Distinctively related to eukaryotic PLPP enzymes.. This family of protens expanded considerably in Kinetoplastids (might be due to metabolic dependence on host lipids)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 23 |
GO:0110165 | cellular anatomical entity | 1 | 23 |
Related structures:
AlphaFold database: A4HA84
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 23 |
GO:0006644 | phospholipid metabolic process | 4 | 23 |
GO:0006793 | phosphorus metabolic process | 3 | 23 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 23 |
GO:0008152 | metabolic process | 1 | 23 |
GO:0009987 | cellular process | 1 | 23 |
GO:0019637 | organophosphate metabolic process | 3 | 23 |
GO:0044237 | cellular metabolic process | 2 | 23 |
GO:0044238 | primary metabolic process | 2 | 23 |
GO:0044255 | cellular lipid metabolic process | 3 | 23 |
GO:0071704 | organic substance metabolic process | 2 | 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008195 | phosphatidate phosphatase activity | 6 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 3 |
GO:0016791 | phosphatase activity | 5 | 3 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.313 |
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.360 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.249 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.788 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.222 |
DEG_APCC_DBOX_1 | 143 | 151 | PF00400 | 0.540 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.341 |
DOC_MAPK_DCC_7 | 248 | 258 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 206 | 214 | PF00069 | 0.464 |
DOC_PP1_RVXF_1 | 209 | 215 | PF00149 | 0.452 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.339 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.670 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.400 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 248 | 254 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 309 | 316 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 367 | 375 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.265 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.317 |
LIG_deltaCOP1_diTrp_1 | 20 | 28 | PF00928 | 0.152 |
LIG_DLG_GKlike_1 | 242 | 249 | PF00625 | 0.301 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.509 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.407 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.390 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.279 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.546 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.657 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.524 |
LIG_IRF3_LxIS_1 | 250 | 257 | PF10401 | 0.327 |
LIG_LIR_Apic_2 | 374 | 378 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 195 | 205 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.176 |
LIG_LIR_Gen_1 | 245 | 254 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 286 | 296 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 313 | 321 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 8 | 12 | PF02991 | 0.509 |
LIG_LYPXL_S_1 | 139 | 143 | PF13949 | 0.383 |
LIG_LYPXL_yS_3 | 140 | 143 | PF13949 | 0.581 |
LIG_MLH1_MIPbox_1 | 229 | 233 | PF16413 | 0.198 |
LIG_PCNA_yPIPBox_3 | 153 | 166 | PF02747 | 0.385 |
LIG_PDZ_Wminus1_1 | 398 | 400 | PF00595 | 0.550 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.341 |
LIG_Pex14_2 | 76 | 80 | PF04695 | 0.384 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.606 |
LIG_PTB_Apo_2 | 190 | 197 | PF02174 | 0.561 |
LIG_PTB_Phospho_1 | 190 | 196 | PF10480 | 0.561 |
LIG_SH2_CRK | 197 | 201 | PF00017 | 0.486 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.535 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 65 | 70 | PF11976 | 0.333 |
LIG_TYR_ITIM | 138 | 143 | PF00017 | 0.612 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.456 |
LIG_WRC_WIRS_1 | 289 | 294 | PF05994 | 0.394 |
LIG_WRC_WIRS_1 | 372 | 377 | PF05994 | 0.430 |
MOD_CDK_SPK_2 | 120 | 125 | PF00069 | 0.691 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.604 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.442 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.480 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.348 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.371 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.251 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.242 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.348 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.152 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.725 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.761 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.749 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.689 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.456 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.345 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.380 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.480 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.376 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.475 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.524 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.508 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.378 |
MOD_LATS_1 | 41 | 47 | PF00433 | 0.325 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.403 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.424 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.247 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.292 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.354 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.434 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.385 |
MOD_PKA_1 | 358 | 364 | PF00069 | 0.571 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.439 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.489 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.561 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.557 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.387 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.302 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.374 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.268 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.315 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.304 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.318 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.611 |
MOD_SUMO_rev_2 | 315 | 325 | PF00179 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.345 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.714 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.275 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.741 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P344 | Leptomonas seymouri | 60% | 100% |
A0A0N1I1J3 | Leptomonas seymouri | 29% | 100% |
A0A0S4JH63 | Bodo saltans | 31% | 100% |
A0A1X0P677 | Trypanosomatidae | 37% | 100% |
A0A1X0P6S8 | Trypanosomatidae | 33% | 100% |
A0A1X0P729 | Trypanosomatidae | 33% | 100% |
A0A3Q8ID01 | Leishmania donovani | 29% | 100% |
A0A3Q8IK66 | Leishmania donovani | 71% | 100% |
A0A3S5IRX0 | Trypanosoma rangeli | 40% | 100% |
A0A422MQK2 | Trypanosoma rangeli | 37% | 100% |
A4H9I2 | Leishmania braziliensis | 31% | 99% |
A4HXR8 | Leishmania infantum | 29% | 100% |
A4HYG7 | Leishmania infantum | 71% | 100% |
C9ZUG5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZZW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A051 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AS87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
E9AS88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
O08564 | Rattus norvegicus | 26% | 100% |
O14494 | Homo sapiens | 27% | 100% |
O88956 | Cavia porcellus | 29% | 100% |
P60588 | Sus scrofa | 26% | 100% |
Q4QD76 | Leishmania major | 70% | 100% |
Q61469 | Mus musculus | 29% | 100% |
Q86AF0 | Dictyostelium discoideum | 24% | 100% |
Q9UUA6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q9ZU49 | Arabidopsis thaliana | 26% | 100% |
V5B5J9 | Trypanosoma cruzi | 40% | 100% |
V5BM01 | Trypanosoma cruzi | 33% | 100% |
V5BWA7 | Trypanosoma cruzi | 31% | 100% |