Potassium in PDB 7jzf: Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site
Enzymatic activity of Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site
All present enzymatic activity of Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site:
4.3.3.7;
Protein crystallography data
The structure of Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site, PDB code: 7jzf
was solved by
A.J.Board,
R.C.J.Dobson,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
33.23 /
1.82
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
120.679,
120.679,
110.571,
90,
90,
120
|
R / Rfree (%)
|
14.4 /
17.4
|
Potassium Binding Sites:
The binding sites of Potassium atom in the Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site
(pdb code 7jzf). 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 Mutant S48F with Pyruvate in the Catalytic Site, PDB code: 7jzf:
Jump to Potassium binding site number:
1;
2;
3;
4;
Potassium binding site 1 out
of 4 in 7jzf
Go back to
Potassium Binding Sites List in 7jzf
Potassium binding site 1 out
of 4 in the Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 1 of Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K301
b:25.3
occ:1.00
|
O
|
A:ILE157
|
2.6
|
19.5
|
1.0
|
O
|
A:VAL154
|
2.6
|
25.0
|
1.0
|
O
|
A:ALA152
|
2.7
|
23.0
|
1.0
|
O
|
A:HOH628
|
2.7
|
32.9
|
1.0
|
O
|
A:HOH658
|
2.8
|
54.6
|
1.0
|
O
|
A:LYS155
|
3.0
|
25.6
|
1.0
|
C
|
A:LYS155
|
3.6
|
26.1
|
1.0
|
C
|
A:ILE157
|
3.7
|
18.9
|
1.0
|
C
|
A:VAL154
|
3.7
|
22.3
|
1.0
|
C
|
A:ALA152
|
3.8
|
22.8
|
1.0
|
CA
|
A:LYS155
|
4.0
|
28.6
|
1.0
|
N
|
A:ILE157
|
4.1
|
20.2
|
1.0
|
O
|
A:HOH623
|
4.3
|
44.1
|
1.0
|
N
|
A:LYS155
|
4.3
|
26.1
|
1.0
|
CA
|
A:ILE157
|
4.4
|
17.9
|
1.0
|
CA
|
A:ALA152
|
4.4
|
19.1
|
1.0
|
N
|
A:ASN156
|
4.5
|
22.5
|
1.0
|
N
|
A:VAL154
|
4.5
|
24.2
|
1.0
|
N
|
A:ILE158
|
4.6
|
18.0
|
1.0
|
C
|
A:LYS153
|
4.6
|
27.2
|
1.0
|
CA
|
A:ILE158
|
4.6
|
19.9
|
1.0
|
CG2
|
A:ILE158
|
4.7
|
29.0
|
1.0
|
N
|
A:LYS153
|
4.8
|
19.5
|
1.0
|
CA
|
A:VAL154
|
4.8
|
23.6
|
1.0
|
CB
|
A:ILE157
|
4.9
|
18.3
|
1.0
|
C
|
A:ASN156
|
4.9
|
24.1
|
1.0
|
CA
|
A:LYS153
|
4.9
|
25.3
|
1.0
|
|
Potassium binding site 2 out
of 4 in 7jzf
Go back to
Potassium Binding Sites List in 7jzf
Potassium binding site 2 out
of 4 in the Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 2 of Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K302
b:27.3
occ:1.00
|
OD1
|
A:ASN80
|
2.6
|
15.3
|
1.0
|
O
|
B:ALA49
|
2.6
|
25.9
|
1.0
|
O
|
A:HOH650
|
2.7
|
31.3
|
1.0
|
O
|
B:HOH479
|
2.8
|
26.2
|
1.0
|
O
|
B:HOH690
|
3.1
|
41.8
|
1.0
|
O
|
A:HOH636
|
3.2
|
37.7
|
1.0
|
O
|
A:HOH606
|
3.3
|
30.4
|
1.0
|
CG
|
A:ASN80
|
3.7
|
16.8
|
1.0
|
C
|
B:ALA49
|
3.8
|
22.5
|
1.0
|
ND2
|
A:ASN80
|
4.2
|
16.1
|
1.0
|
CA
|
B:ALA49
|
4.4
|
22.0
|
1.0
|
CB
|
A:ALA81
|
4.5
|
17.5
|
1.0
|
N
|
A:ALA81
|
4.5
|
15.0
|
1.0
|
N
|
B:THR50
|
4.8
|
17.5
|
1.0
|
O
|
B:HOH674
|
4.8
|
29.7
|
1.0
|
N
|
A:ASN80
|
4.9
|
15.2
|
1.0
|
C
|
A:ASN80
|
4.9
|
18.3
|
1.0
|
CA
|
B:THR50
|
5.0
|
18.9
|
1.0
|
O
|
B:PHE48
|
5.0
|
21.5
|
1.0
|
O
|
B:HOH681
|
5.0
|
44.5
|
1.0
|
|
Potassium binding site 3 out
of 4 in 7jzf
Go back to
Potassium Binding Sites List in 7jzf
Potassium binding site 3 out
of 4 in the Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 3 of Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K301
b:21.0
occ:1.00
|
O
|
B:ILE157
|
2.6
|
13.5
|
1.0
|
O
|
B:ALA152
|
2.7
|
15.8
|
1.0
|
O
|
B:VAL154
|
2.7
|
21.9
|
1.0
|
O
|
B:HOH661
|
2.7
|
29.3
|
1.0
|
O
|
B:HOH667
|
3.0
|
48.0
|
1.0
|
O
|
B:LYS155
|
3.2
|
18.8
|
1.0
|
C
|
B:ALA152
|
3.7
|
16.3
|
1.0
|
C
|
B:LYS155
|
3.7
|
21.9
|
1.0
|
C
|
B:ILE157
|
3.7
|
14.4
|
1.0
|
C
|
B:VAL154
|
3.8
|
22.7
|
1.0
|
CA
|
B:LYS155
|
4.1
|
23.9
|
1.0
|
O
|
B:HOH533
|
4.1
|
40.2
|
1.0
|
N
|
B:ILE157
|
4.2
|
14.4
|
1.0
|
CA
|
B:ALA152
|
4.3
|
15.1
|
1.0
|
N
|
B:LYS155
|
4.4
|
22.6
|
1.0
|
CA
|
B:ILE157
|
4.5
|
14.4
|
1.0
|
O
|
B:HOH663
|
4.6
|
41.0
|
1.0
|
N
|
B:ASN156
|
4.6
|
19.1
|
1.0
|
N
|
B:VAL154
|
4.6
|
21.4
|
1.0
|
C
|
B:LYS153
|
4.6
|
23.0
|
1.0
|
N
|
B:ILE158
|
4.7
|
13.8
|
1.0
|
CA
|
B:ILE158
|
4.7
|
15.8
|
1.0
|
N
|
B:LYS153
|
4.7
|
17.3
|
1.0
|
CA
|
B:VAL154
|
4.8
|
21.4
|
1.0
|
CG2
|
B:ILE158
|
4.8
|
24.9
|
1.0
|
CD1
|
B:PHE181
|
4.9
|
14.1
|
1.0
|
CB
|
B:ILE157
|
4.9
|
13.7
|
1.0
|
O
|
B:LYS153
|
4.9
|
21.0
|
1.0
|
CA
|
B:LYS153
|
5.0
|
18.7
|
1.0
|
CB
|
B:ALA152
|
5.0
|
14.4
|
1.0
|
C
|
B:ASN156
|
5.0
|
14.5
|
1.0
|
|
Potassium binding site 4 out
of 4 in 7jzf
Go back to
Potassium Binding Sites List in 7jzf
Potassium binding site 4 out
of 4 in the Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 4 of Dihydrodipicolinate Synthase Mutant S48F with Pyruvate in the Catalytic Site within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:K302
b:32.6
occ:1.00
|
O
|
B:THR126
|
2.7
|
21.0
|
1.0
|
O
|
B:ALA123
|
2.8
|
16.8
|
1.0
|
O
|
B:HOH678
|
2.8
|
44.0
|
1.0
|
O
|
B:HOH409
|
2.9
|
39.1
|
1.0
|
O
|
B:HOH497
|
2.9
|
24.6
|
1.0
|
O
|
B:GLU124
|
3.2
|
22.7
|
1.0
|
C
|
B:GLU124
|
3.7
|
22.8
|
1.0
|
C
|
B:THR126
|
3.8
|
20.8
|
1.0
|
ND2
|
B:ASN156
|
3.9
|
19.6
|
1.0
|
OD1
|
B:ASN156
|
3.9
|
22.1
|
1.0
|
C
|
B:ALA123
|
3.9
|
16.6
|
1.0
|
CA
|
B:GLU124
|
3.9
|
20.6
|
1.0
|
O
|
B:HOH565
|
4.0
|
38.2
|
1.0
|
CG
|
B:ASN156
|
4.1
|
17.9
|
1.0
|
N
|
B:THR126
|
4.3
|
18.1
|
1.0
|
N
|
B:GLU124
|
4.3
|
16.5
|
1.0
|
OD1
|
B:ASP127
|
4.4
|
34.0
|
1.0
|
N
|
B:HIS125
|
4.6
|
19.2
|
1.0
|
N
|
B:ASP127
|
4.6
|
21.4
|
1.0
|
CA
|
B:ASP127
|
4.7
|
23.1
|
1.0
|
CA
|
B:THR126
|
4.7
|
19.4
|
1.0
|
|
Reference:
A.J.Board,
R.C.J.Dobson.
Mapping the Uncharted Water Channel of Dhdps To Be Published.
Page generated: Mon Aug 12 19:12:51 2024
|