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Fluorine in PDB 4cmt: Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine

Enzymatic activity of Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine

All present enzymatic activity of Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine:
2.7.10.1;

Protein crystallography data

The structure of Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine, PDB code: 4cmt was solved by M.A.Mctigue, Y.L.Deng, W.Liu, A.Brooun, A.E.Stewart, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 52.56 / 1.73
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 51.793, 57.431, 105.120, 90.00, 90.00, 90.00
R / Rfree (%) 21.3 / 24.8

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine (pdb code 4cmt). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total only one binding site of Fluorine was determined in the Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine, PDB code: 4cmt:

Fluorine binding site 1 out of 1 in 4cmt

Go back to Fluorine Binding Sites List in 4cmt
Fluorine binding site 1 out of 1 in the Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F2401

b:23.2
occ:1.00
 F17 A:GWH2401 0.0 23.2 1.0
C15 A:GWH2401 1.3 22.7 1.0
C16 A:GWH2401 2.4 23.4 1.0
C14 A:GWH2401 2.4 25.8 1.0
C A:GLY1269 3.0 20.2 1.0
CA A:GLY1269 3.2 20.6 1.0
N A:ASP1270 3.2 20.2 1.0
O A:ASN1254 3.3 18.8 1.0
O A:GLY1269 3.3 21.8 1.0
C A:ASN1254 3.5 16.8 1.0
CB A:ASP1270 3.6 21.0 1.0
CG A:LEU1256 3.6 18.4 1.0
C13 A:GWH2401 3.7 24.8 1.0
C10 A:GWH2401 3.7 23.5 1.0
N A:GLY1269 3.8 18.1 1.0
CA A:ASN1254 3.8 18.5 1.0
CD1 A:LEU1256 3.9 20.8 1.0
CA A:ASP1270 3.9 20.6 1.0
CD2 A:LEU1256 4.0 18.4 1.0
N A:CYS1255 4.1 16.8 1.0
C12 A:GWH2401 4.2 27.6 1.0
O A:ARG1253 4.3 19.1 1.0
C A:CYS1255 4.5 19.0 1.0
CA A:CYS1255 4.6 16.9 1.0
O A:HOH2143 4.7 41.6 1.0
O A:CYS1255 4.7 20.6 1.0
CB A:ASN1254 4.8 19.0 1.0
N A:LEU1256 4.9 19.0 1.0
N A:ASN1254 4.9 17.4 1.0
CG A:ASP1270 4.9 24.8 1.0
C9 A:GWH2401 4.9 21.7 1.0
CB A:LEU1256 4.9 17.1 1.0

Reference:

T.W.Johnson, P.F.Richardson, S.Bailey, A.Brooun, B.J.Burke, M.R.Collins, J.J.Cui, J.G.Deal, Y.L.Deng, D.M.Dinh, L.D.Engstrom, M.He, J.E.Hoffman, R.L.Hoffman, Q.Huang, J.Kath, R.S.Kania, H.Lam, J.L.Lam, P.T.Le, L.Lingardo, W.Liu, M.A.Mctigue, C.L.Palmer, N.W.Sach, T.Smeal, G.L.Smith, A.E.Stewart, S.L.Timofeevski, H.Zhu, J.Zhu, H.Y.Zou, M.P.Edwards. Discovery of (10R)-7-Amino-12-Fluoro-2,10,16-Trimethyl-15- Oxo-10,15,16,17-Tetrahydro-2H-8,4-(Metheno)Pyrazolo[4,3- H][2,5,11]Benzoxadiazacyclotetradecine-3-Carbonitrile (Pf- 06463922), A Macrocyclic Inhibitor of Alk/ROS1 with Pre- Clinical Brain Exposure and Broad Spectrum Potency Against Alk-Resistant Mutations. J.Med.Chem. V. 57 4720 2014.
ISSN: ISSN 0022-2623
PubMed: 24819116
DOI: 10.1021/JM500261Q
Page generated: Thu Aug 1 00:45:25 2024

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