Potassium in PDB 3i7r: Dihydrodipicolinate Synthase - K161R
Enzymatic activity of Dihydrodipicolinate Synthase - K161R
All present enzymatic activity of Dihydrodipicolinate Synthase - K161R:
4.2.1.52;
Protein crystallography data
The structure of Dihydrodipicolinate Synthase - K161R, PDB code: 3i7r
was solved by
R.C.J.Dobson,
G.B.Jameson,
J.A.Gerrard,
T.P.Soares Da Costa,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
34.92 /
2.10
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
121.435,
121.435,
111.037,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
19.5 /
23
|
Other elements in 3i7r:
The structure of Dihydrodipicolinate Synthase - K161R also contains other interesting chemical elements:
Potassium Binding Sites:
The binding sites of Potassium atom in the Dihydrodipicolinate Synthase - K161R
(pdb code 3i7r). This binding sites where shown within
5.0 Angstroms radius around Potassium atom.
In total 4 binding sites of Potassium where determined in the
Dihydrodipicolinate Synthase - K161R, PDB code: 3i7r:
Jump to Potassium binding site number:
1;
2;
3;
4;
Potassium binding site 1 out
of 4 in 3i7r
Go back to
Potassium Binding Sites List in 3i7r
Potassium binding site 1 out
of 4 in the Dihydrodipicolinate Synthase - K161R
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 1 of Dihydrodipicolinate Synthase - K161R within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K293
b:34.7
occ:1.00
|
O
|
A:VAL154
|
2.8
|
27.9
|
1.0
|
O
|
A:ALA152
|
2.8
|
24.7
|
1.0
|
O
|
A:ILE157
|
2.8
|
22.8
|
1.0
|
O
|
A:HOH428
|
2.9
|
46.8
|
1.0
|
O
|
A:LYS155
|
3.3
|
27.8
|
1.0
|
C
|
A:VAL154
|
3.8
|
27.6
|
1.0
|
C
|
A:LYS155
|
3.8
|
27.6
|
1.0
|
C
|
A:ILE157
|
3.8
|
23.5
|
1.0
|
C
|
A:ALA152
|
3.8
|
24.6
|
1.0
|
CA
|
A:LYS155
|
4.2
|
28.2
|
1.0
|
N
|
A:ILE157
|
4.3
|
24.1
|
1.0
|
N
|
A:LYS155
|
4.4
|
27.8
|
1.0
|
CA
|
A:ALA152
|
4.5
|
24.2
|
1.0
|
N
|
A:VAL154
|
4.6
|
27.2
|
1.0
|
CA
|
A:ILE157
|
4.6
|
23.8
|
1.0
|
N
|
A:ASN156
|
4.7
|
26.3
|
1.0
|
CA
|
A:ILE158
|
4.7
|
23.5
|
1.0
|
C
|
A:LYS153
|
4.7
|
27.0
|
1.0
|
N
|
A:ILE158
|
4.7
|
23.6
|
1.0
|
CG2
|
A:ILE158
|
4.7
|
24.1
|
1.0
|
CA
|
A:VAL154
|
4.8
|
27.3
|
1.0
|
N
|
A:LYS153
|
4.8
|
25.6
|
1.0
|
CD1
|
A:PHE181
|
5.0
|
26.1
|
1.0
|
O
|
A:LYS153
|
5.0
|
27.0
|
1.0
|
|
Potassium binding site 2 out
of 4 in 3i7r
Go back to
Potassium Binding Sites List in 3i7r
Potassium binding site 2 out
of 4 in the Dihydrodipicolinate Synthase - K161R
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 2 of Dihydrodipicolinate Synthase - K161R within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K294
b:40.6
occ:1.00
|
O
|
A:LEU51
|
2.7
|
21.2
|
1.0
|
O
|
A:SER48
|
2.9
|
21.1
|
1.0
|
O3
|
A:GOL295
|
2.9
|
19.9
|
0.5
|
O
|
A:HOH469
|
3.0
|
43.0
|
1.0
|
O
|
A:HOH440
|
3.1
|
45.6
|
1.0
|
O3
|
A:GOL295
|
3.1
|
29.9
|
0.5
|
O
|
A:ALA49
|
3.2
|
20.2
|
1.0
|
C
|
A:ALA49
|
3.7
|
20.4
|
1.0
|
C3
|
A:GOL295
|
3.8
|
24.3
|
0.5
|
C
|
A:LEU51
|
3.9
|
21.6
|
1.0
|
O2
|
A:GOL295
|
3.9
|
24.8
|
0.5
|
C
|
A:SER48
|
4.0
|
20.5
|
1.0
|
CA
|
A:ALA49
|
4.1
|
20.4
|
1.0
|
C3
|
A:GOL295
|
4.2
|
30.3
|
0.5
|
N
|
A:LEU51
|
4.4
|
20.9
|
1.0
|
N
|
A:THR50
|
4.4
|
20.4
|
1.0
|
C2
|
A:GOL295
|
4.5
|
24.4
|
0.5
|
O2
|
A:GOL298
|
4.5
|
43.0
|
1.0
|
N
|
A:ALA49
|
4.6
|
20.3
|
1.0
|
O3
|
A:GOL298
|
4.6
|
34.5
|
1.0
|
CA
|
A:ASN52
|
4.6
|
21.8
|
1.0
|
N
|
A:ASN52
|
4.7
|
21.9
|
1.0
|
CA
|
A:LEU51
|
4.8
|
21.5
|
1.0
|
O
|
A:HOH429
|
4.9
|
30.0
|
1.0
|
C
|
A:THR50
|
4.9
|
21.1
|
1.0
|
CA
|
A:THR50
|
5.0
|
20.8
|
1.0
|
O
|
A:HOH464
|
5.0
|
32.7
|
1.0
|
|
Potassium binding site 3 out
of 4 in 3i7r
Go back to
Potassium Binding Sites List in 3i7r
Potassium binding site 3 out
of 4 in the Dihydrodipicolinate Synthase - K161R
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 3 of Dihydrodipicolinate Synthase - K161R within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K293
b:28.9
occ:1.00
|
O
|
B:ILE157
|
2.7
|
20.8
|
1.0
|
O
|
B:VAL154
|
2.7
|
26.4
|
1.0
|
O
|
B:ALA152
|
2.7
|
22.0
|
1.0
|
O
|
B:LYS155
|
3.1
|
25.4
|
1.0
|
C
|
B:LYS155
|
3.7
|
26.0
|
1.0
|
C
|
B:ILE157
|
3.7
|
21.0
|
1.0
|
C
|
B:VAL154
|
3.7
|
26.4
|
1.0
|
C
|
B:ALA152
|
3.8
|
22.5
|
1.0
|
CA
|
B:LYS155
|
4.1
|
26.9
|
1.0
|
N
|
B:ILE157
|
4.2
|
21.4
|
1.0
|
N
|
B:LYS155
|
4.4
|
26.5
|
1.0
|
CA
|
B:ALA152
|
4.4
|
22.0
|
1.0
|
CA
|
B:ILE157
|
4.5
|
21.1
|
1.0
|
N
|
B:VAL154
|
4.5
|
25.9
|
1.0
|
C
|
B:LYS153
|
4.6
|
25.7
|
1.0
|
N
|
B:ASN156
|
4.6
|
24.4
|
1.0
|
N
|
B:ILE158
|
4.6
|
21.4
|
1.0
|
CA
|
B:ILE158
|
4.7
|
21.4
|
1.0
|
N
|
B:LYS153
|
4.8
|
23.8
|
1.0
|
CA
|
B:VAL154
|
4.8
|
25.7
|
1.0
|
CD1
|
B:PHE181
|
4.9
|
21.0
|
1.0
|
O
|
B:HOH342
|
4.9
|
36.3
|
1.0
|
CB
|
B:ILE157
|
4.9
|
21.0
|
1.0
|
O
|
B:LYS153
|
4.9
|
25.9
|
1.0
|
CA
|
B:LYS153
|
5.0
|
25.4
|
1.0
|
C
|
B:ASN156
|
5.0
|
22.2
|
1.0
|
|
Potassium binding site 4 out
of 4 in 3i7r
Go back to
Potassium Binding Sites List in 3i7r
Potassium binding site 4 out
of 4 in the Dihydrodipicolinate Synthase - K161R
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 4 of Dihydrodipicolinate Synthase - K161R within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K294
b:43.2
occ:1.00
|
O
|
B:THR126
|
2.7
|
25.0
|
1.0
|
O
|
B:HOH438
|
2.8
|
27.4
|
1.0
|
O
|
B:HOH343
|
2.8
|
35.3
|
1.0
|
O
|
B:ALA123
|
2.9
|
19.2
|
1.0
|
O
|
B:HOH378
|
3.0
|
37.2
|
1.0
|
O
|
B:GLU124
|
3.4
|
22.4
|
1.0
|
C
|
B:GLU124
|
3.8
|
22.0
|
1.0
|
C
|
B:THR126
|
3.9
|
24.6
|
1.0
|
ND2
|
B:ASN156
|
3.9
|
26.8
|
1.0
|
OD1
|
B:ASN156
|
3.9
|
26.7
|
1.0
|
C
|
B:ALA123
|
3.9
|
19.0
|
1.0
|
CA
|
B:GLU124
|
4.0
|
21.1
|
1.0
|
CG
|
B:ASN156
|
4.1
|
24.3
|
1.0
|
N
|
B:THR126
|
4.3
|
23.7
|
1.0
|
N
|
B:GLU124
|
4.4
|
19.9
|
1.0
|
OD1
|
B:ASP127
|
4.5
|
32.0
|
1.0
|
N
|
B:HIS125
|
4.6
|
22.6
|
1.0
|
N
|
B:ASP127
|
4.7
|
25.3
|
1.0
|
CA
|
B:THR126
|
4.7
|
24.0
|
1.0
|
CA
|
B:ASP127
|
4.8
|
26.0
|
1.0
|
|
Reference:
T.P.Soares Da Costa,
A.C.Muscroft-Taylor,
R.C.Dobson,
S.R.Devenish,
G.B.Jameson,
J.A.Gerrard.
How Essential Is the 'Essential' Active-Site Lysine in Dihydrodipicolinate Synthase? Biochimie V. 92 837 2010.
ISSN: ISSN 0300-9084
PubMed: 20353808
DOI: 10.1016/J.BIOCHI.2010.03.004
Page generated: Mon Aug 12 08:30:02 2024
|