Hydrolase, Haloacid dehalogenase-like hydrolase-like
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. | yes | yes: 25 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 34 |
NetGPI | no | yes: 0, no: 34 |
Related structures:
AlphaFold database: A4I3L7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 31 |
GO:0016787 | hydrolase activity | 2 | 31 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.461 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.303 |
CLV_PCSK_FUR_1 | 78 | 82 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.290 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.217 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.552 |
DEG_SCF_FBW7_1 | 124 | 131 | PF00400 | 0.504 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 397 | 401 | PF00917 | 0.497 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.502 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.636 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.677 |
DOC_MAPK_DCC_7 | 358 | 368 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 15 | 22 | PF00069 | 0.606 |
DOC_MAPK_gen_1 | 358 | 368 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 78 | 85 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 360 | 368 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 90 | 99 | PF00069 | 0.636 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.774 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 255 | 262 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 379 | 387 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.526 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.572 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.311 |
LIG_EVH1_1 | 124 | 128 | PF00568 | 0.500 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.622 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.571 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.470 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.405 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.550 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.500 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.590 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.510 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.675 |
LIG_IBAR_NPY_1 | 27 | 29 | PF08397 | 0.339 |
LIG_LIR_Gen_1 | 177 | 186 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 240 | 244 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.513 |
LIG_MYND_3 | 363 | 367 | PF01753 | 0.455 |
LIG_NRBOX | 54 | 60 | PF00104 | 0.567 |
LIG_Pex14_1 | 221 | 225 | PF04695 | 0.530 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.564 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.365 |
LIG_SH2_GRB2like | 206 | 209 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 158 | 162 | PF00017 | 0.567 |
LIG_SH2_NCK_1 | 206 | 210 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.495 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.510 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.604 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.641 |
LIG_SUMO_SIM_anti_2 | 339 | 345 | PF11976 | 0.536 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.518 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.521 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.748 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.729 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.584 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.562 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.562 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.428 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.507 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.506 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.548 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.485 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.520 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.665 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.755 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.625 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.330 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.267 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.717 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.738 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.683 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.566 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.529 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.535 |
MOD_N-GLC_1 | 137 | 142 | PF02516 | 0.434 |
MOD_N-GLC_2 | 328 | 330 | PF02516 | 0.216 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.520 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.577 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.558 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.505 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.565 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.496 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.419 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.493 |
MOD_PKA_1 | 379 | 385 | PF00069 | 0.472 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.518 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.569 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.578 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.409 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.445 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.535 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.518 |
MOD_Plk_2-3 | 215 | 221 | PF00069 | 0.567 |
MOD_Plk_2-3 | 267 | 273 | PF00069 | 0.421 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.530 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.506 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.601 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.680 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.504 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.691 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.635 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.612 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.655 |
MOD_SUMO_for_1 | 287 | 290 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 210 | 218 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 282 | 289 | PF00179 | 0.585 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.443 |
TRG_NLS_MonoExtC_3 | 359 | 364 | PF00514 | 0.416 |
TRG_NLS_MonoExtN_4 | 357 | 364 | PF00514 | 0.416 |
TRG_NLS_MonoExtN_4 | 78 | 84 | PF00514 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7I9 | Leptomonas seymouri | 29% | 100% |
A0A0N0P7W9 | Leptomonas seymouri | 24% | 100% |
A0A0N1I1D8 | Leptomonas seymouri | 30% | 100% |
A0A0N1ILU0 | Leptomonas seymouri | 28% | 100% |
A0A0N1PEM6 | Leptomonas seymouri | 65% | 100% |
A0A1X0NRL0 | Trypanosomatidae | 26% | 100% |
A0A1X0NYN3 | Trypanosomatidae | 30% | 100% |
A0A1X0NYY3 | Trypanosomatidae | 29% | 100% |
A0A1X0P2Q4 | Trypanosomatidae | 39% | 100% |
A0A3Q8IDX0 | Leishmania donovani | 28% | 100% |
A0A3Q8IEU6 | Leishmania donovani | 100% | 100% |
A0A3Q8IGR3 | Leishmania donovani | 28% | 100% |
A0A3R7M7Z1 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X1G8 | Leishmania donovani | 32% | 100% |
A0A422MX56 | Trypanosoma rangeli | 26% | 100% |
A0A422N4F0 | Trypanosoma rangeli | 30% | 100% |
A4HGI1 | Leishmania braziliensis | 27% | 90% |
A4HGI6 | Leishmania braziliensis | 30% | 83% |
A4HGI9 | Leishmania braziliensis | 27% | 100% |
A4HGJ0 | Leishmania braziliensis | 31% | 91% |
A4I3L4 | Leishmania infantum | 29% | 85% |
A4I3L6 | Leishmania infantum | 32% | 100% |
D0A7S2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A841 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AZV4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 83% |
E9AZV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AZV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AZV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q8C8 | Leishmania major | 95% | 100% |
Q4Q8C9 | Leishmania major | 29% | 100% |
Q4Q8D1 | Leishmania major | 29% | 83% |
V5BGL5 | Trypanosoma cruzi | 33% | 100% |
V5D8D2 | Trypanosoma cruzi | 27% | 100% |