| 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: 7 | 
| NetGPI | no | yes: 0, no: 7 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 1 | 
| GO:0110165 | cellular anatomical entity | 1 | 1 | 
Related structures:
AlphaFold database: A4IAE0
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 122 | 128 | PF00089 | 0.455 | 
| CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.388 | 
| CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.404 | 
| CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.478 | 
| CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.452 | 
| CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.451 | 
| CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.596 | 
| CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.515 | 
| CLV_PCSK_FUR_1 | 293 | 297 | PF00082 | 0.622 | 
| CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.388 | 
| CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.404 | 
| CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.430 | 
| CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.450 | 
| CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.451 | 
| CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.601 | 
| CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.489 | 
| CLV_PCSK_PC7_1 | 108 | 114 | PF00082 | 0.468 | 
| CLV_PCSK_PC7_1 | 263 | 269 | PF00082 | 0.486 | 
| CLV_PCSK_PC7_1 | 295 | 301 | PF00082 | 0.473 | 
| CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.398 | 
| CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.444 | 
| CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.426 | 
| CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.477 | 
| CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.521 | 
| CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.515 | 
| DEG_APCC_DBOX_1 | 234 | 242 | PF00400 | 0.513 | 
| DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.410 | 
| DOC_CKS1_1 | 16 | 21 | PF01111 | 0.548 | 
| DOC_CYCLIN_yCln2_LP_2 | 245 | 251 | PF00134 | 0.527 | 
| DOC_MAPK_gen_1 | 193 | 201 | PF00069 | 0.422 | 
| DOC_MAPK_gen_1 | 212 | 222 | PF00069 | 0.319 | 
| DOC_MAPK_gen_1 | 276 | 286 | PF00069 | 0.440 | 
| DOC_PP1_RVXF_1 | 117 | 124 | PF00149 | 0.430 | 
| DOC_PP1_RVXF_1 | 163 | 169 | PF00149 | 0.427 | 
| DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.738 | 
| DOC_PP4_FxxP_1 | 16 | 19 | PF00568 | 0.541 | 
| DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.477 | 
| DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.378 | 
| DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.499 | 
| DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.572 | 
| DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.641 | 
| DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.594 | 
| LIG_14-3-3_CanoR_1 | 156 | 160 | PF00244 | 0.494 | 
| LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.494 | 
| LIG_14-3-3_CanoR_1 | 221 | 228 | PF00244 | 0.401 | 
| LIG_14-3-3_CanoR_1 | 230 | 234 | PF00244 | 0.373 | 
| LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.623 | 
| LIG_14-3-3_CanoR_1 | 318 | 325 | PF00244 | 0.620 | 
| LIG_14-3-3_CanoR_1 | 42 | 49 | PF00244 | 0.546 | 
| LIG_14-3-3_CterR_2 | 345 | 348 | PF00244 | 0.564 | 
| LIG_Actin_WH2_2 | 99 | 114 | PF00022 | 0.460 | 
| LIG_APCC_ABBAyCdc20_2 | 144 | 150 | PF00400 | 0.442 | 
| LIG_CaM_IQ_9 | 111 | 127 | PF13499 | 0.398 | 
| LIG_deltaCOP1_diTrp_1 | 169 | 174 | PF00928 | 0.452 | 
| LIG_deltaCOP1_diTrp_1 | 292 | 297 | PF00928 | 0.535 | 
| LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.451 | 
| LIG_FHA_1 | 16 | 22 | PF00498 | 0.571 | 
| LIG_FHA_1 | 4 | 10 | PF00498 | 0.537 | 
| LIG_FHA_1 | 77 | 83 | PF00498 | 0.487 | 
| LIG_FHA_1 | 89 | 95 | PF00498 | 0.365 | 
| LIG_FHA_2 | 156 | 162 | PF00498 | 0.382 | 
| LIG_LIR_Gen_1 | 242 | 251 | PF02991 | 0.566 | 
| LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.571 | 
| LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.484 | 
| LIG_SH2_NCK_1 | 53 | 57 | PF00017 | 0.549 | 
| LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.521 | 
| LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.520 | 
| LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.690 | 
| LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.632 | 
| LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.515 | 
| LIG_SUMO_SIM_par_1 | 90 | 95 | PF11976 | 0.355 | 
| MOD_CDK_SPxxK_3 | 35 | 42 | PF00069 | 0.541 | 
| MOD_CK1_1 | 22 | 28 | PF00069 | 0.577 | 
| MOD_CK1_1 | 74 | 80 | PF00069 | 0.453 | 
| MOD_CK2_1 | 14 | 20 | PF00069 | 0.606 | 
| MOD_CK2_1 | 155 | 161 | PF00069 | 0.336 | 
| MOD_CK2_1 | 22 | 28 | PF00069 | 0.496 | 
| MOD_CMANNOS | 168 | 171 | PF00535 | 0.442 | 
| MOD_CMANNOS | 294 | 297 | PF00535 | 0.410 | 
| MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.447 | 
| MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.644 | 
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.636 | 
| MOD_GSK3_1 | 220 | 227 | PF00069 | 0.453 | 
| MOD_GSK3_1 | 29 | 36 | PF00069 | 0.584 | 
| MOD_GSK3_1 | 41 | 48 | PF00069 | 0.540 | 
| MOD_GSK3_1 | 51 | 58 | PF00069 | 0.488 | 
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.623 | 
| MOD_NEK2_1 | 3 | 8 | PF00069 | 0.562 | 
| MOD_PIKK_1 | 318 | 324 | PF00454 | 0.469 | 
| MOD_PKA_2 | 155 | 161 | PF00069 | 0.362 | 
| MOD_PKA_2 | 220 | 226 | PF00069 | 0.427 | 
| MOD_PKA_2 | 229 | 235 | PF00069 | 0.403 | 
| MOD_PKA_2 | 28 | 34 | PF00069 | 0.658 | 
| MOD_PKA_2 | 41 | 47 | PF00069 | 0.554 | 
| MOD_PKA_2 | 74 | 80 | PF00069 | 0.500 | 
| MOD_PKB_1 | 200 | 208 | PF00069 | 0.398 | 
| MOD_Plk_1 | 224 | 230 | PF00069 | 0.468 | 
| MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.362 | 
| MOD_Plk_4 | 155 | 161 | PF00069 | 0.480 | 
| MOD_Plk_4 | 240 | 246 | PF00069 | 0.471 | 
| MOD_Plk_4 | 88 | 94 | PF00069 | 0.449 | 
| MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.574 | 
| MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.640 | 
| MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.592 | 
| TRG_DiLeu_BaEn_1 | 155 | 160 | PF01217 | 0.402 | 
| TRG_DiLeu_BaEn_1 | 312 | 317 | PF01217 | 0.504 | 
| TRG_DiLeu_BaLyEn_6 | 273 | 278 | PF01217 | 0.466 | 
| TRG_DiLeu_BaLyEn_6 | 311 | 316 | PF01217 | 0.498 | 
| TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.641 | 
| TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.418 | 
| TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.398 | 
| TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.366 | 
| TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.476 | 
| TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.397 | 
| TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.474 | 
| TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.620 | 
| TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.499 | 
| TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.548 | 
| TRG_Pf-PMV_PEXEL_1 | 140 | 145 | PF00026 | 0.481 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1ILB8 | Leptomonas seymouri | 58% | 100% | 
| A0A1X0PA21 | Trypanosomatidae | 28% | 100% | 
| A0A3Q8IFU3 | Leishmania donovani | 99% | 100% | 
| A4HB92 | Leishmania braziliensis | 68% | 93% | 
| E9B5G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% | 
| Q4Q2H1 | Leishmania major | 89% | 100% |