| 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: Q4Q6C7
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 189 | 193 | PF00656 | 0.395 |
| CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.428 |
| CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.569 |
| CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.545 |
| CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.555 |
| CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.506 |
| CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.470 |
| CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.576 |
| CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.533 |
| CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.498 |
| CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.623 |
| CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.620 |
| CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.559 |
| CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.426 |
| CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.466 |
| CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.561 |
| CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.569 |
| CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.483 |
| DEG_APCC_DBOX_1 | 229 | 237 | PF00400 | 0.525 |
| DOC_CKS1_1 | 60 | 65 | PF01111 | 0.482 |
| DOC_MAPK_MEF2A_6 | 190 | 198 | PF00069 | 0.397 |
| DOC_MAPK_MEF2A_6 | 358 | 366 | PF00069 | 0.558 |
| DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.508 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.351 |
| DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.431 |
| DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.721 |
| DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.650 |
| DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.669 |
| DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.512 |
| DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.520 |
| DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.531 |
| DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.482 |
| LIG_14-3-3_CanoR_1 | 117 | 125 | PF00244 | 0.469 |
| LIG_14-3-3_CanoR_1 | 184 | 194 | PF00244 | 0.468 |
| LIG_14-3-3_CanoR_1 | 240 | 247 | PF00244 | 0.482 |
| LIG_14-3-3_CanoR_1 | 65 | 70 | PF00244 | 0.454 |
| LIG_Actin_WH2_2 | 194 | 210 | PF00022 | 0.486 |
| LIG_Actin_WH2_2 | 250 | 267 | PF00022 | 0.440 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.426 |
| LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.442 |
| LIG_DLG_GKlike_1 | 65 | 73 | PF00625 | 0.447 |
| LIG_FHA_1 | 119 | 125 | PF00498 | 0.431 |
| LIG_FHA_1 | 186 | 192 | PF00498 | 0.483 |
| LIG_FHA_2 | 288 | 294 | PF00498 | 0.601 |
| LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.525 |
| LIG_Pex14_2 | 215 | 219 | PF04695 | 0.501 |
| LIG_SH3_3 | 319 | 325 | PF00018 | 0.482 |
| LIG_SH3_3 | 60 | 66 | PF00018 | 0.478 |
| LIG_SUMO_SIM_par_1 | 126 | 133 | PF11976 | 0.469 |
| LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.529 |
| MOD_CDK_SPK_2 | 26 | 31 | PF00069 | 0.428 |
| MOD_CDK_SPxK_1 | 59 | 65 | PF00069 | 0.481 |
| MOD_CK1_1 | 332 | 338 | PF00069 | 0.446 |
| MOD_CK2_1 | 239 | 245 | PF00069 | 0.609 |
| MOD_CK2_1 | 26 | 32 | PF00069 | 0.438 |
| MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.527 |
| MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.630 |
| MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.660 |
| MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.504 |
| MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.556 |
| MOD_GSK3_1 | 136 | 143 | PF00069 | 0.605 |
| MOD_GSK3_1 | 297 | 304 | PF00069 | 0.707 |
| MOD_GSK3_1 | 332 | 339 | PF00069 | 0.491 |
| MOD_GSK3_1 | 39 | 46 | PF00069 | 0.482 |
| MOD_GSK3_1 | 65 | 72 | PF00069 | 0.456 |
| MOD_NEK2_1 | 160 | 165 | PF00069 | 0.644 |
| MOD_NEK2_1 | 247 | 252 | PF00069 | 0.465 |
| MOD_NEK2_1 | 270 | 275 | PF00069 | 0.559 |
| MOD_NEK2_1 | 41 | 46 | PF00069 | 0.487 |
| MOD_NEK2_1 | 69 | 74 | PF00069 | 0.438 |
| MOD_NEK2_2 | 96 | 101 | PF00069 | 0.512 |
| MOD_PIKK_1 | 239 | 245 | PF00454 | 0.564 |
| MOD_PKA_1 | 336 | 342 | PF00069 | 0.551 |
| MOD_PKA_2 | 118 | 124 | PF00069 | 0.574 |
| MOD_PKA_2 | 239 | 245 | PF00069 | 0.455 |
| MOD_PKA_2 | 247 | 253 | PF00069 | 0.405 |
| MOD_PKA_2 | 329 | 335 | PF00069 | 0.669 |
| MOD_PKA_2 | 336 | 342 | PF00069 | 0.591 |
| MOD_Plk_4 | 277 | 283 | PF00069 | 0.522 |
| MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.535 |
| MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.481 |
| MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.431 |
| MOD_SUMO_rev_2 | 192 | 201 | PF00179 | 0.509 |
| MOD_SUMO_rev_2 | 250 | 259 | PF00179 | 0.529 |
| MOD_SUMO_rev_2 | 381 | 390 | PF00179 | 0.617 |
| TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.430 |
| TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.630 |
| TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.588 |
| TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.429 |
| TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.520 |
| TRG_Pf-PMV_PEXEL_1 | 74 | 79 | PF00026 | 0.444 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HXL4 | Leptomonas seymouri | 40% | 100% |
| A0A3S7X4F2 | Leishmania donovani | 91% | 100% |
| A0A422NZ65 | Trypanosoma rangeli | 30% | 100% |
| A4HJB9 | Leishmania braziliensis | 73% | 100% |
| A4I6R2 | Leishmania infantum | 91% | 100% |
| C9ZWT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
| E9B1T4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |