EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
1.14.14.138 | lithocholate + [reduced NADPH-hemoprotein reductase] + O2 |
- |
Rattus norvegicus |
6beta-hydroxylithocholate + [oxidized NADPH-hemoprotein reductase] + H2O |
- |
? |
1.14.14.138 | lithocholate + [reduced NADPH-hemoprotein reductase] + O2 |
- |
Mesocricetus auratus |
6beta-hydroxylithocholate + [oxidized NADPH-hemoprotein reductase] + H2O |
- |
? |
1.14.14.138 | lithocholate + [reduced NADPH-hemoprotein reductase] + O2 |
a STAT factor mediates the sexually dimorphic regulation of hepatic cytochrome P450 3A10/lithocholic acid 6beta-hydroxylase gene expression by growth hormone |
Mesocricetus auratus |
6beta-hydroxylithocholate + [oxidized NADPH-hemoprotein reductase] + H2O |
- |
? |
1.14.14.138 | lithocholate + [reduced NADPH-hemoprotein reductase] + O2 |
in male hamsters, 6beta-hydroxylation is the major pathway for detoxification of lithocholate. Likely CYP3A10 is responsible for this activity |
Mesocricetus auratus |
6beta-hydroxylithocholate + [oxidized NADPH-hemoprotein reductase] + H2O |
- |
? |
1.14.14.138 | lithocholate + [reduced NADPH-hemoprotein reductase] + O2 |
the male-specific P450 catalyzes the reaction. The pattern of growth hormone secretion is directly responsible for male-specific expression of this gene. STAT 5a and STAT 5b mediates GH-dependent regulation of CYP3A10/6beta-hydroxylase promoter activity |
Mesocricetus auratus |
6beta-hydroxylithocholate + [oxidized NADPH-hemoprotein reductase] + H2O |
- |
? |
1.14.14.138 | more |
hydroxylations of bile acids by reconstituted systems from rat liver microsomes |
Rattus norvegicus |
? |
- |
? |