Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase. [electronic resource]
Producer: 19981112Description: 27879-86 p. digitalISSN:- 0021-9258
- Amino Acid Sequence
- Binding Sites
- Biological Transport
- Child, Preschool
- Cytochrome b Group -- biosynthesis
- Cytosol -- metabolism
- Ferredoxin-NADP Reductase -- metabolism
- Flavin-Adenine Dinucleotide -- analysis
- Genetic Linkage
- Granulomatous Disease, Chronic -- genetics
- Heme -- analysis
- Histidine -- genetics
- Humans
- Male
- Membrane Glycoproteins -- genetics
- Membrane Transport Proteins
- Molecular Sequence Data
- Mutation
- NADPH Dehydrogenase -- analysis
- NADPH Oxidase 2
- NADPH Oxidases -- biosynthesis
- Neutrophils -- enzymology
- Phosphoproteins -- analysis
- Sequence Homology, Amino Acid
- Sex Chromosome Aberrations -- genetics
- Superoxides -- metabolism
- X Chromosome
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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