| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8ICV5
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.667 |
| CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.627 |
| CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.511 |
| CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.667 |
| CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.533 |
| CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.562 |
| DEG_COP1_1 | 238 | 246 | PF00400 | 0.376 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.627 |
| DOC_CKS1_1 | 150 | 155 | PF01111 | 0.425 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 310 | 317 | PF00134 | 0.392 |
| DOC_CYCLIN_yCln2_LP_2 | 317 | 323 | PF00134 | 0.482 |
| DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.434 |
| DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.550 |
| DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.317 |
| DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.365 |
| LIG_14-3-3_CanoR_1 | 142 | 147 | PF00244 | 0.343 |
| LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.630 |
| LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.632 |
| LIG_Actin_WH2_2 | 59 | 75 | PF00022 | 0.369 |
| LIG_APCC_ABBA_1 | 16 | 21 | PF00400 | 0.571 |
| LIG_BIR_III_2 | 251 | 255 | PF00653 | 0.330 |
| LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.430 |
| LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.438 |
| LIG_DLG_GKlike_1 | 142 | 150 | PF00625 | 0.357 |
| LIG_FHA_1 | 150 | 156 | PF00498 | 0.334 |
| LIG_FHA_1 | 61 | 67 | PF00498 | 0.518 |
| LIG_FHA_1 | 84 | 90 | PF00498 | 0.439 |
| LIG_FHA_2 | 261 | 267 | PF00498 | 0.490 |
| LIG_LIR_Apic_2 | 101 | 106 | PF02991 | 0.471 |
| LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.355 |
| LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.323 |
| LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.310 |
| LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.351 |
| LIG_MYND_1 | 244 | 248 | PF01753 | 0.313 |
| LIG_MYND_3 | 253 | 257 | PF01753 | 0.379 |
| LIG_Pex14_2 | 201 | 205 | PF04695 | 0.448 |
| LIG_Pex14_2 | 348 | 352 | PF04695 | 0.446 |
| LIG_REV1ctd_RIR_1 | 203 | 211 | PF16727 | 0.441 |
| LIG_REV1ctd_RIR_1 | 231 | 241 | PF16727 | 0.409 |
| LIG_REV1ctd_RIR_1 | 285 | 294 | PF16727 | 0.486 |
| LIG_REV1ctd_RIR_1 | 326 | 335 | PF16727 | 0.354 |
| LIG_SH2_CRK | 103 | 107 | PF00017 | 0.482 |
| LIG_SH2_CRK | 57 | 61 | PF00017 | 0.481 |
| LIG_SH2_NCK_1 | 103 | 107 | PF00017 | 0.482 |
| LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.317 |
| LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.293 |
| LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.412 |
| LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.533 |
| LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.391 |
| LIG_SH3_3 | 147 | 153 | PF00018 | 0.449 |
| LIG_SH3_3 | 74 | 80 | PF00018 | 0.381 |
| LIG_SUMO_SIM_par_1 | 335 | 341 | PF11976 | 0.411 |
| LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.377 |
| MOD_CK1_1 | 149 | 155 | PF00069 | 0.312 |
| MOD_CK1_1 | 260 | 266 | PF00069 | 0.474 |
| MOD_CK1_1 | 87 | 93 | PF00069 | 0.366 |
| MOD_CK2_1 | 142 | 148 | PF00069 | 0.488 |
| MOD_CK2_1 | 260 | 266 | PF00069 | 0.468 |
| MOD_CK2_1 | 283 | 289 | PF00069 | 0.382 |
| MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.466 |
| MOD_GlcNHglycan | 177 | 182 | PF01048 | 0.494 |
| MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.441 |
| MOD_GSK3_1 | 138 | 145 | PF00069 | 0.348 |
| MOD_GSK3_1 | 185 | 192 | PF00069 | 0.426 |
| MOD_GSK3_1 | 268 | 275 | PF00069 | 0.417 |
| MOD_GSK3_1 | 27 | 34 | PF00069 | 0.618 |
| MOD_GSK3_1 | 83 | 90 | PF00069 | 0.326 |
| MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.391 |
| MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.371 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.621 |
| MOD_NEK2_1 | 125 | 130 | PF00069 | 0.428 |
| MOD_NEK2_1 | 146 | 151 | PF00069 | 0.357 |
| MOD_NEK2_1 | 159 | 164 | PF00069 | 0.379 |
| MOD_NEK2_1 | 283 | 288 | PF00069 | 0.457 |
| MOD_NEK2_1 | 62 | 67 | PF00069 | 0.569 |
| MOD_NEK2_1 | 72 | 77 | PF00069 | 0.394 |
| MOD_PIKK_1 | 213 | 219 | PF00454 | 0.461 |
| MOD_PKA_1 | 38 | 44 | PF00069 | 0.425 |
| MOD_PKA_2 | 1 | 7 | PF00069 | 0.635 |
| MOD_PKA_2 | 19 | 25 | PF00069 | 0.438 |
| MOD_PKA_2 | 72 | 78 | PF00069 | 0.459 |
| MOD_Plk_1 | 146 | 152 | PF00069 | 0.358 |
| MOD_Plk_4 | 146 | 152 | PF00069 | 0.453 |
| MOD_Plk_4 | 242 | 248 | PF00069 | 0.342 |
| MOD_Plk_4 | 260 | 266 | PF00069 | 0.343 |
| MOD_Plk_4 | 31 | 37 | PF00069 | 0.419 |
| MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.314 |
| MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.371 |
| TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.545 |
| TRG_DiLeu_BaEn_2 | 120 | 126 | PF01217 | 0.412 |
| TRG_DiLeu_BaEn_4 | 178 | 184 | PF01217 | 0.578 |
| TRG_DiLeu_LyEn_5 | 366 | 371 | PF01217 | 0.635 |
| TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.461 |
| TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.502 |
| TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.672 |
| TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.477 |
| TRG_NLS_MonoCore_2 | 23 | 28 | PF00514 | 0.572 |
| TRG_Pf-PMV_PEXEL_1 | 369 | 374 | PF00026 | 0.594 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I2W1 | Leptomonas seymouri | 74% | 100% |
| A0A0S4ISK5 | Bodo saltans | 46% | 100% |
| A0A1X0NRI0 | Trypanosomatidae | 54% | 100% |
| A4HFZ3 | Leishmania braziliensis | 89% | 100% |
| A4I312 | Leishmania infantum | 100% | 100% |
| C9ZJH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
| E9ADJ6 | Leishmania major | 97% | 100% |
| E9AZC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
| V5BNB6 | Trypanosoma cruzi | 60% | 100% |