Copper in PDB 7bdn: Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
Protein crystallography data
The structure of Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form, PDB code: 7bdn
was solved by
K.Zovo,
S.Majumdar,
T.Lukk,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
29.50 /
2.70
|
Space group
|
P 21 3
|
Cell size a, b, c (Å), α, β, γ (°)
|
176.981,
176.981,
176.981,
90,
90,
90
|
R / Rfree (%)
|
20 /
22.2
|
Copper Binding Sites:
The binding sites of Copper atom in the Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
(pdb code 7bdn). 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 the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form, PDB code: 7bdn:
Jump to Copper binding site number:
1;
2;
3;
4;
5;
6;
Copper binding site 1 out
of 6 in 7bdn
Go back to
Copper Binding Sites List in 7bdn
Copper binding site 1 out
of 6 in the Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 1 of Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu401
b:45.6
occ:1.00
|
NE2
|
A:HIS104
|
2.1
|
32.3
|
1.0
|
NE2
|
A:HIS156
|
2.2
|
37.4
|
1.0
|
CE1
|
A:HIS102
|
2.9
|
36.0
|
1.0
|
CE1
|
A:HIS156
|
3.0
|
34.3
|
1.0
|
CE1
|
A:HIS104
|
3.0
|
31.3
|
1.0
|
CD2
|
A:HIS104
|
3.2
|
30.2
|
1.0
|
CD2
|
A:HIS156
|
3.3
|
33.0
|
1.0
|
ND1
|
A:HIS102
|
3.3
|
35.2
|
1.0
|
CU
|
A:CU402
|
3.4
|
75.3
|
1.0
|
NE2
|
A:HIS102
|
4.1
|
42.2
|
1.0
|
ND1
|
A:HIS156
|
4.1
|
32.0
|
1.0
|
ND1
|
A:HIS104
|
4.2
|
33.6
|
1.0
|
O
|
A:HOH592
|
4.2
|
34.3
|
1.0
|
CG
|
A:HIS104
|
4.3
|
31.6
|
1.0
|
CG
|
A:HIS156
|
4.3
|
34.0
|
1.0
|
CG
|
A:HIS102
|
4.6
|
39.0
|
1.0
|
CB
|
A:ALA266
|
4.7
|
27.4
|
1.0
|
CE1
|
A:HIS154
|
4.7
|
28.3
|
1.0
|
|
Copper binding site 2 out
of 6 in 7bdn
Go back to
Copper Binding Sites List in 7bdn
Copper binding site 2 out
of 6 in the Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 2 of Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu402
b:75.3
occ:1.00
|
NE2
|
A:HIS158
|
2.6
|
38.7
|
1.0
|
O
|
A:HOH592
|
3.3
|
34.3
|
1.0
|
CD2
|
A:HIS158
|
3.4
|
35.8
|
1.0
|
CU
|
A:CU401
|
3.4
|
45.6
|
1.0
|
CE1
|
A:HIS102
|
3.6
|
36.0
|
1.0
|
CE1
|
A:HIS158
|
3.6
|
36.1
|
1.0
|
NE2
|
A:HIS102
|
3.9
|
42.2
|
1.0
|
ND1
|
A:HIS102
|
4.2
|
35.2
|
1.0
|
CG
|
A:HIS158
|
4.5
|
37.2
|
1.0
|
ND1
|
A:HIS158
|
4.6
|
37.0
|
1.0
|
CD2
|
A:HIS102
|
4.6
|
38.2
|
1.0
|
CE1
|
A:HIS156
|
4.7
|
34.3
|
1.0
|
NE2
|
A:HIS156
|
4.8
|
37.4
|
1.0
|
CG
|
A:HIS102
|
4.8
|
39.0
|
1.0
|
|
Copper binding site 3 out
of 6 in 7bdn
Go back to
Copper Binding Sites List in 7bdn
Copper binding site 3 out
of 6 in the Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 3 of Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu403
b:34.6
occ:1.00
|
ND1
|
A:HIS231
|
2.0
|
31.7
|
1.0
|
ND1
|
A:HIS293
|
2.1
|
30.5
|
1.0
|
SG
|
A:CYS288
|
2.2
|
33.2
|
1.0
|
CG
|
A:HIS231
|
2.9
|
31.0
|
1.0
|
CE1
|
A:HIS231
|
3.0
|
29.7
|
1.0
|
CG
|
A:HIS293
|
3.0
|
34.3
|
1.0
|
CE1
|
A:HIS293
|
3.1
|
33.9
|
1.0
|
CB
|
A:CYS288
|
3.1
|
31.8
|
1.0
|
CB
|
A:HIS231
|
3.2
|
28.2
|
1.0
|
CB
|
A:HIS293
|
3.3
|
31.7
|
1.0
|
SD
|
A:MET298
|
3.5
|
36.0
|
1.0
|
CA
|
A:HIS231
|
3.7
|
28.6
|
1.0
|
CE
|
A:MET298
|
3.7
|
30.2
|
1.0
|
CD2
|
A:HIS231
|
4.1
|
31.9
|
1.0
|
NE2
|
A:HIS231
|
4.1
|
33.4
|
1.0
|
O
|
A:TYR230
|
4.1
|
29.2
|
1.0
|
NE2
|
A:HIS293
|
4.2
|
32.9
|
1.0
|
CD2
|
A:HIS293
|
4.2
|
36.2
|
1.0
|
CG2
|
A:VAL290
|
4.2
|
27.6
|
1.0
|
CB
|
A:VAL290
|
4.2
|
30.3
|
1.0
|
CA
|
A:CYS288
|
4.5
|
31.1
|
1.0
|
N
|
A:THR232
|
4.6
|
28.2
|
1.0
|
N
|
A:HIS231
|
4.7
|
29.9
|
1.0
|
C
|
A:HIS231
|
4.7
|
27.6
|
1.0
|
C
|
A:TYR230
|
4.8
|
29.6
|
1.0
|
CA
|
A:HIS293
|
4.8
|
30.8
|
1.0
|
CD2
|
A:PHE195
|
4.9
|
33.1
|
1.0
|
|
Copper binding site 4 out
of 6 in 7bdn
Go back to
Copper Binding Sites List in 7bdn
Copper binding site 4 out
of 6 in the Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 4 of Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu401
b:45.2
occ:1.00
|
NE2
|
B:HIS104
|
2.1
|
32.5
|
1.0
|
NE2
|
B:HIS156
|
2.2
|
36.1
|
1.0
|
CE1
|
B:HIS102
|
2.8
|
36.3
|
1.0
|
CE1
|
B:HIS156
|
2.9
|
33.9
|
1.0
|
CE1
|
B:HIS104
|
3.1
|
30.5
|
1.0
|
CD2
|
B:HIS104
|
3.1
|
31.4
|
1.0
|
ND1
|
B:HIS102
|
3.3
|
34.1
|
1.0
|
CD2
|
B:HIS156
|
3.3
|
31.1
|
1.0
|
CU
|
B:CU402
|
3.5
|
77.7
|
1.0
|
NE2
|
B:HIS102
|
4.0
|
41.3
|
1.0
|
ND1
|
B:HIS156
|
4.1
|
30.9
|
1.0
|
ND1
|
B:HIS104
|
4.2
|
33.4
|
1.0
|
CG
|
B:HIS104
|
4.2
|
32.0
|
1.0
|
O
|
B:HOH600
|
4.3
|
34.9
|
1.0
|
CG
|
B:HIS156
|
4.3
|
33.3
|
1.0
|
CG
|
B:HIS102
|
4.6
|
38.8
|
1.0
|
CB
|
B:ALA266
|
4.7
|
27.3
|
1.0
|
CE1
|
B:HIS154
|
4.7
|
27.5
|
1.0
|
CD2
|
B:HIS102
|
4.9
|
37.5
|
1.0
|
|
Copper binding site 5 out
of 6 in 7bdn
Go back to
Copper Binding Sites List in 7bdn
Copper binding site 5 out
of 6 in the Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 5 of Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu402
b:77.7
occ:1.00
|
NE2
|
B:HIS158
|
2.6
|
39.6
|
1.0
|
CD2
|
B:HIS158
|
3.4
|
34.1
|
1.0
|
O
|
B:HOH600
|
3.4
|
34.9
|
1.0
|
CU
|
B:CU401
|
3.5
|
45.2
|
1.0
|
CE1
|
B:HIS158
|
3.6
|
34.3
|
1.0
|
CE1
|
B:HIS102
|
3.7
|
36.3
|
1.0
|
NE2
|
B:HIS102
|
3.9
|
41.3
|
1.0
|
ND1
|
B:HIS102
|
4.2
|
34.1
|
1.0
|
CG
|
B:HIS158
|
4.5
|
35.3
|
1.0
|
ND1
|
B:HIS158
|
4.6
|
36.2
|
1.0
|
CD2
|
B:HIS102
|
4.7
|
37.5
|
1.0
|
CE1
|
B:HIS156
|
4.8
|
33.9
|
1.0
|
CG
|
B:HIS102
|
4.8
|
38.8
|
1.0
|
CD2
|
B:HIS164
|
4.9
|
35.0
|
1.0
|
NE2
|
B:HIS156
|
5.0
|
36.1
|
1.0
|
|
Copper binding site 6 out
of 6 in 7bdn
Go back to
Copper Binding Sites List in 7bdn
Copper binding site 6 out
of 6 in the Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 6 of Structure of the Streptomyces Coelicolor Small Laccase - Cubic Crystal Form within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu403
b:36.0
occ:1.00
|
ND1
|
B:HIS231
|
2.0
|
31.9
|
1.0
|
ND1
|
B:HIS293
|
2.0
|
28.9
|
1.0
|
SG
|
B:CYS288
|
2.1
|
32.8
|
1.0
|
CG
|
B:HIS231
|
3.0
|
31.7
|
1.0
|
CE1
|
B:HIS231
|
3.0
|
28.8
|
1.0
|
CG
|
B:HIS293
|
3.0
|
34.1
|
1.0
|
CE1
|
B:HIS293
|
3.0
|
34.2
|
1.0
|
CB
|
B:CYS288
|
3.1
|
31.9
|
1.0
|
CB
|
B:HIS231
|
3.3
|
27.4
|
1.0
|
CB
|
B:HIS293
|
3.3
|
31.0
|
1.0
|
SD
|
B:MET298
|
3.5
|
37.0
|
1.0
|
CA
|
B:HIS231
|
3.7
|
28.1
|
1.0
|
CE
|
B:MET298
|
3.7
|
29.6
|
1.0
|
O
|
B:TYR230
|
4.1
|
28.2
|
1.0
|
NE2
|
B:HIS231
|
4.1
|
32.5
|
1.0
|
CD2
|
B:HIS231
|
4.1
|
32.6
|
1.0
|
NE2
|
B:HIS293
|
4.1
|
31.7
|
1.0
|
CD2
|
B:HIS293
|
4.1
|
35.6
|
1.0
|
CB
|
B:VAL290
|
4.2
|
30.4
|
1.0
|
CG2
|
B:VAL290
|
4.2
|
26.4
|
1.0
|
CA
|
B:CYS288
|
4.5
|
29.7
|
1.0
|
N
|
B:THR232
|
4.7
|
28.0
|
1.0
|
N
|
B:HIS231
|
4.7
|
30.0
|
1.0
|
C
|
B:HIS231
|
4.8
|
27.2
|
1.0
|
CA
|
B:HIS293
|
4.8
|
30.5
|
1.0
|
C
|
B:TYR230
|
4.8
|
29.2
|
1.0
|
CD2
|
B:PHE195
|
4.9
|
31.1
|
1.0
|
|
Reference:
K.Zovo,
H.Pupart,
A.Van Wieren,
R.E.Gillilan,
Q.Huang,
S.Majumdar,
T.Lukk.
Substitution of the Methionine Axial Ligand of the T1 Copper For the Fungal-Like Phenylalanine Ligand (M298F) Causes Local Structural Perturbations That Lead to Thermal Instability and Reduced Catalytic Efficiency of the Small Laccase From Streptomyces Coelicolor A3(2). Acs Omega V. 7 6184 2022.
ISSN: ESSN 2470-1343
PubMed: 35224382
DOI: 10.1021/ACSOMEGA.1C06668
Page generated: Wed Jul 31 08:22:01 2024
|