| 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:0005737 | cytoplasm | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q469
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.463 |
| CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.459 |
| CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.459 |
| CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.496 |
| CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.503 |
| CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.541 |
| CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.522 |
| CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.532 |
| CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.473 |
| CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.349 |
| DEG_APCC_DBOX_1 | 131 | 139 | PF00400 | 0.279 |
| DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.342 |
| DEG_SPOP_SBC_1 | 226 | 230 | PF00917 | 0.449 |
| DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.505 |
| DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.611 |
| DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.632 |
| DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.565 |
| DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.560 |
| DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.458 |
| LIG_14-3-3_CanoR_1 | 23 | 27 | PF00244 | 0.412 |
| LIG_14-3-3_CanoR_1 | 276 | 285 | PF00244 | 0.564 |
| LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.564 |
| LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.494 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.437 |
| LIG_BIR_III_4 | 213 | 217 | PF00653 | 0.367 |
| LIG_FHA_1 | 120 | 126 | PF00498 | 0.332 |
| LIG_FHA_1 | 215 | 221 | PF00498 | 0.487 |
| LIG_FHA_1 | 287 | 293 | PF00498 | 0.503 |
| LIG_FHA_1 | 321 | 327 | PF00498 | 0.400 |
| LIG_FHA_2 | 184 | 190 | PF00498 | 0.319 |
| LIG_HCF-1_HBM_1 | 75 | 78 | PF13415 | 0.446 |
| LIG_Integrin_RGD_1 | 256 | 258 | PF01839 | 0.469 |
| LIG_LIR_Gen_1 | 27 | 34 | PF02991 | 0.334 |
| LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.336 |
| LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.311 |
| LIG_SH2_CRK | 29 | 33 | PF00017 | 0.304 |
| LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.417 |
| LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.351 |
| LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.378 |
| LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.442 |
| LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.307 |
| LIG_SH3_3 | 297 | 303 | PF00018 | 0.363 |
| LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.597 |
| LIG_TYR_ITSM | 61 | 68 | PF00017 | 0.334 |
| MOD_CK1_1 | 111 | 117 | PF00069 | 0.403 |
| MOD_CK1_1 | 2 | 8 | PF00069 | 0.368 |
| MOD_CK1_1 | 228 | 234 | PF00069 | 0.662 |
| MOD_CK2_1 | 183 | 189 | PF00069 | 0.388 |
| MOD_CK2_1 | 202 | 208 | PF00069 | 0.468 |
| MOD_CMANNOS | 310 | 313 | PF00535 | 0.374 |
| MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.655 |
| MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.587 |
| MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.590 |
| MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.484 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.368 |
| MOD_GSK3_1 | 183 | 190 | PF00069 | 0.545 |
| MOD_GSK3_1 | 221 | 228 | PF00069 | 0.682 |
| MOD_GSK3_1 | 238 | 245 | PF00069 | 0.577 |
| MOD_GSK3_1 | 28 | 35 | PF00069 | 0.308 |
| MOD_GSK3_1 | 292 | 299 | PF00069 | 0.381 |
| MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.504 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.408 |
| MOD_NEK2_1 | 115 | 120 | PF00069 | 0.333 |
| MOD_NEK2_1 | 202 | 207 | PF00069 | 0.566 |
| MOD_NEK2_1 | 227 | 232 | PF00069 | 0.658 |
| MOD_NEK2_1 | 274 | 279 | PF00069 | 0.559 |
| MOD_NEK2_2 | 322 | 327 | PF00069 | 0.500 |
| MOD_PIKK_1 | 202 | 208 | PF00454 | 0.453 |
| MOD_PIKK_1 | 32 | 38 | PF00454 | 0.300 |
| MOD_PKA_2 | 22 | 28 | PF00069 | 0.351 |
| MOD_PKA_2 | 320 | 326 | PF00069 | 0.386 |
| MOD_PKB_1 | 165 | 173 | PF00069 | 0.348 |
| MOD_Plk_1 | 2 | 8 | PF00069 | 0.526 |
| MOD_Plk_1 | 257 | 263 | PF00069 | 0.470 |
| MOD_Plk_1 | 274 | 280 | PF00069 | 0.310 |
| MOD_Plk_4 | 115 | 121 | PF00069 | 0.474 |
| MOD_Plk_4 | 246 | 252 | PF00069 | 0.488 |
| MOD_Plk_4 | 28 | 34 | PF00069 | 0.318 |
| MOD_Plk_4 | 60 | 66 | PF00069 | 0.330 |
| MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.459 |
| MOD_SUMO_rev_2 | 228 | 237 | PF00179 | 0.615 |
| TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.331 |
| TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.322 |
| TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.488 |
| TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.353 |
| TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.385 |
| TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.353 |
| TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.365 |
| TRG_Pf-PMV_PEXEL_1 | 307 | 312 | PF00026 | 0.501 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P4F8 | Leptomonas seymouri | 80% | 95% |
| A0A0S4J7D5 | Bodo saltans | 52% | 97% |
| A0A1X0P104 | Trypanosomatidae | 64% | 100% |
| A0A3Q8IGJ8 | Leishmania donovani | 97% | 100% |
| A0A3R7N235 | Trypanosoma rangeli | 64% | 100% |
| A4HLH6 | Leishmania braziliensis | 91% | 100% |
| A4I8Y6 | Leishmania infantum | 97% | 100% |
| D0A4Y3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
| E9B3V5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
| V5BZN0 | Trypanosoma cruzi | 63% | 100% |