| 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 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 1 | 
| GO:0110165 | cellular anatomical entity | 1 | 1 | 
Related structures:
AlphaFold database: A4IAE8
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.399 | 
| CLV_C14_Caspase3-7 | 223 | 227 | PF00656 | 0.641 | 
| CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.412 | 
| CLV_MEL_PAP_1 | 66 | 72 | PF00089 | 0.388 | 
| CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.544 | 
| CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.390 | 
| CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.620 | 
| CLV_PCSK_FUR_1 | 2 | 6 | PF00082 | 0.630 | 
| CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.404 | 
| CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.491 | 
| CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.428 | 
| CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.545 | 
| CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.312 | 
| CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.419 | 
| CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.428 | 
| CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.321 | 
| CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.447 | 
| CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.412 | 
| CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.376 | 
| CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.523 | 
| CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.440 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.504 | 
| DOC_CYCLIN_RxL_1 | 202 | 211 | PF00134 | 0.368 | 
| DOC_CYCLIN_yCln2_LP_2 | 315 | 321 | PF00134 | 0.479 | 
| DOC_MAPK_gen_1 | 316 | 327 | PF00069 | 0.521 | 
| DOC_MAPK_gen_1 | 32 | 39 | PF00069 | 0.519 | 
| DOC_MAPK_HePTP_8 | 29 | 41 | PF00069 | 0.420 | 
| DOC_MAPK_MEF2A_6 | 194 | 203 | PF00069 | 0.332 | 
| DOC_MAPK_MEF2A_6 | 32 | 41 | PF00069 | 0.423 | 
| DOC_MAPK_RevD_3 | 17 | 33 | PF00069 | 0.336 | 
| DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.465 | 
| DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.322 | 
| DOC_PP4_FxxP_1 | 76 | 79 | PF00568 | 0.491 | 
| DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.613 | 
| DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.372 | 
| DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.404 | 
| DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.383 | 
| DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.449 | 
| LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.410 | 
| LIG_14-3-3_CanoR_1 | 2 | 12 | PF00244 | 0.479 | 
| LIG_14-3-3_CanoR_1 | 320 | 327 | PF00244 | 0.472 | 
| LIG_14-3-3_CanoR_1 | 60 | 70 | PF00244 | 0.348 | 
| LIG_APCC_ABBA_1 | 246 | 251 | PF00400 | 0.294 | 
| LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.437 | 
| LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.440 | 
| LIG_FHA_1 | 13 | 19 | PF00498 | 0.342 | 
| LIG_FHA_1 | 157 | 163 | PF00498 | 0.410 | 
| LIG_FHA_1 | 25 | 31 | PF00498 | 0.405 | 
| LIG_FHA_1 | 279 | 285 | PF00498 | 0.377 | 
| LIG_FHA_1 | 333 | 339 | PF00498 | 0.376 | 
| LIG_FHA_1 | 49 | 55 | PF00498 | 0.320 | 
| LIG_FHA_1 | 61 | 67 | PF00498 | 0.355 | 
| LIG_FHA_2 | 223 | 229 | PF00498 | 0.651 | 
| LIG_FHA_2 | 26 | 32 | PF00498 | 0.410 | 
| LIG_FHA_2 | 269 | 275 | PF00498 | 0.448 | 
| LIG_FHA_2 | 338 | 344 | PF00498 | 0.413 | 
| LIG_LIR_Apic_2 | 328 | 332 | PF02991 | 0.497 | 
| LIG_LIR_Apic_2 | 74 | 79 | PF02991 | 0.418 | 
| LIG_LIR_Gen_1 | 14 | 24 | PF02991 | 0.332 | 
| LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.342 | 
| LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.328 | 
| LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.371 | 
| LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.338 | 
| LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.336 | 
| LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.413 | 
| LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.400 | 
| LIG_PCNA_PIPBox_1 | 99 | 108 | PF02747 | 0.461 | 
| LIG_PDZ_Class_2 | 350 | 355 | PF00595 | 0.304 | 
| LIG_Pex14_2 | 76 | 80 | PF04695 | 0.494 | 
| LIG_SH2_CRK | 180 | 184 | PF00017 | 0.538 | 
| LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.360 | 
| LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.378 | 
| LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.431 | 
| LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.384 | 
| LIG_SH3_3 | 250 | 256 | PF00018 | 0.375 | 
| LIG_SUMO_SIM_par_1 | 51 | 58 | PF11976 | 0.308 | 
| LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.446 | 
| LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.354 | 
| LIG_WRC_WIRS_1 | 102 | 107 | PF05994 | 0.454 | 
| MOD_CDC14_SPxK_1 | 78 | 81 | PF00782 | 0.392 | 
| MOD_CDK_SPxK_1 | 75 | 81 | PF00069 | 0.386 | 
| MOD_CK1_1 | 104 | 110 | PF00069 | 0.458 | 
| MOD_CK1_1 | 136 | 142 | PF00069 | 0.434 | 
| MOD_CK1_1 | 272 | 278 | PF00069 | 0.369 | 
| MOD_CK1_1 | 65 | 71 | PF00069 | 0.344 | 
| MOD_CK1_1 | 75 | 81 | PF00069 | 0.402 | 
| MOD_CK1_1 | 88 | 94 | PF00069 | 0.587 | 
| MOD_CK2_1 | 136 | 142 | PF00069 | 0.432 | 
| MOD_CK2_1 | 222 | 228 | PF00069 | 0.699 | 
| MOD_CK2_1 | 25 | 31 | PF00069 | 0.415 | 
| MOD_CK2_1 | 268 | 274 | PF00069 | 0.427 | 
| MOD_CK2_1 | 337 | 343 | PF00069 | 0.421 | 
| MOD_DYRK1A_RPxSP_1 | 125 | 129 | PF00069 | 0.374 | 
| MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.613 | 
| MOD_GSK3_1 | 218 | 225 | PF00069 | 0.743 | 
| MOD_GSK3_1 | 268 | 275 | PF00069 | 0.528 | 
| MOD_GSK3_1 | 333 | 340 | PF00069 | 0.371 | 
| MOD_GSK3_1 | 61 | 68 | PF00069 | 0.481 | 
| MOD_GSK3_1 | 71 | 78 | PF00069 | 0.501 | 
| MOD_GSK3_1 | 81 | 88 | PF00069 | 0.421 | 
| MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.599 | 
| MOD_NEK2_1 | 106 | 111 | PF00069 | 0.384 | 
| MOD_NEK2_1 | 220 | 225 | PF00069 | 0.684 | 
| MOD_NEK2_1 | 304 | 309 | PF00069 | 0.467 | 
| MOD_NEK2_1 | 311 | 316 | PF00069 | 0.360 | 
| MOD_NEK2_1 | 61 | 66 | PF00069 | 0.382 | 
| MOD_NEK2_1 | 72 | 77 | PF00069 | 0.392 | 
| MOD_NEK2_2 | 3 | 8 | PF00069 | 0.480 | 
| MOD_PIKK_1 | 107 | 113 | PF00454 | 0.449 | 
| MOD_PIKK_1 | 178 | 184 | PF00454 | 0.358 | 
| MOD_PKA_2 | 3 | 9 | PF00069 | 0.589 | 
| MOD_PKA_2 | 319 | 325 | PF00069 | 0.474 | 
| MOD_PKB_1 | 171 | 179 | PF00069 | 0.401 | 
| MOD_Plk_1 | 173 | 179 | PF00069 | 0.469 | 
| MOD_Plk_4 | 101 | 107 | PF00069 | 0.424 | 
| MOD_Plk_4 | 157 | 163 | PF00069 | 0.479 | 
| MOD_Plk_4 | 25 | 31 | PF00069 | 0.405 | 
| MOD_Plk_4 | 62 | 68 | PF00069 | 0.479 | 
| MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.384 | 
| MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.458 | 
| MOD_SUMO_rev_2 | 296 | 304 | PF00179 | 0.428 | 
| TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.378 | 
| TRG_DiLeu_LyEn_5 | 300 | 305 | PF01217 | 0.470 | 
| TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.351 | 
| TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.416 | 
| TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.428 | 
| TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.654 | 
| TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.450 | 
| TRG_Pf-PMV_PEXEL_1 | 278 | 282 | PF00026 | 0.300 | 
| TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.385 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P771 | Leptomonas seymouri | 58% | 95% | 
| A0A0S4KPS3 | Bodo saltans | 30% | 100% | 
| A0A1X0PA34 | Trypanosomatidae | 40% | 100% | 
| A0A3S7X8E4 | Leishmania donovani | 100% | 100% | 
| A0A422NT02 | Trypanosoma rangeli | 39% | 100% | 
| A4HBA0 | Leishmania braziliensis | 80% | 100% | 
| C9ZLU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% | 
| E9B5H2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% | 
| Q4Q2G3 | Leishmania major | 96% | 100% | 
| V5DMU4 | Trypanosoma cruzi | 41% | 100% |