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Atomistry » Iron » PDB 5g6f-5h8y » 5g6h » |
Iron in PDB 5g6h: Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-AmineEnzymatic activity of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-Amine
All present enzymatic activity of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-Amine:
1.14.13.165; Protein crystallography data
The structure of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-Amine, PDB code: 5g6h
was solved by
J.K.Holden,
T.L.Poulos,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 5g6h:
The structure of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-Amine also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-Amine
(pdb code 5g6h). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total only one binding site of Iron was determined in the Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-Amine, PDB code: 5g6h: Iron binding site 1 out of 1 in 5g6hGo back to![]() ![]()
Iron binding site 1 out
of 1 in the Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 7-((3-(Methylamino)Methyl)Phenoxy)Methyl)Quinolin-2-Amine
![]() Mono view ![]() Stereo pair view
Reference:
J.K.Holden,
M.C.Lewis,
M.A.Cinelli,
Z.Abdullatif,
A.V.Pensa,
R.B.Silverman,
T.L.Poulos.
Targeting Bacterial Nitric Oxide Synthase with Aminoquinoline-Based Inhibitors. Biochemistry V. 55 5587 2016.
Page generated: Tue Aug 5 21:39:48 2025
ISSN: ISSN 1520-4995 PubMed: 27607918 DOI: 10.1021/ACS.BIOCHEM.6B00786 |
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