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Atomistry » Copper » PDB 5i26-5luf » 5i6m | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Copper » PDB 5i26-5luf » 5i6m » |
Copper in PDB 5i6m: Crystal Structure of Copper Nitrite Reductase at 100K After 7.59 MgyEnzymatic activity of Crystal Structure of Copper Nitrite Reductase at 100K After 7.59 Mgy
All present enzymatic activity of Crystal Structure of Copper Nitrite Reductase at 100K After 7.59 Mgy:
1.7.2.1; Protein crystallography data
The structure of Crystal Structure of Copper Nitrite Reductase at 100K After 7.59 Mgy, PDB code: 5i6m
was solved by
S.Horrell,
M.A.Hough,
R.W.Strange,
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 Structure of Copper Nitrite Reductase at 100K After 7.59 Mgy
(pdb code 5i6m). 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 Structure of Copper Nitrite Reductase at 100K After 7.59 Mgy, PDB code: 5i6m: Jump to Copper binding site number: 1; 2; Copper binding site 1 out of 2 in 5i6mGo back to![]() ![]()
Copper binding site 1 out
of 2 in the Crystal Structure of Copper Nitrite Reductase at 100K After 7.59 Mgy
![]() Mono view ![]() Stereo pair view
Copper binding site 2 out of 2 in 5i6mGo back to![]() ![]()
Copper binding site 2 out
of 2 in the Crystal Structure of Copper Nitrite Reductase at 100K After 7.59 Mgy
![]() Mono view ![]() Stereo pair view
Reference:
S.Horrell,
S.V.Antonyuk,
R.R.Eady,
S.S.Hasnain,
M.A.Hough,
R.W.Strange.
Serial Crystallography Captures Enzyme Catalysis in Copper Nitrite Reductase at Atomic Resolution From One Crystal. Iucrj V. 3 271 2016.
Page generated: Mon Jul 14 04:42:25 2025
ISSN: ESSN 2052-2525 PubMed: 27437114 DOI: 10.1107/S205225251600823X |
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