Chlorine in PDB 1ots: Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex
Protein crystallography data
The structure of Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex, PDB code: 1ots
was solved by
R.Dutzler,
E.B.Campbell,
R.Mackinnon,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
24.58 /
2.51
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
229.936,
93.870,
168.536,
90.00,
131.72,
90.00
|
R / Rfree (%)
|
26.4 /
29.9
|
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex
(pdb code 1ots). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 4 binding sites of Chlorine where determined in the
Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex, PDB code: 1ots:
Jump to Chlorine binding site number:
1;
2;
3;
4;
Chlorine binding site 1 out
of 4 in 1ots
Go back to
Chlorine Binding Sites List in 1ots
Chlorine binding site 1 out
of 4 in the Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 1 of Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl466
b:61.4
occ:1.00
|
OH
|
A:TYR445
|
2.9
|
76.4
|
1.0
|
N
|
A:ILE356
|
3.0
|
58.8
|
1.0
|
OG
|
A:SER107
|
3.0
|
67.1
|
1.0
|
CA
|
A:GLY355
|
3.2
|
56.2
|
1.0
|
CB
|
A:SER107
|
3.3
|
61.0
|
1.0
|
N
|
A:PHE357
|
3.6
|
58.0
|
1.0
|
C
|
A:GLY355
|
3.6
|
58.0
|
1.0
|
CD1
|
A:ILE109
|
3.7
|
52.4
|
1.0
|
CG2
|
A:ILE356
|
3.9
|
62.6
|
1.0
|
CB
|
A:PHE357
|
3.9
|
63.4
|
1.0
|
CZ
|
A:TYR445
|
3.9
|
75.2
|
1.0
|
CE2
|
A:TYR445
|
4.0
|
74.0
|
1.0
|
CA
|
A:SER107
|
4.1
|
62.1
|
1.0
|
OE1
|
A:GLU148
|
4.1
|
71.1
|
1.0
|
CA
|
A:GLY149
|
4.1
|
61.9
|
1.0
|
N
|
A:GLY149
|
4.1
|
62.5
|
1.0
|
CA
|
A:ILE356
|
4.2
|
58.6
|
1.0
|
CA
|
A:PHE357
|
4.3
|
59.5
|
1.0
|
C
|
A:ILE356
|
4.3
|
58.7
|
1.0
|
CG1
|
A:ILE109
|
4.4
|
56.0
|
1.0
|
N
|
A:GLY355
|
4.5
|
56.6
|
1.0
|
CB
|
A:ILE356
|
4.5
|
60.3
|
1.0
|
CE1
|
A:PHE348
|
4.7
|
72.1
|
1.0
|
O
|
A:GLY354
|
4.7
|
59.9
|
1.0
|
CB
|
A:GLU148
|
4.8
|
65.2
|
1.0
|
O
|
A:GLY355
|
4.8
|
61.0
|
1.0
|
C
|
A:SER107
|
5.0
|
62.4
|
1.0
|
CG
|
A:PHE357
|
5.0
|
65.8
|
1.0
|
|
Chlorine binding site 2 out
of 4 in 1ots
Go back to
Chlorine Binding Sites List in 1ots
Chlorine binding site 2 out
of 4 in the Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 2 of Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl467
b:63.6
occ:1.00
|
N
|
A:SER107
|
3.1
|
61.0
|
1.0
|
CB
|
A:SER107
|
3.4
|
61.0
|
1.0
|
CG
|
A:PRO110
|
3.5
|
65.1
|
1.0
|
CD
|
A:PRO110
|
3.6
|
65.7
|
1.0
|
CA
|
A:SER107
|
3.7
|
62.1
|
1.0
|
N
|
A:GLY108
|
3.7
|
64.3
|
1.0
|
CG2
|
A:ILE448
|
3.8
|
53.7
|
1.0
|
CZ
|
A:PHE348
|
3.9
|
71.5
|
1.0
|
C
|
A:GLY106
|
4.0
|
60.5
|
1.0
|
CA
|
A:GLY106
|
4.1
|
61.0
|
1.0
|
CD1
|
A:ILE448
|
4.1
|
58.4
|
1.0
|
C
|
A:SER107
|
4.2
|
62.4
|
1.0
|
CB
|
A:PRO110
|
4.3
|
63.0
|
1.0
|
O
|
A:GLY105
|
4.4
|
64.9
|
1.0
|
CE1
|
A:PHE348
|
4.4
|
72.1
|
1.0
|
OG
|
A:SER107
|
4.5
|
67.1
|
1.0
|
CA
|
A:GLY108
|
4.8
|
62.8
|
1.0
|
CB
|
A:ILE448
|
4.8
|
61.4
|
1.0
|
CE2
|
A:PHE348
|
4.9
|
69.8
|
1.0
|
N
|
A:PRO110
|
4.9
|
65.0
|
1.0
|
|
Chlorine binding site 3 out
of 4 in 1ots
Go back to
Chlorine Binding Sites List in 1ots
Chlorine binding site 3 out
of 4 in the Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 3 of Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl466
b:52.5
occ:1.00
|
OH
|
B:TYR445
|
2.8
|
68.9
|
1.0
|
OG
|
B:SER107
|
3.0
|
60.9
|
1.0
|
N
|
B:ILE356
|
3.0
|
53.5
|
1.0
|
CA
|
B:GLY355
|
3.2
|
51.2
|
1.0
|
CB
|
B:SER107
|
3.4
|
58.9
|
1.0
|
N
|
B:PHE357
|
3.6
|
61.5
|
1.0
|
C
|
B:GLY355
|
3.6
|
51.6
|
1.0
|
CD1
|
B:ILE109
|
3.7
|
49.8
|
1.0
|
CZ
|
B:TYR445
|
3.8
|
69.7
|
1.0
|
CB
|
B:PHE357
|
3.9
|
64.4
|
1.0
|
CG2
|
B:ILE356
|
3.9
|
54.7
|
1.0
|
CE2
|
B:TYR445
|
4.0
|
68.5
|
1.0
|
OE1
|
B:GLU148
|
4.1
|
65.0
|
1.0
|
CA
|
B:SER107
|
4.1
|
58.7
|
1.0
|
CA
|
B:ILE356
|
4.2
|
59.1
|
1.0
|
N
|
B:GLY149
|
4.2
|
61.4
|
1.0
|
CA
|
B:GLY149
|
4.2
|
60.2
|
1.0
|
CA
|
B:PHE357
|
4.3
|
62.9
|
1.0
|
C
|
B:ILE356
|
4.3
|
60.6
|
1.0
|
N
|
B:GLY355
|
4.5
|
54.9
|
1.0
|
CG1
|
B:ILE109
|
4.5
|
48.0
|
1.0
|
CB
|
B:ILE356
|
4.5
|
58.2
|
1.0
|
O
|
B:GLY354
|
4.7
|
56.9
|
1.0
|
CE1
|
B:PHE348
|
4.8
|
59.6
|
1.0
|
O
|
B:GLY355
|
4.8
|
49.8
|
1.0
|
CB
|
B:GLU148
|
4.9
|
61.8
|
1.0
|
CG
|
B:PHE357
|
4.9
|
67.8
|
1.0
|
C
|
B:SER107
|
5.0
|
58.6
|
1.0
|
|
Chlorine binding site 4 out
of 4 in 1ots
Go back to
Chlorine Binding Sites List in 1ots
Chlorine binding site 4 out
of 4 in the Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 4 of Structure of the Escherichia Coli Clc Chloride Channel and Fab Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl467
b:60.7
occ:1.00
|
N
|
B:SER107
|
3.1
|
53.4
|
1.0
|
CG
|
B:PRO110
|
3.3
|
56.3
|
1.0
|
CB
|
B:SER107
|
3.4
|
58.9
|
1.0
|
CD
|
B:PRO110
|
3.5
|
55.2
|
1.0
|
CA
|
B:SER107
|
3.7
|
58.7
|
1.0
|
N
|
B:GLY108
|
3.8
|
58.7
|
1.0
|
CG2
|
B:ILE448
|
3.9
|
47.9
|
1.0
|
CZ
|
B:PHE348
|
4.0
|
59.8
|
1.0
|
C
|
B:GLY106
|
4.0
|
51.5
|
1.0
|
CD1
|
B:ILE448
|
4.1
|
51.2
|
1.0
|
CA
|
B:GLY106
|
4.2
|
53.9
|
1.0
|
CB
|
B:PRO110
|
4.2
|
56.6
|
1.0
|
C
|
B:SER107
|
4.3
|
58.6
|
1.0
|
O
|
B:GLY105
|
4.3
|
55.5
|
1.0
|
OG
|
B:SER107
|
4.5
|
60.9
|
1.0
|
CE1
|
B:PHE348
|
4.5
|
59.6
|
1.0
|
O
|
B:HOH492
|
4.8
|
47.6
|
1.0
|
CB
|
B:ILE448
|
4.9
|
55.7
|
1.0
|
N
|
B:PRO110
|
4.9
|
53.6
|
1.0
|
CA
|
B:GLY108
|
4.9
|
59.3
|
1.0
|
CE2
|
B:PHE348
|
5.0
|
58.9
|
1.0
|
|
Reference:
R.Dutzler,
E.B.Campbell,
R.Mackinnon.
Gating the Selectivity Filter in Clc Chloride Channels Science V. 300 108 2003.
ISSN: ISSN 0036-8075
PubMed: 12649487
DOI: 10.1126/SCIENCE.1082708
Page generated: Sat Jul 20 01:01:30 2024
|