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Atomistry » Chlorine » PDB 5x2o-5xif » 5x8k | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Chlorine » PDB 5x2o-5xif » 5x8k » |
Chlorine in PDB 5x8k: V158T Mutant of Thermus Thermophilus HB8 Thymidylate KinaseEnzymatic activity of V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase
All present enzymatic activity of V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase:
2.7.4.9; Protein crystallography data
The structure of V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase, PDB code: 5x8k
was solved by
S.K.Chaudhary,
J.Jeyakanthan,
K.Sekar,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 5x8k:
The structure of V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase
(pdb code 5x8k). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase, PDB code: 5x8k: Jump to Chlorine binding site number: 1; 2; Chlorine binding site 1 out of 2 in 5x8kGo back to Chlorine Binding Sites List in 5x8k
Chlorine binding site 1 out
of 2 in the V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase
Mono view Stereo pair view
Chlorine binding site 2 out of 2 in 5x8kGo back to Chlorine Binding Sites List in 5x8k
Chlorine binding site 2 out
of 2 in the V158T Mutant of Thermus Thermophilus HB8 Thymidylate Kinase
Mono view Stereo pair view
Reference:
S.K.Chaudhary,
J.Jeyakanthan,
K.Sekar.
Structural and Functional Roles of Dynamically Correlated Residues in Thymidylate Kinase. Acta Crystallogr D Struct V. 74 341 2018BIOL.
Page generated: Fri Jul 26 20:51:33 2024
ISSN: ISSN 2059-7983 PubMed: 29652261 DOI: 10.1107/S2059798318002267 |
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