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Atomistry » Chlorine » PDB 6dox-6dy2 » 6ds8 » |
Chlorine in PDB 6ds8: Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active SiteEnzymatic activity of Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site
All present enzymatic activity of Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site:
1.14.14.18; Protein crystallography data
The structure of Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site, PDB code: 6ds8
was solved by
A.Chao,
C.W.Goulding,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 6ds8:
The structure of Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site
(pdb code 6ds8). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site, PDB code: 6ds8: Jump to Chlorine binding site number: 1; 2; Chlorine binding site 1 out of 2 in 6ds8Go back to![]() ![]()
Chlorine binding site 1 out
of 2 in the Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site
![]() Mono view ![]() Stereo pair view
Chlorine binding site 2 out of 2 in 6ds8Go back to![]() ![]()
Chlorine binding site 2 out
of 2 in the Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site
![]() Mono view ![]() Stereo pair view
Reference:
A.Chao,
C.W.Goulding.
Crystal Structure of Mhud R26S Mutant with Two Manganese Protoporphyrin IX Bound Per Active Site To Be Published.
Page generated: Sat Jul 12 13:00:54 2025
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