Hydrolase, Uncharacterized
| 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: 1, no: 5 |
| NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HYN2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 7 |
| GO:0005488 | binding | 1 | 7 |
| GO:0016787 | hydrolase activity | 2 | 7 |
| GO:0043167 | ion binding | 2 | 7 |
| GO:0043169 | cation binding | 3 | 7 |
| GO:0046872 | metal ion binding | 4 | 7 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.511 |
| CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.714 |
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.602 |
| CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.443 |
| CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.560 |
| CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.602 |
| CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.443 |
| CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.560 |
| CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.473 |
| CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.494 |
| CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.650 |
| CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.629 |
| CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.707 |
| CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.730 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.565 |
| DEG_ODPH_VHL_1 | 288 | 301 | PF01847 | 0.565 |
| DEG_SIAH_1 | 58 | 66 | PF03145 | 0.374 |
| DOC_CKS1_1 | 174 | 179 | PF01111 | 0.540 |
| DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.576 |
| DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.472 |
| DOC_PP4_FxxP_1 | 355 | 358 | PF00568 | 0.533 |
| DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.730 |
| DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.364 |
| DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.408 |
| DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.382 |
| DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.709 |
| DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.515 |
| DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.640 |
| DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.500 |
| DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.470 |
| DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.700 |
| LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.473 |
| LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.480 |
| LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.447 |
| LIG_Actin_WH2_2 | 176 | 192 | PF00022 | 0.506 |
| LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.543 |
| LIG_deltaCOP1_diTrp_1 | 146 | 152 | PF00928 | 0.584 |
| LIG_eIF4E_1 | 208 | 214 | PF01652 | 0.438 |
| LIG_FHA_1 | 13 | 19 | PF00498 | 0.452 |
| LIG_FHA_1 | 290 | 296 | PF00498 | 0.457 |
| LIG_FHA_1 | 76 | 82 | PF00498 | 0.544 |
| LIG_FHA_2 | 342 | 348 | PF00498 | 0.691 |
| LIG_FHA_2 | 396 | 402 | PF00498 | 0.708 |
| LIG_Integrin_isoDGR_2 | 348 | 350 | PF01839 | 0.471 |
| LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.473 |
| LIG_LIR_Apic_2 | 354 | 358 | PF02991 | 0.512 |
| LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.594 |
| LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.455 |
| LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.460 |
| LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.504 |
| LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.490 |
| LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.447 |
| LIG_MYND_3 | 255 | 259 | PF01753 | 0.526 |
| LIG_Pex14_2 | 387 | 391 | PF04695 | 0.640 |
| LIG_Rb_LxCxE_1 | 333 | 354 | PF01857 | 0.580 |
| LIG_SH2_CRK | 210 | 214 | PF00017 | 0.437 |
| LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.475 |
| LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.462 |
| LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.410 |
| LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.455 |
| LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.437 |
| LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.437 |
| LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.549 |
| LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.522 |
| LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.636 |
| LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.462 |
| LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.502 |
| LIG_SH3_3 | 171 | 177 | PF00018 | 0.586 |
| LIG_SH3_3 | 313 | 319 | PF00018 | 0.682 |
| LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.466 |
| LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.598 |
| LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.513 |
| LIG_TRFH_1 | 286 | 290 | PF08558 | 0.481 |
| LIG_WW_1 | 290 | 293 | PF00397 | 0.568 |
| MOD_CDK_SPK_2 | 194 | 199 | PF00069 | 0.500 |
| MOD_CK1_1 | 184 | 190 | PF00069 | 0.563 |
| MOD_CK1_1 | 262 | 268 | PF00069 | 0.581 |
| MOD_CK1_1 | 304 | 310 | PF00069 | 0.559 |
| MOD_CK1_1 | 343 | 349 | PF00069 | 0.587 |
| MOD_CK2_1 | 107 | 113 | PF00069 | 0.639 |
| MOD_CK2_1 | 142 | 148 | PF00069 | 0.460 |
| MOD_CK2_1 | 234 | 240 | PF00069 | 0.749 |
| MOD_CK2_1 | 268 | 274 | PF00069 | 0.511 |
| MOD_CK2_1 | 315 | 321 | PF00069 | 0.573 |
| MOD_CK2_1 | 341 | 347 | PF00069 | 0.614 |
| MOD_CMANNOS | 149 | 152 | PF00535 | 0.611 |
| MOD_Cter_Amidation | 348 | 351 | PF01082 | 0.566 |
| MOD_DYRK1A_RPxSP_1 | 173 | 177 | PF00069 | 0.575 |
| MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.684 |
| MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.680 |
| MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.434 |
| MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.486 |
| MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.512 |
| MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.549 |
| MOD_GSK3_1 | 159 | 166 | PF00069 | 0.699 |
| MOD_GSK3_1 | 169 | 176 | PF00069 | 0.757 |
| MOD_GSK3_1 | 181 | 188 | PF00069 | 0.356 |
| MOD_GSK3_1 | 194 | 201 | PF00069 | 0.434 |
| MOD_GSK3_1 | 213 | 220 | PF00069 | 0.336 |
| MOD_GSK3_1 | 229 | 236 | PF00069 | 0.521 |
| MOD_GSK3_1 | 280 | 287 | PF00069 | 0.491 |
| MOD_GSK3_1 | 297 | 304 | PF00069 | 0.477 |
| MOD_NEK2_1 | 102 | 107 | PF00069 | 0.679 |
| MOD_NEK2_1 | 12 | 17 | PF00069 | 0.464 |
| MOD_NEK2_1 | 213 | 218 | PF00069 | 0.473 |
| MOD_NEK2_1 | 362 | 367 | PF00069 | 0.650 |
| MOD_NEK2_2 | 185 | 190 | PF00069 | 0.574 |
| MOD_PIKK_1 | 230 | 236 | PF00454 | 0.773 |
| MOD_PIKK_1 | 96 | 102 | PF00454 | 0.740 |
| MOD_PKA_1 | 95 | 101 | PF00069 | 0.703 |
| MOD_PKA_2 | 198 | 204 | PF00069 | 0.541 |
| MOD_Plk_1 | 181 | 187 | PF00069 | 0.405 |
| MOD_Plk_4 | 12 | 18 | PF00069 | 0.464 |
| MOD_Plk_4 | 204 | 210 | PF00069 | 0.392 |
| MOD_Plk_4 | 289 | 295 | PF00069 | 0.460 |
| MOD_Plk_4 | 331 | 337 | PF00069 | 0.587 |
| MOD_Plk_4 | 407 | 413 | PF00069 | 0.720 |
| MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.626 |
| MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.507 |
| MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.476 |
| MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.709 |
| MOD_SUMO_rev_2 | 91 | 98 | PF00179 | 0.650 |
| TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.498 |
| TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.470 |
| TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.438 |
| TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.507 |
| TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.582 |
| TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.498 |
| TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.587 |
| TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.451 |
| TRG_Pf-PMV_PEXEL_1 | 350 | 354 | PF00026 | 0.495 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IIQ0 | Leptomonas seymouri | 49% | 100% |
| A0A3S7WVU6 | Leishmania donovani | 99% | 100% |
| E9AI97 | Leishmania braziliensis | 72% | 100% |
| E9AUI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
| Q4QD02 | Leishmania major | 93% | 100% |