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FAHD1

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Protein-coding gene in the species Homo sapiens
FAHD1
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1SAW

Identifiers
AliasesFAHD1, C16orf36, YISKL, fumarylacetoacetate hydrolase domain containing 1
External IDsOMIM: 616320; MGI: 1915886; HomoloGene: 6774; GeneCards: FAHD1; OMA:FAHD1 - orthologs
EC number4.1.1.112
Gene location (Mouse)
Chromosome 17 (mouse)
Chr.Chromosome 17 (mouse)
Chromosome 17 (mouse)Genomic location for FAHD1Genomic location for FAHD1
Band17|17 A3.3Start25,067,866 bp
End25,069,338 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • pancreatic ductal cell

  • jejunal mucosa

  • endothelial cell

  • duodenum

  • kidney

  • renal medulla

  • vastus lateralis muscle

  • human penis

  • liver

  • right ventricle
Top expressed in
  • Ileal epithelium

  • right kidney

  • human kidney

  • cardiac muscle tissue of left ventricle

  • duodenum

  • extensor digitorum longus muscle

  • interventricular septum

  • jejunum

  • plantaris muscle

  • left lobe of liver
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

81889

68636

Ensembl

n/a

ENSMUSG00000045316

UniProt

Q6P587

Q8R0F8

RefSeq (mRNA)

NM_031208
NM_001018104
NM_001142398

NM_023480

RefSeq (protein)

NP_001018114
NP_001135870
NP_112485

NP_075969

Location (UCSC)n/aChr 17: 25.07 – 25.07 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Fumarylacetoacetate hydrolase domain-containing protein 1, also known as FLJ36880 protein, is an enzyme that in humans is encoded by the FAHD1 gene on chromosome 16.


Structure

The FAHD1 gene encodes for a 24-kDa protein that is localized to the mitochondrion and belongs to the fumarylacetoacetate hydrolase family of proteins. The structure of FAHD1 has been resolved using X-ray crystallography at 2.2-Å resolution. The overall structure is similar to the C-terminal domain of the bifunctional enzyme HpcE from Escherichia coli C, fumarylacetoacetate hydrolase from Mus musculus and to YcgM (Apc5008) from E. coli 1262. A number of conserved amino acids including Asp-102 and Arg-106 of FAHD1 appear to be important for its catalytic activity.

Function

The FAHD1 protein has been shown to function as an oxaloacetate decarboxylase in eukaryotes. The FAHD1 protein probably also functions as an acylpyruvase, having been shown to catalyze the hydrolysis of acetylpyruvate and fumarylpyruvate in in vitro experiments. Mg(2+) was required for maximal enzyme activity.

References

  1. ^ GRCm38: Ensembl release 89: ENSMUSG00000045316Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Entrez Gene: FAHD1 fumarylacetoacetate hydrolase domain containing 1".
  5. ^ Manjasetty BA, Niesen FH, Delbrück H, Götz F, Sievert V, Büssow K, Behlke J, Heinemann U (2004). "X-ray structure of fumarylacetoacetate hydrolase family member Homo sapiens FLJ36880". Biol. Chem. 385 (10): 935–42. doi:10.1515/BC.2004.122. PMID 15551868. S2CID 16759973.
  6. ^ Pircher H, Straganz GD, Ehehalt D, Morrow G, Tanguay RM, Jansen-Dürr P (2011). "Identification of human fumarylacetoacetate hydrolase domain-containing protein 1 (FAHD1) as a novel mitochondrial acylpyruvase". J. Biol. Chem. 286 (42): 36500–8. doi:10.1074/jbc.M111.264770. PMC 3196145. PMID 21878618.
  7. Pircher H, von Grafenstein S, Diener T, Metzger C, Albertini E, Taferner A, Unterluggauer H, Kramer C, Liedl KR, Jansen-Dürr P (2015). "Identification of FAH domain-containing protein 1 (FAHD1) as oxaloacetate decarboxylase". J. Biol. Chem. 290 (11): 6755–62. doi:10.1074/jbc.M114.609305. PMC 4358102. PMID 25575590.

Further reading

PDB gallery
  • 1saw: X-ray structure of homo sapiens protein FLJ36880 1saw: X-ray structure of homo sapiens protein FLJ36880


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