Fluorine in PDB 4yct: Endothiapepsin in Complex with Fragment 216
Enzymatic activity of Endothiapepsin in Complex with Fragment 216
All present enzymatic activity of Endothiapepsin in Complex with Fragment 216:
3.4.23.22;
Protein crystallography data
The structure of Endothiapepsin in Complex with Fragment 216, PDB code: 4yct
was solved by
M.Stieler,
A.Heine,
G.Klebe,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
34.74 /
1.13
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
45.224,
72.957,
52.636,
90.00,
109.53,
90.00
|
R / Rfree (%)
|
13.8 /
15.7
|
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Endothiapepsin in Complex with Fragment 216
(pdb code 4yct). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the
Endothiapepsin in Complex with Fragment 216, PDB code: 4yct:
Jump to Fluorine binding site number:
1;
2;
3;
Fluorine binding site 1 out
of 3 in 4yct
Go back to
Fluorine Binding Sites List in 4yct
Fluorine binding site 1 out
of 3 in the Endothiapepsin in Complex with Fragment 216
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Endothiapepsin in Complex with Fragment 216 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F401
b:22.3
occ:1.00
|
F11
|
A:FBF401
|
0.0
|
22.3
|
1.0
|
C10
|
A:FBF401
|
1.3
|
22.4
|
1.0
|
F12
|
A:FBF401
|
2.1
|
23.7
|
1.0
|
F13
|
A:FBF401
|
2.1
|
24.7
|
1.0
|
C3
|
A:FBF401
|
2.3
|
18.5
|
1.0
|
HD11
|
A:ILE302
|
2.3
|
19.1
|
0.3
|
HD11
|
A:ILE304
|
2.9
|
11.6
|
1.0
|
C2
|
A:FBF401
|
2.9
|
16.5
|
1.0
|
HG23
|
A:ILE300
|
3.1
|
21.8
|
1.0
|
HD12
|
A:ILE302
|
3.1
|
19.1
|
0.3
|
CD1
|
A:ILE302
|
3.1
|
15.9
|
0.3
|
HG22
|
A:ILE300
|
3.1
|
21.8
|
1.0
|
HG21
|
A:ILE300
|
3.2
|
21.8
|
1.0
|
HG22
|
A:ILE302
|
3.3
|
15.4
|
0.7
|
CG2
|
A:ILE300
|
3.3
|
18.1
|
1.0
|
C4
|
A:FBF401
|
3.4
|
17.2
|
1.0
|
HD13
|
A:ILE302
|
3.5
|
19.1
|
0.3
|
HG21
|
A:ILE302
|
3.5
|
15.4
|
0.7
|
CG2
|
A:ILE302
|
3.8
|
12.9
|
0.7
|
CD1
|
A:ILE304
|
3.8
|
9.6
|
1.0
|
HG23
|
A:ILE302
|
3.9
|
15.4
|
0.7
|
HD13
|
A:ILE304
|
4.0
|
11.6
|
1.0
|
C1
|
A:FBF401
|
4.3
|
14.4
|
1.0
|
CG1
|
A:ILE302
|
4.3
|
15.3
|
0.3
|
HG13
|
A:ILE302
|
4.3
|
18.4
|
0.3
|
HD12
|
A:ILE304
|
4.4
|
11.6
|
1.0
|
HG12
|
A:ILE304
|
4.5
|
9.2
|
1.0
|
C5
|
A:FBF401
|
4.6
|
14.6
|
1.0
|
HG12
|
A:ILE302
|
4.6
|
18.4
|
0.3
|
CG1
|
A:ILE304
|
4.7
|
7.7
|
1.0
|
HD13
|
A:ILE300
|
4.7
|
22.6
|
1.0
|
O
|
A:ILE300
|
4.8
|
20.0
|
1.0
|
CB
|
A:ILE300
|
4.8
|
18.1
|
1.0
|
HG13
|
A:ILE304
|
4.8
|
9.2
|
1.0
|
HD11
|
A:ILE217
|
4.9
|
11.5
|
1.0
|
C6
|
A:FBF401
|
4.9
|
11.5
|
1.0
|
|
Fluorine binding site 2 out
of 3 in 4yct
Go back to
Fluorine Binding Sites List in 4yct
Fluorine binding site 2 out
of 3 in the Endothiapepsin in Complex with Fragment 216
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Endothiapepsin in Complex with Fragment 216 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F401
b:23.7
occ:1.00
|
F12
|
A:FBF401
|
0.0
|
23.7
|
1.0
|
C10
|
A:FBF401
|
1.3
|
22.4
|
1.0
|
F11
|
A:FBF401
|
2.1
|
22.3
|
1.0
|
F13
|
A:FBF401
|
2.1
|
24.7
|
1.0
|
C3
|
A:FBF401
|
2.3
|
18.5
|
1.0
|
C4
|
A:FBF401
|
2.7
|
17.2
|
1.0
|
C2
|
A:FBF401
|
3.6
|
16.5
|
1.0
|
HG23
|
A:ILE300
|
4.0
|
21.8
|
1.0
|
C5
|
A:FBF401
|
4.1
|
14.6
|
1.0
|
HD11
|
A:ILE302
|
4.3
|
19.1
|
0.3
|
HG22
|
A:ILE300
|
4.4
|
21.8
|
1.0
|
HD12
|
A:ILE302
|
4.5
|
19.1
|
0.3
|
CG2
|
A:ILE300
|
4.6
|
18.1
|
1.0
|
HG21
|
A:ILE300
|
4.7
|
21.8
|
1.0
|
C1
|
A:FBF401
|
4.8
|
14.4
|
1.0
|
CD1
|
A:ILE302
|
4.8
|
15.9
|
0.3
|
HD11
|
A:ILE304
|
4.9
|
11.6
|
1.0
|
HG22
|
A:ILE302
|
4.9
|
15.4
|
0.7
|
C6
|
A:FBF401
|
5.0
|
11.5
|
1.0
|
|
Fluorine binding site 3 out
of 3 in 4yct
Go back to
Fluorine Binding Sites List in 4yct
Fluorine binding site 3 out
of 3 in the Endothiapepsin in Complex with Fragment 216
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Endothiapepsin in Complex with Fragment 216 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F401
b:24.7
occ:1.00
|
F13
|
A:FBF401
|
0.0
|
24.7
|
1.0
|
C10
|
A:FBF401
|
1.3
|
22.4
|
1.0
|
F11
|
A:FBF401
|
2.1
|
22.3
|
1.0
|
F12
|
A:FBF401
|
2.1
|
23.7
|
1.0
|
C3
|
A:FBF401
|
2.4
|
18.5
|
1.0
|
C2
|
A:FBF401
|
3.0
|
16.5
|
1.0
|
HZ
|
A:PHE194
|
3.3
|
16.0
|
1.0
|
HD12
|
A:ILE302
|
3.3
|
19.1
|
0.3
|
HD11
|
A:ILE302
|
3.3
|
19.1
|
0.3
|
C4
|
A:FBF401
|
3.4
|
17.2
|
1.0
|
HG21
|
A:ILE302
|
3.6
|
15.4
|
0.7
|
CD1
|
A:ILE302
|
3.8
|
15.9
|
0.3
|
HG22
|
A:ILE302
|
3.9
|
15.4
|
0.7
|
CZ
|
A:PHE194
|
3.9
|
13.3
|
1.0
|
HE1
|
A:PHE194
|
4.2
|
16.5
|
1.0
|
CG2
|
A:ILE302
|
4.2
|
12.9
|
0.7
|
C1
|
A:FBF401
|
4.3
|
14.4
|
1.0
|
HG13
|
A:ILE302
|
4.3
|
18.4
|
0.3
|
CE1
|
A:PHE194
|
4.4
|
13.7
|
1.0
|
HG22
|
A:ILE300
|
4.5
|
21.8
|
1.0
|
HD13
|
A:ILE302
|
4.5
|
19.1
|
0.3
|
C5
|
A:FBF401
|
4.6
|
14.6
|
1.0
|
CG1
|
A:ILE302
|
4.7
|
15.3
|
0.3
|
HG23
|
A:ILE302
|
4.7
|
15.4
|
0.7
|
HD11
|
A:ILE304
|
4.7
|
11.6
|
1.0
|
HG23
|
A:ILE300
|
4.8
|
21.8
|
1.0
|
CE2
|
A:PHE194
|
4.8
|
11.5
|
1.0
|
HE2
|
A:PHE194
|
4.9
|
13.8
|
1.0
|
HD13
|
A:ILE217
|
4.9
|
11.5
|
1.0
|
C6
|
A:FBF401
|
4.9
|
11.5
|
1.0
|
HG23
|
A:ILE302
|
5.0
|
17.3
|
0.3
|
CG2
|
A:ILE300
|
5.0
|
18.1
|
1.0
|
|
Reference:
M.Stieler,
A.Heine,
G.Klebe.
Crystallographic Fragment Screening of An Entire Library To Be Published.
Page generated: Thu Aug 1 06:57:28 2024
|