Copper in PDB 4hak: Multicopper Oxidase Cueo Mutant E506A
Protein crystallography data
The structure of Multicopper Oxidase Cueo Mutant E506A, PDB code: 4hak
was solved by
H.Komori,
K.Kataoka,
T.Sakurai,
Y.Higuchi,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
30.20 /
1.40
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
50.439,
90.867,
53.244,
90.00,
102.70,
90.00
|
R / Rfree (%)
|
15.9 /
18.4
|
Copper Binding Sites:
The binding sites of Copper atom in the Multicopper Oxidase Cueo Mutant E506A
(pdb code 4hak). This binding sites where shown within
5.0 Angstroms radius around Copper atom.
In total 4 binding sites of Copper where determined in the
Multicopper Oxidase Cueo Mutant E506A, PDB code: 4hak:
Jump to Copper binding site number:
1;
2;
3;
4;
Copper binding site 1 out
of 4 in 4hak
Go back to
Copper Binding Sites List in 4hak
Copper binding site 1 out
of 4 in the Multicopper Oxidase Cueo Mutant E506A
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 1 of Multicopper Oxidase Cueo Mutant E506A within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1001
b:10.4
occ:1.00
|
ND1
|
A:HIS505
|
2.0
|
9.8
|
1.0
|
ND1
|
A:HIS443
|
2.0
|
9.8
|
1.0
|
SG
|
A:CYS500
|
2.2
|
10.3
|
1.0
|
CE1
|
A:HIS443
|
3.0
|
10.3
|
1.0
|
CE1
|
A:HIS505
|
3.0
|
9.4
|
1.0
|
CG
|
A:HIS505
|
3.0
|
8.8
|
1.0
|
CG
|
A:HIS443
|
3.1
|
9.7
|
1.0
|
CB
|
A:CYS500
|
3.2
|
9.8
|
1.0
|
SD
|
A:MET510
|
3.3
|
11.3
|
1.0
|
CB
|
A:HIS505
|
3.4
|
9.4
|
1.0
|
CB
|
A:HIS443
|
3.4
|
10.0
|
1.0
|
O
|
A:LEU442
|
3.7
|
12.2
|
1.0
|
CA
|
A:HIS443
|
3.7
|
9.8
|
1.0
|
CE
|
A:MET510
|
4.0
|
11.9
|
1.0
|
CB
|
A:LEU502
|
4.1
|
8.7
|
1.0
|
NE2
|
A:HIS443
|
4.1
|
10.6
|
1.0
|
NE2
|
A:HIS505
|
4.1
|
10.3
|
1.0
|
CD2
|
A:HIS505
|
4.1
|
9.5
|
1.0
|
CD2
|
A:HIS443
|
4.2
|
10.3
|
1.0
|
C
|
A:LEU442
|
4.4
|
10.6
|
1.0
|
N
|
A:HIS443
|
4.4
|
9.7
|
1.0
|
CA
|
A:CYS500
|
4.6
|
9.7
|
1.0
|
CG
|
A:MET510
|
4.8
|
12.3
|
1.0
|
CD1
|
A:LEU502
|
4.8
|
10.3
|
1.0
|
O
|
A:LEU502
|
4.9
|
8.3
|
1.0
|
CA
|
A:HIS505
|
4.9
|
8.8
|
1.0
|
C
|
A:HIS443
|
4.9
|
9.7
|
1.0
|
CG
|
A:LEU502
|
4.9
|
8.8
|
1.0
|
N
|
A:LEU502
|
5.0
|
8.4
|
1.0
|
|
Copper binding site 2 out
of 4 in 4hak
Go back to
Copper Binding Sites List in 4hak
Copper binding site 2 out
of 4 in the Multicopper Oxidase Cueo Mutant E506A
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 2 of Multicopper Oxidase Cueo Mutant E506A within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1002
b:16.3
occ:0.70
|
ND1
|
A:HIS103
|
2.0
|
12.7
|
1.0
|
NE2
|
A:HIS141
|
2.1
|
14.8
|
1.0
|
NE2
|
A:HIS501
|
2.1
|
13.4
|
1.0
|
O
|
A:OH1005
|
2.5
|
22.8
|
0.7
|
CE1
|
A:HIS103
|
2.9
|
11.8
|
1.0
|
CE1
|
A:HIS141
|
3.0
|
14.8
|
1.0
|
CG
|
A:HIS103
|
3.0
|
12.3
|
1.0
|
CE1
|
A:HIS501
|
3.1
|
13.9
|
1.0
|
CD2
|
A:HIS141
|
3.1
|
14.1
|
1.0
|
CD2
|
A:HIS501
|
3.1
|
13.8
|
1.0
|
CB
|
A:HIS103
|
3.4
|
12.6
|
1.0
|
CZ2
|
A:TRP139
|
3.8
|
10.2
|
1.0
|
O
|
A:HOH1101
|
4.0
|
23.0
|
0.5
|
CE2
|
A:TRP139
|
4.0
|
9.8
|
1.0
|
NE2
|
A:HIS103
|
4.1
|
11.9
|
1.0
|
CD2
|
A:HIS103
|
4.1
|
11.9
|
1.0
|
NE1
|
A:TRP139
|
4.1
|
10.9
|
1.0
|
ND1
|
A:HIS141
|
4.1
|
13.8
|
1.0
|
CU
|
A:CU1004
|
4.2
|
19.9
|
0.5
|
ND1
|
A:HIS501
|
4.2
|
13.5
|
1.0
|
CG
|
A:HIS141
|
4.2
|
10.7
|
1.0
|
CG
|
A:HIS501
|
4.3
|
11.9
|
1.0
|
CD2
|
A:HIS101
|
4.3
|
17.8
|
1.0
|
CD2
|
A:HIS446
|
4.5
|
15.3
|
1.0
|
CU
|
A:CU1003
|
4.5
|
17.4
|
0.7
|
CH2
|
A:TRP139
|
4.5
|
12.1
|
1.0
|
NE2
|
A:HIS446
|
4.5
|
15.7
|
1.0
|
CA
|
A:HIS103
|
4.6
|
12.5
|
1.0
|
NE2
|
A:HIS101
|
4.7
|
18.8
|
1.0
|
|
Copper binding site 3 out
of 4 in 4hak
Go back to
Copper Binding Sites List in 4hak
Copper binding site 3 out
of 4 in the Multicopper Oxidase Cueo Mutant E506A
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 3 of Multicopper Oxidase Cueo Mutant E506A within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1003
b:17.4
occ:0.70
|
NE2
|
A:HIS448
|
2.0
|
17.7
|
1.0
|
NE2
|
A:HIS499
|
2.0
|
14.7
|
1.0
|
NE2
|
A:HIS143
|
2.0
|
19.4
|
1.0
|
O
|
A:OH1005
|
2.1
|
22.8
|
0.7
|
CE1
|
A:HIS448
|
2.9
|
19.7
|
1.0
|
CD2
|
A:HIS499
|
2.9
|
14.4
|
1.0
|
CE1
|
A:HIS499
|
3.0
|
15.6
|
1.0
|
CD2
|
A:HIS143
|
3.0
|
18.6
|
1.0
|
CD2
|
A:HIS448
|
3.0
|
17.3
|
1.0
|
CE1
|
A:HIS143
|
3.0
|
19.1
|
1.0
|
O
|
A:HOH1101
|
3.6
|
23.0
|
0.5
|
CD2
|
A:HIS446
|
3.6
|
15.3
|
1.0
|
CU
|
A:CU1004
|
3.7
|
19.9
|
0.5
|
NE2
|
A:HIS101
|
3.9
|
18.8
|
1.0
|
CD2
|
A:HIS101
|
4.0
|
17.8
|
1.0
|
ND1
|
A:HIS448
|
4.0
|
18.0
|
1.0
|
ND1
|
A:HIS499
|
4.1
|
13.8
|
1.0
|
CG
|
A:HIS499
|
4.1
|
13.1
|
1.0
|
CG
|
A:HIS448
|
4.1
|
15.6
|
1.0
|
ND1
|
A:HIS143
|
4.1
|
18.5
|
1.0
|
NE2
|
A:HIS446
|
4.2
|
15.7
|
1.0
|
CG
|
A:HIS143
|
4.2
|
16.4
|
1.0
|
CU
|
A:CU1002
|
4.5
|
16.3
|
0.7
|
CE1
|
A:HIS101
|
4.7
|
18.6
|
1.0
|
CB
|
A:MET497
|
4.7
|
15.6
|
1.0
|
CG
|
A:HIS101
|
4.7
|
15.9
|
1.0
|
O
|
A:HOH1102
|
4.9
|
26.9
|
0.5
|
CG
|
A:HIS446
|
4.9
|
13.3
|
1.0
|
CD2
|
A:HIS501
|
4.9
|
13.8
|
1.0
|
CE1
|
A:HIS141
|
4.9
|
14.8
|
1.0
|
NE2
|
A:HIS501
|
5.0
|
13.4
|
1.0
|
|
Copper binding site 4 out
of 4 in 4hak
Go back to
Copper Binding Sites List in 4hak
Copper binding site 4 out
of 4 in the Multicopper Oxidase Cueo Mutant E506A
Mono view
Stereo pair view
|
A full contact list of Copper with other atoms in the Cu binding
site number 4 of Multicopper Oxidase Cueo Mutant E506A within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cu1004
b:19.9
occ:0.50
|
NE2
|
A:HIS446
|
1.9
|
15.7
|
1.0
|
NE2
|
A:HIS101
|
2.0
|
18.8
|
1.0
|
OXT
|
A:ACT1006
|
2.2
|
31.4
|
0.5
|
O
|
A:HOH1104
|
2.4
|
19.9
|
0.5
|
CD2
|
A:HIS446
|
2.9
|
15.3
|
1.0
|
CE1
|
A:HIS101
|
2.9
|
18.6
|
1.0
|
CE1
|
A:HIS446
|
3.0
|
15.6
|
1.0
|
CD2
|
A:HIS101
|
3.0
|
17.8
|
1.0
|
CD2
|
A:HIS448
|
3.2
|
17.3
|
1.0
|
NE2
|
A:HIS448
|
3.3
|
17.7
|
1.0
|
C
|
A:ACT1006
|
3.4
|
31.2
|
0.5
|
CA
|
A:HIS103
|
3.5
|
12.5
|
1.0
|
CG
|
A:HIS103
|
3.5
|
12.3
|
1.0
|
O
|
A:OH1005
|
3.6
|
22.8
|
0.7
|
CU
|
A:CU1003
|
3.7
|
17.4
|
0.7
|
CB
|
A:HIS103
|
3.7
|
12.6
|
1.0
|
ND1
|
A:HIS103
|
3.7
|
12.7
|
1.0
|
CG
|
A:HIS448
|
3.8
|
15.6
|
1.0
|
CE1
|
A:HIS448
|
3.9
|
19.7
|
1.0
|
CG
|
A:HIS446
|
4.0
|
13.3
|
1.0
|
ND1
|
A:HIS101
|
4.0
|
18.5
|
1.0
|
ND1
|
A:HIS446
|
4.0
|
15.2
|
1.0
|
O
|
A:ACT1006
|
4.1
|
31.3
|
0.5
|
CD2
|
A:HIS103
|
4.1
|
11.9
|
1.0
|
CG
|
A:HIS101
|
4.1
|
15.9
|
1.0
|
CU
|
A:CU1002
|
4.2
|
16.3
|
0.7
|
ND1
|
A:HIS448
|
4.2
|
18.0
|
1.0
|
N
|
A:GLY104
|
4.2
|
13.1
|
1.0
|
CE1
|
A:HIS103
|
4.3
|
11.8
|
1.0
|
N
|
A:HIS103
|
4.3
|
12.4
|
1.0
|
C
|
A:HIS103
|
4.4
|
12.4
|
1.0
|
NE2
|
A:HIS103
|
4.5
|
11.9
|
1.0
|
CH3
|
A:ACT1006
|
4.5
|
31.2
|
0.5
|
CA
|
A:HIS448
|
4.5
|
13.9
|
1.0
|
CB
|
A:HIS448
|
4.7
|
15.0
|
1.0
|
O
|
A:TRP102
|
4.8
|
14.0
|
1.0
|
O
|
A:HOH1106
|
4.8
|
9.9
|
0.5
|
O
|
A:HOH1105
|
4.8
|
19.4
|
0.5
|
C
|
A:TRP102
|
4.9
|
13.0
|
1.0
|
N
|
A:HIS448
|
4.9
|
13.6
|
1.0
|
|
Reference:
H.Komori,
K.Kataoka,
T.Sakurai,
Y.Higuchi.
Multicopper Oxidase Cueo Mutant E506A To Be Published.
Page generated: Wed Jul 31 03:00:47 2024
|