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Atomistry » Chlorine » PDB 2p67-2pg4 » 2pdh » |
Chlorine in PDB 2pdh: Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A.Enzymatic activity of Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A.
All present enzymatic activity of Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A.:
1.1.1.21; Protein crystallography data
The structure of Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A., PDB code: 2pdh
was solved by
H.Steuber,
A.Heine,
G.Klebe,
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 Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A.
(pdb code 2pdh). 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 Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A., PDB code: 2pdh: Chlorine binding site 1 out of 1 in 2pdhGo back to![]() ![]()
Chlorine binding site 1 out
of 1 in the Human Aldose Reductase Mutant L300P Complexed with Uracil- Type Inhibitor at 1.45 A.
![]() Mono view ![]() Stereo pair view
Reference:
H.Steuber,
A.Heine,
A.Podjarny,
G.Klebe.
Merging the Binding Sites of Aldose and Aldehyde Reductase For Detection of Inhibitor Selectivity-Determining Features. J.Mol.Biol. V. 379 991 2008.
Page generated: Sat Jul 20 10:06:19 2024
ISSN: ISSN 0022-2836 PubMed: 18495158 DOI: 10.1016/J.JMB.2008.03.063 |
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