Copper in PDB 1aq8: Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
Enzymatic activity of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
All present enzymatic activity of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate:
1.7.99.3;
Protein crystallography data
The structure of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate, PDB code: 1aq8
was solved by
M.E.P.Murphy,
E.T.Adman,
S.Turley,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
10.00 /
2.00
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
61.790,
102.400,
146.200,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
18.9 /
n/a
|
Copper Binding Sites:
The binding sites of Copper atom in the Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
(pdb code 1aq8). This binding sites where shown within
5.0 Angstroms radius around Copper atom.
In total 6 binding sites of Copper where determined in the
Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate, PDB code: 1aq8:
Jump to Copper binding site number:
1;
2;
3;
4;
5;
6;
Copper binding site 1 out
of 6 in 1aq8
Go back to
Copper Binding Sites List in 1aq8
Copper binding site 1 out
of 6 in the Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 1 of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu501
b:17.8
occ:1.00
|
ND1
|
A:HIS95
|
2.0
|
11.6
|
1.0
|
ND1
|
A:HIS145
|
2.1
|
11.9
|
1.0
|
SG
|
A:CYS136
|
2.1
|
15.1
|
1.0
|
SD
|
A:MET150
|
2.6
|
18.0
|
1.0
|
CE1
|
A:HIS95
|
3.0
|
7.0
|
1.0
|
CE1
|
A:HIS145
|
3.1
|
11.7
|
1.0
|
CB
|
A:CYS136
|
3.1
|
11.6
|
1.0
|
CG
|
A:HIS95
|
3.1
|
7.2
|
1.0
|
CG
|
A:HIS145
|
3.2
|
13.3
|
1.0
|
CE
|
A:MET150
|
3.5
|
11.4
|
1.0
|
CB
|
A:HIS145
|
3.5
|
10.6
|
1.0
|
CB
|
A:HIS95
|
3.5
|
10.0
|
1.0
|
CG
|
A:MET150
|
3.8
|
13.1
|
1.0
|
CA
|
A:HIS95
|
4.0
|
10.8
|
1.0
|
H
|
A:ASN96
|
4.1
|
0.0
|
1.0
|
NE2
|
A:HIS95
|
4.1
|
3.2
|
1.0
|
CG
|
A:PRO138
|
4.2
|
14.8
|
1.0
|
CD2
|
A:HIS95
|
4.2
|
10.7
|
1.0
|
NE2
|
A:HIS145
|
4.2
|
10.8
|
1.0
|
CD2
|
A:HIS145
|
4.3
|
10.7
|
1.0
|
O
|
A:MET94
|
4.3
|
5.7
|
1.0
|
SD
|
A:MET62
|
4.3
|
16.2
|
1.0
|
CB
|
A:MET150
|
4.4
|
8.6
|
1.0
|
CD
|
A:PRO138
|
4.4
|
16.6
|
1.0
|
CA
|
A:CYS136
|
4.5
|
14.0
|
1.0
|
CA
|
A:HIS145
|
4.7
|
12.2
|
1.0
|
CB
|
A:MET62
|
4.7
|
13.9
|
1.0
|
N
|
A:ASN96
|
4.9
|
14.0
|
1.0
|
N
|
A:HIS95
|
5.0
|
12.8
|
1.0
|
HE2
|
A:HIS95
|
5.0
|
0.0
|
1.0
|
|
Copper binding site 2 out
of 6 in 1aq8
Go back to
Copper Binding Sites List in 1aq8
Copper binding site 2 out
of 6 in the Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 2 of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu502
b:16.9
occ:1.00
|
NE2
|
A:HIS100
|
1.9
|
13.8
|
1.0
|
NE2
|
A:HIS135
|
1.9
|
12.2
|
1.0
|
NE2
|
B:HIS306
|
2.0
|
16.7
|
1.0
|
CE1
|
A:HIS100
|
2.7
|
15.2
|
1.0
|
CE1
|
B:HIS306
|
2.8
|
10.9
|
1.0
|
CE1
|
A:HIS135
|
2.9
|
9.3
|
1.0
|
CD2
|
A:HIS135
|
3.0
|
14.6
|
1.0
|
CD2
|
A:HIS100
|
3.1
|
11.3
|
1.0
|
CD2
|
B:HIS306
|
3.3
|
12.6
|
1.0
|
OD1
|
A:ASP98
|
3.6
|
24.6
|
1.0
|
ND1
|
A:HIS100
|
4.0
|
11.9
|
1.0
|
ND1
|
B:HIS306
|
4.0
|
18.7
|
1.0
|
HE2
|
B:HIS255
|
4.1
|
0.0
|
1.0
|
ND1
|
A:HIS135
|
4.1
|
16.6
|
1.0
|
CG
|
A:HIS135
|
4.1
|
9.9
|
1.0
|
NE2
|
B:HIS255
|
4.1
|
8.8
|
1.0
|
CG
|
A:HIS100
|
4.2
|
16.2
|
1.0
|
CG
|
B:HIS306
|
4.3
|
14.0
|
1.0
|
CG
|
A:ASP98
|
4.3
|
19.0
|
1.0
|
CE1
|
B:HIS255
|
4.5
|
12.0
|
1.0
|
CD2
|
B:HIS255
|
4.5
|
10.8
|
1.0
|
H1
|
B:HOH2104
|
4.7
|
0.0
|
1.0
|
HD1
|
A:HIS100
|
4.8
|
0.0
|
1.0
|
HD1
|
B:HIS306
|
4.8
|
0.0
|
1.0
|
OD2
|
A:ASP98
|
4.9
|
18.0
|
1.0
|
HD1
|
A:HIS135
|
5.0
|
0.0
|
1.0
|
CG1
|
B:ILE257
|
5.0
|
23.7
|
1.0
|
ND1
|
B:HIS255
|
5.0
|
13.3
|
1.0
|
CD2
|
B:LEU308
|
5.0
|
8.8
|
1.0
|
|
Copper binding site 3 out
of 6 in 1aq8
Go back to
Copper Binding Sites List in 1aq8
Copper binding site 3 out
of 6 in the Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 3 of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu501
b:22.2
occ:1.00
|
ND1
|
B:HIS95
|
2.1
|
20.6
|
1.0
|
ND1
|
B:HIS145
|
2.1
|
17.4
|
1.0
|
SG
|
B:CYS136
|
2.2
|
18.2
|
1.0
|
SD
|
B:MET150
|
2.6
|
17.8
|
1.0
|
CE1
|
B:HIS145
|
2.9
|
20.8
|
1.0
|
CG
|
B:HIS95
|
3.1
|
24.2
|
1.0
|
CE1
|
B:HIS95
|
3.1
|
22.0
|
1.0
|
CB
|
B:CYS136
|
3.1
|
16.3
|
1.0
|
CG
|
B:HIS145
|
3.3
|
17.7
|
1.0
|
CE
|
B:MET150
|
3.3
|
21.1
|
1.0
|
CB
|
B:HIS95
|
3.4
|
24.0
|
1.0
|
CB
|
B:HIS145
|
3.7
|
17.5
|
1.0
|
CA
|
B:HIS95
|
3.9
|
22.1
|
1.0
|
H
|
B:ASN96
|
4.0
|
0.0
|
1.0
|
CG
|
B:MET150
|
4.0
|
13.8
|
1.0
|
CG
|
B:PRO138
|
4.0
|
21.7
|
1.0
|
NE2
|
B:HIS145
|
4.1
|
17.1
|
1.0
|
NE2
|
B:HIS95
|
4.2
|
24.2
|
1.0
|
CD2
|
B:HIS95
|
4.2
|
19.3
|
1.0
|
O
|
B:MET94
|
4.3
|
20.9
|
1.0
|
CD2
|
B:HIS145
|
4.3
|
21.3
|
1.0
|
SD
|
B:MET62
|
4.3
|
16.9
|
1.0
|
CD
|
B:PRO138
|
4.4
|
19.6
|
1.0
|
CB
|
B:MET150
|
4.5
|
10.3
|
1.0
|
CA
|
B:CYS136
|
4.5
|
17.4
|
1.0
|
N
|
B:ASN96
|
4.7
|
21.8
|
1.0
|
CB
|
B:MET62
|
4.8
|
19.0
|
1.0
|
N
|
B:HIS95
|
4.8
|
22.8
|
1.0
|
C
|
B:HIS95
|
4.9
|
23.1
|
1.0
|
C
|
B:MET94
|
4.9
|
23.1
|
1.0
|
CA
|
B:HIS145
|
4.9
|
19.3
|
1.0
|
HE2
|
B:HIS145
|
5.0
|
0.0
|
1.0
|
O
|
B:ASN96
|
5.0
|
21.8
|
1.0
|
|
Copper binding site 4 out
of 6 in 1aq8
Go back to
Copper Binding Sites List in 1aq8
Copper binding site 4 out
of 6 in the Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 4 of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu502
b:19.4
occ:1.00
|
NE2
|
B:HIS100
|
2.0
|
11.1
|
1.0
|
NE2
|
B:HIS135
|
2.0
|
15.6
|
1.0
|
NE2
|
C:HIS306
|
2.1
|
12.2
|
1.0
|
CE1
|
C:HIS306
|
2.8
|
13.8
|
1.0
|
CE1
|
B:HIS100
|
2.8
|
11.9
|
1.0
|
CE1
|
B:HIS135
|
3.0
|
17.4
|
1.0
|
CD2
|
B:HIS135
|
3.0
|
15.0
|
1.0
|
CD2
|
B:HIS100
|
3.2
|
15.6
|
1.0
|
CD2
|
C:HIS306
|
3.3
|
15.7
|
1.0
|
OD1
|
B:ASP98
|
3.5
|
26.8
|
1.0
|
CD1
|
C:ILE257
|
3.8
|
24.4
|
1.0
|
H1
|
B:HOH1918
|
3.8
|
0.0
|
1.0
|
HE2
|
C:HIS255
|
4.0
|
0.0
|
1.0
|
ND1
|
B:HIS100
|
4.0
|
12.7
|
1.0
|
ND1
|
C:HIS306
|
4.1
|
14.0
|
1.0
|
NE2
|
C:HIS255
|
4.1
|
24.9
|
1.0
|
ND1
|
B:HIS135
|
4.1
|
14.0
|
1.0
|
CG
|
B:HIS135
|
4.2
|
16.8
|
1.0
|
CG
|
B:HIS100
|
4.2
|
12.0
|
1.0
|
CG
|
B:ASP98
|
4.3
|
20.6
|
1.0
|
CG
|
C:HIS306
|
4.3
|
14.6
|
1.0
|
CE1
|
C:HIS255
|
4.4
|
24.2
|
1.0
|
CD2
|
C:HIS255
|
4.5
|
21.7
|
1.0
|
H1
|
C:HOH2740
|
4.6
|
0.0
|
1.0
|
O
|
B:HOH1918
|
4.7
|
36.3
|
1.0
|
O
|
C:HOH2740
|
4.7
|
23.9
|
1.0
|
HD1
|
B:HIS100
|
4.8
|
0.0
|
1.0
|
HD1
|
C:HIS306
|
4.9
|
0.0
|
1.0
|
OD2
|
B:ASP98
|
4.9
|
14.0
|
1.0
|
ND1
|
C:HIS255
|
5.0
|
21.8
|
1.0
|
CD2
|
C:LEU308
|
5.0
|
22.3
|
1.0
|
|
Copper binding site 5 out
of 6 in 1aq8
Go back to
Copper Binding Sites List in 1aq8
Copper binding site 5 out
of 6 in the Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 5 of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Cu501
b:23.8
occ:1.00
|
ND1
|
C:HIS145
|
2.0
|
25.0
|
1.0
|
ND1
|
C:HIS95
|
2.1
|
25.0
|
1.0
|
SG
|
C:CYS136
|
2.2
|
21.5
|
1.0
|
SD
|
C:MET150
|
2.6
|
19.6
|
1.0
|
CE1
|
C:HIS145
|
2.9
|
21.3
|
1.0
|
CE1
|
C:HIS95
|
3.0
|
21.3
|
1.0
|
CG
|
C:HIS95
|
3.1
|
19.4
|
1.0
|
CG
|
C:HIS145
|
3.2
|
22.5
|
1.0
|
CB
|
C:CYS136
|
3.2
|
21.2
|
1.0
|
CB
|
C:HIS95
|
3.5
|
14.7
|
1.0
|
CE
|
C:MET150
|
3.6
|
16.3
|
1.0
|
CB
|
C:HIS145
|
3.6
|
19.7
|
1.0
|
CA
|
C:HIS95
|
3.9
|
18.1
|
1.0
|
CG
|
C:MET150
|
4.0
|
17.6
|
1.0
|
H
|
C:ASN96
|
4.0
|
0.0
|
1.0
|
CG
|
C:PRO138
|
4.0
|
16.5
|
1.0
|
NE2
|
C:HIS145
|
4.1
|
21.5
|
1.0
|
SD
|
C:MET62
|
4.2
|
17.4
|
1.0
|
NE2
|
C:HIS95
|
4.2
|
17.9
|
1.0
|
O
|
C:MET94
|
4.2
|
16.6
|
1.0
|
CD2
|
C:HIS95
|
4.2
|
20.7
|
1.0
|
CD2
|
C:HIS145
|
4.3
|
20.5
|
1.0
|
CD
|
C:PRO138
|
4.5
|
15.2
|
1.0
|
CB
|
C:MET150
|
4.5
|
18.1
|
1.0
|
CA
|
C:CYS136
|
4.6
|
20.7
|
1.0
|
CB
|
C:MET62
|
4.7
|
17.6
|
1.0
|
N
|
C:ASN96
|
4.8
|
19.7
|
1.0
|
CA
|
C:HIS145
|
4.8
|
19.5
|
1.0
|
N
|
C:HIS95
|
4.9
|
19.0
|
1.0
|
C
|
C:MET94
|
4.9
|
20.8
|
1.0
|
C
|
C:HIS95
|
4.9
|
17.8
|
1.0
|
HE2
|
C:HIS145
|
5.0
|
0.0
|
1.0
|
|
Copper binding site 6 out
of 6 in 1aq8
Go back to
Copper Binding Sites List in 1aq8
Copper binding site 6 out
of 6 in the Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 6 of Structure of Alcaligenes Faecalis Nitrite Reductase Reduced with Ascorbate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Cu502
b:19.9
occ:1.00
|
NE2
|
C:HIS100
|
1.9
|
11.0
|
1.0
|
NE2
|
A:HIS306
|
2.1
|
15.3
|
1.0
|
NE2
|
C:HIS135
|
2.1
|
18.0
|
1.0
|
CE1
|
C:HIS100
|
2.7
|
14.1
|
1.0
|
CE1
|
A:HIS306
|
2.8
|
11.3
|
1.0
|
CE1
|
C:HIS135
|
3.1
|
16.8
|
1.0
|
CD2
|
C:HIS100
|
3.1
|
15.2
|
1.0
|
CD2
|
C:HIS135
|
3.1
|
21.1
|
1.0
|
CD2
|
A:HIS306
|
3.3
|
15.5
|
1.0
|
CD1
|
A:ILE257
|
3.6
|
25.5
|
1.0
|
OD1
|
C:ASP98
|
3.7
|
26.0
|
1.0
|
HE2
|
A:HIS255
|
3.9
|
0.0
|
1.0
|
H2
|
C:HOH2530
|
3.9
|
0.0
|
1.0
|
ND1
|
C:HIS100
|
3.9
|
14.4
|
1.0
|
ND1
|
A:HIS306
|
4.0
|
15.3
|
1.0
|
NE2
|
A:HIS255
|
4.0
|
24.3
|
1.0
|
CG
|
C:HIS100
|
4.1
|
13.9
|
1.0
|
ND1
|
C:HIS135
|
4.2
|
18.4
|
1.0
|
CG
|
C:HIS135
|
4.3
|
21.5
|
1.0
|
CG
|
A:HIS306
|
4.3
|
15.9
|
1.0
|
CG
|
C:ASP98
|
4.4
|
22.0
|
1.0
|
CE1
|
A:HIS255
|
4.4
|
26.5
|
1.0
|
CD2
|
A:HIS255
|
4.4
|
23.5
|
1.0
|
HD1
|
C:HIS100
|
4.7
|
0.0
|
1.0
|
HD1
|
A:HIS306
|
4.8
|
0.0
|
1.0
|
O
|
C:HOH2530
|
4.8
|
41.2
|
1.0
|
OD2
|
C:ASP98
|
4.9
|
21.5
|
1.0
|
O
|
A:HOH1369
|
4.9
|
11.5
|
1.0
|
ND1
|
A:HIS255
|
4.9
|
25.6
|
1.0
|
CG
|
A:HIS255
|
5.0
|
24.7
|
1.0
|
|
Reference:
M.E.Murphy,
S.Turley,
E.T.Adman.
Structure of Nitrite Bound to Copper-Containing Nitrite Reductase From Alcaligenes Faecalis. Mechanistic Implications. J.Biol.Chem. V. 272 28455 1997.
ISSN: ISSN 0021-9258
PubMed: 9353305
DOI: 10.1074/JBC.272.45.28455
Page generated: Tue Jul 30 21:29:22 2024
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