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Atomistry » Zinc » PDB 5thi-5tt8 » 5tl7 » |
Zinc in PDB 5tl7: Crystal Structure of Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15Enzymatic activity of Crystal Structure of Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15
All present enzymatic activity of Crystal Structure of Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15:
2.7.7.48; 3.4.19.12; 3.4.22.69; 3.6.4.12; 3.6.4.13; Protein crystallography data
The structure of Crystal Structure of Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15, PDB code: 5tl7
was solved by
C.D.Daczkowski,
J.V.Dzimianski,
S.D.Pegan,
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 Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15
(pdb code 5tl7). 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 Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15, PDB code: 5tl7: Jump to Zinc binding site number: 1; 2; Zinc binding site 1 out of 2 in 5tl7Go back to![]() ![]()
Zinc binding site 1 out
of 2 in the Crystal Structure of Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15
![]() Mono view ![]() Stereo pair view
Zinc binding site 2 out of 2 in 5tl7Go back to![]() ![]()
Zinc binding site 2 out
of 2 in the Crystal Structure of Sars-Cov Papain-Like Protease in Complex with C- Terminal Domain Mouse ISG15
![]() Mono view ![]() Stereo pair view
Reference:
C.M.Daczkowski,
J.V.Dzimianski,
J.R.Clasman,
O.Goodwin,
A.D.Mesecar,
S.D.Pegan.
Structural Insights Into the Interaction of Coronavirus Papain-Like Proteases and Interferon-Stimulated Gene Product 15 From Different Species. J. Mol. Biol. V. 429 1661 2017.
Page generated: Mon Oct 28 08:39:20 2024
ISSN: ESSN 1089-8638 PubMed: 28438633 DOI: 10.1016/J.JMB.2017.04.011 |
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