Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.14.19.69 extracted from

  • Zhao, B.; Waterman, M.R.; Isin, E.M.; Sundaramoorthy, M.; Podust, L.M.
    Ligand-assisted inhibition in cytochrome P450 158A2 from Streptomyces coelicolor A3(2) (2006), Biochemistry, 45, 7493-7500.
    View publication on PubMed

Crystallization (Commentary)

Crystallization (Comment) Organism
in complex with inhibitor 4-phenylimidazole, crystallization in presence of malonic acid. Diffraction to 1.5 A resolution. Presence of malonic acid affects binding behaviour and increases inhibitory potency up to 2fold. Two molecules of malonate are found above the single inhibitor molecule in the active site, linked between the BC loop and beta 1-4/beta6-1 strands via hydrogen bond interactions to stabilize the conformational changes of the BC loop and beta strands that take place upon inhibitor binding. 4-Phenylimidazole can launch an extensive hydrogen-bonding network in the region of the F/G helices which may stabilize the conformational changes Streptomyces coelicolor

Inhibitors

Inhibitors Comment Organism Structure
4-phenylimidazole crystallization data. Presence of malonic acid affects binding behaviour and increases inhibitory potency up to 2fold Streptomyces coelicolor

Organism

Organism UniProt Comment Textmining
Streptomyces coelicolor
-
isoform CYP158A2
-
Streptomyces coelicolor A3(2)
-
isoform CYP158A2
-