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Sodium in PDB 7zkk: A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans

Enzymatic activity of A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans

All present enzymatic activity of A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans:
1.2.7.4; 2.3.1.169;

Protein crystallography data

The structure of A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans, PDB code: 7zkk was solved by J.Ruickoldt, J.-H.Jeoung, Y.Basak, L.Domnik, H.Dobbek, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 45.12 / 1.97
Space group P 61 2 2
Cell size a, b, c (Å), α, β, γ (°) 142.63, 142.63, 291.34, 90, 90, 120
R / Rfree (%) 15.8 / 19.2

Other elements in 7zkk:

The structure of A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans also contains other interesting chemical elements:

Iron (Fe) 14 atoms
Nickel (Ni) 3 atoms

Sodium Binding Sites:

The binding sites of Sodium atom in the A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans (pdb code 7zkk). This binding sites where shown within 5.0 Angstroms radius around Sodium atom.
In total only one binding site of Sodium was determined in the A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans, PDB code: 7zkk:

Sodium binding site 1 out of 1 in 7zkk

Go back to Sodium Binding Sites List in 7zkk
Sodium binding site 1 out of 1 in the A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 1 of A216H Variant of the Codh/Acs Complex of C. Hydrogenoformans within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Na805

b:28.4
occ:1.00
OE1 B:GLU334 2.3 31.4 1.0
O B:ASN415 2.3 24.1 1.0
O B:PHE420 2.4 28.2 1.0
O B:GLY417 2.4 31.5 1.0
O B:HOH1031 2.4 23.4 1.0
O B:PHE331 2.9 25.1 1.0
CD B:GLU334 3.2 38.8 1.0
C B:ASN415 3.3 28.6 1.0
CG B:GLU334 3.4 31.6 1.0
C B:PHE420 3.6 26.5 1.0
C B:GLY417 3.6 27.8 1.0
CA B:ASN415 3.7 28.6 1.0
C B:PHE331 3.8 26.1 1.0
CB B:PHE331 3.9 25.8 1.0
N B:PHE420 4.1 31.0 1.0
N B:GLY417 4.3 25.6 1.0
N B:GLY419 4.3 27.5 1.0
CA B:PHE420 4.4 29.0 1.0
OE2 B:GLU334 4.4 44.0 1.0
N B:TYR416 4.4 29.1 1.0
CB B:ASN415 4.4 26.1 1.0
OD1 B:ASN415 4.4 31.6 1.0
CA B:PHE331 4.4 26.3 1.0
N B:GLU418 4.5 24.3 1.0
C B:TYR416 4.5 24.5 1.0
CB B:GLU334 4.5 32.7 1.0
CA B:GLU418 4.5 25.0 1.0
CA B:GLY417 4.5 26.0 1.0
O B:THR414 4.5 25.9 1.0
N B:TRP421 4.6 27.1 1.0
CA B:TRP421 4.7 25.5 1.0
N B:GLU332 4.7 26.6 1.0
CA B:GLU332 4.8 27.3 1.0
CB B:PHE420 4.8 29.3 1.0
CA B:TYR416 4.8 25.8 1.0
O B:GLU332 4.8 33.3 1.0
C B:GLU418 4.9 25.2 1.0
O B:TYR416 4.9 28.0 1.0
CG B:ASN415 4.9 31.8 1.0
C B:GLU332 5.0 32.4 1.0
N B:ASN415 5.0 23.1 1.0

Reference:

J.Ruickoldt, Y.Basak, L.Domnik, J.H.Jeoung, H.Dobbek. On the Kinetics of CO2 Reduction By Ni, Fe-Co Dehydrogenases Acs Catalysis 2022.
ISSN: ESSN 2155-5435
DOI: 10.1021/ACSCATAL.2C02221
Page generated: Wed Oct 9 10:17:18 2024

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