Copper in PDB 1w8e: 3D Structure of Cota Incubated with Hydrogen Peroxide
Protein crystallography data
The structure of 3D Structure of Cota Incubated with Hydrogen Peroxide, PDB code: 1w8e
was solved by
I.Bento,
L.O.Martins,
G.G.Lopes,
M.A.Carrondo,
P.F.Lindley,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
32.03 /
2.2
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
102.720,
102.720,
137.348,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
16.1 /
19.9
|
Copper Binding Sites:
The binding sites of Copper atom in the 3D Structure of Cota Incubated with Hydrogen Peroxide
(pdb code 1w8e). This binding sites where shown within
5.0 Angstroms radius around Copper atom.
In total 4 binding sites of Copper where determined in the
3D Structure of Cota Incubated with Hydrogen Peroxide, PDB code: 1w8e:
Jump to Copper binding site number:
1;
2;
3;
4;
Copper binding site 1 out
of 4 in 1w8e
Go back to
Copper Binding Sites List in 1w8e
Copper binding site 1 out
of 4 in the 3D Structure of Cota Incubated with Hydrogen Peroxide
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 1 of 3D Structure of Cota Incubated with Hydrogen Peroxide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1512
b:25.6
occ:1.00
|
ND1
|
A:HIS497
|
2.0
|
23.5
|
1.0
|
ND1
|
A:HIS419
|
2.0
|
27.1
|
1.0
|
SG
|
A:CYS492
|
2.2
|
24.9
|
1.0
|
CE1
|
A:HIS419
|
2.9
|
26.6
|
1.0
|
CE1
|
A:HIS497
|
3.0
|
24.5
|
1.0
|
CG
|
A:HIS497
|
3.0
|
24.6
|
1.0
|
CG
|
A:HIS419
|
3.1
|
27.7
|
1.0
|
CB
|
A:CYS492
|
3.3
|
23.8
|
1.0
|
SD
|
A:MET502
|
3.3
|
26.3
|
1.0
|
CB
|
A:HIS497
|
3.4
|
24.6
|
1.0
|
CB
|
A:HIS419
|
3.6
|
26.2
|
1.0
|
CE
|
A:MET502
|
4.0
|
24.8
|
1.0
|
CD1
|
A:ILE494
|
4.0
|
21.6
|
1.0
|
NE2
|
A:HIS419
|
4.0
|
26.1
|
1.0
|
NE2
|
A:HIS497
|
4.1
|
24.5
|
1.0
|
CB
|
A:ILE494
|
4.1
|
22.9
|
1.0
|
CA
|
A:HIS419
|
4.1
|
26.2
|
1.0
|
CD2
|
A:HIS497
|
4.1
|
19.5
|
1.0
|
CD2
|
A:HIS419
|
4.2
|
26.3
|
1.0
|
CG1
|
A:ILE494
|
4.4
|
23.2
|
1.0
|
O
|
A:HOH2401
|
4.5
|
32.5
|
1.0
|
CA
|
A:CYS492
|
4.6
|
24.6
|
1.0
|
CD
|
A:PRO420
|
4.7
|
22.6
|
1.0
|
CD1
|
A:LEU386
|
4.7
|
36.1
|
1.0
|
CG
|
A:MET502
|
4.7
|
25.7
|
1.0
|
CG2
|
A:ILE494
|
4.8
|
22.9
|
1.0
|
CA
|
A:HIS497
|
4.9
|
25.5
|
1.0
|
O
|
A:THR418
|
4.9
|
29.0
|
1.0
|
N
|
A:ILE494
|
5.0
|
24.1
|
1.0
|
|
Copper binding site 2 out
of 4 in 1w8e
Go back to
Copper Binding Sites List in 1w8e
Copper binding site 2 out
of 4 in the 3D Structure of Cota Incubated with Hydrogen Peroxide
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 2 of 3D Structure of Cota Incubated with Hydrogen Peroxide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1513
b:27.8
occ:0.75
|
O1
|
A:PER1516
|
1.9
|
32.0
|
0.8
|
ND1
|
A:HIS107
|
2.0
|
25.4
|
1.0
|
NE2
|
A:HIS493
|
2.0
|
24.2
|
1.0
|
NE2
|
A:HIS153
|
2.0
|
27.1
|
1.0
|
CE1
|
A:HIS107
|
2.9
|
27.7
|
1.0
|
O2
|
A:PER1516
|
2.9
|
35.8
|
0.8
|
CE1
|
A:HIS153
|
2.9
|
23.3
|
1.0
|
CE1
|
A:HIS493
|
3.0
|
20.7
|
1.0
|
CD2
|
A:HIS493
|
3.1
|
24.0
|
1.0
|
CG
|
A:HIS107
|
3.1
|
26.1
|
1.0
|
CD2
|
A:HIS153
|
3.1
|
22.6
|
1.0
|
CB
|
A:HIS107
|
3.5
|
23.9
|
1.0
|
CD2
|
A:HIS105
|
3.9
|
25.3
|
1.0
|
CZ2
|
A:TRP151
|
4.0
|
19.7
|
1.0
|
NE2
|
A:HIS107
|
4.0
|
27.4
|
1.0
|
O
|
A:HOH2449
|
4.1
|
47.3
|
1.0
|
ND1
|
A:HIS153
|
4.1
|
23.7
|
1.0
|
CU
|
A:CU1515
|
4.1
|
27.0
|
0.5
|
ND1
|
A:HIS493
|
4.1
|
24.1
|
1.0
|
CD2
|
A:HIS107
|
4.2
|
25.4
|
1.0
|
CG
|
A:HIS493
|
4.2
|
25.1
|
1.0
|
CG
|
A:HIS153
|
4.2
|
23.7
|
1.0
|
CE2
|
A:TRP151
|
4.3
|
20.0
|
1.0
|
NE2
|
A:HIS105
|
4.3
|
29.2
|
1.0
|
NE1
|
A:TRP151
|
4.4
|
21.8
|
1.0
|
CB
|
A:ALA297
|
4.5
|
21.6
|
1.0
|
CA
|
A:HIS107
|
4.6
|
24.2
|
1.0
|
CD2
|
A:HIS422
|
4.6
|
24.2
|
1.0
|
CU
|
A:CU1514
|
4.6
|
30.6
|
0.7
|
NE2
|
A:HIS422
|
4.7
|
24.2
|
1.0
|
CH2
|
A:TRP151
|
4.7
|
20.1
|
1.0
|
|
Copper binding site 3 out
of 4 in 1w8e
Go back to
Copper Binding Sites List in 1w8e
Copper binding site 3 out
of 4 in the 3D Structure of Cota Incubated with Hydrogen Peroxide
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 3 of 3D Structure of Cota Incubated with Hydrogen Peroxide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1514
b:30.6
occ:0.70
|
O2
|
A:PER1516
|
1.9
|
35.8
|
0.8
|
NE2
|
A:HIS491
|
2.0
|
30.3
|
1.0
|
NE2
|
A:HIS424
|
2.0
|
36.6
|
1.0
|
NE2
|
A:HIS155
|
2.0
|
32.6
|
1.0
|
CE1
|
A:HIS424
|
2.8
|
35.6
|
1.0
|
O1
|
A:PER1516
|
2.9
|
32.0
|
0.8
|
CE1
|
A:HIS491
|
2.9
|
27.3
|
1.0
|
CD2
|
A:HIS155
|
2.9
|
29.9
|
1.0
|
CD2
|
A:HIS491
|
3.0
|
28.2
|
1.0
|
CE1
|
A:HIS155
|
3.1
|
32.3
|
1.0
|
CD2
|
A:HIS424
|
3.2
|
35.8
|
1.0
|
O
|
A:HOH2449
|
3.7
|
47.3
|
1.0
|
CU
|
A:CU1515
|
3.7
|
27.0
|
0.5
|
NE2
|
A:HIS105
|
3.8
|
29.2
|
1.0
|
CD2
|
A:HIS105
|
3.8
|
25.3
|
1.0
|
CD2
|
A:HIS422
|
3.9
|
24.2
|
1.0
|
ND1
|
A:HIS491
|
4.0
|
25.1
|
1.0
|
ND1
|
A:HIS424
|
4.0
|
34.3
|
1.0
|
CG2
|
A:VAL489
|
4.0
|
29.0
|
1.0
|
CG
|
A:HIS491
|
4.1
|
25.5
|
1.0
|
CG
|
A:HIS155
|
4.1
|
27.1
|
1.0
|
ND1
|
A:HIS155
|
4.2
|
32.7
|
1.0
|
CG
|
A:HIS424
|
4.2
|
32.9
|
1.0
|
NE2
|
A:HIS422
|
4.4
|
24.2
|
1.0
|
CE1
|
A:HIS105
|
4.5
|
28.1
|
1.0
|
CG
|
A:HIS105
|
4.5
|
25.4
|
1.0
|
CU
|
A:CU1513
|
4.6
|
27.8
|
0.8
|
O
|
A:HOH2172
|
4.7
|
49.8
|
1.0
|
OE2
|
A:GLU498
|
4.8
|
32.4
|
1.0
|
CD2
|
A:HIS493
|
4.9
|
24.0
|
1.0
|
NE2
|
A:HIS493
|
4.9
|
24.2
|
1.0
|
ND1
|
A:HIS105
|
4.9
|
27.0
|
1.0
|
OE1
|
A:GLU498
|
5.0
|
28.3
|
1.0
|
|
Copper binding site 4 out
of 4 in 1w8e
Go back to
Copper Binding Sites List in 1w8e
Copper binding site 4 out
of 4 in the 3D Structure of Cota Incubated with Hydrogen Peroxide
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 4 of 3D Structure of Cota Incubated with Hydrogen Peroxide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1515
b:27.0
occ:0.50
|
NE2
|
A:HIS422
|
2.0
|
24.2
|
1.0
|
NE2
|
A:HIS105
|
2.0
|
29.2
|
1.0
|
O2
|
A:PER1516
|
2.6
|
35.8
|
0.8
|
O
|
A:HOH2155
|
2.7
|
41.6
|
1.0
|
CD2
|
A:HIS422
|
2.8
|
24.2
|
1.0
|
CE1
|
A:HIS105
|
2.9
|
28.1
|
1.0
|
CE1
|
A:HIS422
|
3.0
|
23.4
|
1.0
|
CD2
|
A:HIS105
|
3.0
|
25.3
|
1.0
|
CD2
|
A:HIS424
|
3.2
|
35.8
|
1.0
|
NE2
|
A:HIS424
|
3.2
|
36.6
|
1.0
|
ND1
|
A:HIS107
|
3.6
|
25.4
|
1.0
|
O1
|
A:PER1516
|
3.7
|
32.0
|
0.8
|
CU
|
A:CU1514
|
3.7
|
30.6
|
0.7
|
CG
|
A:HIS424
|
3.7
|
32.9
|
1.0
|
CE1
|
A:HIS424
|
3.8
|
35.6
|
1.0
|
CG
|
A:HIS107
|
3.8
|
26.1
|
1.0
|
CE1
|
A:HIS107
|
3.9
|
27.7
|
1.0
|
CA
|
A:HIS107
|
3.9
|
24.2
|
1.0
|
ND1
|
A:HIS105
|
4.0
|
27.0
|
1.0
|
CG
|
A:HIS422
|
4.0
|
24.9
|
1.0
|
ND1
|
A:HIS424
|
4.0
|
34.3
|
1.0
|
ND1
|
A:HIS422
|
4.1
|
26.2
|
1.0
|
CU
|
A:CU1513
|
4.1
|
27.8
|
0.8
|
CG
|
A:HIS105
|
4.1
|
25.4
|
1.0
|
CD2
|
A:HIS107
|
4.2
|
25.4
|
1.0
|
CB
|
A:HIS107
|
4.2
|
23.9
|
1.0
|
NE2
|
A:HIS107
|
4.2
|
27.4
|
1.0
|
N
|
A:GLY108
|
4.3
|
24.9
|
1.0
|
CA
|
A:HIS424
|
4.5
|
32.2
|
1.0
|
CB
|
A:HIS424
|
4.6
|
32.3
|
1.0
|
C
|
A:HIS107
|
4.7
|
24.9
|
1.0
|
O
|
A:HOH2156
|
4.7
|
31.9
|
1.0
|
NE2
|
A:HIS491
|
4.8
|
30.3
|
1.0
|
N
|
A:HIS107
|
4.9
|
23.1
|
1.0
|
O
|
A:HOH2404
|
4.9
|
27.1
|
1.0
|
N
|
A:HIS424
|
5.0
|
31.5
|
1.0
|
|
Reference:
I.Bento,
L.O.Martins,
G.G.Lopes,
M.A.Carrondo,
P.F.Lindley.
Dioxygen Reduction By Multi-Copper Oxidases; A Structural Perspective. Dalton Trans. V. 7 3507 2005.
ISSN: ISSN 1477-9226
PubMed: 16234932
DOI: 10.1039/B504806K
Page generated: Tue Jul 30 22:58:18 2024
|