Fluorine in PDB 6hdj: R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.
Enzymatic activity of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.
All present enzymatic activity of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.:
5.4.2.6;
Protein crystallography data
The structure of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A., PDB code: 6hdj
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)
|
48.10 /
1.16
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
104.210,
37.220,
54.220,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
14.3 /
16.6
|
Other elements in 6hdj:
The structure of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A. also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.
(pdb code 6hdj). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 4 binding sites of Fluorine where determined in the
R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A., PDB code: 6hdj:
Jump to Fluorine binding site number:
1;
2;
3;
4;
Fluorine binding site 1 out
of 4 in 6hdj
Go back to
Fluorine Binding Sites List in 6hdj
Fluorine binding site 1 out
of 4 in the R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F305
b:8.9
occ:1.00
|
F1
|
A:ALF305
|
0.0
|
8.9
|
1.0
|
AL
|
A:ALF305
|
1.8
|
8.8
|
1.0
|
O1
|
A:BG6306
|
2.5
|
7.8
|
1.0
|
F3
|
A:ALF305
|
2.5
|
9.9
|
1.0
|
F4
|
A:ALF305
|
2.6
|
8.6
|
1.0
|
OD1
|
A:ASP8
|
2.6
|
8.4
|
1.0
|
N
|
A:ASP10
|
2.8
|
7.8
|
1.0
|
OG
|
A:SER114
|
2.8
|
9.6
|
1.0
|
N
|
A:LEU9
|
2.9
|
8.3
|
1.0
|
OD2
|
A:ASP10
|
3.2
|
9.5
|
1.0
|
CB
|
A:LEU9
|
3.3
|
9.6
|
1.0
|
CA
|
A:LEU9
|
3.4
|
8.2
|
1.0
|
CG
|
A:ASP8
|
3.4
|
8.3
|
1.0
|
C
|
A:LEU9
|
3.5
|
8.1
|
1.0
|
F2
|
A:ALF305
|
3.5
|
9.4
|
1.0
|
CG
|
A:ASP10
|
3.6
|
9.1
|
1.0
|
CB
|
A:SER114
|
3.6
|
10.1
|
1.0
|
OD2
|
A:ASP8
|
3.8
|
9.3
|
1.0
|
CB
|
A:ASP10
|
3.8
|
7.7
|
1.0
|
CA
|
A:ASP10
|
3.9
|
8.0
|
1.0
|
C1
|
A:BG6306
|
3.9
|
8.2
|
1.0
|
C
|
A:ASP8
|
4.0
|
8.3
|
1.0
|
CA
|
A:SER114
|
4.1
|
10.6
|
1.0
|
MG
|
A:MG304
|
4.2
|
8.6
|
1.0
|
CA
|
A:ASP8
|
4.4
|
8.2
|
1.0
|
OD1
|
A:ASP10
|
4.4
|
9.2
|
1.0
|
CB
|
A:ASP8
|
4.4
|
8.7
|
1.0
|
O
|
A:ASP10
|
4.5
|
8.9
|
1.0
|
O5
|
A:BG6306
|
4.6
|
8.7
|
1.0
|
N
|
A:ALA115
|
4.6
|
9.3
|
1.0
|
C2
|
A:BG6306
|
4.7
|
8.0
|
1.0
|
C
|
A:ASP10
|
4.7
|
8.3
|
1.0
|
O
|
A:LEU9
|
4.7
|
8.8
|
1.0
|
O2
|
A:BG6306
|
4.7
|
8.4
|
1.0
|
CG
|
A:LEU9
|
4.7
|
12.2
|
1.0
|
NZ
|
A:LYS145
|
4.8
|
11.6
|
1.0
|
CB
|
A:SER116
|
4.8
|
9.7
|
1.0
|
C
|
A:SER114
|
4.9
|
9.9
|
1.0
|
O
|
A:HOH426
|
4.9
|
9.9
|
1.0
|
N
|
A:SER116
|
5.0
|
9.5
|
1.0
|
|
Fluorine binding site 2 out
of 4 in 6hdj
Go back to
Fluorine Binding Sites List in 6hdj
Fluorine binding site 2 out
of 4 in the R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F305
b:9.4
occ:1.00
|
F2
|
A:ALF305
|
0.0
|
9.4
|
1.0
|
AL
|
A:ALF305
|
1.8
|
8.8
|
1.0
|
F3
|
A:ALF305
|
2.4
|
9.9
|
1.0
|
F4
|
A:ALF305
|
2.5
|
8.6
|
1.0
|
O
|
A:HOH426
|
2.7
|
9.9
|
1.0
|
OD1
|
A:ASP8
|
2.7
|
8.4
|
1.0
|
O1
|
A:BG6306
|
2.8
|
7.8
|
1.0
|
C1
|
A:BG6306
|
3.1
|
8.2
|
1.0
|
CA
|
A:GLY46
|
3.1
|
10.2
|
1.0
|
NZ
|
A:LYS145
|
3.1
|
11.6
|
1.0
|
O2
|
A:BG6306
|
3.1
|
8.4
|
1.0
|
F1
|
A:ALF305
|
3.5
|
8.9
|
1.0
|
CG
|
A:ASP8
|
3.6
|
8.3
|
1.0
|
MG
|
A:MG304
|
3.6
|
8.6
|
1.0
|
C2
|
A:BG6306
|
3.7
|
8.0
|
1.0
|
N
|
A:GLY46
|
3.8
|
9.5
|
1.0
|
OD2
|
A:ASP8
|
3.9
|
9.3
|
1.0
|
C
|
A:GLY46
|
3.9
|
9.9
|
1.0
|
O
|
A:GLY46
|
3.9
|
12.9
|
1.0
|
OE2
|
A:GLU169
|
3.9
|
11.6
|
1.0
|
CD
|
A:LYS145
|
4.0
|
12.7
|
1.0
|
CE
|
A:LYS145
|
4.0
|
12.3
|
1.0
|
O5
|
A:BG6306
|
4.3
|
8.7
|
1.0
|
O
|
A:HOH455
|
4.5
|
9.8
|
1.0
|
OE1
|
A:GLU169
|
4.6
|
12.5
|
1.0
|
CB
|
A:ALA115
|
4.6
|
12.1
|
1.0
|
CD
|
A:GLU169
|
4.7
|
10.7
|
1.0
|
N
|
A:ALA115
|
4.7
|
9.3
|
1.0
|
C3
|
A:BG6306
|
4.8
|
8.1
|
1.0
|
OG
|
A:SER171
|
4.8
|
11.6
|
1.0
|
CB
|
A:ASP8
|
4.8
|
8.7
|
1.0
|
|
Fluorine binding site 3 out
of 4 in 6hdj
Go back to
Fluorine Binding Sites List in 6hdj
Fluorine binding site 3 out
of 4 in the R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F305
b:9.9
occ:1.00
|
F3
|
A:ALF305
|
0.0
|
9.9
|
1.0
|
AL
|
A:ALF305
|
1.7
|
8.8
|
1.0
|
F2
|
A:ALF305
|
2.4
|
9.4
|
1.0
|
F1
|
A:ALF305
|
2.5
|
8.9
|
1.0
|
OD1
|
A:ASP8
|
2.6
|
8.4
|
1.0
|
N
|
A:ALA115
|
2.7
|
9.3
|
1.0
|
O1
|
A:BG6306
|
2.7
|
7.8
|
1.0
|
NZ
|
A:LYS145
|
2.8
|
11.6
|
1.0
|
CA
|
A:SER114
|
3.0
|
10.6
|
1.0
|
OG
|
A:SER114
|
3.1
|
9.6
|
1.0
|
C
|
A:SER114
|
3.3
|
9.9
|
1.0
|
CB
|
A:SER114
|
3.5
|
10.1
|
1.0
|
C1
|
A:BG6306
|
3.5
|
8.2
|
1.0
|
F4
|
A:ALF305
|
3.6
|
8.6
|
1.0
|
CA
|
A:ALA115
|
3.7
|
9.8
|
1.0
|
CB
|
A:ALA115
|
3.7
|
12.1
|
1.0
|
CE
|
A:LYS145
|
3.8
|
12.3
|
1.0
|
CG
|
A:ASP8
|
3.9
|
8.3
|
1.0
|
O
|
A:ALA113
|
3.9
|
11.2
|
1.0
|
N
|
A:SER116
|
4.2
|
9.5
|
1.0
|
N
|
A:SER114
|
4.2
|
9.8
|
1.0
|
O5
|
A:BG6306
|
4.2
|
8.7
|
1.0
|
C
|
A:ALA115
|
4.5
|
9.7
|
1.0
|
C
|
A:ALA113
|
4.5
|
9.5
|
1.0
|
N
|
A:LEU9
|
4.5
|
8.3
|
1.0
|
O
|
A:SER114
|
4.5
|
11.1
|
1.0
|
CD
|
A:LYS145
|
4.5
|
12.7
|
1.0
|
OD2
|
A:ASP8
|
4.7
|
9.3
|
1.0
|
CB
|
A:ASP8
|
4.7
|
8.7
|
1.0
|
O
|
A:HOH426
|
4.7
|
9.9
|
1.0
|
OE2
|
A:GLU169
|
4.8
|
11.6
|
1.0
|
CA
|
A:ASP8
|
4.8
|
8.2
|
1.0
|
OD2
|
A:ASP10
|
4.8
|
9.5
|
1.0
|
C2
|
A:BG6306
|
4.8
|
8.0
|
1.0
|
O2
|
A:BG6306
|
4.8
|
8.4
|
1.0
|
|
Fluorine binding site 4 out
of 4 in 6hdj
Go back to
Fluorine Binding Sites List in 6hdj
Fluorine binding site 4 out
of 4 in the R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A.
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 4 of R49K Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed Aluminium Tetrafluoride and Beta-G6P to 1.2 A. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F305
b:8.6
occ:1.00
|
F4
|
A:ALF305
|
0.0
|
8.6
|
1.0
|
AL
|
A:ALF305
|
1.8
|
8.8
|
1.0
|
MG
|
A:MG304
|
2.0
|
8.6
|
1.0
|
F2
|
A:ALF305
|
2.5
|
9.4
|
1.0
|
F1
|
A:ALF305
|
2.6
|
8.9
|
1.0
|
O1
|
A:BG6306
|
2.6
|
7.8
|
1.0
|
OD1
|
A:ASP8
|
2.7
|
8.4
|
1.0
|
OD2
|
A:ASP8
|
2.8
|
9.3
|
1.0
|
O
|
A:HOH426
|
2.8
|
9.9
|
1.0
|
O2
|
A:BG6306
|
2.8
|
8.4
|
1.0
|
O
|
A:ASP10
|
3.0
|
8.9
|
1.0
|
O
|
A:HOH455
|
3.0
|
9.8
|
1.0
|
CG
|
A:ASP8
|
3.1
|
8.3
|
1.0
|
CB
|
A:ASP10
|
3.2
|
7.7
|
1.0
|
N
|
A:ASP10
|
3.3
|
7.8
|
1.0
|
C1
|
A:BG6306
|
3.5
|
8.2
|
1.0
|
CA
|
A:ASP10
|
3.5
|
8.0
|
1.0
|
C2
|
A:BG6306
|
3.5
|
8.0
|
1.0
|
F3
|
A:ALF305
|
3.6
|
9.9
|
1.0
|
C
|
A:ASP10
|
3.6
|
8.3
|
1.0
|
OD2
|
A:ASP10
|
3.6
|
9.5
|
1.0
|
CG
|
A:ASP10
|
3.8
|
9.1
|
1.0
|
OD1
|
A:ASP170
|
4.0
|
8.7
|
1.0
|
C
|
A:LEU9
|
4.3
|
8.1
|
1.0
|
N
|
A:LEU9
|
4.4
|
8.3
|
1.0
|
O
|
A:HOH497
|
4.5
|
10.7
|
1.0
|
CB
|
A:ASP8
|
4.6
|
8.7
|
1.0
|
O5
|
A:BG6306
|
4.7
|
8.7
|
1.0
|
N
|
A:GLY46
|
4.8
|
9.5
|
1.0
|
CA
|
A:GLY46
|
4.8
|
10.2
|
1.0
|
CA
|
A:LEU9
|
4.9
|
8.2
|
1.0
|
N
|
A:GLY11
|
4.9
|
8.2
|
1.0
|
C3
|
A:BG6306
|
4.9
|
8.1
|
1.0
|
OD1
|
A:ASP10
|
5.0
|
9.2
|
1.0
|
CG
|
A:ASP170
|
5.0
|
9.4
|
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 21:00:41 2024
|