A catalytically active hydrolase 4 domain associated with a multi-pass membrane domain. Probably recognizes membrane-associated substrates.. Distant Eukaryotic relatives typically have signal-anchors and are luminal
| 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: 11 | 
| NetGPI | no | yes: 0, no: 11 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 11 | 
| GO:0110165 | cellular anatomical entity | 1 | 11 | 
Related structures:
AlphaFold database: A0A3S5H7Z7
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 2 | 
| GO:0016787 | hydrolase activity | 2 | 2 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.564 | 
| CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.456 | 
| CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.509 | 
| CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.378 | 
| CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.317 | 
| CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.322 | 
| CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.325 | 
| CLV_PCSK_FUR_1 | 139 | 143 | PF00082 | 0.346 | 
| CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.329 | 
| CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.320 | 
| CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.298 | 
| CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.337 | 
| CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.575 | 
| DEG_COP1_1 | 157 | 166 | PF00400 | 0.594 | 
| DEG_MDM2_SWIB_1 | 109 | 116 | PF02201 | 0.210 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.649 | 
| DEG_ODPH_VHL_1 | 29 | 42 | PF01847 | 0.254 | 
| DEG_SCF_FBW7_1 | 302 | 307 | PF00400 | 0.535 | 
| DOC_CKS1_1 | 301 | 306 | PF01111 | 0.446 | 
| DOC_CYCLIN_RxL_1 | 328 | 337 | PF00134 | 0.565 | 
| DOC_CYCLIN_yClb1_LxF_4 | 255 | 261 | PF00134 | 0.392 | 
| DOC_MAPK_DCC_7 | 93 | 101 | PF00069 | 0.254 | 
| DOC_MAPK_gen_1 | 152 | 160 | PF00069 | 0.553 | 
| DOC_MAPK_HePTP_8 | 150 | 162 | PF00069 | 0.501 | 
| DOC_MAPK_MEF2A_6 | 153 | 162 | PF00069 | 0.594 | 
| DOC_MAPK_MEF2A_6 | 93 | 101 | PF00069 | 0.258 | 
| DOC_PP1_RVXF_1 | 219 | 226 | PF00149 | 0.446 | 
| DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.331 | 
| DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.466 | 
| DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.620 | 
| DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.505 | 
| DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.513 | 
| DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.453 | 
| LIG_14-3-3_CanoR_1 | 287 | 293 | PF00244 | 0.437 | 
| LIG_BRCT_BRCA1_1 | 394 | 398 | PF00533 | 0.509 | 
| LIG_eIF4E_1 | 278 | 284 | PF01652 | 0.535 | 
| LIG_FHA_1 | 102 | 108 | PF00498 | 0.359 | 
| LIG_FHA_1 | 172 | 178 | PF00498 | 0.532 | 
| LIG_FHA_1 | 225 | 231 | PF00498 | 0.512 | 
| LIG_FHA_1 | 301 | 307 | PF00498 | 0.469 | 
| LIG_LIR_Apic_2 | 300 | 304 | PF02991 | 0.446 | 
| LIG_LIR_Apic_2 | 368 | 373 | PF02991 | 0.457 | 
| LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.413 | 
| LIG_LIR_Gen_1 | 286 | 297 | PF02991 | 0.438 | 
| LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.572 | 
| LIG_LIR_Gen_1 | 62 | 70 | PF02991 | 0.447 | 
| LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.379 | 
| LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.494 | 
| LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.583 | 
| LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.385 | 
| LIG_PDZ_Class_2 | 395 | 400 | PF00595 | 0.447 | 
| LIG_Pex14_2 | 109 | 113 | PF04695 | 0.210 | 
| LIG_SH2_GRB2like | 376 | 379 | PF00017 | 0.498 | 
| LIG_SH2_SRC | 21 | 24 | PF00017 | 0.618 | 
| LIG_SH2_SRC | 387 | 390 | PF00017 | 0.517 | 
| LIG_SH2_STAT3 | 229 | 232 | PF00017 | 0.580 | 
| LIG_SH2_STAT3 | 336 | 339 | PF00017 | 0.481 | 
| LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.481 | 
| LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.551 | 
| LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.470 | 
| LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.396 | 
| LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.552 | 
| LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.337 | 
| LIG_SH3_3 | 76 | 82 | PF00018 | 0.459 | 
| LIG_SUMO_SIM_anti_2 | 5 | 11 | PF11976 | 0.596 | 
| LIG_SUMO_SIM_anti_2 | 76 | 82 | PF11976 | 0.383 | 
| LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.280 | 
| LIG_UBA3_1 | 63 | 71 | PF00899 | 0.287 | 
| LIG_WW_1 | 373 | 376 | PF00397 | 0.506 | 
| MOD_CDK_SPK_2 | 300 | 305 | PF00069 | 0.513 | 
| MOD_CK1_1 | 290 | 296 | PF00069 | 0.433 | 
| MOD_CK1_1 | 300 | 306 | PF00069 | 0.441 | 
| MOD_CK1_1 | 379 | 385 | PF00069 | 0.516 | 
| MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.294 | 
| MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.319 | 
| MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.336 | 
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.320 | 
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.561 | 
| MOD_GSK3_1 | 224 | 231 | PF00069 | 0.503 | 
| MOD_GSK3_1 | 300 | 307 | PF00069 | 0.498 | 
| MOD_GSK3_1 | 372 | 379 | PF00069 | 0.497 | 
| MOD_GSK3_1 | 392 | 399 | PF00069 | 0.570 | 
| MOD_GSK3_1 | 69 | 76 | PF00069 | 0.555 | 
| MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.332 | 
| MOD_NEK2_1 | 14 | 19 | PF00069 | 0.494 | 
| MOD_NEK2_1 | 197 | 202 | PF00069 | 0.512 | 
| MOD_NEK2_1 | 261 | 266 | PF00069 | 0.498 | 
| MOD_NEK2_1 | 285 | 290 | PF00069 | 0.431 | 
| MOD_NEK2_1 | 345 | 350 | PF00069 | 0.529 | 
| MOD_NEK2_1 | 59 | 64 | PF00069 | 0.341 | 
| MOD_NEK2_1 | 83 | 88 | PF00069 | 0.329 | 
| MOD_PIKK_1 | 228 | 234 | PF00454 | 0.584 | 
| MOD_PK_1 | 154 | 160 | PF00069 | 0.502 | 
| MOD_PKA_2 | 392 | 398 | PF00069 | 0.526 | 
| MOD_Plk_1 | 154 | 160 | PF00069 | 0.497 | 
| MOD_Plk_1 | 181 | 187 | PF00069 | 0.544 | 
| MOD_Plk_1 | 197 | 203 | PF00069 | 0.451 | 
| MOD_Plk_1 | 285 | 291 | PF00069 | 0.431 | 
| MOD_Plk_1 | 345 | 351 | PF00069 | 0.497 | 
| MOD_Plk_4 | 105 | 111 | PF00069 | 0.227 | 
| MOD_Plk_4 | 279 | 285 | PF00069 | 0.535 | 
| MOD_Plk_4 | 376 | 382 | PF00069 | 0.555 | 
| MOD_Plk_4 | 59 | 65 | PF00069 | 0.324 | 
| MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.453 | 
| MOD_SUMO_rev_2 | 165 | 170 | PF00179 | 0.623 | 
| TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.575 | 
| TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.572 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P8Q9 | Leptomonas seymouri | 63% | 100% | 
| A0A0S4JC83 | Bodo saltans | 32% | 93% | 
| A0A1X0P6X8 | Trypanosomatidae | 35% | 99% | 
| A0A422P2Q7 | Trypanosoma rangeli | 35% | 99% | 
| A4HMU6 | Leishmania braziliensis | 77% | 100% | 
| A4IBE6 | Leishmania infantum | 100% | 100% | 
| C9ZZ74 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 95% | 
| E9AFA4 | Leishmania major | 94% | 100% | 
| E9B6F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% | 
| V5BD21 | Trypanosoma cruzi | 34% | 98% |