| 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 |
Related structures:
AlphaFold database: E9AYP6
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 142 | 146 | PF00656 | 0.610 |
| CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.571 |
| CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.632 |
| CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.554 |
| CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.666 |
| CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.595 |
| CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.599 |
| CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.666 |
| CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.588 |
| CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.599 |
| CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.511 |
| CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.619 |
| DEG_APCC_DBOX_1 | 546 | 554 | PF00400 | 0.614 |
| DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.565 |
| DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.679 |
| DOC_CKS1_1 | 540 | 545 | PF01111 | 0.653 |
| DOC_MAPK_MEF2A_6 | 68 | 75 | PF00069 | 0.608 |
| DOC_MAPK_MEF2A_6 | 77 | 84 | PF00069 | 0.518 |
| DOC_PP1_RVXF_1 | 565 | 571 | PF00149 | 0.510 |
| DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.656 |
| DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.421 |
| DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.398 |
| DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.635 |
| DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.822 |
| DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.717 |
| DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.642 |
| DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.631 |
| DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.557 |
| DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.650 |
| DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.612 |
| DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.607 |
| DOC_USP7_MATH_2 | 543 | 549 | PF00917 | 0.571 |
| DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.518 |
| DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.698 |
| DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.739 |
| DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.603 |
| DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.606 |
| DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.490 |
| DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.694 |
| DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.655 |
| DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.542 |
| LIG_14-3-3_CanoR_1 | 140 | 150 | PF00244 | 0.645 |
| LIG_14-3-3_CanoR_1 | 234 | 238 | PF00244 | 0.696 |
| LIG_14-3-3_CanoR_1 | 312 | 319 | PF00244 | 0.764 |
| LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.664 |
| LIG_14-3-3_CanoR_1 | 440 | 449 | PF00244 | 0.616 |
| LIG_14-3-3_CanoR_1 | 503 | 510 | PF00244 | 0.567 |
| LIG_Actin_WH2_2 | 90 | 108 | PF00022 | 0.556 |
| LIG_APCC_ABBA_1 | 459 | 464 | PF00400 | 0.541 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.718 |
| LIG_FHA_1 | 105 | 111 | PF00498 | 0.662 |
| LIG_FHA_1 | 246 | 252 | PF00498 | 0.835 |
| LIG_FHA_1 | 316 | 322 | PF00498 | 0.741 |
| LIG_FHA_1 | 379 | 385 | PF00498 | 0.425 |
| LIG_FHA_1 | 428 | 434 | PF00498 | 0.661 |
| LIG_FHA_1 | 464 | 470 | PF00498 | 0.563 |
| LIG_FHA_1 | 492 | 498 | PF00498 | 0.579 |
| LIG_FHA_1 | 528 | 534 | PF00498 | 0.404 |
| LIG_FHA_2 | 165 | 171 | PF00498 | 0.708 |
| LIG_FHA_2 | 200 | 206 | PF00498 | 0.509 |
| LIG_FHA_2 | 540 | 546 | PF00498 | 0.519 |
| LIG_FHA_2 | 6 | 12 | PF00498 | 0.623 |
| LIG_FXI_DFP_1 | 217 | 221 | PF00024 | 0.554 |
| LIG_Integrin_isoDGR_2 | 118 | 120 | PF01839 | 0.500 |
| LIG_Integrin_isoDGR_2 | 209 | 211 | PF01839 | 0.616 |
| LIG_IRF3_LxIS_1 | 74 | 81 | PF10401 | 0.551 |
| LIG_LIR_Apic_2 | 191 | 197 | PF02991 | 0.421 |
| LIG_LIR_Apic_2 | 381 | 385 | PF02991 | 0.419 |
| LIG_LIR_Apic_2 | 530 | 534 | PF02991 | 0.399 |
| LIG_LIR_Apic_2 | 538 | 543 | PF02991 | 0.495 |
| LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.487 |
| LIG_LIR_Gen_1 | 504 | 514 | PF02991 | 0.426 |
| LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.601 |
| LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.527 |
| LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.459 |
| LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.456 |
| LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.556 |
| LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.517 |
| LIG_LYPXL_yS_3 | 578 | 581 | PF13949 | 0.581 |
| LIG_PCNA_yPIPBox_3 | 193 | 207 | PF02747 | 0.596 |
| LIG_PROFILIN_1 | 147 | 153 | PF00235 | 0.609 |
| LIG_SH2_NCK_1 | 540 | 544 | PF00017 | 0.602 |
| LIG_SH2_SRC | 462 | 465 | PF00017 | 0.609 |
| LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.589 |
| LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.485 |
| LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.616 |
| LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.574 |
| LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.318 |
| LIG_SH3_3 | 144 | 150 | PF00018 | 0.820 |
| LIG_SH3_3 | 160 | 166 | PF00018 | 0.523 |
| LIG_SH3_3 | 318 | 324 | PF00018 | 0.681 |
| LIG_SH3_3 | 558 | 564 | PF00018 | 0.542 |
| LIG_SUMO_SIM_anti_2 | 69 | 75 | PF11976 | 0.537 |
| LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.531 |
| LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.635 |
| LIG_TRAF2_2 | 561 | 566 | PF00917 | 0.500 |
| LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.631 |
| MOD_CDK_SPxxK_3 | 305 | 312 | PF00069 | 0.753 |
| MOD_CDK_SPxxK_3 | 539 | 546 | PF00069 | 0.570 |
| MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.627 |
| MOD_CK1_1 | 139 | 145 | PF00069 | 0.717 |
| MOD_CK1_1 | 241 | 247 | PF00069 | 0.744 |
| MOD_CK1_1 | 452 | 458 | PF00069 | 0.634 |
| MOD_CK1_1 | 522 | 528 | PF00069 | 0.524 |
| MOD_CK1_1 | 532 | 538 | PF00069 | 0.474 |
| MOD_CK1_1 | 59 | 65 | PF00069 | 0.571 |
| MOD_CK2_1 | 199 | 205 | PF00069 | 0.578 |
| MOD_CK2_1 | 5 | 11 | PF00069 | 0.646 |
| MOD_CK2_1 | 532 | 538 | PF00069 | 0.458 |
| MOD_CK2_1 | 539 | 545 | PF00069 | 0.470 |
| MOD_CK2_1 | 61 | 67 | PF00069 | 0.505 |
| MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.713 |
| MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.591 |
| MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.588 |
| MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.716 |
| MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.587 |
| MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.434 |
| MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.614 |
| MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.567 |
| MOD_GSK3_1 | 104 | 111 | PF00069 | 0.568 |
| MOD_GSK3_1 | 139 | 146 | PF00069 | 0.616 |
| MOD_GSK3_1 | 233 | 240 | PF00069 | 0.669 |
| MOD_GSK3_1 | 241 | 248 | PF00069 | 0.712 |
| MOD_GSK3_1 | 269 | 276 | PF00069 | 0.697 |
| MOD_GSK3_1 | 291 | 298 | PF00069 | 0.633 |
| MOD_GSK3_1 | 311 | 318 | PF00069 | 0.688 |
| MOD_GSK3_1 | 34 | 41 | PF00069 | 0.640 |
| MOD_GSK3_1 | 445 | 452 | PF00069 | 0.533 |
| MOD_GSK3_1 | 487 | 494 | PF00069 | 0.653 |
| MOD_GSK3_1 | 497 | 504 | PF00069 | 0.448 |
| MOD_GSK3_1 | 51 | 58 | PF00069 | 0.644 |
| MOD_GSK3_1 | 529 | 536 | PF00069 | 0.521 |
| MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.662 |
| MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.547 |
| MOD_NEK2_1 | 127 | 132 | PF00069 | 0.767 |
| MOD_NEK2_1 | 378 | 383 | PF00069 | 0.443 |
| MOD_NEK2_1 | 497 | 502 | PF00069 | 0.589 |
| MOD_NEK2_1 | 55 | 60 | PF00069 | 0.610 |
| MOD_NEK2_1 | 78 | 83 | PF00069 | 0.490 |
| MOD_NEK2_2 | 465 | 470 | PF00069 | 0.581 |
| MOD_PIKK_1 | 108 | 114 | PF00454 | 0.729 |
| MOD_PIKK_1 | 233 | 239 | PF00454 | 0.772 |
| MOD_PIKK_1 | 242 | 248 | PF00454 | 0.670 |
| MOD_PK_1 | 429 | 435 | PF00069 | 0.550 |
| MOD_PKA_2 | 119 | 125 | PF00069 | 0.631 |
| MOD_PKA_2 | 139 | 145 | PF00069 | 0.493 |
| MOD_PKA_2 | 233 | 239 | PF00069 | 0.685 |
| MOD_PKA_2 | 29 | 35 | PF00069 | 0.665 |
| MOD_PKA_2 | 311 | 317 | PF00069 | 0.761 |
| MOD_PKA_2 | 339 | 345 | PF00069 | 0.761 |
| MOD_PKA_2 | 502 | 508 | PF00069 | 0.609 |
| MOD_PKA_2 | 545 | 551 | PF00069 | 0.614 |
| MOD_Plk_1 | 158 | 164 | PF00069 | 0.669 |
| MOD_Plk_1 | 292 | 298 | PF00069 | 0.708 |
| MOD_Plk_1 | 353 | 359 | PF00069 | 0.630 |
| MOD_Plk_1 | 38 | 44 | PF00069 | 0.486 |
| MOD_Plk_1 | 50 | 56 | PF00069 | 0.515 |
| MOD_Plk_1 | 69 | 75 | PF00069 | 0.582 |
| MOD_Plk_2-3 | 354 | 360 | PF00069 | 0.643 |
| MOD_Plk_2-3 | 506 | 512 | PF00069 | 0.560 |
| MOD_Plk_4 | 292 | 298 | PF00069 | 0.671 |
| MOD_Plk_4 | 317 | 323 | PF00069 | 0.730 |
| MOD_Plk_4 | 38 | 44 | PF00069 | 0.507 |
| MOD_Plk_4 | 465 | 471 | PF00069 | 0.538 |
| MOD_Plk_4 | 69 | 75 | PF00069 | 0.615 |
| MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.697 |
| MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.740 |
| MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.602 |
| MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.606 |
| MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.490 |
| MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.688 |
| MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.649 |
| MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.536 |
| MOD_SUMO_rev_2 | 185 | 195 | PF00179 | 0.434 |
| MOD_SUMO_rev_2 | 511 | 519 | PF00179 | 0.552 |
| MOD_SUMO_rev_2 | 9 | 15 | PF00179 | 0.666 |
| TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.438 |
| TRG_DiLeu_BaEn_1 | 70 | 75 | PF01217 | 0.535 |
| TRG_DiLeu_BaEn_2 | 167 | 173 | PF01217 | 0.404 |
| TRG_DiLeu_LyEn_5 | 409 | 414 | PF01217 | 0.457 |
| TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.448 |
| TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.503 |
| TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.581 |
| TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.606 |
| TRG_Pf-PMV_PEXEL_1 | 440 | 444 | PF00026 | 0.654 |
| TRG_Pf-PMV_PEXEL_1 | 482 | 486 | PF00026 | 0.511 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I848 | Leptomonas seymouri | 56% | 100% |
| A0A1X0P7D0 | Trypanosomatidae | 33% | 100% |
| A0A3R7MCE3 | Trypanosoma rangeli | 35% | 100% |
| A0A3S7X099 | Leishmania donovani | 89% | 100% |
| A4HFA9 | Leishmania braziliensis | 79% | 100% |
| A4I2J1 | Leishmania infantum | 90% | 100% |
| C9ZWZ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| Q4Q8S6 | Leishmania major | 90% | 100% |
| V5B7P2 | Trypanosoma cruzi | 35% | 100% |