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: 27 |
NetGPI | no | yes: 0, no: 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4QGZ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044255 | cellular lipid metabolic process | 3 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016298 | lipase activity | 4 | 4 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 4 |
GO:0034338 | short-chain carboxylesterase activity | 5 | 4 |
GO:0047372 | acylglycerol lipase activity | 5 | 4 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 79 | 85 | PF00089 | 0.449 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.532 |
CLV_PCSK_FUR_1 | 78 | 82 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.534 |
CLV_Separin_Metazoa | 219 | 223 | PF03568 | 0.376 |
DEG_APCC_DBOX_1 | 343 | 351 | PF00400 | 0.366 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.612 |
DEG_SCF_FBW7_2 | 453 | 459 | PF00400 | 0.365 |
DEG_SPOP_SBC_1 | 145 | 149 | PF00917 | 0.368 |
DOC_CDC14_PxL_1 | 176 | 184 | PF14671 | 0.291 |
DOC_CDC14_PxL_1 | 30 | 38 | PF14671 | 0.344 |
DOC_CKS1_1 | 249 | 254 | PF01111 | 0.367 |
DOC_CKS1_1 | 296 | 301 | PF01111 | 0.368 |
DOC_CKS1_1 | 453 | 458 | PF01111 | 0.374 |
DOC_MAPK_DCC_7 | 248 | 257 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 10 | 19 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.280 |
DOC_MAPK_gen_1 | 78 | 87 | PF00069 | 0.257 |
DOC_MAPK_MEF2A_6 | 22 | 30 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 253 | 262 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 404 | 412 | PF00069 | 0.232 |
DOC_PP1_RVXF_1 | 14 | 20 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 171 | 178 | PF00149 | 0.347 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.278 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.378 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.215 |
DOC_PP2B_PxIxI_1 | 255 | 261 | PF00149 | 0.350 |
DOC_PP4_FxxP_1 | 177 | 180 | PF00568 | 0.330 |
DOC_PP4_FxxP_1 | 359 | 362 | PF00568 | 0.413 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.308 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.323 |
DOC_SPAK_OSR1_1 | 193 | 197 | PF12202 | 0.298 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.299 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.248 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.297 |
LIG_14-3-3_CanoR_1 | 10 | 19 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 368 | 375 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 430 | 440 | PF00244 | 0.217 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.338 |
LIG_CSL_BTD_1 | 400 | 403 | PF09270 | 0.351 |
LIG_eIF4E_1 | 31 | 37 | PF01652 | 0.394 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.565 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.298 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.318 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.221 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.274 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.381 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.361 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.306 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.319 |
LIG_IBAR_NPY_1 | 436 | 438 | PF08397 | 0.206 |
LIG_Integrin_RGD_1 | 461 | 463 | PF01839 | 0.553 |
LIG_LIR_Apic_2 | 135 | 141 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.332 |
LIG_Pex14_2 | 224 | 228 | PF04695 | 0.317 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.359 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.263 |
LIG_SH2_GRB2like | 378 | 381 | PF00017 | 0.400 |
LIG_SH2_NCK_1 | 310 | 314 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 328 | 332 | PF00017 | 0.275 |
LIG_SH2_NCK_1 | 393 | 397 | PF00017 | 0.237 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.229 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.211 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.238 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.342 |
LIG_SH2_STAT3 | 239 | 242 | PF00017 | 0.224 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.286 |
LIG_SH3_1 | 112 | 118 | PF00018 | 0.245 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.307 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.368 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.301 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.239 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.445 |
LIG_SUMO_SIM_anti_2 | 66 | 71 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 301 | 307 | PF11976 | 0.319 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.275 |
LIG_TYR_ITIM | 322 | 327 | PF00017 | 0.367 |
MOD_CDK_SPK_2 | 248 | 253 | PF00069 | 0.286 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.471 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.578 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.460 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.389 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.468 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.346 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.417 |
MOD_CMANNOS | 44 | 47 | PF00535 | 0.305 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.365 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.405 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.500 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.342 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.487 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.357 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.287 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.547 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.516 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.584 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.308 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.328 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.392 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.468 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.209 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.365 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.591 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.328 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.419 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.346 |
MOD_PK_1 | 368 | 374 | PF00069 | 0.372 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.457 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.516 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.376 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.521 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.495 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.295 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.391 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.318 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.335 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.407 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.387 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.478 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.654 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.357 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.502 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.404 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.418 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.409 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.367 |
TRG_DiLeu_BaEn_1 | 466 | 471 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.246 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 356 | 360 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 430 | 435 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L7 | Leptomonas seymouri | 32% | 100% |
A0A0N1HZ60 | Leptomonas seymouri | 64% | 100% |
A0A0N1I523 | Leptomonas seymouri | 29% | 100% |
A0A0N1I5Q2 | Leptomonas seymouri | 36% | 95% |
A0A0N1I7U8 | Leptomonas seymouri | 31% | 100% |
A0A0S4JMS7 | Bodo saltans | 31% | 100% |
A0A0S4JTS9 | Bodo saltans | 30% | 100% |
A0A1X0NEW5 | Trypanosomatidae | 31% | 100% |
A0A1X0NSK7 | Trypanosomatidae | 31% | 100% |
A0A1X0NUZ6 | Trypanosomatidae | 30% | 100% |
A0A3S5H6J1 | Leishmania donovani | 96% | 100% |
A0A3S7X2V6 | Leishmania donovani | 32% | 100% |
A0A422NB49 | Trypanosoma rangeli | 34% | 100% |
A0A422NQC5 | Trypanosoma rangeli | 37% | 100% |
A4H6L0 | Leishmania braziliensis | 34% | 98% |
A4HHU6 | Leishmania braziliensis | 31% | 100% |
A4HUZ4 | Leishmania infantum | 96% | 100% |
A4I4Z6 | Leishmania infantum | 32% | 100% |
C9ZPB9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ANM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ANM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B0C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
Q02891 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
Q0VC00 | Bos taurus | 24% | 100% |
Q18610 | Caenorhabditis elegans | 20% | 100% |
Q24093 | Drosophila melanogaster | 23% | 100% |
Q3T0A0 | Bos taurus | 25% | 100% |
Q40863 | Picea glauca | 28% | 100% |
Q4Q7V8 | Leishmania major | 30% | 98% |
Q4QGZ5 | Leishmania major | 36% | 100% |
Q5RK23 | Rattus norvegicus | 23% | 100% |
Q8WU67 | Homo sapiens | 24% | 100% |
Q91ZH7 | Mus musculus | 24% | 100% |
Q96SE0 | Homo sapiens | 23% | 100% |
Q9QZC8 | Mus musculus | 23% | 100% |
V5AZF4 | Trypanosoma cruzi | 35% | 100% |
V5BBC2 | Trypanosoma cruzi | 37% | 100% |