Home LiteratureArticle Details
PMID: 8940153 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Hormone-sensitive lipase is structurally related to acetylcholinesterase, bile salt-stimulated lipase, and several fungal lipases. Building of a three-dimensional model for the catalytic domain of hormone-sensitive lipase.

The Journal of biological chemistry ·Vol. 271 ·No. 49 ·1996-12-06 ·Pages 31426-30

Contreras JA, Karlsson M, Osterlund T, Laurell H, Svensson A, Holm C

Abstract

Hormone-sensitive lipase is the key enzyme in the mobilization of fatty acids from adipose tissue, thereby playing a crucial role in the overall energy homeostasis in mammals. Its activity is stimulated by catecholamines through cAMP-dependent phosphorylation of a single serine, a process that is prevented by insulin. This regulatory property is unique to this enzyme among all known lipases and has been acquired during evolution through insertion of a regulatory module into an ancestral lipase. Sequence alignments have failed to detect significant homology between hormone-sensitive lipase and the rest of the mammalian lipases and esterases, to which this enzyme is only very distantly related. In the present work, we report the finding of a remarkable secondary structure homology between hormone-sensitive lipase and the enzymes from a superfamily of esterases and lipases that includes acetylcholinesterase, bile salt-stimulated lipase, and several fungal lipases. This finding, based on the identification of the secondary structure elements in the hormone-sensitive lipase sequence, has allowed us to construct a three-dimensional model for the catalytic domain of hormone-sensitive lipase. The model reveals the topological organization, predicts the components of the catalytic triad, suggests a three-dimensional localization of the regulatory module, and provides a valuable tool for the future study of structural and functional aspects of this metabolically important enzyme.

MeSH Terms
Acetylcholinesterase/chemistry Amino Acid Sequence Bile Acids and Salts/pharmacology Binding Sites Lipase/chemistry Models, Chemical Models, Molecular Molecular Sequence Data Protein Conformation Protein Structure, Secondary Sequence Alignment Sterol Esterase
Chemicals
Bile Acids and Salts Sterol Esterase Lipase Acetylcholinesterase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Contreras J A
Department of Cell and Molecular Biology, Lund University, Lund S-221 00, Sweden. cecilia.holm@medkem.lu.se
Karlsson M
Osterlund T
Laurell H
Svensson A
Holm C
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1996-12-06
Pages
31426-30
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com