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 |
Related structures:
AlphaFold database: A4H5S8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.289 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.357 |
DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.308 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.596 |
DOC_CYCLIN_RxL_1 | 178 | 188 | PF00134 | 0.455 |
DOC_MAPK_gen_1 | 31 | 39 | PF00069 | 0.289 |
DOC_MAPK_HePTP_8 | 29 | 41 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 32 | 41 | PF00069 | 0.368 |
DOC_PP1_RVXF_1 | 270 | 277 | PF00149 | 0.388 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.341 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 155 | 159 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 291 | 295 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.368 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.253 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.330 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.417 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.407 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.704 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.592 |
LIG_HCF-1_HBM_1 | 256 | 259 | PF13415 | 0.332 |
LIG_Integrin_isoDGR_2 | 284 | 286 | PF01839 | 0.564 |
LIG_LIR_Apic_2 | 40 | 44 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 224 | 235 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 65 | 75 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 8 | 17 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.402 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.368 |
LIG_PDZ_Class_2 | 307 | 312 | PF00595 | 0.377 |
LIG_PTB_Apo_2 | 190 | 197 | PF02174 | 0.392 |
LIG_PTB_Apo_2 | 40 | 47 | PF02174 | 0.356 |
LIG_REV1ctd_RIR_1 | 193 | 203 | PF16727 | 0.474 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.245 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.364 |
LIG_SH3_2 | 150 | 155 | PF14604 | 0.452 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.463 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.353 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.539 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.350 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.717 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.360 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.379 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.632 |
MOD_GlcNHglycan | 200 | 204 | PF01048 | 0.376 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.476 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.386 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.362 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.438 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.392 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.387 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.284 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.585 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.356 |
MOD_PKA_1 | 128 | 134 | PF00069 | 0.538 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.403 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.504 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.298 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.303 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.495 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.368 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.257 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.371 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.334 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.648 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.253 |
TRG_DiLeu_BaEn_1 | 283 | 288 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_4 | 8 | 14 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.308 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBQ0 | Leptomonas seymouri | 59% | 100% |
A0A0S4IH55 | Bodo saltans | 31% | 80% |
A0A1X0NI65 | Trypanosomatidae | 42% | 100% |
A0A3S7WQS2 | Leishmania donovani | 72% | 100% |
A0A422N3Q8 | Trypanosoma rangeli | 40% | 100% |
A4HU22 | Leishmania infantum | 73% | 100% |
D0A9J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AMV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QHS4 | Leishmania major | 74% | 100% |
V5D6M9 | Trypanosoma cruzi | 39% | 100% |