Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

3-hydroxyisobutyrate dehydrogenase

From Wikipedia, the free encyclopedia
(Redirected from HIBADH)

3-hydroxyisobutyrate dehydrogenase
Identifiers
EC no.1.1.1.31
CAS no.9028-39-1
Databases
BRENDAenzyme data
ExPASyNiceZyme view
KEGGenzyme entry
MetaCycmetabolic pathway
Rheareactions
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
Search
PMCarticles
PubMedarticles
NCBIproteins
HIBADH
Identifiers
AliasesHIBADH, Hibadh, 6430402H10Rik, AI265272, NS5ATP1, 3-hydroxyisobutyrate dehydrogenase
External IDsOMIM: 608475; MGI: 1889802; HomoloGene: 15088; GeneCards: HIBADH; OMA:HIBADH - orthologs
Available structures
PDBOrtholog search: PDBe RCSB
Enzyme activity
EC #BRENDAExPASyKEGGMetaCyc
1.1.1.31
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_152740

NM_145567

RefSeq (protein)

NP_689953

NP_663542

Location (UCSC)Chr 7: 27.53 – 27.66 MbChr 6: 52.52 – 52.62 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

In enzymology, a 3-hydroxyisobutyrate dehydrogenase (EC 1.1.1.31) also known as β-hydroxyisobutyrate dehydrogenase or 3-hydroxyisobutyrate dehydrogenase, mitochondrial (HIBADH) is an enzyme[5] that in humans is encoded by the HIBADH gene.[6]

3-Hydroxyisobutyrate dehydrogenase catalyzes the chemical reaction:

 
 
 
H+
Reversible left-right reaction arrow with minor forward product(s) to top right and minor reverse substrate(s) from bottom right
 
H+
 
 

The two substrates of this enzyme are 3-hydroxyisobutyric acid and oxidised nicotinamide adenine dinucleotide (NAD+). Its products are methylmalonic acid semialdehyde, reduced NADH, and a proton.[7]

This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is 3-hydroxy-2-methylpropanoate:NAD+ oxidoreductase. This enzyme participates in valine, leucine and isoleucine degradation.

Function

[edit]

3-hydroxyisobutyrate dehydrogenase is a tetrameric mitochondrial enzyme that catalyzes the NAD+-dependent, reversible oxidation of 3-hydroxyisobutyrate, an intermediate of valine catabolism, to methylmalonate semialdehyde.[6]

Structural studies

[edit]

As of late 2007, five structures have been solved for this class of enzymes, with PDB accession codes PDB: 1WP4, PDB: 2CVZ, PDB: 2GF2, PDB: 2H78, and PDB: 2I9P.

References

[edit]
  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000106049 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000029776 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Robinson WG, Coon MJ (March 1957). "The purification and properties of beta-hydroxyisobutyric dehydrogenase". The Journal of Biological Chemistry. 225 (1): 511–521. doi:10.1016/S0021-9258(18)64948-8. PMID 13416257.
  6. 1 2 "Entrez Gene: HIBADH 3-hydroxyisobutyrate dehydrogenase".
  7. Enzyme 1.1.1.31 at KEGG Pathway Database.

Further reading

[edit]
[edit]
  • Human HIBADH genome location and HIBADH gene details page in the UCSC Genome Browser.
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human 3-hydroxyisobutyrate dehydrogenase, mitochondrial