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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A0A3S5H6J1
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 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016298 | lipase activity | 4 | 3 |
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_MEL_PAP_1 | 69 | 75 | PF00089 | 0.464 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.536 |
CLV_PCSK_FUR_1 | 68 | 72 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.543 |
CLV_Separin_Metazoa | 209 | 213 | PF03568 | 0.373 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.353 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.574 |
DEG_SCF_FBW7_2 | 443 | 449 | PF00400 | 0.360 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.392 |
DOC_CDC14_PxL_1 | 166 | 174 | PF14671 | 0.306 |
DOC_CDC14_PxL_1 | 20 | 28 | PF14671 | 0.330 |
DOC_CKS1_1 | 239 | 244 | PF01111 | 0.390 |
DOC_CKS1_1 | 286 | 291 | PF01111 | 0.370 |
DOC_CKS1_1 | 443 | 448 | PF01111 | 0.361 |
DOC_MAPK_DCC_7 | 238 | 247 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 394 | 402 | PF00069 | 0.290 |
DOC_MAPK_gen_1 | 68 | 77 | PF00069 | 0.247 |
DOC_MAPK_MEF2A_6 | 12 | 20 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 243 | 252 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 394 | 402 | PF00069 | 0.254 |
DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.342 |
DOC_PP1_RVXF_1 | 23 | 29 | PF00149 | 0.294 |
DOC_PP1_RVXF_1 | 4 | 10 | PF00149 | 0.447 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.223 |
DOC_PP2B_PxIxI_1 | 245 | 251 | PF00149 | 0.371 |
DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.323 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.391 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.304 |
DOC_PP4_FxxP_1 | 73 | 76 | PF00568 | 0.356 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.270 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.237 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.267 |
LIG_14-3-3_CanoR_1 | 2 | 9 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 358 | 365 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 420 | 430 | PF00244 | 0.228 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.335 |
LIG_CSL_BTD_1 | 390 | 393 | PF09270 | 0.345 |
LIG_eIF4E_1 | 21 | 27 | PF01652 | 0.385 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.311 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.558 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.323 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.225 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.233 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.356 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.366 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.304 |
LIG_IBAR_NPY_1 | 426 | 428 | PF08397 | 0.223 |
LIG_Integrin_RGD_1 | 451 | 453 | PF01839 | 0.542 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 297 | 308 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.325 |
LIG_Pex14_2 | 214 | 218 | PF04695 | 0.312 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.329 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.268 |
LIG_SH2_GRB2like | 368 | 371 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 300 | 304 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.244 |
LIG_SH2_SRC | 126 | 129 | PF00017 | 0.300 |
LIG_SH2_SRC | 368 | 371 | PF00017 | 0.222 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 318 | 322 | PF00017 | 0.327 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.204 |
LIG_SH2_STAT3 | 117 | 120 | PF00017 | 0.248 |
LIG_SH2_STAT3 | 229 | 232 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.267 |
LIG_SH3_1 | 102 | 108 | PF00018 | 0.260 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.325 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.383 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.315 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.268 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 56 | 61 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 291 | 297 | PF11976 | 0.315 |
LIG_TRAF2_1 | 378 | 381 | PF00917 | 0.267 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.312 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.311 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.500 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.456 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.564 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.451 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.382 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.351 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.408 |
MOD_CMANNOS | 34 | 37 | PF00535 | 0.323 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.412 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.520 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.349 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.511 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.373 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.459 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.568 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.544 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.662 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.318 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.344 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.462 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.429 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.475 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.380 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.380 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.463 |
MOD_PK_1 | 358 | 364 | PF00069 | 0.360 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.451 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.294 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.415 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.570 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.341 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.521 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.428 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.317 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.406 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.370 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.479 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.336 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.539 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.517 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.370 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.528 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.408 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.412 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.405 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.346 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.322 |
TRG_DiLeu_BaEn_1 | 456 | 461 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 243 | 248 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 385 | 390 | PF01217 | 0.258 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 261 | 265 | PF00026 | 0.298 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 420 | 425 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L7 | Leptomonas seymouri | 30% | 100% |
A0A0N1HZ60 | Leptomonas seymouri | 66% | 100% |
A0A0N1I523 | Leptomonas seymouri | 29% | 100% |
A0A0N1I5Q2 | Leptomonas seymouri | 35% | 93% |
A0A0N1I7U8 | Leptomonas seymouri | 31% | 100% |
A0A0S4JMS7 | Bodo saltans | 32% | 100% |
A0A0S4JTS9 | Bodo saltans | 30% | 100% |
A0A1X0NEW5 | Trypanosomatidae | 31% | 100% |
A0A1X0NSK7 | Trypanosomatidae | 31% | 100% |
A0A1X0NUZ6 | Trypanosomatidae | 30% | 100% |
A0A3S7X2V6 | Leishmania donovani | 32% | 100% |
A0A422NB49 | Trypanosoma rangeli | 34% | 100% |
A0A422NQC5 | Trypanosoma rangeli | 37% | 100% |
A4H6L0 | Leishmania braziliensis | 35% | 97% |
A4HHU6 | Leishmania braziliensis | 31% | 100% |
A4HUZ4 | Leishmania infantum | 100% | 100% |
A4I4Z6 | Leishmania infantum | 31% | 94% |
C9ZPB9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9ANM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9ANM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B0C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
P38295 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q02891 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
Q03649 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
Q0VC00 | Bos taurus | 25% | 100% |
Q18610 | Caenorhabditis elegans | 21% | 100% |
Q24093 | Drosophila melanogaster | 23% | 100% |
Q3T0A0 | Bos taurus | 25% | 100% |
Q40863 | Picea glauca | 28% | 100% |
Q4Q7V8 | Leishmania major | 30% | 98% |
Q4QGZ4 | Leishmania major | 96% | 100% |
Q4QGZ5 | Leishmania major | 35% | 100% |
Q5RK23 | Rattus norvegicus | 24% | 100% |
Q8WU67 | Homo sapiens | 25% | 100% |
Q91ZH7 | Mus musculus | 25% | 100% |
Q96SE0 | Homo sapiens | 24% | 100% |
Q9QZC8 | Mus musculus | 23% | 100% |
V5AZF4 | Trypanosoma cruzi | 34% | 100% |
V5BBC2 | Trypanosoma cruzi | 37% | 100% |