Iron in PDB 3b2g: Leptolyngbya Boryana Ferredoxin
Protein crystallography data
The structure of Leptolyngbya Boryana Ferredoxin, PDB code: 3b2g
was solved by
G.Kurisu,
T.Hase,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
27.83 /
1.76
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
108.141,
34.158,
48.604,
90.00,
107.30,
90.00
|
R / Rfree (%)
|
18.3 /
24.8
|
Iron Binding Sites:
The binding sites of Iron atom in the Leptolyngbya Boryana Ferredoxin
(pdb code 3b2g). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the
Leptolyngbya Boryana Ferredoxin, PDB code: 3b2g:
Jump to Iron binding site number:
1;
2;
3;
4;
Iron binding site 1 out
of 4 in 3b2g
Go back to
Iron Binding Sites List in 3b2g
Iron binding site 1 out
of 4 in the Leptolyngbya Boryana Ferredoxin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Leptolyngbya Boryana Ferredoxin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe99
b:2.5
occ:1.00
|
FE1
|
A:FES99
|
0.0
|
2.5
|
1.0
|
S2
|
A:FES99
|
2.2
|
3.1
|
1.0
|
S1
|
A:FES99
|
2.3
|
2.6
|
1.0
|
SG
|
A:CYS46
|
2.3
|
2.9
|
1.0
|
SG
|
A:CYS41
|
2.3
|
2.5
|
1.0
|
FE2
|
A:FES99
|
2.8
|
2.4
|
1.0
|
CB
|
A:CYS46
|
3.4
|
3.0
|
1.0
|
CB
|
A:CYS41
|
3.5
|
2.4
|
1.0
|
N
|
A:CYS41
|
3.6
|
1.9
|
1.0
|
N
|
A:CYS46
|
3.6
|
2.3
|
1.0
|
N
|
A:ARG42
|
3.8
|
1.8
|
1.0
|
CA
|
A:CYS46
|
3.9
|
2.4
|
1.0
|
OG
|
A:SER40
|
4.0
|
4.8
|
1.0
|
CA
|
A:CYS41
|
4.0
|
2.3
|
1.0
|
C
|
A:CYS46
|
4.1
|
2.1
|
1.0
|
O
|
A:CYS46
|
4.3
|
2.1
|
1.0
|
N
|
A:ALA45
|
4.3
|
3.3
|
1.0
|
C
|
A:CYS41
|
4.3
|
2.2
|
1.0
|
SG
|
A:CYS79
|
4.4
|
2.2
|
1.0
|
N
|
A:ALA43
|
4.5
|
2.2
|
1.0
|
N
|
A:GLY44
|
4.5
|
3.0
|
1.0
|
N
|
A:THR48
|
4.6
|
0.9
|
1.0
|
C
|
A:ALA45
|
4.6
|
3.5
|
1.0
|
SG
|
A:CYS49
|
4.6
|
0.6
|
1.0
|
N
|
A:SER47
|
4.7
|
1.5
|
1.0
|
CA
|
A:ARG42
|
4.7
|
1.8
|
1.0
|
C
|
A:SER40
|
4.7
|
1.9
|
1.0
|
N
|
A:SER40
|
4.8
|
1.3
|
1.0
|
CB
|
A:THR48
|
4.8
|
1.1
|
1.0
|
CA
|
A:GLY44
|
4.9
|
2.8
|
1.0
|
C
|
A:GLY44
|
5.0
|
3.1
|
1.0
|
|
Iron binding site 2 out
of 4 in 3b2g
Go back to
Iron Binding Sites List in 3b2g
Iron binding site 2 out
of 4 in the Leptolyngbya Boryana Ferredoxin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Leptolyngbya Boryana Ferredoxin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe99
b:2.4
occ:1.00
|
FE2
|
A:FES99
|
0.0
|
2.4
|
1.0
|
S2
|
A:FES99
|
2.2
|
3.1
|
1.0
|
S1
|
A:FES99
|
2.2
|
2.6
|
1.0
|
SG
|
A:CYS79
|
2.3
|
2.2
|
1.0
|
SG
|
A:CYS49
|
2.3
|
0.6
|
1.0
|
FE1
|
A:FES99
|
2.8
|
2.5
|
1.0
|
CB
|
A:CYS79
|
3.2
|
1.1
|
1.0
|
CB
|
A:CYS49
|
3.4
|
0.4
|
1.0
|
N
|
A:CYS79
|
4.2
|
0.7
|
1.0
|
N
|
A:CYS49
|
4.3
|
0.5
|
1.0
|
N
|
A:GLY44
|
4.3
|
3.0
|
1.0
|
CA
|
A:CYS79
|
4.3
|
0.9
|
1.0
|
N
|
A:ARG42
|
4.4
|
1.8
|
1.0
|
CA
|
A:ARG42
|
4.4
|
1.8
|
1.0
|
CA
|
A:CYS49
|
4.4
|
0.4
|
1.0
|
SG
|
A:CYS41
|
4.4
|
2.5
|
1.0
|
CA
|
A:GLY44
|
4.6
|
2.8
|
1.0
|
CB
|
A:LEU77
|
4.6
|
0.8
|
1.0
|
N
|
A:ALA43
|
4.7
|
2.2
|
1.0
|
SG
|
A:CYS46
|
4.7
|
2.9
|
1.0
|
C
|
A:ARG42
|
4.8
|
2.0
|
1.0
|
O
|
A:CYS46
|
5.0
|
2.1
|
1.0
|
|
Iron binding site 3 out
of 4 in 3b2g
Go back to
Iron Binding Sites List in 3b2g
Iron binding site 3 out
of 4 in the Leptolyngbya Boryana Ferredoxin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Leptolyngbya Boryana Ferredoxin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe99
b:2.0
occ:1.00
|
FE1
|
B:FES99
|
0.0
|
2.0
|
1.0
|
S2
|
B:FES99
|
2.2
|
2.7
|
1.0
|
S1
|
B:FES99
|
2.2
|
2.2
|
1.0
|
SG
|
B:CYS46
|
2.3
|
1.6
|
1.0
|
SG
|
B:CYS41
|
2.4
|
1.6
|
1.0
|
FE2
|
B:FES99
|
2.8
|
2.4
|
1.0
|
CB
|
B:CYS46
|
3.4
|
1.9
|
1.0
|
CB
|
B:CYS41
|
3.5
|
2.0
|
1.0
|
N
|
B:CYS41
|
3.5
|
1.6
|
1.0
|
N
|
B:CYS46
|
3.6
|
1.8
|
1.0
|
N
|
B:ARG42
|
3.7
|
1.3
|
1.0
|
CA
|
B:CYS46
|
3.8
|
1.9
|
1.0
|
CA
|
B:CYS41
|
3.9
|
1.8
|
1.0
|
C
|
B:CYS46
|
4.0
|
1.6
|
1.0
|
OG
|
B:SER40
|
4.1
|
6.2
|
1.0
|
C
|
B:CYS41
|
4.2
|
1.7
|
1.0
|
O
|
B:CYS46
|
4.3
|
1.4
|
1.0
|
N
|
B:ALA45
|
4.3
|
1.7
|
1.0
|
SG
|
B:CYS79
|
4.4
|
0.6
|
1.0
|
N
|
B:ALA43
|
4.4
|
1.4
|
1.0
|
N
|
B:GLY44
|
4.5
|
1.4
|
1.0
|
C
|
B:ALA45
|
4.5
|
2.1
|
1.0
|
N
|
B:THR48
|
4.6
|
1.3
|
1.0
|
CA
|
B:ARG42
|
4.6
|
1.2
|
1.0
|
N
|
B:SER47
|
4.6
|
1.7
|
1.0
|
SG
|
B:CYS49
|
4.7
|
1.6
|
1.0
|
C
|
B:SER40
|
4.7
|
1.7
|
1.0
|
N
|
B:SER40
|
4.7
|
1.3
|
1.0
|
CB
|
B:THR48
|
4.8
|
1.4
|
1.0
|
N
|
B:CYS49
|
4.9
|
0.9
|
1.0
|
CA
|
B:GLY44
|
4.9
|
1.4
|
1.0
|
C
|
B:GLY44
|
5.0
|
2.1
|
1.0
|
CA
|
B:ALA45
|
5.0
|
2.1
|
1.0
|
|
Iron binding site 4 out
of 4 in 3b2g
Go back to
Iron Binding Sites List in 3b2g
Iron binding site 4 out
of 4 in the Leptolyngbya Boryana Ferredoxin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Leptolyngbya Boryana Ferredoxin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe99
b:2.4
occ:1.00
|
FE2
|
B:FES99
|
0.0
|
2.4
|
1.0
|
S2
|
B:FES99
|
2.2
|
2.7
|
1.0
|
S1
|
B:FES99
|
2.2
|
2.2
|
1.0
|
SG
|
B:CYS79
|
2.3
|
0.6
|
1.0
|
SG
|
B:CYS49
|
2.4
|
1.6
|
1.0
|
FE1
|
B:FES99
|
2.8
|
2.0
|
1.0
|
CB
|
B:CYS79
|
3.3
|
0.4
|
1.0
|
CB
|
B:CYS49
|
3.4
|
1.6
|
1.0
|
O
|
B:CYS49
|
3.9
|
8.3
|
1.0
|
N
|
B:CYS79
|
4.2
|
0.5
|
1.0
|
N
|
B:CYS49
|
4.2
|
0.9
|
1.0
|
N
|
B:GLY44
|
4.3
|
1.4
|
1.0
|
CA
|
B:CYS79
|
4.3
|
0.3
|
1.0
|
N
|
B:ARG42
|
4.3
|
1.3
|
1.0
|
CA
|
B:CYS49
|
4.3
|
2.5
|
1.0
|
CA
|
B:ARG42
|
4.4
|
1.2
|
1.0
|
SG
|
B:CYS41
|
4.5
|
1.6
|
1.0
|
CA
|
B:GLY44
|
4.5
|
1.4
|
1.0
|
C
|
B:CYS49
|
4.6
|
4.2
|
1.0
|
CB
|
B:LEU77
|
4.6
|
0.6
|
1.0
|
SG
|
B:CYS46
|
4.7
|
1.6
|
1.0
|
N
|
B:ALA43
|
4.7
|
1.4
|
1.0
|
C
|
B:ARG42
|
4.8
|
1.3
|
1.0
|
O
|
B:CYS46
|
5.0
|
1.4
|
1.0
|
|
Reference:
Y.Sakakibara,
H.Kimura,
A.Iwamura,
T.Saitoh,
T.Ikegami,
G.Kurisu,
T.Hase.
A New Structural Insight Into Differential Interaction of Cyanobacterial and Plant Ferredoxins with Nitrite Reductase As Revealed By uc(Nmr) and X-Ray Crystallographic Studies J.Biochem. V. 151 483 2012.
ISSN: ISSN 0021-924X
PubMed: 22427434
DOI: 10.1093/JB/MVS028
Page generated: Sun Aug 4 07:35:10 2024
|