592 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.568 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.609 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.668 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.526 |
LIG_LIR_Gen_1 | 147 | 156 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 349 | 357 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 610 | 614 | PF02991 | 0.464 |
LIG_NRBOX | 151 | 157 | PF00104 | 0.661 |
LIG_Pex14_1 | 382 | 386 | PF04695 | 0.556 |
LIG_PTB_Apo_2 | 275 | 282 | PF02174 | 0.547 |
LIG_PTB_Phospho_1 | 275 | 281 | PF10480 | 0.545 |
LIG_RPA_C_Fungi | 453 | 465 | PF08784 | 0.490 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.545 |
LIG_SH2_NCK_1 | 387 | 391 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.557 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.673 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.628 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.458 |
LIG_UBA3_1 | 603 | 612 | PF00899 | 0.247 |
LIG_WRC_WIRS_1 | 608 | 613 | PF05994 | 0.536 |
MOD_CDC14_SPxK_1 | 409 | 412 | PF00782 | 0.621 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.627 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.480 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.573 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.447 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.689 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.447 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.533 |
MOD_Cter_Amidation | 504 | 507 | PF01082 | 0.729 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.693 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.675 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.579 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.693 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.792 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.588 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.598 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.634 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.366 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.516 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.495 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.286 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.456 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.542 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.670 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.685 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.628 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.565 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.632 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.648 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.596 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.671 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.433 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.603 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.430 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.649 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.679 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.668 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.439 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.472 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.583 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.464 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.502 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.521 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.520 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.599 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.573 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.596 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.419 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.490 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.469 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.477 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.543 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.500 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.469 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.439 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.517 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.501 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.490 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.496 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.439 |
MOD_Plk_2-3 | 343 | 349 | PF00069 | 0.517 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.521 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.416 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.496 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.534 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.557 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.351 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.591 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.642 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.589 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.602 |
MOD_SUMO_for_1 | 242 | 245 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 25 | 34 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 261 | 267 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 354 | 364 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 377 | 384 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 71 | 76 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_1 | 24 | 29 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_1 | 249 | 254 | PF01217 | 0.487 |
TRG_DiLeu_BaEn_4 | 24 | 30 | PF01217 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 164 | 169 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 535 | 540 | PF01217 | 0.715 |
TRG_DiLeu_BaLyEn_6 | 553 | 558 | PF01217 | 0.384 |
TRG_DiLeu_LyEn_5 | 24 | 29 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 562 | 564 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 587 | 589 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.665 |
TRG_NLS_MonoExtC_3 | 16 | 21 | PF00514 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 20 | 24 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 531 | 535 | PF00026 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 556 | 561 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHW2 | Leptomonas seymouri | 56% | 96% |
A0A0S4ITZ6 | Bodo saltans | 25% | 100% |
A0A1X0NWL4 | Trypanosomatidae | 35% | 100% |
A0A3R7KMY4 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H6I2 | Leishmania donovani | 88% | 99% |
A4H6F4 | Leishmania braziliensis | 75% | 100% |
A4HUU8 | Leishmania infantum | 89% | 100% |
D0A7K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q4QH43 | Leishmania major | 89% | 100% |
V5BB44 | Trypanosoma cruzi | 34% | 100% |