Chlorine in PDB 3n9j: Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
Enzymatic activity of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
All present enzymatic activity of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin:
2.5.1.18;
Protein crystallography data
The structure of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin, PDB code: 3n9j
was solved by
L.J.Parker,
M.W.Parker,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.28 /
1.85
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
76.806,
89.994,
68.870,
90.00,
98.24,
90.00
|
R / Rfree (%)
|
17.8 /
21.8
|
Other elements in 3n9j:
The structure of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
(pdb code 3n9j). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 5 binding sites of Chlorine where determined in the
Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin, PDB code: 3n9j:
Jump to Chlorine binding site number:
1;
2;
3;
4;
5;
Chlorine binding site 1 out
of 5 in 3n9j
Go back to
Chlorine Binding Sites List in 3n9j
Chlorine binding site 1 out
of 5 in the Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 1 of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl210
b:22.4
occ:0.50
|
CL1
|
A:EAA210
|
0.0
|
22.4
|
0.5
|
C2
|
A:EAA210
|
1.8
|
23.2
|
0.5
|
C3
|
A:EAA210
|
2.8
|
23.1
|
0.5
|
C1
|
A:EAA210
|
2.8
|
23.7
|
0.5
|
OH
|
A:TYR7
|
2.9
|
15.7
|
1.0
|
O
|
A:HOH374
|
3.0
|
24.7
|
1.0
|
O2
|
A:EAA210
|
3.0
|
24.1
|
0.5
|
CL2
|
A:EAA210
|
3.2
|
24.0
|
0.5
|
O
|
A:HOH297
|
3.6
|
22.3
|
1.0
|
O
|
A:HOH304
|
3.6
|
19.4
|
1.0
|
CZ
|
A:TYR7
|
3.7
|
16.6
|
1.0
|
OH
|
A:TYR108
|
3.7
|
26.8
|
1.0
|
CG2
|
A:VAL10
|
4.0
|
19.0
|
1.0
|
C6
|
A:EAA210
|
4.1
|
24.1
|
0.5
|
C4
|
A:EAA210
|
4.1
|
24.6
|
0.5
|
CD2
|
A:PHE8
|
4.2
|
17.7
|
1.0
|
CE1
|
A:TYR7
|
4.3
|
16.4
|
1.0
|
C12
|
A:EAA210
|
4.4
|
21.8
|
0.5
|
OXT
|
A:EAA210
|
4.4
|
21.2
|
0.5
|
CE2
|
A:TYR7
|
4.5
|
15.2
|
1.0
|
C5
|
A:EAA210
|
4.6
|
23.4
|
0.5
|
CE2
|
A:PHE8
|
4.6
|
20.1
|
1.0
|
CZ
|
A:TYR108
|
4.6
|
27.3
|
1.0
|
CA
|
A:GLY12
|
4.9
|
14.1
|
1.0
|
C13
|
A:EAA210
|
4.9
|
21.4
|
0.5
|
|
Chlorine binding site 2 out
of 5 in 3n9j
Go back to
Chlorine Binding Sites List in 3n9j
Chlorine binding site 2 out
of 5 in the Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 2 of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl210
b:24.0
occ:0.50
|
CL2
|
A:EAA210
|
0.0
|
24.0
|
0.5
|
C3
|
A:EAA210
|
1.8
|
23.1
|
0.5
|
C2
|
A:EAA210
|
2.8
|
23.2
|
0.5
|
C4
|
A:EAA210
|
2.9
|
24.6
|
0.5
|
CL1
|
A:EAA210
|
3.2
|
22.4
|
0.5
|
C7
|
A:EAA210
|
3.3
|
25.8
|
0.5
|
CD2
|
A:PHE8
|
3.6
|
17.7
|
1.0
|
CA
|
A:GLY205
|
3.6
|
24.1
|
1.0
|
CG1
|
A:VAL10
|
3.7
|
18.2
|
1.0
|
C11
|
A:EAA210
|
3.7
|
28.2
|
0.5
|
O1
|
A:EAA210
|
3.7
|
27.8
|
0.5
|
CG
|
A:PHE8
|
3.8
|
18.8
|
1.0
|
CB
|
A:PHE8
|
3.8
|
16.2
|
1.0
|
C8
|
A:EAA210
|
3.9
|
28.3
|
0.5
|
N
|
A:GLY205
|
4.1
|
22.8
|
1.0
|
OH
|
A:TYR108
|
4.1
|
26.8
|
1.0
|
CG2
|
A:VAL10
|
4.2
|
19.0
|
1.0
|
C5
|
A:EAA210
|
4.2
|
23.4
|
0.5
|
C1
|
A:EAA210
|
4.2
|
23.7
|
0.5
|
CE2
|
A:PHE8
|
4.3
|
20.1
|
1.0
|
CB
|
A:VAL10
|
4.6
|
17.9
|
1.0
|
C6
|
A:EAA210
|
4.7
|
24.1
|
0.5
|
CD1
|
A:PHE8
|
4.7
|
20.2
|
1.0
|
C
|
A:GLY205
|
4.8
|
25.9
|
1.0
|
|
Chlorine binding site 3 out
of 5 in 3n9j
Go back to
Chlorine Binding Sites List in 3n9j
Chlorine binding site 3 out
of 5 in the Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 3 of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl210
b:26.7
occ:0.20
|
PT
|
A:PT211
|
2.4
|
32.3
|
0.2
|
O
|
A:HOH377
|
2.5
|
43.1
|
1.0
|
O
|
B:HOH322
|
2.6
|
24.7
|
1.0
|
SG
|
B:CYS101
|
3.1
|
19.7
|
0.4
|
CB
|
B:CYS101
|
3.4
|
17.3
|
0.4
|
CB
|
B:CYS101
|
3.4
|
15.8
|
0.6
|
SG
|
B:CYS101
|
3.7
|
14.6
|
0.6
|
SG
|
A:CYS101
|
3.8
|
21.6
|
0.3
|
O
|
A:HOH369
|
3.9
|
40.3
|
1.0
|
OD1
|
B:ASP98
|
4.1
|
21.0
|
1.0
|
SG
|
A:CYS101
|
4.3
|
21.2
|
0.7
|
O
|
B:HOH376
|
4.3
|
44.3
|
1.0
|
O
|
B:ASP98
|
4.6
|
13.1
|
1.0
|
O
|
A:HOH367
|
4.6
|
40.7
|
1.0
|
CA
|
B:ASP98
|
4.7
|
14.0
|
1.0
|
O
|
B:HOH368
|
4.8
|
41.8
|
1.0
|
CA
|
B:CYS101
|
4.9
|
17.3
|
0.4
|
CA
|
B:CYS101
|
4.9
|
16.1
|
0.6
|
CG
|
B:ASP98
|
4.9
|
17.1
|
1.0
|
|
Chlorine binding site 4 out
of 5 in 3n9j
Go back to
Chlorine Binding Sites List in 3n9j
Chlorine binding site 4 out
of 5 in the Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 4 of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl214
b:30.4
occ:0.60
|
CL1
|
B:EAA214
|
0.0
|
30.4
|
0.6
|
C2
|
B:EAA214
|
1.8
|
29.1
|
0.6
|
C3
|
B:EAA214
|
2.8
|
29.7
|
0.6
|
C1
|
B:EAA214
|
2.9
|
30.1
|
0.6
|
OH
|
B:TYR7
|
2.9
|
18.5
|
1.0
|
CL2
|
B:EAA214
|
3.1
|
30.9
|
0.6
|
O2
|
B:EAA214
|
3.1
|
29.1
|
0.6
|
O
|
B:HOH347
|
3.2
|
28.6
|
1.0
|
C12
|
B:EAA214
|
3.4
|
27.4
|
0.6
|
O
|
B:EAA214
|
3.6
|
25.0
|
0.6
|
O
|
B:HOH324
|
3.6
|
16.3
|
1.0
|
C13
|
B:EAA214
|
3.6
|
26.4
|
0.6
|
CZ
|
B:TYR7
|
3.7
|
15.8
|
1.0
|
OH
|
B:TYR108
|
3.8
|
19.8
|
1.0
|
CG2
|
B:VAL10
|
3.8
|
19.2
|
1.0
|
CD2
|
B:PHE8
|
4.0
|
22.1
|
1.0
|
C6
|
B:EAA214
|
4.1
|
30.4
|
0.6
|
C4
|
B:EAA214
|
4.1
|
30.4
|
0.6
|
CE1
|
B:TYR7
|
4.2
|
16.6
|
1.0
|
CE2
|
B:TYR7
|
4.4
|
16.7
|
1.0
|
CE2
|
B:PHE8
|
4.5
|
25.5
|
1.0
|
OXT
|
B:EAA214
|
4.5
|
26.3
|
0.6
|
C5
|
B:EAA214
|
4.6
|
30.8
|
0.6
|
CZ
|
B:TYR108
|
4.7
|
20.1
|
1.0
|
CA
|
B:GLY12
|
4.9
|
14.2
|
1.0
|
|
Chlorine binding site 5 out
of 5 in 3n9j
Go back to
Chlorine Binding Sites List in 3n9j
Chlorine binding site 5 out
of 5 in the Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 5 of Structure of Human Glutathione Transferase Pi Class in Complex with Ethacraplatin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl214
b:30.9
occ:0.60
|
CL2
|
B:EAA214
|
0.0
|
30.9
|
0.6
|
C3
|
B:EAA214
|
1.8
|
29.7
|
0.6
|
C2
|
B:EAA214
|
2.8
|
29.1
|
0.6
|
C4
|
B:EAA214
|
2.9
|
30.4
|
0.6
|
CL1
|
B:EAA214
|
3.1
|
30.4
|
0.6
|
C7
|
B:EAA214
|
3.2
|
30.8
|
0.6
|
O1
|
B:EAA214
|
3.3
|
30.3
|
0.6
|
CD2
|
B:PHE8
|
3.6
|
22.1
|
1.0
|
CA
|
B:GLY205
|
3.6
|
21.8
|
1.0
|
CG
|
B:PHE8
|
3.8
|
20.4
|
1.0
|
CB
|
B:PHE8
|
3.9
|
20.4
|
1.0
|
CG1
|
B:VAL10
|
3.9
|
19.4
|
1.0
|
OH
|
B:TYR108
|
4.0
|
19.8
|
1.0
|
CG2
|
B:VAL10
|
4.0
|
19.2
|
1.0
|
C11
|
B:EAA214
|
4.1
|
32.1
|
0.6
|
C8
|
B:EAA214
|
4.1
|
32.6
|
0.6
|
N
|
B:GLY205
|
4.1
|
19.6
|
1.0
|
C5
|
B:EAA214
|
4.2
|
30.8
|
0.6
|
C1
|
B:EAA214
|
4.2
|
30.1
|
0.6
|
CE2
|
B:PHE8
|
4.3
|
25.5
|
1.0
|
CB
|
B:VAL10
|
4.6
|
18.5
|
1.0
|
C6
|
B:EAA214
|
4.7
|
30.4
|
0.6
|
C
|
B:GLY205
|
4.7
|
22.8
|
1.0
|
CD1
|
B:PHE8
|
4.7
|
23.2
|
1.0
|
CZ
|
B:TYR108
|
4.9
|
20.1
|
1.0
|
O
|
B:GLY205
|
5.0
|
24.3
|
1.0
|
|
Reference:
L.J.Parker,
L.C.Italiano,
C.J.Morton,
N.C.Hancock,
D.B.Ascher,
J.B.Aitken,
H.H.Harris,
P.Campomanes,
U.Rothlisberger,
A.De Luca,
M.Lo Bello,
W.H.Ang,
P.J.Dyson,
M.W.Parker.
Studies of Glutathione Transferase P1-1 Bound to A Platinum(IV)-Based Anticancer Compound Reveal the Molecular Basis of Its Activation. To Be Published.
Page generated: Sun Jul 21 00:45:19 2024
|