Magnesium in PDB 6h07: X-Ray Structure of Lactobacillus Brevis Alcohol Dehydrogenase

Protein crystallography data

The structure of X-Ray Structure of Lactobacillus Brevis Alcohol Dehydrogenase, PDB code: 6h07 was solved by J.Hermann, P.Nowotny, P.Biggel, S.Schneider, D.Hekmat, D.Weuster-Botz, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 47.15 / 1.48
Space group P 21 2 21
Cell size a, b, c (Å), α, β, γ (°) 56.030, 83.310, 114.380, 90.00, 90.00, 90.00
R / Rfree (%) 18 / 20.3

Other elements in 6h07:

The structure of X-Ray Structure of Lactobacillus Brevis Alcohol Dehydrogenase also contains other interesting chemical elements:

Manganese (Mn) 1 atom

Magnesium Binding Sites:

The binding sites of Magnesium atom in the X-Ray Structure of Lactobacillus Brevis Alcohol Dehydrogenase (pdb code 6h07). 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 X-Ray Structure of Lactobacillus Brevis Alcohol Dehydrogenase, PDB code: 6h07:

Magnesium binding site 1 out of 1 in 6h07

Go back to Magnesium Binding Sites List in 6h07
Magnesium binding site 1 out of 1 in the X-Ray Structure of Lactobacillus Brevis Alcohol Dehydrogenase


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of X-Ray Structure of Lactobacillus Brevis Alcohol Dehydrogenase within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg301

b:18.0
occ:0.75
MN B:MN302 0.0 17.9 0.2
O B:HOH526 2.0 18.0 1.0
O B:GLN251 2.0 16.2 1.0
O B:HOH441 2.1 17.6 1.0
C B:GLN251 3.1 16.3 1.0
OXT B:GLN251 3.3 15.7 1.0
O B:TYR248 4.3 17.6 1.0
O B:HOH409 4.4 24.0 1.0
CA B:GLN251 4.4 15.7 1.0
N B:GLN251 4.7 14.5 1.0
CG1 B:VAL147 4.7 16.6 1.0
O B:THR249 4.7 17.7 1.0
O B:HOH475 4.8 19.3 1.0
CG B:GLN251 4.8 16.7 1.0
CA B:THR249 5.0 15.0 1.0

Reference:

J.Hermann, P.Nowotny, T.E.Schrader, P.Biggel, D.Hekmat, D.Weuster-Botz. Neutron and X-Ray Crystal Structures of Lactobacillus Brevis Alcohol Dehydrogenase Reveal New Insights Into Hydrogen-Bonding Pathways. Acta Crystallogr F Struct V. 74 754 2018BIOL Commun.
ISSN: ESSN 2053-230X
PubMed: 30511668
DOI: 10.1107/S2053230X18015273
Page generated: Mon Dec 14 22:47:06 2020

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