Copper in PDB 5zll: Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0
Protein crystallography data
The structure of Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0, PDB code: 5zll
was solved by
T.Xie,
Z.C.Liu,
G.G.Wang,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
29.90 /
2.60
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
101.827,
101.827,
135.439,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
17 /
21.5
|
Copper Binding Sites:
The binding sites of Copper atom in the Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0
(pdb code 5zll). This binding sites where shown within
5.0 Angstroms radius around Copper atom.
In total 3 binding sites of Copper where determined in the
Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0, PDB code: 5zll:
Jump to Copper binding site number:
1;
2;
3;
Copper binding site 1 out
of 3 in 5zll
Go back to
Copper Binding Sites List in 5zll
Copper binding site 1 out
of 3 in the Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 1 of Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu601
b:27.9
occ:0.85
|
ND1
|
A:HIS419
|
2.0
|
31.3
|
1.0
|
ND1
|
A:HIS497
|
2.0
|
27.2
|
1.0
|
SG
|
A:CYS492
|
2.3
|
31.1
|
1.0
|
CE1
|
A:HIS419
|
2.8
|
30.7
|
1.0
|
CE1
|
A:HIS497
|
3.0
|
26.9
|
1.0
|
CG
|
A:HIS497
|
3.0
|
26.1
|
1.0
|
CG
|
A:HIS419
|
3.1
|
31.1
|
1.0
|
SD
|
A:MET502
|
3.2
|
23.5
|
1.0
|
CB
|
A:CYS492
|
3.3
|
26.2
|
1.0
|
CB
|
A:HIS497
|
3.4
|
26.6
|
1.0
|
CB
|
A:HIS419
|
3.6
|
29.3
|
1.0
|
CE
|
A:MET502
|
3.7
|
25.6
|
1.0
|
CD1
|
A:ILE494
|
4.0
|
25.0
|
1.0
|
NE2
|
A:HIS419
|
4.0
|
28.7
|
1.0
|
NE2
|
A:HIS497
|
4.1
|
26.5
|
1.0
|
CB
|
A:ILE494
|
4.1
|
26.3
|
1.0
|
CD2
|
A:HIS497
|
4.2
|
25.6
|
1.0
|
CD2
|
A:HIS419
|
4.2
|
30.8
|
1.0
|
CA
|
A:HIS419
|
4.3
|
27.4
|
1.0
|
CG1
|
A:ILE494
|
4.5
|
25.3
|
1.0
|
CA
|
A:CYS492
|
4.7
|
26.7
|
1.0
|
CD
|
A:PRO420
|
4.7
|
26.4
|
1.0
|
CG
|
A:MET502
|
4.7
|
24.8
|
1.0
|
CG2
|
A:ILE494
|
4.8
|
25.6
|
1.0
|
O
|
A:HOH712
|
4.9
|
30.1
|
1.0
|
N
|
A:ILE494
|
4.9
|
25.7
|
1.0
|
CA
|
A:HIS497
|
4.9
|
27.3
|
1.0
|
O
|
A:THR418
|
4.9
|
23.6
|
1.0
|
O
|
A:ILE494
|
5.0
|
29.1
|
1.0
|
|
Copper binding site 2 out
of 3 in 5zll
Go back to
Copper Binding Sites List in 5zll
Copper binding site 2 out
of 3 in the Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 2 of Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu602
b:34.6
occ:0.29
|
NE2
|
A:HIS424
|
1.8
|
21.4
|
1.0
|
NE2
|
A:HIS491
|
1.9
|
33.1
|
1.0
|
NE2
|
A:HIS155
|
2.5
|
30.5
|
1.0
|
CE1
|
A:HIS424
|
2.6
|
22.4
|
1.0
|
CD2
|
A:HIS491
|
2.7
|
31.5
|
1.0
|
CD2
|
A:HIS424
|
2.9
|
22.6
|
1.0
|
CE1
|
A:HIS491
|
3.0
|
32.4
|
1.0
|
CD2
|
A:HIS155
|
3.3
|
30.8
|
1.0
|
CD2
|
A:HIS422
|
3.4
|
23.9
|
1.0
|
CE1
|
A:HIS155
|
3.6
|
31.2
|
1.0
|
O
|
A:HOH838
|
3.7
|
42.9
|
1.0
|
CU
|
A:CU603
|
3.8
|
27.8
|
0.3
|
ND1
|
A:HIS424
|
3.8
|
23.1
|
1.0
|
CD2
|
A:HIS105
|
3.9
|
19.9
|
1.0
|
CG
|
A:HIS491
|
3.9
|
28.8
|
1.0
|
CG
|
A:HIS424
|
3.9
|
22.9
|
1.0
|
NE2
|
A:HIS422
|
3.9
|
25.1
|
1.0
|
NE2
|
A:HIS105
|
3.9
|
20.0
|
1.0
|
CG2
|
A:VAL489
|
3.9
|
27.4
|
1.0
|
ND1
|
A:HIS491
|
4.0
|
31.7
|
1.0
|
CG
|
A:HIS155
|
4.5
|
26.9
|
1.0
|
CG
|
A:HIS105
|
4.6
|
19.7
|
1.0
|
CG
|
A:HIS422
|
4.6
|
24.4
|
1.0
|
ND1
|
A:HIS155
|
4.6
|
31.1
|
1.0
|
CE1
|
A:HIS105
|
4.7
|
20.7
|
1.0
|
O
|
A:HOH836
|
4.8
|
41.1
|
1.0
|
OE2
|
A:GLU498
|
5.0
|
38.4
|
1.0
|
CE1
|
A:HIS107
|
5.0
|
21.0
|
1.0
|
|
Copper binding site 3 out
of 3 in 5zll
Go back to
Copper Binding Sites List in 5zll
Copper binding site 3 out
of 3 in the Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 3 of Mutation in the Trinuclear Site of Cota-Laccase: H493C Mutant, pH 8.0 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu603
b:27.8
occ:0.26
|
NE2
|
A:HIS422
|
1.8
|
25.1
|
1.0
|
NE2
|
A:HIS105
|
1.9
|
20.0
|
1.0
|
CE1
|
A:HIS422
|
2.7
|
25.5
|
1.0
|
CD2
|
A:HIS422
|
2.8
|
23.9
|
1.0
|
CD2
|
A:HIS105
|
2.8
|
19.9
|
1.0
|
O
|
A:HOH752
|
2.9
|
20.8
|
1.0
|
CE1
|
A:HIS105
|
3.0
|
20.7
|
1.0
|
CG
|
A:HIS107
|
3.2
|
19.6
|
1.0
|
ND1
|
A:HIS107
|
3.4
|
20.2
|
1.0
|
CD2
|
A:HIS107
|
3.4
|
19.3
|
1.0
|
CA
|
A:HIS107
|
3.4
|
19.1
|
1.0
|
NE2
|
A:HIS424
|
3.6
|
21.4
|
1.0
|
CD2
|
A:HIS424
|
3.6
|
22.6
|
1.0
|
CE1
|
A:HIS107
|
3.7
|
21.0
|
1.0
|
NE2
|
A:HIS107
|
3.7
|
20.2
|
1.0
|
CB
|
A:HIS107
|
3.8
|
18.6
|
1.0
|
CU
|
A:CU602
|
3.8
|
34.6
|
0.3
|
ND1
|
A:HIS422
|
3.8
|
25.8
|
1.0
|
N
|
A:GLY108
|
3.8
|
19.3
|
1.0
|
CG
|
A:HIS422
|
3.8
|
24.4
|
1.0
|
CE1
|
A:HIS424
|
3.9
|
22.4
|
1.0
|
CG
|
A:HIS105
|
4.0
|
19.7
|
1.0
|
CG
|
A:HIS424
|
4.0
|
22.9
|
1.0
|
ND1
|
A:HIS105
|
4.0
|
21.1
|
1.0
|
ND1
|
A:HIS424
|
4.1
|
23.1
|
1.0
|
C
|
A:HIS107
|
4.1
|
19.5
|
1.0
|
N
|
A:HIS107
|
4.5
|
18.4
|
1.0
|
CA
|
A:HIS424
|
4.6
|
22.6
|
1.0
|
O
|
A:LEU106
|
4.6
|
19.0
|
1.0
|
CB
|
A:HIS424
|
4.8
|
23.1
|
1.0
|
O
|
A:HOH798
|
4.9
|
19.8
|
1.0
|
C
|
A:LEU106
|
4.9
|
19.3
|
1.0
|
O
|
A:HOH750
|
4.9
|
17.3
|
1.0
|
|
Reference:
T.Xie,
Z.Liu,
G.Wang.
Structural Insight Into the Allosteric Coupling of CU1 Site and Trinuclear Cu Cluster in Cota Laccase Chembiochem 2018.
ISSN: ESSN 1439-7633
PubMed: 29722464
DOI: 10.1002/CBIC.201800236
Page generated: Wed Jul 31 05:36:32 2024
|