| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9B6Y9
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.538 |
| CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.497 |
| CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.500 |
| CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.670 |
| CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.582 |
| CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.493 |
| CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.606 |
| CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.447 |
| CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.570 |
| CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.623 |
| CLV_PCSK_PC1ET2_1 | 127 | 129 | PF00082 | 0.595 |
| CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.447 |
| CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.570 |
| CLV_PCSK_PC7_1 | 457 | 463 | PF00082 | 0.468 |
| CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.708 |
| CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.452 |
| CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.595 |
| CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.614 |
| CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.619 |
| CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.575 |
| DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.589 |
| DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.683 |
| DOC_CKS1_1 | 413 | 418 | PF01111 | 0.483 |
| DOC_CYCLIN_RxL_1 | 197 | 207 | PF00134 | 0.533 |
| DOC_MAPK_gen_1 | 262 | 271 | PF00069 | 0.563 |
| DOC_MAPK_MEF2A_6 | 262 | 271 | PF00069 | 0.388 |
| DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.643 |
| DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.644 |
| DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.651 |
| DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.678 |
| DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.759 |
| DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.638 |
| DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.703 |
| DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.671 |
| DOC_USP7_UBL2_3 | 372 | 376 | PF12436 | 0.547 |
| DOC_USP7_UBL2_3 | 394 | 398 | PF12436 | 0.648 |
| DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.736 |
| DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.652 |
| DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.672 |
| DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.453 |
| DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.672 |
| LIG_14-3-3_CanoR_1 | 128 | 138 | PF00244 | 0.505 |
| LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.635 |
| LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.570 |
| LIG_Actin_WH2_2 | 70 | 85 | PF00022 | 0.627 |
| LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.557 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.634 |
| LIG_eIF4E_1 | 26 | 32 | PF01652 | 0.546 |
| LIG_FHA_1 | 124 | 130 | PF00498 | 0.533 |
| LIG_FHA_1 | 230 | 236 | PF00498 | 0.565 |
| LIG_FHA_1 | 90 | 96 | PF00498 | 0.495 |
| LIG_FHA_2 | 350 | 356 | PF00498 | 0.681 |
| LIG_FHA_2 | 55 | 61 | PF00498 | 0.522 |
| LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.578 |
| LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.476 |
| LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.569 |
| LIG_NRBOX | 112 | 118 | PF00104 | 0.630 |
| LIG_NRBOX | 16 | 22 | PF00104 | 0.549 |
| LIG_NRBOX | 187 | 193 | PF00104 | 0.552 |
| LIG_SH2_CRK | 43 | 47 | PF00017 | 0.592 |
| LIG_SH2_STAT3 | 310 | 313 | PF00017 | 0.579 |
| LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.505 |
| LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.348 |
| LIG_SH3_3 | 117 | 123 | PF00018 | 0.595 |
| LIG_SH3_3 | 153 | 159 | PF00018 | 0.504 |
| LIG_SH3_3 | 287 | 293 | PF00018 | 0.686 |
| LIG_SH3_3 | 337 | 343 | PF00018 | 0.663 |
| LIG_SH3_3 | 410 | 416 | PF00018 | 0.688 |
| LIG_SH3_3 | 417 | 423 | PF00018 | 0.681 |
| LIG_SH3_3 | 74 | 80 | PF00018 | 0.488 |
| LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.640 |
| LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.560 |
| LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.572 |
| LIG_UBA3_1 | 191 | 200 | PF00899 | 0.640 |
| LIG_UBA3_1 | 78 | 83 | PF00899 | 0.517 |
| MOD_CDC14_SPxK_1 | 155 | 158 | PF00782 | 0.581 |
| MOD_CDK_SPxK_1 | 152 | 158 | PF00069 | 0.737 |
| MOD_CDK_SPxK_1 | 412 | 418 | PF00069 | 0.660 |
| MOD_CK1_1 | 194 | 200 | PF00069 | 0.535 |
| MOD_CK1_1 | 349 | 355 | PF00069 | 0.636 |
| MOD_CK1_1 | 401 | 407 | PF00069 | 0.667 |
| MOD_CK1_1 | 497 | 503 | PF00069 | 0.664 |
| MOD_CK1_1 | 89 | 95 | PF00069 | 0.566 |
| MOD_CK2_1 | 217 | 223 | PF00069 | 0.542 |
| MOD_CK2_1 | 293 | 299 | PF00069 | 0.654 |
| MOD_CK2_1 | 327 | 333 | PF00069 | 0.633 |
| MOD_CK2_1 | 349 | 355 | PF00069 | 0.600 |
| MOD_CK2_1 | 54 | 60 | PF00069 | 0.605 |
| MOD_CK2_1 | 95 | 101 | PF00069 | 0.671 |
| MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.784 |
| MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.589 |
| MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.604 |
| MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.522 |
| MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.713 |
| MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.682 |
| MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.680 |
| MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.699 |
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.714 |
| MOD_GSK3_1 | 397 | 404 | PF00069 | 0.645 |
| MOD_GSK3_1 | 418 | 425 | PF00069 | 0.752 |
| MOD_GSK3_1 | 494 | 501 | PF00069 | 0.598 |
| MOD_GSK3_1 | 82 | 89 | PF00069 | 0.648 |
| MOD_GSK3_1 | 91 | 98 | PF00069 | 0.659 |
| MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.752 |
| MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.799 |
| MOD_NEK2_1 | 129 | 134 | PF00069 | 0.654 |
| MOD_NEK2_1 | 177 | 182 | PF00069 | 0.594 |
| MOD_NEK2_1 | 191 | 196 | PF00069 | 0.559 |
| MOD_NEK2_1 | 209 | 214 | PF00069 | 0.441 |
| MOD_NEK2_1 | 499 | 504 | PF00069 | 0.592 |
| MOD_NEK2_2 | 385 | 390 | PF00069 | 0.459 |
| MOD_NEK2_2 | 69 | 74 | PF00069 | 0.498 |
| MOD_PIKK_1 | 194 | 200 | PF00454 | 0.513 |
| MOD_PIKK_1 | 327 | 333 | PF00454 | 0.631 |
| MOD_PIKK_1 | 494 | 500 | PF00454 | 0.454 |
| MOD_PKA_2 | 141 | 147 | PF00069 | 0.749 |
| MOD_Plk_1 | 101 | 107 | PF00069 | 0.770 |
| MOD_Plk_1 | 163 | 169 | PF00069 | 0.504 |
| MOD_Plk_1 | 398 | 404 | PF00069 | 0.689 |
| MOD_Plk_1 | 494 | 500 | PF00069 | 0.412 |
| MOD_Plk_4 | 177 | 183 | PF00069 | 0.590 |
| MOD_Plk_4 | 293 | 299 | PF00069 | 0.601 |
| MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.737 |
| MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.655 |
| MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.673 |
| MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.457 |
| MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.671 |
| MOD_SUMO_rev_2 | 119 | 129 | PF00179 | 0.591 |
| MOD_SUMO_rev_2 | 421 | 429 | PF00179 | 0.676 |
| TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.624 |
| TRG_DiLeu_BaEn_4 | 299 | 305 | PF01217 | 0.594 |
| TRG_DiLeu_LyEn_5 | 125 | 130 | PF01217 | 0.562 |
| TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.588 |
| TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.504 |
| TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.575 |
| TRG_NES_CRM1_1 | 380 | 395 | PF08389 | 0.530 |
| TRG_NES_CRM1_1 | 442 | 456 | PF08389 | 0.579 |
| TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.599 |
| TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.575 |
| TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.607 |
| TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.576 |
| TRG_Pf-PMV_PEXEL_1 | 491 | 495 | PF00026 | 0.359 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P962 | Leptomonas seymouri | 48% | 91% |
| A0A1X0P582 | Trypanosomatidae | 26% | 100% |
| A0A3S7X9X8 | Leishmania donovani | 89% | 100% |
| A4HNC7 | Leishmania braziliensis | 69% | 100% |
| A4IC00 | Leishmania infantum | 89% | 100% |
| E9AFT7 | Leishmania major | 88% | 100% |
| V5C2K9 | Trypanosoma cruzi | 24% | 100% |