Atomistry » Magnesium » PDB 1dam-1dtw » 1dtw
Atomistry »
  Magnesium »
    PDB 1dam-1dtw »
      1dtw »

Magnesium in PDB 1dtw: Human Branched-Chain Alpha-Keto Acid Dehydrogenase

Enzymatic activity of Human Branched-Chain Alpha-Keto Acid Dehydrogenase

All present enzymatic activity of Human Branched-Chain Alpha-Keto Acid Dehydrogenase:
1.2.4.4;

Protein crystallography data

The structure of Human Branched-Chain Alpha-Keto Acid Dehydrogenase, PDB code: 1dtw was solved by A.Aevarsson, J.L.Chuang, R.M.Wynn, S.Turley, D.T.Chuang, W.G.J.Hol, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.00 / 2.70
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 143.760, 143.760, 69.160, 90.00, 90.00, 120.00
R / Rfree (%) 22.4 / 27.9

Other elements in 1dtw:

The structure of Human Branched-Chain Alpha-Keto Acid Dehydrogenase also contains other interesting chemical elements:

Potassium (K) 2 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Human Branched-Chain Alpha-Keto Acid Dehydrogenase (pdb code 1dtw). 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 Human Branched-Chain Alpha-Keto Acid Dehydrogenase, PDB code: 1dtw:

Magnesium binding site 1 out of 1 in 1dtw

Go back to Magnesium Binding Sites List in 1dtw
Magnesium binding site 1 out of 1 in the Human Branched-Chain Alpha-Keto Acid Dehydrogenase


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Human Branched-Chain Alpha-Keto Acid Dehydrogenase within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg401

b:28.3
occ:1.00
O A:TYR224 2.1 35.0 1.0
OD1 A:ASN222 2.1 34.1 1.0
O12 A:TDP403 2.1 40.2 1.0
O A:HOH417 2.2 16.8 1.0
O23 A:TDP403 2.4 40.1 1.0
OE1 A:GLU193 2.5 27.6 1.0
CG A:ASN222 3.0 34.0 1.0
CD A:GLU193 3.2 27.6 1.0
P1 A:TDP403 3.2 40.3 1.0
OE2 A:GLU193 3.2 27.6 1.0
P2 A:TDP403 3.3 40.2 1.0
O11 A:TDP403 3.3 40.2 1.0
ND2 A:ASN222 3.3 34.0 1.0
C A:TYR224 3.3 35.0 1.0
O21 A:TDP403 3.5 40.0 1.0
O A:ARG220 4.1 32.9 1.0
N A:TYR224 4.2 34.8 1.0
N A:GLU193 4.2 27.4 1.0
N A:ALA225 4.2 35.0 1.0
N A:ASN222 4.3 33.7 1.0
O13 A:TDP403 4.3 40.2 1.0
CA A:TYR224 4.3 34.9 1.0
CB A:ASN222 4.3 34.0 1.0
O5G A:TDP403 4.3 40.2 1.0
CA A:ALA225 4.4 35.1 1.0
CA A:GLY192 4.5 27.6 1.0
N A:GLY194 4.6 27.0 1.0
O22 A:TDP403 4.6 40.1 1.0
CG A:GLU193 4.6 27.4 1.0
CA A:ASN222 4.7 33.9 1.0
C A:GLY192 4.8 27.5 1.0
C A:ASN222 4.8 34.1 1.0
NH1 A:ARG220 5.0 33.0 1.0
CB A:ALA225 5.0 35.1 1.0

Reference:

A.Aevarsson, J.L.Chuang, R.M.Wynn, S.Turley, D.T.Chuang, W.G.Hol. Crystal Structure of Human Branched-Chain Alpha-Ketoacid Dehydrogenase and the Molecular Basis of Multienzyme Complex Deficiency in Maple Syrup Urine Disease. Structure Fold.Des. V. 8 277 2000.
ISSN: ISSN 0969-2126
PubMed: 10745006
DOI: 10.1016/S0969-2126(00)00105-2
Page generated: Tue Aug 13 02:43:54 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy