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Chlorine in PDB 4i24: Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib

Enzymatic activity of Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib

All present enzymatic activity of Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib:
2.7.10.1;

Protein crystallography data

The structure of Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib, PDB code: 4i24 was solved by K.S.Gajiwala, J.Feng, R.Ferre, K.Ryan, O.Brodsky, A.Stewart, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 42.55 / 1.80
Space group P 1
Cell size a, b, c (Å), α, β, γ (°) 35.848, 76.385, 77.961, 67.17, 80.53, 85.67
R / Rfree (%) 20.9 / 23.9

Other elements in 4i24:

The structure of Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib also contains other interesting chemical elements:

Fluorine (F) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib (pdb code 4i24). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib, PDB code: 4i24:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 4i24

Go back to Chlorine Binding Sites List in 4i24
Chlorine binding site 1 out of 2 in the Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl9001

b:31.7
occ:1.00
CL A:1C99001 0.0 31.7 1.0
C17 A:1C99001 1.7 28.3 1.0
C16 A:1C99001 2.7 25.1 1.0
C18 A:1C99001 2.7 25.6 1.0
F21 A:1C99001 3.0 27.2 1.0
O A:LEU788 3.2 26.1 1.0
N A:LYS745 3.4 31.0 1.0
CB A:LYS745 3.5 33.3 1.0
O A:ALA743 3.6 27.0 1.0
CG A:MET790 3.8 25.8 1.0
C A:LEU788 3.8 26.8 1.0
C A:ILE744 3.9 31.3 1.0
SD A:MET790 3.9 27.6 1.0
CB A:MET790 4.0 23.3 1.0
N A:MET790 4.0 23.1 1.0
C A:ALA743 4.0 27.8 1.0
C15 A:1C99001 4.0 24.2 1.0
C19 A:1C99001 4.1 24.7 1.0
CA A:LYS745 4.1 33.2 1.0
CA A:ILE744 4.1 30.3 1.0
CB A:LEU788 4.2 26.4 1.0
N A:ILE744 4.2 28.0 1.0
N A:ILE789 4.4 26.6 1.0
C A:ILE789 4.4 23.4 1.0
CA A:ILE789 4.4 24.4 1.0
CB A:ALA743 4.4 28.2 1.0
C20 A:1C99001 4.6 24.3 1.0
CA A:MET790 4.6 22.5 1.0
O A:ILE744 4.6 29.4 1.0
CA A:LEU788 4.6 27.6 1.0
CG A:LYS745 4.8 36.2 1.0
CA A:ALA743 4.9 28.1 1.0
CD A:LYS745 5.0 37.5 1.0

Chlorine binding site 2 out of 2 in 4i24

Go back to Chlorine Binding Sites List in 4i24
Chlorine binding site 2 out of 2 in the Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Structure of T790M Egfr Kinase Domain Co-Crystallized with Dacomitinib within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl9001

b:27.4
occ:1.00
CL B:1C99001 0.0 27.4 1.0
C17 B:1C99001 1.7 23.1 1.0
C16 B:1C99001 2.7 22.7 1.0
C18 B:1C99001 2.7 22.3 1.0
F21 B:1C99001 3.0 23.6 1.0
O B:LEU788 3.2 26.8 1.0
N B:LYS745 3.4 26.7 1.0
CB B:LYS745 3.6 28.1 1.0
O B:ALA743 3.6 23.3 1.0
CG B:MET790 3.7 22.9 1.0
SD B:MET790 3.7 27.3 1.0
C B:LEU788 3.8 23.4 1.0
C B:ILE744 3.9 24.9 1.0
CB B:MET790 3.9 21.6 1.0
N B:MET790 4.0 20.8 1.0
C B:ALA743 4.0 25.9 1.0
C15 B:1C99001 4.0 21.0 1.0
C19 B:1C99001 4.1 21.3 1.0
CB B:LEU788 4.1 22.8 1.0
CA B:ILE744 4.1 24.7 1.0
CA B:LYS745 4.1 27.6 1.0
N B:ILE744 4.3 24.9 1.0
C B:ILE789 4.3 20.7 1.0
N B:ILE789 4.4 23.4 1.0
CA B:ILE789 4.4 22.3 1.0
CB B:ALA743 4.4 25.9 1.0
C20 B:1C99001 4.6 23.3 1.0
CA B:LEU788 4.6 24.4 1.0
CA B:MET790 4.6 20.9 1.0
O B:ILE744 4.7 26.0 1.0
CA B:ALA743 4.9 25.7 1.0
CG B:LYS745 4.9 28.9 1.0
O B:HOH9104 4.9 17.9 1.0

Reference:

K.S.Gajiwala, J.Feng, R.Ferre, K.Ryan, O.Brodsky, S.Weinrich, J.C.Kath, A.Stewart. Insights Into the Aberrant Activity of Mutant Egfr Kinase Domain and Drug Recognition. Structure V. 21 209 2013.
ISSN: ISSN 0969-2126
PubMed: 23273428
DOI: 10.1016/J.STR.2012.11.014
Page generated: Sun Jul 21 16:20:55 2024

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