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Atomistry » Chlorine » PDB 3nb5-3nnu » 3nf7 » |
Chlorine in PDB 3nf7: Structural Basis For A New Mechanism of Inhibition of Hiv Integrase Identified By Fragment Screening and Structure Based DesignProtein crystallography data
The structure of Structural Basis For A New Mechanism of Inhibition of Hiv Integrase Identified By Fragment Screening and Structure Based Design, PDB code: 3nf7
was solved by
T.S.Peat,
J.Newman,
J.J.Deadman,
D.Rhodes,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Structural Basis For A New Mechanism of Inhibition of Hiv Integrase Identified By Fragment Screening and Structure Based Design
(pdb code 3nf7). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Structural Basis For A New Mechanism of Inhibition of Hiv Integrase Identified By Fragment Screening and Structure Based Design, PDB code: 3nf7: Jump to Chlorine binding site number: 1; 2; Chlorine binding site 1 out of 2 in 3nf7Go back to Chlorine Binding Sites List in 3nf7
Chlorine binding site 1 out
of 2 in the Structural Basis For A New Mechanism of Inhibition of Hiv Integrase Identified By Fragment Screening and Structure Based Design
Mono view Stereo pair view
Chlorine binding site 2 out of 2 in 3nf7Go back to Chlorine Binding Sites List in 3nf7
Chlorine binding site 2 out
of 2 in the Structural Basis For A New Mechanism of Inhibition of Hiv Integrase Identified By Fragment Screening and Structure Based Design
Mono view Stereo pair view
Reference:
D.I.Rhodes,
T.S.Peat,
N.Vandegraaff,
D.Jeevarajah,
G.Le,
E.D.Jones,
J.A.Smith,
J.A.Coates,
L.J.Winfield,
N.Thienthong,
J.Newman,
D.Lucent,
J.H.Ryan,
G.P.Savage,
C.L.Francis,
J.J.Deadman.
Structural Basis For A New Mechanism of Inhibition of Hiv-1 Integrase Identified By Fragment Screening and Structure-Based Design Antivir.Chem.Chemother. V. 21 155 2011.
Page generated: Sun Jul 21 01:00:52 2024
ISSN: ISSN 0956-3202 PubMed: 21602613 DOI: 10.3851/IMP1716 |
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