Copper in PDB 4hd7: Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4
Enzymatic activity of Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4
All present enzymatic activity of Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4:
1.14.18.1;
Protein crystallography data
The structure of Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4, PDB code: 4hd7
was solved by
M.Goldfeder,
M.Kanteev,
N.Adir,
A.Fishman,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
36.21 /
2.10
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
47.900,
78.670,
85.770,
90.00,
105.91,
90.00
|
R / Rfree (%)
|
25.4 /
28.2
|
Copper Binding Sites:
The binding sites of Copper atom in the Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4
(pdb code 4hd7). 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 Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4, PDB code: 4hd7:
Jump to Copper binding site number:
1;
2;
3;
4;
Copper binding site 1 out
of 4 in 4hd7
Go back to
Copper Binding Sites List in 4hd7
Copper binding site 1 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4
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 Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu401
b:26.4
occ:0.90
|
NE2
|
A:HIS60
|
2.0
|
19.4
|
0.7
|
O
|
A:HOH607
|
2.0
|
30.0
|
1.0
|
NE2
|
A:HIS69
|
2.1
|
9.5
|
1.0
|
NE2
|
A:HIS42
|
2.1
|
19.6
|
1.0
|
CE1
|
A:HIS60
|
2.8
|
18.7
|
0.7
|
CE1
|
A:HIS69
|
2.9
|
12.0
|
1.0
|
CD2
|
A:HIS42
|
2.9
|
17.1
|
1.0
|
CD2
|
A:HIS60
|
3.1
|
18.6
|
0.7
|
CD2
|
A:HIS69
|
3.2
|
12.8
|
1.0
|
CE1
|
A:HIS42
|
3.3
|
20.6
|
1.0
|
CZ
|
A:PHE227
|
3.9
|
15.2
|
1.0
|
CU
|
A:CU402
|
3.9
|
48.2
|
0.7
|
ND1
|
A:HIS60
|
4.0
|
18.7
|
0.7
|
ND1
|
A:HIS69
|
4.1
|
16.0
|
1.0
|
CG
|
A:HIS60
|
4.1
|
18.2
|
0.7
|
CG
|
A:HIS42
|
4.1
|
12.4
|
1.0
|
ND1
|
A:HIS42
|
4.2
|
15.9
|
1.0
|
CG
|
A:HIS69
|
4.3
|
12.5
|
1.0
|
NE2
|
A:HIS231
|
4.3
|
20.2
|
1.0
|
CE2
|
A:PHE227
|
4.3
|
11.3
|
1.0
|
CE1
|
A:HIS231
|
4.4
|
18.2
|
1.0
|
O
|
A:ALA59
|
4.4
|
14.8
|
1.0
|
CZ3
|
A:TRP68
|
4.7
|
14.7
|
1.0
|
CB
|
A:ALA59
|
4.7
|
18.4
|
1.0
|
CE3
|
A:TRP68
|
5.0
|
14.1
|
1.0
|
|
Copper binding site 2 out
of 4 in 4hd7
Go back to
Copper Binding Sites List in 4hd7
Copper binding site 2 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4
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 Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu402
b:48.2
occ:0.73
|
NE2
|
A:HIS204
|
2.0
|
11.8
|
1.0
|
NE2
|
A:HIS231
|
2.2
|
20.2
|
1.0
|
O
|
A:HOH607
|
2.2
|
30.0
|
1.0
|
NE2
|
A:HIS208
|
2.3
|
19.1
|
1.0
|
CE1
|
A:HIS204
|
2.7
|
14.2
|
1.0
|
CE1
|
A:HIS231
|
2.9
|
18.2
|
1.0
|
CD2
|
A:HIS204
|
3.1
|
14.2
|
1.0
|
CE1
|
A:HIS208
|
3.1
|
17.1
|
1.0
|
CD2
|
A:HIS208
|
3.3
|
15.2
|
1.0
|
CD2
|
A:HIS231
|
3.4
|
12.4
|
1.0
|
ND1
|
A:HIS204
|
3.9
|
16.3
|
1.0
|
CU
|
A:CU401
|
3.9
|
26.4
|
0.9
|
ND1
|
A:HIS231
|
4.1
|
13.2
|
1.0
|
CG
|
A:HIS204
|
4.2
|
13.0
|
1.0
|
CE2
|
A:PHE227
|
4.2
|
11.3
|
1.0
|
ND1
|
A:HIS208
|
4.3
|
19.4
|
1.0
|
CE1
|
A:HIS230
|
4.3
|
13.6
|
1.0
|
CG
|
A:HIS208
|
4.4
|
14.6
|
1.0
|
CG
|
A:HIS231
|
4.4
|
13.3
|
1.0
|
NE2
|
A:HIS69
|
4.4
|
9.5
|
1.0
|
ND1
|
A:HIS230
|
4.5
|
15.2
|
1.0
|
CE1
|
A:PHE65
|
4.5
|
11.6
|
1.0
|
CZ
|
A:PHE227
|
4.6
|
15.2
|
1.0
|
NE2
|
A:HIS60
|
4.7
|
19.4
|
0.7
|
CZ
|
A:PHE65
|
4.8
|
14.9
|
1.0
|
CD2
|
A:HIS60
|
4.8
|
18.6
|
0.7
|
CD2
|
A:HIS69
|
4.9
|
12.8
|
1.0
|
CE1
|
A:HIS69
|
4.9
|
12.0
|
1.0
|
|
Copper binding site 3 out
of 4 in 4hd7
Go back to
Copper Binding Sites List in 4hd7
Copper binding site 3 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4
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 Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu401
b:34.7
occ:0.80
|
NE2
|
B:HIS42
|
2.0
|
17.1
|
1.0
|
O
|
B:HOH502
|
2.1
|
26.4
|
1.0
|
NE2
|
B:HIS60
|
2.1
|
24.4
|
1.0
|
NE2
|
B:HIS69
|
2.2
|
18.9
|
1.0
|
CD2
|
B:HIS42
|
2.8
|
16.8
|
1.0
|
CE1
|
B:HIS60
|
2.8
|
23.4
|
1.0
|
CE1
|
B:HIS69
|
3.0
|
15.1
|
1.0
|
CE1
|
B:HIS42
|
3.0
|
22.5
|
1.0
|
CD2
|
B:HIS60
|
3.2
|
17.3
|
1.0
|
CD2
|
B:HIS69
|
3.3
|
15.2
|
1.0
|
CZ
|
B:PHE227
|
3.9
|
16.5
|
1.0
|
ND1
|
B:HIS60
|
4.0
|
20.6
|
1.0
|
CG
|
B:HIS42
|
4.0
|
21.2
|
1.0
|
CU
|
B:CU402
|
4.0
|
48.5
|
0.7
|
ND1
|
B:HIS42
|
4.1
|
20.7
|
1.0
|
CE2
|
B:PHE227
|
4.1
|
16.3
|
1.0
|
CG
|
B:HIS60
|
4.2
|
26.2
|
1.0
|
ND1
|
B:HIS69
|
4.2
|
14.0
|
1.0
|
NE2
|
B:HIS231
|
4.2
|
22.2
|
1.0
|
CG
|
B:HIS69
|
4.4
|
12.5
|
1.0
|
CE1
|
B:HIS231
|
4.5
|
18.6
|
1.0
|
CB
|
B:ALA59
|
5.0
|
20.3
|
1.0
|
O
|
B:ALA59
|
5.0
|
17.1
|
1.0
|
|
Copper binding site 4 out
of 4 in 4hd7
Go back to
Copper Binding Sites List in 4hd7
Copper binding site 4 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4
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 Tyrosinase From Bacillus Megaterium V218G Mutant Soaked in CUSO4 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu402
b:48.5
occ:0.72
|
NE2
|
B:HIS208
|
2.1
|
19.4
|
1.0
|
NE2
|
B:HIS231
|
2.1
|
22.2
|
1.0
|
NE2
|
B:HIS204
|
2.1
|
25.6
|
1.0
|
O
|
B:HOH502
|
2.4
|
26.4
|
1.0
|
CE1
|
B:HIS231
|
2.7
|
18.6
|
1.0
|
CE1
|
B:HIS208
|
3.0
|
17.8
|
1.0
|
CD2
|
B:HIS208
|
3.0
|
21.1
|
1.0
|
CD2
|
B:HIS204
|
3.1
|
18.5
|
1.0
|
CE1
|
B:HIS204
|
3.1
|
21.7
|
1.0
|
CD2
|
B:HIS231
|
3.2
|
19.5
|
1.0
|
ND1
|
B:HIS231
|
3.9
|
15.2
|
1.0
|
CU
|
B:CU401
|
4.0
|
34.7
|
0.8
|
CE1
|
B:HIS230
|
4.0
|
23.0
|
1.0
|
ND1
|
B:HIS208
|
4.1
|
23.1
|
1.0
|
CE2
|
B:PHE227
|
4.1
|
16.3
|
1.0
|
CG
|
B:HIS208
|
4.1
|
24.2
|
1.0
|
ND1
|
B:HIS230
|
4.2
|
25.5
|
1.0
|
ND1
|
B:HIS204
|
4.2
|
20.9
|
1.0
|
CG
|
B:HIS231
|
4.2
|
19.3
|
1.0
|
CG
|
B:HIS204
|
4.2
|
20.4
|
1.0
|
CZ
|
B:PHE227
|
4.4
|
16.5
|
1.0
|
NE2
|
B:HIS69
|
4.5
|
18.9
|
1.0
|
CD2
|
B:HIS69
|
4.7
|
15.2
|
1.0
|
CE1
|
B:PHE65
|
4.7
|
17.8
|
1.0
|
CD2
|
B:PHE227
|
4.8
|
21.5
|
1.0
|
NE2
|
B:HIS60
|
5.0
|
24.4
|
1.0
|
|
Reference:
M.Goldfeder,
M.Kanteev,
N.Adir,
A.Fishman.
Influencing the Monophenolase/Diphenolase Activity Ratio in Tyrosinase. Biochim.Biophys.Acta V.1834 629 2013.
ISSN: ISSN 0006-3002
PubMed: 23305929
DOI: 10.1016/J.BBAPAP.2012.12.021
Page generated: Wed Jul 31 03:01:56 2024
|