Copper in PDB 4a2e: Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5
Enzymatic activity of Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5
All present enzymatic activity of Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5:
1.10.3.2;
Protein crystallography data
The structure of Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5, PDB code: 4a2e
was solved by
E.De La Mora,
B.Valderrama,
E.Horjales,
E.Rudino-Pinera,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
25.63 /
1.80
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
56.385,
86.127,
152.637,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
15.4 /
18.7
|
Copper Binding Sites:
The binding sites of Copper atom in the Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5
(pdb code 4a2e). This binding sites where shown within
5.0 Angstroms radius around Copper atom.
In total 4 binding sites of Copper where determined in the
Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5, PDB code: 4a2e:
Jump to Copper binding site number:
1;
2;
3;
4;
Copper binding site 1 out
of 4 in 4a2e
Go back to
Copper Binding Sites List in 4a2e
Copper binding site 1 out
of 4 in the Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 1 of Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1518
b:14.4
occ:0.80
|
ND1
|
A:HIS87
|
2.0
|
10.7
|
1.0
|
NE2
|
A:HIS472
|
2.1
|
15.2
|
1.0
|
NE2
|
A:HIS130
|
2.1
|
11.3
|
1.0
|
O
|
A:HOH2200
|
2.7
|
24.7
|
1.0
|
CE1
|
A:HIS87
|
2.9
|
11.3
|
1.0
|
CG
|
A:HIS87
|
3.1
|
9.6
|
1.0
|
CE1
|
A:HIS472
|
3.1
|
17.4
|
1.0
|
CE1
|
A:HIS130
|
3.1
|
11.3
|
1.0
|
CD2
|
A:HIS130
|
3.1
|
12.2
|
1.0
|
CD2
|
A:HIS472
|
3.2
|
14.7
|
1.0
|
CB
|
A:HIS87
|
3.5
|
8.4
|
1.0
|
CZ2
|
A:TRP128
|
3.6
|
11.4
|
1.0
|
CD2
|
A:HIS85
|
3.6
|
10.2
|
1.0
|
CE2
|
A:TRP128
|
3.9
|
10.9
|
1.0
|
CU
|
A:CU1520
|
4.0
|
17.3
|
0.5
|
NE2
|
A:HIS87
|
4.1
|
11.0
|
1.0
|
NE1
|
A:TRP128
|
4.1
|
11.1
|
1.0
|
CD2
|
A:HIS87
|
4.2
|
10.3
|
1.0
|
NE2
|
A:HIS85
|
4.2
|
12.1
|
1.0
|
ND1
|
A:HIS472
|
4.2
|
13.9
|
1.0
|
ND1
|
A:HIS130
|
4.2
|
10.8
|
1.0
|
CB
|
A:ALA261
|
4.3
|
10.0
|
1.0
|
O
|
A:HOH2205
|
4.3
|
32.1
|
1.0
|
CG
|
A:HIS130
|
4.3
|
10.7
|
1.0
|
CG
|
A:HIS472
|
4.3
|
17.6
|
1.0
|
CD2
|
A:HIS418
|
4.3
|
9.9
|
0.8
|
CH2
|
A:TRP128
|
4.3
|
10.7
|
1.0
|
NE2
|
A:HIS418
|
4.4
|
6.7
|
0.2
|
NE2
|
A:HIS418
|
4.5
|
12.1
|
0.8
|
CA
|
A:HIS87
|
4.6
|
7.4
|
1.0
|
CE1
|
A:HIS418
|
4.7
|
7.4
|
0.2
|
CD2
|
A:HIS418
|
4.7
|
7.0
|
0.2
|
CG
|
A:HIS85
|
4.8
|
11.6
|
1.0
|
CD2
|
A:TRP128
|
4.9
|
10.4
|
1.0
|
|
Copper binding site 2 out
of 4 in 4a2e
Go back to
Copper Binding Sites List in 4a2e
Copper binding site 2 out
of 4 in the Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 2 of Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1519
b:12.8
occ:0.81
|
NE2
|
A:HIS420
|
2.0
|
11.6
|
1.0
|
NE2
|
A:HIS470
|
2.0
|
18.8
|
1.0
|
NE2
|
A:HIS132
|
2.0
|
9.9
|
1.0
|
O
|
A:HOH2200
|
2.3
|
24.7
|
1.0
|
NE2
|
A:HIS418
|
2.4
|
6.7
|
0.2
|
CE1
|
A:HIS420
|
2.8
|
10.2
|
1.0
|
CE1
|
A:HIS470
|
2.9
|
20.6
|
1.0
|
CD2
|
A:HIS132
|
3.0
|
9.3
|
1.0
|
CE1
|
A:HIS418
|
3.0
|
7.4
|
0.2
|
CE1
|
A:HIS132
|
3.0
|
13.2
|
1.0
|
CD2
|
A:HIS470
|
3.0
|
15.1
|
1.0
|
CD2
|
A:HIS420
|
3.2
|
11.3
|
1.0
|
CD2
|
A:HIS418
|
3.6
|
7.0
|
0.2
|
O
|
A:HOH2205
|
3.7
|
32.1
|
1.0
|
CD2
|
A:HIS418
|
4.0
|
9.9
|
0.8
|
ND1
|
A:HIS420
|
4.0
|
9.2
|
1.0
|
ND1
|
A:HIS470
|
4.1
|
16.1
|
1.0
|
ND1
|
A:HIS132
|
4.1
|
9.5
|
1.0
|
CG
|
A:HIS132
|
4.1
|
10.8
|
1.0
|
CG
|
A:HIS470
|
4.1
|
14.7
|
1.0
|
CG
|
A:HIS420
|
4.2
|
8.6
|
1.0
|
CD2
|
A:PHE468
|
4.2
|
11.0
|
1.0
|
ND1
|
A:HIS418
|
4.3
|
9.2
|
0.2
|
CB
|
A:PHE468
|
4.4
|
8.5
|
1.0
|
CU
|
A:CU1520
|
4.4
|
17.3
|
0.5
|
CD2
|
A:HIS85
|
4.5
|
10.2
|
1.0
|
CG
|
A:HIS418
|
4.6
|
6.6
|
0.2
|
CG
|
A:PRO100
|
4.6
|
11.4
|
1.0
|
NE2
|
A:HIS85
|
4.7
|
12.1
|
1.0
|
CG
|
A:PHE468
|
4.7
|
8.7
|
1.0
|
NE2
|
A:HIS418
|
4.7
|
12.1
|
0.8
|
CD2
|
A:HIS472
|
5.0
|
14.7
|
1.0
|
NE2
|
A:HIS472
|
5.0
|
15.2
|
1.0
|
|
Copper binding site 3 out
of 4 in 4a2e
Go back to
Copper Binding Sites List in 4a2e
Copper binding site 3 out
of 4 in the Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 3 of Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1520
b:17.3
occ:0.46
|
NE2
|
A:HIS85
|
1.7
|
12.1
|
1.0
|
NE2
|
A:HIS418
|
1.8
|
12.1
|
0.8
|
CD2
|
A:HIS418
|
2.7
|
9.9
|
0.8
|
CE1
|
A:HIS85
|
2.7
|
9.4
|
1.0
|
CD2
|
A:HIS85
|
2.8
|
10.2
|
1.0
|
O
|
A:HOH2138
|
2.8
|
11.7
|
1.0
|
CE1
|
A:HIS418
|
2.9
|
7.7
|
0.8
|
ND1
|
A:HIS87
|
3.4
|
10.7
|
1.0
|
CE1
|
A:HIS420
|
3.4
|
10.2
|
1.0
|
CD2
|
A:HIS418
|
3.4
|
7.0
|
0.2
|
NE2
|
A:HIS420
|
3.4
|
11.6
|
1.0
|
O
|
A:HOH2200
|
3.5
|
24.7
|
1.0
|
ND1
|
A:HIS420
|
3.6
|
9.2
|
1.0
|
CD2
|
A:HIS420
|
3.6
|
11.3
|
1.0
|
CG
|
A:HIS87
|
3.7
|
9.6
|
1.0
|
CE1
|
A:HIS87
|
3.7
|
11.3
|
1.0
|
NE2
|
A:HIS418
|
3.7
|
6.7
|
0.2
|
CG
|
A:HIS420
|
3.8
|
8.6
|
1.0
|
ND1
|
A:HIS85
|
3.8
|
10.4
|
1.0
|
CG
|
A:HIS418
|
3.8
|
7.8
|
0.8
|
CG
|
A:HIS85
|
3.9
|
11.6
|
1.0
|
ND1
|
A:HIS418
|
3.9
|
10.1
|
0.8
|
CU
|
A:CU1518
|
4.0
|
14.4
|
0.8
|
CA
|
A:HIS87
|
4.0
|
7.4
|
1.0
|
NE2
|
A:HIS87
|
4.1
|
11.0
|
1.0
|
CD2
|
A:HIS87
|
4.1
|
10.3
|
1.0
|
CB
|
A:HIS87
|
4.2
|
8.4
|
1.0
|
N
|
A:GLY88
|
4.3
|
8.1
|
1.0
|
CU
|
A:CU1519
|
4.4
|
12.8
|
0.8
|
CA
|
A:HIS420
|
4.6
|
8.7
|
1.0
|
CG
|
A:HIS418
|
4.6
|
6.6
|
0.2
|
C
|
A:HIS87
|
4.6
|
9.7
|
1.0
|
O
|
A:HOH2141
|
4.7
|
12.6
|
1.0
|
CB
|
A:HIS420
|
4.7
|
9.5
|
1.0
|
O
|
A:HOH2516
|
4.9
|
14.2
|
1.0
|
CE1
|
A:HIS418
|
4.9
|
7.4
|
0.2
|
|
Copper binding site 4 out
of 4 in 4a2e
Go back to
Copper Binding Sites List in 4a2e
Copper binding site 4 out
of 4 in the Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 4 of Crystal Structure of A Coriolopsis Gallica Laccase at 1.7 A Resolution pH 5.5 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1521
b:12.7
occ:0.70
|
ND1
|
A:HIS415
|
2.0
|
14.3
|
1.0
|
ND1
|
A:HIS476
|
2.1
|
18.4
|
1.0
|
SG
|
A:CYS471
|
2.2
|
14.2
|
1.0
|
CE1
|
A:HIS415
|
2.9
|
19.4
|
1.0
|
CG
|
A:HIS415
|
3.0
|
14.4
|
1.0
|
CE1
|
A:HIS476
|
3.1
|
20.5
|
1.0
|
CG
|
A:HIS476
|
3.1
|
19.2
|
1.0
|
CB
|
A:CYS471
|
3.3
|
11.2
|
1.0
|
CD1
|
A:ILE473
|
3.4
|
15.4
|
1.0
|
CB
|
A:HIS476
|
3.4
|
16.0
|
1.0
|
CB
|
A:HIS415
|
3.4
|
12.5
|
1.0
|
CD2
|
A:PHE481
|
3.7
|
10.9
|
1.0
|
CB
|
A:ILE473
|
3.8
|
15.8
|
1.0
|
CE2
|
A:PHE481
|
3.9
|
12.8
|
1.0
|
CA
|
A:HIS415
|
4.0
|
12.0
|
1.0
|
CG1
|
A:ILE473
|
4.0
|
15.4
|
1.0
|
NE2
|
A:HIS415
|
4.1
|
14.4
|
1.0
|
CD2
|
A:HIS415
|
4.1
|
11.9
|
1.0
|
NE2
|
A:HIS476
|
4.2
|
18.9
|
1.0
|
CD2
|
A:HIS476
|
4.2
|
15.6
|
1.0
|
CG2
|
A:ILE473
|
4.6
|
16.6
|
1.0
|
CA
|
A:CYS471
|
4.6
|
12.0
|
1.0
|
CD
|
A:PRO416
|
4.7
|
9.7
|
1.0
|
O
|
A:GLY412
|
4.8
|
16.4
|
1.0
|
N
|
A:ILE473
|
4.8
|
17.3
|
1.0
|
CA
|
A:ILE473
|
4.9
|
16.3
|
1.0
|
O
|
A:ILE473
|
4.9
|
16.3
|
1.0
|
CA
|
A:HIS476
|
4.9
|
16.1
|
1.0
|
C
|
A:HIS415
|
4.9
|
10.5
|
1.0
|
CG
|
A:PHE481
|
5.0
|
12.8
|
1.0
|
|
Reference:
E.De La Mora,
J.E.Lovett,
C.F.Blanford,
E.F.Garman,
B.Valderrama,
E.Rudino-Pinera.
Structural Changes Caused By Radiation-Induced Reduction and Radiolysis: the Effect of X-Ray Absorbed Dose in A Fungal Multicopper Oxidase Acta Crystallogr.,Sect.D V. 68 564 2012.
ISSN: ISSN 0907-4449
PubMed: 22525754
DOI: 10.1107/S0907444912005343
Page generated: Wed Jul 31 02:31:14 2024
|