Magnesium in PDB 8r3p: Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate
Enzymatic activity of Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate
All present enzymatic activity of Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate:
2.2.1.1;
Protein crystallography data
The structure of Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate, PDB code: 8r3p
was solved by
L.Ballut,
R.N.Georges,
N.Aghajari,
L.Hecquet,
F.Charmantray,
B.Doumeche,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
34.94 /
2.90
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
249.66,
68.22,
165.46,
90,
110.71,
90
|
R / Rfree (%)
|
20.8 /
24.3
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate
(pdb code 8r3p). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the
Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate, PDB code: 8r3p:
Jump to Magnesium binding site number:
1;
2;
3;
4;
Magnesium binding site 1 out
of 4 in 8r3p
Go back to
Magnesium Binding Sites List in 8r3p
Magnesium binding site 1 out
of 4 in the Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_01.jpg) Mono view
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_01_stereo.jpg) Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg702
b:96.1
occ:1.00
|
OD1
|
A:ASP158
|
1.9
|
72.1
|
1.0
|
O2A
|
A:TPP701
|
2.0
|
72.8
|
1.0
|
OD1
|
A:ASN188
|
2.1
|
78.8
|
1.0
|
ND2
|
A:ASN188
|
2.1
|
79.6
|
1.0
|
CG
|
A:ASN188
|
2.4
|
71.6
|
1.0
|
O
|
A:ILE190
|
2.6
|
67.1
|
1.0
|
O2B
|
A:TPP701
|
2.8
|
67.7
|
1.0
|
O1B
|
A:TPP701
|
2.9
|
80.0
|
1.0
|
CG
|
A:ASP158
|
3.0
|
69.4
|
1.0
|
PB
|
A:TPP701
|
3.1
|
84.3
|
1.0
|
PA
|
A:TPP701
|
3.3
|
78.1
|
1.0
|
O3A
|
A:TPP701
|
3.4
|
77.0
|
1.0
|
N
|
A:ASP158
|
3.7
|
56.8
|
1.0
|
C
|
A:ILE190
|
3.8
|
68.0
|
1.0
|
CB
|
A:ASP158
|
3.8
|
58.8
|
1.0
|
O
|
A:ASP186
|
3.9
|
64.4
|
1.0
|
OD2
|
A:ASP158
|
3.9
|
73.2
|
1.0
|
CB
|
A:ASN188
|
3.9
|
63.9
|
1.0
|
N
|
A:ILE190
|
4.1
|
67.3
|
1.0
|
O1A
|
A:TPP701
|
4.2
|
73.8
|
1.0
|
O7
|
A:TPP701
|
4.3
|
64.6
|
1.0
|
CA
|
A:ASP158
|
4.4
|
60.1
|
1.0
|
N
|
A:ASN188
|
4.4
|
70.6
|
1.0
|
CA
|
A:ILE190
|
4.5
|
66.0
|
1.0
|
CA
|
A:GLY157
|
4.6
|
57.5
|
1.0
|
N
|
A:ASP189
|
4.6
|
69.0
|
1.0
|
CA
|
A:ASN188
|
4.6
|
63.6
|
1.0
|
C
|
A:GLY157
|
4.6
|
57.2
|
1.0
|
O3B
|
A:TPP701
|
4.6
|
77.5
|
1.0
|
N
|
A:SER191
|
4.8
|
71.7
|
1.0
|
C
|
A:ASN188
|
4.9
|
66.0
|
1.0
|
|
Magnesium binding site 2 out
of 4 in 8r3p
Go back to
Magnesium Binding Sites List in 8r3p
Magnesium binding site 2 out
of 4 in the Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_02.jpg) Mono view
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_02_stereo.jpg) Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg702
b:47.7
occ:1.00
|
O2A
|
B:TPP701
|
1.8
|
60.8
|
1.0
|
OD1
|
B:ASP158
|
1.9
|
53.8
|
1.0
|
OD1
|
B:ASN188
|
2.0
|
54.1
|
1.0
|
ND2
|
B:ASN188
|
2.6
|
62.9
|
1.0
|
CG
|
B:ASN188
|
2.6
|
51.4
|
1.0
|
O
|
B:ILE190
|
2.7
|
48.4
|
1.0
|
CG
|
B:ASP158
|
3.0
|
51.8
|
1.0
|
O2B
|
B:TPP701
|
3.0
|
54.3
|
1.0
|
PA
|
B:TPP701
|
3.1
|
60.1
|
1.0
|
O1B
|
B:TPP701
|
3.1
|
62.9
|
1.0
|
PB
|
B:TPP701
|
3.3
|
55.1
|
1.0
|
O3A
|
B:TPP701
|
3.4
|
60.7
|
1.0
|
O
|
B:ASP186
|
3.6
|
59.7
|
1.0
|
N
|
B:ASP158
|
3.6
|
42.9
|
1.0
|
CB
|
B:ASP158
|
3.7
|
45.9
|
1.0
|
O1A
|
B:TPP701
|
3.9
|
57.9
|
1.0
|
C
|
B:ILE190
|
3.9
|
57.0
|
1.0
|
OD2
|
B:ASP158
|
3.9
|
56.0
|
1.0
|
CB
|
B:ASN188
|
4.0
|
47.6
|
1.0
|
O7
|
B:TPP701
|
4.2
|
56.2
|
1.0
|
N
|
B:ASN188
|
4.2
|
54.7
|
1.0
|
CA
|
B:ASP158
|
4.3
|
40.5
|
1.0
|
N
|
B:ILE190
|
4.4
|
53.0
|
1.0
|
CA
|
B:GLY157
|
4.5
|
50.1
|
1.0
|
C
|
B:GLY157
|
4.6
|
50.6
|
1.0
|
CA
|
B:ASN188
|
4.6
|
53.6
|
1.0
|
CA
|
B:ILE190
|
4.8
|
54.6
|
1.0
|
N
|
B:ASP189
|
4.8
|
49.9
|
1.0
|
O3B
|
B:TPP701
|
4.8
|
59.7
|
1.0
|
C
|
B:ASP186
|
4.8
|
60.0
|
1.0
|
N
|
B:SER191
|
4.9
|
58.8
|
1.0
|
C
|
B:ASN188
|
4.9
|
52.2
|
1.0
|
CA
|
B:SER191
|
4.9
|
58.9
|
1.0
|
|
Magnesium binding site 3 out
of 4 in 8r3p
Go back to
Magnesium Binding Sites List in 8r3p
Magnesium binding site 3 out
of 4 in the Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_03.jpg) Mono view
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_03_stereo.jpg) Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg702
b:74.8
occ:1.00
|
O2A
|
C:TPP701
|
1.9
|
77.4
|
1.0
|
OD1
|
C:ASP158
|
2.5
|
80.1
|
1.0
|
O2B
|
C:TPP701
|
2.6
|
87.0
|
1.0
|
ND2
|
C:ASN188
|
2.6
|
82.8
|
1.0
|
OD1
|
C:ASN188
|
3.0
|
75.4
|
1.0
|
PA
|
C:TPP701
|
3.0
|
79.3
|
1.0
|
N
|
C:ASP158
|
3.1
|
70.6
|
1.0
|
CG
|
C:ASN188
|
3.1
|
80.6
|
1.0
|
O3A
|
C:TPP701
|
3.4
|
77.8
|
1.0
|
PB
|
C:TPP701
|
3.4
|
81.2
|
1.0
|
CA
|
C:GLY157
|
3.5
|
73.0
|
1.0
|
O1A
|
C:TPP701
|
3.5
|
73.0
|
1.0
|
CG
|
C:ASP158
|
3.5
|
78.9
|
1.0
|
O
|
C:ASP186
|
3.5
|
70.5
|
1.0
|
O3B
|
C:TPP701
|
3.6
|
81.4
|
1.0
|
O
|
C:ILE190
|
3.7
|
76.5
|
1.0
|
OD1
|
C:ASP186
|
3.7
|
90.2
|
1.0
|
C
|
C:GLY157
|
3.8
|
73.7
|
1.0
|
CB
|
C:ASP158
|
3.9
|
74.3
|
1.0
|
CA
|
C:ASP158
|
4.1
|
75.5
|
1.0
|
CG
|
C:ASP186
|
4.3
|
86.2
|
1.0
|
O7
|
C:TPP701
|
4.3
|
86.5
|
1.0
|
OD2
|
C:ASP158
|
4.6
|
79.2
|
1.0
|
CB
|
C:ASN188
|
4.6
|
71.1
|
1.0
|
OD2
|
C:ASP186
|
4.6
|
87.6
|
1.0
|
N
|
C:ASN188
|
4.7
|
72.6
|
1.0
|
C
|
C:ASP186
|
4.7
|
75.3
|
1.0
|
N
|
C:GLY157
|
4.8
|
74.7
|
1.0
|
O1B
|
C:TPP701
|
4.9
|
76.7
|
1.0
|
C
|
C:ILE190
|
4.9
|
80.1
|
1.0
|
N
|
C:GLY159
|
4.9
|
75.1
|
1.0
|
|
Magnesium binding site 4 out
of 4 in 8r3p
Go back to
Magnesium Binding Sites List in 8r3p
Magnesium binding site 4 out
of 4 in the Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_04.jpg) Mono view
![](/pictures/MG/pdb/r3/8r3p-MG-sphere_04_stereo.jpg) Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Transketolase From Enterococcus Faecium in Complex with Thiamin Pyrophosphate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg702
b:64.7
occ:1.00
|
O2A
|
D:TPP701
|
1.9
|
72.2
|
1.0
|
OD1
|
D:ASP158
|
1.9
|
70.0
|
1.0
|
ND2
|
D:ASN188
|
2.1
|
76.2
|
1.0
|
OD1
|
D:ASN188
|
2.3
|
70.3
|
1.0
|
CG
|
D:ASN188
|
2.5
|
66.2
|
1.0
|
O2B
|
D:TPP701
|
2.7
|
78.2
|
1.0
|
PA
|
D:TPP701
|
3.0
|
83.6
|
1.0
|
CG
|
D:ASP158
|
3.1
|
68.0
|
1.0
|
O3B
|
D:TPP701
|
3.2
|
77.7
|
1.0
|
O
|
D:ILE190
|
3.2
|
73.5
|
1.0
|
PB
|
D:TPP701
|
3.3
|
77.4
|
1.0
|
O3A
|
D:TPP701
|
3.3
|
74.2
|
1.0
|
N
|
D:ASP158
|
3.4
|
61.2
|
1.0
|
O
|
D:ASP186
|
3.5
|
60.9
|
1.0
|
CB
|
D:ASP158
|
3.7
|
63.4
|
1.0
|
O1A
|
D:TPP701
|
3.7
|
74.7
|
1.0
|
CB
|
D:ASN188
|
4.0
|
61.1
|
1.0
|
OD2
|
D:ASP158
|
4.1
|
67.8
|
1.0
|
CA
|
D:ASP158
|
4.2
|
61.0
|
1.0
|
N
|
D:ASN188
|
4.3
|
66.6
|
1.0
|
O7
|
D:TPP701
|
4.3
|
79.3
|
1.0
|
CA
|
D:GLY157
|
4.3
|
55.2
|
1.0
|
C
|
D:GLY157
|
4.4
|
60.7
|
1.0
|
C
|
D:ILE190
|
4.4
|
72.6
|
1.0
|
C
|
D:ASP186
|
4.7
|
61.6
|
1.0
|
CA
|
D:ASN188
|
4.7
|
67.3
|
1.0
|
O1B
|
D:TPP701
|
4.8
|
70.1
|
1.0
|
N
|
D:ILE190
|
4.9
|
68.5
|
1.0
|
|
Reference:
R.N.Georges,
L.Ballut,
N.Aghajari,
L.Hecquet,
F.Charmantray,
B.Doumeche.
Are Transketolases Relevant Targets Fighting Human Pathogens? A Comparative Biochemical, Bioinformatic and Structural Study To Be Published.
Page generated: Fri Oct 4 17:25:31 2024
|