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Magnesium in PDB 4l9w: Crystal Structure of H-Ras G12C, Gmppnp-Bound

Enzymatic activity of Crystal Structure of H-Ras G12C, Gmppnp-Bound

All present enzymatic activity of Crystal Structure of H-Ras G12C, Gmppnp-Bound:
3.6.5.2;

Protein crystallography data

The structure of Crystal Structure of H-Ras G12C, Gmppnp-Bound, PDB code: 4l9w was solved by J.M.Ostrem, U.Peters, M.L.Sos, J.A.Wells, K.M.Shokat, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 1.95
Space group H 3 2
Cell size a, b, c (Å), α, β, γ (°) 89.148, 89.148, 136.314, 90.00, 90.00, 120.00
R / Rfree (%) 15.6 / 18.9

Other elements in 4l9w:

The structure of Crystal Structure of H-Ras G12C, Gmppnp-Bound also contains other interesting chemical elements:

Calcium (Ca) 2 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of H-Ras G12C, Gmppnp-Bound (pdb code 4l9w). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total only one binding site of Magnesium was determined in the Crystal Structure of H-Ras G12C, Gmppnp-Bound, PDB code: 4l9w:

Magnesium binding site 1 out of 1 in 4l9w

Go back to Magnesium Binding Sites List in 4l9w
Magnesium binding site 1 out of 1 in the Crystal Structure of H-Ras G12C, Gmppnp-Bound


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Crystal Structure of H-Ras G12C, Gmppnp-Bound within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg202

b:25.2
occ:1.00
O A:HOH301 2.0 24.5 1.0
O2B A:GNP201 2.0 21.1 1.0
O1G A:GNP201 2.1 24.8 1.0
OG1 A:THR35 2.1 25.1 1.0
O A:HOH312 2.1 23.7 1.0
OG A:SER17 2.1 25.6 1.0
CB A:THR35 3.1 25.3 1.0
CB A:SER17 3.2 24.0 1.0
PG A:GNP201 3.2 25.6 1.0
PB A:GNP201 3.2 22.5 1.0
N3B A:GNP201 3.3 28.3 1.0
N A:THR35 3.8 27.7 1.0
N A:SER17 3.9 19.9 1.0
O3G A:GNP201 4.0 30.1 1.0
CA A:THR35 4.0 26.0 1.0
O2A A:GNP201 4.1 26.2 1.0
OD2 A:ASP57 4.1 32.8 1.0
CA A:SER17 4.1 22.4 1.0
O A:HOH320 4.1 29.1 1.0
CG2 A:THR35 4.2 24.9 1.0
OD1 A:ASP57 4.2 29.9 1.0
O1B A:GNP201 4.2 22.2 1.0
O3A A:GNP201 4.2 23.8 1.0
O2G A:GNP201 4.3 21.2 1.0
O A:ASP33 4.4 23.8 1.0
O A:THR58 4.4 27.7 1.0
PA A:GNP201 4.5 23.7 1.0
CG A:ASP57 4.5 34.0 1.0
O1A A:GNP201 4.6 22.6 1.0
C A:PRO34 4.7 29.9 1.0
CB A:LYS16 4.8 20.8 1.0
CE A:LYS16 4.9 20.6 1.0
C A:LYS16 5.0 22.0 1.0

Reference:

J.M.Ostrem, U.Peters, M.L.Sos, J.A.Wells, K.M.Shokat. K-Ras(G12C) Inhibitors Allosterically Control Gtp Affinity and Effector Interactions. Nature V. 503 548 2013.
ISSN: ISSN 0028-0836
PubMed: 24256730
DOI: 10.1038/NATURE12796
Page generated: Sat Aug 17 04:29:27 2024

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