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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HGR4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009395 | phospholipid catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044242 | cellular lipid catabolic process | 4 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046475 | glycerophospholipid catabolic process | 6 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0046503 | glycerolipid catabolic process | 5 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 11 |
GO:0008889 | glycerophosphodiester phosphodiesterase activity | 6 | 5 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.472 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.307 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.310 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.188 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.245 |
DEG_SPOP_SBC_1 | 260 | 264 | PF00917 | 0.329 |
DOC_MAPK_DCC_7 | 163 | 171 | PF00069 | 0.358 |
DOC_MAPK_FxFP_2 | 39 | 42 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 125 | 132 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 339 | 348 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 80 | 89 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 125 | 132 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 163 | 171 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 339 | 348 | PF00069 | 0.433 |
DOC_MAPK_NFAT4_5 | 125 | 133 | PF00069 | 0.510 |
DOC_MAPK_RevD_3 | 17 | 30 | PF00069 | 0.401 |
DOC_PP4_FxxP_1 | 228 | 231 | PF00568 | 0.470 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.248 |
DOC_PP4_FxxP_1 | 39 | 42 | PF00568 | 0.553 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.454 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.565 |
DOC_USP7_UBL2_3 | 174 | 178 | PF12436 | 0.554 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.291 |
LIG_APCC_ABBA_1 | 167 | 172 | PF00400 | 0.429 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.298 |
LIG_EVH1_1 | 164 | 168 | PF00568 | 0.358 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.439 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.451 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.502 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.414 |
LIG_LIR_Apic_2 | 254 | 259 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 158 | 169 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 250 | 261 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 59 | 67 | PF02991 | 0.453 |
LIG_LIR_LC3C_4 | 109 | 113 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 102 | 106 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.192 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.369 |
LIG_MLH1_MIPbox_1 | 210 | 214 | PF16413 | 0.404 |
LIG_PCNA_yPIPBox_3 | 317 | 330 | PF02747 | 0.296 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.172 |
LIG_Pex14_2 | 249 | 253 | PF04695 | 0.230 |
LIG_REV1ctd_RIR_1 | 232 | 240 | PF16727 | 0.418 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.499 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.464 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 308 | 314 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 5 | 11 | PF11976 | 0.160 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 73 | 78 | PF11976 | 0.429 |
LIG_TYR_ITIM | 240 | 245 | PF00017 | 0.352 |
LIG_TYR_ITIM | 246 | 251 | PF00017 | 0.434 |
LIG_WRC_WIRS_1 | 60 | 65 | PF05994 | 0.464 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.293 |
MOD_Cter_Amidation | 175 | 178 | PF01082 | 0.395 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.410 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.488 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.315 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.462 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.500 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.414 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.388 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.365 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.358 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.246 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.450 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.409 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.358 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.460 |
MOD_PKA_1 | 339 | 345 | PF00069 | 0.279 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.279 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.464 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.445 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.409 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.445 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.454 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.290 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.294 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.390 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.399 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.286 |
TRG_DiLeu_BaEn_1 | 183 | 188 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 285 | 290 | PF01217 | 0.310 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 221 | 224 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.484 |
TRG_NES_CRM1_1 | 69 | 81 | PF08389 | 0.507 |
TRG_NLS_MonoCore_2 | 27 | 32 | PF00514 | 0.500 |
TRG_NLS_MonoExtC_3 | 221 | 226 | PF00514 | 0.519 |
TRG_NLS_MonoExtN_4 | 219 | 226 | PF00514 | 0.560 |
TRG_NLS_MonoExtN_4 | 27 | 33 | PF00514 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.227 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8E4 | Leptomonas seymouri | 55% | 99% |
A0A0S4IJ80 | Bodo saltans | 37% | 85% |
A0A1X0NRF0 | Trypanosomatidae | 45% | 98% |
A0A3R7NHN9 | Trypanosoma rangeli | 46% | 99% |
A0A3S7X1Q6 | Leishmania donovani | 79% | 100% |
A4I3T9 | Leishmania infantum | 79% | 100% |
D0A869 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9B031 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q0VGK4 | Rattus norvegicus | 30% | 100% |
Q4Q855 | Leishmania major | 77% | 100% |
Q7L5L3 | Homo sapiens | 26% | 100% |
Q8N9F7 | Homo sapiens | 30% | 100% |
Q99LY2 | Mus musculus | 26% | 100% |
Q9CRY7 | Mus musculus | 30% | 100% |