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Function

PDE5 is an phosphodiesterase : this enzyme catalyzes the hydrolysis of cGMP into 5'GMP. CGMP is an usual second messager in cell transduction. PDE5 regulates its concentration by hydrolysis. Human PDE5 is a PDE of class I. PDE5 function affects the smooth muscle, blood vessels or penis, uterus and intestines.

Structural highlights

PDE5 is a homodimeric protein of 875 amino acids long. This protein is composed of several important domains: pol-GLY (10-24 amino acids) in Ntermini (structural importance).

• • GAFA (164-314 amino acids)
  • GAFB (346-503 amino acids)
  • Catalytic domain (588-853 amino acids) in Ctermini involved in cGMP hydrolysis.

The full structure of PDE5 has not been crystallized contrary to this of isolated domains of the protein. GAFA and GAFB are homologous domains and allosteric binding site of cGMP.

Catalytic activity

PDE5 is a phosphodiesterase. cGMP could bind the catalytic domain thanks to hydrogen bonds made with Gln775 and Gln817 and coordination bonds made with Zn2+ and Mg2+ in the catalytic site. To see these interactions, report to Sildenafil in Inhibitors and medical application. cGMP is hydrolyzed in GMP. The catalytic chemical reaction deals with breaking a phosphodiester bound in cGMP between the 3'O of the guanoside and the phosphate of cGMP: cGMP + H20 => GMP.

Some residues could be affected by post traductional modifications :

phosphorylation : S60, S86, S92, S102, S104, S108, T111, T127, T137, S869. acylation : K364. ubiquitinylation : K714. The ubiquitinylation of (in fushia) and the phosphorylation of are involved in the binding of cGMP to PDE5 catalytic domain.

Inhibitors and medical application

Inhibitors of PDE5 prevent cGMP from binding the catalytic site by competititve inhibition. They have more affinity for this domain than cGMP. Sildenafil (active substance of Viagra) binds to PDE5 catalytic domain through: hydrogen bonds made between Gln775 and Gln817 of PDE5 (green) and (red) coordination bond made with coordination made with

Allosteric activation

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