| 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: Q4Q5T0
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.475 |
| CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.571 |
| CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.434 |
| CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.617 |
| CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.471 |
| CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.594 |
| CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.545 |
| CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.568 |
| CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.455 |
| CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.615 |
| CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.405 |
| CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.572 |
| CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.564 |
| CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.545 |
| CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.564 |
| CLV_PCSK_PC7_1 | 315 | 321 | PF00082 | 0.475 |
| CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.538 |
| CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.521 |
| CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.462 |
| CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.529 |
| DEG_SPOP_SBC_1 | 288 | 292 | PF00917 | 0.465 |
| DOC_CDC14_PxL_1 | 224 | 232 | PF14671 | 0.633 |
| DOC_CYCLIN_yCln2_LP_2 | 242 | 248 | PF00134 | 0.474 |
| DOC_CYCLIN_yCln2_LP_2 | 31 | 37 | PF00134 | 0.578 |
| DOC_MAPK_gen_1 | 108 | 114 | PF00069 | 0.646 |
| DOC_MAPK_gen_1 | 128 | 134 | PF00069 | 0.305 |
| DOC_MAPK_gen_1 | 256 | 264 | PF00069 | 0.652 |
| DOC_PP4_FxxP_1 | 368 | 371 | PF00568 | 0.564 |
| DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.677 |
| DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.647 |
| DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.615 |
| DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.642 |
| DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.557 |
| DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.581 |
| DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.673 |
| LIG_14-3-3_CanoR_1 | 324 | 333 | PF00244 | 0.578 |
| LIG_Actin_WH2_2 | 202 | 218 | PF00022 | 0.508 |
| LIG_Clathr_ClatBox_1 | 88 | 92 | PF01394 | 0.532 |
| LIG_FHA_1 | 161 | 167 | PF00498 | 0.442 |
| LIG_FHA_1 | 218 | 224 | PF00498 | 0.583 |
| LIG_FHA_1 | 25 | 31 | PF00498 | 0.655 |
| LIG_FHA_1 | 291 | 297 | PF00498 | 0.548 |
| LIG_FHA_2 | 169 | 175 | PF00498 | 0.385 |
| LIG_FHA_2 | 231 | 237 | PF00498 | 0.627 |
| LIG_FHA_2 | 329 | 335 | PF00498 | 0.479 |
| LIG_FHA_2 | 370 | 376 | PF00498 | 0.468 |
| LIG_LIR_Apic_2 | 259 | 263 | PF02991 | 0.679 |
| LIG_LIR_Apic_2 | 375 | 380 | PF02991 | 0.762 |
| LIG_LIR_Gen_1 | 167 | 177 | PF02991 | 0.421 |
| LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.436 |
| LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.458 |
| LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.637 |
| LIG_MYND_1 | 5 | 9 | PF01753 | 0.603 |
| LIG_SH2_CRK | 191 | 195 | PF00017 | 0.530 |
| LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.585 |
| LIG_SH2_NCK_1 | 333 | 337 | PF00017 | 0.549 |
| LIG_SH2_PTP2 | 261 | 264 | PF00017 | 0.679 |
| LIG_SH2_SRC | 261 | 264 | PF00017 | 0.679 |
| LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.670 |
| LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.529 |
| LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.582 |
| LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.337 |
| LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.640 |
| LIG_SH3_3 | 222 | 228 | PF00018 | 0.515 |
| LIG_SH3_3 | 31 | 37 | PF00018 | 0.630 |
| LIG_SH3_3 | 55 | 61 | PF00018 | 0.629 |
| LIG_SH3_3 | 92 | 98 | PF00018 | 0.559 |
| LIG_SUMO_SIM_par_1 | 85 | 92 | PF11976 | 0.586 |
| LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.556 |
| LIG_TRFH_1 | 94 | 98 | PF08558 | 0.553 |
| LIG_WRC_WIRS_1 | 20 | 25 | PF05994 | 0.686 |
| MOD_CK1_1 | 159 | 165 | PF00069 | 0.498 |
| MOD_CK1_1 | 19 | 25 | PF00069 | 0.663 |
| MOD_CK1_1 | 290 | 296 | PF00069 | 0.580 |
| MOD_CK1_1 | 337 | 343 | PF00069 | 0.594 |
| MOD_CK1_1 | 359 | 365 | PF00069 | 0.592 |
| MOD_CK1_1 | 42 | 48 | PF00069 | 0.703 |
| MOD_CK1_1 | 53 | 59 | PF00069 | 0.640 |
| MOD_CK2_1 | 161 | 167 | PF00069 | 0.393 |
| MOD_CK2_1 | 168 | 174 | PF00069 | 0.364 |
| MOD_CK2_1 | 230 | 236 | PF00069 | 0.673 |
| MOD_CK2_1 | 328 | 334 | PF00069 | 0.477 |
| MOD_CK2_1 | 337 | 343 | PF00069 | 0.479 |
| MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.714 |
| MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.610 |
| MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.632 |
| MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.604 |
| MOD_GSK3_1 | 156 | 163 | PF00069 | 0.497 |
| MOD_GSK3_1 | 288 | 295 | PF00069 | 0.644 |
| MOD_GSK3_1 | 352 | 359 | PF00069 | 0.638 |
| MOD_GSK3_1 | 49 | 56 | PF00069 | 0.642 |
| MOD_GSK3_1 | 64 | 71 | PF00069 | 0.529 |
| MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.455 |
| MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.610 |
| MOD_N-GLC_2 | 46 | 48 | PF02516 | 0.614 |
| MOD_NEK2_1 | 101 | 106 | PF00069 | 0.550 |
| MOD_NEK2_1 | 161 | 166 | PF00069 | 0.513 |
| MOD_NEK2_1 | 215 | 220 | PF00069 | 0.586 |
| MOD_NEK2_1 | 230 | 235 | PF00069 | 0.522 |
| MOD_NEK2_1 | 44 | 49 | PF00069 | 0.606 |
| MOD_NEK2_1 | 62 | 67 | PF00069 | 0.730 |
| MOD_PIKK_1 | 325 | 331 | PF00454 | 0.502 |
| MOD_PIKK_1 | 7 | 13 | PF00454 | 0.574 |
| MOD_PKA_2 | 215 | 221 | PF00069 | 0.608 |
| MOD_PKA_2 | 230 | 236 | PF00069 | 0.573 |
| MOD_Plk_1 | 166 | 172 | PF00069 | 0.515 |
| MOD_Plk_1 | 207 | 213 | PF00069 | 0.340 |
| MOD_Plk_1 | 238 | 244 | PF00069 | 0.509 |
| MOD_Plk_1 | 53 | 59 | PF00069 | 0.713 |
| MOD_Plk_1 | 63 | 69 | PF00069 | 0.735 |
| MOD_Plk_1 | 84 | 90 | PF00069 | 0.531 |
| MOD_Plk_4 | 161 | 167 | PF00069 | 0.448 |
| MOD_Plk_4 | 26 | 32 | PF00069 | 0.692 |
| MOD_Plk_4 | 328 | 334 | PF00069 | 0.517 |
| MOD_Plk_4 | 69 | 75 | PF00069 | 0.644 |
| MOD_Plk_4 | 84 | 90 | PF00069 | 0.612 |
| MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.643 |
| MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.558 |
| MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.669 |
| TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.539 |
| TRG_DiLeu_BaLyEn_6 | 34 | 39 | PF01217 | 0.674 |
| TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.516 |
| TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.609 |
| TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.615 |
| TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.654 |
| TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.499 |
| TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.591 |
| TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.549 |
| TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.511 |
| TRG_NLS_Bipartite_1 | 267 | 284 | PF00514 | 0.624 |
| TRG_NLS_MonoCore_2 | 279 | 284 | PF00514 | 0.568 |
| TRG_NLS_MonoExtC_3 | 279 | 285 | PF00514 | 0.599 |
| TRG_NLS_MonoExtN_4 | 277 | 284 | PF00514 | 0.691 |
| TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.554 |
| TRG_Pf-PMV_PEXEL_1 | 294 | 299 | PF00026 | 0.641 |
| TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.545 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P875 | Leptomonas seymouri | 60% | 100% |
| A0A0S4JFY4 | Bodo saltans | 31% | 100% |
| A0A1X0P6X1 | Trypanosomatidae | 35% | 87% |
| A0A3R7M1V0 | Trypanosoma rangeli | 31% | 83% |
| A0A3S7X519 | Leishmania donovani | 92% | 86% |
| A4HJY6 | Leishmania braziliensis | 77% | 100% |
| A4I7G9 | Leishmania infantum | 91% | 100% |
| C9ZZZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 83% |
| E9B2C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
| V5DTD7 | Trypanosoma cruzi | 30% | 82% |