Functional Characterization of Drosophila melanogaster CYP6A8 Fatty Acid Hydroxylase
Author:
Affiliation:
1. Department of Biological Sciences, Konkuk University, Seoul 05025, Republic of Korea
2. College of Pharmacy, Chung Ang University, Seoul 06974, Republic of Korea
Funder
National Research Foundation of Korea
Publisher
The Korean Society of Applied Pharmacology
Subject
Drug Discovery,Pharmacology,Molecular Medicine,Biochemistry
Link
http://pdf.medrang.co.kr/BT2/2023/031/BT031-01-82.pdf
Reference27 articles.
1. Requirement for ω and (ω–1)-hydroxylations of fatty acids by human cytochromes P450 2E1 and 4A11
2. Point mutations associated with insecticide resistance in the Drosophila cytochrome P450 Cyp6a2 enable DDT metabolism
3. CYP4A11 is repressed by retinoic acid in human liver cells
4. The catalytic site of rat hepatic lauric acid omega-hydroxylase. Protein versus prosthetic heme alkylation in the omega-hydroxylation of acetylenic fatty acids.
5. The Hinge Segment of Human NADPH-Cytochrome P450 Reductase in Conformational Switching: The Critical Role of Ionic Strength
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