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: Q4QHS4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.317 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.262 |
DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.292 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.586 |
DOC_CYCLIN_RxL_1 | 178 | 188 | PF00134 | 0.450 |
DOC_MAPK_gen_1 | 31 | 39 | PF00069 | 0.319 |
DOC_MAPK_HePTP_8 | 29 | 41 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 32 | 41 | PF00069 | 0.394 |
DOC_PP1_RVXF_1 | 270 | 277 | PF00149 | 0.371 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.406 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.650 |
DOC_USP7_UBL2_3 | 291 | 295 | PF12436 | 0.448 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.406 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.251 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 58 | 64 | PF00244 | 0.329 |
LIG_BRCT_BRCA1_1 | 266 | 270 | PF00533 | 0.500 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.406 |
LIG_BRCT_BRCA1_2 | 266 | 272 | PF00533 | 0.498 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.731 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.410 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.530 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.513 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.386 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.605 |
LIG_HCF-1_HBM_1 | 256 | 259 | PF13415 | 0.344 |
LIG_Integrin_isoDGR_2 | 284 | 286 | PF01839 | 0.579 |
LIG_LIR_Apic_2 | 40 | 44 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 224 | 235 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.555 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.352 |
LIG_PDZ_Class_2 | 307 | 312 | PF00595 | 0.377 |
LIG_PTB_Apo_2 | 190 | 197 | PF02174 | 0.409 |
LIG_REV1ctd_RIR_1 | 193 | 203 | PF16727 | 0.475 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.461 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.476 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.600 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.360 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.341 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.668 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.391 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.658 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.485 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.467 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.411 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.414 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.376 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.585 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.638 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.451 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.370 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.259 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.681 |
MOD_PK_1 | 199 | 205 | PF00069 | 0.402 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.412 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.386 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.465 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.532 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.490 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.495 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.251 |
TRG_DiLeu_BaEn_1 | 283 | 288 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_4 | 8 | 14 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 246 | 251 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.292 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.273 |
TRG_NES_CRM1_1 | 118 | 131 | PF08389 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBQ0 | Leptomonas seymouri | 60% | 100% |
A0A1X0NI65 | Trypanosomatidae | 39% | 100% |
A0A3S7WQS2 | Leishmania donovani | 90% | 100% |
A0A422N3Q8 | Trypanosoma rangeli | 39% | 100% |
A4H5S8 | Leishmania braziliensis | 74% | 100% |
A4HU22 | Leishmania infantum | 91% | 100% |
D0A9J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AMV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5D6M9 | Trypanosoma cruzi | 41% | 100% |