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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
Related structures:
AlphaFold database: A4HXR8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 19 |
GO:0006644 | phospholipid metabolic process | 4 | 19 |
GO:0006793 | phosphorus metabolic process | 3 | 19 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 19 |
GO:0008152 | metabolic process | 1 | 19 |
GO:0009987 | cellular process | 1 | 19 |
GO:0019637 | organophosphate metabolic process | 3 | 19 |
GO:0044237 | cellular metabolic process | 2 | 19 |
GO:0044238 | primary metabolic process | 2 | 19 |
GO:0044255 | cellular lipid metabolic process | 3 | 19 |
GO:0071704 | organic substance metabolic process | 2 | 19 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.604 |
DEG_APCC_DBOX_1 | 203 | 211 | PF00400 | 0.268 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.372 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 211 | 217 | PF00134 | 0.337 |
DOC_MAPK_gen_1 | 165 | 174 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 198 | 207 | PF00069 | 0.321 |
DOC_MAPK_MEF2A_6 | 102 | 109 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 204 | 212 | PF00069 | 0.258 |
DOC_MAPK_MEF2A_6 | 27 | 36 | PF00069 | 0.521 |
DOC_MAPK_NFAT4_5 | 102 | 110 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 169 | 175 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 51 | 58 | PF00149 | 0.387 |
DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.337 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.315 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.365 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 171 | 175 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 225 | 233 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 281 | 290 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 308 | 314 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 187 | 203 | PF00022 | 0.406 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.322 |
LIG_eIF4E_1 | 87 | 93 | PF01652 | 0.393 |
LIG_EVH1_2 | 19 | 23 | PF00568 | 0.443 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.682 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.521 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.403 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.405 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.465 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.284 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.409 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.704 |
LIG_LIR_Apic_2 | 184 | 189 | PF02991 | 0.234 |
LIG_LIR_Apic_2 | 264 | 269 | PF02991 | 0.261 |
LIG_LIR_Apic_2 | 54 | 60 | PF02991 | 0.291 |
LIG_LIR_Apic_2 | 94 | 99 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 121 | 132 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 152 | 161 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 74 | 83 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.317 |
LIG_NRBOX | 206 | 212 | PF00104 | 0.214 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.358 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.340 |
LIG_SH2_NCK_1 | 266 | 270 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 300 | 304 | PF00017 | 0.358 |
LIG_SH2_PTP2 | 186 | 189 | PF00017 | 0.453 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.258 |
LIG_SH2_SRC | 266 | 269 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.150 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.304 |
LIG_SH3_1 | 300 | 306 | PF00018 | 0.353 |
LIG_SH3_2 | 303 | 308 | PF14604 | 0.353 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.503 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.436 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 30 | 36 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 125 | 130 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 219 | 224 | PF11976 | 0.352 |
LIG_UBA3_1 | 13 | 17 | PF00899 | 0.519 |
LIG_WRC_WIRS_1 | 252 | 257 | PF05994 | 0.369 |
LIG_WRC_WIRS_1 | 79 | 84 | PF05994 | 0.176 |
MOD_CDK_SPK_2 | 324 | 329 | PF00069 | 0.361 |
MOD_CDK_SPxxK_3 | 301 | 308 | PF00069 | 0.352 |
MOD_CDK_SPxxK_3 | 324 | 331 | PF00069 | 0.540 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.511 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.444 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.557 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.417 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.359 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.377 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.715 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.244 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.295 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.351 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.754 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.526 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.552 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.428 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.503 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.472 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.455 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.659 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.407 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.381 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.362 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.384 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.696 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.433 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.314 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.306 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.376 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.506 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.482 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.311 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.444 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.418 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.340 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.601 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.480 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.398 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.345 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.307 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.285 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.653 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.525 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.549 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.536 |
TRG_DiLeu_BaEn_1 | 274 | 279 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.313 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P344 | Leptomonas seymouri | 30% | 94% |
A0A0N1I1J3 | Leptomonas seymouri | 65% | 100% |
A0A0S4IVL2 | Bodo saltans | 32% | 100% |
A0A0S4JH63 | Bodo saltans | 39% | 100% |
A0A1X0P677 | Trypanosomatidae | 34% | 100% |
A0A1X0P729 | Trypanosomatidae | 48% | 100% |
A0A3Q8ID01 | Leishmania donovani | 100% | 100% |
A0A3Q8IK66 | Leishmania donovani | 29% | 92% |
A4H9I2 | Leishmania braziliensis | 73% | 100% |
A4HA84 | Leishmania braziliensis | 29% | 100% |
A4HYG7 | Leishmania infantum | 28% | 92% |
C9ZUG5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZZW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ARI0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9AS87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AS88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
O08564 | Rattus norvegicus | 27% | 100% |
O14494 | Homo sapiens | 27% | 100% |
O88956 | Cavia porcellus | 29% | 100% |
P60588 | Sus scrofa | 26% | 100% |
Q4QD76 | Leishmania major | 28% | 100% |
Q61469 | Mus musculus | 28% | 100% |
Q9UUA6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
V5BM01 | Trypanosoma cruzi | 39% | 100% |
V5BWA7 | Trypanosoma cruzi | 45% | 100% |