Protein family
Protein sequence
Protein function
Catalytic activity
EC number
EC number description
3.1.1.-
Hydrolases;
Acting on ester bonds;
Carboxylic-ester hydrolases;
3.1.1.5
Hydrolases;
Acting on ester bonds;
Carboxylic-ester hydrolases;
lysophospholipase
PDB | Resolution (Å) | PDB name |
---|
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0019369 | arachidonic acid metabolic process |
Biological Process | GO:0050482 | arachidonic acid secretion |
Biological Process | GO:0032048 | cardiolipin metabolic process |
Biological Process | GO:0006631 | fatty acid metabolic process |
Biological Process | GO:0035556 | intracellular signal transduction |
Biological Process | GO:0043651 | linoleic acid metabolic process |
Biological Process | GO:0055088 | lipid homeostasis |
Biological Process | GO:0034638 | phosphatidylcholine catabolic process |
Biological Process | GO:0046338 | phosphatidylethanolamine catabolic process |
Biological Process | GO:0001516 | prostaglandin biosynthetic process |
Biological Process | GO:1900407 | regulation of cellular response to oxidative stress |
Biological Process | GO:0070328 | triglyceride homeostasis |
Molecular Function | GO:0005524 | ATP binding |
Molecular Function | GO:0047499 | calcium-independent phospholipase A2 activity |
Molecular Function | GO:0004622 | lysophospholipase activity |
Molecular Function | GO:0102545 | phosphatidyl phospholipase B activity |
Molecular Function | GO:0008970 | phospholipase A1 activity |
Cellular Component | GO:0005789 | endoplasmic reticulum membrane |
Cellular Component | GO:0016020 | membrane |
Cellular Component | GO:0031966 | mitochondrial membrane |
Cellular Component | GO:0005739 | mitochondrion |
Cellular Component | GO:0005778 | peroxisomal membrane |
Cellular Component | GO:0005777 | peroxisome |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-1482788 | Acyl chain remodelling of PC | Leaf | R-HSA-1430728 | Metabolism |
R-HSA-1482839 | Acyl chain remodelling of PE | Leaf | R-HSA-1430728 | Metabolism |
Location | ECO term | Pubmed |
---|---|---|
Endoplasmic reticulum membrane | ECO:0000250 | PubMed:10744668 |
Endoplasmic reticulum membrane | ECO:0000250 | PubMed:10833412 |
Mitochondrion membrane | ECO:0000305 | PubMed:10744668 |
Mitochondrion membrane | ECO:0000305 | PubMed:10833412 |
Mitochondrion membrane | ECO:0000305 | PubMed:17213206 |
Peroxisome membrane | ECO:0000269 | PubMed:10744668 |
Peroxisome membrane | ECO:0000269 | PubMed:10833412 |
Peroxisome membrane | ECO:0000269 | PubMed:15695510 |
HPO ID | HPO name |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001257 | Spasticity |
HP:0001260 | Dysarthria |
HP:0001310 | Dysmetria |
HP:0001332 | Dystonia |
HP:0002151 | Increased serum lactate |
HP:0002384 | Focal impaired awareness seizure |
HP:0003128 | Lactic acidosis |
HP:0003391 | Gowers sign |
HP:0003542 | Increased serum pyruvate |
HP:0003676 | Progressive |
HP:0003701 | Proximal muscle weakness |
HP:0003737 | Mitochondrial myopathy |
HP:0011463 | Childhood onset |
HP:0012378 | Fatigue |
HP:0012446 | Decreased CSF 5-methyltetrahydrofolate concentration |
HP:0030051 | Tip-toe gait |
HP:0031962 | Elevated serum anion gap |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
mitochondrial myopathy-lactic acidosis-deafness syndrome | MONDO:0016825 | G71 | chapter6, Diseases of the nervous system | OMIM:251950 | Orphanet:2597 |