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Atomistry » Nickel » PDB 2pr0-2w3u » 2uuh » |
Nickel in PDB 2uuh: Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate GlutathioneEnzymatic activity of Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate Glutathione
All present enzymatic activity of Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate Glutathione:
4.4.1.20; Protein crystallography data
The structure of Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate Glutathione, PDB code: 2uuh
was solved by
D.Martinez Molina,
A.Wetterholm,
A.Kohl,
A.A.Mccarthy,
D.Niegowski,
E.Ohlson,
T.Hammarberg,
S.Eshaghi,
J.Z.Haeggstrom,
P.Nordlund,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Nickel Binding Sites:
The binding sites of Nickel atom in the Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate Glutathione
(pdb code 2uuh). This binding sites where shown within
5.0 Angstroms radius around Nickel atom.
In total 2 binding sites of Nickel where determined in the Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate Glutathione, PDB code: 2uuh: Jump to Nickel binding site number: 1; 2; Nickel binding site 1 out of 2 in 2uuhGo back to Nickel Binding Sites List in 2uuh
Nickel binding site 1 out
of 2 in the Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate Glutathione
Mono view Stereo pair view
Nickel binding site 2 out of 2 in 2uuhGo back to Nickel Binding Sites List in 2uuh
Nickel binding site 2 out
of 2 in the Crystal Structure of Human Leukotriene C4 Synthase in Complex with Substrate Glutathione
Mono view Stereo pair view
Reference:
D.Martinez Molina,
A.Wetterholm,
A.Kohl,
A.A.Mccarthy,
D.Niegowski,
E.Ohlson,
T.Hammarberg,
S.Eshaghi,
J.Z.Haeggstrom,
P.Nordlund.
Structural Basis For Synthesis of Inflammatory Mediators By Human Leukotriene C4 Synthase. Nature V. 448 613 2007.
Page generated: Wed Oct 9 16:58:08 2024
ISSN: ISSN 0028-0836 PubMed: 17632546 DOI: 10.1038/NATURE06009 |
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