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. | no | yes: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 43, no: 4 |
NetGPI | no | yes: 0, no: 47 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 36 |
GO:0110165 | cellular anatomical entity | 1 | 36 |
Related structures:
AlphaFold database: A4HPC5
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 | 9 |
GO:0003993 | acid phosphatase activity | 6 | 4 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016791 | phosphatase activity | 5 | 9 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.413 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 397 | 399 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.704 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.517 |
DEG_APCC_KENBOX_2 | 386 | 390 | PF00400 | 0.199 |
DOC_CDC14_PxL_1 | 237 | 245 | PF14671 | 0.433 |
DOC_CKS1_1 | 431 | 436 | PF01111 | 0.319 |
DOC_CYCLIN_RxL_1 | 217 | 226 | PF00134 | 0.372 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.313 |
DOC_PP1_RVXF_1 | 396 | 403 | PF00149 | 0.395 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.345 |
DOC_PP4_MxPP_1 | 326 | 329 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.260 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.339 |
DOC_USP7_UBL2_3 | 397 | 401 | PF12436 | 0.230 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 554 | 563 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.385 |
LIG_APCC_ABBA_1 | 390 | 395 | PF00400 | 0.318 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BIR_III_4 | 378 | 382 | PF00653 | 0.419 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.401 |
LIG_deltaCOP1_diTrp_1 | 365 | 372 | PF00928 | 0.290 |
LIG_EH1_1 | 523 | 531 | PF00400 | 0.377 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.338 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.320 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.341 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.322 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.463 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.690 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.420 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.378 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.370 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.358 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.429 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.366 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.262 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.538 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.389 |
LIG_GBD_Chelix_1 | 9 | 17 | PF00786 | 0.559 |
LIG_LIR_Apic_2 | 105 | 111 | PF02991 | 0.350 |
LIG_LIR_Apic_2 | 428 | 434 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 165 | 173 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 395 | 399 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.411 |
LIG_LYPXL_yS_3 | 240 | 243 | PF13949 | 0.430 |
LIG_PDZ_Class_3 | 573 | 578 | PF00595 | 0.790 |
LIG_Pex14_1 | 168 | 172 | PF04695 | 0.353 |
LIG_Pex14_1 | 546 | 550 | PF04695 | 0.496 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.387 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.415 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.413 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.451 |
LIG_SH2_GRB2like | 173 | 176 | PF00017 | 0.395 |
LIG_SH2_PTP2 | 348 | 351 | PF00017 | 0.384 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.242 |
LIG_SH2_SRC | 260 | 263 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.316 |
LIG_SH2_STAT3 | 413 | 416 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.337 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.414 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.352 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.415 |
LIG_Sin3_3 | 14 | 21 | PF02671 | 0.569 |
LIG_TRAF2_2 | 356 | 361 | PF00917 | 0.376 |
LIG_UBA3_1 | 224 | 232 | PF00899 | 0.401 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.367 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.369 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.267 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.387 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.418 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.502 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.670 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.421 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.401 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.439 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.394 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.535 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.510 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.488 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.539 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.616 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.561 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.662 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.718 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.392 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.351 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.363 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.313 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.404 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.475 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.578 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.386 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.365 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.561 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.601 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.507 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.704 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.579 |
MOD_N-GLC_2 | 389 | 391 | PF02516 | 0.525 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.353 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.376 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.398 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.356 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.326 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.371 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.354 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.575 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.571 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.333 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.329 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.366 |
MOD_OFUCOSY | 468 | 475 | PF10250 | 0.616 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.361 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.344 |
MOD_PK_1 | 249 | 255 | PF00069 | 0.181 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.340 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.560 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.434 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.387 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.320 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.372 |
MOD_Plk_2-3 | 415 | 421 | PF00069 | 0.238 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.382 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.374 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.372 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.313 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.336 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.428 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.386 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.382 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.325 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.326 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.396 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.409 |
MOD_SUMO_rev_2 | 359 | 364 | PF00179 | 0.251 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.203 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.672 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.359 |
TRG_NES_CRM1_1 | 324 | 337 | PF08389 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 572 | 576 | PF00026 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 61% | 100% |
A0A0N1I756 | Leptomonas seymouri | 40% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 38% | 100% |
A0A0S4IV77 | Bodo saltans | 34% | 100% |
A0A0S4JEA9 | Bodo saltans | 27% | 100% |
A0A0S4JJK3 | Bodo saltans | 27% | 100% |
A0A0S4JW09 | Bodo saltans | 31% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 34% | 100% |
A0A1X0NQL4 | Trypanosomatidae | 30% | 100% |
A0A1X0NY34 | Trypanosomatidae | 24% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 46% | 100% |
A0A3Q8IR23 | Leishmania donovani | 80% | 100% |
A0A3R7KGH3 | Trypanosoma rangeli | 23% | 100% |
A0A3R7KSH4 | Trypanosoma rangeli | 24% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 43% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H827 | Leishmania donovani | 38% | 100% |
A0A3S7WXU0 | Leishmania donovani | 50% | 100% |
A0A3S7X1W4 | Leishmania donovani | 42% | 100% |
A4HCZ0 | Leishmania braziliensis | 50% | 100% |
A4HGW8 | Leishmania braziliensis | 45% | 100% |
A4HPC1 | Leishmania braziliensis | 40% | 100% |
A4HQG6 | Leishmania braziliensis | 37% | 100% |
A4HQG9 | Leishmania braziliensis | 37% | 100% |
A4I0H5 | Leishmania infantum | 50% | 100% |
A4I3Z8 | Leishmania infantum | 42% | 100% |
A4ICA5 | Leishmania infantum | 39% | 87% |
A4ICG3 | Leishmania infantum | 38% | 100% |
A4ICG5 | Leishmania infantum | 81% | 100% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q4Q0A9 | Leishmania major | 29% | 98% |
Q4Q1G2 | Leishmania major | 80% | 99% |
Q4Q1G4 | Leishmania major | 39% | 100% |
Q4Q7Z7 | Leishmania major | 45% | 100% |
Q4QB35 | Leishmania major | 50% | 100% |
V5BCI2 | Trypanosoma cruzi | 25% | 100% |
V5BIM1 | Trypanosoma cruzi | 25% | 100% |
V5BK91 | Trypanosoma cruzi | 41% | 100% |
V5BL75 | Trypanosoma cruzi | 30% | 100% |