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Atomistry » Sodium » PDB 8bh0-8c9f » 8byk » |
Sodium in PDB 8byk: The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide CyclasesProtein crystallography data
The structure of The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide Cyclases, PDB code: 8byk
was solved by
C.V.Knospe,
M.Kamel,
O.Spitz,
A.Hoeppner,
S.Galle,
J.Reiners,
A.Kedrov,
S.H.Smits,
L.Schmitt,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 8byk:
The structure of The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide Cyclases also contains other interesting chemical elements:
Sodium Binding Sites:
The binding sites of Sodium atom in the The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide Cyclases
(pdb code 8byk). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide Cyclases, PDB code: 8byk: Jump to Sodium binding site number: 1; 2; Sodium binding site 1 out of 2 in 8bykGo back to![]() ![]()
Sodium binding site 1 out
of 2 in the The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide Cyclases
![]() Mono view ![]() Stereo pair view
Sodium binding site 2 out of 2 in 8bykGo back to![]() ![]()
Sodium binding site 2 out
of 2 in the The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide Cyclases
![]() Mono view ![]() Stereo pair view
Reference:
C.V.Knospe,
M.Kamel,
O.Spitz,
A.Hoeppner,
S.Galle,
J.Reiners,
A.Kedrov,
S.H.J.Smits,
L.Schmitt.
The Structure of Madc From Clostridium Maddingley Reveals New Insights Into Class I Lanthipeptide Cyclases. Front Microbiol V. 13 57217 2022.
Page generated: Mon Aug 18 13:23:00 2025
ISSN: ESSN 1664-302X PubMed: 36741885 DOI: 10.3389/FMICB.2022.1057217 |
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