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PMID: 10320667 Published · ppublish English Journal Article Review

Guanylate cyclase and the .NO/cGMP signaling pathway.

Biochimica et biophysica acta ·Vol. 1411 ·No. 2-3 ·1999-05-05 ·Pages 334-50

Denninger JW, Marletta MA

Abstract

Signal transduction with the diatomic radical nitric oxide (NO) is involved in a number of important physiological processes, including smooth muscle relaxation and neurotransmission. Soluble guanylate cyclase (sGC), a heterodimeric enzyme that converts guanosine triphosphate to cyclic guanosine monophosphate, is a critical component of this signaling pathway. sGC is a hemoprotein; it is through the specific interaction of NO with the sGC heme that sGC is activated. Over the last decade, much has been learned about the unique heme environment of sGC and its interaction with ligands like NO and carbon monoxide. This review will focus on the role of sGC in signaling, its relationship to the other nucleotide cyclases, and on what is known about sGC genetics, heme environment and catalysis. The latest understanding in regard to sGC will be incorporated to build a model of sGC structure, activation, catalytic mechanism and deactivation.

MeSH Terms
Animals Catalysis Cell Line Cyclic GMP/chemistry,metabolism Enzyme Activation Free Radicals/chemistry Gene Expression Guanylate Cyclase/chemistry,genetics,metabolism Humans Models, Chemical Nitric Oxide/chemistry,metabolism Nitric Oxide Synthase/chemistry Signal Transduction Structure-Activity Relationship
Chemicals
Free Radicals Nitric Oxide Nitric Oxide Synthase Guanylate Cyclase Cyclic GMP
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Denninger J W
5315A Medical Sciences I, Department of Biological Chemistry, University of Michigan Medical School, 1150 West Medical Center Drive, Ann Arbor, MI 48109-0606, USA.
Marletta M A
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1999-05-05
Pages
334-50
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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