Chlorine in PDB 6vdx: Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
Protein crystallography data
The structure of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol, PDB code: 6vdx
was solved by
R.A.Ghiladi,
V.S.De Serrano,
A.Mcguire,
T.Malewschik,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
44.64 /
1.53
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
59.365,
67.585,
67.626,
90,
90,
90
|
R / Rfree (%)
|
16.5 /
23.7
|
Other elements in 6vdx:
The structure of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
(pdb code 6vdx). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 6 binding sites of Chlorine where determined in the
Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol, PDB code: 6vdx:
Jump to Chlorine binding site number:
1;
2;
3;
4;
5;
6;
Chlorine binding site 1 out
of 6 in 6vdx
Go back to
Chlorine Binding Sites List in 6vdx
Chlorine binding site 1 out
of 6 in the Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 1 of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl301
b:48.0
occ:0.85
|
CL2
|
A:T6C301
|
0.0
|
48.0
|
0.8
|
C2
|
A:T6C301
|
1.7
|
31.7
|
0.8
|
C1
|
A:T6C301
|
2.6
|
34.5
|
0.8
|
C3
|
A:T6C301
|
2.7
|
37.3
|
0.8
|
O1
|
A:T6C301
|
2.8
|
33.1
|
0.8
|
OH
|
A:TYR38
|
3.0
|
27.0
|
1.0
|
CG2
|
A:THR56
|
3.2
|
16.8
|
1.0
|
CE2
|
A:TYR38
|
3.3
|
18.8
|
1.0
|
CZ
|
A:TYR38
|
3.5
|
23.4
|
1.0
|
CB
|
A:HIS55
|
3.8
|
16.4
|
1.0
|
O
|
A:PHE52
|
3.8
|
16.0
|
1.0
|
CE2
|
A:PHE21
|
3.9
|
21.1
|
1.0
|
CD1
|
A:PHE52
|
3.9
|
14.2
|
1.0
|
C6
|
A:T6C301
|
3.9
|
44.0
|
0.8
|
C4
|
A:T6C301
|
4.0
|
39.2
|
0.8
|
N
|
A:THR56
|
4.0
|
15.2
|
1.0
|
CA
|
A:PHE52
|
4.1
|
15.3
|
1.0
|
CD2
|
A:PHE21
|
4.2
|
18.1
|
1.0
|
CE1
|
A:PHE52
|
4.2
|
15.6
|
1.0
|
O
|
A:LYS51
|
4.3
|
17.1
|
0.7
|
O1D
|
A:MNR305
|
4.3
|
11.8
|
0.1
|
CB
|
A:THR56
|
4.4
|
15.4
|
1.0
|
CZ
|
A:PHE21
|
4.4
|
22.2
|
1.0
|
C5
|
A:T6C301
|
4.4
|
37.2
|
0.8
|
CA
|
A:THR56
|
4.4
|
14.0
|
1.0
|
CG
|
A:PHE52
|
4.5
|
15.6
|
1.0
|
C
|
A:PHE52
|
4.5
|
15.4
|
1.0
|
CD2
|
A:TYR38
|
4.5
|
20.4
|
1.0
|
C
|
A:HIS55
|
4.6
|
15.1
|
1.0
|
CA
|
A:HIS55
|
4.7
|
16.0
|
1.0
|
O
|
A:LYS51
|
4.7
|
15.0
|
0.3
|
CE1
|
A:TYR38
|
4.8
|
20.5
|
1.0
|
CB
|
A:PHE52
|
4.8
|
16.6
|
1.0
|
CG
|
A:HIS55
|
4.9
|
19.2
|
1.0
|
O2D
|
A:MNR305
|
4.9
|
10.9
|
0.1
|
CG
|
A:PHE21
|
5.0
|
16.0
|
1.0
|
CZ
|
A:PHE52
|
5.0
|
15.0
|
1.0
|
|
Chlorine binding site 2 out
of 6 in 6vdx
Go back to
Chlorine Binding Sites List in 6vdx
Chlorine binding site 2 out
of 6 in the Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 2 of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl301
b:53.9
occ:0.85
|
CL6
|
A:T6C301
|
0.0
|
53.9
|
0.8
|
CGD
|
A:MNR305
|
0.2
|
12.5
|
0.1
|
CBD
|
A:MNR305
|
1.3
|
14.2
|
0.1
|
O2D
|
A:MNR305
|
1.4
|
10.9
|
0.1
|
O1D
|
A:MNR305
|
1.4
|
11.8
|
0.1
|
C6
|
A:T6C301
|
1.7
|
44.0
|
0.8
|
CAD
|
A:MNR305
|
2.4
|
20.3
|
1.0
|
C1
|
A:T6C301
|
2.7
|
34.5
|
0.8
|
C5
|
A:T6C301
|
2.7
|
37.2
|
0.8
|
C3D
|
A:MNR305
|
3.0
|
23.9
|
1.0
|
O1
|
A:T6C301
|
3.0
|
33.1
|
0.8
|
ND1
|
A:HIS55
|
3.3
|
26.6
|
1.0
|
C2D
|
A:MNR305
|
3.7
|
25.8
|
1.0
|
C4D
|
A:MNR305
|
3.8
|
25.0
|
1.0
|
C2
|
A:T6C301
|
4.0
|
31.7
|
0.8
|
CE1
|
A:HIS55
|
4.0
|
22.8
|
1.0
|
C4
|
A:T6C301
|
4.0
|
39.2
|
0.8
|
CHA
|
A:MNR305
|
4.1
|
20.1
|
1.0
|
CMD
|
A:MNR305
|
4.2
|
28.9
|
1.0
|
O
|
A:HOH423
|
4.3
|
37.9
|
1.0
|
CE1
|
A:PHE35
|
4.3
|
23.5
|
1.0
|
CG
|
A:HIS55
|
4.4
|
19.2
|
1.0
|
CD1
|
A:PHE35
|
4.5
|
21.2
|
1.0
|
C3
|
A:T6C301
|
4.5
|
37.3
|
0.8
|
CB
|
A:HIS55
|
4.7
|
16.4
|
1.0
|
C1D
|
A:MNR305
|
4.7
|
24.9
|
1.0
|
ND
|
A:MNR305
|
4.8
|
23.2
|
1.0
|
|
Chlorine binding site 3 out
of 6 in 6vdx
Go back to
Chlorine Binding Sites List in 6vdx
Chlorine binding site 3 out
of 6 in the Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 3 of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl301
b:42.1
occ:0.85
|
CL4
|
A:T6C301
|
0.0
|
42.1
|
0.8
|
C4
|
A:T6C301
|
1.7
|
39.2
|
0.8
|
C5
|
A:T6C301
|
2.7
|
37.2
|
0.8
|
C3
|
A:T6C301
|
2.7
|
37.3
|
0.8
|
NC
|
A:MNR305
|
3.3
|
21.5
|
1.0
|
ND
|
A:MNR305
|
3.3
|
23.2
|
1.0
|
MN
|
A:MNR305
|
3.4
|
22.5
|
1.0
|
C4C
|
A:MNR305
|
3.5
|
26.2
|
1.0
|
CG2
|
A:VAL59
|
3.6
|
16.4
|
1.0
|
C1D
|
A:MNR305
|
3.6
|
24.9
|
1.0
|
CE1
|
A:PHE21
|
3.7
|
25.2
|
1.0
|
CHD
|
A:MNR305
|
3.8
|
23.3
|
1.0
|
CE1
|
A:PHE35
|
3.9
|
23.5
|
1.0
|
CZ
|
A:PHE35
|
3.9
|
23.0
|
1.0
|
C1C
|
A:MNR305
|
3.9
|
20.3
|
1.0
|
C2
|
A:T6C301
|
4.0
|
31.7
|
0.8
|
C4D
|
A:MNR305
|
4.0
|
25.0
|
1.0
|
C6
|
A:T6C301
|
4.0
|
44.0
|
0.8
|
CZ
|
A:PHE21
|
4.1
|
22.2
|
1.0
|
NB
|
A:MNR305
|
4.2
|
20.3
|
1.0
|
CG1
|
A:VAL59
|
4.2
|
16.3
|
1.0
|
NA
|
A:MNR305
|
4.2
|
20.5
|
1.0
|
C3C
|
A:MNR305
|
4.4
|
23.0
|
1.0
|
CB
|
A:VAL59
|
4.4
|
14.6
|
1.0
|
C2D
|
A:MNR305
|
4.5
|
25.8
|
1.0
|
CHA
|
A:MNR305
|
4.5
|
20.1
|
1.0
|
C1
|
A:T6C301
|
4.5
|
34.5
|
0.8
|
CHC
|
A:MNR305
|
4.6
|
23.2
|
1.0
|
C2C
|
A:MNR305
|
4.6
|
19.5
|
1.0
|
C1A
|
A:MNR305
|
4.6
|
22.4
|
1.0
|
CD1
|
A:PHE21
|
4.6
|
20.1
|
1.0
|
C4B
|
A:MNR305
|
4.7
|
22.4
|
1.0
|
C3D
|
A:MNR305
|
4.7
|
23.9
|
1.0
|
O2D
|
A:MNR305
|
4.8
|
10.9
|
0.1
|
|
Chlorine binding site 4 out
of 6 in 6vdx
Go back to
Chlorine Binding Sites List in 6vdx
Chlorine binding site 4 out
of 6 in the Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 4 of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl301
b:50.6
occ:0.75
|
CL2
|
B:T6C301
|
0.0
|
50.6
|
0.8
|
CGD
|
B:MNR304
|
0.5
|
8.2
|
0.2
|
O1D
|
B:MNR304
|
1.2
|
7.3
|
0.2
|
O2D
|
B:MNR304
|
1.5
|
6.9
|
0.2
|
CBD
|
B:MNR304
|
1.6
|
9.8
|
0.2
|
C2
|
B:T6C301
|
1.7
|
33.7
|
0.8
|
CAD
|
B:MNR304
|
2.6
|
15.3
|
1.0
|
C3
|
B:T6C301
|
2.7
|
35.0
|
0.8
|
C1
|
B:T6C301
|
2.7
|
32.3
|
0.8
|
ND1
|
B:HIS55
|
2.9
|
22.4
|
1.0
|
O1
|
B:T6C301
|
3.1
|
36.4
|
0.8
|
C3D
|
B:MNR304
|
3.3
|
16.7
|
1.0
|
O
|
B:HOH413
|
3.5
|
38.4
|
1.0
|
CE1
|
B:HIS55
|
3.7
|
26.6
|
1.0
|
C4
|
B:T6C301
|
4.0
|
26.8
|
0.8
|
C6
|
B:T6C301
|
4.0
|
35.0
|
0.8
|
C4D
|
B:MNR304
|
4.0
|
14.7
|
1.0
|
CG
|
B:HIS55
|
4.1
|
17.8
|
1.0
|
CHA
|
B:MNR304
|
4.1
|
14.5
|
1.0
|
C2D
|
B:MNR304
|
4.1
|
16.1
|
1.0
|
CE1
|
B:PHE35
|
4.3
|
22.9
|
0.4
|
CB
|
B:HIS55
|
4.4
|
16.6
|
1.0
|
CD1
|
B:PHE35
|
4.5
|
18.6
|
0.4
|
C5
|
B:T6C301
|
4.5
|
34.9
|
0.8
|
CMD
|
B:MNR304
|
4.6
|
20.8
|
1.0
|
CD1
|
B:PHE35
|
4.8
|
16.9
|
0.6
|
CE1
|
B:PHE35
|
4.9
|
18.4
|
0.6
|
NE2
|
B:HIS55
|
4.9
|
19.7
|
1.0
|
|
Chlorine binding site 5 out
of 6 in 6vdx
Go back to
Chlorine Binding Sites List in 6vdx
Chlorine binding site 5 out
of 6 in the Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 5 of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl301
b:52.5
occ:0.75
|
CL6
|
B:T6C301
|
0.0
|
52.5
|
0.8
|
C6
|
B:T6C301
|
1.7
|
35.0
|
0.8
|
C1
|
B:T6C301
|
2.6
|
32.3
|
0.8
|
C5
|
B:T6C301
|
2.7
|
34.9
|
0.8
|
O1
|
B:T6C301
|
2.8
|
36.4
|
0.8
|
OH
|
B:TYR38
|
2.9
|
19.1
|
1.0
|
CG2
|
B:THR56
|
3.0
|
15.6
|
1.0
|
CE2
|
B:TYR38
|
3.3
|
17.4
|
1.0
|
CZ
|
B:TYR38
|
3.5
|
17.6
|
1.0
|
CE2
|
B:PHE21
|
3.7
|
13.1
|
0.5
|
CD1
|
B:PHE52
|
3.7
|
14.2
|
1.0
|
O
|
B:PHE52
|
3.7
|
13.8
|
1.0
|
CB
|
B:HIS55
|
3.8
|
16.6
|
1.0
|
N
|
B:THR56
|
3.9
|
11.7
|
1.0
|
C2
|
B:T6C301
|
3.9
|
33.7
|
0.8
|
C4
|
B:T6C301
|
4.0
|
26.8
|
0.8
|
CD2
|
B:PHE21
|
4.0
|
14.6
|
0.5
|
CE1
|
B:PHE52
|
4.0
|
13.9
|
1.0
|
CA
|
B:PHE52
|
4.1
|
18.5
|
1.0
|
CE2
|
B:PHE21
|
4.2
|
15.7
|
0.6
|
CB
|
B:THR56
|
4.3
|
13.0
|
1.0
|
CA
|
B:THR56
|
4.3
|
11.3
|
1.0
|
CD2
|
B:PHE21
|
4.4
|
14.4
|
0.6
|
CZ
|
B:PHE21
|
4.4
|
15.1
|
0.5
|
CG
|
B:PHE52
|
4.4
|
14.0
|
1.0
|
C
|
B:HIS55
|
4.4
|
12.7
|
1.0
|
C
|
B:PHE52
|
4.4
|
15.8
|
1.0
|
C3
|
B:T6C301
|
4.4
|
35.0
|
0.8
|
O
|
B:LYS51
|
4.5
|
20.1
|
0.5
|
O2D
|
B:MNR304
|
4.5
|
6.9
|
0.2
|
CD2
|
B:TYR38
|
4.5
|
17.5
|
1.0
|
CA
|
B:HIS55
|
4.6
|
15.6
|
1.0
|
CZ
|
B:PHE21
|
4.7
|
15.8
|
0.6
|
CE1
|
B:TYR38
|
4.8
|
19.5
|
1.0
|
CB
|
B:PHE52
|
4.8
|
16.2
|
1.0
|
CZ
|
B:PHE52
|
4.8
|
14.2
|
1.0
|
CG
|
B:PHE21
|
4.9
|
13.7
|
0.5
|
O
|
B:LYS51
|
4.9
|
16.9
|
0.5
|
CG
|
B:HIS55
|
4.9
|
17.8
|
1.0
|
OG1
|
B:THR56
|
5.0
|
16.0
|
1.0
|
CG
|
B:PHE21
|
5.0
|
13.6
|
0.6
|
|
Chlorine binding site 6 out
of 6 in 6vdx
Go back to
Chlorine Binding Sites List in 6vdx
Chlorine binding site 6 out
of 6 in the Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 6 of Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate Trichlorophenol within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl301
b:43.4
occ:0.75
|
CL4
|
B:T6C301
|
0.0
|
43.4
|
0.8
|
C4
|
B:T6C301
|
1.7
|
26.8
|
0.8
|
C3
|
B:T6C301
|
2.7
|
35.0
|
0.8
|
C5
|
B:T6C301
|
2.7
|
34.9
|
0.8
|
CG2
|
B:VAL59
|
3.3
|
13.8
|
1.0
|
ND
|
B:MNR304
|
3.3
|
14.9
|
1.0
|
CZ
|
B:PHE21
|
3.4
|
15.8
|
0.6
|
CE1
|
B:PHE21
|
3.4
|
16.0
|
0.6
|
NC
|
B:MNR304
|
3.5
|
16.5
|
1.0
|
MN
|
B:MNR304
|
3.5
|
16.2
|
1.0
|
CZ
|
B:PHE35
|
3.6
|
25.3
|
0.4
|
C1D
|
B:MNR304
|
3.6
|
12.8
|
1.0
|
CE1
|
B:PHE35
|
3.7
|
18.4
|
0.6
|
C4C
|
B:MNR304
|
3.8
|
16.0
|
1.0
|
CE1
|
B:PHE35
|
3.9
|
22.9
|
0.4
|
C4D
|
B:MNR304
|
3.9
|
14.7
|
1.0
|
C2
|
B:T6C301
|
4.0
|
33.7
|
0.8
|
CHD
|
B:MNR304
|
4.0
|
16.9
|
1.0
|
C6
|
B:T6C301
|
4.0
|
35.0
|
0.8
|
CZ
|
B:PHE35
|
4.0
|
17.4
|
0.6
|
CG1
|
B:VAL59
|
4.1
|
13.8
|
1.0
|
CE1
|
B:PHE21
|
4.1
|
17.5
|
0.5
|
CB
|
B:VAL59
|
4.2
|
12.0
|
1.0
|
NA
|
B:MNR304
|
4.2
|
13.8
|
1.0
|
C1C
|
B:MNR304
|
4.2
|
14.3
|
1.0
|
NB
|
B:MNR304
|
4.3
|
13.4
|
1.0
|
CHA
|
B:MNR304
|
4.5
|
14.5
|
1.0
|
C2D
|
B:MNR304
|
4.5
|
16.1
|
1.0
|
CZ
|
B:PHE21
|
4.5
|
15.1
|
0.5
|
C1A
|
B:MNR304
|
4.5
|
15.4
|
1.0
|
C1
|
B:T6C301
|
4.5
|
32.3
|
0.8
|
O1D
|
B:MNR304
|
4.6
|
7.3
|
0.2
|
C3D
|
B:MNR304
|
4.6
|
16.7
|
1.0
|
CD1
|
B:PHE21
|
4.6
|
15.3
|
0.6
|
CE2
|
B:PHE21
|
4.6
|
15.7
|
0.6
|
C3C
|
B:MNR304
|
4.7
|
18.1
|
1.0
|
CE2
|
B:PHE35
|
4.7
|
21.1
|
0.4
|
CD1
|
B:PHE21
|
4.8
|
14.6
|
0.5
|
CHC
|
B:MNR304
|
4.8
|
15.2
|
1.0
|
C4B
|
B:MNR304
|
4.9
|
14.2
|
1.0
|
CD1
|
B:PHE35
|
4.9
|
16.9
|
0.6
|
C2C
|
B:MNR304
|
5.0
|
17.0
|
1.0
|
|
Reference:
A.H.Mcguire,
A.R.Petit,
J.Kang,
T.Malewschik,
V.De Serrano,
L.M.Carey,
R.A.Ghiladi.
Nonnative Heme Incorporation Into Multifunctional Globin Increases Peroxygenase Activity An Order and Magnitude Compared to Native Enzyme To Be Published.
Page generated: Mon Jul 29 16:14:58 2024
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