Fluorine in PDB 7sq2: Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
Enzymatic activity of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
All present enzymatic activity of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex:
3.1.4.11;
Protein crystallography data
The structure of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex, PDB code: 7sq2
was solved by
S.T.Endo-Streeter,
J.Sondek,
T.K.Harden,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
40.55 /
2.60
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
202.837,
90.817,
93.135,
90,
101.19,
90
|
R / Rfree (%)
|
19.9 /
26.3
|
Other elements in 7sq2:
The structure of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
(pdb code 7sq2). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 4 binding sites of Fluorine where determined in the
Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex, PDB code: 7sq2:
Jump to Fluorine binding site number:
1;
2;
3;
4;
Fluorine binding site 1 out
of 4 in 7sq2
Go back to
Fluorine Binding Sites List in 7sq2
Fluorine binding site 1 out
of 4 in the Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F401
b:103.3
occ:1.00
|
F1
|
A:ALF401
|
0.0
|
103.3
|
1.0
|
AL
|
A:ALF401
|
1.8
|
67.5
|
1.0
|
O1B
|
A:GDP403
|
2.0
|
35.2
|
1.0
|
NZ
|
A:LYS52
|
2.3
|
77.8
|
1.0
|
F3
|
A:ALF401
|
2.5
|
75.6
|
1.0
|
F4
|
A:ALF401
|
2.6
|
85.8
|
1.0
|
N
|
A:GLY208
|
3.1
|
64.6
|
1.0
|
MG
|
A:MG402
|
3.1
|
59.1
|
1.0
|
PB
|
A:GDP403
|
3.2
|
65.8
|
1.0
|
CE
|
A:LYS52
|
3.3
|
73.2
|
1.0
|
O3B
|
A:GDP403
|
3.5
|
70.8
|
1.0
|
F2
|
A:ALF401
|
3.6
|
129.7
|
1.0
|
CA
|
A:GLY208
|
3.7
|
72.2
|
1.0
|
CA
|
A:GLY48
|
3.8
|
76.1
|
1.0
|
O2B
|
A:GDP403
|
3.9
|
44.4
|
1.0
|
N
|
A:GLU49
|
3.9
|
68.3
|
1.0
|
O
|
A:VAL206
|
4.0
|
68.2
|
1.0
|
C
|
A:GLY207
|
4.0
|
68.8
|
1.0
|
CA
|
A:GLY207
|
4.2
|
73.0
|
1.0
|
C
|
A:GLY48
|
4.4
|
69.4
|
1.0
|
OE1
|
A:GLN209
|
4.4
|
70.9
|
1.0
|
O3A
|
A:GDP403
|
4.5
|
45.4
|
1.0
|
NE2
|
A:GLN209
|
4.6
|
61.3
|
1.0
|
N
|
A:GLY48
|
4.6
|
81.6
|
1.0
|
CD
|
A:LYS52
|
4.7
|
75.8
|
1.0
|
CB
|
A:THR186
|
4.8
|
69.1
|
1.0
|
OG1
|
A:THR186
|
4.8
|
65.5
|
1.0
|
C
|
A:GLY208
|
4.8
|
70.8
|
1.0
|
CD
|
A:GLN209
|
4.8
|
61.9
|
1.0
|
O
|
A:HOH503
|
4.9
|
54.8
|
1.0
|
O
|
A:THR186
|
4.9
|
66.8
|
1.0
|
C
|
A:VAL206
|
4.9
|
71.8
|
1.0
|
N
|
A:GLN209
|
4.9
|
69.3
|
1.0
|
|
Fluorine binding site 2 out
of 4 in 7sq2
Go back to
Fluorine Binding Sites List in 7sq2
Fluorine binding site 2 out
of 4 in the Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F401
b:129.7
occ:1.00
|
F2
|
A:ALF401
|
0.0
|
129.7
|
1.0
|
AL
|
A:ALF401
|
1.8
|
67.5
|
1.0
|
F3
|
A:ALF401
|
2.5
|
75.6
|
1.0
|
F4
|
A:ALF401
|
2.5
|
85.8
|
1.0
|
NH1
|
A:ARG183
|
2.9
|
54.9
|
1.0
|
NH2
|
A:ARG183
|
2.9
|
61.8
|
1.0
|
N
|
A:THR186
|
3.0
|
67.8
|
1.0
|
CA
|
A:PRO185
|
3.0
|
73.3
|
1.0
|
O1B
|
A:GDP403
|
3.2
|
35.2
|
1.0
|
CZ
|
A:ARG183
|
3.3
|
56.0
|
1.0
|
C
|
A:PRO185
|
3.5
|
67.9
|
1.0
|
F1
|
A:ALF401
|
3.6
|
103.3
|
1.0
|
CB
|
A:PRO185
|
3.6
|
77.5
|
1.0
|
OE1
|
A:GLN209
|
3.8
|
70.9
|
1.0
|
NE2
|
A:GLN209
|
3.8
|
61.3
|
1.0
|
O
|
A:THR186
|
3.9
|
66.8
|
1.0
|
CA
|
A:THR186
|
4.1
|
64.2
|
1.0
|
OG1
|
A:THR186
|
4.2
|
65.5
|
1.0
|
CD
|
A:GLN209
|
4.2
|
61.9
|
1.0
|
N
|
A:PRO185
|
4.2
|
67.4
|
1.0
|
MG
|
A:MG402
|
4.3
|
59.1
|
1.0
|
O
|
A:HOH503
|
4.3
|
54.8
|
1.0
|
CB
|
A:THR186
|
4.4
|
69.1
|
1.0
|
C
|
A:THR186
|
4.5
|
61.6
|
1.0
|
NE
|
A:ARG183
|
4.5
|
61.1
|
1.0
|
O
|
A:VAL184
|
4.5
|
68.8
|
1.0
|
PB
|
A:GDP403
|
4.6
|
65.8
|
1.0
|
O
|
A:PRO185
|
4.7
|
67.5
|
1.0
|
CG
|
A:PRO185
|
4.7
|
71.8
|
1.0
|
C
|
A:VAL184
|
4.8
|
65.2
|
1.0
|
O1A
|
A:GDP403
|
4.9
|
41.7
|
1.0
|
|
Fluorine binding site 3 out
of 4 in 7sq2
Go back to
Fluorine Binding Sites List in 7sq2
Fluorine binding site 3 out
of 4 in the Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F401
b:75.6
occ:1.00
|
F3
|
A:ALF401
|
0.0
|
75.6
|
1.0
|
AL
|
A:ALF401
|
1.8
|
67.5
|
1.0
|
O
|
A:THR186
|
2.4
|
66.8
|
1.0
|
F2
|
A:ALF401
|
2.5
|
129.7
|
1.0
|
F1
|
A:ALF401
|
2.5
|
103.3
|
1.0
|
CB
|
A:THR186
|
2.9
|
69.1
|
1.0
|
N
|
A:THR186
|
3.0
|
67.8
|
1.0
|
MG
|
A:MG402
|
3.1
|
59.1
|
1.0
|
CA
|
A:THR186
|
3.1
|
64.2
|
1.0
|
C
|
A:THR186
|
3.1
|
61.6
|
1.0
|
CA
|
A:GLY207
|
3.3
|
73.0
|
1.0
|
O1B
|
A:GDP403
|
3.4
|
35.2
|
1.0
|
OG1
|
A:THR186
|
3.4
|
65.5
|
1.0
|
F4
|
A:ALF401
|
3.6
|
85.8
|
1.0
|
OE1
|
A:GLN209
|
3.7
|
70.9
|
1.0
|
N
|
A:GLY208
|
3.7
|
64.6
|
1.0
|
O
|
A:VAL206
|
3.8
|
68.2
|
1.0
|
C
|
A:GLY207
|
4.0
|
68.8
|
1.0
|
CG2
|
A:THR186
|
4.1
|
70.3
|
1.0
|
C
|
A:PRO185
|
4.2
|
67.9
|
1.0
|
N
|
A:GLY207
|
4.3
|
73.5
|
1.0
|
N
|
A:THR187
|
4.4
|
62.6
|
1.0
|
C
|
A:VAL206
|
4.5
|
71.8
|
1.0
|
CD
|
A:GLN209
|
4.6
|
61.9
|
1.0
|
NZ
|
A:LYS52
|
4.6
|
77.8
|
1.0
|
O
|
A:HOH503
|
4.6
|
54.8
|
1.0
|
CA
|
A:PRO185
|
4.6
|
73.3
|
1.0
|
PB
|
A:GDP403
|
4.7
|
65.8
|
1.0
|
NE2
|
A:GLN209
|
4.7
|
61.3
|
1.0
|
O2B
|
A:GDP403
|
4.8
|
44.4
|
1.0
|
CA
|
A:GLY208
|
4.9
|
72.2
|
1.0
|
ND2
|
B:ASN260
|
5.0
|
79.5
|
1.0
|
NH1
|
A:ARG183
|
5.0
|
54.9
|
1.0
|
|
Fluorine binding site 4 out
of 4 in 7sq2
Go back to
Fluorine Binding Sites List in 7sq2
Fluorine binding site 4 out
of 4 in the Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 4 of Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F401
b:85.8
occ:1.00
|
F4
|
A:ALF401
|
0.0
|
85.8
|
1.0
|
AL
|
A:ALF401
|
1.8
|
67.5
|
1.0
|
O1B
|
A:GDP403
|
2.0
|
35.2
|
1.0
|
F2
|
A:ALF401
|
2.5
|
129.7
|
1.0
|
F1
|
A:ALF401
|
2.6
|
103.3
|
1.0
|
N
|
A:GLU49
|
2.6
|
68.3
|
1.0
|
NH1
|
A:ARG183
|
3.2
|
54.9
|
1.0
|
NH2
|
A:ARG183
|
3.2
|
61.8
|
1.0
|
PB
|
A:GDP403
|
3.3
|
65.8
|
1.0
|
CA
|
A:GLU49
|
3.3
|
64.7
|
1.0
|
NE2
|
A:GLN209
|
3.3
|
61.3
|
1.0
|
C
|
A:GLY48
|
3.3
|
69.4
|
1.0
|
CZ
|
A:ARG183
|
3.6
|
56.0
|
1.0
|
CA
|
A:GLY48
|
3.6
|
76.1
|
1.0
|
F3
|
A:ALF401
|
3.6
|
75.6
|
1.0
|
O3A
|
A:GDP403
|
3.8
|
45.4
|
1.0
|
O3B
|
A:GDP403
|
4.0
|
70.8
|
1.0
|
CB
|
A:GLU49
|
4.1
|
74.5
|
1.0
|
CD
|
A:GLN209
|
4.2
|
61.9
|
1.0
|
OE1
|
A:GLN209
|
4.3
|
70.9
|
1.0
|
NZ
|
A:LYS52
|
4.3
|
77.8
|
1.0
|
O2B
|
A:GDP403
|
4.4
|
44.4
|
1.0
|
O
|
A:GLY48
|
4.5
|
68.1
|
1.0
|
MG
|
A:MG402
|
4.5
|
59.1
|
1.0
|
C
|
A:GLU49
|
4.6
|
70.1
|
1.0
|
N
|
A:SER50
|
4.8
|
70.5
|
1.0
|
O1A
|
A:GDP403
|
4.8
|
41.7
|
1.0
|
NE
|
A:ARG183
|
4.8
|
61.1
|
1.0
|
N
|
A:GLY48
|
4.9
|
81.6
|
1.0
|
O
|
A:HOH503
|
4.9
|
54.8
|
1.0
|
O
|
A:HOH531
|
4.9
|
61.2
|
1.0
|
O
|
A:HOH512
|
5.0
|
68.8
|
1.0
|
N
|
A:GLY208
|
5.0
|
64.6
|
1.0
|
CG
|
A:GLU49
|
5.0
|
75.0
|
1.0
|
|
Reference:
S.T.Endo-Streeter,
J.Sondek,
T.K.Harden.
Kinetic Scaffolding Mediated By A Phospholipase C-{Beta} and Gq Signaling Complex Science V. 330 974 2010.
ISSN: ISSN 0036-8075
PubMed: 20966218
DOI: 10.1126/SCIENCE.1193438
Page generated: Fri Aug 2 13:03:25 2024
|