An extensively expanded family of exophosphatase enzymes presumed to be active at acidic pH
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 1 |
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: 65 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 22, no: 4 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: Q4Q0A9
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 5 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016311 | dephosphorylation | 5 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 6 |
GO:0016791 | phosphatase activity | 5 | 6 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 6 |
GO:0003993 | acid phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.378 |
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.359 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.335 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.235 |
DEG_COP1_1 | 115 | 122 | PF00400 | 0.300 |
DEG_SPOP_SBC_1 | 357 | 361 | PF00917 | 0.455 |
DOC_MAPK_gen_1 | 238 | 247 | PF00069 | 0.325 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.296 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.448 |
DOC_PP4_MxPP_1 | 213 | 216 | PF00568 | 0.410 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.263 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.595 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 108 | 114 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 270 | 280 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 382 | 386 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.384 |
LIG_BIR_III_2 | 117 | 121 | PF00653 | 0.292 |
LIG_BIR_III_4 | 231 | 235 | PF00653 | 0.305 |
LIG_BIR_III_4 | 265 | 269 | PF00653 | 0.381 |
LIG_eIF4E_1 | 51 | 57 | PF01652 | 0.315 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.369 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.318 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.411 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.374 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.490 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.360 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.348 |
LIG_LIR_Apic_2 | 371 | 376 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 70 | 76 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 96 | 101 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 220 | 230 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 233 | 244 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 49 | 57 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.384 |
LIG_LYPXL_S_1 | 133 | 137 | PF13949 | 0.560 |
LIG_LYPXL_yS_3 | 134 | 137 | PF13949 | 0.426 |
LIG_MYND_1 | 180 | 184 | PF01753 | 0.370 |
LIG_Pex14_1 | 326 | 330 | PF04695 | 0.258 |
LIG_Pex14_2 | 145 | 149 | PF04695 | 0.336 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.355 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.298 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.270 |
LIG_SH2_GRB2like | 306 | 309 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 330 | 334 | PF00017 | 0.301 |
LIG_SH2_NCK_1 | 73 | 77 | PF00017 | 0.270 |
LIG_SH2_PTP2 | 236 | 239 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.411 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.516 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.428 |
LIG_SUMO_SIM_anti_2 | 220 | 229 | PF11976 | 0.264 |
LIG_SUMO_SIM_anti_2 | 53 | 59 | PF11976 | 0.326 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.248 |
LIG_WRC_WIRS_1 | 370 | 375 | PF05994 | 0.437 |
LIG_WW_3 | 178 | 182 | PF00397 | 0.357 |
MOD_CDC14_SPxK_1 | 385 | 388 | PF00782 | 0.426 |
MOD_CDK_SPK_2 | 308 | 313 | PF00069 | 0.305 |
MOD_CDK_SPxK_1 | 382 | 388 | PF00069 | 0.437 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.379 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.304 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.568 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.564 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.475 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.441 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.508 |
MOD_DYRK1A_RPxSP_1 | 382 | 386 | PF00069 | 0.436 |
MOD_GlcNHglycan | 10 | 14 | PF01048 | 0.619 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.520 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.588 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.528 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.579 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.681 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.592 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.573 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.375 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.338 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.349 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.508 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.497 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.477 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.558 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.571 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.448 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.440 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.358 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.616 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.576 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.638 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.520 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.684 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.678 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.320 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.372 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.353 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.376 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.445 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.354 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.335 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.399 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.405 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.256 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.317 |
MOD_OFUCOSY | 332 | 337 | PF10250 | 0.553 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.371 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.314 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.295 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.395 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.321 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.362 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.541 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.396 |
MOD_PKB_1 | 270 | 278 | PF00069 | 0.299 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.351 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.395 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.662 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.407 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.400 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.403 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.338 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.347 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.445 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.326 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.288 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.527 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.436 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.446 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.510 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.355 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.409 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.480 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.436 |
MOD_SUMO_rev_2 | 12 | 20 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 311 | 321 | PF00179 | 0.298 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.311 |
TRG_DiLeu_BaLyEn_6 | 235 | 240 | PF01217 | 0.326 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.290 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 26% | 73% |
A0A3Q8ILZ1 | Leishmania donovani | 63% | 100% |
A0A3Q8IR23 | Leishmania donovani | 27% | 74% |
A0A3R7MEN7 | Trypanosoma rangeli | 30% | 81% |
A0A3S5H827 | Leishmania donovani | 29% | 82% |
A0A3S7WXU0 | Leishmania donovani | 30% | 79% |
A4HCZ0 | Leishmania braziliensis | 31% | 68% |
A4HGW8 | Leishmania braziliensis | 26% | 77% |
A4HPC1 | Leishmania braziliensis | 32% | 81% |
A4HPC5 | Leishmania braziliensis | 29% | 73% |
A4HQG6 | Leishmania braziliensis | 58% | 95% |
A4HQG9 | Leishmania braziliensis | 57% | 81% |
A4I0H5 | Leishmania infantum | 30% | 79% |
A4ICA2 | Leishmania infantum | 63% | 100% |
A4ICG3 | Leishmania infantum | 29% | 82% |
A4ICG5 | Leishmania infantum | 27% | 74% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 80% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 80% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 81% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 74% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 79% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 76% |
Q4Q1G2 | Leishmania major | 27% | 74% |
Q4Q1G4 | Leishmania major | 29% | 82% |
Q4QB35 | Leishmania major | 30% | 77% |