Fluorine in PDB 6h8x: Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
Enzymatic activity of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
All present enzymatic activity of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.:
5.4.2.6;
Protein crystallography data
The structure of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A., PDB code: 6h8x
was solved by
A.J.Robertson,
C.Bisson,
J.P.Waltho,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
23.31 /
1.83
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
38.160,
116.980,
53.110,
90.00,
98.93,
90.00
|
R / Rfree (%)
|
18.3 /
22.6
|
Other elements in 6h8x:
The structure of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A. also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
(pdb code 6h8x). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 6 binding sites of Fluorine where determined in the
Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A., PDB code: 6h8x:
Jump to Fluorine binding site number:
1;
2;
3;
4;
5;
6;
Fluorine binding site 1 out
of 6 in 6h8x
Go back to
Fluorine Binding Sites List in 6h8x
Fluorine binding site 1 out
of 6 in the Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F305
b:38.0
occ:1.00
|
F1
|
A:MGF305
|
0.0
|
38.0
|
1.0
|
MG
|
A:MGF305
|
2.0
|
38.8
|
1.0
|
MG
|
A:MG301
|
2.1
|
29.0
|
1.0
|
O
|
A:HOH460
|
2.4
|
28.2
|
1.0
|
OD2
|
A:ASP8
|
2.7
|
30.4
|
1.0
|
OD1
|
A:ASP8
|
2.8
|
27.7
|
1.0
|
O
|
A:HOH403
|
2.9
|
28.0
|
1.0
|
O
|
A:ASP10
|
3.1
|
21.2
|
1.0
|
CG
|
A:ASP8
|
3.1
|
26.4
|
1.0
|
F3
|
A:MGF305
|
3.2
|
32.8
|
1.0
|
CB
|
A:ASP10
|
3.5
|
22.3
|
1.0
|
F2
|
A:MGF305
|
3.7
|
33.8
|
1.0
|
C
|
A:ASP10
|
3.9
|
21.5
|
1.0
|
N
|
A:ASP10
|
3.9
|
20.0
|
1.0
|
CA
|
A:ASP10
|
3.9
|
20.6
|
1.0
|
OD2
|
A:ASP10
|
4.0
|
29.7
|
1.0
|
OD1
|
A:ASP170
|
4.1
|
22.8
|
1.0
|
CG
|
A:ASP10
|
4.3
|
24.7
|
1.0
|
CB
|
A:ASP8
|
4.7
|
24.3
|
1.0
|
OE2
|
A:GLU169
|
4.7
|
24.3
|
1.0
|
OE1
|
A:GLU169
|
4.7
|
25.8
|
1.0
|
CH3
|
A:ACT306
|
4.8
|
48.5
|
1.0
|
NZ
|
A:LYS145
|
4.8
|
23.3
|
1.0
|
C
|
A:LEU9
|
4.8
|
20.9
|
1.0
|
N
|
A:LEU9
|
4.9
|
20.4
|
1.0
|
|
Fluorine binding site 2 out
of 6 in 6h8x
Go back to
Fluorine Binding Sites List in 6h8x
Fluorine binding site 2 out
of 6 in the Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F305
b:33.8
occ:1.00
|
F2
|
A:MGF305
|
0.0
|
33.8
|
1.0
|
MG
|
A:MGF305
|
2.0
|
38.8
|
1.0
|
NZ
|
A:LYS145
|
2.7
|
23.3
|
1.0
|
N
|
A:ALA115
|
2.9
|
20.5
|
1.0
|
OD1
|
A:ASP8
|
2.9
|
27.7
|
1.0
|
F3
|
A:MGF305
|
3.3
|
32.8
|
1.0
|
CE
|
A:LYS145
|
3.4
|
25.5
|
1.0
|
CA
|
A:SER114
|
3.4
|
19.1
|
1.0
|
C
|
A:SER114
|
3.6
|
18.7
|
1.0
|
F1
|
A:MGF305
|
3.7
|
38.0
|
1.0
|
CB
|
A:ALA115
|
3.7
|
24.9
|
1.0
|
OG
|
A:SER114
|
3.7
|
18.3
|
1.0
|
CA
|
A:ALA115
|
3.8
|
21.9
|
1.0
|
CD
|
A:LYS145
|
3.9
|
25.2
|
1.0
|
CG
|
A:ASP8
|
4.0
|
26.4
|
1.0
|
CB
|
A:SER114
|
4.0
|
18.7
|
1.0
|
O
|
A:ALA113
|
4.2
|
21.0
|
1.0
|
CH3
|
A:ACT306
|
4.5
|
48.5
|
1.0
|
N
|
A:SER114
|
4.6
|
19.4
|
1.0
|
OE2
|
A:GLU169
|
4.6
|
24.3
|
1.0
|
OD2
|
A:ASP8
|
4.7
|
30.4
|
1.0
|
N
|
A:SER116
|
4.7
|
20.2
|
1.0
|
O
|
A:HOH460
|
4.8
|
28.2
|
1.0
|
C
|
A:ALA115
|
4.8
|
21.1
|
1.0
|
O
|
A:SER114
|
4.8
|
18.9
|
1.0
|
O
|
A:HOH498
|
4.8
|
40.5
|
1.0
|
C
|
A:ALA113
|
4.8
|
20.3
|
1.0
|
O
|
A:HOH475
|
4.9
|
35.8
|
1.0
|
|
Fluorine binding site 3 out
of 6 in 6h8x
Go back to
Fluorine Binding Sites List in 6h8x
Fluorine binding site 3 out
of 6 in the Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F305
b:32.8
occ:1.00
|
F3
|
A:MGF305
|
0.0
|
32.8
|
1.0
|
MG
|
A:MGF305
|
2.0
|
38.8
|
1.0
|
OG
|
A:SER114
|
2.7
|
18.3
|
1.0
|
N
|
A:ASP10
|
2.9
|
20.0
|
1.0
|
OD1
|
A:ASP8
|
3.1
|
27.7
|
1.0
|
F1
|
A:MGF305
|
3.2
|
38.0
|
1.0
|
F2
|
A:MGF305
|
3.3
|
33.8
|
1.0
|
OXT
|
A:ACT306
|
3.3
|
48.4
|
1.0
|
CB
|
A:LEU9
|
3.3
|
21.3
|
1.0
|
CH3
|
A:ACT306
|
3.4
|
48.5
|
1.0
|
N
|
A:LEU9
|
3.5
|
20.4
|
1.0
|
CB
|
A:ASP10
|
3.6
|
22.3
|
1.0
|
CB
|
A:SER114
|
3.6
|
18.7
|
1.0
|
CA
|
A:LEU9
|
3.7
|
21.0
|
1.0
|
C
|
A:LEU9
|
3.7
|
20.9
|
1.0
|
C
|
A:ACT306
|
3.8
|
51.5
|
1.0
|
CA
|
A:ASP10
|
3.9
|
20.6
|
1.0
|
CG
|
A:ASP8
|
4.0
|
26.4
|
1.0
|
CA
|
A:SER114
|
4.3
|
19.1
|
1.0
|
CG
|
A:LEU9
|
4.3
|
23.2
|
1.0
|
N
|
A:ALA115
|
4.4
|
20.5
|
1.0
|
N
|
A:SER116
|
4.5
|
20.2
|
1.0
|
OD2
|
A:ASP8
|
4.5
|
30.4
|
1.0
|
CD2
|
A:LEU9
|
4.5
|
26.0
|
1.0
|
CB
|
A:SER116
|
4.6
|
21.7
|
1.0
|
O
|
A:ASP10
|
4.7
|
21.2
|
1.0
|
C
|
A:ASP8
|
4.7
|
20.8
|
1.0
|
C
|
A:ASP10
|
4.8
|
21.5
|
1.0
|
C
|
A:SER114
|
4.8
|
18.7
|
1.0
|
MG
|
A:MG301
|
4.9
|
29.0
|
1.0
|
O
|
A:LEU9
|
4.9
|
22.6
|
1.0
|
|
Fluorine binding site 4 out
of 6 in 6h8x
Go back to
Fluorine Binding Sites List in 6h8x
Fluorine binding site 4 out
of 6 in the Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 4 of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F308
b:33.7
occ:1.00
|
F1
|
B:MGF308
|
0.0
|
33.7
|
1.0
|
MG
|
B:MGF308
|
2.0
|
37.5
|
1.0
|
OG
|
B:SER114
|
2.5
|
19.3
|
1.0
|
O
|
B:HOH495
|
2.7
|
36.1
|
1.0
|
N
|
B:ASP10
|
2.9
|
20.5
|
1.0
|
OD1
|
B:ASP8
|
3.0
|
24.7
|
1.0
|
F3
|
B:MGF308
|
3.2
|
34.1
|
1.0
|
CB
|
B:LEU9
|
3.3
|
24.4
|
1.0
|
F2
|
B:MGF308
|
3.3
|
33.5
|
1.0
|
N
|
B:LEU9
|
3.3
|
19.9
|
1.0
|
O
|
B:HOH493
|
3.5
|
49.0
|
1.0
|
CB
|
B:SER114
|
3.5
|
20.1
|
1.0
|
CA
|
B:LEU9
|
3.6
|
21.8
|
1.0
|
C
|
B:LEU9
|
3.7
|
20.5
|
1.0
|
CB
|
B:ASP10
|
3.8
|
24.1
|
1.0
|
CA
|
B:ASP10
|
3.9
|
22.1
|
1.0
|
CG
|
B:ASP8
|
3.9
|
24.2
|
1.0
|
CA
|
B:SER114
|
4.2
|
21.0
|
1.0
|
CG
|
B:LEU9
|
4.2
|
28.6
|
1.0
|
N
|
B:ALA115
|
4.3
|
21.2
|
1.0
|
OD2
|
B:ASP8
|
4.4
|
30.8
|
1.0
|
N
|
B:SER116
|
4.4
|
22.6
|
1.0
|
C
|
B:ASP8
|
4.5
|
20.8
|
1.0
|
CB
|
B:SER116
|
4.5
|
23.0
|
1.0
|
O
|
B:ASP10
|
4.7
|
24.6
|
1.0
|
C
|
B:SER114
|
4.7
|
20.1
|
1.0
|
CD2
|
B:LEU9
|
4.8
|
31.6
|
1.0
|
C
|
B:ASP10
|
4.8
|
22.5
|
1.0
|
CA
|
B:ASP8
|
4.9
|
20.0
|
1.0
|
O
|
B:LEU9
|
4.9
|
22.5
|
1.0
|
MG
|
B:MG301
|
4.9
|
27.2
|
1.0
|
|
Fluorine binding site 5 out
of 6 in 6h8x
Go back to
Fluorine Binding Sites List in 6h8x
Fluorine binding site 5 out
of 6 in the Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 5 of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F308
b:33.5
occ:1.00
|
F2
|
B:MGF308
|
0.0
|
33.5
|
1.0
|
MG
|
B:MG301
|
1.9
|
27.2
|
1.0
|
MG
|
B:MGF308
|
2.0
|
37.5
|
1.0
|
OD2
|
B:ASP8
|
2.6
|
30.8
|
1.0
|
O
|
B:HOH495
|
2.7
|
36.1
|
1.0
|
O
|
B:HOH408
|
2.7
|
30.4
|
1.0
|
O
|
B:HOH432
|
2.8
|
29.1
|
1.0
|
O
|
B:ASP10
|
2.8
|
24.6
|
1.0
|
OD1
|
B:ASP8
|
2.9
|
24.7
|
1.0
|
CG
|
B:ASP8
|
3.1
|
24.2
|
1.0
|
F1
|
B:MGF308
|
3.3
|
33.7
|
1.0
|
CB
|
B:ASP10
|
3.3
|
24.1
|
1.0
|
C
|
B:ASP10
|
3.6
|
22.5
|
1.0
|
CA
|
B:ASP10
|
3.7
|
22.1
|
1.0
|
N
|
B:ASP10
|
3.7
|
20.5
|
1.0
|
F3
|
B:MGF308
|
3.7
|
34.1
|
1.0
|
OD1
|
B:ASP170
|
4.0
|
24.8
|
1.0
|
OD2
|
B:ASP10
|
4.0
|
27.8
|
1.0
|
CG
|
B:ASP10
|
4.2
|
26.4
|
1.0
|
CB
|
B:ASP8
|
4.6
|
21.6
|
1.0
|
C
|
B:LEU9
|
4.7
|
20.5
|
1.0
|
OE1
|
B:GLU169
|
4.7
|
27.3
|
1.0
|
N
|
B:LEU9
|
4.8
|
19.9
|
1.0
|
N
|
B:GLY11
|
4.9
|
22.8
|
1.0
|
OE2
|
B:GLU169
|
4.9
|
25.4
|
1.0
|
O
|
B:HOH493
|
4.9
|
49.0
|
1.0
|
NZ
|
B:LYS145
|
4.9
|
24.3
|
1.0
|
CG
|
B:ASP170
|
5.0
|
25.7
|
1.0
|
|
Fluorine binding site 6 out
of 6 in 6h8x
Go back to
Fluorine Binding Sites List in 6h8x
Fluorine binding site 6 out
of 6 in the Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 6 of Beta-Phosphoglucomutase From Lactococcus Lactis in An Open Conformer Complexed with Magnesium Trifluoride to 1.8 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F308
b:34.1
occ:1.00
|
F3
|
B:MGF308
|
0.0
|
34.1
|
1.0
|
MG
|
B:MGF308
|
2.0
|
37.5
|
1.0
|
NZ
|
B:LYS145
|
2.5
|
24.3
|
1.0
|
OD1
|
B:ASP8
|
2.6
|
24.7
|
1.0
|
O
|
B:HOH495
|
2.7
|
36.1
|
1.0
|
N
|
B:ALA115
|
2.9
|
21.2
|
1.0
|
F1
|
B:MGF308
|
3.2
|
33.7
|
1.0
|
CE
|
B:LYS145
|
3.3
|
25.6
|
1.0
|
CA
|
B:SER114
|
3.4
|
21.0
|
1.0
|
C
|
B:SER114
|
3.7
|
20.1
|
1.0
|
CB
|
B:ALA115
|
3.7
|
23.0
|
1.0
|
CG
|
B:ASP8
|
3.7
|
24.2
|
1.0
|
F2
|
B:MGF308
|
3.7
|
33.5
|
1.0
|
OG
|
B:SER114
|
3.8
|
19.3
|
1.0
|
CA
|
B:ALA115
|
3.9
|
22.6
|
1.0
|
CD
|
B:LYS145
|
4.0
|
26.0
|
1.0
|
CB
|
B:SER114
|
4.1
|
20.1
|
1.0
|
O
|
B:ALA113
|
4.2
|
21.3
|
1.0
|
OD2
|
B:ASP8
|
4.4
|
30.8
|
1.0
|
OE2
|
B:GLU169
|
4.5
|
25.4
|
1.0
|
O
|
B:HOH408
|
4.6
|
30.4
|
1.0
|
N
|
B:SER114
|
4.6
|
20.3
|
1.0
|
O
|
B:HOH493
|
4.7
|
49.0
|
1.0
|
CB
|
B:ASP8
|
4.7
|
21.6
|
1.0
|
N
|
B:SER116
|
4.8
|
22.6
|
1.0
|
O
|
B:SER114
|
4.9
|
19.8
|
1.0
|
C
|
B:ALA115
|
4.9
|
21.9
|
1.0
|
C
|
B:ALA113
|
4.9
|
20.1
|
1.0
|
|
Reference:
A.J.Robertson,
C.Bisson,
J.P.Waltho.
Transition State of Phospho-Enzyme Hydrolysis in Beta-Phosphoglucomutase. To Be Published.
Page generated: Thu Aug 1 20:54:58 2024
|