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: 60 |
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: 31, no: 3 |
NetGPI | no | yes: 0, no: 34 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
Related structures:
AlphaFold database: Q4Q7Z7
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: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 |
GO:0003993 | acid phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.682 |
DEG_Kelch_Keap1_1 | 337 | 342 | PF01344 | 0.235 |
DOC_CKS1_1 | 31 | 36 | PF01111 | 0.404 |
DOC_CYCLIN_RxL_1 | 3 | 12 | PF00134 | 0.606 |
DOC_MAPK_MEF2A_6 | 14 | 22 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 392 | 399 | PF00149 | 0.357 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.182 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.173 |
DOC_PP4_MxPP_1 | 322 | 325 | PF00568 | 0.321 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.242 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 292 | 296 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.319 |
LIG_APCC_Cbox_2 | 187 | 193 | PF00515 | 0.173 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.378 |
LIG_EH1_1 | 2 | 10 | PF00400 | 0.355 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.528 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.377 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.312 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.277 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.308 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.337 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.364 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.391 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.289 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.297 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.382 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.303 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.309 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.296 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.422 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.383 |
LIG_HP1_1 | 165 | 169 | PF01393 | 0.182 |
LIG_LIR_Apic_2 | 161 | 165 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 163 | 174 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.294 |
LIG_PCNA_PIPBox_1 | 83 | 92 | PF02747 | 0.290 |
LIG_PCNA_yPIPBox_3 | 181 | 190 | PF02747 | 0.246 |
LIG_PCNA_yPIPBox_3 | 328 | 336 | PF02747 | 0.320 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.316 |
LIG_Pex14_1 | 204 | 208 | PF04695 | 0.355 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.310 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.405 |
LIG_SH2_NCK_1 | 223 | 227 | PF00017 | 0.206 |
LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.247 |
LIG_SH2_SRC | 223 | 226 | PF00017 | 0.299 |
LIG_SH2_SRC | 260 | 263 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.320 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.422 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.279 |
LIG_SH3_5 | 107 | 111 | PF00018 | 0.217 |
LIG_SUMO_SIM_anti_2 | 514 | 519 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 18 | 23 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 218 | 224 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 328 | 333 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 516 | 522 | PF11976 | 0.523 |
LIG_SxIP_EBH_1 | 51 | 64 | PF03271 | 0.303 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.261 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.318 |
LIG_WRC_WIRS_1 | 500 | 505 | PF05994 | 0.320 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.310 |
MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.403 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.311 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.345 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.284 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.322 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.427 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.377 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.470 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.462 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.415 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.291 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.243 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.410 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.451 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.583 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.499 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.516 |
MOD_GlcNHglycan | 411 | 417 | PF01048 | 0.552 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.524 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.516 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.523 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.641 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.528 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.223 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.252 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.303 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.303 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.376 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.402 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.494 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.362 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.343 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.459 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.464 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.510 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.532 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.575 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.545 |
MOD_N-GLC_2 | 385 | 387 | PF02516 | 0.489 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.309 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.324 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.292 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.329 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.366 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.296 |
MOD_OFUCOSY | 462 | 469 | PF10250 | 0.637 |
MOD_OGLYCOS | 67 | 72 | PF02709 | 0.471 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.359 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.359 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.426 |
MOD_PK_1 | 534 | 540 | PF00069 | 0.565 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.267 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.350 |
MOD_PKB_1 | 91 | 99 | PF00069 | 0.349 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.253 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.309 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.275 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.383 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.369 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.363 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.703 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.328 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.281 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.298 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.277 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.296 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.296 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.713 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.263 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.291 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.579 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.391 |
TRG_DiLeu_BaEn_1 | 413 | 418 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.182 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 543 | 546 | PF00400 | 0.731 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 283 | 287 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 46% | 96% |
A0A0N1I756 | Leptomonas seymouri | 38% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 31% | 100% |
A0A0S4IRF5 | Bodo saltans | 24% | 82% |
A0A0S4IUV8 | Bodo saltans | 23% | 100% |
A0A0S4IV77 | Bodo saltans | 33% | 100% |
A0A0S4IXN9 | Bodo saltans | 22% | 100% |
A0A0S4JEA9 | Bodo saltans | 25% | 100% |
A0A0S4JJK3 | Bodo saltans | 28% | 100% |
A0A0S4JW09 | Bodo saltans | 26% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 36% | 99% |
A0A1X0NQL4 | Trypanosomatidae | 28% | 100% |
A0A1X0NY34 | Trypanosomatidae | 25% | 100% |
A0A1X0P3J2 | Trypanosomatidae | 23% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 38% | 100% |
A0A3Q8IR23 | Leishmania donovani | 47% | 96% |
A0A3R7KGH3 | Trypanosoma rangeli | 24% | 100% |
A0A3R7KSH4 | Trypanosoma rangeli | 24% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 38% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 28% | 100% |
A0A3S5H827 | Leishmania donovani | 34% | 100% |
A0A3S7WXU0 | Leishmania donovani | 44% | 100% |
A0A3S7X1W4 | Leishmania donovani | 94% | 100% |
A4HCZ0 | Leishmania braziliensis | 42% | 89% |
A4HGW8 | Leishmania braziliensis | 72% | 100% |
A4HPC1 | Leishmania braziliensis | 35% | 100% |
A4HPC5 | Leishmania braziliensis | 45% | 95% |
A4HQG6 | Leishmania braziliensis | 34% | 100% |
A4HQG9 | Leishmania braziliensis | 34% | 100% |
A4I0H5 | Leishmania infantum | 44% | 100% |
A4I3Z8 | Leishmania infantum | 94% | 100% |
A4ICA5 | Leishmania infantum | 34% | 82% |
A4ICG3 | Leishmania infantum | 34% | 100% |
A4ICG5 | Leishmania infantum | 47% | 96% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 96% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q3KQG9 | Xenopus laevis | 28% | 100% |
Q4Q1G2 | Leishmania major | 45% | 100% |
Q4Q1G4 | Leishmania major | 33% | 100% |
Q4QB35 | Leishmania major | 44% | 100% |
V5BCI2 | Trypanosoma cruzi | 24% | 100% |
V5BIM1 | Trypanosoma cruzi | 22% | 100% |
V5BK91 | Trypanosoma cruzi | 38% | 100% |
V5BL75 | Trypanosoma cruzi | 27% | 100% |