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Atomistry » Iron » PDB 4ud6-4uh0 » 4ug7 » |
Iron in PDB 4ug7: Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)BenzonitrileEnzymatic activity of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)Benzonitrile
All present enzymatic activity of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)Benzonitrile:
1.14.13.165; Protein crystallography data
The structure of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)Benzonitrile, PDB code: 4ug7
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 4ug7:
The structure of Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)Benzonitrile 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 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)Benzonitrile
(pdb code 4ug7). 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 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)Benzonitrile, PDB code: 4ug7: Iron binding site 1 out of 1 in 4ug7Go back to Iron Binding Sites List in 4ug7
Iron binding site 1 out
of 1 in the Structure of Bacillus Subtilis Nitric Oxide Synthase in Complex with 3,5-Bis(2-(6-Amino-4-Methylpyridin-2-Yl)Ethyl)Benzonitrile
Mono view Stereo pair view
Reference:
J.K.Holden,
D.Dejam,
M.C.Lewis,
H.Huang,
S.Kang,
Q.Jing,
F.Xue,
R.B.Silverman,
T.L.Poulos.
Inhibitor Bound Crystal Structures of Bacterial Nitric Oxide Synthase. Biochemistry V. 54 4075 2015.
Page generated: Mon Aug 5 12:38:04 2024
ISSN: ISSN 0006-2960 PubMed: 26062720 DOI: 10.1021/ACS.BIOCHEM.5B00431 |
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