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Atomistry » Sodium » PDB 5b15-5bph » 5bmw » |
Sodium in PDB 5bmw: Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium FalciparumEnzymatic activity of Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum
All present enzymatic activity of Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum:
5.3.1.1; Protein crystallography data
The structure of Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum, PDB code: 5bmw
was solved by
D.Bandyopadhyay,
M.R.N.Murthy,
H.Balaram,
P.Balaram,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 5bmw:
The structure of Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum also contains other interesting chemical elements:
Sodium Binding Sites:
The binding sites of Sodium atom in the Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum
(pdb code 5bmw). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum, PDB code: 5bmw: Jump to Sodium binding site number: 1; 2; Sodium binding site 1 out of 2 in 5bmwGo back to Sodium Binding Sites List in 5bmw
Sodium binding site 1 out
of 2 in the Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum
Mono view Stereo pair view
Sodium binding site 2 out of 2 in 5bmwGo back to Sodium Binding Sites List in 5bmw
Sodium binding site 2 out
of 2 in the Crystal Structure of T75V Mutant of Triosephosphate Isomerase From Plasmodium Falciparum
Mono view Stereo pair view
Reference:
D.Bandyopadhyay,
M.R.Murthy,
H.Balaram,
P.Balaram.
Probing the Role of Highly Conserved Residues in Triosephosphate Isomerase - Analysis of Site Specific Mutants at Positions 64 and 75 in the Plasmodial Enzyme Febs J. V. 282 3863 2015.
Page generated: Mon Oct 7 20:05:30 2024
ISSN: ISSN 1742-464X PubMed: 26206206 DOI: 10.1111/FEBS.13384 |
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