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Magnesium in PDB 4le0: Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium

Protein crystallography data

The structure of Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium, PDB code: 4le0 was solved by F.Trajtenberg, N.Larrieux, A.Buschiazzo, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.94 / 2.27
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 43.945, 71.782, 52.193, 90.00, 104.25, 90.00
R / Rfree (%) 17.7 / 21.3

Other elements in 4le0:

The structure of Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium also contains other interesting chemical elements:

Fluorine (F) 6 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium (pdb code 4le0). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium, PDB code: 4le0:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 4le0

Go back to Magnesium Binding Sites List in 4le0
Magnesium binding site 1 out of 2 in the Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium


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 the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg201

b:22.3
occ:1.00
F2 A:BEF202 2.0 22.3 1.0
OD2 A:ASP54 2.1 12.7 1.0
OD1 A:ASP9 2.1 18.9 1.0
O A:GLU56 2.1 22.2 1.0
O A:HOH307 2.1 25.3 1.0
O A:HOH301 2.2 26.6 1.0
CG A:ASP54 3.0 14.8 1.0
CG A:ASP9 3.2 19.7 1.0
BE A:BEF202 3.2 20.3 1.0
C A:GLU56 3.3 23.1 1.0
OD1 A:ASP54 3.4 18.2 1.0
OD2 A:ASP9 3.7 27.8 1.0
O A:HOH362 3.8 57.6 1.0
OE2 A:GLU8 3.9 26.1 1.0
O A:HOH361 4.0 30.2 1.0
CA A:GLU56 4.1 19.4 1.0
F3 A:BEF202 4.2 21.4 1.0
N A:MET57 4.3 18.4 1.0
N A:GLU56 4.3 18.4 1.0
CB A:GLU56 4.3 21.6 1.0
CG A:MET57 4.4 18.5 1.0
CB A:ASP54 4.4 14.0 1.0
CB A:ASP9 4.4 15.2 1.0
F1 A:BEF202 4.4 18.6 1.0
NZ A:LYS102 4.5 14.1 1.0
N A:ASP9 4.5 15.2 1.0
CA A:MET57 4.6 17.0 1.0
CD A:GLU8 4.6 21.9 1.0
O A:HOH355 4.6 42.5 1.0
OE1 A:GLU8 4.6 24.9 1.0
CG A:GLN10 4.8 43.9 1.0
CA A:ASP9 5.0 14.7 1.0

Magnesium binding site 2 out of 2 in 4le0

Go back to Magnesium Binding Sites List in 4le0
Magnesium binding site 2 out of 2 in the Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg201

b:17.1
occ:1.00
F1 B:BEF202 2.0 23.4 1.0
O B:GLU56 2.1 18.8 1.0
O B:HOH335 2.1 24.6 1.0
O B:HOH301 2.1 13.6 1.0
OD1 B:ASP9 2.1 16.9 1.0
OD2 B:ASP54 2.2 22.2 1.0
CG B:ASP54 3.1 19.2 1.0
BE B:BEF202 3.2 22.8 1.0
CG B:ASP9 3.2 20.9 1.0
C B:GLU56 3.3 19.2 1.0
OD1 B:ASP54 3.4 19.8 1.0
OD2 B:ASP9 3.7 28.5 1.0
OE2 B:GLU8 4.0 18.5 1.0
CA B:GLU56 4.0 17.2 1.0
CB B:GLU56 4.2 18.4 1.0
O B:HOH305 4.2 23.9 1.0
F3 B:BEF202 4.3 21.8 1.0
N B:MET57 4.3 15.4 1.0
N B:GLU56 4.3 17.8 1.0
O B:HOH310 4.3 44.6 1.0
F2 B:BEF202 4.4 23.1 1.0
CG B:MET57 4.4 18.4 1.0
CB B:ASP9 4.5 17.9 1.0
NZ B:LYS102 4.5 24.4 1.0
CB B:ASP54 4.5 16.5 1.0
O B:HOH354 4.5 45.2 1.0
CA B:MET57 4.6 14.8 1.0
N B:ASP9 4.6 15.6 1.0
CD B:GLU8 4.7 30.5 1.0
OE1 B:GLU8 4.7 18.9 1.0
CG B:GLN10 4.8 39.4 1.0

Reference:

F.Trajtenberg, A.Albanesi, N.Ruetalo, H.Botti, A.Mechaly, L.Cybulski, N.Larrieux, D.De Mendoza, A.Buschiazzo. A Non-Canonical Protein Surface Is Key in Allosteric Control of Response Regulators To Be Published.
Page generated: Sat Aug 17 04:53:31 2024

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