Structural characterization of nitric oxide synthase isoforms reveals striking active-site conservation.

Article Details

Citation

Fischmann TO, Hruza A, Niu XD, Fossetta JD, Lunn CA, Dolphin E, Prongay AJ, Reichert P, Lundell DJ, Narula SK, Weber PC

Structural characterization of nitric oxide synthase isoforms reveals striking active-site conservation.

Nat Struct Biol. 1999 Mar;6(3):233-42.

PubMed ID
10074942 [ View in PubMed
]
Abstract

Crystal structures of human endothelial nitric oxide synthase (eNOS) and human inducible NOS (iNOS) catalytic domains were solved in complex with the arginine substrate and an inhibitor S-ethylisothiourea (SEITU), respectively. The small molecules bind in a narrow cleft within the larger active-site cavity containing heme and tetrahydrobiopterin. Both are hydrogen-bonded to a conserved glutamate (eNOS E361, iNOS E377). The active-site residues of iNOS and eNOS are nearly identical. Nevertheless, structural comparisons provide a basis for design of isozyme-selective inhibitors. The high-resolution, refined structures of eNOS (2.4 A resolution) and iNOS (2.25 A resolution) reveal an unexpected structural zinc situated at the intermolecular interface and coordinated by four cysteines, two from each monomer.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Nitric oxide synthase, inducibleP35228Details
Nitric oxide synthase, endothelialP29474Details