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Atomistry » Zinc » PDB 1sdx-1sx1 » 1sg6 » |
Zinc in PDB 1sg6: Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7DEnzymatic activity of Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7D
All present enzymatic activity of Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7D:
4.2.3.4; Protein crystallography data
The structure of Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7D, PDB code: 1sg6
was solved by
C.E.Nichols,
A.R.Hawkins,
D.K.Stammers,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7D
(pdb code 1sg6). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7D, PDB code: 1sg6: Jump to Zinc binding site number: 1; 2; Zinc binding site 1 out of 2 in 1sg6Go back to Zinc Binding Sites List in 1sg6
Zinc binding site 1 out
of 2 in the Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7D
Mono view Stereo pair view
Zinc binding site 2 out of 2 in 1sg6Go back to Zinc Binding Sites List in 1sg6
Zinc binding site 2 out
of 2 in the Crystal Structure of Aspergillus Nidulans 3-Dehydroquinate Synthase (Andhqs) in Complex with ZN2+ and Nad+, at 1.7D
Mono view Stereo pair view
Reference:
C.E.Nichols,
A.R.Hawkins,
D.K.Stammers.
Structure of the 'Open' Form of Aspergillus Nidulans 3-Dehydroquinate Synthase at 1.7 A Resolution From Crystals Grown Following Enzyme Turnover. Acta Crystallogr.,Sect.D V. 60 971 2004.
Page generated: Wed Oct 16 18:50:24 2024
ISSN: ISSN 0907-4449 PubMed: 15103156 DOI: 10.1107/S0907444904004743 |
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