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Atomistry » Zinc » PDB 1sdx-1sx1 » 1sr9 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Zinc » PDB 1sdx-1sx1 » 1sr9 » |
Zinc in PDB 1sr9: Crystal Structure of Leua From Mycobacterium TuberculosisEnzymatic activity of Crystal Structure of Leua From Mycobacterium Tuberculosis
All present enzymatic activity of Crystal Structure of Leua From Mycobacterium Tuberculosis:
2.3.3.13; Protein crystallography data
The structure of Crystal Structure of Leua From Mycobacterium Tuberculosis, PDB code: 1sr9
was solved by
N.Koon,
C.J.Squire,
E.N.Baker,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 1sr9:
The structure of Crystal Structure of Leua From Mycobacterium Tuberculosis also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Leua From Mycobacterium Tuberculosis
(pdb code 1sr9). 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 Leua From Mycobacterium Tuberculosis, PDB code: 1sr9: Jump to Zinc binding site number: 1; 2; Zinc binding site 1 out of 2 in 1sr9Go back to Zinc Binding Sites List in 1sr9
Zinc binding site 1 out
of 2 in the Crystal Structure of Leua From Mycobacterium Tuberculosis
Mono view Stereo pair view
Zinc binding site 2 out of 2 in 1sr9Go back to Zinc Binding Sites List in 1sr9
Zinc binding site 2 out
of 2 in the Crystal Structure of Leua From Mycobacterium Tuberculosis
Mono view Stereo pair view
Reference:
N.Koon,
C.J.Squire,
E.N.Baker.
Crystal Structure of Leua From Mycobacterium Tuberculosis, A Key Enzyme in Leucine Biosynthesis Proc.Natl.Acad.Sci.Usa V. 101 8295 2004.
Page generated: Wed Oct 16 18:54:22 2024
ISSN: ISSN 0027-8424 PubMed: 15159544 DOI: 10.1073/PNAS.0400820101 |
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