| 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 | 
Related structures:
AlphaFold database: A0A3Q8IAW5
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.423 | 
| CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.541 | 
| CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.421 | 
| CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.621 | 
| CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.551 | 
| CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.478 | 
| CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.495 | 
| DEG_APCC_KENBOX_2 | 49 | 53 | PF00400 | 0.451 | 
| DOC_CKS1_1 | 170 | 175 | PF01111 | 0.470 | 
| DOC_PP1_RVXF_1 | 54 | 60 | PF00149 | 0.467 | 
| DOC_PP1_RVXF_1 | 87 | 94 | PF00149 | 0.362 | 
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.604 | 
| DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.689 | 
| DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.540 | 
| DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.456 | 
| DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.462 | 
| DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.571 | 
| LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.529 | 
| LIG_deltaCOP1_diTrp_1 | 178 | 187 | PF00928 | 0.439 | 
| LIG_deltaCOP1_diTrp_1 | 231 | 241 | PF00928 | 0.411 | 
| LIG_FHA_2 | 170 | 176 | PF00498 | 0.476 | 
| LIG_FHA_2 | 237 | 243 | PF00498 | 0.257 | 
| LIG_FHA_2 | 24 | 30 | PF00498 | 0.580 | 
| LIG_LIR_Apic_2 | 364 | 369 | PF02991 | 0.512 | 
| LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.358 | 
| LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.560 | 
| LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.334 | 
| LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.266 | 
| LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.538 | 
| LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.574 | 
| LIG_Pex14_2 | 221 | 225 | PF04695 | 0.281 | 
| LIG_SH2_CRK | 166 | 170 | PF00017 | 0.355 | 
| LIG_SH2_CRK | 258 | 262 | PF00017 | 0.411 | 
| LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.347 | 
| LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.527 | 
| LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.443 | 
| LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.371 | 
| LIG_SH3_1 | 167 | 173 | PF00018 | 0.370 | 
| LIG_SH3_3 | 167 | 173 | PF00018 | 0.308 | 
| LIG_SH3_3 | 201 | 207 | PF00018 | 0.265 | 
| LIG_SH3_3 | 379 | 385 | PF00018 | 0.575 | 
| LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.493 | 
| LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.445 | 
| MOD_CDK_SPxK_1 | 100 | 106 | PF00069 | 0.441 | 
| MOD_CK1_1 | 136 | 142 | PF00069 | 0.554 | 
| MOD_CK1_1 | 190 | 196 | PF00069 | 0.325 | 
| MOD_CK1_1 | 219 | 225 | PF00069 | 0.369 | 
| MOD_CK1_1 | 295 | 301 | PF00069 | 0.602 | 
| MOD_CK1_1 | 41 | 47 | PF00069 | 0.407 | 
| MOD_CK2_1 | 169 | 175 | PF00069 | 0.466 | 
| MOD_CK2_1 | 23 | 29 | PF00069 | 0.591 | 
| MOD_CK2_1 | 236 | 242 | PF00069 | 0.293 | 
| MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.687 | 
| MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.358 | 
| MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.360 | 
| MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.360 | 
| MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.591 | 
| MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.523 | 
| MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.709 | 
| MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.673 | 
| MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.410 | 
| MOD_GSK3_1 | 133 | 140 | PF00069 | 0.583 | 
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.356 | 
| MOD_GSK3_1 | 236 | 243 | PF00069 | 0.360 | 
| MOD_GSK3_1 | 310 | 317 | PF00069 | 0.683 | 
| MOD_GSK3_1 | 8 | 15 | PF00069 | 0.518 | 
| MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.653 | 
| MOD_NEK2_1 | 301 | 306 | PF00069 | 0.723 | 
| MOD_NEK2_1 | 361 | 366 | PF00069 | 0.543 | 
| MOD_OFUCOSY | 156 | 163 | PF10250 | 0.358 | 
| MOD_PIKK_1 | 8 | 14 | PF00454 | 0.470 | 
| MOD_PKA_2 | 293 | 299 | PF00069 | 0.605 | 
| MOD_PKA_2 | 321 | 327 | PF00069 | 0.618 | 
| MOD_PKA_2 | 73 | 79 | PF00069 | 0.530 | 
| MOD_Plk_1 | 274 | 280 | PF00069 | 0.475 | 
| MOD_Plk_1 | 302 | 308 | PF00069 | 0.482 | 
| MOD_Plk_4 | 12 | 18 | PF00069 | 0.594 | 
| MOD_Plk_4 | 236 | 242 | PF00069 | 0.300 | 
| MOD_Plk_4 | 284 | 290 | PF00069 | 0.529 | 
| MOD_Plk_4 | 361 | 367 | PF00069 | 0.503 | 
| MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.470 | 
| MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.465 | 
| MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.566 | 
| TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.436 | 
| TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.300 | 
| TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.513 | 
| TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.449 | 
| TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.454 | 
| TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.547 | 
| TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.348 | 
| TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.445 | 
| TRG_Pf-PMV_PEXEL_1 | 7 | 12 | PF00026 | 0.547 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P400 | Leptomonas seymouri | 61% | 92% | 
| A0A1X0P6R6 | Trypanosomatidae | 44% | 100% | 
| A0A422NWL4 | Trypanosoma rangeli | 42% | 100% | 
| A4H9D8 | Leishmania braziliensis | 79% | 100% | 
| A4HXQ9 | Leishmania infantum | 100% | 100% | 
| B6DTF3 | Bodo saltans | 31% | 100% | 
| D0A041 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% | 
| E9ARH1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% | 
| Q4QE08 | Leishmania major | 96% | 100% | 
| V5DN00 | Trypanosoma cruzi | 40% | 100% |