| 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: A4H712
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.566 |
| CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.495 |
| CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.484 |
| CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.413 |
| CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.539 |
| CLV_PCSK_FUR_1 | 177 | 181 | PF00082 | 0.423 |
| CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.678 |
| CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.467 |
| CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.537 |
| CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.614 |
| CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.539 |
| CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.614 |
| CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.372 |
| CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.520 |
| CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.707 |
| CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.498 |
| DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.450 |
| DOC_CYCLIN_RxL_1 | 223 | 234 | PF00134 | 0.353 |
| DOC_MAPK_gen_1 | 179 | 188 | PF00069 | 0.510 |
| DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.527 |
| DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.572 |
| DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.383 |
| DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.655 |
| DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.747 |
| DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.482 |
| LIG_14-3-3_CanoR_1 | 116 | 120 | PF00244 | 0.517 |
| LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.591 |
| LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.545 |
| LIG_14-3-3_CanoR_1 | 268 | 276 | PF00244 | 0.625 |
| LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.475 |
| LIG_14-3-3_CanoR_1 | 339 | 346 | PF00244 | 0.469 |
| LIG_FHA_1 | 148 | 154 | PF00498 | 0.541 |
| LIG_FHA_1 | 181 | 187 | PF00498 | 0.637 |
| LIG_FHA_1 | 216 | 222 | PF00498 | 0.485 |
| LIG_FHA_1 | 230 | 236 | PF00498 | 0.401 |
| LIG_FHA_1 | 27 | 33 | PF00498 | 0.480 |
| LIG_FHA_2 | 101 | 107 | PF00498 | 0.648 |
| LIG_FHA_2 | 260 | 266 | PF00498 | 0.558 |
| LIG_FHA_2 | 320 | 326 | PF00498 | 0.493 |
| LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.549 |
| LIG_LIR_Gen_1 | 321 | 332 | PF02991 | 0.620 |
| LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.634 |
| LIG_PTAP_UEV_1 | 345 | 350 | PF05743 | 0.474 |
| LIG_SH2_GRB2like | 217 | 220 | PF00017 | 0.538 |
| LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.535 |
| LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.538 |
| LIG_SH3_1 | 201 | 207 | PF00018 | 0.472 |
| LIG_SH3_3 | 201 | 207 | PF00018 | 0.499 |
| LIG_SH3_3 | 343 | 349 | PF00018 | 0.499 |
| LIG_SH3_3 | 93 | 99 | PF00018 | 0.521 |
| LIG_SUMO_SIM_par_1 | 289 | 295 | PF11976 | 0.332 |
| LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.482 |
| MOD_CK1_1 | 306 | 312 | PF00069 | 0.482 |
| MOD_CK1_1 | 58 | 64 | PF00069 | 0.529 |
| MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.492 |
| MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.492 |
| MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.413 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.558 |
| MOD_GSK3_1 | 12 | 19 | PF00069 | 0.572 |
| MOD_GSK3_1 | 143 | 150 | PF00069 | 0.510 |
| MOD_GSK3_1 | 186 | 193 | PF00069 | 0.512 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.436 |
| MOD_GSK3_1 | 61 | 68 | PF00069 | 0.455 |
| MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.368 |
| MOD_NEK2_1 | 235 | 240 | PF00069 | 0.514 |
| MOD_NEK2_1 | 26 | 31 | PF00069 | 0.461 |
| MOD_NEK2_1 | 354 | 359 | PF00069 | 0.599 |
| MOD_NEK2_1 | 55 | 60 | PF00069 | 0.550 |
| MOD_PIKK_1 | 109 | 115 | PF00454 | 0.673 |
| MOD_PIKK_1 | 2 | 8 | PF00454 | 0.575 |
| MOD_PIKK_1 | 235 | 241 | PF00454 | 0.461 |
| MOD_PIKK_1 | 61 | 67 | PF00454 | 0.567 |
| MOD_PKA_1 | 108 | 114 | PF00069 | 0.460 |
| MOD_PKA_1 | 180 | 186 | PF00069 | 0.451 |
| MOD_PKA_2 | 108 | 114 | PF00069 | 0.729 |
| MOD_PKA_2 | 11 | 17 | PF00069 | 0.567 |
| MOD_PKA_2 | 115 | 121 | PF00069 | 0.583 |
| MOD_PKA_2 | 147 | 153 | PF00069 | 0.433 |
| MOD_PKA_2 | 215 | 221 | PF00069 | 0.507 |
| MOD_PKA_2 | 267 | 273 | PF00069 | 0.659 |
| MOD_PKA_2 | 282 | 288 | PF00069 | 0.474 |
| MOD_PKA_2 | 70 | 76 | PF00069 | 0.450 |
| MOD_Plk_1 | 235 | 241 | PF00069 | 0.483 |
| MOD_Plk_1 | 276 | 282 | PF00069 | 0.503 |
| MOD_Plk_1 | 318 | 324 | PF00069 | 0.370 |
| MOD_Plk_2-3 | 97 | 103 | PF00069 | 0.518 |
| MOD_Plk_4 | 115 | 121 | PF00069 | 0.590 |
| MOD_Plk_4 | 282 | 288 | PF00069 | 0.474 |
| MOD_Plk_4 | 319 | 325 | PF00069 | 0.518 |
| MOD_Plk_4 | 349 | 355 | PF00069 | 0.574 |
| MOD_Plk_4 | 65 | 71 | PF00069 | 0.571 |
| MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.743 |
| MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.481 |
| MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.365 |
| MOD_SUMO_rev_2 | 152 | 158 | PF00179 | 0.485 |
| TRG_DiLeu_BaLyEn_6 | 163 | 168 | PF01217 | 0.623 |
| TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.490 |
| TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.374 |
| TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.467 |
| TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.491 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P2V4 | Leptomonas seymouri | 50% | 100% |
| A0A3Q8IBM3 | Leishmania donovani | 70% | 100% |
| A4HVE0 | Leishmania infantum | 70% | 100% |
| E9AP38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
| Q4QGF0 | Leishmania major | 69% | 96% |
| V5ATU2 | Trypanosoma cruzi | 30% | 70% |