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. | yes | 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 | 35 |
GO:0110165 | cellular anatomical entity | 1 | 35 |
Related structures:
AlphaFold database: Q4Q1G2
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016311 | dephosphorylation | 5 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
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 |
GO:0003993 | acid phosphatase activity | 6 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.674 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.476 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 397 | 399 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 535 | 537 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.606 |
DOC_CDC14_PxL_1 | 237 | 245 | PF14671 | 0.446 |
DOC_CKS1_1 | 431 | 436 | PF01111 | 0.392 |
DOC_CYCLIN_RxL_1 | 217 | 226 | PF00134 | 0.417 |
DOC_PP1_RVXF_1 | 396 | 403 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 4 | 10 | PF00149 | 0.726 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.351 |
DOC_PP4_MxPP_1 | 326 | 329 | PF00568 | 0.413 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.478 |
DOC_USP7_UBL2_3 | 196 | 200 | PF12436 | 0.373 |
DOC_USP7_UBL2_3 | 397 | 401 | PF12436 | 0.302 |
DOC_USP7_UBL2_3 | 40 | 44 | PF12436 | 0.328 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 536 | 544 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 545 | 551 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.406 |
LIG_APCC_ABBA_1 | 390 | 395 | PF00400 | 0.392 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.688 |
LIG_BIR_III_4 | 378 | 382 | PF00653 | 0.492 |
LIG_BIR_III_4 | 407 | 411 | PF00653 | 0.419 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.400 |
LIG_deltaCOP1_diTrp_1 | 365 | 372 | PF00928 | 0.365 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.372 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.334 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.340 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.396 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.556 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.540 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.479 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.381 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.374 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.357 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.449 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.371 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.522 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.606 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.469 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.591 |
LIG_LIR_Apic_2 | 105 | 111 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 165 | 173 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 395 | 399 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.449 |
LIG_LYPXL_yS_3 | 240 | 243 | PF13949 | 0.452 |
LIG_PDZ_Class_3 | 566 | 571 | PF00595 | 0.816 |
LIG_Pex14_1 | 168 | 172 | PF04695 | 0.434 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.431 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.493 |
LIG_Rb_pABgroove_1 | 219 | 227 | PF01858 | 0.431 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.403 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.526 |
LIG_SH2_GRB2like | 173 | 176 | PF00017 | 0.415 |
LIG_SH2_PTP2 | 348 | 351 | PF00017 | 0.425 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.261 |
LIG_SH2_SRC | 260 | 263 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.393 |
LIG_SH2_STAT3 | 413 | 416 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.368 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.402 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.379 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.437 |
LIG_TRAF2_1 | 480 | 483 | PF00917 | 0.444 |
LIG_TRAF2_1 | 549 | 552 | PF00917 | 0.725 |
LIG_TRAF2_2 | 356 | 361 | PF00917 | 0.457 |
LIG_UBA3_1 | 224 | 232 | PF00899 | 0.442 |
LIG_WRC_WIRS_1 | 514 | 519 | PF05994 | 0.460 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.372 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.450 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.420 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.384 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.479 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.491 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.549 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.407 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.457 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.407 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.476 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.472 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.581 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.452 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.737 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.556 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.574 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.627 |
MOD_GlcNHglycan | 482 | 487 | PF01048 | 0.757 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.789 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.643 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.365 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.389 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.350 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.484 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.552 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.658 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.462 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.413 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.372 |
MOD_LATS_1 | 543 | 549 | PF00433 | 0.584 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.563 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.561 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.653 |
MOD_N-GLC_2 | 389 | 391 | PF02516 | 0.602 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.395 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.444 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.392 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.477 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.442 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.649 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.373 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.412 |
MOD_OFUCOSY | 468 | 475 | PF10250 | 0.692 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.447 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.692 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.252 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.464 |
MOD_PKA_1 | 535 | 541 | PF00069 | 0.642 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.372 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.391 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.610 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.662 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.693 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.446 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.417 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.360 |
MOD_Plk_2-3 | 415 | 421 | PF00069 | 0.310 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.381 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.373 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.383 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.389 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.333 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.354 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.414 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.519 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.451 |
MOD_SUMO_rev_2 | 34 | 42 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 359 | 364 | PF00179 | 0.333 |
MOD_SUMO_rev_2 | 487 | 497 | PF00179 | 0.469 |
TRG_DiLeu_BaEn_4 | 551 | 557 | PF01217 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.403 |
TRG_NES_CRM1_1 | 324 | 337 | PF08389 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 62% | 100% |
A0A0N1I756 | Leptomonas seymouri | 40% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 39% | 100% |
A0A0S4IRF5 | Bodo saltans | 23% | 85% |
A0A0S4IV77 | Bodo saltans | 35% | 100% |
A0A0S4JEA9 | Bodo saltans | 27% | 100% |
A0A0S4JJK3 | Bodo saltans | 26% | 100% |
A0A0S4JW09 | Bodo saltans | 30% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 34% | 100% |
A0A1X0NQL4 | Trypanosomatidae | 30% | 100% |
A0A1X0NY34 | Trypanosomatidae | 25% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 45% | 100% |
A0A3Q8IR23 | Leishmania donovani | 94% | 100% |
A0A3R7KSH4 | Trypanosoma rangeli | 25% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 42% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H827 | Leishmania donovani | 38% | 100% |
A0A3S7WXU0 | Leishmania donovani | 51% | 100% |
A0A3S7X1W4 | Leishmania donovani | 45% | 100% |
A4HCZ0 | Leishmania braziliensis | 49% | 93% |
A4HGW8 | Leishmania braziliensis | 46% | 100% |
A4HPC1 | Leishmania braziliensis | 37% | 100% |
A4HPC5 | Leishmania braziliensis | 80% | 99% |
A4HQG6 | Leishmania braziliensis | 38% | 100% |
A4HQG9 | Leishmania braziliensis | 37% | 100% |
A4I0H5 | Leishmania infantum | 51% | 100% |
A4I3Z8 | Leishmania infantum | 45% | 100% |
A4ICA5 | Leishmania infantum | 39% | 86% |
A4ICG3 | Leishmania infantum | 38% | 100% |
A4ICG5 | Leishmania infantum | 94% | 100% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 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) | 40% | 100% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q4Q0A9 | Leishmania major | 27% | 92% |
Q4Q1G4 | Leishmania major | 36% | 100% |
Q4Q7Z7 | Leishmania major | 45% | 100% |
Q4QB35 | Leishmania major | 49% | 100% |
V5BCI2 | Trypanosoma cruzi | 27% | 100% |
V5BIM1 | Trypanosoma cruzi | 25% | 100% |
V5BK91 | Trypanosoma cruzi | 41% | 100% |
V5BL75 | Trypanosoma cruzi | 30% | 100% |