Iron in PDB 1dy7: Cytochrome CD1 Nitrite Reductase, Co Complex
Enzymatic activity of Cytochrome CD1 Nitrite Reductase, Co Complex
All present enzymatic activity of Cytochrome CD1 Nitrite Reductase, Co Complex:
1.7.2.1;
1.7.99.1;
Protein crystallography data
The structure of Cytochrome CD1 Nitrite Reductase, Co Complex, PDB code: 1dy7
was solved by
T.Sjogren,
M.Svensson-Ek,
J.Hajdu,
P.Brzezinski,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
30.00 /
1.60
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
106.940,
61.040,
100.390,
90.00,
111.77,
90.00
|
R / Rfree (%)
|
17.8 /
19.9
|
Iron Binding Sites:
The binding sites of Iron atom in the Cytochrome CD1 Nitrite Reductase, Co Complex
(pdb code 1dy7). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 3 binding sites of Iron where determined in the
Cytochrome CD1 Nitrite Reductase, Co Complex, PDB code: 1dy7:
Jump to Iron binding site number:
1;
2;
3;
Iron binding site 1 out
of 3 in 1dy7
Go back to
Iron Binding Sites List in 1dy7
Iron binding site 1 out
of 3 in the Cytochrome CD1 Nitrite Reductase, Co Complex
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Cytochrome CD1 Nitrite Reductase, Co Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe602
b:11.7
occ:1.00
|
FE
|
A:DHE602
|
0.0
|
11.7
|
1.0
|
NE2
|
A:HIS200
|
2.0
|
12.5
|
1.0
|
NB
|
A:DHE602
|
2.0
|
12.2
|
1.0
|
ND
|
A:DHE602
|
2.0
|
11.5
|
1.0
|
NC
|
A:DHE602
|
2.0
|
11.6
|
1.0
|
C
|
A:CMO603
|
2.0
|
17.3
|
1.0
|
NA
|
A:DHE602
|
2.0
|
10.7
|
1.0
|
CE1
|
A:HIS200
|
3.0
|
12.0
|
1.0
|
C1C
|
A:DHE602
|
3.0
|
13.9
|
1.0
|
C1B
|
A:DHE602
|
3.0
|
12.9
|
1.0
|
CD2
|
A:HIS200
|
3.0
|
11.3
|
1.0
|
O
|
A:CMO603
|
3.0
|
20.4
|
1.0
|
C1D
|
A:DHE602
|
3.0
|
11.1
|
1.0
|
C4B
|
A:DHE602
|
3.0
|
14.0
|
1.0
|
C4D
|
A:DHE602
|
3.0
|
11.5
|
1.0
|
C1A
|
A:DHE602
|
3.0
|
11.0
|
1.0
|
C4C
|
A:DHE602
|
3.0
|
12.1
|
1.0
|
C4A
|
A:DHE602
|
3.0
|
11.1
|
1.0
|
CHB
|
A:DHE602
|
3.4
|
13.0
|
1.0
|
CHC
|
A:DHE602
|
3.4
|
14.1
|
1.0
|
CHA
|
A:DHE602
|
3.4
|
11.1
|
1.0
|
CHD
|
A:DHE602
|
3.4
|
12.0
|
1.0
|
ND1
|
A:HIS200
|
4.1
|
11.2
|
1.0
|
CG
|
A:HIS200
|
4.1
|
12.0
|
1.0
|
C3B
|
A:DHE602
|
4.2
|
14.8
|
1.0
|
C2B
|
A:DHE602
|
4.2
|
15.7
|
1.0
|
C2C
|
A:DHE602
|
4.2
|
14.6
|
1.0
|
C3D
|
A:DHE602
|
4.2
|
11.1
|
1.0
|
C2D
|
A:DHE602
|
4.2
|
10.6
|
1.0
|
C2A
|
A:DHE602
|
4.2
|
11.6
|
1.0
|
C3A
|
A:DHE602
|
4.3
|
11.3
|
1.0
|
C3C
|
A:DHE602
|
4.3
|
12.8
|
1.0
|
O
|
A:HOH2252
|
4.4
|
22.1
|
1.0
|
O2C
|
A:DHE602
|
4.9
|
16.6
|
1.0
|
O2B
|
A:DHE602
|
4.9
|
19.1
|
1.0
|
|
Iron binding site 2 out
of 3 in 1dy7
Go back to
Iron Binding Sites List in 1dy7
Iron binding site 2 out
of 3 in the Cytochrome CD1 Nitrite Reductase, Co Complex
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Cytochrome CD1 Nitrite Reductase, Co Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe601
b:19.7
occ:1.00
|
FE
|
B:HEC601
|
0.0
|
19.7
|
1.0
|
NB
|
B:HEC601
|
2.0
|
18.3
|
1.0
|
NC
|
B:HEC601
|
2.0
|
20.8
|
1.0
|
NA
|
B:HEC601
|
2.0
|
20.5
|
1.0
|
ND
|
B:HEC601
|
2.0
|
21.5
|
1.0
|
NE2
|
B:HIS69
|
2.1
|
18.5
|
1.0
|
SD
|
B:MET106
|
2.3
|
19.2
|
1.0
|
CE1
|
B:HIS69
|
2.9
|
19.3
|
1.0
|
C1D
|
B:HEC601
|
3.0
|
23.1
|
1.0
|
C1B
|
B:HEC601
|
3.0
|
17.6
|
1.0
|
C4B
|
B:HEC601
|
3.0
|
17.6
|
1.0
|
C4A
|
B:HEC601
|
3.0
|
19.1
|
1.0
|
C4D
|
B:HEC601
|
3.0
|
23.2
|
1.0
|
C1C
|
B:HEC601
|
3.0
|
19.9
|
1.0
|
C4C
|
B:HEC601
|
3.1
|
22.0
|
1.0
|
C1A
|
B:HEC601
|
3.1
|
20.2
|
1.0
|
CD2
|
B:HIS69
|
3.2
|
18.4
|
1.0
|
CHD
|
B:HEC601
|
3.4
|
22.4
|
1.0
|
CHB
|
B:HEC601
|
3.4
|
16.7
|
1.0
|
CE
|
B:MET106
|
3.4
|
20.0
|
1.0
|
CHA
|
B:HEC601
|
3.4
|
22.1
|
1.0
|
CHC
|
B:HEC601
|
3.4
|
19.6
|
1.0
|
CG
|
B:MET106
|
3.5
|
22.6
|
1.0
|
CB
|
B:MET106
|
4.1
|
24.7
|
1.0
|
ND1
|
B:HIS69
|
4.1
|
18.3
|
1.0
|
CG
|
B:HIS69
|
4.2
|
18.6
|
1.0
|
C3B
|
B:HEC601
|
4.2
|
17.9
|
1.0
|
C2B
|
B:HEC601
|
4.2
|
17.8
|
1.0
|
C2D
|
B:HEC601
|
4.3
|
24.4
|
1.0
|
C3C
|
B:HEC601
|
4.3
|
21.6
|
1.0
|
C3A
|
B:HEC601
|
4.3
|
19.5
|
1.0
|
C3D
|
B:HEC601
|
4.3
|
25.2
|
1.0
|
C2A
|
B:HEC601
|
4.3
|
20.5
|
1.0
|
C2C
|
B:HEC601
|
4.3
|
21.4
|
1.0
|
CA
|
B:MET106
|
4.6
|
26.4
|
1.0
|
CD
|
B:PRO107
|
5.0
|
22.9
|
1.0
|
|
Iron binding site 3 out
of 3 in 1dy7
Go back to
Iron Binding Sites List in 1dy7
Iron binding site 3 out
of 3 in the Cytochrome CD1 Nitrite Reductase, Co Complex
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Cytochrome CD1 Nitrite Reductase, Co Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe602
b:12.2
occ:1.00
|
FE
|
B:DHE602
|
0.0
|
12.2
|
1.0
|
C
|
B:CMO603
|
1.9
|
14.1
|
1.0
|
NC
|
B:DHE602
|
2.0
|
12.2
|
1.0
|
ND
|
B:DHE602
|
2.0
|
11.7
|
1.0
|
NB
|
B:DHE602
|
2.0
|
12.6
|
1.0
|
NA
|
B:DHE602
|
2.0
|
11.4
|
1.0
|
NE2
|
B:HIS200
|
2.1
|
11.9
|
1.0
|
O
|
B:CMO603
|
3.0
|
19.3
|
1.0
|
C1C
|
B:DHE602
|
3.0
|
14.3
|
1.0
|
C4B
|
B:DHE602
|
3.0
|
14.0
|
1.0
|
C4D
|
B:DHE602
|
3.0
|
11.6
|
1.0
|
C1D
|
B:DHE602
|
3.0
|
11.6
|
1.0
|
C1B
|
B:DHE602
|
3.0
|
13.6
|
1.0
|
C1A
|
B:DHE602
|
3.0
|
12.6
|
1.0
|
C4C
|
B:DHE602
|
3.0
|
13.6
|
1.0
|
C4A
|
B:DHE602
|
3.0
|
12.1
|
1.0
|
CE1
|
B:HIS200
|
3.1
|
12.2
|
1.0
|
CD2
|
B:HIS200
|
3.1
|
11.4
|
1.0
|
CHC
|
B:DHE602
|
3.4
|
14.5
|
1.0
|
CHB
|
B:DHE602
|
3.4
|
12.5
|
1.0
|
CHA
|
B:DHE602
|
3.4
|
12.2
|
1.0
|
CHD
|
B:DHE602
|
3.4
|
12.9
|
1.0
|
ND1
|
B:HIS200
|
4.2
|
12.2
|
1.0
|
C2C
|
B:DHE602
|
4.2
|
15.0
|
1.0
|
C3D
|
B:DHE602
|
4.2
|
11.7
|
1.0
|
CG
|
B:HIS200
|
4.2
|
11.2
|
1.0
|
C3B
|
B:DHE602
|
4.2
|
14.2
|
1.0
|
C2D
|
B:DHE602
|
4.2
|
11.6
|
1.0
|
C2B
|
B:DHE602
|
4.2
|
15.0
|
1.0
|
C2A
|
B:DHE602
|
4.3
|
12.1
|
1.0
|
C3C
|
B:DHE602
|
4.3
|
13.8
|
1.0
|
C3A
|
B:DHE602
|
4.3
|
12.3
|
1.0
|
O
|
B:HOH2287
|
4.4
|
21.9
|
1.0
|
O2B
|
B:DHE602
|
4.9
|
18.4
|
1.0
|
O2C
|
B:DHE602
|
4.9
|
17.1
|
1.0
|
|
Reference:
T.Sjogren,
M.Svensson-Ek,
J.Hajdu,
P.Brzezinski.
Proton-Coupled Structural Changes Upon Binding of Carbon Monoxide to Cytochrome Cd(1): A Combined Flash Photolysis and X-Ray Crystallography Study Biochemistry V. 39 10967 2000.
ISSN: ISSN 0006-2960
PubMed: 10998233
DOI: 10.1021/BI000179Q
Page generated: Sat Aug 3 04:07:38 2024
|