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Chlorine in PDB 6gqm: Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229

Enzymatic activity of Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229

All present enzymatic activity of Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229:
2.7.10.1;

Protein crystallography data

The structure of Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229, PDB code: 6gqm was solved by M.Schimpl, C.J.Hardy, D.J.Ogg, R.C.Overman, M.J.Packer, J.G.Kettle, R.Anjum, E.Barry, D.Bhavsar, C.Brown, A.Campbell, K.Goldberg, M.Grondine, S.Guichard, T.Hunt, O.Jones, X.Li, O.Moleva, S.Pearson, W.Shao, A.Smith, J.Smith, D.Stead, S.Stokes, M.Tucker, Y.Ye, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 40.00 / 2.00
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 87.970, 90.180, 91.150, 90.00, 90.00, 90.00
R / Rfree (%) 20.3 / 23

Other elements in 6gqm:

The structure of Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229 also contains other interesting chemical elements:

Fluorine (F) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229 (pdb code 6gqm). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229, PDB code: 6gqm:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 6gqm

Go back to Chlorine Binding Sites List in 6gqm
Chlorine binding site 1 out of 2 in the Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1002

b:30.5
occ:1.00
CD A:PRO627 3.7 37.4 1.0
CB A:LYS626 3.8 36.7 1.0
CB A:SER628 3.9 35.2 1.0
N A:SER628 3.9 34.4 1.0
OG A:SER628 4.0 34.9 1.0
N A:PRO627 4.1 35.6 1.0
CD A:LYS626 4.3 52.3 1.0
CG A:PRO627 4.4 44.5 1.0
CG A:LYS626 4.5 45.2 1.0
CA A:SER628 4.5 34.2 1.0
CB A:PRO627 4.6 40.1 1.0
O A:HOH1133 4.6 39.6 1.0
C A:LYS626 4.6 38.4 1.0
C A:PRO627 4.7 38.3 1.0
CA A:PRO627 4.7 36.6 1.0
CA A:LYS626 4.8 35.4 1.0

Chlorine binding site 2 out of 2 in 6gqm

Go back to Chlorine Binding Sites List in 6gqm
Chlorine binding site 2 out of 2 in the Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Crystal Structure of Human C-Kit Kinase Domain in Complex with A Small Molecule Inhibitor, AZD3229 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1003

b:36.2
occ:1.00
O A:HOH1134 3.1 49.2 1.0
O A:HOH1101 3.3 29.5 1.0
N A:THR666 3.5 39.1 1.0
CG A:ARG634 3.8 38.7 1.0
CD1 A:LEU625 3.8 37.2 1.0
OG1 A:THR666 3.9 46.8 1.0
CD A:ARG634 4.0 33.9 1.0
CB A:THR666 4.0 43.3 1.0
CA A:PRO665 4.1 44.6 1.0
CB A:PRO665 4.2 46.9 1.0
C A:PRO665 4.3 43.8 1.0
CA A:THR666 4.3 37.6 1.0
CB A:ARG634 4.4 35.1 1.0
CG A:LEU625 4.5 36.6 1.0
CA A:ARG634 4.6 36.4 1.0
CB A:LEU625 4.7 34.4 1.0
O A:THR666 4.8 40.5 1.0
CD2 A:LEU637 4.9 36.1 1.0

Reference:

J.G.Kettle, R.Anjum, E.Barry, D.Bhavsar, C.Brown, S.Boyd, A.Campbell, K.Goldberg, M.Grondine, S.Guichard, C.J.Hardy, T.Hunt, R.D.O.Jones, X.Li, O.Moleva, D.Ogg, R.C.Overman, M.J.Packer, S.Pearson, M.Schimpl, W.Shao, A.Smith, J.M.Smith, D.Stead, S.Stokes, M.Tucker, Y.Ye. Discovery of N-(4-{[5-Fluoro-7-(2-Methoxyethoxy) Quinazolin-4-Yl]Amino}Phenyl)-2-[4-(Propan-2-Yl)-1 H-1,2,3-Triazol-1-Yl]Acetamide (AZD3229), A Potent Pan-Kit Mutant Inhibitor For the Treatment of Gastrointestinal Stromal Tumors. J. Med. Chem. V. 61 8797 2018.
ISSN: ISSN 1520-4804
PubMed: 30204441
DOI: 10.1021/ACS.JMEDCHEM.8B00938
Page generated: Sat Jul 12 14:40:37 2025

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