Fluorine in PDB 8fww: Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel
Other elements in 8fww:
The structure of Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel
(pdb code 8fww). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 4 binding sites of Fluorine where determined in the
Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel, PDB code: 8fww:
Jump to Fluorine binding site number:
1;
2;
3;
4;
Fluorine binding site 1 out
of 4 in 8fww
Go back to
Fluorine Binding Sites List in 8fww
Fluorine binding site 1 out
of 4 in the Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F1001
b:21.0
occ:1.00
|
FAC
|
A:2J91001
|
0.0
|
21.0
|
1.0
|
CAK
|
A:2J91001
|
1.4
|
21.0
|
1.0
|
CAD
|
A:2J91001
|
2.4
|
21.0
|
1.0
|
CAF
|
A:2J91001
|
2.4
|
21.0
|
1.0
|
CG2
|
D:THR535
|
3.3
|
48.6
|
1.0
|
CA
|
D:GLY763
|
3.3
|
44.2
|
1.0
|
CB
|
D:PRO532
|
3.3
|
43.4
|
1.0
|
CG
|
D:PRO532
|
3.4
|
43.4
|
1.0
|
O
|
D:LYS762
|
3.5
|
46.8
|
1.0
|
CAE
|
A:2J91001
|
3.6
|
21.0
|
1.0
|
CAM
|
A:2J91001
|
3.7
|
21.0
|
1.0
|
CB
|
D:THR535
|
3.9
|
48.6
|
1.0
|
N
|
D:GLY763
|
3.9
|
44.2
|
1.0
|
CA
|
D:THR535
|
4.0
|
48.6
|
1.0
|
C
|
D:LYS762
|
4.0
|
46.8
|
1.0
|
O
|
D:MET534
|
4.0
|
49.3
|
1.0
|
CAL
|
A:2J91001
|
4.1
|
21.0
|
1.0
|
CAD
|
A:2J91009
|
4.4
|
13.6
|
1.0
|
C
|
D:GLY763
|
4.5
|
44.2
|
1.0
|
C
|
D:MET534
|
4.5
|
49.3
|
1.0
|
N
|
D:THR535
|
4.6
|
48.6
|
1.0
|
CAK
|
A:2J91009
|
4.6
|
13.6
|
1.0
|
CD
|
D:PRO532
|
4.6
|
43.4
|
1.0
|
FAC
|
A:2J91009
|
4.8
|
13.6
|
1.0
|
CAE
|
A:2J91009
|
4.8
|
13.6
|
1.0
|
CA
|
D:PRO532
|
4.9
|
43.4
|
1.0
|
N
|
D:TYR764
|
4.9
|
50.5
|
1.0
|
|
Fluorine binding site 2 out
of 4 in 8fww
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Fluorine Binding Sites List in 8fww
Fluorine binding site 2 out
of 4 in the Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F1009
b:13.6
occ:1.00
|
FAC
|
A:2J91009
|
0.0
|
13.6
|
1.0
|
CAK
|
A:2J91009
|
1.4
|
13.6
|
1.0
|
CAD
|
A:2J91009
|
2.4
|
13.6
|
1.0
|
CAF
|
A:2J91009
|
2.4
|
13.6
|
1.0
|
CG
|
A:PRO532
|
3.3
|
41.9
|
1.0
|
CG2
|
A:THR535
|
3.3
|
49.5
|
1.0
|
CB
|
A:PRO532
|
3.3
|
41.9
|
1.0
|
O
|
A:LYS762
|
3.4
|
54.5
|
1.0
|
CA
|
A:GLY763
|
3.4
|
48.1
|
1.0
|
CAE
|
A:2J91009
|
3.6
|
13.6
|
1.0
|
CAM
|
A:2J91009
|
3.7
|
13.6
|
1.0
|
O
|
A:MET534
|
3.8
|
44.7
|
1.0
|
C
|
A:LYS762
|
4.0
|
54.5
|
1.0
|
N
|
A:GLY763
|
4.0
|
48.1
|
1.0
|
CB
|
A:THR535
|
4.1
|
49.5
|
1.0
|
CAL
|
A:2J91009
|
4.1
|
13.6
|
1.0
|
CA
|
A:THR535
|
4.2
|
49.5
|
1.0
|
CAD
|
A:2J91001
|
4.3
|
21.0
|
1.0
|
C
|
A:MET534
|
4.5
|
44.7
|
1.0
|
C
|
A:GLY763
|
4.5
|
48.1
|
1.0
|
CAK
|
A:2J91001
|
4.6
|
21.0
|
1.0
|
CD
|
A:PRO532
|
4.6
|
41.9
|
1.0
|
CAE
|
A:2J91001
|
4.7
|
21.0
|
1.0
|
N
|
A:THR535
|
4.7
|
49.5
|
1.0
|
FAC
|
A:2J91001
|
4.8
|
21.0
|
1.0
|
CA
|
A:PRO532
|
4.8
|
41.9
|
1.0
|
N
|
A:TYR764
|
4.9
|
49.0
|
1.0
|
|
Fluorine binding site 3 out
of 4 in 8fww
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Fluorine Binding Sites List in 8fww
Fluorine binding site 3 out
of 4 in the Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F1001
b:0.1
occ:1.00
|
FAC
|
B:2J91001
|
0.0
|
0.1
|
1.0
|
CAK
|
B:2J91001
|
1.4
|
0.1
|
1.0
|
CAF
|
B:2J91001
|
2.4
|
0.1
|
1.0
|
CAD
|
B:2J91001
|
2.4
|
0.1
|
1.0
|
CG2
|
C:THR535
|
3.3
|
48.4
|
1.0
|
CG
|
C:PRO532
|
3.3
|
43.1
|
1.0
|
CB
|
C:PRO532
|
3.3
|
43.1
|
1.0
|
O
|
C:LYS762
|
3.4
|
54.0
|
1.0
|
CA
|
C:GLY763
|
3.5
|
46.6
|
1.0
|
CAE
|
B:2J91001
|
3.6
|
0.1
|
1.0
|
CAM
|
B:2J91001
|
3.6
|
0.1
|
1.0
|
O
|
C:MET534
|
3.9
|
43.8
|
1.0
|
C
|
C:LYS762
|
4.1
|
54.0
|
1.0
|
CB
|
C:THR535
|
4.1
|
48.4
|
1.0
|
CAL
|
B:2J91001
|
4.1
|
0.1
|
1.0
|
N
|
C:GLY763
|
4.2
|
46.6
|
1.0
|
CA
|
C:THR535
|
4.2
|
48.4
|
1.0
|
CAD
|
B:2J91004
|
4.3
|
20.7
|
1.0
|
CAK
|
B:2J91004
|
4.5
|
20.7
|
1.0
|
C
|
C:MET534
|
4.6
|
43.8
|
1.0
|
CD
|
C:PRO532
|
4.6
|
43.1
|
1.0
|
C
|
C:GLY763
|
4.7
|
46.6
|
1.0
|
CAE
|
B:2J91004
|
4.7
|
20.7
|
1.0
|
FAC
|
B:2J91004
|
4.7
|
20.7
|
1.0
|
N
|
C:THR535
|
4.7
|
48.4
|
1.0
|
CA
|
C:PRO532
|
4.8
|
43.1
|
1.0
|
|
Fluorine binding site 4 out
of 4 in 8fww
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Fluorine Binding Sites List in 8fww
Fluorine binding site 4 out
of 4 in the Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 4 of Structure of the Ligand-Binding and Transmembrane Domains of Kainate Receptor GLUK2 in Complex with the Positive Allosteric Modulator BPAM344 and Noncompetitive Inhibitor Perampanel within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F1004
b:20.7
occ:1.00
|
FAC
|
B:2J91004
|
0.0
|
20.7
|
1.0
|
CAK
|
B:2J91004
|
1.4
|
20.7
|
1.0
|
CAD
|
B:2J91004
|
2.4
|
20.7
|
1.0
|
CAF
|
B:2J91004
|
2.4
|
20.7
|
1.0
|
CG2
|
B:THR535
|
3.2
|
49.2
|
1.0
|
CA
|
B:GLY763
|
3.3
|
47.1
|
1.0
|
CB
|
B:PRO532
|
3.4
|
45.3
|
1.0
|
CG
|
B:PRO532
|
3.4
|
45.3
|
1.0
|
O
|
B:LYS762
|
3.4
|
49.4
|
1.0
|
CAE
|
B:2J91004
|
3.6
|
20.7
|
1.0
|
CAM
|
B:2J91004
|
3.6
|
20.7
|
1.0
|
CB
|
B:THR535
|
3.9
|
49.2
|
1.0
|
N
|
B:GLY763
|
3.9
|
47.1
|
1.0
|
C
|
B:LYS762
|
3.9
|
49.4
|
1.0
|
CA
|
B:THR535
|
3.9
|
49.2
|
1.0
|
O
|
B:MET534
|
4.0
|
50.9
|
1.0
|
CAL
|
B:2J91004
|
4.1
|
20.7
|
1.0
|
CAD
|
B:2J91001
|
4.4
|
0.1
|
1.0
|
C
|
B:GLY763
|
4.5
|
47.1
|
1.0
|
C
|
B:MET534
|
4.5
|
50.9
|
1.0
|
N
|
B:THR535
|
4.6
|
49.2
|
1.0
|
CAK
|
B:2J91001
|
4.6
|
0.1
|
1.0
|
CD
|
B:PRO532
|
4.7
|
45.3
|
1.0
|
FAC
|
B:2J91001
|
4.7
|
0.1
|
1.0
|
CAE
|
B:2J91001
|
4.8
|
0.1
|
1.0
|
CA
|
B:PRO532
|
4.9
|
45.3
|
1.0
|
N
|
B:TYR764
|
4.9
|
52.2
|
1.0
|
|
Reference:
S.P.Gangwar,
L.Y.Yen,
M.V.Yelshanskaya,
A.I.Sobolevsky.
Positive and Negative Allosteric Modulation of GLUK2 Kainate Receptors By BPAM344 and Antiepileptic Perampanel. Cell Rep V. 42 12124 2023.
ISSN: ESSN 2211-1247
PubMed: 36857176
DOI: 10.1016/J.CELREP.2023.112124
Page generated: Fri Aug 2 19:30:11 2024
|