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 |
Related structures:
AlphaFold database: E9B5L0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.392 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.752 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 613 | 615 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.405 |
CLV_Separin_Metazoa | 487 | 491 | PF03568 | 0.342 |
DEG_APCC_DBOX_1 | 402 | 410 | PF00400 | 0.457 |
DEG_APCC_DBOX_1 | 489 | 497 | PF00400 | 0.433 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.495 |
DOC_CDC14_PxL_1 | 584 | 592 | PF14671 | 0.362 |
DOC_CYCLIN_RxL_1 | 221 | 231 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 348 | 356 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 463 | 470 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 27 | 36 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 463 | 472 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 528 | 537 | PF00069 | 0.243 |
DOC_MAPK_MEF2A_6 | 583 | 591 | PF00069 | 0.376 |
DOC_MAPK_NFAT4_5 | 463 | 471 | PF00069 | 0.488 |
DOC_PP1_RVXF_1 | 186 | 192 | PF00149 | 0.317 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.337 |
DOC_SPAK_OSR1_1 | 54 | 58 | PF12202 | 0.368 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.413 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 212 | 222 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 348 | 354 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 403 | 413 | PF00244 | 0.382 |
LIG_APCC_ABBA_1 | 489 | 494 | PF00400 | 0.391 |
LIG_BIR_III_2 | 444 | 448 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.402 |
LIG_deltaCOP1_diTrp_1 | 23 | 29 | PF00928 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 388 | 392 | PF00928 | 0.347 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.575 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.460 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.416 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.493 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.521 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.406 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.503 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.463 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.484 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 629 | 638 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.305 |
LIG_LYPXL_yS_3 | 42 | 45 | PF13949 | 0.552 |
LIG_SH2_GRB2like | 115 | 118 | PF00017 | 0.499 |
LIG_SH2_PTP2 | 326 | 329 | PF00017 | 0.414 |
LIG_SH2_PTP2 | 56 | 59 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 569 | 572 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.360 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.365 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.444 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.544 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.698 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.500 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.360 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.390 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.385 |
LIG_SUMO_SIM_anti_2 | 313 | 320 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 313 | 320 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 468 | 474 | PF11976 | 0.440 |
LIG_SxIP_EBH_1 | 509 | 523 | PF03271 | 0.330 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.459 |
LIG_WRC_WIRS_1 | 628 | 633 | PF05994 | 0.596 |
MOD_CDK_SPK_2 | 216 | 221 | PF00069 | 0.625 |
MOD_CDK_SPxxK_3 | 430 | 437 | PF00069 | 0.690 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.528 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.319 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.465 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.679 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.690 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.412 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.528 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.451 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.716 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.495 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.455 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.534 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.444 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.435 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.574 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.315 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.521 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.444 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.580 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.625 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.428 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.518 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.552 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.717 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.581 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.382 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.608 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.524 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.568 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.594 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.631 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.435 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.442 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.396 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.368 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.513 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.480 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.298 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.573 |
MOD_LATS_1 | 402 | 408 | PF00433 | 0.311 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.624 |
MOD_N-GLC_2 | 182 | 184 | PF02516 | 0.497 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.498 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.472 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.374 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.473 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.466 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.283 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.462 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.533 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.467 |
MOD_PK_1 | 509 | 515 | PF00069 | 0.394 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.661 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.383 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.661 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.521 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.445 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.357 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.515 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.530 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.389 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.399 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.378 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.618 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.370 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.542 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.670 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.612 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.746 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.752 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.461 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7E9 | Leptomonas seymouri | 52% | 98% |
A0A0S4KIT9 | Bodo saltans | 27% | 94% |
A0A1X0PA76 | Trypanosomatidae | 32% | 100% |
A0A3Q8IHL1 | Leishmania donovani | 87% | 98% |
A0A422NVA9 | Trypanosoma rangeli | 35% | 100% |
A4HBD8 | Leishmania braziliensis | 75% | 100% |
A4IAI6 | Leishmania infantum | 87% | 98% |
C9ZLQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4Q2C6 | Leishmania major | 88% | 100% |
V5DMS9 | Trypanosoma cruzi | 34% | 100% |