A functional heme-binding site of soluble guanylyl cyclase requires intact N-termini of α1 and β1 subunits

European Journal of Biochemistry

Volumn 240, Issue 2, 1996, Pages 380-386

  Koesling, D ^a  

^a FREIE UNIVERSITÄT BERLIN   (Germany)

Author keywords

cGMP; Guanylyl cyclase; Heme proteins; Nitric oxide

Indexed keywords

GUANYLATE CYCLASE; HEME; NITRIC OXIDE; PROTOPORPHYRIN;

ANIMAL TISSUE; ARTICLE; CATTLE; CONTROLLED STUDY; DELETION MUTANT; ENZYME ACTIVITY; ENZYME BINDING; ENZYME PURIFICATION; ENZYME SUBUNIT; GENE CONSTRUCT; LUNG; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; ULTRAVIOLET SPECTROPHOTOMETRY;

ANIMALIA; BOS TAURUS; HUMBERT;

EID: 0029808345     PISSN: 00142956     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1432-1033.1996.0380h.x     Document Type: Article

References (4)

1. Garbers, D. L., Koesling, D. & Schultz, G. (1994) Mol. Biol. Cell 5, 1-5.
2. Garbers, D. L. & Löwe, D. G. (1994) J. Biol. Chem. 269, 30741-30744.
3. Stone, J. R. & Marletta, M. A. (1994) Biochemistry 33, 5636-5640.
4. Stone, J. R., Sands, R. H., Dunham, W. R. & Marletta, M. A. (1995) Biochem. Biophys. Res. Commun. 207, 572-577.