Iron in PDB 1frh: Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Protein crystallography data
The structure of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential, PDB code: 1frh
was solved by
C.D.Stout,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
8.00 /
2.30
|
Space group
|
P 41 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
55.250,
55.250,
95.270,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
22.4 /
n/a
|
Iron Binding Sites:
The binding sites of Iron atom in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
(pdb code 1frh). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 7 binding sites of Iron where determined in the
Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential, PDB code: 1frh:
Jump to Iron binding site number:
1;
2;
3;
4;
5;
6;
7;
Iron binding site 1 out
of 7 in 1frh
Go back to
Iron Binding Sites List in 1frh
Iron binding site 1 out
of 7 in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe107
b:14.9
occ:1.00
|
FE1
|
A:SF4107
|
0.0
|
14.9
|
1.0
|
S2
|
A:SF4107
|
2.3
|
20.4
|
1.0
|
SG
|
A:CYS39
|
2.3
|
16.6
|
1.0
|
S4
|
A:SF4107
|
2.3
|
18.9
|
1.0
|
S3
|
A:SF4107
|
2.3
|
15.5
|
1.0
|
FE3
|
A:SF4107
|
2.5
|
19.4
|
1.0
|
FE2
|
A:SF4107
|
2.6
|
17.6
|
1.0
|
FE4
|
A:SF4107
|
2.8
|
19.8
|
1.0
|
CB
|
A:CYS39
|
3.5
|
15.6
|
1.0
|
S1
|
A:SF4107
|
3.8
|
18.6
|
1.0
|
CA
|
A:CYS39
|
3.9
|
17.3
|
1.0
|
N
|
A:ASP41
|
4.1
|
16.3
|
1.0
|
SG
|
A:CYS24
|
4.1
|
17.1
|
1.0
|
N
|
A:ILE40
|
4.2
|
16.4
|
1.0
|
CB
|
A:TYR2
|
4.4
|
11.7
|
1.0
|
C
|
A:CYS39
|
4.5
|
17.5
|
1.0
|
CG2
|
A:ILE34
|
4.5
|
10.8
|
1.0
|
SG
|
A:CYS45
|
4.5
|
19.5
|
1.0
|
CA
|
A:ASP41
|
4.6
|
16.5
|
1.0
|
N
|
A:CYS42
|
4.8
|
16.3
|
1.0
|
SG
|
A:CYS20
|
4.8
|
16.8
|
1.0
|
CD1
|
A:TYR2
|
4.8
|
12.4
|
1.0
|
SG
|
A:CYS42
|
4.9
|
18.6
|
1.0
|
CG
|
A:TYR2
|
4.9
|
12.6
|
1.0
|
N
|
A:TYR2
|
4.9
|
13.7
|
1.0
|
C
|
A:ILE40
|
5.0
|
17.2
|
1.0
|
|
Iron binding site 2 out
of 7 in 1frh
Go back to
Iron Binding Sites List in 1frh
Iron binding site 2 out
of 7 in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe107
b:17.6
occ:1.00
|
FE2
|
A:SF4107
|
0.0
|
17.6
|
1.0
|
S3
|
A:SF4107
|
2.3
|
15.5
|
1.0
|
S1
|
A:SF4107
|
2.3
|
18.6
|
1.0
|
S4
|
A:SF4107
|
2.3
|
18.9
|
1.0
|
SG
|
A:CYS42
|
2.3
|
18.6
|
1.0
|
FE3
|
A:SF4107
|
2.6
|
19.4
|
1.0
|
FE1
|
A:SF4107
|
2.6
|
14.9
|
1.0
|
FE4
|
A:SF4107
|
2.7
|
19.8
|
1.0
|
CB
|
A:CYS42
|
3.6
|
15.3
|
1.0
|
N
|
A:CYS42
|
3.7
|
16.3
|
1.0
|
S2
|
A:SF4107
|
3.8
|
20.4
|
1.0
|
N
|
A:ALA43
|
3.9
|
17.9
|
1.0
|
CA
|
A:CYS42
|
4.1
|
16.8
|
1.0
|
C
|
A:CYS42
|
4.3
|
18.1
|
1.0
|
CD
|
A:PRO21
|
4.3
|
17.1
|
1.0
|
N
|
A:LEU44
|
4.3
|
19.0
|
1.0
|
SG
|
A:CYS45
|
4.5
|
19.5
|
1.0
|
SG
|
A:CYS39
|
4.5
|
16.6
|
1.0
|
N
|
A:ASP41
|
4.5
|
16.3
|
1.0
|
C
|
A:ASP41
|
4.6
|
16.5
|
1.0
|
SG
|
A:CYS20
|
4.7
|
16.8
|
1.0
|
CA
|
A:ALA43
|
4.7
|
18.4
|
1.0
|
CG
|
A:PRO21
|
4.8
|
15.9
|
1.0
|
CA
|
A:ASP41
|
4.8
|
16.5
|
1.0
|
CG1
|
A:ILE40
|
4.8
|
14.1
|
1.0
|
C
|
A:ALA43
|
5.0
|
18.4
|
1.0
|
N
|
A:CYS45
|
5.0
|
20.4
|
1.0
|
|
Iron binding site 3 out
of 7 in 1frh
Go back to
Iron Binding Sites List in 1frh
Iron binding site 3 out
of 7 in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe107
b:19.4
occ:1.00
|
FE3
|
A:SF4107
|
0.0
|
19.4
|
1.0
|
S2
|
A:SF4107
|
2.3
|
20.4
|
1.0
|
S4
|
A:SF4107
|
2.3
|
18.9
|
1.0
|
S1
|
A:SF4107
|
2.3
|
18.6
|
1.0
|
SG
|
A:CYS45
|
2.3
|
19.5
|
1.0
|
FE1
|
A:SF4107
|
2.5
|
14.9
|
1.0
|
FE2
|
A:SF4107
|
2.6
|
17.6
|
1.0
|
FE4
|
A:SF4107
|
2.6
|
19.8
|
1.0
|
CB
|
A:CYS45
|
3.4
|
19.4
|
1.0
|
S3
|
A:SF4107
|
3.7
|
15.5
|
1.0
|
N
|
A:CYS45
|
4.2
|
20.4
|
1.0
|
CA
|
A:CYS45
|
4.4
|
20.1
|
1.0
|
CB
|
A:TYR2
|
4.4
|
11.7
|
1.0
|
CZ
|
A:PHE25
|
4.4
|
12.6
|
1.0
|
CE1
|
A:PHE25
|
4.5
|
13.1
|
1.0
|
SG
|
A:CYS39
|
4.5
|
16.6
|
1.0
|
SG
|
A:CYS42
|
4.6
|
18.6
|
1.0
|
CD1
|
A:ILE34
|
4.6
|
8.4
|
1.0
|
CG
|
A:TYR2
|
4.7
|
12.6
|
1.0
|
SG
|
A:CYS20
|
4.8
|
16.8
|
1.0
|
N
|
A:LEU44
|
4.9
|
19.0
|
1.0
|
N
|
A:ALA43
|
5.0
|
17.9
|
1.0
|
|
Iron binding site 4 out
of 7 in 1frh
Go back to
Iron Binding Sites List in 1frh
Iron binding site 4 out
of 7 in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe107
b:19.8
occ:1.00
|
FE4
|
A:SF4107
|
0.0
|
19.8
|
1.0
|
S3
|
A:SF4107
|
2.3
|
15.5
|
1.0
|
SG
|
A:CYS20
|
2.3
|
16.8
|
1.0
|
S2
|
A:SF4107
|
2.3
|
20.4
|
1.0
|
S1
|
A:SF4107
|
2.3
|
18.6
|
1.0
|
FE3
|
A:SF4107
|
2.6
|
19.4
|
1.0
|
FE2
|
A:SF4107
|
2.7
|
17.6
|
1.0
|
FE1
|
A:SF4107
|
2.8
|
14.9
|
1.0
|
CB
|
A:CYS20
|
3.3
|
16.1
|
1.0
|
SG
|
A:CYS24
|
3.7
|
17.1
|
1.0
|
CA
|
A:CYS20
|
3.7
|
20.3
|
1.0
|
S4
|
A:SF4107
|
4.0
|
18.9
|
1.0
|
CE1
|
A:PHE25
|
4.1
|
13.1
|
1.0
|
CD
|
A:PRO21
|
4.3
|
17.1
|
1.0
|
CG2
|
A:VAL22
|
4.4
|
17.7
|
1.0
|
C
|
A:CYS20
|
4.5
|
19.3
|
1.0
|
N
|
A:PRO21
|
4.6
|
18.3
|
1.0
|
SG
|
A:CYS42
|
4.6
|
18.6
|
1.0
|
SG
|
A:CYS45
|
4.7
|
19.5
|
1.0
|
CD1
|
A:PHE25
|
4.8
|
13.6
|
1.0
|
N
|
A:CYS20
|
4.9
|
20.9
|
1.0
|
CZ
|
A:PHE25
|
4.9
|
12.6
|
1.0
|
SG
|
A:CYS39
|
4.9
|
16.6
|
1.0
|
|
Iron binding site 5 out
of 7 in 1frh
Go back to
Iron Binding Sites List in 1frh
Iron binding site 5 out
of 7 in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 5 of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe108
b:21.1
occ:1.00
|
FE1
|
A:F3S108
|
0.0
|
21.1
|
1.0
|
S2
|
A:F3S108
|
2.2
|
16.1
|
1.0
|
S3
|
A:F3S108
|
2.3
|
14.9
|
1.0
|
S1
|
A:F3S108
|
2.3
|
15.9
|
1.0
|
SG
|
A:CYS16
|
2.4
|
18.6
|
1.0
|
FE4
|
A:F3S108
|
2.5
|
20.8
|
1.0
|
FE3
|
A:F3S108
|
2.6
|
17.2
|
1.0
|
CB
|
A:CYS16
|
3.3
|
19.5
|
1.0
|
S4
|
A:F3S108
|
3.9
|
16.3
|
1.0
|
N
|
A:THR14
|
4.1
|
17.4
|
1.0
|
CA
|
A:THR14
|
4.1
|
18.3
|
1.0
|
N
|
A:CYS16
|
4.1
|
21.6
|
1.0
|
CA
|
A:CYS16
|
4.4
|
20.8
|
1.0
|
CD2
|
A:LEU32
|
4.4
|
11.2
|
1.0
|
C
|
A:THR14
|
4.5
|
19.6
|
1.0
|
CD1
|
A:ILE54
|
4.6
|
13.0
|
1.0
|
SG
|
A:CYS49
|
4.6
|
14.1
|
1.0
|
N
|
A:ASP15
|
4.6
|
21.4
|
1.0
|
SG
|
A:CYS8
|
4.7
|
13.8
|
1.0
|
N
|
A:TYR13
|
4.9
|
15.0
|
1.0
|
CB
|
A:LEU32
|
5.0
|
11.5
|
1.0
|
|
Iron binding site 6 out
of 7 in 1frh
Go back to
Iron Binding Sites List in 1frh
Iron binding site 6 out
of 7 in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 6 of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe108
b:17.2
occ:1.00
|
FE3
|
A:F3S108
|
0.0
|
17.2
|
1.0
|
SG
|
A:CYS8
|
2.2
|
13.8
|
1.0
|
S3
|
A:F3S108
|
2.3
|
14.9
|
1.0
|
S1
|
A:F3S108
|
2.3
|
15.9
|
1.0
|
S4
|
A:F3S108
|
2.3
|
16.3
|
1.0
|
FE4
|
A:F3S108
|
2.6
|
20.8
|
1.0
|
FE1
|
A:F3S108
|
2.6
|
21.1
|
1.0
|
CB
|
A:CYS8
|
3.2
|
14.2
|
1.0
|
S2
|
A:F3S108
|
3.9
|
16.1
|
1.0
|
CA
|
A:CYS8
|
3.9
|
15.5
|
1.0
|
CA
|
A:LYS12
|
4.1
|
13.4
|
1.0
|
N
|
A:TYR13
|
4.3
|
15.0
|
1.0
|
N
|
A:LYS12
|
4.4
|
14.2
|
1.0
|
CG1
|
A:VAL4
|
4.5
|
9.2
|
1.0
|
SG
|
A:CYS49
|
4.6
|
14.1
|
1.0
|
O
|
A:CYS8
|
4.6
|
16.1
|
1.0
|
C
|
A:CYS8
|
4.7
|
15.8
|
1.0
|
C
|
A:LYS12
|
4.7
|
14.8
|
1.0
|
CB
|
A:LEU32
|
4.7
|
11.5
|
1.0
|
SG
|
A:CYS16
|
4.8
|
18.6
|
1.0
|
N
|
A:THR14
|
4.9
|
17.4
|
1.0
|
|
Iron binding site 7 out
of 7 in 1frh
Go back to
Iron Binding Sites List in 1frh
Iron binding site 7 out
of 7 in the Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 7 of Azotobacter Vinelandii Ferredoxin I: Alteration of Individual Surface Charges and the [4FE-4S] Cluster Reduction Potential within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe108
b:20.8
occ:1.00
|
FE4
|
A:F3S108
|
0.0
|
20.8
|
1.0
|
S3
|
A:F3S108
|
2.2
|
14.9
|
1.0
|
S2
|
A:F3S108
|
2.3
|
16.1
|
1.0
|
S4
|
A:F3S108
|
2.3
|
16.3
|
1.0
|
SG
|
A:CYS49
|
2.3
|
14.1
|
1.0
|
FE1
|
A:F3S108
|
2.5
|
21.1
|
1.0
|
FE3
|
A:F3S108
|
2.6
|
17.2
|
1.0
|
CB
|
A:CYS49
|
3.4
|
15.2
|
1.0
|
CA
|
A:CYS49
|
3.8
|
17.0
|
1.0
|
S1
|
A:F3S108
|
3.9
|
15.9
|
1.0
|
CD
|
A:PRO50
|
4.4
|
15.7
|
1.0
|
C
|
A:CYS49
|
4.5
|
16.5
|
1.0
|
N
|
A:PRO50
|
4.6
|
16.3
|
1.0
|
SG
|
A:CYS8
|
4.6
|
13.8
|
1.0
|
CB
|
A:ALA51
|
4.6
|
15.5
|
1.0
|
CB
|
A:ALA53
|
4.7
|
13.7
|
1.0
|
SG
|
A:CYS16
|
4.7
|
18.6
|
1.0
|
CD2
|
A:TYR13
|
4.7
|
17.1
|
1.0
|
N
|
A:ALA51
|
4.7
|
17.1
|
1.0
|
CB
|
A:CYS8
|
4.8
|
14.2
|
1.0
|
CB
|
A:TYR13
|
4.8
|
15.2
|
1.0
|
N
|
A:TYR13
|
4.9
|
15.0
|
1.0
|
CD1
|
A:ILE54
|
4.9
|
13.0
|
1.0
|
CG1
|
A:ILE54
|
5.0
|
13.3
|
1.0
|
CB
|
A:CYS16
|
5.0
|
19.5
|
1.0
|
|
Reference:
B.Shen,
D.R.Jollie,
C.D.Stout,
T.C.Diller,
F.A.Armstrong,
C.M.Gorst,
G.N.La Mar,
P.J.Stephens,
B.K.Burgess.
Azotobacter Vinelandii Ferredoxin I. Alteration of Individual Surface Charges and the [4FE-4S]2+/+ Cluster Reduction Potential. J.Biol.Chem. V. 269 8564 1994.
ISSN: ISSN 0021-9258
PubMed: 8132582
Page generated: Sat Aug 3 05:13:51 2024
|