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: 42, no: 5 |
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: E9AT34
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 | 308 | 312 | PF00656 | 0.340 |
CLV_C14_Caspase3-7 | 331 | 335 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.427 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.595 |
DOC_CDC14_PxL_1 | 226 | 234 | PF14671 | 0.488 |
DOC_MAPK_gen_1 | 145 | 151 | PF00069 | 0.269 |
DOC_MAPK_gen_1 | 507 | 516 | PF00069 | 0.695 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.638 |
DOC_PP1_RVXF_1 | 1 | 8 | PF00149 | 0.754 |
DOC_PP4_MxPP_1 | 317 | 320 | PF00568 | 0.429 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.550 |
DOC_USP7_UBL2_3 | 505 | 509 | PF12436 | 0.652 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.605 |
LIG_14-3-3_CanoR_1 | 111 | 119 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 180 | 185 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 392 | 402 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 427 | 436 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 85 | 93 | PF00244 | 0.437 |
LIG_APCC_ABBA_1 | 384 | 389 | PF00400 | 0.382 |
LIG_BIR_III_4 | 372 | 376 | PF00653 | 0.497 |
LIG_BRCT_BRCA1_1 | 133 | 137 | PF00533 | 0.364 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.369 |
LIG_Clathr_ClatBox_1 | 181 | 185 | PF01394 | 0.282 |
LIG_Clathr_ClatBox_1 | 413 | 417 | PF01394 | 0.305 |
LIG_deltaCOP1_diTrp_1 | 498 | 506 | PF00928 | 0.537 |
LIG_DLG_GKlike_1 | 180 | 187 | PF00625 | 0.266 |
LIG_eIF4E_1 | 268 | 274 | PF01652 | 0.426 |
LIG_eIF4E_1 | 407 | 413 | PF01652 | 0.281 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.413 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.444 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.386 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.426 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.459 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.419 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.415 |
LIG_GBD_Chelix_1 | 270 | 278 | PF00786 | 0.535 |
LIG_LIR_Apic_2 | 153 | 157 | PF02991 | 0.404 |
LIG_LIR_Apic_2 | 405 | 410 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 183 | 192 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 340 | 347 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 389 | 398 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 101 | 105 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 389 | 393 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.456 |
LIG_MLH1_MIPbox_1 | 133 | 137 | PF16413 | 0.407 |
LIG_MLH1_MIPbox_1 | 245 | 249 | PF16413 | 0.232 |
LIG_NRBOX | 269 | 275 | PF00104 | 0.424 |
LIG_PCNA_yPIPBox_3 | 117 | 130 | PF02747 | 0.287 |
LIG_PDZ_Class_2 | 511 | 516 | PF00595 | 0.601 |
LIG_Pex14_2 | 321 | 325 | PF04695 | 0.343 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.286 |
LIG_Pex14_2 | 98 | 102 | PF04695 | 0.288 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.257 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.555 |
LIG_SH2_PTP2 | 343 | 346 | PF00017 | 0.451 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.393 |
LIG_SH2_SRC | 407 | 410 | PF00017 | 0.365 |
LIG_SH2_SRC | 450 | 453 | PF00017 | 0.462 |
LIG_SH2_SRC | 81 | 84 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 69 | 72 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.454 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.308 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.345 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.446 |
LIG_Sin3_3 | 271 | 278 | PF02671 | 0.268 |
LIG_SUMO_SIM_par_1 | 303 | 308 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 325 | 331 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 417 | 425 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 479 | 484 | PF11976 | 0.329 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.418 |
LIG_UBA3_1 | 74 | 80 | PF00899 | 0.258 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.420 |
LIG_WRC_WIRS_1 | 181 | 186 | PF05994 | 0.267 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.425 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.390 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.537 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.466 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.505 |
MOD_Cter_Amidation | 143 | 146 | PF01082 | 0.674 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.583 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.686 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.646 |
MOD_GlcNHglycan | 294 | 298 | PF01048 | 0.594 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.594 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.754 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.352 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.378 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.369 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.430 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.301 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.311 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.368 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.531 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.431 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.604 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.611 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.638 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.608 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.580 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.499 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.592 |
MOD_N-GLC_1 | 441 | 446 | PF02516 | 0.664 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.768 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.618 |
MOD_N-GLC_2 | 383 | 385 | PF02516 | 0.597 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.382 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.419 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.417 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.348 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.439 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.303 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.318 |
MOD_NEK2_2 | 201 | 206 | PF00069 | 0.454 |
MOD_NEK2_2 | 402 | 407 | PF00069 | 0.403 |
MOD_OFUCOSY | 440 | 445 | PF10250 | 0.585 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.470 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.397 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.512 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.399 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.367 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.478 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.436 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.369 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.389 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.389 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.454 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.406 |
MOD_Plk_2-3 | 328 | 334 | PF00069 | 0.292 |
MOD_Plk_2-3 | 425 | 431 | PF00069 | 0.310 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.425 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.361 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.327 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.436 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.395 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.407 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.437 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.407 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.349 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.376 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.323 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.601 |
MOD_SUMO_for_1 | 166 | 169 | PF00179 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.455 |
TRG_DiLeu_LyEn_5 | 227 | 232 | PF01217 | 0.429 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.744 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.524 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.621 |
TRG_NES_CRM1_1 | 315 | 328 | PF08389 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.679 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 34% | 90% |
A0A0N1I756 | Leptomonas seymouri | 65% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 38% | 100% |
A0A0S4IRF5 | Bodo saltans | 24% | 77% |
A0A0S4IUV8 | Bodo saltans | 24% | 100% |
A0A0S4IV77 | Bodo saltans | 34% | 99% |
A0A0S4JEA9 | Bodo saltans | 25% | 100% |
A0A0S4JJK3 | Bodo saltans | 29% | 100% |
A0A0S4JW09 | Bodo saltans | 28% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 36% | 93% |
A0A1X0NQL4 | Trypanosomatidae | 27% | 94% |
A0A1X0NY34 | Trypanosomatidae | 28% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 39% | 99% |
A0A3Q8IR23 | Leishmania donovani | 39% | 90% |
A0A3R7KSH4 | Trypanosoma rangeli | 26% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 38% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 25% | 100% |
A0A3S5H827 | Leishmania donovani | 89% | 100% |
A0A3S7WXU0 | Leishmania donovani | 38% | 97% |
A0A3S7X1W4 | Leishmania donovani | 34% | 94% |
A4HCZ0 | Leishmania braziliensis | 37% | 100% |
A4HGW8 | Leishmania braziliensis | 35% | 100% |
A4HPC1 | Leishmania braziliensis | 68% | 100% |
A4HPC5 | Leishmania braziliensis | 37% | 100% |
A4HQG6 | Leishmania braziliensis | 39% | 100% |
A4HQG9 | Leishmania braziliensis | 38% | 100% |
A4I0H5 | Leishmania infantum | 38% | 97% |
A4I3Z8 | Leishmania infantum | 34% | 94% |
A4ICA5 | Leishmania infantum | 36% | 77% |
A4ICG3 | Leishmania infantum | 89% | 100% |
A4ICG5 | Leishmania infantum | 39% | 90% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 98% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 98% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 90% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 97% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 94% |
Q4Q0A9 | Leishmania major | 30% | 96% |
Q4Q1G2 | Leishmania major | 37% | 100% |
Q4Q1G4 | Leishmania major | 86% | 100% |
Q4Q7Z7 | Leishmania major | 34% | 100% |
Q4QB35 | Leishmania major | 38% | 100% |
V5BCI2 | Trypanosoma cruzi | 26% | 100% |
V5BK91 | Trypanosoma cruzi | 37% | 100% |
V5BL75 | Trypanosoma cruzi | 27% | 100% |