Magnesium in PDB 1ao0: Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp
Enzymatic activity of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp
All present enzymatic activity of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp:
2.4.2.14;
Protein crystallography data
The structure of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp, PDB code: 1ao0
was solved by
D.R.Tomchick,
J.L.Smith,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
15.00 /
2.80
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
160.300,
70.400,
182.700,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
21.4 /
26.4
|
Other elements in 1ao0:
The structure of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp
(pdb code 1ao0). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the
Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp, PDB code: 1ao0:
Jump to Magnesium binding site number:
1;
2;
3;
4;
Magnesium binding site 1 out
of 4 in 1ao0
Go back to
Magnesium Binding Sites List in 1ao0
Magnesium binding site 1 out
of 4 in the Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg469
b:10.1
occ:1.00
|
OD1
|
A:ASP346
|
2.0
|
19.2
|
1.0
|
OD1
|
A:ASP345
|
2.1
|
15.3
|
1.0
|
O
|
A:HOH470
|
2.1
|
11.7
|
1.0
|
O2'
|
A:5GP467
|
2.1
|
13.3
|
1.0
|
OG
|
A:SER283
|
2.2
|
23.6
|
1.0
|
CB
|
A:SER283
|
2.3
|
13.0
|
1.0
|
O3'
|
A:5GP467
|
2.5
|
17.5
|
1.0
|
CG
|
A:ASP345
|
3.2
|
17.9
|
1.0
|
CG
|
A:ASP346
|
3.2
|
22.0
|
1.0
|
C2'
|
A:5GP467
|
3.3
|
17.5
|
1.0
|
OD2
|
A:ASP345
|
3.6
|
18.3
|
1.0
|
C3'
|
A:5GP467
|
3.6
|
20.2
|
1.0
|
CA
|
A:SER283
|
3.6
|
15.3
|
1.0
|
C
|
A:SER283
|
3.9
|
18.2
|
1.0
|
N
|
A:ASP346
|
3.9
|
20.9
|
1.0
|
OD2
|
A:ASP346
|
4.0
|
11.9
|
1.0
|
O1B
|
A:ADP468
|
4.1
|
60.0
|
1.0
|
N
|
A:SER284
|
4.1
|
11.7
|
1.0
|
CB
|
A:ASP346
|
4.2
|
17.4
|
1.0
|
CB
|
A:SER284
|
4.3
|
10.0
|
1.0
|
C4'
|
A:5GP467
|
4.3
|
14.7
|
1.0
|
N
|
A:SER283
|
4.4
|
15.5
|
1.0
|
O
|
A:SER283
|
4.4
|
24.9
|
1.0
|
C1'
|
A:5GP467
|
4.5
|
23.5
|
1.0
|
OG
|
A:SER284
|
4.5
|
13.5
|
1.0
|
CB
|
A:ASP345
|
4.5
|
16.3
|
1.0
|
CB
|
A:VAL280
|
4.6
|
10.1
|
1.0
|
CA
|
A:ASP346
|
4.6
|
21.6
|
1.0
|
CA
|
A:ASP345
|
4.7
|
23.3
|
1.0
|
C
|
A:ASP345
|
4.8
|
23.4
|
1.0
|
CA
|
A:SER284
|
4.8
|
11.2
|
1.0
|
N
|
A:SER347
|
4.9
|
12.6
|
1.0
|
CG1
|
A:VAL280
|
4.9
|
10.2
|
1.0
|
CE1
|
A:TYR242
|
4.9
|
19.5
|
1.0
|
CD1
|
A:TYR242
|
5.0
|
19.2
|
1.0
|
|
Magnesium binding site 2 out
of 4 in 1ao0
Go back to
Magnesium Binding Sites List in 1ao0
Magnesium binding site 2 out
of 4 in the Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg469
b:22.9
occ:1.00
|
OD1
|
B:ASP346
|
2.0
|
20.9
|
1.0
|
O
|
B:HOH470
|
2.0
|
10.1
|
1.0
|
OD1
|
B:ASP345
|
2.1
|
18.6
|
1.0
|
O2'
|
B:5GP467
|
2.1
|
20.3
|
1.0
|
OG
|
B:SER283
|
2.2
|
24.3
|
1.0
|
CB
|
B:SER283
|
2.3
|
14.2
|
1.0
|
O3'
|
B:5GP467
|
2.6
|
16.2
|
1.0
|
CG
|
B:ASP345
|
3.2
|
23.8
|
1.0
|
CG
|
B:ASP346
|
3.2
|
15.8
|
1.0
|
C2'
|
B:5GP467
|
3.3
|
19.7
|
1.0
|
C3'
|
B:5GP467
|
3.6
|
14.8
|
1.0
|
OD2
|
B:ASP345
|
3.6
|
19.6
|
1.0
|
CA
|
B:SER283
|
3.6
|
20.9
|
1.0
|
C
|
B:SER283
|
3.9
|
24.8
|
1.0
|
N
|
B:ASP346
|
4.0
|
27.4
|
1.0
|
O1B
|
B:ADP468
|
4.0
|
53.6
|
1.0
|
OD2
|
B:ASP346
|
4.0
|
18.6
|
1.0
|
N
|
B:SER284
|
4.1
|
19.8
|
1.0
|
CB
|
B:ASP346
|
4.2
|
18.2
|
1.0
|
C4'
|
B:5GP467
|
4.3
|
12.9
|
1.0
|
CB
|
B:SER284
|
4.3
|
24.0
|
1.0
|
N
|
B:SER283
|
4.4
|
21.4
|
1.0
|
C1'
|
B:5GP467
|
4.4
|
20.4
|
1.0
|
O
|
B:SER283
|
4.4
|
31.2
|
1.0
|
OG
|
B:SER284
|
4.5
|
24.1
|
1.0
|
CB
|
B:ASP345
|
4.5
|
26.5
|
1.0
|
CB
|
B:VAL280
|
4.6
|
15.0
|
1.0
|
CA
|
B:ASP346
|
4.7
|
22.7
|
1.0
|
CA
|
B:ASP345
|
4.7
|
29.4
|
1.0
|
CA
|
B:SER284
|
4.8
|
19.6
|
1.0
|
CG1
|
B:VAL280
|
4.8
|
10.2
|
1.0
|
C
|
B:ASP345
|
4.8
|
30.5
|
1.0
|
CE1
|
B:TYR242
|
4.9
|
19.4
|
1.0
|
N
|
B:SER347
|
4.9
|
21.2
|
1.0
|
CD1
|
B:TYR242
|
4.9
|
25.5
|
1.0
|
O4'
|
B:5GP467
|
4.9
|
12.3
|
1.0
|
|
Magnesium binding site 3 out
of 4 in 1ao0
Go back to
Magnesium Binding Sites List in 1ao0
Magnesium binding site 3 out
of 4 in the Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg469
b:12.9
occ:1.00
|
OD1
|
C:ASP346
|
2.0
|
22.5
|
1.0
|
O2'
|
C:5GP467
|
2.0
|
20.4
|
1.0
|
O
|
C:HOH470
|
2.1
|
10.0
|
1.0
|
OD1
|
C:ASP345
|
2.2
|
16.3
|
1.0
|
OG
|
C:SER283
|
2.2
|
26.2
|
1.0
|
CB
|
C:SER283
|
2.3
|
13.9
|
1.0
|
O3'
|
C:5GP467
|
2.5
|
18.1
|
1.0
|
CG
|
C:ASP345
|
3.2
|
21.3
|
1.0
|
CG
|
C:ASP346
|
3.2
|
17.0
|
1.0
|
C2'
|
C:5GP467
|
3.2
|
25.9
|
1.0
|
C3'
|
C:5GP467
|
3.5
|
22.7
|
1.0
|
OD2
|
C:ASP345
|
3.6
|
17.7
|
1.0
|
CA
|
C:SER283
|
3.6
|
17.3
|
1.0
|
O3B
|
C:ADP468
|
3.9
|
65.3
|
1.0
|
C
|
C:SER283
|
3.9
|
22.7
|
1.0
|
N
|
C:ASP346
|
4.0
|
26.1
|
1.0
|
OD2
|
C:ASP346
|
4.0
|
18.4
|
1.0
|
N
|
C:SER284
|
4.2
|
19.4
|
1.0
|
CB
|
C:ASP346
|
4.2
|
12.6
|
1.0
|
C4'
|
C:5GP467
|
4.2
|
14.5
|
1.0
|
C1'
|
C:5GP467
|
4.3
|
26.5
|
1.0
|
N
|
C:SER283
|
4.4
|
18.7
|
1.0
|
CB
|
C:SER284
|
4.4
|
13.8
|
1.0
|
O
|
C:SER283
|
4.4
|
31.9
|
1.0
|
CB
|
C:ASP345
|
4.5
|
18.2
|
1.0
|
OG
|
C:SER284
|
4.6
|
16.2
|
1.0
|
CB
|
C:VAL280
|
4.7
|
18.0
|
1.0
|
CA
|
C:ASP346
|
4.7
|
20.7
|
1.0
|
CA
|
C:ASP345
|
4.8
|
26.8
|
1.0
|
C
|
C:ASP345
|
4.8
|
29.9
|
1.0
|
CG1
|
C:VAL280
|
4.9
|
10.1
|
1.0
|
CA
|
C:SER284
|
4.9
|
12.0
|
1.0
|
N
|
C:SER347
|
4.9
|
17.9
|
1.0
|
O4'
|
C:5GP467
|
4.9
|
26.5
|
1.0
|
CE1
|
C:TYR242
|
4.9
|
22.1
|
1.0
|
CD1
|
C:TYR242
|
4.9
|
19.1
|
1.0
|
|
Magnesium binding site 4 out
of 4 in 1ao0
Go back to
Magnesium Binding Sites List in 1ao0
Magnesium binding site 4 out
of 4 in the Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Glutamine Phosphoribosylpyrophosphate (Prpp) Amidotransferase From B. Subtilis Complexed with Adp and Gmp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg469
b:10.3
occ:1.00
|
OD1
|
D:ASP346
|
1.9
|
17.3
|
1.0
|
O2'
|
D:5GP467
|
2.0
|
13.4
|
1.0
|
OD1
|
D:ASP345
|
2.1
|
13.7
|
1.0
|
O
|
D:HOH470
|
2.1
|
13.9
|
1.0
|
CB
|
D:SER283
|
2.2
|
14.8
|
1.0
|
OG
|
D:SER283
|
2.2
|
18.5
|
1.0
|
O3'
|
D:5GP467
|
2.5
|
12.0
|
1.0
|
CG
|
D:ASP346
|
3.2
|
19.5
|
1.0
|
CG
|
D:ASP345
|
3.2
|
23.8
|
1.0
|
C2'
|
D:5GP467
|
3.3
|
17.2
|
1.0
|
CA
|
D:SER283
|
3.5
|
10.6
|
1.0
|
C3'
|
D:5GP467
|
3.6
|
10.1
|
1.0
|
OD2
|
D:ASP345
|
3.6
|
21.3
|
1.0
|
C
|
D:SER283
|
3.8
|
13.9
|
1.0
|
N
|
D:ASP346
|
3.9
|
28.0
|
1.0
|
O3B
|
D:ADP468
|
4.0
|
57.7
|
1.0
|
OD2
|
D:ASP346
|
4.0
|
13.9
|
1.0
|
N
|
D:SER284
|
4.0
|
14.1
|
1.0
|
CB
|
D:ASP346
|
4.1
|
21.2
|
1.0
|
CB
|
D:SER284
|
4.3
|
16.3
|
1.0
|
C4'
|
D:5GP467
|
4.3
|
10.0
|
1.0
|
O
|
D:SER283
|
4.3
|
17.8
|
1.0
|
C1'
|
D:5GP467
|
4.3
|
25.0
|
1.0
|
N
|
D:SER283
|
4.3
|
18.7
|
1.0
|
OG
|
D:SER284
|
4.4
|
14.7
|
1.0
|
CB
|
D:ASP345
|
4.5
|
25.1
|
1.0
|
CA
|
D:ASP346
|
4.6
|
24.7
|
1.0
|
CB
|
D:VAL280
|
4.7
|
10.3
|
1.0
|
CA
|
D:ASP345
|
4.7
|
28.1
|
1.0
|
CA
|
D:SER284
|
4.8
|
17.9
|
1.0
|
C
|
D:ASP345
|
4.8
|
29.4
|
1.0
|
CD1
|
D:TYR242
|
4.9
|
23.2
|
1.0
|
N
|
D:SER347
|
4.9
|
17.1
|
1.0
|
CE1
|
D:TYR242
|
4.9
|
25.2
|
1.0
|
O4'
|
D:5GP467
|
4.9
|
14.2
|
1.0
|
CG1
|
D:VAL280
|
4.9
|
10.0
|
1.0
|
|
Reference:
S.Chen,
D.R.Tomchick,
D.Wolle,
P.Hu,
J.L.Smith,
R.L.Switzer,
H.Zalkin.
Mechanism of the Synergistic End-Product Regulation of Bacillus Subtilis Glutamine Phosphoribosylpyrophosphate Amidotransferase By Nucleotides. Biochemistry V. 36 10718 1997.
ISSN: ISSN 0006-2960
PubMed: 9271502
DOI: 10.1021/BI9711893
Page generated: Tue Aug 13 02:07:24 2024
|