Atomic structure of PDE4: insights into phosphodiesterase mechanism and specificity.

Article Details

Citation

Xu RX, Hassell AM, Vanderwall D, Lambert MH, Holmes WD, Luther MA, Rocque WJ, Milburn MV, Zhao Y, Ke H, Nolte RT

Atomic structure of PDE4: insights into phosphodiesterase mechanism and specificity.

Science. 2000 Jun 9;288(5472):1822-5.

PubMed ID
10846163 [ View in PubMed
]
Abstract

Cyclic nucleotides are second messengers that are essential in vision, muscle contraction, neurotransmission, exocytosis, cell growth, and differentiation. These molecules are degraded by a family of enzymes known as phosphodiesterases, which serve a critical function by regulating the intracellular concentration of cyclic nucleotides. We have determined the three-dimensional structure of the catalytic domain of phosphodiesterase 4B2B to 1.77 angstrom resolution. The active site has been identified and contains a cluster of two metal atoms. The structure suggests the mechanism of action and basis for specificity and will provide a framework for structure-assisted drug design for members of the phosphodiesterase family.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
cAMP-specific 3',5'-cyclic phosphodiesterase 4BQ07343Details