Copper in PDB 4j6t: Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant
Enzymatic activity of Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant
All present enzymatic activity of Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant:
1.14.18.1;
Protein crystallography data
The structure of Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant, PDB code: 4j6t
was solved by
M.Kanteev,
M.Goldfeder,
N.Adir,
A.Fishman,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
27.48 /
2.43
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
55.010,
78.810,
84.340,
90.00,
106.62,
90.00
|
R / Rfree (%)
|
19.6 /
23.7
|
Copper Binding Sites:
The binding sites of Copper atom in the Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant
(pdb code 4j6t). 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 F197A Mutant, PDB code: 4j6t:
Jump to Copper binding site number:
1;
2;
3;
4;
Copper binding site 1 out
of 4 in 4j6t
Go back to
Copper Binding Sites List in 4j6t
Copper binding site 1 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant
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 F197A Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu401
b:35.3
occ:0.80
|
NE2
|
A:HIS60
|
2.0
|
28.0
|
1.0
|
NE2
|
A:HIS42
|
2.2
|
24.5
|
1.0
|
NE2
|
A:HIS69
|
2.3
|
20.4
|
1.0
|
O
|
A:HOH575
|
2.7
|
28.4
|
1.0
|
CD2
|
A:HIS60
|
3.0
|
26.3
|
1.0
|
CE1
|
A:HIS69
|
3.0
|
20.6
|
1.0
|
CE1
|
A:HIS42
|
3.0
|
22.9
|
1.0
|
CU
|
A:CU402
|
3.0
|
58.5
|
0.7
|
CE1
|
A:HIS60
|
3.1
|
26.5
|
1.0
|
CD2
|
A:HIS42
|
3.2
|
21.2
|
1.0
|
CD2
|
A:HIS69
|
3.4
|
19.7
|
1.0
|
CZ
|
A:PHE227
|
3.7
|
17.1
|
1.0
|
NE2
|
A:HIS231
|
3.8
|
19.4
|
1.0
|
CE2
|
A:PHE227
|
4.0
|
18.7
|
1.0
|
CE1
|
A:HIS231
|
4.1
|
19.3
|
1.0
|
ND1
|
A:HIS42
|
4.2
|
23.0
|
1.0
|
CG
|
A:HIS60
|
4.2
|
28.0
|
1.0
|
ND1
|
A:HIS60
|
4.2
|
26.1
|
1.0
|
ND1
|
A:HIS69
|
4.2
|
22.4
|
1.0
|
O
|
A:HOH580
|
4.3
|
31.4
|
1.0
|
CG
|
A:HIS42
|
4.3
|
22.7
|
1.0
|
CG1
|
A:VAL218
|
4.3
|
31.7
|
1.0
|
CG
|
A:HIS69
|
4.4
|
21.5
|
1.0
|
NE2
|
A:HIS204
|
4.7
|
20.2
|
1.0
|
CD2
|
A:HIS231
|
4.8
|
18.3
|
1.0
|
CE1
|
A:PHE65
|
4.9
|
20.2
|
1.0
|
CE1
|
A:HIS204
|
5.0
|
20.1
|
1.0
|
|
Copper binding site 2 out
of 4 in 4j6t
Go back to
Copper Binding Sites List in 4j6t
Copper binding site 2 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant
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 F197A Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu402
b:58.5
occ:0.70
|
NE2
|
A:HIS208
|
2.2
|
21.8
|
1.0
|
NE2
|
A:HIS204
|
2.2
|
20.2
|
1.0
|
O
|
A:HOH575
|
2.2
|
28.4
|
1.0
|
NE2
|
A:HIS231
|
2.3
|
19.4
|
1.0
|
CE1
|
A:HIS208
|
2.9
|
22.4
|
1.0
|
CE1
|
A:HIS231
|
3.0
|
19.3
|
1.0
|
CE1
|
A:HIS204
|
3.0
|
20.1
|
1.0
|
CU
|
A:CU401
|
3.0
|
35.3
|
0.8
|
CD2
|
A:HIS208
|
3.3
|
22.5
|
1.0
|
CD2
|
A:HIS204
|
3.4
|
19.1
|
1.0
|
CD2
|
A:HIS231
|
3.4
|
18.3
|
1.0
|
CE2
|
A:PHE227
|
3.6
|
18.7
|
1.0
|
O
|
A:HOH580
|
3.9
|
31.4
|
1.0
|
ND1
|
A:HIS208
|
4.1
|
22.1
|
1.0
|
CZ
|
A:PHE227
|
4.1
|
17.1
|
1.0
|
NE2
|
A:HIS69
|
4.2
|
20.4
|
1.0
|
ND1
|
A:HIS231
|
4.2
|
16.5
|
1.0
|
ND1
|
A:HIS204
|
4.2
|
20.9
|
1.0
|
CG
|
A:HIS208
|
4.3
|
23.2
|
1.0
|
CG
|
A:HIS204
|
4.4
|
20.6
|
1.0
|
CG
|
A:HIS231
|
4.4
|
18.2
|
1.0
|
CE1
|
A:HIS230
|
4.5
|
19.8
|
1.0
|
CD2
|
A:PHE227
|
4.5
|
17.4
|
1.0
|
NE2
|
A:HIS60
|
4.5
|
28.0
|
1.0
|
CD2
|
A:HIS69
|
4.6
|
19.7
|
1.0
|
CE1
|
A:PHE65
|
4.7
|
20.2
|
1.0
|
ND1
|
A:HIS230
|
4.7
|
21.1
|
1.0
|
CD2
|
A:HIS60
|
4.7
|
26.3
|
1.0
|
NE2
|
A:HIS42
|
4.8
|
24.5
|
1.0
|
CE1
|
A:HIS69
|
4.9
|
20.6
|
1.0
|
|
Copper binding site 3 out
of 4 in 4j6t
Go back to
Copper Binding Sites List in 4j6t
Copper binding site 3 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant
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 F197A Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu401
b:40.2
occ:0.80
|
O
|
B:HOH573
|
2.1
|
21.9
|
1.0
|
NE2
|
B:HIS60
|
2.1
|
31.3
|
1.0
|
NE2
|
B:HIS69
|
2.2
|
27.3
|
1.0
|
NE2
|
B:HIS42
|
2.3
|
28.1
|
1.0
|
CE1
|
B:HIS60
|
2.8
|
30.9
|
1.0
|
CE1
|
B:HIS69
|
3.0
|
26.3
|
1.0
|
CD2
|
B:HIS42
|
3.1
|
25.6
|
1.0
|
CD2
|
B:HIS60
|
3.3
|
30.6
|
1.0
|
CD2
|
B:HIS69
|
3.3
|
25.9
|
1.0
|
CE1
|
B:HIS42
|
3.4
|
25.2
|
1.0
|
CU
|
B:CU402
|
3.6
|
68.6
|
0.6
|
CZ
|
B:PHE227
|
3.8
|
23.9
|
1.0
|
NE2
|
B:HIS231
|
3.9
|
25.3
|
1.0
|
ND1
|
B:HIS60
|
4.0
|
30.1
|
1.0
|
ND1
|
B:HIS69
|
4.2
|
27.5
|
1.0
|
CE1
|
B:HIS231
|
4.2
|
24.7
|
1.0
|
CE2
|
B:PHE227
|
4.2
|
24.1
|
1.0
|
CG
|
B:HIS60
|
4.3
|
30.2
|
1.0
|
CG
|
B:HIS42
|
4.3
|
25.0
|
1.0
|
CG
|
B:HIS69
|
4.3
|
25.7
|
1.0
|
ND1
|
B:HIS42
|
4.4
|
25.3
|
1.0
|
CG1
|
B:VAL218
|
4.5
|
38.6
|
1.0
|
CD2
|
B:HIS231
|
4.9
|
24.6
|
1.0
|
O
|
B:ALA59
|
5.0
|
25.2
|
1.0
|
CE1
|
B:PHE65
|
5.0
|
32.2
|
1.0
|
|
Copper binding site 4 out
of 4 in 4j6t
Go back to
Copper Binding Sites List in 4j6t
Copper binding site 4 out
of 4 in the Crystal Structure of Tyrosinase From Bacillus Megaterium F197A Mutant
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 F197A Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cu402
b:68.6
occ:0.60
|
NE2
|
B:HIS231
|
2.1
|
25.3
|
1.0
|
NE2
|
B:HIS204
|
2.1
|
29.9
|
1.0
|
O
|
B:HOH573
|
2.1
|
21.9
|
1.0
|
NE2
|
B:HIS208
|
2.4
|
29.2
|
1.0
|
CE1
|
B:HIS231
|
2.7
|
24.7
|
1.0
|
CE1
|
B:HIS204
|
3.0
|
30.4
|
1.0
|
CD2
|
B:HIS204
|
3.2
|
28.8
|
1.0
|
CD2
|
B:HIS231
|
3.2
|
24.6
|
1.0
|
CE1
|
B:HIS208
|
3.3
|
26.4
|
1.0
|
CD2
|
B:HIS208
|
3.3
|
28.8
|
1.0
|
CU
|
B:CU401
|
3.6
|
40.2
|
0.8
|
CE2
|
B:PHE227
|
3.8
|
24.1
|
1.0
|
ND1
|
B:HIS231
|
3.9
|
23.8
|
1.0
|
ND1
|
B:HIS204
|
4.2
|
31.0
|
1.0
|
CG
|
B:HIS231
|
4.2
|
25.9
|
1.0
|
CZ
|
B:PHE227
|
4.2
|
23.9
|
1.0
|
CG
|
B:HIS204
|
4.3
|
30.1
|
1.0
|
CE1
|
B:HIS230
|
4.3
|
35.3
|
1.0
|
ND1
|
B:HIS208
|
4.4
|
28.4
|
1.0
|
CG
|
B:HIS208
|
4.4
|
26.8
|
1.0
|
ND1
|
B:HIS230
|
4.4
|
34.9
|
1.0
|
NE2
|
B:HIS69
|
4.4
|
27.3
|
1.0
|
CE1
|
B:PHE65
|
4.7
|
32.2
|
1.0
|
CD2
|
B:PHE227
|
4.7
|
22.6
|
1.0
|
NE2
|
B:HIS60
|
4.7
|
31.3
|
1.0
|
CD2
|
B:HIS69
|
4.8
|
25.9
|
1.0
|
|
Reference:
M.Kanteev,
M.Goldfeder,
M.Chojnacki,
N.Adir,
A.Fishman.
The Mechanism of Copper Uptake By Tyrosinase From Bacillus Megaterium. J.Biol.Inorg.Chem. V. 18 895 2013.
ISSN: ISSN 0949-8257
PubMed: 24061559
DOI: 10.1007/S00775-013-1034-0
Page generated: Wed Jul 31 03:06:15 2024
|