Iron in PDB 1h32: Reduced Soxax Complex From Rhodovulum Sulfidophilum
Protein crystallography data
The structure of Reduced Soxax Complex From Rhodovulum Sulfidophilum, PDB code: 1h32
was solved by
V.A.Bamford,
S.Bruno,
T.Rasmussen,
C.Appia-Ayme,
M.R.Cheesman,
B.C.Berks,
A.M.Hemmings,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
25.0 /
1.5
|
Space group
|
P 21 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
65.795,
87.186,
71.459,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
19.9 /
23.5
|
Iron Binding Sites:
The binding sites of Iron atom in the Reduced Soxax Complex From Rhodovulum Sulfidophilum
(pdb code 1h32). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 3 binding sites of Iron where determined in the
Reduced Soxax Complex From Rhodovulum Sulfidophilum, PDB code: 1h32:
Jump to Iron binding site number:
1;
2;
3;
Iron binding site 1 out
of 3 in 1h32
Go back to
Iron Binding Sites List in 1h32
Iron binding site 1 out
of 3 in the Reduced Soxax Complex From Rhodovulum Sulfidophilum
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Reduced Soxax Complex From Rhodovulum Sulfidophilum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1263
b:10.7
occ:1.00
|
FE
|
A:HEC1263
|
0.0
|
10.7
|
1.0
|
NB
|
A:HEC1263
|
2.0
|
11.1
|
1.0
|
NC
|
A:HEC1263
|
2.0
|
11.3
|
1.0
|
ND
|
A:HEC1263
|
2.0
|
11.6
|
1.0
|
NA
|
A:HEC1263
|
2.0
|
9.6
|
1.0
|
NE2
|
A:HIS80
|
2.1
|
9.1
|
1.0
|
SG
|
A:CYS114
|
2.3
|
12.3
|
1.0
|
CE1
|
A:HIS80
|
3.0
|
8.5
|
1.0
|
C4D
|
A:HEC1263
|
3.0
|
8.8
|
1.0
|
C1A
|
A:HEC1263
|
3.0
|
8.7
|
1.0
|
C1B
|
A:HEC1263
|
3.0
|
10.6
|
1.0
|
C1D
|
A:HEC1263
|
3.1
|
12.5
|
1.0
|
C4A
|
A:HEC1263
|
3.1
|
10.7
|
1.0
|
C4B
|
A:HEC1263
|
3.1
|
11.2
|
1.0
|
C1C
|
A:HEC1263
|
3.1
|
12.3
|
1.0
|
C4C
|
A:HEC1263
|
3.1
|
11.6
|
1.0
|
CD2
|
A:HIS80
|
3.1
|
11.5
|
1.0
|
CHA
|
A:HEC1263
|
3.4
|
11.2
|
1.0
|
CHB
|
A:HEC1263
|
3.4
|
9.5
|
1.0
|
CHD
|
A:HEC1263
|
3.4
|
11.4
|
1.0
|
CB
|
A:CYS114
|
3.4
|
12.3
|
1.0
|
CHC
|
A:HEC1263
|
3.4
|
9.7
|
1.0
|
O
|
A:HOH2262
|
3.7
|
0.3
|
1.0
|
ND1
|
A:HIS80
|
4.2
|
8.7
|
1.0
|
CG
|
A:HIS80
|
4.2
|
9.6
|
1.0
|
C2A
|
A:HEC1263
|
4.3
|
11.1
|
1.0
|
C3C
|
A:HEC1263
|
4.3
|
15.0
|
1.0
|
C3D
|
A:HEC1263
|
4.3
|
13.9
|
1.0
|
C3A
|
A:HEC1263
|
4.3
|
10.5
|
1.0
|
C2B
|
A:HEC1263
|
4.3
|
9.0
|
1.0
|
C2C
|
A:HEC1263
|
4.3
|
11.9
|
1.0
|
C2D
|
A:HEC1263
|
4.3
|
12.2
|
1.0
|
C3B
|
A:HEC1263
|
4.3
|
10.5
|
1.0
|
O
|
A:HOH2263
|
4.7
|
12.9
|
1.0
|
CA
|
A:CYS114
|
4.8
|
10.8
|
1.0
|
|
Iron binding site 2 out
of 3 in 1h32
Go back to
Iron Binding Sites List in 1h32
Iron binding site 2 out
of 3 in the Reduced Soxax Complex From Rhodovulum Sulfidophilum
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Reduced Soxax Complex From Rhodovulum Sulfidophilum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1264
b:6.7
occ:1.00
|
FE
|
A:HEC1264
|
0.0
|
6.7
|
1.0
|
NC
|
A:HEC1264
|
2.0
|
5.0
|
1.0
|
ND
|
A:HEC1264
|
2.0
|
7.1
|
1.0
|
NB
|
A:HEC1264
|
2.0
|
7.0
|
1.0
|
NA
|
A:HEC1264
|
2.0
|
6.5
|
1.0
|
NE2
|
A:HIS181
|
2.1
|
7.5
|
1.0
|
SD
|
A:CSS222
|
2.3
|
8.1
|
1.0
|
CE1
|
A:HIS181
|
3.0
|
5.6
|
1.0
|
C4C
|
A:HEC1264
|
3.0
|
6.5
|
1.0
|
C1D
|
A:HEC1264
|
3.0
|
6.1
|
1.0
|
C1C
|
A:HEC1264
|
3.0
|
7.6
|
1.0
|
C4D
|
A:HEC1264
|
3.0
|
5.4
|
1.0
|
C4A
|
A:HEC1264
|
3.0
|
5.7
|
1.0
|
C1B
|
A:HEC1264
|
3.0
|
6.3
|
1.0
|
C1A
|
A:HEC1264
|
3.1
|
4.7
|
1.0
|
C4B
|
A:HEC1264
|
3.1
|
7.3
|
1.0
|
CD2
|
A:HIS181
|
3.1
|
7.2
|
1.0
|
CHD
|
A:HEC1264
|
3.4
|
7.2
|
1.0
|
CHB
|
A:HEC1264
|
3.4
|
6.3
|
1.0
|
CHA
|
A:HEC1264
|
3.4
|
5.5
|
1.0
|
CHC
|
A:HEC1264
|
3.4
|
8.9
|
1.0
|
SG
|
A:CSS222
|
3.6
|
8.7
|
1.0
|
ND1
|
A:HIS181
|
4.2
|
7.5
|
1.0
|
CG
|
A:HIS181
|
4.2
|
6.3
|
1.0
|
C3C
|
A:HEC1264
|
4.2
|
6.7
|
1.0
|
C2C
|
A:HEC1264
|
4.3
|
7.8
|
1.0
|
C3D
|
A:HEC1264
|
4.3
|
6.9
|
1.0
|
C2D
|
A:HEC1264
|
4.3
|
6.1
|
1.0
|
C3A
|
A:HEC1264
|
4.3
|
5.9
|
1.0
|
C2A
|
A:HEC1264
|
4.3
|
5.2
|
1.0
|
C2B
|
A:HEC1264
|
4.3
|
6.1
|
1.0
|
C3B
|
A:HEC1264
|
4.3
|
6.1
|
1.0
|
CB
|
A:CSS222
|
4.5
|
7.8
|
1.0
|
O
|
A:HOH2208
|
4.5
|
16.6
|
1.0
|
|
Iron binding site 3 out
of 3 in 1h32
Go back to
Iron Binding Sites List in 1h32
Iron binding site 3 out
of 3 in the Reduced Soxax Complex From Rhodovulum Sulfidophilum
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Reduced Soxax Complex From Rhodovulum Sulfidophilum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1139
b:13.9
occ:1.00
|
FE
|
B:HEC1139
|
0.0
|
13.9
|
1.0
|
NB
|
B:HEC1139
|
2.0
|
16.2
|
1.0
|
ND
|
B:HEC1139
|
2.0
|
18.1
|
1.0
|
NC
|
B:HEC1139
|
2.0
|
9.6
|
1.0
|
NA
|
B:HEC1139
|
2.0
|
12.1
|
1.0
|
NE2
|
B:HIS46
|
2.0
|
14.3
|
1.0
|
SD
|
B:MET92
|
2.4
|
14.6
|
1.0
|
CE1
|
B:HIS46
|
3.0
|
12.3
|
1.0
|
C1D
|
B:HEC1139
|
3.0
|
14.1
|
1.0
|
C1B
|
B:HEC1139
|
3.0
|
13.6
|
1.0
|
C4C
|
B:HEC1139
|
3.0
|
12.7
|
1.0
|
C4D
|
B:HEC1139
|
3.0
|
16.1
|
1.0
|
CD2
|
B:HIS46
|
3.0
|
13.3
|
1.0
|
C1C
|
B:HEC1139
|
3.0
|
15.8
|
1.0
|
C4B
|
B:HEC1139
|
3.0
|
10.3
|
1.0
|
C4A
|
B:HEC1139
|
3.1
|
23.2
|
1.0
|
C1A
|
B:HEC1139
|
3.1
|
17.5
|
1.0
|
CE
|
B:MET92
|
3.2
|
9.7
|
1.0
|
CG
|
B:MET92
|
3.3
|
13.5
|
1.0
|
CHD
|
B:HEC1139
|
3.4
|
13.6
|
1.0
|
CHB
|
B:HEC1139
|
3.4
|
13.1
|
1.0
|
CHC
|
B:HEC1139
|
3.4
|
14.4
|
1.0
|
CHA
|
B:HEC1139
|
3.4
|
19.9
|
1.0
|
CB
|
B:MET92
|
4.0
|
13.4
|
1.0
|
ND1
|
B:HIS46
|
4.1
|
13.6
|
1.0
|
CG
|
B:HIS46
|
4.2
|
12.5
|
1.0
|
C3C
|
B:HEC1139
|
4.3
|
11.4
|
1.0
|
C2B
|
B:HEC1139
|
4.3
|
12.0
|
1.0
|
C3B
|
B:HEC1139
|
4.3
|
14.0
|
1.0
|
C2D
|
B:HEC1139
|
4.3
|
13.5
|
1.0
|
C2C
|
B:HEC1139
|
4.3
|
10.4
|
1.0
|
C2A
|
B:HEC1139
|
4.3
|
21.7
|
1.0
|
C3D
|
B:HEC1139
|
4.3
|
15.4
|
1.0
|
C3A
|
B:HEC1139
|
4.3
|
17.8
|
1.0
|
|
Reference:
V.A.Bamford,
S.Bruno,
T.Rasmussen,
C.Appia-Ayme,
M.R.Cheesman,
B.C.Berks,
A.M.Hemmings.
Structural Basis For the Oxidation of Thiosulfate By A Sulfur Cycle Enzyme Embo J. V. 21 5599 2002.
ISSN: ISSN 0261-4189
PubMed: 12411478
DOI: 10.1093/EMBOJ/CDF566
Page generated: Sat Aug 3 06:53:48 2024
|