Biology:Biliverdin reductase A

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Short description: Protein-coding gene in the species Homo sapiens
biliverdin reductase A
Bilivra.jpg
Biliverdin reductase A dimer, Human
Identifiers
EC number1.3.1.24
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Biliverdin reductase A is a protein that in humans is encoded by the BLVRA gene.[1][2]

Function

The protein encoded by this gene belongs to the biliverdin reductase family, members of which catalyze the conversion of biliverdin to bilirubin in the presence of NADPH or NADH.[1]

Clinical significance

Mutations in this gene are associated with hyperbiliverdinemia.[1]

References

  1. 1.0 1.1 1.2 "Entrez Gene: Biliverdin reductase A". https://www.ncbi.nlm.nih.gov/gene/644. 
  2. Class 1 Oxidoreductases V. Springer Handbook of Enzymes. 21 (2nd ed.). Springer Science & Business Media. 2004. pp. 140–. ISBN 978-3-540-22515-7. 

External links

  • Human BLVRA genome location and BLVRA gene details page in the UCSC Genome Browser.
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Biliverdin reductase A

This article incorporates text from the United States National Library of Medicine, which is in the public domain.