Fluorine in PDB 4n5v: Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase
Enzymatic activity of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase
All present enzymatic activity of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase:
2.4.2.18;
Protein crystallography data
The structure of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase, PDB code: 4n5v
was solved by
A.Castell,
T.V.M.Cookson,
E.J.Parker,
E.N.Baker,
S.J.Lott,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
73.52 /
1.90
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
79.595,
92.542,
121.063,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
18.2 /
21.8
|
Other elements in 4n5v:
The structure of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase
(pdb code 4n5v). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 4 binding sites of Fluorine where determined in the
Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase, PDB code: 4n5v:
Jump to Fluorine binding site number:
1;
2;
3;
4;
Fluorine binding site 1 out
of 4 in 4n5v
Go back to
Fluorine Binding Sites List in 4n5v
Fluorine binding site 1 out
of 4 in the Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 1 of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F404
b:21.6
occ:1.00
|
FAH
|
A:FA0404
|
0.0
|
21.6
|
1.0
|
CAG
|
A:FA0404
|
1.3
|
21.0
|
1.0
|
CAF
|
A:FA0404
|
2.3
|
16.8
|
1.0
|
CAI
|
A:FA0404
|
2.4
|
17.6
|
1.0
|
ND1
|
A:HIS136
|
3.1
|
13.5
|
1.0
|
CG2
|
A:VAL106
|
3.2
|
19.7
|
1.0
|
CG
|
A:HIS136
|
3.3
|
16.4
|
1.0
|
CB
|
A:HIS136
|
3.3
|
17.1
|
1.0
|
C
|
A:HIS136
|
3.4
|
19.0
|
1.0
|
N
|
A:GLY137
|
3.5
|
19.1
|
1.0
|
O
|
A:HIS136
|
3.5
|
19.0
|
1.0
|
CAE
|
A:FA0404
|
3.6
|
18.4
|
1.0
|
CAJ
|
A:FA0404
|
3.6
|
19.4
|
1.0
|
O
|
A:GLY206
|
3.7
|
19.4
|
1.0
|
CA
|
A:GLY137
|
3.7
|
19.9
|
1.0
|
C
|
A:GLY206
|
3.7
|
18.0
|
1.0
|
O
|
A:HOH536
|
3.8
|
24.8
|
1.0
|
CG1
|
A:VAL106
|
3.9
|
19.8
|
1.0
|
CE1
|
A:HIS136
|
3.9
|
16.8
|
1.0
|
CA
|
A:HIS136
|
4.0
|
18.4
|
1.0
|
N
|
A:PRO207
|
4.0
|
17.7
|
1.0
|
CB
|
A:VAL106
|
4.1
|
17.4
|
1.0
|
CAD
|
A:FA0404
|
4.1
|
19.5
|
1.0
|
CA
|
A:PRO207
|
4.2
|
17.5
|
1.0
|
CD2
|
A:HIS136
|
4.2
|
13.7
|
1.0
|
CA
|
A:GLY206
|
4.3
|
19.0
|
1.0
|
NE2
|
A:HIS136
|
4.5
|
15.7
|
1.0
|
C
|
A:GLY137
|
4.6
|
19.8
|
1.0
|
CD
|
A:PRO207
|
4.6
|
19.0
|
1.0
|
NAK
|
A:FA0404
|
4.7
|
18.8
|
1.0
|
CG
|
A:PRO207
|
4.9
|
17.1
|
1.0
|
N
|
A:HIS136
|
4.9
|
19.7
|
1.0
|
O
|
A:GLY137
|
5.0
|
19.8
|
1.0
|
|
Fluorine binding site 2 out
of 4 in 4n5v
Go back to
Fluorine Binding Sites List in 4n5v
Fluorine binding site 2 out
of 4 in the Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 2 of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:F405
b:24.9
occ:1.00
|
FAH
|
A:FA0405
|
0.0
|
24.9
|
1.0
|
CAG
|
A:FA0405
|
1.3
|
21.8
|
1.0
|
CAI
|
A:FA0405
|
2.3
|
23.2
|
1.0
|
CAF
|
A:FA0405
|
2.4
|
21.6
|
1.0
|
CB
|
A:ALA179
|
3.2
|
18.4
|
1.0
|
O
|
A:HOH769
|
3.5
|
36.8
|
1.0
|
CAJ
|
A:FA0405
|
3.6
|
23.5
|
1.0
|
CAE
|
A:FA0405
|
3.6
|
22.1
|
1.0
|
CD2
|
A:TYR186
|
3.7
|
21.4
|
1.0
|
C
|
A:ALA179
|
3.9
|
18.9
|
1.0
|
CB
|
A:HIS183
|
3.9
|
16.6
|
1.0
|
O
|
A:ALA179
|
4.0
|
19.9
|
1.0
|
CAD
|
A:FA0405
|
4.1
|
23.2
|
1.0
|
CA
|
A:ALA179
|
4.1
|
18.3
|
1.0
|
ND1
|
A:HIS183
|
4.2
|
19.1
|
1.0
|
CE
|
A:MET86
|
4.2
|
20.4
|
1.0
|
N
|
A:PRO180
|
4.2
|
19.4
|
1.0
|
CE2
|
A:TYR186
|
4.3
|
20.9
|
1.0
|
CG
|
A:HIS183
|
4.4
|
18.6
|
1.0
|
CG
|
A:TYR186
|
4.4
|
19.6
|
1.0
|
OAA
|
A:FA0404
|
4.6
|
21.3
|
1.0
|
CB
|
A:TYR186
|
4.6
|
19.4
|
1.0
|
NAK
|
A:FA0405
|
4.7
|
22.0
|
1.0
|
CAE
|
A:FA0404
|
4.7
|
18.4
|
1.0
|
CD
|
A:PRO180
|
4.8
|
19.0
|
1.0
|
CA
|
A:PRO180
|
4.8
|
19.8
|
1.0
|
O
|
A:HIS183
|
4.8
|
17.4
|
1.0
|
ND2
|
A:ASN138
|
4.9
|
16.9
|
1.0
|
|
Fluorine binding site 3 out
of 4 in 4n5v
Go back to
Fluorine Binding Sites List in 4n5v
Fluorine binding site 3 out
of 4 in the Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 3 of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F404
b:26.5
occ:1.00
|
FAH
|
B:FA0404
|
0.0
|
26.5
|
1.0
|
CAG
|
B:FA0404
|
1.3
|
25.0
|
1.0
|
CAI
|
B:FA0404
|
2.3
|
22.7
|
1.0
|
CAF
|
B:FA0404
|
2.4
|
23.8
|
1.0
|
O
|
B:HOH623
|
3.0
|
38.5
|
1.0
|
CB
|
B:ALA179
|
3.3
|
16.7
|
1.0
|
CAE
|
B:FA0404
|
3.6
|
22.6
|
1.0
|
CAJ
|
B:FA0404
|
3.6
|
23.4
|
1.0
|
CD2
|
B:TYR186
|
3.7
|
20.8
|
1.0
|
CB
|
B:HIS183
|
3.9
|
16.9
|
1.0
|
C
|
B:ALA179
|
3.9
|
18.5
|
1.0
|
O
|
B:ALA179
|
4.0
|
18.4
|
1.0
|
CAD
|
B:FA0404
|
4.1
|
22.7
|
1.0
|
ND1
|
B:HIS183
|
4.1
|
20.8
|
1.0
|
CA
|
B:ALA179
|
4.2
|
18.0
|
1.0
|
CE
|
B:MET86
|
4.2
|
22.9
|
1.0
|
CG
|
B:HIS183
|
4.3
|
17.4
|
1.0
|
CE2
|
B:TYR186
|
4.4
|
22.1
|
1.0
|
N
|
B:PRO180
|
4.4
|
19.6
|
1.0
|
CG
|
B:TYR186
|
4.4
|
19.7
|
1.0
|
CB
|
B:TYR186
|
4.6
|
19.3
|
1.0
|
OAC
|
B:FA0405
|
4.7
|
27.3
|
1.0
|
NAK
|
B:FA0404
|
4.7
|
23.2
|
1.0
|
CAE
|
B:FA0405
|
4.7
|
24.1
|
1.0
|
O
|
B:HIS183
|
4.8
|
18.9
|
1.0
|
CA
|
B:PRO180
|
4.9
|
19.8
|
1.0
|
CD
|
B:PRO180
|
4.9
|
19.7
|
1.0
|
ND2
|
B:ASN138
|
4.9
|
20.6
|
1.0
|
|
Fluorine binding site 4 out
of 4 in 4n5v
Go back to
Fluorine Binding Sites List in 4n5v
Fluorine binding site 4 out
of 4 in the Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase
Mono view
Stereo pair view
|
A full contact list of Fluorine with other atoms in the F binding
site number 4 of Alternative Substrates of Mycobacterium Tuberculosis Anthranilate Phosphoribosyl Transferase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:F405
b:25.6
occ:1.00
|
FAH
|
B:FA0405
|
0.0
|
25.6
|
1.0
|
CAG
|
B:FA0405
|
1.3
|
24.0
|
1.0
|
CAF
|
B:FA0405
|
2.3
|
22.8
|
1.0
|
CAI
|
B:FA0405
|
2.4
|
24.3
|
1.0
|
ND1
|
B:HIS136
|
3.2
|
19.2
|
1.0
|
CG
|
B:HIS136
|
3.3
|
17.7
|
1.0
|
CB
|
B:HIS136
|
3.3
|
18.9
|
1.0
|
C
|
B:HIS136
|
3.3
|
20.1
|
1.0
|
CG2
|
B:VAL106
|
3.3
|
22.6
|
1.0
|
O
|
B:HIS136
|
3.4
|
20.5
|
1.0
|
N
|
B:GLY137
|
3.4
|
20.1
|
1.0
|
CAE
|
B:FA0405
|
3.6
|
24.1
|
1.0
|
CAJ
|
B:FA0405
|
3.6
|
25.0
|
1.0
|
O
|
B:GLY206
|
3.6
|
22.3
|
1.0
|
O
|
B:HOH616
|
3.7
|
35.6
|
1.0
|
CA
|
B:GLY137
|
3.7
|
20.4
|
1.0
|
C
|
B:GLY206
|
3.7
|
21.6
|
1.0
|
CA
|
B:HIS136
|
3.9
|
18.9
|
1.0
|
CE1
|
B:HIS136
|
4.0
|
14.6
|
1.0
|
N
|
B:PRO207
|
4.1
|
21.9
|
1.0
|
CG1
|
B:VAL106
|
4.1
|
20.4
|
1.0
|
CAD
|
B:FA0405
|
4.1
|
24.2
|
1.0
|
CD2
|
B:HIS136
|
4.1
|
18.7
|
1.0
|
CA
|
B:GLY206
|
4.2
|
22.1
|
1.0
|
CB
|
B:VAL106
|
4.2
|
21.1
|
1.0
|
CA
|
B:PRO207
|
4.5
|
21.9
|
1.0
|
NE2
|
B:HIS136
|
4.5
|
19.7
|
1.0
|
C
|
B:GLY137
|
4.5
|
20.4
|
1.0
|
NAK
|
B:FA0405
|
4.7
|
24.3
|
1.0
|
CD
|
B:PRO207
|
4.7
|
21.9
|
1.0
|
N
|
B:HIS136
|
4.8
|
19.4
|
1.0
|
O
|
B:GLY137
|
4.9
|
19.5
|
1.0
|
|
Reference:
T.V.Cookson,
A.Castell,
E.M.Bulloch,
G.L.Evans,
F.L.Short,
E.N.Baker,
J.S.Lott,
E.J.Parker.
Alternative Substrates Reveal Catalytic Cycle and Key Binding Events in the Reaction Catalysed By Anthranilate Phosphoribosyltransferase From Mycobacterium Tuberculosis. Biochem.J. V. 461 87 2014.
ISSN: ISSN 0264-6021
PubMed: 24712732
DOI: 10.1042/BJ20140209
Page generated: Thu Aug 1 04:07:07 2024
|