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Atomistry » Iron » PDB 3ebd-3esf » 3ekd | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Iron » PDB 3ebd-3esf » 3ekd » |
Iron in PDB 3ekd: Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3Enzymatic activity of Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3
All present enzymatic activity of Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3:
1.14.14.1; Protein crystallography data
The structure of Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3, PDB code: 3ekd
was solved by
H.S.Toogood,
D.Leys,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Iron Binding Sites:
The binding sites of Iron atom in the Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3
(pdb code 3ekd). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3, PDB code: 3ekd: Jump to Iron binding site number: 1; 2; Iron binding site 1 out of 2 in 3ekdGo back to![]() ![]()
Iron binding site 1 out
of 2 in the Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3
![]() Mono view ![]() Stereo pair view
Iron binding site 2 out of 2 in 3ekdGo back to![]() ![]()
Iron binding site 2 out
of 2 in the Crystal Structure of the A264M Heme Domain of Cytochrome P450 BM3
![]() Mono view ![]() Stereo pair view
Reference:
H.M.Girvan,
H.S.Toogood,
R.E.Littleford,
H.E.Seward,
W.E.Smith,
I.S.Ekanem,
D.Leys,
M.R.Cheesman,
A.W.Munro.
Novel Haem Co-Ordination Variants of Flavocytochrome P450BM3. Biochem.J. V. 417 65 2009.
Page generated: Sun Aug 4 09:46:48 2024
ISSN: ISSN 0264-6021 PubMed: 18721129 DOI: 10.1042/BJ20081133 |
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