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 | no | yes: 44, no: 5 |
NetGPI | no | yes: 0, no: 49 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 37 |
GO:0110165 | cellular anatomical entity | 1 | 37 |
Related structures:
AlphaFold database: A4HCZ0
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 | 8 |
GO:0003993 | acid phosphatase activity | 6 | 3 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016791 | phosphatase activity | 5 | 8 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 552 | 556 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.480 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.588 |
DEG_SCF_FBW7_2 | 49 | 56 | PF00400 | 0.406 |
DOC_ANK_TNKS_1 | 489 | 496 | PF00023 | 0.307 |
DOC_CDC14_PxL_1 | 304 | 312 | PF14671 | 0.428 |
DOC_CKS1_1 | 34 | 39 | PF01111 | 0.361 |
DOC_CYCLIN_yCln2_LP_2 | 393 | 396 | PF00134 | 0.238 |
DOC_MAPK_RevD_3 | 589 | 604 | PF00069 | 0.282 |
DOC_PP1_RVXF_1 | 463 | 470 | PF00149 | 0.446 |
DOC_PP2B_LxvP_1 | 393 | 396 | PF13499 | 0.400 |
DOC_PP2B_LxvP_1 | 98 | 101 | PF13499 | 0.486 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.529 |
DOC_USP7_UBL2_3 | 511 | 515 | PF12436 | 0.305 |
DOC_USP7_UBL2_3 | 603 | 607 | PF12436 | 0.696 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.373 |
LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 283 | 291 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 380 | 386 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 457 | 467 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 606 | 610 | PF00244 | 0.729 |
LIG_BIR_III_4 | 445 | 449 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.380 |
LIG_deltaCOP1_diTrp_1 | 256 | 262 | PF00928 | 0.331 |
LIG_deltaCOP1_diTrp_1 | 432 | 439 | PF00928 | 0.334 |
LIG_EH1_1 | 584 | 592 | PF00400 | 0.420 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.383 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.331 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.374 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.380 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.550 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.429 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.514 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.503 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.425 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.365 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.349 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.586 |
LIG_GBD_Chelix_1 | 401 | 409 | PF00786 | 0.438 |
LIG_GBD_Chelix_1 | 89 | 97 | PF00786 | 0.574 |
LIG_LIR_Apic_2 | 256 | 260 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 10 | 21 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 261 | 269 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 286 | 297 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 461 | 471 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 476 | 486 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.358 |
LIG_LYPXL_S_1 | 1 | 5 | PF13949 | 0.377 |
LIG_LYPXL_S_1 | 213 | 217 | PF13949 | 0.567 |
LIG_LYPXL_yS_3 | 2 | 5 | PF13949 | 0.574 |
LIG_LYPXL_yS_3 | 214 | 217 | PF13949 | 0.351 |
LIG_LYPXL_yS_3 | 307 | 310 | PF13949 | 0.434 |
LIG_NRBOX | 90 | 96 | PF00104 | 0.357 |
LIG_PCNA_yPIPBox_3 | 346 | 354 | PF02747 | 0.331 |
LIG_PDZ_Class_1 | 609 | 614 | PF00595 | 0.795 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.206 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.414 |
LIG_Pex14_2 | 236 | 240 | PF04695 | 0.353 |
LIG_Pex14_2 | 431 | 435 | PF04695 | 0.462 |
LIG_Pex14_2 | 65 | 69 | PF04695 | 0.380 |
LIG_REV1ctd_RIR_1 | 62 | 71 | PF16727 | 0.378 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.206 |
LIG_SH2_CRK | 486 | 490 | PF00017 | 0.381 |
LIG_SH2_GRB2like | 229 | 232 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 232 | 235 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.348 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.386 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.358 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.730 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.546 |
LIG_SH3_5 | 176 | 180 | PF00018 | 0.275 |
LIG_SUMO_SIM_par_1 | 399 | 404 | PF11976 | 0.347 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.407 |
LIG_UBA3_1 | 291 | 299 | PF00899 | 0.424 |
LIG_WRC_WIRS_1 | 582 | 587 | PF05994 | 0.418 |
MOD_CDC14_SPxK_1 | 544 | 547 | PF00782 | 0.338 |
MOD_CDK_SPK_2 | 49 | 54 | PF00069 | 0.404 |
MOD_CDK_SPxK_1 | 541 | 547 | PF00069 | 0.309 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.400 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.364 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.370 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.366 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.381 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.345 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.460 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.443 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.391 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.453 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.405 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.535 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.590 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.552 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.585 |
MOD_GlcNHglycan | 445 | 449 | PF01048 | 0.493 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.588 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.612 |
MOD_GlcNHglycan | 571 | 575 | PF01048 | 0.783 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.340 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.645 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.564 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.432 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.380 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.334 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.302 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.383 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.304 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.458 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.617 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.670 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.635 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.542 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.585 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.540 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.482 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.586 |
MOD_N-GLC_2 | 456 | 458 | PF02516 | 0.594 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.341 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.361 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.372 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.206 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.374 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.324 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.333 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.454 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.387 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.495 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.473 |
MOD_OFUCOSY | 517 | 522 | PF10250 | 0.567 |
MOD_OFUCOSY | 535 | 542 | PF10250 | 0.641 |
MOD_OGLYCOS | 136 | 141 | PF02709 | 0.517 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.402 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.337 |
MOD_PK_1 | 45 | 51 | PF00069 | 0.396 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.355 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.387 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.424 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.672 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.442 |
MOD_PKB_1 | 160 | 168 | PF00069 | 0.428 |
MOD_PKB_1 | 514 | 522 | PF00069 | 0.272 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.417 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.376 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.388 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.333 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.312 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.379 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.364 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.402 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.376 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.332 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.453 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.449 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.425 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.400 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.443 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.743 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.372 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.340 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.202 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 513 | 516 | PF00400 | 0.357 |
TRG_NES_CRM1_1 | 391 | 404 | PF08389 | 0.414 |
TRG_NES_CRM1_1 | 88 | 102 | PF08389 | 0.307 |
TRG_NLS_MonoExtC_3 | 513 | 518 | PF00514 | 0.261 |
TRG_NLS_MonoExtC_3 | 602 | 607 | PF00514 | 0.749 |
TRG_NLS_MonoExtN_4 | 511 | 518 | PF00514 | 0.243 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 45% | 100% |
A0A0N1I756 | Leptomonas seymouri | 42% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 37% | 100% |
A0A0S4IRF5 | Bodo saltans | 24% | 92% |
A0A0S4IUV8 | Bodo saltans | 23% | 100% |
A0A0S4IV77 | Bodo saltans | 35% | 100% |
A0A0S4IXN9 | Bodo saltans | 23% | 100% |
A0A0S4JEA9 | Bodo saltans | 27% | 100% |
A0A0S4JJK3 | Bodo saltans | 28% | 100% |
A0A0S4JW09 | Bodo saltans | 27% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 37% | 100% |
A0A1X0NQL4 | Trypanosomatidae | 28% | 100% |
A0A1X0NY34 | Trypanosomatidae | 24% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 44% | 100% |
A0A3Q8IR23 | Leishmania donovani | 50% | 100% |
A0A3R7KSH4 | Trypanosoma rangeli | 25% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 43% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H827 | Leishmania donovani | 39% | 100% |
A0A3S7WXU0 | Leishmania donovani | 85% | 100% |
A0A3S7X1W4 | Leishmania donovani | 41% | 100% |
A4HGW8 | Leishmania braziliensis | 42% | 100% |
A4HPC1 | Leishmania braziliensis | 39% | 100% |
A4HPC5 | Leishmania braziliensis | 50% | 100% |
A4HQG6 | Leishmania braziliensis | 34% | 100% |
A4HQG9 | Leishmania braziliensis | 35% | 100% |
A4I0H5 | Leishmania infantum | 85% | 100% |
A4I3Z8 | Leishmania infantum | 41% | 100% |
A4ICA5 | Leishmania infantum | 36% | 92% |
A4ICG3 | Leishmania infantum | 39% | 100% |
A4ICG5 | Leishmania infantum | 50% | 100% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 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) | 50% | 100% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
Q4Q0A9 | Leishmania major | 31% | 99% |
Q4Q1G2 | Leishmania major | 49% | 100% |
Q4Q1G4 | Leishmania major | 38% | 100% |
Q4Q7Z7 | Leishmania major | 42% | 100% |
Q4QB35 | Leishmania major | 87% | 100% |
V5BCI2 | Trypanosoma cruzi | 27% | 100% |
V5BIM1 | Trypanosoma cruzi | 22% | 100% |
V5BK91 | Trypanosoma cruzi | 42% | 100% |
V5BL75 | Trypanosoma cruzi | 28% | 100% |