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Atomistry » Manganese » PDB 5ekw-5fxv » 5fh1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Manganese » PDB 5ekw-5fxv » 5fh1 » |
Manganese in PDB 5fh1: The Structure of Rat Cytosolic Pepck Variant E89D in Complex with GtpEnzymatic activity of The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp
All present enzymatic activity of The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp:
4.1.1.32; Protein crystallography data
The structure of The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp, PDB code: 5fh1
was solved by
T.A.Johnson,
T.Holyoak,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 5fh1:
The structure of The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp also contains other interesting chemical elements:
Manganese Binding Sites:
The binding sites of Manganese atom in the The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp
(pdb code 5fh1). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp, PDB code: 5fh1: Jump to Manganese binding site number: 1; 2; Manganese binding site 1 out of 2 in 5fh1Go back to![]() ![]()
Manganese binding site 1 out
of 2 in the The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp
![]() Mono view ![]() Stereo pair view
Manganese binding site 2 out of 2 in 5fh1Go back to![]() ![]()
Manganese binding site 2 out
of 2 in the The Structure of Rat Cytosolic Pepck Variant E89D in Complex with Gtp
![]() Mono view ![]() Stereo pair view
Reference:
T.A.Johnson,
M.J.Mcleod,
T.Holyoak.
Utilization of Substrate Intrinsic Binding Energy For Conformational Change and Catalytic Function in Phosphoenolpyruvate Carboxykinase. Biochemistry V. 55 575 2016.
Page generated: Sun Oct 6 00:12:52 2024
ISSN: ISSN 1520-4995 PubMed: 26709450 DOI: 10.1021/ACS.BIOCHEM.5B01215 |
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