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: 40, no: 4 |
NetGPI | no | yes: 0, no: 44 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 32 |
GO:0110165 | cellular anatomical entity | 1 | 32 |
Related structures:
AlphaFold database: A4HQG9
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 | 154 | 158 | PF00656 | 0.305 |
CLV_C14_Caspase3-7 | 264 | 268 | PF00656 | 0.270 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.710 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 66 | 70 | PF03568 | 0.215 |
DEG_COP1_1 | 138 | 150 | PF00400 | 0.285 |
DEG_SCF_FBW7_1 | 467 | 473 | PF00400 | 0.499 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.320 |
DEG_SPOP_SBC_1 | 451 | 455 | PF00917 | 0.732 |
DOC_CKS1_1 | 254 | 259 | PF01111 | 0.281 |
DOC_CKS1_1 | 467 | 472 | PF01111 | 0.501 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.265 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.529 |
DOC_PP4_MxPP_1 | 305 | 308 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.410 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.369 |
LIG_APCC_ABBA_1 | 311 | 316 | PF00400 | 0.255 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.557 |
LIG_BIR_III_4 | 323 | 327 | PF00653 | 0.313 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.414 |
LIG_CtBP_PxDLS_1 | 479 | 483 | PF00389 | 0.509 |
LIG_eIF4E_1 | 79 | 85 | PF01652 | 0.370 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.345 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.399 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.535 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.573 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.440 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.463 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.452 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.569 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.450 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.465 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.539 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.499 |
LIG_LIR_Apic_2 | 123 | 129 | PF02991 | 0.379 |
LIG_LIR_Apic_2 | 380 | 384 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 77 | 82 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 174 | 182 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 312 | 318 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.443 |
LIG_LIR_LC3C_4 | 22 | 27 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.397 |
LIG_LYPXL_yS_3 | 227 | 230 | PF13949 | 0.528 |
LIG_Rb_pABgroove_1 | 199 | 207 | PF01858 | 0.500 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.340 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.506 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.354 |
LIG_SH2_GRB2like | 398 | 401 | PF00017 | 0.440 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 381 | 385 | PF00017 | 0.506 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.354 |
LIG_SH2_PTP2 | 328 | 331 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.377 |
LIG_SH2_STAT3 | 344 | 347 | PF00017 | 0.323 |
LIG_SH2_STAT3 | 516 | 519 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.306 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.524 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.415 |
LIG_Sin3_3 | 10 | 17 | PF02671 | 0.499 |
LIG_SUMO_SIM_par_1 | 291 | 296 | PF11976 | 0.471 |
LIG_TRAF2_1 | 512 | 515 | PF00917 | 0.486 |
MOD_CDC14_SPxK_1 | 488 | 491 | PF00782 | 0.514 |
MOD_CDK_SPxK_1 | 485 | 491 | PF00069 | 0.519 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.449 |
MOD_CDK_SPxxK_3 | 485 | 492 | PF00069 | 0.496 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.420 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.437 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.380 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.750 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.761 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.492 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.433 |
MOD_DYRK1A_RPxSP_1 | 485 | 489 | PF00069 | 0.508 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.343 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.567 |
MOD_GlcNHglycan | 212 | 216 | PF01048 | 0.362 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.432 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.380 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.347 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.468 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.439 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.704 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.532 |
MOD_GlcNHglycan | 472 | 476 | PF01048 | 0.520 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.422 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.432 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.377 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.495 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.619 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.712 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.697 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.382 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.269 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.471 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.468 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.394 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.468 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.780 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.374 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.517 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.594 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.486 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.452 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.444 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.436 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.372 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.523 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.469 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.390 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.307 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.236 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.374 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.412 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.451 |
MOD_PIKK_1 | 445 | 451 | PF00454 | 0.663 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.438 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.372 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.402 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.392 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.419 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.452 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.521 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.322 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.430 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.391 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.506 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.381 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.506 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.401 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.394 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.434 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.371 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.448 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.504 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.509 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.410 |
MOD_SUMO_rev_2 | 218 | 226 | PF00179 | 0.285 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 405 | 409 | PF00026 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 485 | 490 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 34% | 91% |
A0A0N1I756 | Leptomonas seymouri | 38% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 63% | 100% |
A0A0S4IRF5 | Bodo saltans | 23% | 78% |
A0A0S4IV77 | Bodo saltans | 33% | 100% |
A0A0S4JEA9 | Bodo saltans | 27% | 100% |
A0A0S4JJK3 | Bodo saltans | 27% | 100% |
A0A0S4JW09 | Bodo saltans | 25% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 35% | 94% |
A0A1X0NQL4 | Trypanosomatidae | 29% | 95% |
A0A1X0NY34 | Trypanosomatidae | 24% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 38% | 100% |
A0A3Q8IR23 | Leishmania donovani | 36% | 91% |
A0A3R7KSH4 | Trypanosoma rangeli | 26% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 39% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H827 | Leishmania donovani | 38% | 100% |
A0A3S7WXU0 | Leishmania donovani | 35% | 98% |
A0A3S7X1W4 | Leishmania donovani | 33% | 95% |
A4HCZ0 | Leishmania braziliensis | 35% | 100% |
A4HGW8 | Leishmania braziliensis | 35% | 100% |
A4HPC1 | Leishmania braziliensis | 37% | 100% |
A4HPC5 | Leishmania braziliensis | 37% | 100% |
A4HQG6 | Leishmania braziliensis | 99% | 100% |
A4I0H5 | Leishmania infantum | 35% | 98% |
A4I3Z8 | Leishmania infantum | 33% | 95% |
A4ICA5 | Leishmania infantum | 79% | 78% |
A4ICG3 | Leishmania infantum | 38% | 100% |
A4ICG5 | Leishmania infantum | 36% | 91% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 98% |
D0A947 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A948 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A9J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 99% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 91% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 98% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 95% |
P24638 | Mus musculus | 24% | 100% |
Q4Q0A9 | Leishmania major | 57% | 86% |
Q4Q1G2 | Leishmania major | 37% | 100% |
Q4Q1G4 | Leishmania major | 39% | 100% |
Q4Q7Z7 | Leishmania major | 34% | 100% |
Q4QB35 | Leishmania major | 34% | 100% |
Q5R8C0 | Pongo abelii | 24% | 100% |
Q9NPH0 | Homo sapiens | 24% | 100% |
V5BCI2 | Trypanosoma cruzi | 28% | 100% |
V5BIM1 | Trypanosoma cruzi | 24% | 100% |
V5BK91 | Trypanosoma cruzi | 37% | 100% |
V5BL75 | Trypanosoma cruzi | 28% | 100% |