Selective Oxidation of Vitamin D<sub>3</sub> Enhanced by Long-Range Effects of a Substrate Channel Mutation in Cytochrome P450<sub>BM3</sub> (CYP102A1). [PDF]
Chen W +4 more
europepmc +1 more source
Diversity of estrogen biodegradation pathways and application in environmental bioremediation. [PDF]
Hashem JS +3 more
europepmc +1 more source
Immunomodulatory Mechanisms and Therapeutic Potential of Vitamin D in Immune Thrombocytopenia. [PDF]
Ma Y +9 more
europepmc +1 more source
Salicylic acid modulates its catabolic enzymes via proteasomal degradation linked to SCF-associated proximity networks. [PDF]
Hamada N +10 more
europepmc +1 more source
Immunometabolic programming of macrophages in asthma pathogenesis and therapy. [PDF]
Lu L +5 more
europepmc +1 more source
Studies on adrenal steroid hydroxylases. Complex formation of the hydroxylase components.
J W, Chu, T, Kimura
openaire +1 more source
Molecular Cloning of Steroid Hydroxylases
Endocrine Research, 1984Recombinant plasmids specific for bovine adrenocortical cytochromes P-450scc and P-45011 beta have been identified and characterized. Using these cDNA inserts as probes, it is found that tissue specificity of gene expression for these two proteins is as expected. Cytochrome P-450scc mRNA is found in adrenocortical and corpus luteum RNA while cytochrome
Vijayakumar Boggaram +2 more
exaly +3 more sources
Studies on Adrenal Steroid Hydroxylases
Tokuji Kimura
exaly +4 more sources
Role of microsomal steroid hydroxylases in Δ7-steroid biosynthesis
Biochemistry (Moscow), 2013CYP17 (steroid 17α-hydroxylase/17,20-lyase) is a key enzyme in steroid hormone biosynthesis. It catalyzes two independent reactions at the same active center and has a unique ability to differentiate Δ(4)-steroids and Δ(5)-steroids in the 17,20-lyase reaction.
T A, Sushko +3 more
openaire +2 more sources
Enzyme-activated inhibitors of steroidal hydroxylases
The Journal of Steroid Biochemistry and Molecular Biology, 1995Cytochrome P450 monooxygenases (CYP450) of the steroid biosynthetic pathways are highly substrate specific in comparison to the variable specificities of hepatic CYP450 enzymes. Both groups of enzymes catalyze the reductive cleavage of molecular oxygen with transfer of oxygen to the substrate to form hydroxylated derivatives.
J O, Johnston, C L, Wright, G W, Holbert
openaire +2 more sources

