pyruvate dehydrogenase E1 subunit beta
| UniProt | Protein Name |
|---|---|
| A0A384MDR8 |
|
| P11177 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose metabolic process |
|
|
| pyruvate decarboxylation to acetyl-CoA |
|
|
| pyruvate decarboxylation to acetyl-CoA |
|
|
| pyruvate decarboxylation to acetyl-CoA |
|
|
| pyruvate decarboxylation to acetyl-CoA |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus |
|
|
| nucleoplasm |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| pyruvate dehydrogenase (acetyl-transferring) activity |
|
|
| pyruvate dehydrogenase (acetyl-transferring) activity |
|
|
| pyruvate dehydrogenase (acetyl-transferring) activity |
|
|
| protein binding |
|
|
| metal ion binding |
|
|
| Gene Ontology |
|---|
| acetyl-CoA biosynthetic process from pyruvate |
| catalytic activity |
| oxidoreductase activity |
| pyruvate dehydrogenase (acetyl-transferring) activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:3649 | pyruvate decarboxylase deficiency |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001252 | Hypotonia |
| HP:0001263 | Global developmental delay |
| HP:0001265 | Hyporeflexia |
| HP:0001274 | Agenesis of corpus callosum |
| HP:0001290 | Generalized hypotonia |
| HP:0001302 | Pachygyria |
| HP:0001315 | Reduced tendon reflexes |
| Disease ID | Disease Name |
|---|---|
| ORPHA:255138 |
|
| OMIM:614111 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.5.0
Last updated: April 6, 2026