Iron in PDB 2fkz: Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Protein crystallography data
The structure of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin, PDB code: 2fkz
was solved by
L.Swartz,
M.Kunchinskas,
H.Li,
T.L.Poulos,
W.N.Lanzilotta,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
29.55 /
2.00
|
Space group
|
H 3
|
Cell size a, b, c (Å), α, β, γ (°)
|
123.676,
123.676,
284.279,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
21.6 /
24.7
|
Other elements in 2fkz:
The structure of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin also contains other interesting chemical elements:
Iron Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
20;
Page 3, Binding sites: 21 -
22;
Binding sites:
The binding sites of Iron atom in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
(pdb code 2fkz). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 22 binding sites of Iron where determined in the
Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin, PDB code: 2fkz:
Jump to Iron binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Iron binding site 1 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 1 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1600
b:24.0
occ:1.00
|
OE2
|
A:GLU127
|
1.9
|
28.0
|
1.0
|
OE1
|
A:GLU51
|
2.0
|
24.5
|
1.0
|
OE1
|
A:GLU18
|
2.0
|
25.1
|
1.0
|
ND1
|
A:HIS54
|
2.1
|
22.3
|
1.0
|
CD
|
A:GLU18
|
2.9
|
24.9
|
1.0
|
CE1
|
A:HIS54
|
3.0
|
22.8
|
1.0
|
CD
|
A:GLU127
|
3.0
|
27.4
|
1.0
|
CD
|
A:GLU51
|
3.0
|
24.0
|
1.0
|
CG
|
A:HIS54
|
3.2
|
22.0
|
1.0
|
OE2
|
A:GLU18
|
3.2
|
25.8
|
1.0
|
OE2
|
A:GLU51
|
3.3
|
24.6
|
1.0
|
OE1
|
A:GLU127
|
3.3
|
29.1
|
1.0
|
CB
|
A:HIS54
|
3.6
|
20.8
|
1.0
|
FE
|
A:FE21601
|
3.9
|
34.9
|
1.0
|
CG2
|
A:ILE123
|
4.0
|
24.5
|
1.0
|
NE2
|
A:HIS54
|
4.1
|
22.4
|
1.0
|
CD2
|
A:HIS54
|
4.2
|
22.2
|
1.0
|
CG
|
A:GLU18
|
4.3
|
24.6
|
1.0
|
CG
|
A:GLU127
|
4.3
|
26.6
|
1.0
|
CG
|
A:GLU51
|
4.4
|
24.0
|
1.0
|
CA
|
A:GLU51
|
4.4
|
23.7
|
1.0
|
CB
|
A:GLU51
|
4.7
|
23.8
|
1.0
|
O
|
A:HOH1772
|
4.7
|
40.4
|
1.0
|
CB
|
A:GLU18
|
5.0
|
24.1
|
1.0
|
|
Iron binding site 2 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 2 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1601
b:34.9
occ:1.00
|
OE1
|
A:GLU127
|
1.9
|
29.1
|
1.0
|
OE2
|
A:GLU94
|
2.0
|
35.1
|
1.0
|
OE2
|
A:GLU51
|
2.2
|
24.6
|
1.0
|
OE1
|
A:GLU94
|
2.3
|
34.5
|
1.0
|
CD
|
A:GLU94
|
2.4
|
34.9
|
1.0
|
O
|
A:HOH1772
|
2.8
|
40.4
|
1.0
|
CD
|
A:GLU127
|
3.1
|
27.4
|
1.0
|
CD
|
A:GLU51
|
3.3
|
24.0
|
1.0
|
OE2
|
A:GLU127
|
3.6
|
28.0
|
1.0
|
ND1
|
A:HIS130
|
3.7
|
26.8
|
1.0
|
OE1
|
A:GLU51
|
3.8
|
24.5
|
1.0
|
FE
|
A:FE21600
|
3.9
|
24.0
|
1.0
|
CG
|
A:GLU94
|
3.9
|
34.7
|
1.0
|
CB
|
A:HIS130
|
4.0
|
26.8
|
1.0
|
CA
|
A:GLU127
|
4.2
|
25.8
|
1.0
|
CG
|
A:GLU127
|
4.3
|
26.6
|
1.0
|
CG
|
A:HIS130
|
4.3
|
26.9
|
1.0
|
CB
|
A:GLU127
|
4.4
|
26.2
|
1.0
|
OH
|
A:TYR25
|
4.5
|
24.9
|
1.0
|
CE2
|
A:TYR25
|
4.6
|
23.6
|
1.0
|
CG
|
A:GLU51
|
4.6
|
24.0
|
1.0
|
CE1
|
A:HIS130
|
4.8
|
26.8
|
1.0
|
CB
|
A:GLU94
|
4.9
|
34.3
|
1.0
|
O
|
A:GLU127
|
5.0
|
25.2
|
1.0
|
N
|
A:GLU127
|
5.0
|
25.8
|
1.0
|
CE1
|
A:HIS54
|
5.0
|
22.8
|
1.0
|
|
Iron binding site 3 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 3 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1600
b:22.8
occ:1.00
|
OE2
|
B:GLU127
|
1.9
|
27.2
|
1.0
|
OE1
|
B:GLU18
|
2.0
|
24.5
|
1.0
|
OE2
|
B:GLU51
|
2.1
|
23.5
|
1.0
|
ND1
|
B:HIS54
|
2.1
|
20.6
|
1.0
|
CD
|
B:GLU18
|
2.8
|
24.0
|
1.0
|
OE2
|
B:GLU18
|
2.9
|
24.9
|
1.0
|
CE1
|
B:HIS54
|
3.0
|
20.7
|
1.0
|
CD
|
B:GLU127
|
3.0
|
26.8
|
1.0
|
CD
|
B:GLU51
|
3.1
|
23.2
|
1.0
|
CG
|
B:HIS54
|
3.2
|
20.4
|
1.0
|
OE1
|
B:GLU51
|
3.5
|
23.4
|
1.0
|
OE1
|
B:GLU127
|
3.5
|
28.6
|
1.0
|
CB
|
B:HIS54
|
3.6
|
19.6
|
1.0
|
FE
|
B:FE21601
|
3.7
|
34.4
|
1.0
|
CG2
|
B:ILE123
|
4.0
|
22.6
|
1.0
|
NE2
|
B:HIS54
|
4.1
|
20.2
|
1.0
|
CG
|
B:GLU18
|
4.2
|
24.1
|
1.0
|
CG
|
B:GLU127
|
4.3
|
25.9
|
1.0
|
CD2
|
B:HIS54
|
4.3
|
20.1
|
1.0
|
CA
|
B:GLU51
|
4.4
|
22.3
|
1.0
|
CG
|
B:GLU51
|
4.4
|
22.6
|
1.0
|
CB
|
B:GLU51
|
4.7
|
22.6
|
1.0
|
O
|
B:HOH3066
|
4.9
|
34.7
|
1.0
|
CB
|
B:GLU18
|
4.9
|
23.7
|
1.0
|
|
Iron binding site 4 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 4 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1601
b:34.4
occ:1.00
|
OE1
|
B:GLU127
|
1.9
|
28.6
|
1.0
|
OE1
|
B:GLU51
|
2.0
|
23.4
|
1.0
|
OE2
|
B:GLU94
|
2.3
|
34.7
|
1.0
|
OE1
|
B:GLU94
|
2.5
|
34.8
|
1.0
|
O
|
B:HOH3066
|
2.7
|
34.7
|
1.0
|
CD
|
B:GLU94
|
2.8
|
34.6
|
1.0
|
CD
|
B:GLU127
|
2.9
|
26.8
|
1.0
|
CD
|
B:GLU51
|
3.1
|
23.2
|
1.0
|
OE2
|
B:GLU127
|
3.3
|
27.2
|
1.0
|
OE2
|
B:GLU51
|
3.5
|
23.5
|
1.0
|
ND1
|
B:HIS130
|
3.7
|
26.4
|
1.0
|
FE
|
B:FE21600
|
3.7
|
22.8
|
1.0
|
CB
|
B:HIS130
|
4.2
|
26.2
|
1.0
|
CG
|
B:GLU127
|
4.2
|
25.9
|
1.0
|
CG
|
B:GLU94
|
4.3
|
34.7
|
1.0
|
CA
|
B:GLU127
|
4.4
|
25.3
|
1.0
|
CG
|
B:GLU51
|
4.4
|
22.6
|
1.0
|
CG
|
B:HIS130
|
4.4
|
26.4
|
1.0
|
CB
|
B:GLU127
|
4.5
|
25.6
|
1.0
|
CE2
|
B:TYR25
|
4.6
|
24.1
|
1.0
|
OH
|
B:TYR25
|
4.6
|
25.1
|
1.0
|
CE1
|
B:HIS130
|
4.8
|
26.5
|
1.0
|
CE1
|
B:HIS54
|
4.9
|
20.7
|
1.0
|
ND1
|
B:HIS54
|
5.0
|
20.6
|
1.0
|
|
Iron binding site 5 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 5 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 5 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1602
b:20.8
occ:1.00
|
OD1
|
D:ASN148
|
2.9
|
18.8
|
1.0
|
OE1
|
D:GLN151
|
2.9
|
20.5
|
1.0
|
OE1
|
B:GLN151
|
2.9
|
20.1
|
1.0
|
OD1
|
B:ASN148
|
3.0
|
18.1
|
1.0
|
CG
|
D:ASN148
|
3.8
|
18.8
|
1.0
|
CD
|
D:GLN151
|
3.9
|
21.0
|
1.0
|
CG
|
B:ASN148
|
3.9
|
18.8
|
1.0
|
CD
|
B:GLN151
|
3.9
|
20.2
|
1.0
|
NE2
|
D:GLN151
|
4.1
|
20.4
|
1.0
|
NE2
|
B:GLN151
|
4.2
|
19.4
|
1.0
|
ND2
|
D:ASN148
|
4.3
|
19.3
|
1.0
|
ND2
|
B:ASN148
|
4.4
|
18.9
|
1.0
|
CB
|
D:ASN148
|
4.9
|
17.9
|
1.0
|
CB
|
B:ASN148
|
5.0
|
18.8
|
1.0
|
|
Iron binding site 6 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 6 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 6 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe3001
b:29.5
occ:1.00
|
FE
|
B:HEM3001
|
0.0
|
29.5
|
1.0
|
ND
|
B:HEM3001
|
2.0
|
30.5
|
1.0
|
NA
|
B:HEM3001
|
2.0
|
30.4
|
1.0
|
NC
|
B:HEM3001
|
2.0
|
30.0
|
1.0
|
NB
|
B:HEM3001
|
2.1
|
30.1
|
1.0
|
SD
|
A:MET52
|
2.1
|
29.2
|
1.0
|
SD
|
B:MET52
|
2.3
|
28.5
|
1.0
|
C4D
|
B:HEM3001
|
3.0
|
31.1
|
1.0
|
CE
|
B:MET52
|
3.0
|
28.0
|
1.0
|
C1A
|
B:HEM3001
|
3.0
|
31.1
|
1.0
|
C1D
|
B:HEM3001
|
3.0
|
30.8
|
1.0
|
C4A
|
B:HEM3001
|
3.1
|
30.9
|
1.0
|
C1C
|
B:HEM3001
|
3.1
|
30.0
|
1.0
|
C4C
|
B:HEM3001
|
3.1
|
30.2
|
1.0
|
C4B
|
B:HEM3001
|
3.1
|
30.1
|
1.0
|
C1B
|
B:HEM3001
|
3.1
|
30.4
|
1.0
|
CHA
|
B:HEM3001
|
3.3
|
31.2
|
1.0
|
CG
|
B:MET52
|
3.4
|
25.7
|
1.0
|
CHC
|
B:HEM3001
|
3.4
|
29.9
|
1.0
|
CHD
|
B:HEM3001
|
3.4
|
30.6
|
1.0
|
CHB
|
B:HEM3001
|
3.5
|
30.6
|
1.0
|
CG
|
A:MET52
|
3.5
|
26.8
|
1.0
|
CE
|
A:MET52
|
3.6
|
29.1
|
1.0
|
CB
|
B:MET52
|
4.1
|
23.1
|
1.0
|
C3D
|
B:HEM3001
|
4.3
|
31.6
|
1.0
|
C2A
|
B:HEM3001
|
4.3
|
31.6
|
1.0
|
C2D
|
B:HEM3001
|
4.3
|
31.1
|
1.0
|
CB
|
A:MET52
|
4.3
|
24.4
|
1.0
|
C3A
|
B:HEM3001
|
4.3
|
31.3
|
1.0
|
C2C
|
B:HEM3001
|
4.3
|
30.1
|
1.0
|
C3C
|
B:HEM3001
|
4.4
|
30.4
|
1.0
|
C3B
|
B:HEM3001
|
4.4
|
30.5
|
1.0
|
C2B
|
B:HEM3001
|
4.4
|
30.6
|
1.0
|
|
Iron binding site 7 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 7 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 7 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe1600
b:22.4
occ:1.00
|
OE2
|
C:GLU127
|
1.9
|
25.0
|
1.0
|
OE1
|
C:GLU51
|
2.0
|
21.6
|
1.0
|
ND1
|
C:HIS54
|
2.1
|
19.9
|
1.0
|
OE1
|
C:GLU18
|
2.2
|
22.3
|
1.0
|
OE2
|
C:GLU18
|
2.4
|
22.5
|
1.0
|
CD
|
C:GLU18
|
2.6
|
21.7
|
1.0
|
CE1
|
C:HIS54
|
3.0
|
19.9
|
1.0
|
CD
|
C:GLU51
|
3.0
|
21.2
|
1.0
|
CD
|
C:GLU127
|
3.1
|
23.6
|
1.0
|
CG
|
C:HIS54
|
3.1
|
19.0
|
1.0
|
OE2
|
C:GLU51
|
3.5
|
22.9
|
1.0
|
CB
|
C:HIS54
|
3.5
|
17.5
|
1.0
|
OE1
|
C:GLU127
|
3.6
|
24.9
|
1.0
|
O
|
C:HOH1735
|
3.7
|
38.0
|
1.0
|
FE
|
C:FE21601
|
4.0
|
36.4
|
1.0
|
CG2
|
C:ILE123
|
4.1
|
22.6
|
1.0
|
CG
|
C:GLU18
|
4.1
|
20.6
|
1.0
|
NE2
|
C:HIS54
|
4.1
|
18.9
|
1.0
|
O
|
C:HOH1782
|
4.1
|
34.6
|
1.0
|
CD2
|
C:HIS54
|
4.2
|
19.1
|
1.0
|
CA
|
C:GLU51
|
4.2
|
17.6
|
1.0
|
CG
|
C:GLU127
|
4.3
|
23.6
|
1.0
|
CG
|
C:GLU51
|
4.3
|
20.0
|
1.0
|
CB
|
C:GLU51
|
4.5
|
18.4
|
1.0
|
O
|
C:HOH1793
|
4.6
|
22.2
|
1.0
|
CB
|
C:GLU18
|
4.9
|
18.8
|
1.0
|
O
|
C:ASP50
|
5.0
|
17.6
|
1.0
|
|
Iron binding site 8 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 8 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 8 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe1601
b:36.4
occ:1.00
|
O
|
C:HOH1793
|
1.7
|
22.2
|
1.0
|
OE1
|
C:GLU127
|
1.8
|
24.9
|
1.0
|
OE2
|
C:GLU94
|
1.9
|
34.4
|
1.0
|
OE2
|
C:GLU51
|
2.2
|
22.9
|
1.0
|
OE1
|
C:GLU94
|
2.3
|
34.0
|
1.0
|
CD
|
C:GLU94
|
2.4
|
33.5
|
1.0
|
O
|
C:HOH1735
|
2.7
|
38.0
|
1.0
|
CD
|
C:GLU127
|
2.8
|
23.6
|
1.0
|
OE2
|
C:GLU127
|
3.3
|
25.0
|
1.0
|
CD
|
C:GLU51
|
3.3
|
21.2
|
1.0
|
OE1
|
C:GLU51
|
3.7
|
21.6
|
1.0
|
ND1
|
C:HIS130
|
3.8
|
22.6
|
1.0
|
CG
|
C:GLU94
|
3.9
|
31.0
|
1.0
|
CG
|
C:GLU127
|
4.0
|
23.6
|
1.0
|
FE
|
C:FE21600
|
4.0
|
22.4
|
1.0
|
CA
|
C:GLU127
|
4.1
|
22.4
|
1.0
|
CB
|
C:GLU127
|
4.2
|
22.6
|
1.0
|
OH
|
C:TYR25
|
4.4
|
17.6
|
1.0
|
CB
|
C:HIS130
|
4.4
|
22.5
|
1.0
|
CE2
|
C:TYR25
|
4.5
|
16.8
|
1.0
|
CG
|
C:HIS130
|
4.6
|
22.8
|
1.0
|
CG
|
C:GLU51
|
4.6
|
20.0
|
1.0
|
CE1
|
C:HIS130
|
4.9
|
22.6
|
1.0
|
CB
|
C:GLU94
|
4.9
|
28.1
|
1.0
|
O
|
C:GLU127
|
4.9
|
22.3
|
1.0
|
CZ
|
C:TYR25
|
4.9
|
16.9
|
1.0
|
|
Iron binding site 9 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 9 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 9 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Fe1600
b:22.1
occ:1.00
|
OE1
|
D:GLU51
|
1.9
|
21.1
|
1.0
|
OE1
|
D:GLU127
|
1.9
|
24.5
|
1.0
|
ND1
|
D:HIS54
|
2.1
|
19.0
|
1.0
|
OE1
|
D:GLU18
|
2.2
|
22.5
|
1.0
|
OE2
|
D:GLU18
|
2.3
|
22.5
|
1.0
|
CD
|
D:GLU18
|
2.6
|
21.9
|
1.0
|
CD
|
D:GLU127
|
3.0
|
23.4
|
1.0
|
CD
|
D:GLU51
|
3.0
|
20.6
|
1.0
|
CE1
|
D:HIS54
|
3.0
|
19.8
|
1.0
|
CG
|
D:HIS54
|
3.1
|
18.5
|
1.0
|
OE2
|
D:GLU127
|
3.4
|
24.2
|
1.0
|
OE2
|
D:GLU51
|
3.4
|
22.4
|
1.0
|
CB
|
D:HIS54
|
3.5
|
16.8
|
1.0
|
O
|
D:HOH3073
|
4.1
|
34.0
|
1.0
|
CG
|
D:GLU18
|
4.1
|
20.8
|
1.0
|
FE
|
D:FE21601
|
4.1
|
33.4
|
1.0
|
CG2
|
D:ILE123
|
4.1
|
19.2
|
1.0
|
NE2
|
D:HIS54
|
4.1
|
19.2
|
1.0
|
CA
|
D:GLU51
|
4.2
|
17.9
|
1.0
|
CD2
|
D:HIS54
|
4.2
|
18.7
|
1.0
|
CG
|
D:GLU127
|
4.2
|
22.8
|
1.0
|
CG
|
D:GLU51
|
4.3
|
19.8
|
1.0
|
CB
|
D:GLU51
|
4.5
|
18.3
|
1.0
|
CB
|
D:GLU18
|
4.9
|
19.5
|
1.0
|
O
|
D:GLU51
|
5.0
|
16.8
|
1.0
|
|
Iron binding site 10 out
of 22 in 2fkz
Go back to
Iron Binding Sites List in 2fkz
Iron binding site 10 out
of 22 in the Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 10 of Reduced (All Ferrous) Form of the Azotobacter Vinelandii Bacterioferritin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Fe1601
b:33.4
occ:1.00
|
OE2
|
D:GLU127
|
1.8
|
24.2
|
1.0
|
OE1
|
D:GLU94
|
2.0
|
30.6
|
1.0
|
OE2
|
D:GLU51
|
2.1
|
22.4
|
1.0
|
OE2
|
D:GLU94
|
2.3
|
29.9
|
1.0
|
CD
|
D:GLU94
|
2.4
|
29.8
|
1.0
|
CD
|
D:GLU127
|
3.0
|
23.4
|
1.0
|
CD
|
D:GLU51
|
3.2
|
20.6
|
1.0
|
OE1
|
D:GLU127
|
3.6
|
24.5
|
1.0
|
OE1
|
D:GLU51
|
3.7
|
21.1
|
1.0
|
ND1
|
D:HIS130
|
3.7
|
15.0
|
1.0
|
CG
|
D:GLU94
|
3.9
|
27.5
|
1.0
|
FE
|
D:FE21600
|
4.1
|
22.1
|
1.0
|
CA
|
D:GLU127
|
4.2
|
20.9
|
1.0
|
CG
|
D:GLU127
|
4.2
|
22.8
|
1.0
|
CB
|
D:HIS130
|
4.2
|
15.8
|
1.0
|
CB
|
D:GLU127
|
4.3
|
21.6
|
1.0
|
CG
|
D:HIS130
|
4.4
|
15.3
|
1.0
|
CG
|
D:GLU51
|
4.5
|
19.8
|
1.0
|
CE2
|
D:TYR25
|
4.5
|
18.3
|
1.0
|
OH
|
D:TYR25
|
4.5
|
19.2
|
1.0
|
CE1
|
D:HIS130
|
4.8
|
14.9
|
1.0
|
O
|
D:GLU127
|
4.9
|
20.3
|
1.0
|
CB
|
D:GLU94
|
4.9
|
25.6
|
1.0
|
|
Reference:
L.Swartz,
M.Kuchinskas,
H.Li,
T.L.Poulos,
W.N.Lanzilotta.
Redox-Dependent Structural Changes in the Azotobacter Vinelandii Bacterioferritin: New Insights Into the Ferroxidase and Iron Transport Mechanism(,). Biochemistry V. 45 4421 2006.
ISSN: ISSN 0006-2960
PubMed: 16584178
DOI: 10.1021/BI060146W
Page generated: Sat Aug 3 21:29:13 2024
|