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: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 38, no: 4 |
NetGPI | no | yes: 0, no: 42 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 32 |
GO:0110165 | cellular anatomical entity | 1 | 32 |
Related structures:
AlphaFold database: E9AT36
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 | 7 |
GO:0003993 | acid phosphatase activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.448 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 397 | 399 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.624 |
DOC_CDC14_PxL_1 | 237 | 245 | PF14671 | 0.459 |
DOC_CKS1_1 | 431 | 436 | PF01111 | 0.365 |
DOC_CYCLIN_RxL_1 | 217 | 226 | PF00134 | 0.394 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.341 |
DOC_PP1_RVXF_1 | 396 | 403 | PF00149 | 0.427 |
DOC_PP1_RVXF_1 | 4 | 10 | PF00149 | 0.689 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.383 |
DOC_PP4_MxPP_1 | 326 | 329 | PF00568 | 0.404 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.741 |
DOC_USP7_UBL2_3 | 397 | 401 | PF12436 | 0.272 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.433 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 252 | 257 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 545 | 551 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.429 |
LIG_APCC_ABBA_1 | 390 | 395 | PF00400 | 0.345 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.669 |
LIG_BIR_III_4 | 378 | 382 | PF00653 | 0.455 |
LIG_BIR_III_4 | 407 | 411 | PF00653 | 0.377 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.427 |
LIG_deltaCOP1_diTrp_1 | 365 | 372 | PF00928 | 0.338 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.373 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.338 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.385 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.504 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.505 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.450 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.411 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.362 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.337 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.453 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.391 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.483 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.570 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.443 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.555 |
LIG_LIR_Apic_2 | 105 | 111 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 165 | 173 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 395 | 399 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.448 |
LIG_LYPXL_yS_3 | 240 | 243 | PF13949 | 0.345 |
LIG_PCNA_yPIPBox_3 | 332 | 342 | PF02747 | 0.394 |
LIG_PDZ_Class_3 | 566 | 571 | PF00595 | 0.628 |
LIG_Pex14_1 | 168 | 172 | PF04695 | 0.396 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.410 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.468 |
LIG_Rb_pABgroove_1 | 219 | 227 | PF01858 | 0.409 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.439 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.484 |
LIG_SH2_GRB2like | 173 | 176 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 348 | 351 | PF00017 | 0.437 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.282 |
LIG_SH2_SRC | 260 | 263 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.345 |
LIG_SH2_STAT3 | 413 | 416 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.356 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.442 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.368 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.369 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.410 |
LIG_SUMO_SIM_anti_2 | 155 | 161 | PF11976 | 0.278 |
LIG_TRAF2_1 | 480 | 483 | PF00917 | 0.417 |
LIG_TRAF2_2 | 356 | 361 | PF00917 | 0.415 |
LIG_UBA3_1 | 224 | 232 | PF00899 | 0.422 |
LIG_WRC_WIRS_1 | 514 | 519 | PF05994 | 0.415 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.406 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.460 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.395 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.449 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.463 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.582 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.567 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.510 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.441 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.468 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.261 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.543 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.712 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.543 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.572 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.597 |
MOD_GlcNHglycan | 482 | 487 | PF01048 | 0.740 |
MOD_GlcNHglycan | 500 | 504 | PF01048 | 0.783 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.735 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.597 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.322 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.391 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.335 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.517 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.422 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.406 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.604 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.587 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.578 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.778 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.373 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.614 |
MOD_N-GLC_2 | 389 | 391 | PF02516 | 0.562 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.369 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.397 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.412 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.421 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.375 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.420 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.389 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.466 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.614 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.373 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.389 |
MOD_OFUCOSY | 468 | 475 | PF10250 | 0.650 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.418 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.407 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.246 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.436 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.366 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.374 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.463 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.344 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.452 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.372 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.353 |
MOD_Plk_2-3 | 415 | 421 | PF00069 | 0.284 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.435 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.343 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.426 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.419 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.364 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.370 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.421 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.427 |
MOD_SUMO_rev_2 | 359 | 364 | PF00179 | 0.302 |
MOD_SUMO_rev_2 | 487 | 497 | PF00179 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.370 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.714 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.402 |
TRG_NES_CRM1_1 | 324 | 337 | PF08389 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 63% | 100% |
A0A0N1I756 | Leptomonas seymouri | 40% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 38% | 100% |
A0A0S4IRF5 | Bodo saltans | 23% | 85% |
A0A0S4IUV8 | Bodo saltans | 22% | 100% |
A0A0S4IV77 | Bodo saltans | 36% | 100% |
A0A0S4JEA9 | Bodo saltans | 27% | 100% |
A0A0S4JJK3 | Bodo saltans | 25% | 100% |
A0A0S4JW09 | Bodo saltans | 30% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 34% | 100% |
A0A1X0NQL4 | Trypanosomatidae | 30% | 100% |
A0A1X0NY34 | Trypanosomatidae | 25% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 46% | 100% |
A0A3Q8IR23 | Leishmania donovani | 92% | 100% |
A0A3R7KSH4 | Trypanosoma rangeli | 24% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 42% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H827 | Leishmania donovani | 38% | 100% |
A0A3S7WXU0 | Leishmania donovani | 51% | 100% |
A0A3S7X1W4 | Leishmania donovani | 46% | 100% |
A4HCZ0 | Leishmania braziliensis | 50% | 100% |
A4HGW8 | Leishmania braziliensis | 46% | 100% |
A4HPC1 | Leishmania braziliensis | 40% | 100% |
A4HPC5 | Leishmania braziliensis | 80% | 100% |
A4HQG6 | Leishmania braziliensis | 37% | 100% |
A4HQG9 | Leishmania braziliensis | 35% | 100% |
A4I0H5 | Leishmania infantum | 50% | 100% |
A4I3Z8 | Leishmania infantum | 46% | 100% |
A4ICA5 | Leishmania infantum | 39% | 86% |
A4ICG3 | Leishmania infantum | 38% | 100% |
A4ICG5 | Leishmania infantum | 93% | 100% |
B1H1P9 | Xenopus laevis | 26% | 100% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q4Q0A9 | Leishmania major | 26% | 92% |
Q4Q1G2 | Leishmania major | 91% | 100% |
Q4Q1G4 | Leishmania major | 38% | 100% |
Q4Q7Z7 | Leishmania major | 47% | 100% |
Q4QB35 | Leishmania major | 50% | 100% |
V5BCI2 | Trypanosoma cruzi | 27% | 100% |
V5BIM1 | Trypanosoma cruzi | 24% | 100% |
V5BK91 | Trypanosoma cruzi | 41% | 100% |
V5BL75 | Trypanosoma cruzi | 29% | 100% |