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Atomistry » Bromine » PDB 1z76-2cej » 2c69 » |
Bromine in PDB 2c69: Crystal Structure of the Human CDK2 Complexed with the Triazolopyrimidine InhibitorEnzymatic activity of Crystal Structure of the Human CDK2 Complexed with the Triazolopyrimidine Inhibitor
All present enzymatic activity of Crystal Structure of the Human CDK2 Complexed with the Triazolopyrimidine Inhibitor:
2.7.1.37; Protein crystallography data
The structure of Crystal Structure of the Human CDK2 Complexed with the Triazolopyrimidine Inhibitor, PDB code: 2c69
was solved by
C.M.Richardson,
P.Dokurno,
J.B.Murray,
A.E.Surgenor,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Bromine Binding Sites:
The binding sites of Bromine atom in the Crystal Structure of the Human CDK2 Complexed with the Triazolopyrimidine Inhibitor
(pdb code 2c69). This binding sites where shown within
5.0 Angstroms radius around Bromine atom.
In total only one binding site of Bromine was determined in the Crystal Structure of the Human CDK2 Complexed with the Triazolopyrimidine Inhibitor, PDB code: 2c69: Bromine binding site 1 out of 1 in 2c69Go back to Bromine Binding Sites List in 2c69
Bromine binding site 1 out
of 1 in the Crystal Structure of the Human CDK2 Complexed with the Triazolopyrimidine Inhibitor
Mono view Stereo pair view
Reference:
C.M.Richardson,
D.S.Williamson,
M.J.Parratt,
J.Borgognoni,
A.D.Cansfield,
P.Dokurno,
G.L.Francis,
R.Howes,
J.D.Moore,
J.B.Murray,
A.Robertson,
A.E.Surgenor,
C.J.Torrance.
Triazolo[1,5-A]Pyrimidines As Novel CDK2 Inhibitors: Protein Structure-Guided Design and Sar. Bioorg. Med. Chem. Lett. V. 16 1353 2006.
Page generated: Sat Dec 12 02:05:23 2020
ISSN: ISSN 0960-894X PubMed: 16325401 DOI: 10.1016/J.BMCL.2005.11.048 |
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