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Fluorine in PDB 4lmn: Crystal Structure of MEK1 Kinase Bound to GDC0973

Enzymatic activity of Crystal Structure of MEK1 Kinase Bound to GDC0973

All present enzymatic activity of Crystal Structure of MEK1 Kinase Bound to GDC0973:
2.7.12.2;

Protein crystallography data

The structure of Crystal Structure of MEK1 Kinase Bound to GDC0973, PDB code: 4lmn was solved by M.H.Ultsch, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.69 / 2.80
Space group P 62
Cell size a, b, c (Å), α, β, γ (°) 81.610, 81.610, 129.809, 90.00, 90.00, 120.00
R / Rfree (%) 19.1 / 23.3

Other elements in 4lmn:

The structure of Crystal Structure of MEK1 Kinase Bound to GDC0973 also contains other interesting chemical elements:

Magnesium (Mg) 1 atom
Iodine (I) 1 atom

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Crystal Structure of MEK1 Kinase Bound to GDC0973 (pdb code 4lmn). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the Crystal Structure of MEK1 Kinase Bound to GDC0973, PDB code: 4lmn:
Jump to Fluorine binding site number: 1; 2; 3;

Fluorine binding site 1 out of 3 in 4lmn

Go back to Fluorine Binding Sites List in 4lmn
Fluorine binding site 1 out of 3 in the Crystal Structure of MEK1 Kinase Bound to GDC0973


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Crystal Structure of MEK1 Kinase Bound to GDC0973 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F503

b:62.0
occ:1.00
F17 A:EUI503 0.0 62.0 1.0
C12 A:EUI503 1.3 58.8 1.0
C13 A:EUI503 2.4 56.7 1.0
C11 A:EUI503 2.4 58.8 1.0
F16 A:EUI503 2.7 59.6 1.0
N A:SER212 2.9 73.5 1.0
N A:VAL211 3.2 67.6 1.0
O A:SER212 3.5 76.2 1.0
C14 A:EUI503 3.6 58.3 1.0
CB A:SER212 3.6 78.4 1.0
CA A:SER212 3.7 74.7 1.0
C10 A:EUI503 3.7 59.5 1.0
O A:PHE209 3.7 56.4 1.0
C A:VAL211 3.8 77.7 1.0
C A:GLY210 3.9 70.7 1.0
CA A:VAL211 3.9 69.5 1.0
CA A:GLY210 3.9 61.9 1.0
CD2 A:LEU215 4.0 79.8 1.0
C A:SER212 4.0 78.6 1.0
CG1 A:VAL211 4.0 74.8 1.0
CB A:LEU215 4.1 79.7 1.0
C15 A:EUI503 4.1 60.7 1.0
CB A:VAL211 4.2 73.1 1.0
CD2 A:LEU115 4.4 76.6 1.0
CG A:LEU215 4.4 81.7 1.0
C A:PHE209 4.6 58.4 1.0
OG A:SER212 4.6 80.5 1.0
CG1 A:ILE216 4.6 84.9 1.0
N A:GLY210 4.7 59.4 1.0
N9 A:EUI503 4.8 63.1 1.0
O A:GLY210 4.8 73.4 1.0
N A:ILE216 4.8 83.8 1.0

Fluorine binding site 2 out of 3 in 4lmn

Go back to Fluorine Binding Sites List in 4lmn
Fluorine binding site 2 out of 3 in the Crystal Structure of MEK1 Kinase Bound to GDC0973


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Crystal Structure of MEK1 Kinase Bound to GDC0973 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F503

b:59.6
occ:1.00
F16 A:EUI503 0.0 59.6 1.0
C11 A:EUI503 1.3 58.8 1.0
C12 A:EUI503 2.3 58.8 1.0
C10 A:EUI503 2.4 59.5 1.0
F17 A:EUI503 2.7 62.0 1.0
C4 A:EUI503 2.7 68.8 1.0
N9 A:EUI503 2.8 63.1 1.0
C5 A:EUI503 3.0 69.3 1.0
CD2 A:LEU115 3.4 76.6 1.0
O A:PHE209 3.6 56.4 1.0
C13 A:EUI503 3.6 56.7 1.0
C15 A:EUI503 3.6 60.7 1.0
C3 A:EUI503 3.8 70.6 1.0
CG1 A:VAL211 4.0 74.8 1.0
C14 A:EUI503 4.1 58.3 1.0
CD1 A:LEU118 4.2 67.8 1.0
C6 A:EUI503 4.2 70.7 1.0
CD1 A:ILE141 4.3 73.9 1.0
CD2 A:LEU215 4.3 79.8 1.0
CB A:VAL211 4.3 73.1 1.0
N A:VAL211 4.4 67.6 1.0
C2 A:EUI503 4.8 72.6 1.0
C A:PHE209 4.8 58.4 1.0
CG A:LEU115 4.8 77.4 1.0
N A:SER212 4.9 73.5 1.0
CA A:VAL211 4.9 69.5 1.0
C1 A:EUI503 4.9 72.2 1.0
C18 A:EUI503 5.0 63.1 1.0
F7 A:EUI503 5.0 69.6 1.0

Fluorine binding site 3 out of 3 in 4lmn

Go back to Fluorine Binding Sites List in 4lmn
Fluorine binding site 3 out of 3 in the Crystal Structure of MEK1 Kinase Bound to GDC0973


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 3 of Crystal Structure of MEK1 Kinase Bound to GDC0973 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F503

b:69.6
occ:1.00
F7 A:EUI503 0.0 69.6 1.0
C6 A:EUI503 1.3 70.7 1.0
C1 A:EUI503 2.4 72.2 1.0
C5 A:EUI503 2.4 69.3 1.0
N9 A:EUI503 2.7 63.1 1.0
OD1 A:ASP208 3.3 70.1 1.0
CD1 A:ILE141 3.4 73.9 1.0
CE A:LYS97 3.6 65.3 1.0
CE A:MET143 3.6 62.8 1.0
C4 A:EUI503 3.6 68.8 1.0
C2 A:EUI503 3.7 72.6 1.0
CD A:LYS97 3.7 68.1 1.0
O20 A:EUI503 3.8 64.1 1.0
CG2 A:ILE141 3.9 67.9 1.0
CB A:ILE141 3.9 68.7 1.0
C10 A:EUI503 4.1 59.5 1.0
SD A:MET143 4.1 66.3 1.0
C3 A:EUI503 4.1 70.6 1.0
CG1 A:ILE141 4.3 69.4 1.0
CG A:ASP208 4.4 66.1 1.0
CB A:LYS97 4.5 64.9 1.0
C18 A:EUI503 4.7 63.1 1.0
CG A:LYS97 4.7 71.5 1.0
N A:ASP208 4.7 60.1 1.0
CA A:ASP208 4.8 59.5 1.0
NZ A:LYS97 4.8 79.5 1.0
C15 A:EUI503 4.9 60.7 1.0
F16 A:EUI503 5.0 59.6 1.0

Reference:

G.Hatzivassiliou, J.R.Haling, H.Chen, K.Song, S.Price, R.Heald, J.F.Hewitt, M.Zak, A.Peck, C.Orr, M.Merchant, K.P.Hoeflich, J.Chan, S.M.Luoh, D.J.Anderson, M.J.Ludlam, C.Wiesmann, M.Ultsch, L.S.Friedman, S.Malek, M.Belvin. Mechanism of Mek Inhibition Determines Efficacy in Mutant Kras- Versus Braf-Driven Cancers. Nature V. 501 232 2013.
ISSN: ISSN 0028-0836
PubMed: 23934108
DOI: 10.1038/NATURE12441
Page generated: Thu Aug 1 03:27:55 2024

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