Chlorine in PDB 2df7: Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Protein crystallography data
The structure of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle, PDB code: 2df7
was solved by
T.P.Ko,
C.C.Lee,
M.Y.Wang,
A.H.Wang,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
40.00 /
2.60
|
Space group
|
P 21 3 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
316.412,
316.412,
316.412,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
16.5 /
21.5
|
Other elements in 2df7:
The structure of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
(pdb code 2df7). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 8 binding sites of Chlorine where determined in the
Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle, PDB code: 2df7:
Jump to Chlorine binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
Chlorine binding site 1 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 1 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 1 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl5503
b:32.0
occ:1.00
|
N
|
F:ARG202
|
3.1
|
31.6
|
1.0
|
N
|
A:ARG202
|
3.2
|
28.7
|
1.0
|
CA
|
F:ARG202
|
3.7
|
30.5
|
1.0
|
CA
|
A:ARG202
|
3.8
|
29.6
|
1.0
|
CD
|
F:PRO203
|
3.9
|
27.4
|
1.0
|
CD
|
A:PRO203
|
3.9
|
27.1
|
1.0
|
C
|
F:ASP201
|
4.2
|
32.2
|
1.0
|
C
|
A:ASP201
|
4.2
|
30.7
|
1.0
|
CA
|
F:ASP201
|
4.3
|
33.0
|
1.0
|
CA
|
A:ASP201
|
4.4
|
30.7
|
1.0
|
CG
|
F:ARG202
|
4.6
|
27.7
|
1.0
|
CG
|
A:ARG202
|
4.6
|
28.2
|
1.0
|
CB
|
F:ARG202
|
4.7
|
30.5
|
1.0
|
N
|
F:PRO203
|
4.7
|
28.9
|
1.0
|
CB
|
A:ARG202
|
4.8
|
30.0
|
1.0
|
C
|
F:ARG202
|
4.8
|
29.6
|
1.0
|
N
|
A:PRO203
|
4.8
|
30.6
|
1.0
|
CB
|
F:ASP201
|
4.8
|
34.2
|
1.0
|
CB
|
A:ASP201
|
4.8
|
32.2
|
1.0
|
C
|
A:ARG202
|
4.9
|
30.2
|
1.0
|
CG
|
F:PRO203
|
5.0
|
27.6
|
1.0
|
|
Chlorine binding site 2 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 2 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 2 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl5501
b:26.5
occ:0.33
|
N
|
B:ARG202
|
3.1
|
27.8
|
1.0
|
CA
|
B:ARG202
|
3.7
|
26.6
|
1.0
|
CD
|
B:PRO203
|
3.9
|
23.5
|
1.0
|
C
|
B:ASP201
|
4.2
|
29.4
|
1.0
|
CA
|
B:ASP201
|
4.4
|
31.0
|
1.0
|
CG
|
B:ARG202
|
4.5
|
22.8
|
1.0
|
CB
|
B:ARG202
|
4.6
|
25.5
|
1.0
|
N
|
B:PRO203
|
4.8
|
24.4
|
1.0
|
C
|
B:ARG202
|
4.8
|
26.4
|
1.0
|
CB
|
B:ASP201
|
4.9
|
32.4
|
1.0
|
|
Chlorine binding site 3 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 3 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 3 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Cl5504
b:30.2
occ:1.00
|
N
|
L:ARG202
|
3.1
|
33.0
|
1.0
|
N
|
E:ARG202
|
3.2
|
29.7
|
1.0
|
N
|
C:ARG202
|
3.2
|
31.9
|
1.0
|
O
|
L:HOH470
|
3.5
|
36.2
|
1.0
|
CA
|
L:ARG202
|
3.7
|
32.0
|
1.0
|
CA
|
C:ARG202
|
3.7
|
30.7
|
1.0
|
CA
|
E:ARG202
|
3.8
|
28.4
|
1.0
|
CD
|
C:PRO203
|
4.0
|
29.8
|
1.0
|
CD
|
L:PRO203
|
4.0
|
30.7
|
1.0
|
CD
|
E:PRO203
|
4.1
|
27.9
|
1.0
|
C
|
L:ASP201
|
4.1
|
33.0
|
1.0
|
C
|
E:ASP201
|
4.2
|
30.6
|
1.0
|
C
|
C:ASP201
|
4.3
|
32.0
|
1.0
|
CA
|
L:ASP201
|
4.3
|
34.0
|
1.0
|
CA
|
E:ASP201
|
4.4
|
30.7
|
1.0
|
CA
|
C:ASP201
|
4.4
|
33.5
|
1.0
|
CG
|
L:ARG202
|
4.5
|
31.1
|
1.0
|
CG
|
E:ARG202
|
4.5
|
30.8
|
1.0
|
CG
|
C:ARG202
|
4.6
|
30.1
|
1.0
|
CB
|
L:ARG202
|
4.6
|
31.5
|
1.0
|
CB
|
L:ASP201
|
4.7
|
37.0
|
1.0
|
CB
|
E:ARG202
|
4.7
|
30.0
|
1.0
|
CB
|
C:ARG202
|
4.7
|
30.0
|
1.0
|
CB
|
E:ASP201
|
4.8
|
31.3
|
1.0
|
C
|
L:ARG202
|
4.8
|
32.5
|
1.0
|
N
|
L:PRO203
|
4.8
|
31.0
|
1.0
|
N
|
C:PRO203
|
4.8
|
30.3
|
1.0
|
C
|
C:ARG202
|
4.9
|
31.8
|
1.0
|
N
|
E:PRO203
|
4.9
|
29.2
|
1.0
|
C
|
E:ARG202
|
4.9
|
29.3
|
1.0
|
CB
|
C:ASP201
|
4.9
|
36.7
|
1.0
|
|
Chlorine binding site 4 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 4 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 4 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
G:Cl5505
b:33.6
occ:1.00
|
N
|
M:ARG202
|
3.1
|
31.0
|
1.0
|
N
|
G:ARG202
|
3.2
|
30.4
|
1.0
|
N
|
K:ARG202
|
3.2
|
34.0
|
1.0
|
CA
|
G:ARG202
|
3.7
|
29.7
|
1.0
|
CA
|
M:ARG202
|
3.8
|
32.1
|
1.0
|
CA
|
K:ARG202
|
3.8
|
33.6
|
1.0
|
CD
|
M:PRO203
|
3.8
|
27.1
|
1.0
|
CD
|
G:PRO203
|
3.9
|
26.3
|
1.0
|
CD
|
K:PRO203
|
3.9
|
30.3
|
1.0
|
C
|
M:ASP201
|
4.2
|
32.1
|
1.0
|
C
|
G:ASP201
|
4.2
|
29.9
|
1.0
|
C
|
K:ASP201
|
4.3
|
33.9
|
1.0
|
CA
|
M:ASP201
|
4.3
|
33.2
|
1.0
|
CA
|
G:ASP201
|
4.4
|
30.2
|
1.0
|
CA
|
K:ASP201
|
4.4
|
35.1
|
1.0
|
CG
|
M:ARG202
|
4.6
|
34.8
|
1.0
|
CG
|
K:ARG202
|
4.7
|
33.9
|
1.0
|
CG
|
G:ARG202
|
4.7
|
30.8
|
1.0
|
N
|
G:PRO203
|
4.7
|
28.7
|
1.0
|
N
|
M:PRO203
|
4.8
|
29.6
|
1.0
|
CB
|
G:ARG202
|
4.8
|
31.5
|
1.0
|
CB
|
M:ASP201
|
4.8
|
34.4
|
1.0
|
C
|
G:ARG202
|
4.8
|
28.9
|
1.0
|
CB
|
M:ARG202
|
4.8
|
32.6
|
1.0
|
N
|
K:PRO203
|
4.8
|
31.6
|
1.0
|
CB
|
K:ARG202
|
4.8
|
34.7
|
1.0
|
C
|
M:ARG202
|
4.8
|
31.3
|
1.0
|
C
|
K:ARG202
|
4.9
|
32.5
|
1.0
|
CB
|
G:ASP201
|
4.9
|
31.8
|
1.0
|
CG
|
G:PRO203
|
4.9
|
25.0
|
1.0
|
CB
|
K:ASP201
|
4.9
|
37.1
|
1.0
|
CG
|
M:PRO203
|
5.0
|
29.5
|
1.0
|
|
Chlorine binding site 5 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 5 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 5 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
H:Cl5506
b:31.2
occ:1.00
|
N
|
H:ARG202
|
3.1
|
29.9
|
1.0
|
N
|
N:ARG202
|
3.2
|
30.9
|
1.0
|
N
|
O:ARG202
|
3.2
|
32.4
|
1.0
|
CA
|
H:ARG202
|
3.6
|
31.3
|
1.0
|
CA
|
O:ARG202
|
3.8
|
32.2
|
1.0
|
CA
|
N:ARG202
|
3.8
|
30.8
|
1.0
|
CD
|
H:PRO203
|
3.8
|
33.1
|
1.0
|
CD
|
O:PRO203
|
3.8
|
30.9
|
1.0
|
CD
|
N:PRO203
|
3.9
|
29.9
|
1.0
|
C
|
H:ASP201
|
4.1
|
29.9
|
1.0
|
C
|
N:ASP201
|
4.2
|
31.4
|
1.0
|
C
|
O:ASP201
|
4.3
|
33.1
|
1.0
|
CA
|
H:ASP201
|
4.3
|
30.1
|
1.0
|
CA
|
N:ASP201
|
4.4
|
31.4
|
1.0
|
CA
|
O:ASP201
|
4.4
|
33.7
|
1.0
|
CG
|
H:ARG202
|
4.6
|
31.1
|
1.0
|
CG
|
N:ARG202
|
4.6
|
29.7
|
1.0
|
N
|
H:PRO203
|
4.6
|
33.9
|
1.0
|
CB
|
H:ARG202
|
4.7
|
32.3
|
1.0
|
CG
|
O:ARG202
|
4.7
|
35.3
|
1.0
|
N
|
O:PRO203
|
4.7
|
32.4
|
1.0
|
C
|
H:ARG202
|
4.7
|
32.9
|
1.0
|
N
|
N:PRO203
|
4.8
|
31.6
|
1.0
|
CB
|
N:ARG202
|
4.8
|
30.5
|
1.0
|
CB
|
O:ARG202
|
4.8
|
34.1
|
1.0
|
C
|
O:ARG202
|
4.8
|
32.9
|
1.0
|
CB
|
H:ASP201
|
4.9
|
31.9
|
1.0
|
CG
|
H:PRO203
|
4.9
|
32.8
|
1.0
|
C
|
N:ARG202
|
4.9
|
31.5
|
1.0
|
CB
|
N:ASP201
|
4.9
|
33.2
|
1.0
|
CG
|
O:PRO203
|
4.9
|
32.1
|
1.0
|
CB
|
O:ASP201
|
4.9
|
35.8
|
1.0
|
CG
|
N:PRO203
|
5.0
|
28.7
|
1.0
|
|
Chlorine binding site 6 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 6 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 6 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
I:Cl5507
b:33.5
occ:1.00
|
N
|
Q:ARG202
|
3.1
|
34.1
|
1.0
|
N
|
J:ARG202
|
3.2
|
33.1
|
1.0
|
N
|
I:ARG202
|
3.2
|
32.7
|
1.0
|
CA
|
Q:ARG202
|
3.7
|
34.0
|
1.0
|
CA
|
J:ARG202
|
3.7
|
33.5
|
1.0
|
CA
|
I:ARG202
|
3.8
|
32.6
|
1.0
|
CD
|
Q:PRO203
|
3.9
|
32.9
|
1.0
|
CD
|
J:PRO203
|
3.9
|
33.2
|
1.0
|
CD
|
I:PRO203
|
3.9
|
29.3
|
1.0
|
C
|
Q:ASP201
|
4.2
|
35.3
|
1.0
|
C
|
J:ASP201
|
4.2
|
34.6
|
1.0
|
C
|
I:ASP201
|
4.2
|
32.2
|
1.0
|
CA
|
Q:ASP201
|
4.3
|
36.7
|
1.0
|
CA
|
I:ASP201
|
4.3
|
32.6
|
1.0
|
CA
|
J:ASP201
|
4.4
|
35.8
|
1.0
|
CG
|
Q:ARG202
|
4.6
|
36.7
|
1.0
|
CG
|
J:ARG202
|
4.7
|
33.6
|
1.0
|
CG
|
I:ARG202
|
4.7
|
32.6
|
1.0
|
N
|
Q:PRO203
|
4.7
|
34.8
|
1.0
|
CB
|
Q:ARG202
|
4.7
|
34.7
|
1.0
|
CB
|
J:ARG202
|
4.8
|
35.2
|
1.0
|
N
|
J:PRO203
|
4.8
|
34.5
|
1.0
|
CB
|
Q:ASP201
|
4.8
|
39.4
|
1.0
|
CB
|
I:ARG202
|
4.8
|
32.2
|
1.0
|
N
|
I:PRO203
|
4.8
|
32.3
|
1.0
|
C
|
Q:ARG202
|
4.8
|
34.1
|
1.0
|
C
|
J:ARG202
|
4.8
|
35.2
|
1.0
|
CB
|
I:ASP201
|
4.8
|
33.6
|
1.0
|
C
|
I:ARG202
|
4.9
|
33.8
|
1.0
|
CB
|
J:ASP201
|
4.9
|
38.8
|
1.0
|
|
Chlorine binding site 7 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 7 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 7 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
P:Cl5502
b:26.0
occ:0.33
|
N
|
P:ARG202
|
3.1
|
33.6
|
1.0
|
CA
|
P:ARG202
|
3.7
|
33.0
|
1.0
|
CD
|
P:PRO203
|
3.9
|
34.3
|
1.0
|
C
|
P:ASP201
|
4.2
|
33.5
|
1.0
|
CA
|
P:ASP201
|
4.3
|
33.3
|
1.0
|
CG
|
P:ARG202
|
4.5
|
36.2
|
1.0
|
CB
|
P:ARG202
|
4.7
|
35.7
|
1.0
|
CB
|
P:ASP201
|
4.8
|
36.3
|
1.0
|
N
|
P:PRO203
|
4.8
|
35.0
|
1.0
|
C
|
P:ARG202
|
4.8
|
33.6
|
1.0
|
|
Chlorine binding site 8 out
of 8 in 2df7
Go back to
Chlorine Binding Sites List in 2df7
Chlorine binding site 8 out
of 8 in the Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 8 of Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
R:Cl5508
b:27.7
occ:1.00
|
N
|
R:ARG202
|
3.1
|
31.2
|
1.0
|
N
|
T:ARG202
|
3.1
|
28.0
|
1.0
|
N
|
S:ARG202
|
3.2
|
27.2
|
1.0
|
O
|
R:HOH5956
|
3.5
|
41.7
|
1.0
|
CA
|
R:ARG202
|
3.7
|
30.0
|
1.0
|
CA
|
T:ARG202
|
3.7
|
27.2
|
1.0
|
CA
|
S:ARG202
|
3.8
|
26.7
|
1.0
|
CD
|
R:PRO203
|
3.9
|
29.7
|
1.0
|
CD
|
S:PRO203
|
3.9
|
23.7
|
1.0
|
CD
|
T:PRO203
|
3.9
|
24.3
|
1.0
|
C
|
R:ASP201
|
4.2
|
31.7
|
1.0
|
C
|
T:ASP201
|
4.2
|
29.6
|
1.0
|
C
|
S:ASP201
|
4.2
|
27.9
|
1.0
|
CA
|
R:ASP201
|
4.4
|
32.7
|
1.0
|
CA
|
S:ASP201
|
4.4
|
29.4
|
1.0
|
CA
|
T:ASP201
|
4.4
|
30.0
|
1.0
|
CG
|
R:ARG202
|
4.5
|
31.6
|
1.0
|
CG
|
T:ARG202
|
4.6
|
30.6
|
1.0
|
CG
|
S:ARG202
|
4.6
|
28.5
|
1.0
|
CB
|
R:ARG202
|
4.7
|
31.5
|
1.0
|
CB
|
T:ARG202
|
4.7
|
28.1
|
1.0
|
CB
|
S:ARG202
|
4.7
|
27.0
|
1.0
|
N
|
R:PRO203
|
4.8
|
29.4
|
1.0
|
C
|
R:ARG202
|
4.8
|
29.5
|
1.0
|
CB
|
T:ASP201
|
4.8
|
31.0
|
1.0
|
N
|
T:PRO203
|
4.8
|
26.0
|
1.0
|
N
|
S:PRO203
|
4.8
|
27.4
|
1.0
|
C
|
T:ARG202
|
4.8
|
26.6
|
1.0
|
C
|
S:ARG202
|
4.8
|
28.4
|
1.0
|
CB
|
S:ASP201
|
4.9
|
31.9
|
1.0
|
CB
|
R:ASP201
|
4.9
|
35.8
|
1.0
|
CG
|
S:PRO203
|
5.0
|
22.1
|
1.0
|
|
Reference:
C.C.Lee,
T.P.Ko,
C.C.Chou,
M.Yoshimura,
S.R.Doong,
M.Y.Wang,
A.H.Wang.
Crystal Structure of Infectious Bursal Disease Virus VP2 Subviral Particle at 2.6A Resolution: Implications in Virion Assembly and Immunogenicity. J.Struct.Biol. V. 155 74 2006.
ISSN: ISSN 1047-8477
PubMed: 16677827
DOI: 10.1016/J.JSB.2006.02.014
Page generated: Sat Jul 20 06:31:35 2024
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