Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
dihydrolipoamide S-acetyltransferase
Summary
- Gene Symbol
-
- DLAT
- Aliases
-
- E2
- E2 component of pyruvate dehydrogenase complex
- PDC-E2
- dihydrolipoyllysine-residue acetyltransferase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Acyltransferase
- Glucose metabolism
- Lipoyl
- Mitochondrion
- Phosphoprotein
- Pyruvate
- Reference proteome
- Repeat
- Transit peptide
- Tricarboxylic acid cycle
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose metabolic process | ||
| acetyl-CoA biosynthetic process from pyruvate | ||
| tricarboxylic acid cycle |
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound biosynthetic process [inference]
organonitrogen compound metabolic process [inference]
biosynthetic process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound biosynthetic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound biosynthetic process [inference]
cellular biosynthetic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle biosynthetic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
organophosphate metabolic process [inference]
organic cyclic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
purine-containing compound metabolic process [inference]
organonitrogen compound metabolic process [inference]
organic substance biosynthetic process [inference]
cellular process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound biosynthetic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound biosynthetic process [inference]
cellular biosynthetic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle biosynthetic process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| intracellular membrane-bounded organelle | ||
| mitochondrial pyruvate dehydrogenase complex |
|
|
| pyruvate dehydrogenase complex | ||
| mitochondrial matrix | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| dihydrolipoyllysine-residue acetyltransferase activity | ||
| pyruvate dehydrogenase (NAD+) activity | ||
| protein binding | ||
| identical protein binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:3459 | breast carcinoma | |
| DOID:3571 | liver cancer | |
| DOID:3649 | pyruvate decarboxylase deficiency | |
| DOID:3650 | lactic acidosis | |
| DOID:3651 | pyruvate carboxylase deficiency disease | |
| DOID:3891 | placental insufficiency | |
| DOID:409 | liver disease | |
| DOID:417 | autoimmune disease | |
| DOID:418 | systemic scleroderma | |
| DOID:419 | scleroderma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002355 | Difficulty walking |
| HP:0002395 | Lower limb hyperreflexia |
| HP:0002454 | Eye of the tiger anomaly of globus pallidus |
| HP:0002465 | Poor speech |
| HP:0002928 | Decreased activity of the pyruvate dehydrogenase complex |
| HP:0003128 | Lactic acidosis |
| HP:0003487 | Babinski sign |
| HP:0003593 | Infantile onset |
| HP:0004302 | Functional motor deficit |
| HP:0005656 | Positional foot deformity |
| Disease ID | Disease Name |
|---|---|
| ORPHA:79244 |
|
| OMIM:245348 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002413
- Gene Name
- dihydrolipoamide S-acetyltransferase
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 549074 | Xenbase:XB-GENE-982534 | ||
| 101941556 | CHRPI18059 | ||
| 109318080 | CROPO23367 | ||
| 100549645 | MELGA08147 | ||
| 100078104 | ORNAN03269 | ||
| 100412039 | CALJA04831 | ||
| 102131289 | MACFA10342 | ||
| 710930 | MACMU10947 | ||
| 101010313 | PAPAN07312 | ||
| 101137170 | GORGO02579 |
