Atomistry » Manganese » PDB 8iri-8kft » 8jdz
Atomistry »
  Manganese »
    PDB 8iri-8kft »
      8jdz »

Manganese in PDB 8jdz: Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid

Enzymatic activity of Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid

All present enzymatic activity of Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid:
1.1.2.4;

Protein crystallography data

The structure of Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid, PDB code: 8jdz was solved by S.Jin, X.Chen, J.Yang, J.Ding, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 34.13 / 1.56
Space group I 2 2 2
Cell size a, b, c (Å), α, β, γ (°) 82.07, 102.58, 122.94, 90, 90, 90
R / Rfree (%) 18 / 20.5

Manganese Binding Sites:

The binding sites of Manganese atom in the Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid (pdb code 8jdz). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total only one binding site of Manganese was determined in the Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid, PDB code: 8jdz:

Manganese binding site 1 out of 1 in 8jdz

Go back to Manganese Binding Sites List in 8jdz
Manganese binding site 1 out of 1 in the Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Crystal Structure of Mldhd in Complex with 2-Keto-3-Methylvaleric Acid within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn502

b:24.1
occ:0.56
OE2 A:GLU442 2.1 26.4 1.0
O43 A:1QQ503 2.2 26.4 1.0
NE2 A:HIS398 2.4 27.4 1.0
NE2 A:HIS405 2.4 28.7 1.0
O45 A:1QQ503 2.6 28.4 1.0
O4 A:FAD501 2.7 27.8 1.0
C42 A:1QQ503 3.0 32.0 1.0
C4 A:FAD501 3.1 25.4 1.0
C44 A:1QQ503 3.1 33.6 1.0
CD A:GLU442 3.2 26.6 1.0
CD2 A:HIS398 3.3 25.9 1.0
CE1 A:HIS398 3.3 26.0 1.0
CE1 A:HIS405 3.3 25.7 1.0
CD2 A:HIS405 3.4 27.3 1.0
N3 A:FAD501 3.5 23.4 1.0
OE1 A:GLU442 3.6 25.9 1.0
C4X A:FAD501 3.9 26.2 1.0
OXT A:1QQ503 4.2 30.1 1.0
NE2 A:HIS443 4.2 25.0 1.0
NH2 A:ARG347 4.2 27.4 1.0
N5 A:FAD501 4.3 27.4 1.0
ND1 A:HIS398 4.4 24.2 1.0
O A:HOH770 4.4 26.9 1.0
CG A:HIS398 4.4 23.4 1.0
O A:HOH629 4.4 28.7 1.0
ND1 A:HIS405 4.4 27.3 1.0
CG A:GLU442 4.4 22.9 1.0
CG A:HIS405 4.5 25.5 1.0
C2 A:FAD501 4.5 23.0 1.0
C46 A:1QQ503 4.6 34.5 1.0
C10 A:FAD501 4.8 22.7 1.0
CE1 A:HIS443 4.9 24.6 1.0
CD2 A:HIS443 4.9 25.1 1.0

Reference:

S.Jin, X.Chen, J.Yang, J.Ding. Lactate Dehydrogenase D Is A General Dehydrogenase For D-2-Hydroxyacids Containing Hydrophobic Moieties and Plays An Important Role in the Pathogenesis of D-Lactic Acidosis To Be Published.
Page generated: Sun Oct 6 13:01:19 2024

Last articles

Zn in 9J0N
Zn in 9J0O
Zn in 9J0P
Zn in 9FJX
Zn in 9EKB
Zn in 9C0F
Zn in 9CAH
Zn in 9CH0
Zn in 9CH3
Zn in 9CH1
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy