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 | 33 |
GO:0110165 | cellular anatomical entity | 1 | 33 |
Related structures:
AlphaFold database: Q4QB35
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 | 8 |
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 |
GO:0003993 | acid phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.367 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.645 |
DEG_APCC_DBOX_1 | 1 | 9 | PF00400 | 0.567 |
DEG_APCC_DBOX_1 | 230 | 238 | PF00400 | 0.310 |
DEG_APCC_DBOX_1 | 446 | 454 | PF00400 | 0.209 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.608 |
DOC_ANK_TNKS_1 | 406 | 413 | PF00023 | 0.270 |
DOC_CDC14_PxL_1 | 221 | 229 | PF14671 | 0.388 |
DOC_CYCLIN_yCln2_LP_2 | 15 | 21 | PF00134 | 0.608 |
DOC_CYCLIN_yCln2_LP_2 | 310 | 313 | PF00134 | 0.201 |
DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.600 |
DOC_MAPK_NFAT4_5 | 2 | 10 | PF00069 | 0.354 |
DOC_PP1_RVXF_1 | 380 | 387 | PF00149 | 0.401 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.585 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.201 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.564 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.422 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 200 | 208 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 374 | 378 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 447 | 451 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 79 | 87 | PF00244 | 0.379 |
LIG_deltaCOP1_diTrp_1 | 349 | 356 | PF00928 | 0.295 |
LIG_EH1_1 | 501 | 509 | PF00400 | 0.370 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.312 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.284 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.327 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.333 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.285 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.360 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.450 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.328 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.295 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.283 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.317 |
LIG_GBD_Chelix_1 | 318 | 326 | PF00786 | 0.401 |
LIG_GSK3_LRP6_1 | 525 | 530 | PF00069 | 0.535 |
LIG_LIR_Gen_1 | 178 | 186 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 203 | 213 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 379 | 388 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 393 | 403 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 62 | 66 | PF02991 | 0.390 |
LIG_LYPXL_S_1 | 130 | 134 | PF13949 | 0.518 |
LIG_LYPXL_yS_3 | 131 | 134 | PF13949 | 0.300 |
LIG_LYPXL_yS_3 | 224 | 227 | PF13949 | 0.394 |
LIG_NRBOX | 4 | 10 | PF00104 | 0.412 |
LIG_PCNA_yPIPBox_3 | 263 | 271 | PF02747 | 0.280 |
LIG_Pex14_2 | 119 | 123 | PF04695 | 0.370 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.320 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.416 |
LIG_SH2_CRK | 403 | 407 | PF00017 | 0.338 |
LIG_SH2_GRB2like | 146 | 149 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 97 | 101 | PF00017 | 0.306 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.296 |
LIG_SH3_1 | 523 | 529 | PF00018 | 0.529 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.309 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.574 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.558 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.598 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.337 |
LIG_SH3_5 | 93 | 97 | PF00018 | 0.238 |
LIG_SH3_CIN85_PxpxPR_1 | 525 | 530 | PF14604 | 0.535 |
LIG_SUMO_SIM_par_1 | 316 | 321 | PF11976 | 0.306 |
LIG_UBA3_1 | 208 | 215 | PF00899 | 0.383 |
LIG_WRC_WIRS_1 | 460 | 465 | PF05994 | 0.309 |
LIG_WRC_WIRS_1 | 499 | 504 | PF05994 | 0.391 |
MOD_CDK_SPK_2 | 525 | 530 | PF00069 | 0.664 |
MOD_CDK_SPxK_1 | 479 | 485 | PF00069 | 0.391 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.327 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.338 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.344 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.309 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.402 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.556 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.368 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.365 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.416 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.784 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.187 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.497 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.542 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.519 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.573 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.457 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.499 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.530 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.574 |
MOD_GlcNHglycan | 488 | 492 | PF01048 | 0.717 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.579 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.292 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.294 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.337 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.382 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.391 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.526 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.371 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.504 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.560 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.507 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.541 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.581 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.827 |
MOD_N-GLC_2 | 373 | 375 | PF02516 | 0.547 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.331 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.287 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.305 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.411 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.333 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.314 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.328 |
MOD_NEK2_2 | 204 | 209 | PF00069 | 0.349 |
MOD_OFUCOSY | 434 | 439 | PF10250 | 0.534 |
MOD_OFUCOSY | 452 | 459 | PF10250 | 0.600 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.301 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.363 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.307 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.339 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.365 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.388 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.564 |
MOD_PKB_1 | 431 | 439 | PF00069 | 0.236 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.390 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.362 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.294 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.343 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.326 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.371 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.342 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.352 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.314 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.284 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.331 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.354 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.541 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.410 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.683 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.379 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.343 |
TRG_NES_CRM1_1 | 308 | 321 | PF08389 | 0.373 |
TRG_NLS_MonoExtC_3 | 430 | 435 | PF00514 | 0.226 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y5 | Leptomonas seymouri | 45% | 95% |
A0A0N1I756 | Leptomonas seymouri | 42% | 100% |
A0A0N1PEH4 | Leptomonas seymouri | 37% | 100% |
A0A0S4IRF5 | Bodo saltans | 24% | 81% |
A0A0S4IUV8 | Bodo saltans | 22% | 100% |
A0A0S4IV77 | Bodo saltans | 34% | 100% |
A0A0S4IXN9 | Bodo saltans | 23% | 100% |
A0A0S4JEA9 | Bodo saltans | 27% | 100% |
A0A0S4JJK3 | Bodo saltans | 27% | 100% |
A0A0S4JW09 | Bodo saltans | 28% | 100% |
A0A1X0NNY4 | Trypanosomatidae | 36% | 98% |
A0A1X0NQL4 | Trypanosomatidae | 28% | 99% |
A0A1X0NY34 | Trypanosomatidae | 25% | 100% |
A0A1X0P7V5 | Trypanosomatidae | 45% | 100% |
A0A3Q8IR23 | Leishmania donovani | 50% | 95% |
A0A3R7KSH4 | Trypanosoma rangeli | 24% | 100% |
A0A3R7MEN7 | Trypanosoma rangeli | 43% | 100% |
A0A3R7MHJ7 | Trypanosoma rangeli | 28% | 100% |
A0A3S5H827 | Leishmania donovani | 39% | 100% |
A0A3S7WXU0 | Leishmania donovani | 95% | 100% |
A0A3S7X1W4 | Leishmania donovani | 43% | 99% |
A4HCZ0 | Leishmania braziliensis | 87% | 88% |
A4HGW8 | Leishmania braziliensis | 42% | 99% |
A4HPC1 | Leishmania braziliensis | 39% | 100% |
A4HPC5 | Leishmania braziliensis | 50% | 94% |
A4HQG6 | Leishmania braziliensis | 34% | 100% |
A4HQG9 | Leishmania braziliensis | 34% | 100% |
A4I0H5 | Leishmania infantum | 95% | 100% |
A4I3Z8 | Leishmania infantum | 43% | 99% |
A4ICA5 | Leishmania infantum | 36% | 81% |
A4ICG3 | Leishmania infantum | 39% | 100% |
A4ICG5 | Leishmania infantum | 50% | 95% |
B1H1P9 | Xenopus laevis | 25% | 100% |
D0A3E0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
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) | 41% | 100% |
E9AT34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AT36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 95% |
E9AWD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B088 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 99% |
Q4Q0A9 | Leishmania major | 30% | 99% |
Q4Q1G2 | Leishmania major | 49% | 100% |
Q4Q1G4 | Leishmania major | 39% | 100% |
Q4Q7Z7 | Leishmania major | 44% | 100% |
V5BCI2 | Trypanosoma cruzi | 26% | 100% |
V5BK91 | Trypanosoma cruzi | 41% | 100% |
V5BL75 | Trypanosoma cruzi | 29% | 100% |