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PMID: 16287987 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

New insights into biliverdin reductase functions: linking heme metabolism to cell signaling.

Physiology (Bethesda, Md.) ·Vol. 20 ·2005-12-00 ·Pages 382-9

Maines MD

Abstract

Biliverdin reductase (BVR) functions in cell signaling through three distinct tracks: a dual-specificity kinase that functions in the insulin receptor/MAPK pathways (25, 29, 51); a bzip-type transcription factor for ATF-2/CREB and HO-1 regulation (1, 25); and a reductase that catalyzes the conversion of biliverdin to bilirubin (27). These, together with the protein's primary and secondary features, intimately link BVR to the entire spectrum of cell-signaling cascades.

MeSH Terms
Amino Acid Sequence Animals Cell Physiological Phenomena Heme/metabolism Humans Molecular Sequence Data Oxidoreductases Acting on CH-CH Group Donors/genetics,physiology Signal Transduction/physiology
Chemicals
Heme Oxidoreductases Acting on CH-CH Group Donors biliverdin reductase
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Maines Mahin D
Department of Biochemistry and Biophysics, University of Rochester Medical Center, New York, USA. [email protected]
Article Info
Journal
Physiology (Bethesda, Md.)
Abbr.
Physiology (Bethesda)
ISSN
1548-9213
Published
2005-12-00
Pages
382-9
Language
English
Region
United States
NLM ID
101208185
Subset
IM
Grants
NIEHS NIH HHS · R01-ES-04066 · United States
NIEHS NIH HHS · R01-ES-12187 · United States
NINDS NIH HHS · R01-NS-41043 · United States
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