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Magnesium in PDB 6rm7: Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface

Protein crystallography data

The structure of Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface, PDB code: 6rm7 was solved by B.Somsen, M.Wolter, X.Guillory, S.Genet, S.Leysen, J.Patel, P.Castaldi, C.Ottmann, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 45.53 / 1.60
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 82.135, 111.973, 62.706, 90.00, 90.00, 90.00
R / Rfree (%) 14.5 / 16.9

Other elements in 6rm7:

The structure of Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface also contains other interesting chemical elements:

Chlorine (Cl) 1 atom

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface (pdb code 6rm7). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface, PDB code: 6rm7:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 6rm7

Go back to Magnesium Binding Sites List in 6rm7
Magnesium binding site 1 out of 2 in the Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg301

b:30.4
occ:1.00
O A:HOH552 3.1 21.4 1.0
OE2 A:GLU188 4.6 17.5 1.0

Magnesium binding site 2 out of 2 in 6rm7

Go back to Magnesium Binding Sites List in 6rm7
Magnesium binding site 2 out of 2 in the Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Fragment Az-026 Binding at the P53PT387/14-3-3 Sigma Interface within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg302

b:18.8
occ:1.00
O A:HOH419 2.2 25.8 1.0
OE1 A:GLU86 2.4 19.6 0.5
OE2 A:GLU86 2.4 21.8 0.5
OE2 A:GLU89 2.4 16.8 1.0
O A:HOH612 2.4 31.1 1.0
CD A:GLU86 2.7 15.9 0.5
CD A:GLU89 3.5 11.3 1.0
HG2 A:GLU89 3.7 14.0 1.0
HH12 A:ARG85 3.8 21.6 1.0
HG2 A:GLU86 4.0 16.5 0.5
HE22 A:GLN93 4.0 18.9 1.0
O A:HOH503 4.1 29.9 1.0
CG A:GLU89 4.1 11.6 1.0
HH11 A:ARG85 4.2 21.6 1.0
CG A:GLU86 4.3 16.4 0.5
HB3 A:GLU89 4.3 15.9 1.0
NH1 A:ARG85 4.4 18.0 1.0
OE1 A:GLU89 4.4 13.5 1.0
O A:HOH501 4.4 27.8 1.0
HA A:GLU86 4.4 15.6 0.5
HA A:GLU86 4.4 15.7 0.5
OE1 A:GLN93 4.5 15.8 1.0
HG1 A:THR90 4.5 18.9 1.0
O A:HOH568 4.6 29.4 1.0
HG2 A:GLU86 4.6 19.6 0.5
HG3 A:GLU86 4.7 19.6 0.5
NE2 A:GLN93 4.7 15.8 1.0
HB3 A:GLU86 4.7 17.2 0.5
CB A:GLU89 4.8 13.2 1.0
OG1 A:THR90 4.8 15.8 1.0
CG A:GLU86 4.8 13.8 0.5
HG3 A:GLU89 5.0 14.0 1.0
HB3 A:GLU86 5.0 17.5 0.5
CD A:GLN93 5.0 17.2 1.0

Reference:

X.Guillory, M.Wolter, S.Leysen, J.F.Neves, A.Kuusk, S.Genet, B.Somsen, J.Morrow, E.Rivers, L.Van Beek, J.Patel, R.Goodnow, H.Schoenherr, N.Fuller, Q.Cao, R.G.Doveston, L.Brunsveld, M.R.Arkin, M.P.Castaldi, H.Boyd, I.Landrieu, H.Chen, C.Ottmann. Fragment-Based Differential Targeting of Ppi Stabilizer Interfaces. J.Med.Chem. 2020.
ISSN: ISSN 0022-2623
PubMed: 32501690
DOI: 10.1021/ACS.JMEDCHEM.9B01942
Page generated: Tue Oct 1 17:25:27 2024

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