Atomistry » Chlorine » PDB 3o6o-3oht » 3og7
Atomistry »
  Chlorine »
    PDB 3o6o-3oht »
      3og7 »

Chlorine in PDB 3og7: B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032

Enzymatic activity of B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032

All present enzymatic activity of B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032:
2.7.11.1;

Protein crystallography data

The structure of B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032, PDB code: 3og7 was solved by Y.Zhang, K.Y.Zhang, C.Zhang, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 21.30 / 2.45
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 50.770, 104.424, 110.128, 90.00, 90.00, 90.00
R / Rfree (%) 21.3 / 25.8

Other elements in 3og7:

The structure of B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032 also contains other interesting chemical elements:

Fluorine (F) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032 (pdb code 3og7). 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 B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032, PDB code: 3og7:

Chlorine binding site 1 out of 1 in 3og7

Go back to Chlorine Binding Sites List in 3og7
Chlorine binding site 1 out of 1 in the B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of B-Raf Kinase V600E Oncogenic Mutant in Complex with PLX4032 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1

b:67.3
occ:1.00
CL13 A:0321 0.0 67.3 1.0
C10 A:0321 1.7 58.4 1.0
C11 A:0321 2.7 48.5 1.0
C09 A:0321 2.7 62.1 1.0
C12 A:0321 4.0 48.2 1.0
C08 A:0321 4.0 58.7 1.0
C07 A:0321 4.5 54.3 1.0
CG2 A:ILE463 5.0 60.9 1.0
CB A:SER535 5.0 67.8 1.0

Reference:

G.Bollag, P.Hirth, J.Tsai, J.Zhang, P.N.Ibrahim, H.Cho, W.Spevak, C.Zhang, Y.Zhang, G.Habets, E.A.Burton, B.Wong, G.Tsang, B.L.West, B.Powell, R.Shellooe, A.Marimuthu, H.Nguyen, K.Y.Zhang, D.R.Artis, J.Schlessinger, F.Su, B.Higgins, R.Iyer, K.D'andrea, A.Koehler, M.Stumm, P.S.Lin, R.J.Lee, J.Grippo, I.Puzanov, K.B.Kim, A.Ribas, G.A.Mcarthur, J.A.Sosman, P.B.Chapman, K.T.Flaherty, X.Xu, K.L.Nathanson, K.Nolop. Clinical Efficacy of A Raf Inhibitor Needs Broad Target Blockade in Braf-Mutant Melanoma. Nature V. 467 596 2010.
ISSN: ISSN 0028-0836
PubMed: 20823850
DOI: 10.1038/NATURE09454
Page generated: Sun Jul 21 01:38:42 2024

Last articles

Zn in 9J0N
Zn in 9J0O
Zn in 9J0P
Zn in 9FJX
Zn in 9EKB
Zn in 9C0F
Zn in 9CAH
Zn in 9CH0
Zn in 9CH3
Zn in 9CH1
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy