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: 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. | yes | yes: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 34, no: 4 |
NetGPI | no | yes: 0, no: 38 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
Related structures:
AlphaFold database: A0A3S5H827
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:0003993 | acid phosphatase activity | 6 | 1 |
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 | 306 | 310 | PF00656 | 0.257 |
CLV_C14_Caspase3-7 | 329 | 333 | PF00656 | 0.412 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 499 | 501 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.380 |
DEG_MDM2_SWIB_1 | 96 | 103 | PF02201 | 0.183 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.554 |
DOC_CDC14_PxL_1 | 224 | 232 | PF14671 | 0.418 |
DOC_CYCLIN_RxL_1 | 122 | 132 | PF00134 | 0.295 |
DOC_MAPK_gen_1 | 505 | 514 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.603 |
DOC_PP1_RVXF_1 | 1 | 8 | PF00149 | 0.471 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.486 |
DOC_PP4_MxPP_1 | 315 | 318 | PF00568 | 0.341 |
DOC_SPAK_OSR1_1 | 339 | 343 | PF12202 | 0.213 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.473 |
DOC_USP7_UBL2_3 | 499 | 503 | PF12436 | 0.603 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.288 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 109 | 117 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 390 | 400 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 81 | 91 | PF00244 | 0.389 |
LIG_APCC_ABBA_1 | 382 | 387 | PF00400 | 0.351 |
LIG_BIR_III_4 | 370 | 374 | PF00653 | 0.419 |
LIG_BIR_III_4 | 419 | 423 | PF00653 | 0.342 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.292 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.370 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.324 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.401 |
LIG_Clathr_ClatBox_1 | 179 | 183 | PF01394 | 0.221 |
LIG_Clathr_ClatBox_1 | 411 | 415 | PF01394 | 0.241 |
LIG_eIF4E_1 | 266 | 272 | PF01652 | 0.339 |
LIG_eIF4E_1 | 405 | 411 | PF01652 | 0.217 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.339 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.368 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.312 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.319 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.344 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.334 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.320 |
LIG_GBD_Chelix_1 | 268 | 276 | PF00786 | 0.498 |
LIG_LIR_Apic_2 | 403 | 408 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 338 | 345 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 386 | 396 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 496 | 501 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 99 | 103 | PF02991 | 0.336 |
LIG_MLH1_MIPbox_1 | 131 | 135 | PF16413 | 0.347 |
LIG_NRBOX | 267 | 273 | PF00104 | 0.296 |
LIG_PCNA_yPIPBox_3 | 115 | 128 | PF02747 | 0.226 |
LIG_PDZ_Class_2 | 509 | 514 | PF00595 | 0.541 |
LIG_Pex14_2 | 319 | 323 | PF04695 | 0.255 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.222 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.395 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.633 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 341 | 344 | PF00017 | 0.367 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.302 |
LIG_SH2_SRC | 405 | 408 | PF00017 | 0.304 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.345 |
LIG_SH2_STAT3 | 67 | 70 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.276 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.262 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.478 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.352 |
LIG_Sin3_3 | 269 | 276 | PF02671 | 0.203 |
LIG_SUMO_SIM_par_1 | 301 | 306 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 323 | 329 | PF11976 | 0.312 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.375 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.354 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.323 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.458 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.660 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.381 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.217 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.197 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.505 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.614 |
MOD_GlcNHglycan | 292 | 296 | PF01048 | 0.513 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.550 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.669 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.275 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.294 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.295 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.281 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.347 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.287 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.263 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.454 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.373 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.526 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.546 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.579 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.542 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.502 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.455 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.532 |
MOD_N-GLC_1 | 439 | 444 | PF02516 | 0.391 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.742 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.534 |
MOD_N-GLC_2 | 381 | 383 | PF02516 | 0.506 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.305 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.348 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.345 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.256 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.350 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.248 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.293 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.370 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.306 |
MOD_OFUCOSY | 438 | 443 | PF10250 | 0.516 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.226 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.305 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.461 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.375 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.298 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.365 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.293 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.311 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.290 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.367 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.515 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.316 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.347 |
MOD_Plk_2-3 | 326 | 332 | PF00069 | 0.223 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.320 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.300 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.322 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.337 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.288 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.301 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.260 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.227 |
TRG_DiLeu_BaEn_1 | 144 | 149 | PF01217 | 0.318 |
TRG_DiLeu_BaEn_4 | 144 | 150 | PF01217 | 0.188 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.178 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.377 |
TRG_DiLeu_LyEn_5 | 225 | 230 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.214 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.338 |
TRG_NES_CRM1_1 | 313 | 326 | PF08389 | 0.298 |
TRG_NLS_MonoExtC_3 | 498 | 503 | PF00514 | 0.504 |
TRG_NLS_MonoExtN_4 | 499 | 506 | PF00514 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 425 | 430 | PF00026 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 36% | 90% |
A0A0N1I756 | Leptomonas seymouri | 65% | 99% |
A0A0N1PEH4 | Leptomonas seymouri | 38% | 100% |
A0A0S4IRF5 | Bodo saltans | 26% | 77% |
A0A0S4IUV8 | Bodo saltans | 26% | 100% |
A0A0S4IV77 | Bodo saltans | 34% | 99% |
A0A0S4JEA9 | Bodo saltans | 24% | 100% |
A0A0S4JJK3 | Bodo saltans | 29% | 100% |
A0A0S4JW09 | Bodo saltans | 27% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 36% | 93% |
A0A1X0NQL4 | Trypanosomatidae | 27% | 94% |
A0A1X0NY34 | Trypanosomatidae | 27% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 40% | 98% |
A0A3Q8IR23 | Leishmania donovani | 38% | 100% |
A0A3R7KSH4 | Trypanosoma rangeli | 25% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 38% | 99% |
A0A3R7MHJ7 | Trypanosoma rangeli | 26% | 100% |
A0A3S7WXU0 | Leishmania donovani | 39% | 97% |
A0A3S7X1W4 | Leishmania donovani | 35% | 94% |
A4HCZ0 | Leishmania braziliensis | 39% | 100% |
A4HGW8 | Leishmania braziliensis | 36% | 100% |
A4HPC1 | Leishmania braziliensis | 70% | 100% |
A4HPC5 | Leishmania braziliensis | 38% | 100% |
A4HQG6 | Leishmania braziliensis | 39% | 100% |
A4HQG9 | Leishmania braziliensis | 38% | 100% |
A4I0H5 | Leishmania infantum | 39% | 100% |
A4I3Z8 | Leishmania infantum | 35% | 100% |
A4ICA5 | Leishmania infantum | 36% | 100% |
A4ICG3 | Leishmania infantum | 100% | 100% |
A4ICG5 | Leishmania infantum | 38% | 100% |
B1H1P9 | Xenopus laevis | 27% | 100% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 97% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 98% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
P11117 | Homo sapiens | 26% | 100% |
P24638 | Mus musculus | 26% | 100% |
Q0P5F0 | Bos taurus | 26% | 100% |
Q4Q0A9 | Leishmania major | 29% | 100% |
Q4Q1G2 | Leishmania major | 38% | 100% |
Q4Q1G4 | Leishmania major | 93% | 100% |
Q4Q7Z7 | Leishmania major | 34% | 100% |
Q4QB35 | Leishmania major | 39% | 100% |
V5BCI2 | Trypanosoma cruzi | 27% | 100% |
V5BK91 | Trypanosoma cruzi | 39% | 100% |
V5BL75 | Trypanosoma cruzi | 28% | 100% |