| 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 |
Related structures:
AlphaFold database: A4I482
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 10 | 14 | PF00656 | 0.617 |
| CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.533 |
| CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.650 |
| CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.742 |
| CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.687 |
| CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.536 |
| CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.627 |
| CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.742 |
| CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.601 |
| CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.546 |
| DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.522 |
| DEG_SPOP_SBC_1 | 203 | 207 | PF00917 | 0.482 |
| DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.611 |
| DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.725 |
| DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.604 |
| DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.308 |
| DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.527 |
| DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.549 |
| DOC_USP7_UBL2_3 | 275 | 279 | PF12436 | 0.625 |
| DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.637 |
| DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.485 |
| LIG_14-3-3_CanoR_1 | 132 | 141 | PF00244 | 0.602 |
| LIG_14-3-3_CanoR_1 | 19 | 29 | PF00244 | 0.519 |
| LIG_14-3-3_CanoR_1 | 266 | 272 | PF00244 | 0.591 |
| LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.466 |
| LIG_14-3-3_CanoR_1 | 9 | 16 | PF00244 | 0.613 |
| LIG_Actin_WH2_2 | 33 | 48 | PF00022 | 0.489 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.688 |
| LIG_FHA_1 | 166 | 172 | PF00498 | 0.613 |
| LIG_FHA_1 | 24 | 30 | PF00498 | 0.545 |
| LIG_FHA_2 | 272 | 278 | PF00498 | 0.615 |
| LIG_FHA_2 | 31 | 37 | PF00498 | 0.461 |
| LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.610 |
| LIG_LIR_Gen_1 | 168 | 178 | PF02991 | 0.603 |
| LIG_LIR_Gen_1 | 36 | 47 | PF02991 | 0.427 |
| LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.560 |
| LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.676 |
| LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.607 |
| LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.424 |
| LIG_SH2_NCK_1 | 209 | 213 | PF00017 | 0.569 |
| LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.613 |
| LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.530 |
| LIG_SH3_2 | 314 | 319 | PF14604 | 0.674 |
| LIG_SH3_3 | 136 | 142 | PF00018 | 0.596 |
| LIG_SH3_3 | 186 | 192 | PF00018 | 0.628 |
| LIG_SH3_3 | 197 | 203 | PF00018 | 0.495 |
| LIG_SH3_3 | 225 | 231 | PF00018 | 0.647 |
| LIG_SH3_3 | 311 | 317 | PF00018 | 0.681 |
| LIG_SH3_3 | 351 | 357 | PF00018 | 0.317 |
| LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.607 |
| LIG_TRFH_1 | 199 | 203 | PF08558 | 0.578 |
| MOD_CK1_1 | 103 | 109 | PF00069 | 0.577 |
| MOD_CK1_1 | 117 | 123 | PF00069 | 0.590 |
| MOD_CK1_1 | 165 | 171 | PF00069 | 0.594 |
| MOD_CK1_1 | 20 | 26 | PF00069 | 0.508 |
| MOD_CK1_1 | 205 | 211 | PF00069 | 0.591 |
| MOD_CK2_1 | 171 | 177 | PF00069 | 0.602 |
| MOD_CK2_1 | 94 | 100 | PF00069 | 0.563 |
| MOD_Cter_Amidation | 285 | 288 | PF01082 | 0.581 |
| MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.622 |
| MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.693 |
| MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.637 |
| MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.640 |
| MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.621 |
| MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.674 |
| MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.494 |
| MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.405 |
| MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.743 |
| MOD_GSK3_1 | 116 | 123 | PF00069 | 0.629 |
| MOD_GSK3_1 | 172 | 179 | PF00069 | 0.563 |
| MOD_GSK3_1 | 203 | 210 | PF00069 | 0.724 |
| MOD_GSK3_1 | 267 | 274 | PF00069 | 0.614 |
| MOD_GSK3_1 | 299 | 306 | PF00069 | 0.632 |
| MOD_GSK3_1 | 90 | 97 | PF00069 | 0.679 |
| MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.621 |
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.599 |
| MOD_NEK2_1 | 131 | 136 | PF00069 | 0.650 |
| MOD_NEK2_1 | 204 | 209 | PF00069 | 0.597 |
| MOD_NEK2_1 | 29 | 34 | PF00069 | 0.470 |
| MOD_NEK2_1 | 45 | 50 | PF00069 | 0.342 |
| MOD_PIKK_1 | 182 | 188 | PF00454 | 0.660 |
| MOD_PKA_1 | 187 | 193 | PF00069 | 0.663 |
| MOD_PKA_1 | 332 | 338 | PF00069 | 0.471 |
| MOD_PKA_2 | 131 | 137 | PF00069 | 0.613 |
| MOD_PKA_2 | 187 | 193 | PF00069 | 0.745 |
| MOD_PKA_2 | 29 | 35 | PF00069 | 0.528 |
| MOD_PKA_2 | 45 | 51 | PF00069 | 0.357 |
| MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.637 |
| MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.482 |
| MOD_SUMO_for_1 | 326 | 329 | PF00179 | 0.587 |
| MOD_SUMO_rev_2 | 233 | 240 | PF00179 | 0.600 |
| TRG_AP2beta_CARGO_1 | 36 | 46 | PF09066 | 0.479 |
| TRG_DiLeu_BaEn_1 | 24 | 29 | PF01217 | 0.463 |
| TRG_DiLeu_BaEn_2 | 165 | 171 | PF01217 | 0.569 |
| TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.667 |
| TRG_Pf-PMV_PEXEL_1 | 19 | 24 | PF00026 | 0.523 |
| TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.440 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IM20 | Leptomonas seymouri | 39% | 100% |
| A0A3S7X263 | Leishmania donovani | 100% | 100% |
| A4HH62 | Leishmania braziliensis | 67% | 98% |
| E9ADN1 | Leishmania major | 85% | 100% |
| E9AM49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
| V5BIK2 | Trypanosoma cruzi | 30% | 68% |