Magnesium in PDB 3r88: Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145)
Enzymatic activity of Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145)
All present enzymatic activity of Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145):
2.4.2.18;
Protein crystallography data
The structure of Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145), PDB code: 3r88
was solved by
A.Castell,
F.L.Short,
J.S.Lott,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
58.86 /
1.73
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
94.312,
78.849,
100.494,
90.00,
110.27,
90.00
|
R / Rfree (%)
|
17.5 /
21.4
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145)
(pdb code 3r88). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the
Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145), PDB code: 3r88:
Jump to Magnesium binding site number:
1;
2;
3;
4;
Magnesium binding site 1 out
of 4 in 3r88
Go back to
Magnesium Binding Sites List in 3r88
Magnesium binding site 1 out
of 4 in the Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145)
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg402
b:13.3
occ:1.00
|
OE2
|
A:GLU252
|
2.0
|
17.2
|
1.0
|
O1A
|
A:PRP401
|
2.0
|
13.8
|
1.0
|
O
|
A:HOH770
|
2.1
|
13.1
|
1.0
|
OG
|
A:SER119
|
2.1
|
11.6
|
1.0
|
O3B
|
A:PRP401
|
2.1
|
13.7
|
1.0
|
O
|
A:HOH773
|
2.2
|
18.4
|
1.0
|
CD
|
A:GLU252
|
3.0
|
17.5
|
1.0
|
CB
|
A:SER119
|
3.1
|
13.3
|
1.0
|
OE1
|
A:GLU252
|
3.3
|
18.5
|
1.0
|
PB
|
A:PRP401
|
3.3
|
16.6
|
1.0
|
PA
|
A:PRP401
|
3.3
|
16.5
|
1.0
|
MG
|
A:MG403
|
3.4
|
23.2
|
1.0
|
O3A
|
A:PRP401
|
3.6
|
19.2
|
1.0
|
O
|
A:HOH772
|
3.8
|
28.4
|
1.0
|
N
|
A:GLY107
|
3.9
|
12.4
|
1.0
|
O1
|
A:PRP401
|
4.0
|
19.8
|
1.0
|
N
|
A:SER119
|
4.0
|
13.8
|
1.0
|
OD2
|
A:ASP251
|
4.0
|
14.4
|
1.0
|
CA
|
A:SER119
|
4.1
|
13.3
|
1.0
|
O
|
A:ASP251
|
4.2
|
16.4
|
1.0
|
O
|
A:HOH553
|
4.2
|
14.7
|
1.0
|
CA
|
A:GLY107
|
4.3
|
11.6
|
1.0
|
OD1
|
A:ASP251
|
4.3
|
20.4
|
1.0
|
O1B
|
A:PRP401
|
4.3
|
15.1
|
1.0
|
CG
|
A:GLU252
|
4.3
|
16.2
|
1.0
|
O2B
|
A:PRP401
|
4.4
|
19.5
|
1.0
|
CG
|
A:ASP251
|
4.4
|
17.7
|
1.0
|
O2A
|
A:PRP401
|
4.5
|
21.7
|
1.0
|
C
|
A:VAL106
|
4.6
|
11.9
|
1.0
|
O
|
A:HOH771
|
4.7
|
31.7
|
1.0
|
O4
|
A:PRP401
|
4.8
|
23.1
|
0.5
|
C1
|
A:PRP401
|
4.9
|
21.8
|
0.5
|
CA
|
A:VAL106
|
5.0
|
12.8
|
1.0
|
|
Magnesium binding site 2 out
of 4 in 3r88
Go back to
Magnesium Binding Sites List in 3r88
Magnesium binding site 2 out
of 4 in the Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145)
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg403
b:23.2
occ:1.00
|
O
|
A:HOH771
|
2.0
|
31.7
|
1.0
|
O
|
A:HOH620
|
2.0
|
30.1
|
1.0
|
O
|
A:HOH773
|
2.3
|
18.4
|
1.0
|
OD1
|
A:ASP251
|
2.3
|
20.4
|
1.0
|
O
|
A:HOH772
|
2.3
|
28.4
|
1.0
|
OE2
|
A:GLU252
|
2.3
|
17.2
|
1.0
|
CD
|
A:GLU252
|
3.3
|
17.5
|
1.0
|
CG
|
A:ASP251
|
3.3
|
17.7
|
1.0
|
MG
|
A:MG402
|
3.4
|
13.3
|
1.0
|
CG
|
A:GLU252
|
3.5
|
16.2
|
1.0
|
O3B
|
A:PRP401
|
3.6
|
13.7
|
1.0
|
OD2
|
A:ASP251
|
3.6
|
14.4
|
1.0
|
OD2
|
A:ASP111
|
3.9
|
25.9
|
1.0
|
O
|
A:HOH563
|
4.0
|
41.7
|
1.0
|
O
|
A:HOH733
|
4.1
|
45.5
|
1.0
|
O
|
A:HOH633
|
4.2
|
34.5
|
1.0
|
OG1
|
A:THR115
|
4.2
|
25.4
|
1.0
|
O
|
A:HOH770
|
4.3
|
13.1
|
1.0
|
O
|
A:ASP251
|
4.4
|
16.4
|
1.0
|
OE1
|
A:GLU252
|
4.4
|
18.5
|
1.0
|
C
|
A:ASP251
|
4.6
|
16.2
|
1.0
|
CB
|
A:ASP251
|
4.7
|
17.3
|
1.0
|
PB
|
A:PRP401
|
4.7
|
16.6
|
1.0
|
CG
|
A:ASP111
|
4.8
|
26.7
|
1.0
|
O2B
|
A:PRP401
|
4.8
|
19.5
|
1.0
|
N
|
A:ASP251
|
4.8
|
17.5
|
1.0
|
O1A
|
A:PRP401
|
4.9
|
13.8
|
1.0
|
CA
|
A:ASP251
|
4.9
|
17.0
|
1.0
|
CB
|
A:GLU252
|
4.9
|
15.5
|
1.0
|
|
Magnesium binding site 3 out
of 4 in 3r88
Go back to
Magnesium Binding Sites List in 3r88
Magnesium binding site 3 out
of 4 in the Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145)
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg402
b:29.4
occ:1.00
|
O
|
B:HOH767
|
2.2
|
25.2
|
1.0
|
OE2
|
B:GLU252
|
2.3
|
15.0
|
1.0
|
O
|
B:HOH539
|
2.4
|
14.0
|
1.0
|
OD1
|
B:ASP251
|
2.5
|
19.7
|
1.0
|
O
|
B:HOH619
|
3.0
|
40.0
|
1.0
|
O
|
B:HOH774
|
3.1
|
40.7
|
1.0
|
CD
|
B:GLU252
|
3.3
|
16.8
|
1.0
|
MG
|
B:MG403
|
3.4
|
13.7
|
1.0
|
CG
|
B:ASP251
|
3.4
|
16.4
|
1.0
|
CG
|
B:GLU252
|
3.5
|
18.1
|
1.0
|
O3B
|
B:PRP401
|
3.5
|
14.9
|
1.0
|
O
|
B:HOH537
|
3.6
|
39.5
|
1.0
|
O
|
B:HOH521
|
3.6
|
40.3
|
1.0
|
OD2
|
B:ASP251
|
3.7
|
13.7
|
1.0
|
OD2
|
B:ASP111
|
4.0
|
22.0
|
1.0
|
OG1
|
B:THR115
|
4.2
|
23.4
|
1.0
|
O
|
B:HOH503
|
4.3
|
13.5
|
1.0
|
O
|
B:ASP251
|
4.3
|
14.9
|
1.0
|
O
|
B:HOH709
|
4.4
|
42.6
|
1.0
|
OE1
|
B:GLU252
|
4.4
|
20.4
|
1.0
|
O
|
B:HOH689
|
4.5
|
32.4
|
1.0
|
PB
|
B:PRP401
|
4.6
|
13.9
|
1.0
|
C
|
B:ASP251
|
4.6
|
15.5
|
1.0
|
O2B
|
B:PRP401
|
4.7
|
16.3
|
1.0
|
CB
|
B:ASP251
|
4.8
|
15.9
|
1.0
|
CG
|
B:ASP111
|
4.8
|
23.4
|
1.0
|
N
|
B:ASP251
|
4.9
|
16.6
|
1.0
|
CB
|
B:GLU252
|
5.0
|
15.5
|
1.0
|
CA
|
B:ASP251
|
5.0
|
15.7
|
1.0
|
O1A
|
B:PRP401
|
5.0
|
13.8
|
1.0
|
|
Magnesium binding site 4 out
of 4 in 3r88
Go back to
Magnesium Binding Sites List in 3r88
Magnesium binding site 4 out
of 4 in the Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145)
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor ACS145) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg403
b:13.7
occ:1.00
|
O3B
|
B:PRP401
|
2.0
|
14.9
|
1.0
|
O1A
|
B:PRP401
|
2.1
|
13.8
|
1.0
|
O
|
B:HOH503
|
2.1
|
13.5
|
1.0
|
OG
|
B:SER119
|
2.1
|
15.1
|
1.0
|
OE2
|
B:GLU252
|
2.1
|
15.0
|
1.0
|
O
|
B:HOH539
|
2.2
|
14.0
|
1.0
|
CB
|
B:SER119
|
3.0
|
13.7
|
1.0
|
CD
|
B:GLU252
|
3.1
|
16.8
|
1.0
|
PB
|
B:PRP401
|
3.2
|
13.9
|
1.0
|
PA
|
B:PRP401
|
3.2
|
16.3
|
1.0
|
OE1
|
B:GLU252
|
3.4
|
20.4
|
1.0
|
MG
|
B:MG402
|
3.4
|
29.4
|
1.0
|
O3A
|
B:PRP401
|
3.5
|
16.5
|
1.0
|
O
|
B:HOH767
|
3.8
|
25.2
|
1.0
|
O1
|
B:PRP401
|
3.9
|
18.5
|
1.0
|
N
|
B:GLY107
|
4.0
|
14.6
|
1.0
|
N
|
B:SER119
|
4.0
|
13.0
|
1.0
|
OD2
|
B:ASP251
|
4.1
|
13.7
|
1.0
|
CA
|
B:SER119
|
4.1
|
13.9
|
1.0
|
O
|
B:ASP251
|
4.2
|
14.9
|
1.0
|
O
|
B:HOH774
|
4.2
|
40.7
|
1.0
|
O2B
|
B:PRP401
|
4.3
|
16.3
|
1.0
|
O1B
|
B:PRP401
|
4.3
|
15.1
|
1.0
|
CA
|
B:GLY107
|
4.3
|
13.3
|
1.0
|
O
|
B:HOH528
|
4.4
|
17.2
|
1.0
|
CG
|
B:GLU252
|
4.4
|
18.1
|
1.0
|
O2A
|
B:PRP401
|
4.5
|
21.8
|
1.0
|
OD1
|
B:ASP251
|
4.5
|
19.7
|
1.0
|
CG
|
B:ASP251
|
4.5
|
16.4
|
1.0
|
C
|
B:VAL106
|
4.6
|
13.9
|
1.0
|
CA
|
B:VAL106
|
5.0
|
14.4
|
1.0
|
|
Reference:
A.Castell,
F.L.Short,
G.L.Evans,
T.V.Cookson,
E.M.Bulloch,
D.D.Joseph,
C.E.Lee,
E.J.Parker,
E.N.Baker,
J.S.Lott.
The Substrate Capture Mechanism of Mycobacterium Tuberculosis Anthranilate Phosphoribosyltransferase Provides A Mode For Inhibition. Biochemistry V. 52 1776 2013.
ISSN: ISSN 0006-2960
PubMed: 23363292
DOI: 10.1021/BI301387M
Page generated: Thu Aug 15 10:20:08 2024
|