Yoshida, L S <br/><br/>
Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase.  [electronic resource] 

 -  The Journal of biological chemistry  Oct 1998 
 - 27879-86 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-9258 
<br/><br/><label>Standard No.: </label>10.1074/jbc.273.43.27879  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Binding Sites<br/>Biological Transport<br/>Child, Preschool<br/>Cytochrome b Group--biosynthesis<br/>Cytosol--metabolism<br/>Ferredoxin-NADP Reductase--metabolism<br/>Flavin-Adenine Dinucleotide--analysis<br/>Genetic Linkage<br/>Granulomatous Disease, Chronic--genetics<br/>Heme--analysis<br/>Histidine--genetics<br/>Humans<br/>Male<br/>Membrane Glycoproteins--genetics<br/>Membrane Transport Proteins<br/>Molecular Sequence Data<br/>Mutation<br/>NADPH Dehydrogenase--analysis<br/>NADPH Oxidase 2<br/>NADPH Oxidases--biosynthesis<br/>Neutrophils--enzymology<br/>Phosphoproteins--analysis<br/>Sequence Homology, Amino Acid<br/>Sex Chromosome Aberrations--genetics<br/>Superoxides--metabolism<br/>X Chromosome