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Chlorine in PDB 5aaa: Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib

Enzymatic activity of Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib

All present enzymatic activity of Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib:
2.7.10.1;

Protein crystallography data

The structure of Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib, PDB code: 5aaa was solved by M.Mctigue, Y.Deng, W.Liu, A.Brooun, A.Stewart, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 52.35 / 1.73
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 51.471, 57.281, 104.702, 90.00, 90.00, 90.00
R / Rfree (%) 20 / 20.6

Other elements in 5aaa:

The structure of Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib also contains other interesting chemical elements:

Fluorine (F) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib (pdb code 5aaa). 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 L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib, PDB code: 5aaa:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 5aaa

Go back to Chlorine Binding Sites List in 5aaa
Chlorine binding site 1 out of 2 in the Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl9000

b:34.9
occ:1.00
CL A:VGH9000 0.0 34.9 1.0
C13 A:VGH9000 1.7 34.6 1.0
C3 A:VGH9000 2.7 34.1 1.0
C17 A:VGH9000 2.8 34.7 1.0
C21 A:VGH9000 3.2 32.4 1.0
C4 A:VGH9000 3.8 27.3 1.0
C2 A:VGH9000 4.0 34.0 1.0
C18 A:VGH9000 4.1 37.7 1.0
C6 A:VGH9000 4.2 33.4 1.0
CG2 A:VAL1130 4.2 30.4 1.0
O27 A:VGH9000 4.2 28.5 1.0
C1 A:VGH9000 4.3 31.4 1.0
C15 A:VGH9000 4.5 26.5 1.0
CG1 A:VAL1130 4.5 29.0 1.0
O A:GLY1123 4.5 61.3 1.0
CB A:VAL1130 4.5 29.4 1.0
C12 A:VGH9000 4.6 36.8 1.0
C14 A:VGH9000 4.8 28.4 1.0
C16 A:VGH9000 4.9 30.0 1.0

Chlorine binding site 2 out of 2 in 5aaa

Go back to Chlorine Binding Sites List in 5aaa
Chlorine binding site 2 out of 2 in the Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl9000

b:52.7
occ:1.00
CL2 A:VGH9000 0.0 52.7 1.0
C18 A:VGH9000 1.8 37.7 1.0
C12 A:VGH9000 2.7 36.8 1.0
C17 A:VGH9000 2.8 34.7 1.0
O A:GLY1269 2.9 31.7 1.0
F A:VGH9000 3.0 37.5 1.0
O A:HOH2064 3.2 37.0 1.0
C A:GLY1269 3.3 27.0 1.0
C1 A:VGH9000 3.3 31.4 1.0
C21 A:VGH9000 3.3 32.4 1.0
O27 A:VGH9000 3.3 28.5 1.0
CD1 A:LEU1256 3.4 24.6 1.0
CA A:GLY1269 3.6 24.6 1.0
O A:HOH2139 3.7 42.3 1.0
N A:ASP1270 4.0 24.8 1.0
C2 A:VGH9000 4.1 34.0 1.0
C15 A:VGH9000 4.1 26.5 1.0
C13 A:VGH9000 4.2 34.6 1.0
CG A:LEU1256 4.2 22.5 1.0
N22 A:VGH9000 4.3 24.8 1.0
CD1 A:LEU1196 4.3 22.8 1.0
CA A:ASP1270 4.4 24.6 1.0
C19 A:VGH9000 4.6 26.6 1.0
CD2 A:LEU1256 4.6 22.9 1.0
C3 A:VGH9000 4.6 34.1 1.0
CB A:ASP1270 4.7 26.9 1.0
N A:GLY1269 4.9 20.5 1.0

Reference:

A.T.Shaw, L.Friboulet, I.Leshchiner, J.F.Gainor, S.Bergqvist, A.Brooun, B.J.Burke, Y.Deng, W.Liu, L.Dardaei, R.L.Frias, K.R.Schultz, J.Logan, L.P.James, T.Smeal, S.Timofeevski, R.Katayama, A.J.Iafrate, L.Le, M.Mctigue, G.Getz, T.W.Johnson, J.A.Engelman. Resensitization to Crizotinib By the Lorlatinib Alk Resistance Mutation L1198F. N.Engl.J.Med. V. 374 54 2016.
ISSN: ISSN 0028-4793
PubMed: 26698910
DOI: 10.1056/NEJMOA1508887
Page generated: Fri Jul 26 05:04:23 2024

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