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Atomistry » Chlorine » PDB 4p9d-4pk0 » 4pd4 » |
Chlorine in PDB 4pd4: Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug ActionEnzymatic activity of Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action
All present enzymatic activity of Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action:
1.10.2.2; Protein crystallography data
The structure of Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action, PDB code: 4pd4
was solved by
D.Birth,
W.-C.Kao,
C.Hunte,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 4pd4:
The structure of Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action
(pdb code 4pd4). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action, PDB code: 4pd4: Chlorine binding site 1 out of 1 in 4pd4Go back to![]() ![]()
Chlorine binding site 1 out
of 1 in the Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action
![]() Mono view ![]() Stereo pair view
Reference:
D.Birth,
W.C.Kao,
C.Hunte.
Structural Analysis of Atovaquone-Inhibited Cytochrome BC1 Complex Reveals the Molecular Basis of Antimalarial Drug Action. Nat Commun V. 5 4029 2014.
Page generated: Thu Jul 25 23:56:07 2024
ISSN: ESSN 2041-1723 PubMed: 24893593 DOI: 10.1038/NCOMMS5029 |
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