Iron in PDB 1vzh: Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
Enzymatic activity of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
All present enzymatic activity of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction:
1.15.1.2;
Protein crystallography data
The structure of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction, PDB code: 1vzh
was solved by
V.Adam,
A.Royant,
V.Niviere,
F.P.Molina-Heredia,
D.Bourgeois,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
37.49 /
1.69
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
42.130,
67.650,
82.190,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
20.7 /
25
|
Other elements in 1vzh:
The structure of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
(pdb code 1vzh). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 6 binding sites of Iron where determined in the
Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction, PDB code: 1vzh:
Jump to Iron binding site number:
1;
2;
3;
4;
5;
6;
Iron binding site 1 out
of 6 in 1vzh
Go back to
Iron Binding Sites List in 1vzh
Iron binding site 1 out
of 6 in the Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1127
b:18.7
occ:0.37
|
SG
|
A:CYS10
|
1.7
|
16.4
|
0.3
|
SG
|
A:CYS29
|
1.9
|
14.8
|
0.3
|
SG
|
A:CYS13
|
2.0
|
22.9
|
0.4
|
SG
|
A:CYS10
|
2.1
|
12.7
|
0.4
|
CB
|
A:CYS13
|
2.3
|
13.4
|
0.6
|
SG
|
A:CYS30
|
2.3
|
18.6
|
0.4
|
SG
|
A:CYS29
|
2.3
|
19.8
|
0.3
|
SG
|
A:CYS29
|
2.3
|
8.6
|
0.4
|
SG
|
A:CYS30
|
2.6
|
14.4
|
0.6
|
SG
|
A:CYS13
|
3.1
|
17.6
|
0.6
|
CB
|
A:CYS10
|
3.1
|
14.3
|
0.3
|
CB
|
A:CYS13
|
3.1
|
19.5
|
0.4
|
CB
|
A:CYS10
|
3.2
|
16.4
|
0.3
|
CB
|
A:CYS30
|
3.2
|
14.8
|
0.6
|
CB
|
A:CYS10
|
3.2
|
10.9
|
0.4
|
CB
|
A:CYS30
|
3.3
|
14.4
|
0.4
|
SG
|
A:CYS10
|
3.4
|
19.9
|
0.3
|
CB
|
A:CYS29
|
3.5
|
11.8
|
0.4
|
CB
|
A:CYS29
|
3.5
|
15.3
|
0.3
|
CA
|
B:GLY25
|
3.5
|
17.9
|
1.0
|
CA
|
A:CYS13
|
3.6
|
13.3
|
0.6
|
CB
|
A:CYS29
|
3.6
|
17.3
|
0.3
|
ND2
|
A:ASN15
|
3.6
|
14.7
|
0.6
|
C
|
A:CYS29
|
3.6
|
14.5
|
0.3
|
N
|
A:CYS30
|
3.6
|
13.1
|
0.4
|
C
|
A:CYS29
|
3.7
|
15.4
|
0.3
|
N
|
A:CYS30
|
3.7
|
14.5
|
0.6
|
C
|
A:CYS29
|
3.7
|
12.9
|
0.4
|
O
|
A:CYS29
|
3.9
|
15.2
|
0.3
|
O
|
A:GLU11
|
4.0
|
16.2
|
0.4
|
N
|
A:CYS13
|
4.0
|
14.0
|
0.6
|
CA
|
A:CYS30
|
4.0
|
13.8
|
0.4
|
O
|
A:CYS29
|
4.0
|
12.5
|
0.4
|
CA
|
A:CYS30
|
4.1
|
14.4
|
0.6
|
N
|
B:GLY25
|
4.1
|
19.1
|
1.0
|
CA
|
A:CYS29
|
4.1
|
14.9
|
0.3
|
CA
|
A:CYS29
|
4.1
|
16.1
|
0.3
|
N
|
A:CYS13
|
4.1
|
18.0
|
0.4
|
CA
|
A:CYS29
|
4.1
|
13.0
|
0.4
|
CA
|
A:CYS13
|
4.2
|
18.5
|
0.4
|
C
|
A:CYS13
|
4.2
|
13.7
|
0.6
|
ND2
|
A:ASN15
|
4.3
|
12.6
|
0.4
|
CG
|
A:ASN15
|
4.3
|
10.9
|
0.4
|
CA
|
A:CYS10
|
4.4
|
15.6
|
0.3
|
C
|
B:GLY25
|
4.4
|
19.4
|
1.0
|
CA
|
A:CYS10
|
4.4
|
14.5
|
0.3
|
O
|
A:CYS29
|
4.4
|
13.5
|
0.3
|
O
|
A:GLU11
|
4.5
|
18.9
|
0.6
|
OD1
|
A:ASN15
|
4.5
|
9.4
|
0.4
|
CA
|
A:CYS10
|
4.5
|
11.6
|
0.4
|
C
|
A:CYS10
|
4.6
|
11.7
|
0.4
|
N
|
A:GLY14
|
4.6
|
16.5
|
0.4
|
O
|
A:CYS10
|
4.7
|
11.8
|
0.4
|
N
|
A:GLY14
|
4.7
|
13.5
|
0.6
|
C
|
A:CYS10
|
4.7
|
15.6
|
0.3
|
O
|
A:CYS13
|
4.7
|
14.2
|
0.6
|
CG
|
A:ASN15
|
4.8
|
15.5
|
0.6
|
C
|
A:CYS10
|
4.8
|
14.7
|
0.3
|
CB
|
A:ASN15
|
4.9
|
11.7
|
0.4
|
O
|
A:CYS10
|
4.9
|
15.9
|
0.3
|
C
|
A:CYS13
|
4.9
|
18.3
|
0.4
|
N
|
A:ASN15
|
5.0
|
12.2
|
0.4
|
N
|
B:GLU26
|
5.0
|
18.1
|
1.0
|
O
|
B:GLY25
|
5.0
|
17.1
|
1.0
|
|
Iron binding site 2 out
of 6 in 1vzh
Go back to
Iron Binding Sites List in 1vzh
Iron binding site 2 out
of 6 in the Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1129
b:18.5
occ:1.00
|
ND1
|
A:HIS119
|
2.2
|
15.1
|
1.0
|
NE2
|
A:HIS75
|
2.2
|
17.7
|
1.0
|
NE2
|
A:HIS49
|
2.2
|
16.7
|
1.0
|
NE2
|
A:HIS69
|
2.2
|
14.5
|
1.0
|
N24
|
A:FC61130
|
2.4
|
29.3
|
1.0
|
SG
|
A:CYS116
|
2.7
|
17.1
|
1.0
|
CE1
|
A:HIS119
|
3.0
|
18.3
|
1.0
|
CE1
|
A:HIS75
|
3.1
|
18.2
|
1.0
|
CE1
|
A:HIS49
|
3.1
|
17.7
|
1.0
|
CD2
|
A:HIS69
|
3.2
|
14.6
|
1.0
|
CE1
|
A:HIS69
|
3.2
|
15.0
|
1.0
|
CD2
|
A:HIS49
|
3.3
|
17.2
|
1.0
|
CG
|
A:HIS119
|
3.3
|
17.3
|
1.0
|
CD2
|
A:HIS75
|
3.3
|
18.1
|
1.0
|
C24
|
A:FC61130
|
3.4
|
28.9
|
1.0
|
CB
|
A:HIS119
|
3.8
|
15.8
|
1.0
|
CB
|
A:CYS116
|
3.9
|
15.2
|
1.0
|
NE2
|
A:HIS119
|
4.2
|
17.8
|
1.0
|
ND1
|
A:HIS75
|
4.3
|
19.7
|
1.0
|
ND1
|
A:HIS49
|
4.3
|
18.4
|
1.0
|
ND1
|
A:HIS69
|
4.3
|
12.8
|
1.0
|
CD2
|
A:HIS119
|
4.3
|
19.3
|
1.0
|
CG
|
A:HIS69
|
4.4
|
14.4
|
1.0
|
CG
|
A:HIS49
|
4.4
|
16.6
|
1.0
|
N
|
A:HIS119
|
4.4
|
15.4
|
1.0
|
CG
|
A:HIS75
|
4.4
|
18.9
|
1.0
|
CA
|
A:HIS119
|
4.7
|
15.8
|
1.0
|
CB
|
A:ILE118
|
4.9
|
19.2
|
1.0
|
|
Iron binding site 3 out
of 6 in 1vzh
Go back to
Iron Binding Sites List in 1vzh
Iron binding site 3 out
of 6 in the Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1130
b:30.5
occ:1.00
|
FE2
|
A:FC61130
|
0.0
|
30.5
|
1.0
|
C22
|
A:FC61130
|
1.9
|
30.1
|
1.0
|
C26
|
A:FC61130
|
1.9
|
29.6
|
1.0
|
C23
|
A:FC61130
|
1.9
|
30.6
|
1.0
|
C11
|
A:FC61130
|
1.9
|
30.5
|
1.0
|
C24
|
A:FC61130
|
1.9
|
28.9
|
1.0
|
C21
|
A:FC61130
|
1.9
|
29.6
|
1.0
|
N22
|
A:FC61130
|
3.0
|
33.2
|
1.0
|
N21
|
A:FC61130
|
3.1
|
32.0
|
1.0
|
N23
|
A:FC61130
|
3.1
|
30.2
|
1.0
|
N11
|
A:FC61130
|
3.1
|
33.0
|
1.0
|
N24
|
A:FC61130
|
3.1
|
29.3
|
1.0
|
N25
|
A:FC61130
|
3.1
|
29.6
|
1.0
|
CE1
|
A:HIS119
|
4.4
|
18.3
|
1.0
|
CD
|
A:LYS48
|
4.6
|
23.6
|
1.0
|
CE1
|
A:HIS75
|
4.6
|
18.2
|
1.0
|
NZ
|
A:LYS48
|
4.8
|
27.2
|
1.0
|
CE1
|
A:HIS49
|
4.8
|
17.7
|
1.0
|
NE2
|
A:HIS119
|
4.9
|
17.8
|
1.0
|
|
Iron binding site 4 out
of 6 in 1vzh
Go back to
Iron Binding Sites List in 1vzh
Iron binding site 4 out
of 6 in the Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1127
b:18.8
occ:0.70
|
SG
|
B:CYS29
|
1.9
|
18.6
|
0.3
|
SG
|
B:CYS10
|
2.2
|
17.4
|
0.7
|
SG
|
B:CYS13
|
2.2
|
20.5
|
0.7
|
CB
|
B:CYS13
|
2.3
|
23.6
|
0.3
|
SG
|
B:CYS29
|
2.3
|
14.8
|
0.7
|
SG
|
B:CYS30
|
2.5
|
22.5
|
0.7
|
SG
|
B:CYS30
|
2.7
|
23.4
|
0.3
|
SG
|
B:CYS10
|
3.0
|
18.6
|
0.3
|
SG
|
B:CYS13
|
3.1
|
24.9
|
0.3
|
CB
|
B:CYS10
|
3.2
|
17.2
|
0.7
|
CB
|
B:CYS10
|
3.2
|
18.4
|
0.3
|
CB
|
B:CYS30
|
3.3
|
21.4
|
0.3
|
CB
|
B:CYS30
|
3.3
|
19.6
|
0.7
|
CB
|
B:CYS13
|
3.4
|
21.4
|
0.7
|
CB
|
B:CYS29
|
3.4
|
15.8
|
0.7
|
CB
|
B:CYS29
|
3.5
|
18.1
|
0.3
|
CA
|
B:CYS13
|
3.6
|
23.2
|
0.3
|
N
|
B:CYS30
|
3.6
|
19.6
|
0.3
|
N
|
B:CYS30
|
3.7
|
18.8
|
0.7
|
CA
|
A:GLY25
|
3.7
|
25.5
|
1.0
|
N
|
B:CYS13
|
3.7
|
21.2
|
0.7
|
C
|
B:CYS29
|
3.8
|
18.3
|
0.3
|
C
|
B:CYS29
|
3.8
|
16.7
|
0.7
|
ND2
|
B:ASN15
|
3.9
|
21.3
|
0.3
|
N
|
B:CYS13
|
4.0
|
23.8
|
0.3
|
CA
|
B:CYS30
|
4.1
|
20.2
|
0.3
|
CA
|
B:CYS29
|
4.1
|
17.9
|
0.3
|
CA
|
B:CYS30
|
4.1
|
19.2
|
0.7
|
CA
|
B:CYS29
|
4.1
|
16.8
|
0.7
|
CA
|
B:CYS13
|
4.1
|
20.4
|
0.7
|
ND2
|
B:ASN15
|
4.1
|
15.6
|
0.7
|
O
|
B:CYS29
|
4.2
|
17.4
|
0.7
|
C
|
B:CYS13
|
4.2
|
22.7
|
0.3
|
O
|
B:CYS29
|
4.2
|
18.6
|
0.3
|
N
|
A:GLY25
|
4.3
|
27.2
|
1.0
|
O
|
B:CYS13
|
4.4
|
22.5
|
0.3
|
C
|
A:GLY25
|
4.5
|
24.8
|
1.0
|
CB
|
B:VAL12
|
4.5
|
21.4
|
0.7
|
CA
|
B:CYS10
|
4.6
|
18.6
|
0.3
|
CA
|
B:CYS10
|
4.6
|
17.4
|
0.7
|
CG
|
B:ASN15
|
4.8
|
16.8
|
0.7
|
C
|
B:VAL12
|
4.8
|
22.8
|
0.7
|
CB
|
B:ASN15
|
4.8
|
14.7
|
0.7
|
CG
|
B:ASN15
|
4.9
|
20.2
|
0.3
|
C
|
B:CYS13
|
4.9
|
20.1
|
0.7
|
N
|
B:GLY14
|
4.9
|
17.8
|
0.7
|
CB
|
B:ASN15
|
5.0
|
18.8
|
0.3
|
|
Iron binding site 5 out
of 6 in 1vzh
Go back to
Iron Binding Sites List in 1vzh
Iron binding site 5 out
of 6 in the Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 5 of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1128
b:17.0
occ:1.00
|
ND1
|
B:HIS119
|
2.2
|
18.7
|
1.0
|
NE2
|
B:HIS69
|
2.2
|
13.1
|
1.0
|
N24
|
B:FC61129
|
2.2
|
23.4
|
1.0
|
NE2
|
B:HIS49
|
2.2
|
13.2
|
1.0
|
NE2
|
B:HIS75
|
2.3
|
16.6
|
1.0
|
SG
|
B:CYS116
|
2.6
|
15.6
|
1.0
|
CE1
|
B:HIS119
|
3.0
|
20.6
|
1.0
|
CE1
|
B:HIS49
|
3.1
|
14.4
|
1.0
|
CE1
|
B:HIS75
|
3.1
|
16.0
|
1.0
|
CE1
|
B:HIS69
|
3.1
|
11.9
|
1.0
|
CD2
|
B:HIS69
|
3.2
|
14.1
|
1.0
|
CG
|
B:HIS119
|
3.2
|
19.3
|
1.0
|
CD2
|
B:HIS49
|
3.3
|
11.3
|
1.0
|
C24
|
B:FC61129
|
3.3
|
24.2
|
1.0
|
CD2
|
B:HIS75
|
3.4
|
15.6
|
1.0
|
CB
|
B:HIS119
|
3.7
|
16.6
|
1.0
|
CB
|
B:CYS116
|
3.8
|
12.4
|
1.0
|
NE2
|
B:HIS119
|
4.1
|
19.8
|
1.0
|
ND1
|
B:HIS69
|
4.3
|
14.0
|
1.0
|
CD2
|
B:HIS119
|
4.3
|
21.7
|
1.0
|
ND1
|
B:HIS49
|
4.3
|
12.3
|
1.0
|
ND1
|
B:HIS75
|
4.3
|
16.4
|
1.0
|
CG
|
B:HIS69
|
4.3
|
13.1
|
1.0
|
N
|
B:HIS119
|
4.4
|
15.4
|
1.0
|
CG
|
B:HIS49
|
4.4
|
13.1
|
1.0
|
CG
|
B:HIS75
|
4.4
|
16.1
|
1.0
|
CA
|
B:HIS119
|
4.7
|
16.7
|
1.0
|
CB
|
B:ILE118
|
5.0
|
19.9
|
1.0
|
|
Iron binding site 6 out
of 6 in 1vzh
Go back to
Iron Binding Sites List in 1vzh
Iron binding site 6 out
of 6 in the Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 6 of Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray Induced Photoreduction within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1129
b:22.7
occ:1.00
|
FE2
|
B:FC61129
|
0.0
|
22.7
|
1.0
|
C22
|
B:FC61129
|
1.9
|
25.4
|
1.0
|
C23
|
B:FC61129
|
1.9
|
24.9
|
1.0
|
C26
|
B:FC61129
|
1.9
|
25.3
|
1.0
|
C11
|
B:FC61129
|
1.9
|
24.0
|
1.0
|
C24
|
B:FC61129
|
1.9
|
24.2
|
1.0
|
C21
|
B:FC61129
|
1.9
|
24.5
|
1.0
|
N22
|
B:FC61129
|
3.0
|
26.8
|
1.0
|
N23
|
B:FC61129
|
3.1
|
28.0
|
1.0
|
N21
|
B:FC61129
|
3.1
|
24.3
|
1.0
|
N11
|
B:FC61129
|
3.1
|
25.5
|
1.0
|
N24
|
B:FC61129
|
3.1
|
23.4
|
1.0
|
N25
|
B:FC61129
|
3.1
|
25.0
|
1.0
|
CE1
|
B:HIS119
|
4.5
|
20.6
|
1.0
|
CE1
|
B:HIS75
|
4.6
|
16.0
|
1.0
|
CD
|
B:LYS48
|
4.8
|
19.7
|
1.0
|
CE1
|
B:HIS49
|
4.8
|
14.4
|
1.0
|
NE2
|
B:HIS119
|
4.9
|
19.8
|
1.0
|
|
Reference:
V.Adam,
A.Royant,
V.Niviere,
F.P.Molina-Heredia,
D.Bourgeois.
Structure of Superoxide Reductase Bound to Ferrocyanide and Active Site Expansion Upon X-Ray-Induced Photo-Reduction. Structure V. 12 1729 2004.
ISSN: ISSN 0969-2126
PubMed: 15341736
DOI: 10.1016/J.STR.2004.07.013
Page generated: Sat Aug 3 16:23:58 2024
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