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. | no | yes: 60 |
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: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 35, no: 3 |
NetGPI | no | yes: 0, no: 38 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 28 |
GO:0110165 | cellular anatomical entity | 1 | 28 |
Related structures:
AlphaFold database: A4HGW8
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 4 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016311 | dephosphorylation | 5 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0003993 | acid phosphatase activity | 6 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.145 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.530 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.569 |
DOC_MAPK_MEF2A_6 | 478 | 487 | PF00069 | 0.330 |
DOC_PP1_RVXF_1 | 392 | 399 | PF00149 | 0.370 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.624 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.212 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.180 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.333 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 119 | 127 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 292 | 296 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 393 | 399 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 91 | 101 | PF00244 | 0.330 |
LIG_Actin_WH2_2 | 506 | 524 | PF00022 | 0.215 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.403 |
LIG_deltaCOP1_diTrp_1 | 252 | 258 | PF00928 | 0.277 |
LIG_EH_1 | 263 | 267 | PF12763 | 0.199 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.300 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.508 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.288 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.299 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.357 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.346 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.306 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.385 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.463 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.390 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.308 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.215 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.381 |
LIG_HP1_1 | 165 | 169 | PF01393 | 0.199 |
LIG_LIR_Apic_2 | 161 | 165 | PF02991 | 0.353 |
LIG_LIR_Apic_2 | 527 | 533 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 163 | 174 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.328 |
LIG_PCNA_yPIPBox_3 | 125 | 138 | PF02747 | 0.191 |
LIG_PCNA_yPIPBox_3 | 181 | 190 | PF02747 | 0.299 |
LIG_PDZ_Class_3 | 543 | 548 | PF00595 | 0.533 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.348 |
LIG_Pex14_1 | 204 | 208 | PF04695 | 0.419 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.354 |
LIG_Pex14_2 | 254 | 258 | PF04695 | 0.258 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.390 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.273 |
LIG_SH2_CRK | 530 | 534 | PF00017 | 0.649 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.239 |
LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.247 |
LIG_SH2_STAP1 | 111 | 115 | PF00017 | 0.278 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.253 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.190 |
LIG_SH2_STAT3 | 320 | 323 | PF00017 | 0.173 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.235 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.361 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.343 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.298 |
LIG_SH3_5 | 107 | 111 | PF00018 | 0.219 |
LIG_Sin3_3 | 130 | 137 | PF02671 | 0.145 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.367 |
LIG_SUMO_SIM_anti_2 | 514 | 520 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 408 | 415 | PF11976 | 0.190 |
LIG_TRAF2_2 | 352 | 357 | PF00917 | 0.349 |
LIG_UBA3_1 | 221 | 229 | PF00899 | 0.360 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.363 |
LIG_WRC_WIRS_1 | 500 | 505 | PF05994 | 0.349 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.356 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.308 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.348 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.341 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.343 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.647 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.412 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.236 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.361 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.459 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.501 |
MOD_GlcNHglycan | 316 | 320 | PF01048 | 0.555 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.525 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.509 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.530 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.533 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.365 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.467 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.482 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.541 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.230 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.326 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.328 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.291 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.389 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.318 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.396 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.452 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.577 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.359 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.319 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.716 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.549 |
MOD_N-GLC_2 | 385 | 387 | PF02516 | 0.511 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.355 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.382 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.303 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.326 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.381 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.585 |
MOD_OGLYCOS | 67 | 72 | PF02709 | 0.482 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.399 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.358 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.266 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.366 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.628 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.209 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.643 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.652 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.328 |
MOD_PKB_1 | 373 | 381 | PF00069 | 0.223 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.246 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.281 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.305 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.378 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.492 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.289 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.306 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.322 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.280 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.263 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.325 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.259 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.288 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.312 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.368 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.393 |
MOD_SUMO_rev_2 | 472 | 479 | PF00179 | 0.305 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.274 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.219 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.207 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 197 | 202 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 43% | 96% |
A0A0N1I756 | Leptomonas seymouri | 38% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 34% | 100% |
A0A0S4IRF5 | Bodo saltans | 23% | 82% |
A0A0S4IUV8 | Bodo saltans | 23% | 100% |
A0A0S4IV77 | Bodo saltans | 33% | 100% |
A0A0S4IXN9 | Bodo saltans | 22% | 100% |
A0A0S4JEA9 | Bodo saltans | 23% | 100% |
A0A0S4JJK3 | Bodo saltans | 29% | 100% |
A0A0S4JW09 | Bodo saltans | 27% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 37% | 99% |
A0A1X0NQL4 | Trypanosomatidae | 28% | 100% |
A0A1X0NY34 | Trypanosomatidae | 25% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 38% | 100% |
A0A3Q8IR23 | Leishmania donovani | 46% | 96% |
A0A3R7KSH4 | Trypanosoma rangeli | 25% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 40% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H827 | Leishmania donovani | 36% | 100% |
A0A3S7WXU0 | Leishmania donovani | 43% | 100% |
A0A3S7X1W4 | Leishmania donovani | 72% | 100% |
A4HCZ0 | Leishmania braziliensis | 42% | 100% |
A4HPC1 | Leishmania braziliensis | 37% | 100% |
A4HPC5 | Leishmania braziliensis | 45% | 95% |
A4HQG6 | Leishmania braziliensis | 35% | 100% |
A4HQG9 | Leishmania braziliensis | 35% | 100% |
A4I0H5 | Leishmania infantum | 43% | 100% |
A4I3Z8 | Leishmania infantum | 73% | 100% |
A4ICA5 | Leishmania infantum | 34% | 82% |
A4ICG3 | Leishmania infantum | 36% | 100% |
A4ICG5 | Leishmania infantum | 46% | 96% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 96% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
P11117 | Homo sapiens | 26% | 100% |
P20611 | Rattus norvegicus | 26% | 100% |
P24638 | Mus musculus | 26% | 100% |
Q4Q0A9 | Leishmania major | 26% | 100% |
Q4Q1G2 | Leishmania major | 46% | 100% |
Q4Q1G4 | Leishmania major | 37% | 100% |
Q4Q7Z7 | Leishmania major | 72% | 100% |
Q4QB35 | Leishmania major | 42% | 100% |
Q9USS6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
V5BCI2 | Trypanosoma cruzi | 26% | 100% |
V5BIM1 | Trypanosoma cruzi | 23% | 100% |
V5BK91 | Trypanosoma cruzi | 39% | 100% |
V5BL75 | Trypanosoma cruzi | 30% | 100% |