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Atomistry » Chlorine » PDB 2dct-2dxa » 2dhc | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Chlorine » PDB 2dct-2dxa » 2dhc » |
Chlorine in PDB 2dhc: Crystallographic Analysis of the Catalytic Mechanism of Haloalkane DehalogenaseEnzymatic activity of Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase
All present enzymatic activity of Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase:
3.8.1.5; Protein crystallography data
The structure of Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase, PDB code: 2dhc
was solved by
K.H.G.Verschueren,
B.W.Dijkstra,
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 Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase
(pdb code 2dhc). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase, PDB code: 2dhc: Jump to Chlorine binding site number: 1; 2; Chlorine binding site 1 out of 2 in 2dhcGo back to![]() ![]()
Chlorine binding site 1 out
of 2 in the Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase
![]() Mono view ![]() Stereo pair view
Chlorine binding site 2 out of 2 in 2dhcGo back to![]() ![]()
Chlorine binding site 2 out
of 2 in the Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase
![]() Mono view ![]() Stereo pair view
Reference:
K.H.Verschueren,
F.Seljee,
H.J.Rozeboom,
K.H.Kalk,
B.W.Dijkstra.
Crystallographic Analysis of the Catalytic Mechanism of Haloalkane Dehalogenase. Nature V. 363 693 1993.
Page generated: Sat Jul 20 06:32:55 2024
ISSN: ISSN 0028-0836 PubMed: 8515812 DOI: 10.1038/363693A0 |
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