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: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
Related structures:
AlphaFold database: Q4QD76
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 22 |
GO:0006644 | phospholipid metabolic process | 4 | 22 |
GO:0006793 | phosphorus metabolic process | 3 | 22 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 22 |
GO:0008152 | metabolic process | 1 | 22 |
GO:0009987 | cellular process | 1 | 22 |
GO:0019637 | organophosphate metabolic process | 3 | 22 |
GO:0044237 | cellular metabolic process | 2 | 22 |
GO:0044238 | primary metabolic process | 2 | 22 |
GO:0044255 | cellular lipid metabolic process | 3 | 22 |
GO:0071704 | organic substance metabolic process | 2 | 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0008195 | phosphatidate phosphatase activity | 6 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 4 |
GO:0016791 | phosphatase activity | 5 | 4 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.422 |
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.351 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.701 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.701 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.664 |
DEG_APCC_DBOX_1 | 143 | 151 | PF00400 | 0.510 |
DOC_MAPK_DCC_7 | 248 | 258 | PF00069 | 0.292 |
DOC_PP1_RVXF_1 | 209 | 215 | PF00149 | 0.422 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.656 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.569 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.243 |
LIG_14-3-3_CanoR_1 | 358 | 365 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.253 |
LIG_BIR_III_2 | 202 | 206 | PF00653 | 0.423 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.281 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.334 |
LIG_DLG_GKlike_1 | 242 | 249 | PF00625 | 0.289 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.505 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.367 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.502 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.425 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.422 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.385 |
LIG_GBD_Chelix_1 | 24 | 32 | PF00786 | 0.294 |
LIG_IRF3_LxIS_1 | 24 | 31 | PF10401 | 0.400 |
LIG_IRF3_LxIS_1 | 250 | 257 | PF10401 | 0.300 |
LIG_LIR_Gen_1 | 195 | 205 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 245 | 254 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 313 | 324 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.584 |
LIG_LYPXL_S_1 | 139 | 143 | PF13949 | 0.373 |
LIG_LYPXL_yS_3 | 140 | 143 | PF13949 | 0.571 |
LIG_NRBOX | 23 | 29 | PF00104 | 0.411 |
LIG_PDZ_Wminus1_1 | 398 | 400 | PF00595 | 0.532 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.326 |
LIG_Pex14_2 | 72 | 76 | PF04695 | 0.372 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.589 |
LIG_PTB_Apo_2 | 190 | 197 | PF02174 | 0.553 |
LIG_PTB_Phospho_1 | 190 | 196 | PF10480 | 0.553 |
LIG_SH2_CRK | 197 | 201 | PF00017 | 0.474 |
LIG_SH2_NCK_1 | 115 | 119 | PF00017 | 0.718 |
LIG_SH2_SRC | 115 | 118 | PF00017 | 0.744 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.524 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.514 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.421 |
LIG_Sin3_3 | 25 | 32 | PF02671 | 0.359 |
LIG_SUMO_SIM_anti_2 | 257 | 262 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 65 | 70 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 254 | 259 | PF11976 | 0.365 |
LIG_TYR_ITIM | 138 | 143 | PF00017 | 0.599 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.447 |
LIG_WRC_WIRS_1 | 289 | 294 | PF05994 | 0.355 |
LIG_WRC_WIRS_1 | 372 | 377 | PF05994 | 0.416 |
MOD_CDK_SPxxK_3 | 360 | 367 | PF00069 | 0.530 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.423 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.502 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.412 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.546 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.530 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.501 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.492 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.505 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.288 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.212 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.314 |
MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.671 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.692 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.693 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.729 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.500 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.484 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.427 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.352 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.339 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.535 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.548 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.317 |
MOD_LATS_1 | 41 | 47 | PF00433 | 0.305 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.622 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.276 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.330 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.321 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.553 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.360 |
MOD_PKA_1 | 380 | 386 | PF00069 | 0.421 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.412 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.546 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.556 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.294 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.233 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.267 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.332 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.278 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.276 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.345 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.535 |
MOD_SUMO_rev_2 | 315 | 325 | PF00179 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.312 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.258 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.724 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.297 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P344 | Leptomonas seymouri | 58% | 100% |
A0A0N1I1J3 | Leptomonas seymouri | 30% | 100% |
A0A0S4JH63 | Bodo saltans | 33% | 100% |
A0A1X0P677 | Trypanosomatidae | 38% | 100% |
A0A1X0P6S8 | Trypanosomatidae | 32% | 100% |
A0A1X0P729 | Trypanosomatidae | 30% | 100% |
A0A3Q8ID01 | Leishmania donovani | 28% | 100% |
A0A3Q8IK66 | Leishmania donovani | 92% | 100% |
A0A3S5IRX0 | Trypanosoma rangeli | 40% | 100% |
A0A422MQK2 | Trypanosoma rangeli | 35% | 100% |
A4H9I2 | Leishmania braziliensis | 30% | 100% |
A4HA84 | Leishmania braziliensis | 70% | 100% |
A4HXR8 | Leishmania infantum | 28% | 100% |
A4HYG7 | Leishmania infantum | 92% | 100% |
C9ZUG5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZZW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A051 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AS87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9AS88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O08564 | Rattus norvegicus | 26% | 100% |
O14494 | Homo sapiens | 27% | 100% |
O88956 | Cavia porcellus | 28% | 100% |
P60588 | Sus scrofa | 27% | 100% |
Q10022 | Caenorhabditis elegans | 26% | 100% |
Q61469 | Mus musculus | 28% | 100% |
Q8K593 | Rattus norvegicus | 24% | 100% |
Q8LFD1 | Arabidopsis thaliana | 23% | 100% |
Q99JY8 | Mus musculus | 27% | 100% |
Q9DAX2 | Mus musculus | 24% | 100% |
Q9UUA6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
V5B5J9 | Trypanosoma cruzi | 37% | 100% |
V5BM01 | Trypanosoma cruzi | 34% | 100% |
V5BWA7 | Trypanosoma cruzi | 30% | 100% |