Fluorine in PDB 4d4v: Focal Adhesion Kinase Catalytic Domain
Enzymatic activity of Focal Adhesion Kinase Catalytic Domain
All present enzymatic activity of Focal Adhesion Kinase Catalytic Domain:
2.7.10.2;
Protein crystallography data
The structure of Focal Adhesion Kinase Catalytic Domain, PDB code: 4d4v
was solved by
J.Le Coq,
A.Lin,
D.Lietha,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
50.85 /
2.10
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
44.996,
123.597,
51.008,
90.00,
94.49,
90.00
|
R / Rfree (%)
|
19.184 /
22.704
|
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Focal Adhesion Kinase Catalytic Domain
(pdb code 4d4v). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the
Focal Adhesion Kinase Catalytic Domain, PDB code: 4d4v:
Jump to Fluorine binding site number:
1;
2;
3;
Fluorine binding site 1 out
of 3 in 4d4v
Go back to
Fluorine Binding Sites List in 4d4v
Fluorine binding site 1 out
of 3 in the Focal Adhesion Kinase Catalytic Domain
 Mono view
 Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Focal Adhesion Kinase Catalytic Domain within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F1691
b:50.7
occ:1.00
|
FAB
|
B:KB81691
|
0.0
|
50.7
|
1.0
|
CAU
|
B:KB81691
|
1.4
|
58.6
|
1.0
|
CAP
|
B:KB81691
|
2.2
|
55.1
|
1.0
|
FAC
|
B:KB81691
|
2.3
|
60.0
|
1.0
|
FAD
|
B:KB81691
|
2.3
|
57.9
|
1.0
|
NAM
|
B:KB81691
|
2.5
|
52.8
|
1.0
|
O
|
B:HOH2010
|
2.7
|
34.6
|
1.0
|
CG
|
B:MET499
|
3.3
|
51.3
|
1.0
|
O
|
B:GLU500
|
3.4
|
42.1
|
1.0
|
CAG
|
B:KB81691
|
3.5
|
56.8
|
1.0
|
CB
|
B:ALA452
|
3.6
|
47.2
|
1.0
|
SD
|
B:MET499
|
3.7
|
55.8
|
1.0
|
CD1
|
B:LEU553
|
3.8
|
40.0
|
1.0
|
CAR
|
B:KB81691
|
3.8
|
55.3
|
1.0
|
CG1
|
B:VAL484
|
4.1
|
41.3
|
1.0
|
CB
|
B:MET499
|
4.1
|
47.7
|
1.0
|
CAF
|
B:KB81691
|
4.6
|
55.6
|
1.0
|
CG2
|
B:VAL484
|
4.6
|
40.0
|
1.0
|
CAQ
|
B:KB81691
|
4.6
|
58.7
|
1.0
|
C
|
B:GLU500
|
4.7
|
44.9
|
1.0
|
CAS
|
B:KB81691
|
4.7
|
55.8
|
1.0
|
O
|
B:GLY563
|
4.9
|
40.0
|
1.0
|
CB
|
B:VAL484
|
5.0
|
39.0
|
1.0
|
|
Fluorine binding site 2 out
of 3 in 4d4v
Go back to
Fluorine Binding Sites List in 4d4v
Fluorine binding site 2 out
of 3 in the Focal Adhesion Kinase Catalytic Domain
 Mono view
 Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Focal Adhesion Kinase Catalytic Domain within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F1691
b:60.0
occ:1.00
|
FAC
|
B:KB81691
|
0.0
|
60.0
|
1.0
|
CAU
|
B:KB81691
|
1.4
|
58.6
|
1.0
|
CAP
|
B:KB81691
|
2.2
|
55.1
|
1.0
|
FAB
|
B:KB81691
|
2.3
|
50.7
|
1.0
|
FAD
|
B:KB81691
|
2.3
|
57.9
|
1.0
|
SD
|
B:MET499
|
2.9
|
55.8
|
1.0
|
CG
|
B:MET499
|
3.0
|
51.3
|
1.0
|
CAG
|
B:KB81691
|
3.0
|
56.8
|
1.0
|
NAM
|
B:KB81691
|
3.1
|
52.8
|
1.0
|
CE
|
B:LYS454
|
3.2
|
52.3
|
1.0
|
CG
|
B:LYS454
|
3.6
|
49.7
|
1.0
|
CB
|
B:ALA452
|
3.7
|
47.2
|
1.0
|
CD
|
B:LYS454
|
4.0
|
51.5
|
1.0
|
CAR
|
B:KB81691
|
4.2
|
55.3
|
1.0
|
CAQ
|
B:KB81691
|
4.3
|
58.7
|
1.0
|
NZ
|
B:LYS454
|
4.3
|
52.9
|
1.0
|
CB
|
B:MET499
|
4.4
|
47.7
|
1.0
|
CG1
|
B:VAL436
|
4.4
|
54.2
|
1.0
|
CE
|
B:MET499
|
4.6
|
55.9
|
1.0
|
O
|
B:HOH2010
|
4.6
|
34.6
|
1.0
|
CAS
|
B:KB81691
|
4.7
|
55.8
|
1.0
|
C
|
B:ALA452
|
4.8
|
47.6
|
1.0
|
CA
|
B:ALA452
|
4.9
|
48.3
|
1.0
|
|
Fluorine binding site 3 out
of 3 in 4d4v
Go back to
Fluorine Binding Sites List in 4d4v
Fluorine binding site 3 out
of 3 in the Focal Adhesion Kinase Catalytic Domain
 Mono view
 Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Focal Adhesion Kinase Catalytic Domain within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F1691
b:57.9
occ:1.00
|
FAD
|
B:KB81691
|
0.0
|
57.9
|
1.0
|
CAU
|
B:KB81691
|
1.4
|
58.6
|
1.0
|
FAB
|
B:KB81691
|
2.3
|
50.7
|
1.0
|
FAC
|
B:KB81691
|
2.3
|
60.0
|
1.0
|
CAP
|
B:KB81691
|
2.3
|
55.1
|
1.0
|
CAG
|
B:KB81691
|
2.8
|
56.8
|
1.0
|
O
|
B:GLY563
|
2.9
|
40.0
|
1.0
|
SD
|
B:MET499
|
3.1
|
55.8
|
1.0
|
CE
|
B:LYS454
|
3.4
|
52.3
|
1.0
|
NAM
|
B:KB81691
|
3.5
|
52.8
|
1.0
|
NZ
|
B:LYS454
|
3.8
|
52.9
|
1.0
|
CD1
|
B:LEU553
|
3.8
|
40.0
|
1.0
|
CG
|
B:MET499
|
3.9
|
51.3
|
1.0
|
C
|
B:GLY563
|
4.0
|
40.4
|
1.0
|
CAQ
|
B:KB81691
|
4.1
|
58.7
|
1.0
|
CG1
|
B:VAL484
|
4.4
|
41.3
|
1.0
|
CA
|
B:GLY563
|
4.6
|
36.6
|
1.0
|
CAR
|
B:KB81691
|
4.6
|
55.3
|
1.0
|
O
|
B:HOH2010
|
4.7
|
34.6
|
1.0
|
CG2
|
B:VAL484
|
4.7
|
40.0
|
1.0
|
CD
|
B:LYS454
|
4.8
|
51.5
|
1.0
|
CE
|
B:MET499
|
4.9
|
55.9
|
1.0
|
CAS
|
B:KB81691
|
4.9
|
55.8
|
1.0
|
CB
|
B:MET499
|
4.9
|
47.7
|
1.0
|
NAT
|
B:KB81691
|
4.9
|
61.4
|
1.0
|
CB
|
B:VAL484
|
4.9
|
39.0
|
1.0
|
|
Reference:
J.Zhou,
A.Bronowska,
J.Le Coq,
D.Lietha,
F.Grater.
Allosteric Regulation of Focal Adhesion Kinase By PIP2 and Atp. Biophys.J. V. 108 698 2015.
ISSN: ISSN 0006-3495
PubMed: 25650936
DOI: 10.1016/J.BPJ.2014.11.3454
Page generated: Thu Aug 1 00:51:28 2024
|