Posesses a conserved AB hydrolase domain. Due to the distribution of hydrophilic / hydrophobic amino acids, it likely only has a perimembrane helix, not a full TM one.
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9B0C6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044255 | cellular lipid metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016298 | lipase activity | 4 | 3 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 3 |
GO:0034338 | short-chain carboxylesterase activity | 5 | 3 |
GO:0047372 | acylglycerol lipase activity | 5 | 3 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.321 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.472 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.484 |
DEG_SCF_FBW7_1 | 169 | 176 | PF00400 | 0.267 |
DOC_CDC14_PxL_1 | 132 | 140 | PF14671 | 0.272 |
DOC_CDC14_PxL_1 | 15 | 23 | PF14671 | 0.429 |
DOC_CDC14_PxL_1 | 287 | 295 | PF14671 | 0.332 |
DOC_CDC14_PxL_1 | 322 | 330 | PF14671 | 0.332 |
DOC_CKS1_1 | 174 | 179 | PF01111 | 0.291 |
DOC_CKS1_1 | 330 | 335 | PF01111 | 0.302 |
DOC_MAPK_DCC_7 | 205 | 215 | PF00069 | 0.337 |
DOC_MAPK_DCC_7 | 96 | 106 | PF00069 | 0.178 |
DOC_MAPK_gen_1 | 126 | 135 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 204 | 212 | PF00069 | 0.223 |
DOC_MAPK_gen_1 | 23 | 31 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 96 | 106 | PF00069 | 0.178 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 23 | 31 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 99 | 106 | PF00069 | 0.331 |
DOC_PP1_RVXF_1 | 21 | 27 | PF00149 | 0.494 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.255 |
DOC_PP2B_LxvP_1 | 385 | 388 | PF13499 | 0.248 |
DOC_PP2B_PxIxI_1 | 210 | 216 | PF00149 | 0.353 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.267 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.124 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.199 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.200 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.242 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.251 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.283 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.270 |
LIG_14-3-3_CanoR_1 | 321 | 326 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.310 |
LIG_Actin_WH2_2 | 27 | 44 | PF00022 | 0.250 |
LIG_deltaCOP1_diTrp_1 | 344 | 349 | PF00928 | 0.191 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.274 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.291 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.213 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.145 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.324 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.313 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.306 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.252 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.195 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.353 |
LIG_IRF3_LxIS_1 | 351 | 357 | PF10401 | 0.196 |
LIG_LIR_Apic_2 | 327 | 333 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 148 | 155 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 318 | 326 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.165 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 318 | 322 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.169 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.232 |
LIG_MYND_1 | 291 | 295 | PF01753 | 0.218 |
LIG_NRBOX | 117 | 123 | PF00104 | 0.193 |
LIG_Pex14_1 | 345 | 349 | PF04695 | 0.332 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.196 |
LIG_PTB_Apo_2 | 111 | 118 | PF02174 | 0.357 |
LIG_PTB_Phospho_1 | 111 | 117 | PF10480 | 0.233 |
LIG_REV1ctd_RIR_1 | 44 | 53 | PF16727 | 0.425 |
LIG_SH2_NCK_1 | 415 | 419 | PF00017 | 0.253 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.296 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.332 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.322 |
LIG_SH2_SRC | 79 | 82 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.215 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.184 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.327 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.289 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.274 |
LIG_SUMO_SIM_anti_2 | 241 | 248 | PF11976 | 0.196 |
LIG_SUMO_SIM_par_1 | 33 | 38 | PF11976 | 0.384 |
LIG_TYR_ITIM | 101 | 106 | PF00017 | 0.367 |
LIG_UBA3_1 | 70 | 76 | PF00899 | 0.272 |
LIG_WRC_WIRS_1 | 43 | 48 | PF05994 | 0.238 |
MOD_CDK_SPK_2 | 173 | 178 | PF00069 | 0.291 |
MOD_CDK_SPK_2 | 419 | 424 | PF00069 | 0.270 |
MOD_CDK_SPxxK_3 | 291 | 298 | PF00069 | 0.224 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.290 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.311 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.260 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.325 |
MOD_CMANNOS | 400 | 403 | PF00535 | 0.513 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.565 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.467 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.463 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.491 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.492 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.493 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.212 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.256 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.244 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.239 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.285 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.539 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.365 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.320 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.258 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.280 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.171 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.468 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.181 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.190 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.583 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.179 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.268 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.305 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.320 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.265 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.242 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.251 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.233 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.283 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.284 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.285 |
TRG_DiLeu_BaEn_1 | 175 | 180 | PF01217 | 0.332 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.237 |
TRG_Pf-PMV_PEXEL_1 | 236 | 241 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L7 | Leptomonas seymouri | 32% | 93% |
A0A0N1HZ60 | Leptomonas seymouri | 33% | 92% |
A0A0N1I523 | Leptomonas seymouri | 29% | 96% |
A0A0N1I5Q2 | Leptomonas seymouri | 31% | 84% |
A0A0N1I7U8 | Leptomonas seymouri | 66% | 100% |
A0A0S4JMS7 | Bodo saltans | 37% | 98% |
A0A0S4JTS9 | Bodo saltans | 37% | 99% |
A0A1X0NEW5 | Trypanosomatidae | 43% | 100% |
A0A1X0NSK7 | Trypanosomatidae | 43% | 100% |
A0A1X0NUZ6 | Trypanosomatidae | 26% | 100% |
A0A3S5H6J1 | Leishmania donovani | 31% | 90% |
A0A3S7X2V6 | Leishmania donovani | 91% | 100% |
A0A422NB49 | Trypanosoma rangeli | 45% | 100% |
A0A422NQC5 | Trypanosoma rangeli | 36% | 97% |
A4H6L0 | Leishmania braziliensis | 33% | 100% |
A4HHU6 | Leishmania braziliensis | 77% | 100% |
A4HUZ4 | Leishmania infantum | 31% | 90% |
A4I4Z6 | Leishmania infantum | 91% | 100% |
C9ZPB9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9ANM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ANM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
P73879 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 25% | 100% |
Q05AK6 | Danio rerio | 26% | 100% |
Q0VC00 | Bos taurus | 25% | 100% |
Q18610 | Caenorhabditis elegans | 26% | 100% |
Q24093 | Drosophila melanogaster | 24% | 100% |
Q3T0A0 | Bos taurus | 27% | 100% |
Q40863 | Picea glauca | 30% | 93% |
Q4Q7V8 | Leishmania major | 88% | 100% |
Q4QGZ4 | Leishmania major | 32% | 100% |
Q4QGZ5 | Leishmania major | 31% | 100% |
Q54H38 | Dictyostelium discoideum | 29% | 100% |
Q5F2F2 | Mus musculus | 26% | 93% |
Q5RK23 | Rattus norvegicus | 26% | 100% |
Q6UXT9 | Homo sapiens | 25% | 91% |
Q802V6 | Danio rerio | 23% | 98% |
Q8WU67 | Homo sapiens | 25% | 100% |
Q91ZH7 | Mus musculus | 26% | 100% |
Q96SE0 | Homo sapiens | 26% | 100% |
Q9QZC8 | Mus musculus | 26% | 100% |
V5AZF4 | Trypanosoma cruzi | 41% | 100% |
V5BBC2 | Trypanosoma cruzi | 36% | 100% |