| 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: A4HMT7
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.610 |
| CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.398 |
| CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.563 |
| CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.667 |
| CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.775 |
| CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.396 |
| CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.667 |
| CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.775 |
| CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.575 |
| CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.602 |
| CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.549 |
| CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.418 |
| CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.517 |
| CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.517 |
| CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.418 |
| CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.722 |
| CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.539 |
| CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.653 |
| CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.442 |
| DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.574 |
| DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.582 |
| DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.434 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.633 |
| DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.660 |
| DEG_SPOP_SBC_1 | 452 | 456 | PF00917 | 0.559 |
| DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.727 |
| DOC_CYCLIN_RxL_1 | 136 | 146 | PF00134 | 0.538 |
| DOC_CYCLIN_RxL_1 | 154 | 163 | PF00134 | 0.643 |
| DOC_MAPK_gen_1 | 137 | 144 | PF00069 | 0.537 |
| DOC_MAPK_gen_1 | 8 | 16 | PF00069 | 0.329 |
| DOC_PP1_RVXF_1 | 137 | 144 | PF00149 | 0.459 |
| DOC_PP1_RVXF_1 | 362 | 368 | PF00149 | 0.528 |
| DOC_PP2B_LxvP_1 | 205 | 208 | PF13499 | 0.528 |
| DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.532 |
| DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.738 |
| DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.573 |
| DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.711 |
| DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.590 |
| DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.658 |
| DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.802 |
| DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.584 |
| DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.607 |
| DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.536 |
| DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.579 |
| DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.550 |
| DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.626 |
| LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.528 |
| LIG_14-3-3_CanoR_1 | 320 | 326 | PF00244 | 0.462 |
| LIG_14-3-3_CanoR_1 | 364 | 370 | PF00244 | 0.475 |
| LIG_14-3-3_CanoR_1 | 481 | 486 | PF00244 | 0.506 |
| LIG_14-3-3_CanoR_1 | 55 | 65 | PF00244 | 0.769 |
| LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.659 |
| LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.436 |
| LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.545 |
| LIG_FHA_1 | 101 | 107 | PF00498 | 0.542 |
| LIG_FHA_1 | 154 | 160 | PF00498 | 0.565 |
| LIG_FHA_1 | 197 | 203 | PF00498 | 0.648 |
| LIG_FHA_1 | 221 | 227 | PF00498 | 0.777 |
| LIG_FHA_1 | 295 | 301 | PF00498 | 0.467 |
| LIG_FHA_1 | 58 | 64 | PF00498 | 0.522 |
| LIG_FHA_2 | 169 | 175 | PF00498 | 0.573 |
| LIG_FHA_2 | 233 | 239 | PF00498 | 0.651 |
| LIG_FHA_2 | 297 | 303 | PF00498 | 0.559 |
| LIG_FHA_2 | 324 | 330 | PF00498 | 0.568 |
| LIG_FHA_2 | 344 | 350 | PF00498 | 0.300 |
| LIG_FHA_2 | 375 | 381 | PF00498 | 0.612 |
| LIG_FHA_2 | 454 | 460 | PF00498 | 0.779 |
| LIG_IRF3_LxIS_1 | 160 | 167 | PF10401 | 0.704 |
| LIG_LIR_Gen_1 | 389 | 399 | PF02991 | 0.427 |
| LIG_LIR_Gen_1 | 423 | 434 | PF02991 | 0.658 |
| LIG_LIR_LC3C_4 | 383 | 387 | PF02991 | 0.559 |
| LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.425 |
| LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.605 |
| LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.539 |
| LIG_MLH1_MIPbox_1 | 483 | 487 | PF16413 | 0.528 |
| LIG_NRBOX | 496 | 502 | PF00104 | 0.528 |
| LIG_PCNA_yPIPBox_3 | 139 | 152 | PF02747 | 0.607 |
| LIG_Pex14_2 | 291 | 295 | PF04695 | 0.537 |
| LIG_Pex14_2 | 30 | 34 | PF04695 | 0.633 |
| LIG_Pex14_2 | 363 | 367 | PF04695 | 0.412 |
| LIG_Pex14_2 | 483 | 487 | PF04695 | 0.419 |
| LIG_PTB_Apo_2 | 385 | 392 | PF02174 | 0.454 |
| LIG_SH2_CRK | 138 | 142 | PF00017 | 0.576 |
| LIG_SH2_CRK | 7 | 11 | PF00017 | 0.432 |
| LIG_SH2_SRC | 407 | 410 | PF00017 | 0.539 |
| LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.634 |
| LIG_SH2_STAP1 | 422 | 426 | PF00017 | 0.436 |
| LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.559 |
| LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.578 |
| LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.527 |
| LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.405 |
| LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.539 |
| LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.497 |
| LIG_SH3_3 | 368 | 374 | PF00018 | 0.487 |
| LIG_SUMO_SIM_anti_2 | 383 | 389 | PF11976 | 0.531 |
| LIG_SUMO_SIM_par_1 | 296 | 302 | PF11976 | 0.496 |
| LIG_SUMO_SIM_par_1 | 383 | 389 | PF11976 | 0.557 |
| LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.561 |
| LIG_TRFH_1 | 367 | 371 | PF08558 | 0.447 |
| LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.576 |
| LIG_TYR_ITIM | 500 | 505 | PF00017 | 0.532 |
| MOD_CK1_1 | 153 | 159 | PF00069 | 0.535 |
| MOD_CK1_1 | 186 | 192 | PF00069 | 0.729 |
| MOD_CK1_1 | 197 | 203 | PF00069 | 0.770 |
| MOD_CK1_1 | 464 | 470 | PF00069 | 0.767 |
| MOD_CK1_1 | 49 | 55 | PF00069 | 0.733 |
| MOD_CK1_1 | 59 | 65 | PF00069 | 0.644 |
| MOD_CK1_1 | 71 | 77 | PF00069 | 0.512 |
| MOD_CK2_1 | 227 | 233 | PF00069 | 0.539 |
| MOD_CK2_1 | 296 | 302 | PF00069 | 0.575 |
| MOD_CK2_1 | 343 | 349 | PF00069 | 0.606 |
| MOD_CK2_1 | 374 | 380 | PF00069 | 0.711 |
| MOD_Cter_Amidation | 448 | 451 | PF01082 | 0.526 |
| MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.764 |
| MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.776 |
| MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.635 |
| MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.717 |
| MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.628 |
| MOD_GSK3_1 | 160 | 167 | PF00069 | 0.706 |
| MOD_GSK3_1 | 183 | 190 | PF00069 | 0.703 |
| MOD_GSK3_1 | 192 | 199 | PF00069 | 0.726 |
| MOD_GSK3_1 | 211 | 218 | PF00069 | 0.673 |
| MOD_GSK3_1 | 228 | 235 | PF00069 | 0.699 |
| MOD_GSK3_1 | 323 | 330 | PF00069 | 0.483 |
| MOD_GSK3_1 | 370 | 377 | PF00069 | 0.665 |
| MOD_GSK3_1 | 420 | 427 | PF00069 | 0.490 |
| MOD_GSK3_1 | 451 | 458 | PF00069 | 0.711 |
| MOD_GSK3_1 | 459 | 466 | PF00069 | 0.782 |
| MOD_GSK3_1 | 46 | 53 | PF00069 | 0.647 |
| MOD_GSK3_1 | 477 | 484 | PF00069 | 0.536 |
| MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.660 |
| MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.556 |
| MOD_NEK2_1 | 159 | 164 | PF00069 | 0.633 |
| MOD_NEK2_1 | 227 | 232 | PF00069 | 0.669 |
| MOD_NEK2_1 | 30 | 35 | PF00069 | 0.534 |
| MOD_NEK2_1 | 36 | 41 | PF00069 | 0.568 |
| MOD_NEK2_1 | 429 | 434 | PF00069 | 0.690 |
| MOD_NEK2_1 | 51 | 56 | PF00069 | 0.474 |
| MOD_NEK2_1 | 57 | 62 | PF00069 | 0.500 |
| MOD_PKA_2 | 153 | 159 | PF00069 | 0.565 |
| MOD_PKA_2 | 215 | 221 | PF00069 | 0.725 |
| MOD_PKA_2 | 365 | 371 | PF00069 | 0.536 |
| MOD_PKA_2 | 92 | 98 | PF00069 | 0.703 |
| MOD_PKB_1 | 418 | 426 | PF00069 | 0.427 |
| MOD_Plk_1 | 101 | 107 | PF00069 | 0.614 |
| MOD_Plk_4 | 102 | 108 | PF00069 | 0.607 |
| MOD_Plk_4 | 386 | 392 | PF00069 | 0.434 |
| MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.590 |
| MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.604 |
| MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.539 |
| MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.590 |
| MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.550 |
| MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.625 |
| TRG_DiLeu_BaEn_1 | 397 | 402 | PF01217 | 0.540 |
| TRG_DiLeu_BaEn_4 | 403 | 409 | PF01217 | 0.590 |
| TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.570 |
| TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.573 |
| TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.413 |
| TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.440 |
| TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.568 |
| TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.558 |
| TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.484 |
| TRG_Pf-PMV_PEXEL_1 | 415 | 419 | PF00026 | 0.624 |
| TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.487 |
| TRG_Pf-PMV_PEXEL_1 | 9 | 13 | PF00026 | 0.324 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IBR0 | Leptomonas seymouri | 50% | 100% |
| A0A1X0P6J4 | Trypanosomatidae | 21% | 100% |
| A0A3S7X9M3 | Leishmania donovani | 75% | 100% |
| A0A422P2R2 | Trypanosoma rangeli | 26% | 100% |
| A4IBD8 | Leishmania infantum | 75% | 100% |
| C9ZZ79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
| E9AF94 | Leishmania major | 72% | 97% |
| E9B6E9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
| V5BTJ6 | Trypanosoma cruzi | 27% | 100% |