Search Results
Overview
| Uniprot ID | Q02218 |
|---|---|
| Protein Name | 2-oxoglutarate dehydrogenase complex component E1 |
| Gene Name | OGDH |
| Organism | Homo sapiens |
Kla Sites from experimental identification
| Position | Flanking peptide |
|---|---|
| 1000 | APATGNKKTHLTELQ |
| 488 | EAVMYVCKVAAEWRS |
| 561 | EYEEEISKYDKICEE |
| 564 | EEISKYDKICEEAFA |
| 852 | QILLPFRKPLIIFTP |
| 899 | AQNPENVKRLLFCTG |
| 970 | QGYYDYVKPRLRTTI |
Function
2-oxoglutarate dehydrogenase (E1o) component of the 2-oxoglutarate dehydrogenase complex (OGDHC) (PubMed:24495017, PubMed:25210035, PubMed:28435050). Participates in the first step, rate limiting for the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) catalyzed by the whole OGDHC (PubMed:24495017, PubMed:25210035, PubMed:28435050). Catalyzes the irreversible decarboxylation of 2-oxoglutarate (alpha-ketoglutarate) via the thiamine diphosphate (ThDP) cofactor and subsequent transfer of the decarboxylated acyl intermediate on an oxidized dihydrolipoyl group that is covalently amidated to the E2 enzyme (dihydrolipoyllysine-residue succinyltransferase or DLST) (PubMed:24495017, PubMed:25210035, PubMed:28435050, PubMed:35272141). Plays a key role in the Krebs (citric acid) cycle, which is a common pathway for oxidation of fuel molecules, including carbohydrates, fatty acids, and amino acids (PubMed:25210035). Can catalyze the decarboxylation of 2-oxoadipate in vitro, but at a much lower rate than 2-oxoglutarate (PubMed:28435050). Can also convert 2-keto-4-hydroxyglutarate (KHG) and CoA into malyl-CoA (By similarity). Mainly active in the mitochondrion (PubMed:29211711). A fraction of the 2-oxoglutarate dehydrogenase complex also localizes in the nucleus and is required for lysine succinylation of histones: associates with KAT2A on chromatin and provides succinyl-CoA to histone succinyltransferase KAT2A (PubMed:29211711)
Protein Sequence
Gene Ontology
| Classification | GO ID | Description |
|---|---|---|
| Cellular Component | GO:0005759 | mitochondrial matrix |
| Cellular Component | GO:0031966 | mitochondrial membrane |
| Cellular Component | GO:0005739 | mitochondrion |
| Cellular Component | GO:0005634 | nucleus |
| Cellular Component | GO:0045252 | oxoglutarate dehydrogenase complex |
| Molecular Function | GO:0016831 | carboxy-lyase activity |
| Molecular Function | GO:0031072 | heat shock protein binding |
| Molecular Function | GO:0046872 | metal ion binding |
| Molecular Function | GO:0004591 | oxoglutarate dehydrogenase (succinyl-transferring) activity |
| Molecular Function | GO:0051087 | protein-folding chaperone binding |
| Molecular Function | GO:0030976 | thiamine pyrophosphate binding |
| Biological Process | GO:0120551 | 2-oxoglutarate decarboxylation to succinyl-CoA |
| Biological Process | GO:0006103 | 2-oxoglutarate metabolic process |
| Biological Process | GO:0021695 | cerebellar cortex development |
| Biological Process | GO:0006091 | generation of precursor metabolites and energy |
| Biological Process | GO:0006096 | glycolytic process |
| Biological Process | GO:0021766 | hippocampus development |
| Biological Process | GO:0061034 | olfactory bulb mitral cell layer development |
| Biological Process | GO:0021860 | pyramidal neuron development |
| Biological Process | GO:0021756 | striatum development |
| Biological Process | GO:0006104 | succinyl-CoA metabolic process |
| Biological Process | GO:0022028 | tangential migration from the subventricular zone to the olfactory bulb |
| Biological Process | GO:0021794 | thalamus development |
| Biological Process | GO:0006099 | tricarboxylic acid cycle |
Reference
[1] Yang Z, Yan C, Ma J, Peng P, Ren X et al.. Lactylome analysis suggests lactylation-dependent mechanisms of metabolic adaptation in hepatocellular carcinoma.. Nat Metab 5(1):61-79. 2023 Jan. PMID: 36593272.
[2] Shi CM, Wang QC, Li XL, Yang YH, Tang XY et al.. Global Profiling of Protein Lactylation in Human Hippocampi.. Proteomics Clin Appl 19(2):e202400061. 2025 Mar. PMID: 39610256.
[3] He J, Lai T, Zhou Z, Yang H, Lei Z et al.. Multiomics profiling reveals the involvement of protein lactylation in nonhomologous end joining pathway conferring radioresistance in lung adenocarcinoma cell.. Sci Rep 15(1):24651. 2025 Jul 9. PMID: 40634431.