Sodium in PDB 5t25: Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Enzymatic activity of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
All present enzymatic activity of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.:
4.3.3.7;
Protein crystallography data
The structure of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli., PDB code: 5t25
was solved by
L.Chooback,
L.M.Thomas,
W.E.Karsten,
C.D.Fleming,
P.Seabourn,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
26.81 /
1.99
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
136.647,
56.385,
101.530,
90.00,
127.62,
90.00
|
R / Rfree (%)
|
15.8 /
21.1
|
Sodium Binding Sites:
The binding sites of Sodium atom in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
(pdb code 5t25). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 10 binding sites of Sodium where determined in the
Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli., PDB code: 5t25:
Jump to Sodium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Sodium binding site 1 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 1 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 1 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na302
b:18.9
occ:1.00
|
OG
|
A:SER185
|
2.5
|
13.2
|
1.0
|
OG
|
A:SER190
|
2.7
|
14.7
|
1.0
|
O
|
A:HOH518
|
2.8
|
12.1
|
1.0
|
CB
|
A:SER185
|
3.3
|
12.9
|
1.0
|
CD2
|
A:PHE194
|
3.3
|
13.0
|
1.0
|
CB
|
A:PHE194
|
3.4
|
11.1
|
1.0
|
O
|
A:SER190
|
3.6
|
12.8
|
1.0
|
O
|
A:ASP187
|
3.6
|
14.2
|
1.0
|
C
|
A:SER190
|
3.7
|
11.8
|
1.0
|
CG
|
A:PHE194
|
3.7
|
11.4
|
1.0
|
CB
|
A:SER190
|
3.8
|
10.9
|
1.0
|
CB
|
A:ASP187
|
3.9
|
14.5
|
1.0
|
N
|
A:ALA191
|
4.0
|
12.7
|
1.0
|
CA
|
A:ALA191
|
4.0
|
14.3
|
1.0
|
CA
|
A:SER185
|
4.1
|
12.1
|
1.0
|
N
|
A:ASP187
|
4.2
|
14.2
|
1.0
|
CA
|
A:SER190
|
4.3
|
11.5
|
1.0
|
CD2
|
A:LEU167
|
4.3
|
10.6
|
1.0
|
CE2
|
A:PHE194
|
4.3
|
10.6
|
1.0
|
O
|
A:GLU162
|
4.4
|
11.1
|
1.0
|
CA
|
A:ASP187
|
4.4
|
13.7
|
1.0
|
C
|
A:ASP187
|
4.5
|
13.0
|
1.0
|
OD2
|
A:ASP187
|
4.5
|
14.9
|
1.0
|
CA
|
A:GLY165
|
4.7
|
15.6
|
1.0
|
N
|
A:GLY186
|
4.7
|
13.9
|
1.0
|
CG
|
A:ASP187
|
4.7
|
19.3
|
1.0
|
CA
|
A:PHE194
|
4.7
|
12.3
|
1.0
|
CD1
|
A:PHE194
|
4.8
|
11.9
|
1.0
|
N
|
A:SER190
|
4.8
|
13.4
|
1.0
|
O
|
A:HOH560
|
4.8
|
12.4
|
1.0
|
C
|
A:SER185
|
4.8
|
9.6
|
1.0
|
N
|
A:PHE194
|
4.9
|
14.2
|
1.0
|
CB
|
A:ALA191
|
5.0
|
12.1
|
1.0
|
N
|
A:GLY165
|
5.0
|
17.7
|
1.0
|
|
Sodium binding site 2 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 2 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 2 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na303
b:23.3
occ:1.00
|
OG1
|
A:THR77
|
2.6
|
16.5
|
1.0
|
O
|
A:HOH452
|
2.7
|
16.7
|
1.0
|
OG1
|
A:THR89
|
2.7
|
17.8
|
1.0
|
OE1
|
A:GLN130
|
2.7
|
17.6
|
1.0
|
CB
|
A:THR77
|
3.4
|
16.1
|
1.0
|
CG2
|
A:ILE122
|
3.4
|
14.2
|
1.0
|
CB
|
A:CYS100
|
3.5
|
17.8
|
1.0
|
CD
|
A:GLN130
|
3.6
|
17.6
|
1.0
|
CB
|
A:THR89
|
3.8
|
19.0
|
1.0
|
NE2
|
A:GLN130
|
3.9
|
17.0
|
1.0
|
CB
|
A:THR102
|
3.9
|
14.1
|
1.0
|
CG2
|
A:THR89
|
3.9
|
19.3
|
1.0
|
SG
|
A:CYS100
|
3.9
|
18.4
|
1.0
|
CG2
|
A:THR77
|
4.2
|
12.3
|
1.0
|
OG1
|
A:THR102
|
4.2
|
16.4
|
1.0
|
CG2
|
A:THR102
|
4.3
|
11.7
|
1.0
|
O
|
A:THR77
|
4.4
|
14.6
|
1.0
|
CA
|
A:THR77
|
4.6
|
14.8
|
1.0
|
CA
|
A:THR89
|
4.7
|
17.8
|
1.0
|
C
|
A:THR77
|
4.7
|
17.6
|
1.0
|
O
|
A:ALA85
|
4.8
|
17.7
|
1.0
|
CB
|
A:ILE122
|
4.8
|
16.1
|
1.0
|
CA
|
A:CYS100
|
4.9
|
11.3
|
1.0
|
|
Sodium binding site 3 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 3 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 3 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na304
b:22.9
occ:1.00
|
O
|
A:HOH611
|
2.3
|
35.4
|
1.0
|
O
|
A:ILE157
|
2.7
|
18.4
|
1.0
|
O
|
A:ALA152
|
2.7
|
20.6
|
1.0
|
O
|
A:VAL154
|
2.9
|
23.9
|
1.0
|
O
|
A:LYS155
|
2.9
|
25.6
|
1.0
|
O
|
A:HOH403
|
3.0
|
40.2
|
1.0
|
C
|
A:LYS155
|
3.4
|
32.5
|
1.0
|
CA
|
A:LYS155
|
3.6
|
34.2
|
1.0
|
C
|
A:VAL154
|
3.7
|
26.8
|
1.0
|
C
|
A:ILE157
|
3.7
|
19.4
|
1.0
|
C
|
A:ALA152
|
3.8
|
16.9
|
1.0
|
N
|
A:ILE157
|
4.1
|
20.6
|
1.0
|
N
|
A:LYS155
|
4.2
|
31.9
|
1.0
|
N
|
A:ASN156
|
4.4
|
25.7
|
1.0
|
CA
|
A:ILE157
|
4.4
|
19.5
|
1.0
|
CA
|
A:ALA152
|
4.5
|
20.5
|
1.0
|
O
|
A:HOH444
|
4.5
|
30.3
|
1.0
|
CG2
|
A:ILE158
|
4.5
|
25.8
|
1.0
|
O
|
A:HOH622
|
4.5
|
38.9
|
1.0
|
N
|
A:VAL154
|
4.6
|
22.8
|
1.0
|
CD
|
A:LYS155
|
4.7
|
48.4
|
1.0
|
N
|
A:ILE158
|
4.7
|
17.1
|
1.0
|
CA
|
A:ILE158
|
4.7
|
18.9
|
1.0
|
C
|
A:LYS153
|
4.7
|
29.3
|
1.0
|
NZ
|
A:LYS155
|
4.8
|
53.6
|
1.0
|
N
|
A:LYS153
|
4.8
|
20.0
|
1.0
|
CA
|
A:VAL154
|
4.8
|
20.1
|
1.0
|
C
|
A:ASN156
|
4.8
|
21.9
|
1.0
|
CB
|
A:ILE157
|
4.8
|
19.4
|
1.0
|
CA
|
A:LYS153
|
4.9
|
23.5
|
1.0
|
CB
|
A:LYS155
|
4.9
|
40.7
|
1.0
|
CA
|
A:ASN156
|
5.0
|
22.9
|
1.0
|
|
Sodium binding site 4 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 4 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 4 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na305
b:33.1
occ:1.00
|
O
|
A:HOH507
|
2.5
|
19.5
|
1.0
|
OD2
|
A:ASP265
|
3.0
|
25.3
|
1.0
|
N
|
A:ILE274
|
3.0
|
13.7
|
1.0
|
O
|
A:HOH627
|
3.0
|
21.6
|
1.0
|
O
|
A:HOH405
|
3.4
|
37.3
|
1.0
|
CA
|
A:PRO273
|
3.4
|
16.8
|
1.0
|
CG
|
A:ASP265
|
3.4
|
18.2
|
1.0
|
CG2
|
A:ILE274
|
3.5
|
18.4
|
1.0
|
C
|
A:PRO273
|
3.7
|
17.2
|
1.0
|
CB
|
A:PRO273
|
3.8
|
16.4
|
1.0
|
CB
|
A:ILE274
|
3.9
|
14.5
|
1.0
|
O
|
A:ASP265
|
3.9
|
18.9
|
1.0
|
OD1
|
A:ASP265
|
4.0
|
19.5
|
1.0
|
CB
|
A:ASP265
|
4.1
|
19.8
|
1.0
|
CA
|
A:ILE274
|
4.1
|
14.6
|
1.0
|
O
|
A:HOH596
|
4.3
|
33.2
|
1.0
|
O
|
A:HOH542
|
4.3
|
35.7
|
1.0
|
CD1
|
A:LEU267
|
4.4
|
17.2
|
1.0
|
CG2
|
A:ILE250
|
4.6
|
13.0
|
1.0
|
O
|
A:HOH706
|
4.7
|
43.1
|
1.0
|
N
|
A:PRO273
|
4.7
|
16.9
|
1.0
|
CB
|
A:TRP254
|
4.7
|
16.2
|
1.0
|
C
|
A:ASP265
|
4.7
|
18.8
|
1.0
|
O
|
A:ILE250
|
4.8
|
16.1
|
1.0
|
CG
|
A:PRO273
|
4.8
|
18.4
|
1.0
|
O
|
A:THR272
|
4.9
|
15.4
|
1.0
|
CD1
|
A:TRP254
|
4.9
|
16.3
|
1.0
|
O
|
A:PRO273
|
5.0
|
14.8
|
1.0
|
|
Sodium binding site 5 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 5 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 5 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na306
b:35.5
occ:1.00
|
O
|
A:HOH692
|
2.9
|
40.2
|
1.0
|
O
|
A:HOH711
|
3.0
|
35.6
|
1.0
|
N
|
A:ALA22
|
3.0
|
19.4
|
1.0
|
O
|
A:HOH674
|
3.3
|
29.4
|
1.0
|
CB
|
A:ALA22
|
3.3
|
21.7
|
1.0
|
N
|
A:ARG21
|
3.5
|
18.8
|
1.0
|
CA
|
A:ALA22
|
3.7
|
23.6
|
1.0
|
C
|
A:ARG21
|
3.9
|
18.1
|
1.0
|
CA
|
A:ARG21
|
4.0
|
19.7
|
1.0
|
CB
|
A:ARG21
|
4.0
|
20.7
|
1.0
|
SG
|
A:CYS20
|
4.1
|
23.4
|
1.0
|
C
|
A:CYS20
|
4.2
|
17.8
|
1.0
|
CA
|
A:CYS20
|
4.5
|
21.3
|
1.0
|
O
|
A:HOH615
|
4.7
|
39.8
|
1.0
|
O
|
A:HOH650
|
4.9
|
25.7
|
1.0
|
O
|
A:HOH652
|
4.9
|
39.1
|
1.0
|
O
|
A:HOH697
|
4.9
|
42.5
|
1.0
|
O
|
A:CYS20
|
4.9
|
17.4
|
1.0
|
CB
|
A:CYS20
|
5.0
|
18.6
|
1.0
|
C
|
A:ALA22
|
5.0
|
21.4
|
1.0
|
|
Sodium binding site 6 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 6 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 6 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na302
b:26.0
occ:1.00
|
O
|
B:HOH652
|
2.4
|
34.0
|
1.0
|
O
|
B:ILE157
|
2.7
|
18.8
|
1.0
|
O
|
B:ALA152
|
2.8
|
19.7
|
1.0
|
O
|
B:VAL154
|
2.9
|
26.6
|
1.0
|
O
|
B:HOH671
|
3.0
|
34.1
|
1.0
|
O
|
B:LYS155
|
3.1
|
30.0
|
1.0
|
C
|
B:ILE157
|
3.7
|
17.5
|
1.0
|
C
|
B:LYS155
|
3.9
|
31.2
|
1.0
|
C
|
B:ALA152
|
3.9
|
21.3
|
1.0
|
C
|
B:VAL154
|
4.0
|
27.9
|
1.0
|
N
|
B:ILE157
|
4.1
|
20.0
|
1.0
|
O
|
B:HOH642
|
4.3
|
42.7
|
1.0
|
CA
|
B:ILE157
|
4.4
|
18.4
|
1.0
|
CA
|
B:LYS155
|
4.5
|
29.9
|
1.0
|
CA
|
B:ALA152
|
4.5
|
18.9
|
1.0
|
O
|
B:HOH564
|
4.5
|
34.0
|
1.0
|
N
|
B:ILE158
|
4.6
|
17.2
|
1.0
|
CA
|
B:ILE158
|
4.6
|
18.6
|
1.0
|
N
|
B:ASN156
|
4.7
|
26.8
|
1.0
|
N
|
B:VAL154
|
4.7
|
20.6
|
1.0
|
N
|
B:LYS155
|
4.7
|
27.1
|
1.0
|
C
|
B:LYS153
|
4.8
|
28.0
|
1.0
|
CB
|
B:ILE157
|
4.8
|
18.8
|
1.0
|
C
|
B:ASN156
|
4.8
|
23.1
|
1.0
|
CG2
|
B:ILE158
|
4.8
|
22.1
|
1.0
|
N
|
B:LYS153
|
4.9
|
18.2
|
1.0
|
|
Sodium binding site 7 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 7 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 7 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na303
b:27.0
occ:1.00
|
N
|
B:GLU146
|
2.9
|
14.9
|
1.0
|
O
|
B:HOH416
|
3.1
|
35.5
|
1.0
|
CB
|
B:GLU146
|
3.3
|
27.0
|
1.0
|
N
|
B:PRO145
|
3.5
|
15.1
|
1.0
|
CD
|
B:PRO145
|
3.5
|
12.4
|
1.0
|
CB
|
B:LEU144
|
3.6
|
13.6
|
1.0
|
CA
|
B:GLU146
|
3.7
|
16.9
|
1.0
|
CB
|
B:PRO145
|
3.8
|
14.1
|
1.0
|
C
|
B:PRO145
|
3.8
|
16.0
|
1.0
|
CA
|
B:PRO145
|
3.9
|
13.8
|
1.0
|
C
|
B:LEU144
|
4.0
|
13.3
|
1.0
|
CG
|
B:PRO145
|
4.1
|
15.9
|
1.0
|
CA
|
B:LEU144
|
4.4
|
12.4
|
1.0
|
CD1
|
B:LEU144
|
4.5
|
18.8
|
1.0
|
CG
|
B:GLU146
|
4.6
|
36.1
|
1.0
|
CG
|
B:LEU144
|
4.6
|
15.8
|
1.0
|
O
|
B:LEU144
|
4.7
|
13.3
|
1.0
|
CD
|
B:GLU146
|
4.8
|
44.6
|
1.0
|
OE1
|
B:GLU146
|
4.9
|
53.9
|
1.0
|
C
|
B:GLU146
|
4.9
|
20.0
|
1.0
|
|
Sodium binding site 8 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 8 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 8 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na304
b:27.5
occ:1.00
|
O
|
B:HOH711
|
2.5
|
31.3
|
1.0
|
O
|
B:HOH683
|
2.8
|
34.7
|
1.0
|
N
|
B:GLU113
|
2.9
|
15.8
|
1.0
|
O
|
B:HOH594
|
3.1
|
21.9
|
1.0
|
N
|
B:GLN112
|
3.4
|
15.0
|
1.0
|
CB
|
B:GLN112
|
3.6
|
16.1
|
1.0
|
CB
|
B:GLU113
|
3.6
|
16.5
|
1.0
|
CB
|
B:SER111
|
3.7
|
15.6
|
1.0
|
CA
|
B:GLN112
|
3.7
|
20.6
|
1.0
|
C
|
B:GLN112
|
3.7
|
17.2
|
1.0
|
OG
|
B:SER111
|
3.8
|
12.5
|
1.0
|
O
|
B:HOH640
|
3.8
|
31.4
|
1.0
|
CA
|
B:GLU113
|
3.8
|
16.3
|
1.0
|
O
|
A:HOH690
|
4.1
|
36.5
|
1.0
|
C
|
B:SER111
|
4.2
|
14.9
|
1.0
|
O
|
B:HOH491
|
4.5
|
30.7
|
1.0
|
CA
|
B:SER111
|
4.5
|
18.0
|
1.0
|
CG
|
B:GLN112
|
4.5
|
18.2
|
1.0
|
O
|
B:GLN112
|
4.9
|
15.1
|
1.0
|
O
|
B:HOH720
|
5.0
|
29.4
|
1.0
|
|
Sodium binding site 9 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 9 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 9 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na305
b:31.6
occ:1.00
|
O
|
B:HOH707
|
2.6
|
34.9
|
1.0
|
O
|
B:PRO110
|
2.8
|
12.8
|
1.0
|
O
|
B:HOH540
|
2.9
|
17.7
|
1.0
|
NE2
|
B:GLN112
|
3.1
|
15.2
|
1.0
|
CA
|
B:SER111
|
3.6
|
18.0
|
1.0
|
C
|
B:SER111
|
3.7
|
14.9
|
1.0
|
N
|
B:GLN112
|
3.7
|
15.0
|
1.0
|
O
|
B:HOH666
|
3.8
|
30.4
|
1.0
|
O
|
B:HOH535
|
3.8
|
15.6
|
1.0
|
C
|
B:PRO110
|
3.8
|
13.0
|
1.0
|
O
|
B:HOH594
|
4.0
|
21.9
|
1.0
|
N
|
B:SER111
|
4.2
|
14.2
|
1.0
|
CD
|
B:GLN112
|
4.2
|
18.3
|
1.0
|
O
|
B:HOH720
|
4.3
|
29.4
|
1.0
|
O
|
B:SER111
|
4.4
|
13.3
|
1.0
|
CG
|
B:GLN112
|
4.5
|
18.2
|
1.0
|
CA
|
B:GLN112
|
4.7
|
20.6
|
1.0
|
CB
|
B:CYS141
|
4.7
|
24.6
|
1.0
|
O
|
B:ASP142
|
4.7
|
12.7
|
1.0
|
CB
|
B:SER111
|
4.8
|
15.6
|
1.0
|
CD1
|
B:LEU115
|
4.9
|
13.4
|
1.0
|
|
Sodium binding site 10 out
of 10 in 5t25
Go back to
Sodium Binding Sites List in 5t25
Sodium binding site 10 out
of 10 in the Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli.
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 10 of Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na306
b:32.2
occ:1.00
|
N
|
B:ALA22
|
2.9
|
22.4
|
1.0
|
O
|
B:HOH689
|
3.2
|
27.7
|
1.0
|
CB
|
B:ALA22
|
3.4
|
26.3
|
1.0
|
N
|
B:ARG21
|
3.5
|
20.3
|
1.0
|
O
|
B:HOH615
|
3.5
|
30.2
|
1.0
|
CA
|
B:ALA22
|
3.7
|
19.5
|
1.0
|
C
|
B:ARG21
|
3.9
|
18.0
|
1.0
|
CB
|
B:ARG21
|
3.9
|
19.3
|
1.0
|
CA
|
B:ARG21
|
3.9
|
21.1
|
1.0
|
SG
|
B:CYS20
|
4.2
|
24.8
|
1.0
|
C
|
B:CYS20
|
4.2
|
21.5
|
1.0
|
CA
|
B:CYS20
|
4.6
|
21.2
|
1.0
|
O
|
B:HOH573
|
4.8
|
36.6
|
1.0
|
O
|
B:HOH677
|
4.9
|
21.5
|
1.0
|
C
|
B:ALA22
|
5.0
|
19.4
|
1.0
|
|
Reference:
L.Chooback,
L.M.Thomas,
W.E.Karsten,
C.D.Fleming,
P.Seabourn.
Kinetic, Spectral and Structural Characterization of the Slow Binding Inhibitor Acetopyruvate with Dihydrodipicolinate Synthase From Escherichia Coli. To Be Published.
Page generated: Tue Oct 8 00:00:53 2024
|