| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q9K1
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.575 |
| CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.615 |
| CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.715 |
| CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.591 |
| CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.530 |
| CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.442 |
| CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.651 |
| CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.500 |
| CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.602 |
| CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.591 |
| CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.476 |
| CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.387 |
| CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.578 |
| CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.520 |
| CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.633 |
| CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.358 |
| CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.555 |
| CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.526 |
| DEG_SCF_FBW7_2 | 182 | 187 | PF00400 | 0.560 |
| DEG_SIAH_1 | 16 | 24 | PF03145 | 0.587 |
| DOC_CDC14_PxL_1 | 78 | 86 | PF14671 | 0.725 |
| DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.690 |
| DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.657 |
| DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.642 |
| DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.578 |
| DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.713 |
| DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.639 |
| DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.485 |
| DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.624 |
| DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.706 |
| DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.751 |
| LIG_14-3-3_CanoR_1 | 220 | 229 | PF00244 | 0.536 |
| LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.668 |
| LIG_14-3-3_CanoR_1 | 356 | 363 | PF00244 | 0.707 |
| LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.561 |
| LIG_APCC_ABBA_1 | 75 | 80 | PF00400 | 0.514 |
| LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.588 |
| LIG_FHA_1 | 194 | 200 | PF00498 | 0.600 |
| LIG_FHA_1 | 260 | 266 | PF00498 | 0.715 |
| LIG_FHA_1 | 292 | 298 | PF00498 | 0.512 |
| LIG_FHA_2 | 158 | 164 | PF00498 | 0.534 |
| LIG_FHA_2 | 181 | 187 | PF00498 | 0.638 |
| LIG_FHA_2 | 202 | 208 | PF00498 | 0.613 |
| LIG_FHA_2 | 68 | 74 | PF00498 | 0.668 |
| LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.473 |
| LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.499 |
| LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.473 |
| LIG_NRBOX | 302 | 308 | PF00104 | 0.587 |
| LIG_Rb_pABgroove_1 | 23 | 31 | PF01858 | 0.589 |
| LIG_SH2_CRK | 14 | 18 | PF00017 | 0.619 |
| LIG_SH2_PTP2 | 296 | 299 | PF00017 | 0.560 |
| LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.433 |
| LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.697 |
| LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.531 |
| LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.579 |
| LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.560 |
| LIG_SH3_3 | 17 | 23 | PF00018 | 0.507 |
| LIG_SH3_3 | 62 | 68 | PF00018 | 0.779 |
| LIG_SUMO_SIM_anti_2 | 300 | 309 | PF11976 | 0.556 |
| LIG_SUMO_SIM_par_1 | 276 | 283 | PF11976 | 0.579 |
| LIG_TRAF2_1 | 184 | 187 | PF00917 | 0.562 |
| LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.573 |
| LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.590 |
| MOD_CK1_1 | 124 | 130 | PF00069 | 0.621 |
| MOD_CK1_1 | 132 | 138 | PF00069 | 0.515 |
| MOD_CK1_1 | 178 | 184 | PF00069 | 0.709 |
| MOD_CK1_1 | 243 | 249 | PF00069 | 0.615 |
| MOD_CK1_1 | 60 | 66 | PF00069 | 0.749 |
| MOD_CK2_1 | 161 | 167 | PF00069 | 0.541 |
| MOD_CK2_1 | 180 | 186 | PF00069 | 0.786 |
| MOD_CK2_1 | 222 | 228 | PF00069 | 0.509 |
| MOD_CK2_1 | 37 | 43 | PF00069 | 0.535 |
| MOD_GlcNHglycan | 176 | 180 | PF01048 | 0.596 |
| MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.566 |
| MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.782 |
| MOD_GSK3_1 | 117 | 124 | PF00069 | 0.583 |
| MOD_GSK3_1 | 125 | 132 | PF00069 | 0.676 |
| MOD_GSK3_1 | 138 | 145 | PF00069 | 0.410 |
| MOD_GSK3_1 | 157 | 164 | PF00069 | 0.583 |
| MOD_GSK3_1 | 239 | 246 | PF00069 | 0.472 |
| MOD_GSK3_1 | 254 | 261 | PF00069 | 0.680 |
| MOD_GSK3_1 | 34 | 41 | PF00069 | 0.561 |
| MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.606 |
| MOD_NEK2_1 | 161 | 166 | PF00069 | 0.524 |
| MOD_NEK2_1 | 199 | 204 | PF00069 | 0.571 |
| MOD_NEK2_1 | 221 | 226 | PF00069 | 0.538 |
| MOD_NEK2_1 | 229 | 234 | PF00069 | 0.575 |
| MOD_NEK2_1 | 34 | 39 | PF00069 | 0.512 |
| MOD_PIKK_1 | 121 | 127 | PF00454 | 0.582 |
| MOD_PIKK_1 | 351 | 357 | PF00454 | 0.410 |
| MOD_PK_1 | 107 | 113 | PF00069 | 0.435 |
| MOD_PK_1 | 260 | 266 | PF00069 | 0.571 |
| MOD_PKA_1 | 356 | 362 | PF00069 | 0.472 |
| MOD_PKA_2 | 239 | 245 | PF00069 | 0.470 |
| MOD_PKA_2 | 356 | 362 | PF00069 | 0.519 |
| MOD_Plk_1 | 107 | 113 | PF00069 | 0.629 |
| MOD_Plk_1 | 161 | 167 | PF00069 | 0.660 |
| MOD_Plk_1 | 185 | 191 | PF00069 | 0.720 |
| MOD_Plk_1 | 34 | 40 | PF00069 | 0.575 |
| MOD_Plk_2-3 | 157 | 163 | PF00069 | 0.567 |
| MOD_Plk_2-3 | 277 | 283 | PF00069 | 0.624 |
| MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.554 |
| MOD_Plk_4 | 117 | 123 | PF00069 | 0.538 |
| MOD_Plk_4 | 138 | 144 | PF00069 | 0.529 |
| MOD_Plk_4 | 23 | 29 | PF00069 | 0.558 |
| MOD_Plk_4 | 260 | 266 | PF00069 | 0.712 |
| MOD_Plk_4 | 34 | 40 | PF00069 | 0.341 |
| MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.616 |
| MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.706 |
| MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.751 |
| MOD_SUMO_rev_2 | 224 | 232 | PF00179 | 0.520 |
| TRG_Cilium_Arf4_1 | 360 | 364 | PF00025 | 0.510 |
| TRG_DiLeu_BaEn_4 | 276 | 282 | PF01217 | 0.616 |
| TRG_DiLeu_BaLyEn_6 | 20 | 25 | PF01217 | 0.505 |
| TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.497 |
| TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.526 |
| TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.476 |
| TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.560 |
| TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.587 |
| TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.439 |
| TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.481 |
| TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.511 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IKE1 | Leptomonas seymouri | 44% | 100% |
| A0A1X0NZJ6 | Trypanosomatidae | 29% | 100% |
| A0A3R7KZA5 | Trypanosoma rangeli | 27% | 91% |
| A0A3S5H7F3 | Leishmania donovani | 86% | 100% |
| A4HED8 | Leishmania braziliensis | 71% | 100% |
| A4I1T5 | Leishmania infantum | 85% | 100% |
| C9ZKE3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
| E9AXW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |