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Atomistry » Copper » PDB 7a8v-7ev7 » 7eut | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Copper » PDB 7a8v-7ev7 » 7eut » |
Copper in PDB 7eut: Crystal Structures of 2-Oxoglutarate Dependent Dioxygenase (CTB9) in Complex with N-OxalylglycineProtein crystallography data
The structure of Crystal Structures of 2-Oxoglutarate Dependent Dioxygenase (CTB9) in Complex with N-Oxalylglycine, PDB code: 7eut
was solved by
X.D.Hou,
X.Z.Liu,
Z.B.Yuan,
D.J.Yin,
Y.J.Rao,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Copper Binding Sites:
The binding sites of Copper atom in the Crystal Structures of 2-Oxoglutarate Dependent Dioxygenase (CTB9) in Complex with N-Oxalylglycine
(pdb code 7eut). This binding sites where shown within
5.0 Angstroms radius around Copper atom.
In total 2 binding sites of Copper where determined in the Crystal Structures of 2-Oxoglutarate Dependent Dioxygenase (CTB9) in Complex with N-Oxalylglycine, PDB code: 7eut: Jump to Copper binding site number: 1; 2; Copper binding site 1 out of 2 in 7eutGo back to Copper Binding Sites List in 7eut
Copper binding site 1 out
of 2 in the Crystal Structures of 2-Oxoglutarate Dependent Dioxygenase (CTB9) in Complex with N-Oxalylglycine
Mono view Stereo pair view
Copper binding site 2 out of 2 in 7eutGo back to Copper Binding Sites List in 7eut
Copper binding site 2 out
of 2 in the Crystal Structures of 2-Oxoglutarate Dependent Dioxygenase (CTB9) in Complex with N-Oxalylglycine
Mono view Stereo pair view
Reference:
X.Z.Liu,
Z.B.Yuan,
H.Su,
X.D.Hou,
Z.W.Deng,
H.B.Xu,
B.D.Guo,
D.Yin,
X.Sheng,
Y.J.Rao.
Molecular Basis of the Unusual Seven-Membered Methylenedioxy Bridge Formation Catalyzed By Fe(II)/Alpha-Kg-Dependent Oxygenase CTB9 Acs Catalysis V. 12 3689 2022.
Page generated: Wed Jul 31 08:29:18 2024
ISSN: ESSN 2155-5435 DOI: DOI.ORG/10.1021/ACSCATAL.1C04627 |
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