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Magnesium in PDB 6r5o: The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules

Protein crystallography data

The structure of The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules, PDB code: 6r5o was solved by M.T.Batuecas, J.A.Hermoso, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 46.72 / 2.40
Space group P 1
Cell size a, b, c (Å), α, β, γ (°) 73.505, 74.907, 82.102, 65.64, 74.18, 68.90
R / Rfree (%) 23.8 / 27.6

Magnesium Binding Sites:

The binding sites of Magnesium atom in the The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules (pdb code 6r5o). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules, PDB code: 6r5o:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 6r5o

Go back to Magnesium Binding Sites List in 6r5o
Magnesium binding site 1 out of 2 in the The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg803

b:61.4
occ:1.00
O B:HOH985 2.0 36.0 1.0
O B:HOH942 2.3 40.4 1.0
O B:VAL694 2.5 30.8 1.0
OD1 B:ASP692 2.6 39.4 1.0
O B:GLU744 3.5 50.5 1.0
C B:VAL694 3.7 34.3 1.0
CG B:ASP692 3.7 41.6 1.0
O B:PRO742 3.8 48.9 1.0
CA B:GLY743 3.8 46.5 1.0
C B:GLY743 4.0 49.2 1.0
OD2 B:ASP692 4.2 42.4 1.0
N B:GLU744 4.3 50.1 1.0
C B:PRO742 4.3 45.0 1.0
N B:GLY743 4.3 46.0 1.0
O B:GLU741 4.3 48.2 1.0
N B:VAL694 4.4 39.2 1.0
CA B:VAL694 4.4 35.2 1.0
CB B:VAL694 4.4 35.6 1.0
O B:GLY743 4.5 49.8 1.0
C B:GLU744 4.6 50.8 1.0
O B:HOH1075 4.6 34.2 1.0
CE1 B:PHE745 4.7 47.7 1.0
N B:ALA695 4.8 35.6 1.0
O B:HOH1099 4.8 45.4 1.0
CZ B:PHE745 4.8 48.9 1.0
CB B:GLU741 4.9 57.8 1.0
C B:GLU741 4.9 48.5 1.0
CB B:ASP692 5.0 40.2 1.0
CA B:ALA695 5.0 37.2 1.0

Magnesium binding site 2 out of 2 in 6r5o

Go back to Magnesium Binding Sites List in 6r5o
Magnesium binding site 2 out of 2 in the The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of The Crystal Structure the Glycoside Hydrolase Bglx Inactive Mutant D286N From P. Aeruginosa in Complex with Two Glucose Molecules within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg803

b:40.9
occ:1.00
O A:HOH971 1.9 38.5 1.0
O A:HOH977 2.5 38.9 1.0
OD1 A:ASP692 2.7 50.7 1.0
O A:HOH918 2.8 38.4 1.0
O A:GLU744 2.9 67.7 1.0
C A:GLY743 3.4 65.4 1.0
O A:VAL694 3.4 40.3 1.0
CA A:GLY743 3.4 67.2 1.0
O A:GLY743 3.7 63.7 1.0
CG A:ASP692 3.7 54.3 1.0
O A:GLU741 3.8 48.2 1.0
N A:GLU744 3.8 70.7 1.0
O A:PRO742 3.9 63.7 1.0
C A:GLU744 3.9 67.5 1.0
N A:GLY743 3.9 68.4 1.0
CE2 A:PHE745 4.0 57.1 1.0
C A:PRO742 4.1 63.8 1.0
CZ A:PHE745 4.1 57.2 1.0
OD2 A:ASP692 4.2 51.2 1.0
CD2 A:PHE745 4.3 55.7 1.0
CA A:GLU744 4.5 69.5 1.0
C A:GLU741 4.6 51.1 1.0
C A:VAL694 4.6 41.1 1.0
CE1 A:PHE745 4.6 52.8 1.0
CG A:PHE745 4.8 54.2 1.0
N A:PHE745 4.9 61.4 1.0
CD1 A:PHE745 4.9 54.6 1.0
CB A:ASP692 4.9 56.1 1.0
CB A:GLU741 5.0 55.5 1.0

Reference:

K.V.Mahasenan, M.T.Batuecas, S.De Benedetti, C.Kim, N.Rana, M.Lee, D.Hesek, J.F.Fisher, J.Sanz-Aparicio, J.A.Hermoso, S.Mobashery. Catalytic Cycle of Glycoside Hydrolase Bglx Frompseudomonas Aeruginosaand Its Implications For Biofilm Formation. Acs Chem.Biol. V. 15 189 2020.
ISSN: ESSN 1554-8937
PubMed: 31877028
DOI: 10.1021/ACSCHEMBIO.9B00754
Page generated: Tue Oct 1 16:37:29 2024

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