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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 10 |
GO:0006644 | phospholipid metabolic process | 4 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019637 | organophosphate metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044255 | cellular lipid metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008195 | phosphatidate phosphatase activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.466 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.238 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.238 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.247 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.536 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.432 |
DOC_MAPK_DCC_7 | 178 | 188 | PF00069 | 0.395 |
DOC_PP1_RVXF_1 | 139 | 145 | PF00149 | 0.508 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.497 |
LIG_14-3-3_CanoR_1 | 141 | 145 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 172 | 177 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 288 | 295 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 297 | 305 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.437 |
LIG_BIR_III_2 | 132 | 136 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.356 |
LIG_DLG_GKlike_1 | 172 | 179 | PF00625 | 0.336 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.324 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.593 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.568 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.412 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.465 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.591 |
LIG_IRF3_LxIS_1 | 180 | 187 | PF10401 | 0.440 |
LIG_LIR_Apic_2 | 251 | 255 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 243 | 251 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 43 | 52 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.659 |
LIG_LYPXL_S_1 | 69 | 73 | PF13949 | 0.358 |
LIG_LYPXL_yS_3 | 70 | 73 | PF13949 | 0.556 |
LIG_MLH1_MIPbox_1 | 159 | 163 | PF16413 | 0.286 |
LIG_PDZ_Wminus1_1 | 328 | 330 | PF00595 | 0.445 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.349 |
LIG_PTB_Apo_2 | 120 | 127 | PF02174 | 0.568 |
LIG_PTB_Phospho_1 | 120 | 126 | PF10480 | 0.568 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.536 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 45 | 49 | PF00017 | 0.605 |
LIG_SH2_SRC | 45 | 48 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.372 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.482 |
LIG_SUMO_SIM_anti_2 | 187 | 192 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 184 | 189 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 299 | 308 | PF11976 | 0.374 |
LIG_TYR_ITIM | 244 | 249 | PF00017 | 0.398 |
LIG_TYR_ITIM | 68 | 73 | PF00017 | 0.618 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.366 |
MOD_CDK_SPxxK_3 | 290 | 297 | PF00069 | 0.487 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.544 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.508 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.545 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.538 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.639 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.237 |
MOD_DYRK1A_RPxSP_1 | 290 | 294 | PF00069 | 0.449 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.308 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.413 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.683 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.673 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.236 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.548 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.508 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.351 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.475 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.459 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.467 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.583 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.666 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.397 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.290 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.342 |
MOD_PKA_1 | 310 | 316 | PF00069 | 0.492 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.508 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.445 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.544 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.467 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.406 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.436 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.383 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.337 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.343 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.491 |
MOD_SUMO_rev_2 | 245 | 255 | PF00179 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 318 | 322 | PF00026 | 0.688 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P344 | Leptomonas seymouri | 59% | 84% |
A0A3Q8ID01 | Leishmania donovani | 32% | 89% |
A0A3Q8IK66 | Leishmania donovani | 88% | 82% |
A4HA84 | Leishmania braziliensis | 72% | 100% |
A4HXR8 | Leishmania infantum | 32% | 89% |
A4HYG7 | Leishmania infantum | 88% | 82% |
E9AS87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
Q4QD76 | Leishmania major | 85% | 100% |