Copper in PDB 3qpk: Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Enzymatic activity of Probing Oxygen Channels in Melanocarpus Albomyces Laccase
All present enzymatic activity of Probing Oxygen Channels in Melanocarpus Albomyces Laccase:
1.10.3.2;
Protein crystallography data
The structure of Probing Oxygen Channels in Melanocarpus Albomyces Laccase, PDB code: 3qpk
was solved by
J.P.Kallio,
J.Rouvinen,
N.Hakulinen,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
43.83 /
1.90
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
174.150,
60.200,
114.440,
90.00,
99.79,
90.00
|
R / Rfree (%)
|
21.4 /
27
|
Other elements in 3qpk:
The structure of Probing Oxygen Channels in Melanocarpus Albomyces Laccase also contains other interesting chemical elements:
Copper Binding Sites:
The binding sites of Copper atom in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
(pdb code 3qpk). This binding sites where shown within
5.0 Angstroms radius around Copper atom.
In total 8 binding sites of Copper where determined in the
Probing Oxygen Channels in Melanocarpus Albomyces Laccase, PDB code: 3qpk:
Jump to Copper binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
Copper binding site 1 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 1 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 1 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu601
b:15.0
occ:1.00
|
ND1
|
A:HIS431
|
2.0
|
11.3
|
1.0
|
SG
|
A:CYS503
|
2.1
|
12.0
|
1.0
|
ND1
|
A:HIS508
|
2.2
|
11.1
|
1.0
|
CG
|
A:HIS431
|
3.0
|
11.1
|
1.0
|
CE1
|
A:HIS431
|
3.0
|
10.4
|
1.0
|
CB
|
A:CYS503
|
3.1
|
12.1
|
1.0
|
CG
|
A:HIS508
|
3.1
|
14.3
|
1.0
|
CE1
|
A:HIS508
|
3.3
|
14.5
|
1.0
|
CB
|
A:HIS508
|
3.3
|
12.3
|
1.0
|
CB
|
A:HIS431
|
3.3
|
10.8
|
1.0
|
CD1
|
A:ILE505
|
3.8
|
7.1
|
1.0
|
CD1
|
A:LEU513
|
3.8
|
11.3
|
1.0
|
CA
|
A:HIS431
|
3.8
|
9.0
|
1.0
|
NE2
|
A:HIS431
|
4.1
|
14.9
|
1.0
|
CD2
|
A:HIS431
|
4.1
|
11.7
|
1.0
|
CB
|
A:ILE505
|
4.1
|
8.7
|
1.0
|
CD
|
A:PRO432
|
4.3
|
8.1
|
1.0
|
CG1
|
A:ILE505
|
4.3
|
8.5
|
1.0
|
CD2
|
A:HIS508
|
4.3
|
15.5
|
1.0
|
O
|
A:PRO430
|
4.3
|
9.0
|
1.0
|
NE2
|
A:HIS508
|
4.4
|
10.7
|
1.0
|
CA
|
A:CYS503
|
4.5
|
11.3
|
1.0
|
C
|
A:HIS431
|
4.8
|
8.9
|
1.0
|
CA
|
A:HIS508
|
4.8
|
9.3
|
1.0
|
N
|
A:HIS431
|
4.8
|
9.2
|
1.0
|
N
|
A:PRO432
|
4.8
|
9.4
|
1.0
|
N
|
A:ILE505
|
4.9
|
10.7
|
1.0
|
CG2
|
A:ILE505
|
5.0
|
10.3
|
1.0
|
|
Copper binding site 2 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 2 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 2 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu602
b:17.2
occ:1.00
|
NE2
|
A:HIS436
|
2.1
|
10.9
|
1.0
|
NE2
|
A:HIS140
|
2.1
|
12.6
|
1.0
|
NE2
|
A:HIS502
|
2.2
|
12.3
|
1.0
|
O
|
A:HOH1100
|
2.4
|
9.9
|
1.0
|
CE1
|
A:HIS436
|
2.9
|
10.8
|
1.0
|
CE1
|
A:HIS140
|
3.0
|
16.8
|
1.0
|
CE1
|
A:HIS502
|
3.1
|
12.3
|
1.0
|
CD2
|
A:HIS140
|
3.2
|
11.6
|
1.0
|
CD2
|
A:HIS502
|
3.2
|
12.5
|
1.0
|
CD2
|
A:HIS436
|
3.2
|
10.0
|
1.0
|
CU
|
A:CU604
|
4.0
|
17.4
|
1.0
|
ND1
|
A:HIS436
|
4.1
|
12.2
|
1.0
|
CD2
|
A:HIS434
|
4.1
|
10.4
|
1.0
|
CD2
|
A:HIS93
|
4.2
|
11.9
|
1.0
|
ND1
|
A:HIS140
|
4.2
|
14.0
|
1.0
|
ND1
|
A:HIS502
|
4.2
|
9.5
|
1.0
|
CG
|
A:HIS436
|
4.3
|
8.6
|
1.0
|
CG
|
A:HIS140
|
4.3
|
12.9
|
1.0
|
NE2
|
A:HIS93
|
4.3
|
14.9
|
1.0
|
CG
|
A:HIS502
|
4.3
|
9.7
|
1.0
|
O
|
A:HOH1236
|
4.5
|
16.7
|
1.0
|
CD1
|
A:LEU500
|
4.5
|
8.3
|
1.0
|
NE2
|
A:HIS434
|
4.7
|
10.6
|
1.0
|
CB
|
A:LEU500
|
4.7
|
9.8
|
1.0
|
CG
|
A:HIS93
|
4.8
|
12.3
|
1.0
|
CE1
|
A:HIS138
|
4.9
|
11.0
|
1.0
|
CE1
|
A:HIS93
|
5.0
|
13.6
|
1.0
|
CU
|
A:CU603
|
5.0
|
16.4
|
1.0
|
|
Copper binding site 3 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 3 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 3 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu603
b:16.4
occ:1.00
|
NE2
|
A:HIS138
|
2.1
|
10.9
|
1.0
|
NE2
|
A:HIS504
|
2.1
|
9.1
|
1.0
|
ND1
|
A:HIS95
|
2.1
|
14.5
|
1.0
|
O
|
A:HOH1100
|
2.6
|
9.9
|
1.0
|
CE1
|
A:HIS138
|
3.0
|
11.0
|
1.0
|
CE1
|
A:HIS504
|
3.0
|
10.8
|
1.0
|
CD2
|
A:HIS138
|
3.0
|
10.2
|
1.0
|
CD2
|
A:HIS504
|
3.1
|
10.9
|
1.0
|
CG
|
A:HIS95
|
3.1
|
14.7
|
1.0
|
CE1
|
A:HIS95
|
3.1
|
12.3
|
1.0
|
CB
|
A:HIS95
|
3.4
|
10.8
|
1.0
|
CZ2
|
A:TRP136
|
3.5
|
11.3
|
1.0
|
CE2
|
A:TRP136
|
4.0
|
12.2
|
1.0
|
CU
|
A:CU604
|
4.0
|
17.4
|
1.0
|
CD2
|
A:HIS93
|
4.0
|
11.9
|
1.0
|
ND1
|
A:HIS138
|
4.1
|
9.0
|
1.0
|
CH2
|
A:TRP136
|
4.1
|
12.0
|
1.0
|
ND1
|
A:HIS504
|
4.1
|
10.5
|
1.0
|
CG
|
A:HIS138
|
4.1
|
8.6
|
1.0
|
CG
|
A:HIS504
|
4.2
|
9.8
|
1.0
|
NE1
|
A:TRP136
|
4.2
|
11.4
|
1.0
|
NE2
|
A:HIS95
|
4.3
|
11.4
|
1.0
|
CD2
|
A:HIS95
|
4.3
|
10.2
|
1.0
|
NE2
|
A:HIS434
|
4.5
|
10.6
|
1.0
|
NE2
|
A:HIS93
|
4.5
|
14.9
|
1.0
|
CD2
|
A:HIS434
|
4.5
|
10.4
|
1.0
|
CA
|
A:HIS95
|
4.6
|
10.1
|
1.0
|
CD2
|
A:TRP136
|
4.9
|
9.1
|
1.0
|
O
|
A:HOH1034
|
4.9
|
12.4
|
1.0
|
CU
|
A:CU602
|
5.0
|
17.2
|
1.0
|
O
|
A:HOH1236
|
5.0
|
16.7
|
1.0
|
CZ3
|
A:TRP136
|
5.0
|
11.0
|
1.0
|
|
Copper binding site 4 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 4 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 4 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu604
b:17.4
occ:1.00
|
NE2
|
A:HIS93
|
1.9
|
14.9
|
1.0
|
NE2
|
A:HIS434
|
1.9
|
10.6
|
1.0
|
CD2
|
A:HIS434
|
2.8
|
10.4
|
1.0
|
CD2
|
A:HIS93
|
2.8
|
11.9
|
1.0
|
CL
|
A:CL610
|
2.9
|
23.3
|
1.0
|
CE1
|
A:HIS93
|
2.9
|
13.6
|
1.0
|
CE1
|
A:HIS434
|
3.0
|
15.0
|
1.0
|
O
|
A:HOH1100
|
3.2
|
9.9
|
1.0
|
NE2
|
A:HIS436
|
3.3
|
10.9
|
1.0
|
CD2
|
A:HIS436
|
3.4
|
10.0
|
1.0
|
ND1
|
A:HIS95
|
3.7
|
14.5
|
1.0
|
CE1
|
A:HIS436
|
3.8
|
10.8
|
1.0
|
CA
|
A:HIS95
|
3.9
|
10.1
|
1.0
|
CG
|
A:HIS95
|
3.9
|
14.7
|
1.0
|
CG
|
A:HIS436
|
3.9
|
8.6
|
1.0
|
ND1
|
A:HIS93
|
3.9
|
12.3
|
1.0
|
CG
|
A:HIS93
|
3.9
|
12.3
|
1.0
|
CG
|
A:HIS434
|
4.0
|
9.5
|
1.0
|
CU
|
A:CU603
|
4.0
|
16.4
|
1.0
|
ND1
|
A:HIS434
|
4.0
|
12.5
|
1.0
|
CU
|
A:CU602
|
4.0
|
17.2
|
1.0
|
CB
|
A:HIS95
|
4.1
|
10.8
|
1.0
|
ND1
|
A:HIS436
|
4.1
|
12.2
|
1.0
|
CE1
|
A:HIS95
|
4.3
|
12.3
|
1.0
|
O
|
A:HOH1232
|
4.5
|
25.8
|
1.0
|
N
|
A:GLY96
|
4.6
|
15.2
|
1.0
|
CD2
|
A:HIS95
|
4.6
|
10.2
|
1.0
|
CA
|
A:HIS436
|
4.7
|
11.1
|
1.0
|
C
|
A:HIS95
|
4.7
|
14.6
|
1.0
|
N
|
A:HIS95
|
4.8
|
11.7
|
1.0
|
NE2
|
A:HIS95
|
4.8
|
11.4
|
1.0
|
CB
|
A:HIS436
|
4.8
|
7.2
|
1.0
|
O
|
A:LEU435
|
5.0
|
8.9
|
1.0
|
|
Copper binding site 5 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 5 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 5 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu601
b:14.7
occ:1.00
|
ND1
|
B:HIS431
|
2.0
|
11.2
|
1.0
|
ND1
|
B:HIS508
|
2.1
|
12.7
|
1.0
|
SG
|
B:CYS503
|
2.2
|
8.9
|
1.0
|
CE1
|
B:HIS431
|
2.9
|
11.4
|
1.0
|
CG
|
B:HIS508
|
3.0
|
12.9
|
1.0
|
CG
|
B:HIS431
|
3.1
|
13.8
|
1.0
|
CE1
|
B:HIS508
|
3.1
|
18.2
|
1.0
|
CB
|
B:CYS503
|
3.1
|
12.0
|
1.0
|
CB
|
B:HIS508
|
3.2
|
11.7
|
1.0
|
CB
|
B:HIS431
|
3.5
|
10.3
|
1.0
|
CD1
|
B:ILE505
|
3.8
|
6.9
|
1.0
|
CA
|
B:HIS431
|
3.9
|
11.6
|
1.0
|
CB
|
B:ILE505
|
4.0
|
10.4
|
1.0
|
NE2
|
B:HIS431
|
4.1
|
12.0
|
1.0
|
CD1
|
B:LEU513
|
4.1
|
12.5
|
1.0
|
CD2
|
B:HIS431
|
4.2
|
12.4
|
1.0
|
CG1
|
B:ILE505
|
4.2
|
9.4
|
1.0
|
CD2
|
B:HIS508
|
4.2
|
13.7
|
1.0
|
NE2
|
B:HIS508
|
4.2
|
12.1
|
1.0
|
CD
|
B:PRO432
|
4.4
|
10.5
|
1.0
|
O
|
B:PRO430
|
4.4
|
7.9
|
1.0
|
CA
|
B:CYS503
|
4.5
|
13.1
|
1.0
|
CA
|
B:HIS508
|
4.7
|
9.5
|
1.0
|
N
|
B:ILE505
|
4.8
|
8.9
|
1.0
|
C
|
B:HIS431
|
4.9
|
8.5
|
1.0
|
CG2
|
B:ILE505
|
4.9
|
7.9
|
1.0
|
N
|
B:HIS431
|
4.9
|
6.6
|
1.0
|
N
|
B:PRO432
|
4.9
|
8.2
|
1.0
|
C
|
B:CYS503
|
5.0
|
8.5
|
1.0
|
|
Copper binding site 6 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 6 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 6 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu602
b:15.1
occ:1.00
|
NE2
|
B:HIS502
|
2.1
|
13.8
|
1.0
|
NE2
|
B:HIS140
|
2.1
|
14.2
|
1.0
|
NE2
|
B:HIS436
|
2.1
|
14.6
|
1.0
|
O
|
B:HOH579
|
2.2
|
9.3
|
1.0
|
CE1
|
B:HIS436
|
2.8
|
10.7
|
1.0
|
CE1
|
B:HIS502
|
3.0
|
12.2
|
1.0
|
CE1
|
B:HIS140
|
3.0
|
14.5
|
1.0
|
CD2
|
B:HIS502
|
3.1
|
12.2
|
1.0
|
CD2
|
B:HIS140
|
3.2
|
14.4
|
1.0
|
CD2
|
B:HIS436
|
3.3
|
9.9
|
1.0
|
CU
|
B:CU604
|
4.0
|
15.8
|
1.0
|
ND1
|
B:HIS436
|
4.1
|
13.3
|
1.0
|
CD2
|
B:HIS434
|
4.1
|
8.6
|
1.0
|
ND1
|
B:HIS502
|
4.1
|
12.2
|
1.0
|
ND1
|
B:HIS140
|
4.2
|
12.6
|
1.0
|
CG
|
B:HIS502
|
4.2
|
14.1
|
1.0
|
CG
|
B:HIS140
|
4.3
|
15.1
|
1.0
|
CD2
|
B:HIS93
|
4.3
|
14.0
|
1.0
|
O
|
B:HOH1148
|
4.3
|
18.2
|
1.0
|
CG
|
B:HIS436
|
4.3
|
11.5
|
1.0
|
NE2
|
B:HIS93
|
4.4
|
15.6
|
1.0
|
NE2
|
B:HIS434
|
4.6
|
14.1
|
1.0
|
CD1
|
B:LEU500
|
4.6
|
8.5
|
1.0
|
CG
|
B:HIS93
|
4.8
|
14.2
|
1.0
|
CU
|
B:CU603
|
4.9
|
15.0
|
1.0
|
CB
|
B:LEU500
|
4.9
|
13.7
|
1.0
|
CE1
|
B:HIS138
|
4.9
|
10.4
|
1.0
|
CE1
|
B:HIS93
|
5.0
|
11.8
|
1.0
|
|
Copper binding site 7 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 7 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 7 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu603
b:15.0
occ:1.00
|
ND1
|
B:HIS95
|
1.9
|
15.7
|
1.0
|
NE2
|
B:HIS138
|
2.1
|
16.3
|
1.0
|
NE2
|
B:HIS504
|
2.1
|
10.6
|
1.0
|
O
|
B:HOH579
|
2.7
|
9.3
|
1.0
|
CE1
|
B:HIS95
|
2.9
|
12.2
|
1.0
|
CG
|
B:HIS95
|
2.9
|
12.4
|
1.0
|
CE1
|
B:HIS138
|
3.0
|
10.4
|
1.0
|
CD2
|
B:HIS138
|
3.0
|
11.4
|
1.0
|
CD2
|
B:HIS504
|
3.1
|
14.4
|
1.0
|
CE1
|
B:HIS504
|
3.1
|
11.8
|
1.0
|
CB
|
B:HIS95
|
3.3
|
13.1
|
1.0
|
CZ2
|
B:TRP136
|
3.6
|
11.8
|
1.0
|
NE2
|
B:HIS95
|
4.0
|
13.5
|
1.0
|
CU
|
B:CU604
|
4.0
|
15.8
|
1.0
|
CD2
|
B:HIS93
|
4.0
|
14.0
|
1.0
|
CD2
|
B:HIS95
|
4.0
|
13.4
|
1.0
|
CE2
|
B:TRP136
|
4.1
|
10.9
|
1.0
|
ND1
|
B:HIS138
|
4.1
|
8.6
|
1.0
|
CG
|
B:HIS138
|
4.2
|
11.4
|
1.0
|
CH2
|
B:TRP136
|
4.2
|
12.7
|
1.0
|
ND1
|
B:HIS504
|
4.2
|
9.7
|
1.0
|
CG
|
B:HIS504
|
4.2
|
8.5
|
1.0
|
NE1
|
B:TRP136
|
4.4
|
9.7
|
1.0
|
NE2
|
B:HIS434
|
4.4
|
14.1
|
1.0
|
CA
|
B:HIS95
|
4.5
|
12.4
|
1.0
|
CD2
|
B:HIS434
|
4.5
|
8.6
|
1.0
|
NE2
|
B:HIS93
|
4.7
|
15.6
|
1.0
|
O
|
B:HOH1148
|
4.8
|
18.2
|
1.0
|
CU
|
B:CU602
|
4.9
|
15.1
|
1.0
|
CD2
|
B:TRP136
|
5.0
|
10.5
|
1.0
|
|
Copper binding site 8 out
of 8 in 3qpk
Go back to
Copper Binding Sites List in 3qpk
Copper binding site 8 out
of 8 in the Probing Oxygen Channels in Melanocarpus Albomyces Laccase
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 8 of Probing Oxygen Channels in Melanocarpus Albomyces Laccase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu604
b:15.8
occ:1.00
|
NE2
|
B:HIS93
|
1.9
|
15.6
|
1.0
|
NE2
|
B:HIS434
|
2.0
|
14.1
|
1.0
|
CL
|
B:CL610
|
2.6
|
25.6
|
1.0
|
CD2
|
B:HIS93
|
2.7
|
14.0
|
1.0
|
CD2
|
B:HIS434
|
2.9
|
8.6
|
1.0
|
O
|
B:HOH579
|
3.0
|
9.3
|
1.0
|
CE1
|
B:HIS434
|
3.0
|
10.2
|
1.0
|
CE1
|
B:HIS93
|
3.0
|
11.8
|
1.0
|
NE2
|
B:HIS436
|
3.3
|
14.6
|
1.0
|
CD2
|
B:HIS436
|
3.4
|
9.9
|
1.0
|
CE1
|
B:HIS436
|
3.7
|
10.7
|
1.0
|
CA
|
B:HIS95
|
3.8
|
12.4
|
1.0
|
CG
|
B:HIS95
|
3.8
|
12.4
|
1.0
|
ND1
|
B:HIS95
|
3.8
|
15.7
|
1.0
|
CG
|
B:HIS436
|
3.9
|
11.5
|
1.0
|
CG
|
B:HIS93
|
3.9
|
14.2
|
1.0
|
ND1
|
B:HIS93
|
4.0
|
9.9
|
1.0
|
CB
|
B:HIS95
|
4.0
|
13.1
|
1.0
|
CU
|
B:CU603
|
4.0
|
15.0
|
1.0
|
CU
|
B:CU602
|
4.0
|
15.1
|
1.0
|
ND1
|
B:HIS434
|
4.0
|
11.1
|
1.0
|
CG
|
B:HIS434
|
4.1
|
7.6
|
1.0
|
ND1
|
B:HIS436
|
4.1
|
13.3
|
1.0
|
CD2
|
B:HIS95
|
4.2
|
13.4
|
1.0
|
CE1
|
B:HIS95
|
4.2
|
12.2
|
1.0
|
N
|
B:GLY96
|
4.3
|
14.1
|
1.0
|
NE2
|
B:HIS95
|
4.5
|
13.5
|
1.0
|
C
|
B:HIS95
|
4.6
|
13.5
|
1.0
|
N
|
B:HIS95
|
4.7
|
11.2
|
1.0
|
CA
|
B:HIS436
|
4.7
|
10.4
|
1.0
|
CB
|
B:HIS436
|
4.8
|
8.8
|
1.0
|
O
|
B:HOH1053
|
4.8
|
14.9
|
1.0
|
O
|
B:LEU435
|
4.9
|
10.3
|
1.0
|
O
|
B:TRP94
|
5.0
|
14.8
|
1.0
|
O
|
B:HOH754
|
5.0
|
18.6
|
1.0
|
|
Reference:
J.P.Kallio,
J.Rouvinen,
K.Kruus,
N.Hakulinen.
Probing the Dioxygen Route in Melanocarpus Albomyces Laccase with Pressurized Xenon Gas. Biochemistry V. 50 4396 2011.
ISSN: ISSN 0006-2960
PubMed: 21524088
DOI: 10.1021/BI200486B
Page generated: Wed Jul 31 01:37:12 2024
|