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Chlorine in PDB 6gva: CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455

Enzymatic activity of CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455

All present enzymatic activity of CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455:
2.7.11.22;

Protein crystallography data

The structure of CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455, PDB code: 6gva was solved by J.Skerlova, P.Rezacova, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 48.00 / 2.15
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 71.015, 112.642, 159.690, 90.00, 90.00, 90.00
R / Rfree (%) 19.4 / 24

Other elements in 6gva:

The structure of CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455 also contains other interesting chemical elements:

Bromine (Br) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455 (pdb code 6gva). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455, PDB code: 6gva:

Chlorine binding site 1 out of 1 in 6gva

Go back to Chlorine Binding Sites List in 6gva
Chlorine binding site 1 out of 1 in the CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of CDK2/Cyclin A2 in Complex with Pyrazolo[4,3-D]Pyrimidine Inhibitor LGR4455 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl304

b:57.2
occ:1.00
CD A:PRO254 3.8 36.7 1.0
CG A:PRO254 4.0 36.4 1.0
O A:VAL197 4.0 42.1 1.0
CA A:THR198 4.0 41.0 1.0
CD A:PRO253 4.1 40.5 1.0
CG2 A:THR198 4.3 42.6 1.0
CB A:THR198 4.4 43.0 1.0
CG A:PRO253 4.6 38.6 1.0
C A:VAL197 4.7 38.3 1.0
N A:THR198 4.7 39.1 1.0
N A:PRO253 5.0 38.1 1.0
O A:THR198 5.0 50.2 1.0
C A:THR198 5.0 45.1 1.0

Reference:

R.Jorda, L.Havlicek, A.Sturc, D.Tuskova, L.Daumova, M.Alam, J.Skerlova, M.Nekardova, M.Perina, T.Pospisil, J.Siroka, L.Urbanek, P.Pachl, P.Rezacova, M.Strnad, P.Klener, V.Krystof. 3,5,7-Substituted Pyrazolo[4,3- D]Pyrimidine Inhibitors of Cyclin-Dependent Kinases and Their Evaluation in Lymphoma Models. J.Med.Chem. V. 62 4606 2019.
ISSN: ISSN 0022-2623
PubMed: 30943029
DOI: 10.1021/ACS.JMEDCHEM.9B00189
Page generated: Sun Jul 28 00:14:53 2024

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