Magnesium in PDB 2i19: T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
Enzymatic activity of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
All present enzymatic activity of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate:
2.5.1.10;
Protein crystallography data
The structure of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate, PDB code: 2i19
was solved by
R.Cao,
J.Mao,
Y.Gao,
H.Robinson,
S.Odeh,
A.Goddard,
E.Oldfield,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
30.00 /
2.28
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
133.214,
119.551,
62.438,
90.00,
111.93,
90.00
|
R / Rfree (%)
|
21.7 /
24.4
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
(pdb code 2i19). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 6 binding sites of Magnesium where determined in the
T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate, PDB code: 2i19:
Jump to Magnesium binding site number:
1;
2;
3;
4;
5;
6;
Magnesium binding site 1 out
of 6 in 2i19
Go back to
Magnesium Binding Sites List in 2i19
Magnesium binding site 1 out
of 6 in the T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg3002
b:25.7
occ:1.00
|
O
|
A:HOH5286
|
1.9
|
26.1
|
1.0
|
O4
|
A:1BY3001
|
2.1
|
36.1
|
1.0
|
O2
|
A:1BY3001
|
2.1
|
39.1
|
1.0
|
OD2
|
A:ASP107
|
2.3
|
21.1
|
1.0
|
OD1
|
A:ASP103
|
2.4
|
27.1
|
1.0
|
P2
|
A:1BY3001
|
3.1
|
40.4
|
1.0
|
MG
|
A:MG3003
|
3.2
|
21.1
|
1.0
|
P1
|
A:1BY3001
|
3.3
|
35.2
|
1.0
|
CG
|
A:ASP103
|
3.3
|
26.3
|
1.0
|
CG
|
A:ASP107
|
3.4
|
20.6
|
1.0
|
OD2
|
A:ASP103
|
3.4
|
29.8
|
1.0
|
O6
|
A:1BY3001
|
3.5
|
40.6
|
1.0
|
C1
|
A:1BY3001
|
3.6
|
36.6
|
1.0
|
O
|
A:HOH5204
|
3.9
|
61.6
|
1.0
|
CB
|
A:ASP107
|
4.0
|
22.8
|
1.0
|
C2
|
A:1BY3001
|
4.0
|
36.7
|
1.0
|
NH2
|
A:ARG112
|
4.1
|
19.7
|
1.0
|
O3
|
A:1BY3001
|
4.1
|
41.8
|
1.0
|
OG
|
A:SER109
|
4.3
|
35.0
|
1.0
|
O1
|
A:1BY3001
|
4.3
|
38.3
|
1.0
|
O5
|
A:1BY3001
|
4.4
|
34.6
|
1.0
|
OD1
|
A:ASP107
|
4.4
|
15.1
|
1.0
|
OD2
|
A:ASP104
|
4.5
|
30.2
|
1.0
|
O
|
A:HOH5332
|
4.6
|
61.5
|
1.0
|
O
|
A:HOH5343
|
4.6
|
56.1
|
1.0
|
O
|
A:HOH5036
|
4.6
|
30.5
|
1.0
|
O
|
A:ASP103
|
4.7
|
22.3
|
1.0
|
CB
|
A:ASP103
|
4.7
|
21.0
|
1.0
|
C
|
A:ASP103
|
4.9
|
18.6
|
1.0
|
NZ
|
A:LYS269
|
4.9
|
54.2
|
1.0
|
|
Magnesium binding site 2 out
of 6 in 2i19
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Magnesium Binding Sites List in 2i19
Magnesium binding site 2 out
of 6 in the T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg3003
b:21.1
occ:1.00
|
OD2
|
A:ASP107
|
2.0
|
21.1
|
1.0
|
OD2
|
A:ASP103
|
2.2
|
29.8
|
1.0
|
O4
|
A:1BY3001
|
2.2
|
36.1
|
1.0
|
O
|
A:HOH5036
|
2.4
|
30.5
|
1.0
|
CG
|
A:ASP107
|
2.7
|
20.6
|
1.0
|
OD1
|
A:ASP107
|
2.7
|
15.1
|
1.0
|
MG
|
A:MG3002
|
3.2
|
25.7
|
1.0
|
CG
|
A:ASP103
|
3.2
|
26.3
|
1.0
|
P2
|
A:1BY3001
|
3.6
|
40.4
|
1.0
|
OD1
|
A:ASP103
|
3.6
|
27.1
|
1.0
|
O5
|
A:1BY3001
|
3.8
|
34.6
|
1.0
|
OD2
|
A:ASP175
|
4.0
|
32.2
|
1.0
|
CB
|
A:ASP107
|
4.1
|
22.8
|
1.0
|
OE1
|
A:GLN172
|
4.4
|
35.5
|
1.0
|
NE2
|
A:GLN172
|
4.4
|
20.4
|
1.0
|
O6
|
A:1BY3001
|
4.4
|
40.6
|
1.0
|
O
|
A:HOH5286
|
4.5
|
26.1
|
1.0
|
CB
|
A:ASP103
|
4.6
|
21.0
|
1.0
|
CG
|
A:ASP175
|
4.6
|
27.5
|
1.0
|
NZ
|
A:LYS278
|
4.6
|
45.3
|
1.0
|
OD1
|
A:ASP175
|
4.7
|
26.2
|
1.0
|
CD
|
A:GLN172
|
4.8
|
27.1
|
1.0
|
C1
|
A:1BY3001
|
4.8
|
36.6
|
1.0
|
O
|
A:ASP103
|
4.8
|
22.3
|
1.0
|
C2
|
A:1BY3001
|
4.9
|
36.7
|
1.0
|
O2
|
A:1BY3001
|
4.9
|
39.1
|
1.0
|
|
Magnesium binding site 3 out
of 6 in 2i19
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Magnesium Binding Sites List in 2i19
Magnesium binding site 3 out
of 6 in the T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg3004
b:29.4
occ:1.00
|
O3
|
A:1BY3001
|
2.4
|
41.8
|
1.0
|
O6
|
A:1BY3001
|
2.5
|
40.6
|
1.0
|
O
|
A:HOH5204
|
2.9
|
61.6
|
1.0
|
OD2
|
A:ASP255
|
3.0
|
39.4
|
1.0
|
OD1
|
A:ASP259
|
3.4
|
51.9
|
1.0
|
P1
|
A:1BY3001
|
3.6
|
35.2
|
1.0
|
P2
|
A:1BY3001
|
3.7
|
40.4
|
1.0
|
NZ
|
A:LYS269
|
3.9
|
54.2
|
1.0
|
C1
|
A:1BY3001
|
3.9
|
36.6
|
1.0
|
CG
|
A:ASP255
|
4.0
|
34.9
|
1.0
|
O2
|
A:1BY3001
|
4.3
|
39.1
|
1.0
|
CG
|
A:ASP259
|
4.3
|
38.3
|
1.0
|
O5
|
A:1BY3001
|
4.5
|
34.6
|
1.0
|
OD1
|
A:ASP255
|
4.6
|
37.2
|
1.0
|
O
|
A:ASP255
|
4.6
|
41.0
|
1.0
|
CE
|
A:LYS269
|
4.7
|
53.3
|
1.0
|
O1
|
A:1BY3001
|
4.8
|
38.3
|
1.0
|
O4
|
A:1BY3001
|
4.8
|
36.1
|
1.0
|
OE1
|
A:GLN252
|
4.8
|
32.6
|
1.0
|
OD2
|
A:ASP273
|
4.8
|
38.5
|
1.0
|
CB
|
A:ASP259
|
4.9
|
33.6
|
1.0
|
O
|
A:HOH5046
|
4.9
|
48.9
|
1.0
|
OD1
|
A:ASP273
|
4.9
|
37.4
|
1.0
|
OD1
|
A:ASP256
|
5.0
|
31.4
|
1.0
|
O
|
A:HOH5332
|
5.0
|
61.5
|
1.0
|
|
Magnesium binding site 4 out
of 6 in 2i19
Go back to
Magnesium Binding Sites List in 2i19
Magnesium binding site 4 out
of 6 in the T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg4002
b:27.6
occ:1.00
|
OD1
|
B:ASP103
|
2.0
|
38.2
|
1.0
|
O2
|
B:1BY4001
|
2.0
|
30.8
|
1.0
|
O
|
B:HOH5284
|
2.1
|
22.7
|
1.0
|
O4
|
B:1BY4001
|
2.3
|
36.0
|
1.0
|
OD2
|
B:ASP107
|
2.3
|
24.1
|
1.0
|
P1
|
B:1BY4001
|
3.0
|
31.1
|
1.0
|
P2
|
B:1BY4001
|
3.0
|
35.6
|
1.0
|
CG
|
B:ASP103
|
3.1
|
33.3
|
1.0
|
C1
|
B:1BY4001
|
3.2
|
33.2
|
1.0
|
O6
|
B:1BY4001
|
3.4
|
38.7
|
1.0
|
CG
|
B:ASP107
|
3.4
|
27.8
|
1.0
|
MG
|
B:MG4004
|
3.5
|
23.4
|
1.0
|
C2
|
B:1BY4001
|
3.6
|
36.4
|
1.0
|
O3
|
B:1BY4001
|
3.7
|
32.3
|
1.0
|
OD2
|
B:ASP103
|
3.7
|
33.5
|
1.0
|
CB
|
B:ASP107
|
4.0
|
31.0
|
1.0
|
O1
|
B:1BY4001
|
4.2
|
28.2
|
1.0
|
CB
|
B:ASP103
|
4.3
|
27.2
|
1.0
|
O
|
B:HOH5203
|
4.3
|
4.2
|
0.5
|
OG
|
B:SER109
|
4.4
|
34.4
|
1.0
|
O
|
B:ASP103
|
4.4
|
21.9
|
1.0
|
OD2
|
B:ASP104
|
4.4
|
26.8
|
1.0
|
O5
|
B:1BY4001
|
4.4
|
28.1
|
1.0
|
O
|
B:HOH5288
|
4.4
|
42.8
|
1.0
|
OD1
|
B:ASP107
|
4.5
|
28.5
|
1.0
|
O
|
B:HOH5031
|
4.6
|
18.7
|
1.0
|
O
|
B:HOH5182
|
4.6
|
45.6
|
1.0
|
C
|
B:ASP103
|
4.7
|
22.8
|
1.0
|
NH2
|
B:ARG112
|
4.8
|
38.0
|
1.0
|
N1
|
B:1BY4001
|
4.9
|
32.9
|
1.0
|
|
Magnesium binding site 5 out
of 6 in 2i19
Go back to
Magnesium Binding Sites List in 2i19
Magnesium binding site 5 out
of 6 in the T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 5 of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg4003
b:33.6
occ:1.00
|
O
|
B:HOH5203
|
2.3
|
4.2
|
0.5
|
O
|
B:HOH5060
|
2.7
|
31.5
|
1.0
|
O3
|
B:1BY4001
|
2.9
|
32.3
|
1.0
|
O6
|
B:1BY4001
|
3.0
|
38.7
|
1.0
|
OD2
|
B:ASP255
|
3.2
|
45.9
|
1.0
|
O
|
B:HOH5065
|
3.5
|
41.6
|
1.0
|
OD2
|
B:ASP273
|
3.9
|
41.7
|
1.0
|
P1
|
B:1BY4001
|
4.1
|
31.1
|
1.0
|
CG
|
B:ASP255
|
4.1
|
43.1
|
1.0
|
P2
|
B:1BY4001
|
4.2
|
35.6
|
1.0
|
NE2
|
B:GLN252
|
4.2
|
31.3
|
1.0
|
C1
|
B:1BY4001
|
4.3
|
33.2
|
1.0
|
O
|
B:ASP255
|
4.4
|
42.5
|
1.0
|
CB
|
B:ASP255
|
4.5
|
42.0
|
1.0
|
C
|
B:ASP255
|
4.6
|
41.4
|
1.0
|
CB
|
B:ASP259
|
4.7
|
36.0
|
1.0
|
OD1
|
B:ASP259
|
4.7
|
37.7
|
1.0
|
O5
|
B:1BY4001
|
4.8
|
28.1
|
1.0
|
O
|
B:HOH5116
|
4.8
|
44.7
|
1.0
|
OD1
|
B:ASP256
|
4.9
|
36.9
|
1.0
|
CG
|
B:ASP273
|
4.9
|
41.1
|
1.0
|
O1
|
B:1BY4001
|
4.9
|
28.2
|
1.0
|
|
Magnesium binding site 6 out
of 6 in 2i19
Go back to
Magnesium Binding Sites List in 2i19
Magnesium binding site 6 out
of 6 in the T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 6 of T. Brucei Farnesyl Diphosphate Synthase Complexed with Bisphosphonate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg4004
b:23.4
occ:1.00
|
O4
|
B:1BY4001
|
2.2
|
36.0
|
1.0
|
OD2
|
B:ASP103
|
2.2
|
33.5
|
1.0
|
O
|
B:HOH5031
|
2.3
|
18.7
|
1.0
|
OD2
|
B:ASP107
|
2.4
|
24.1
|
1.0
|
OD1
|
B:ASP107
|
2.9
|
28.5
|
1.0
|
CG
|
B:ASP103
|
3.0
|
33.3
|
1.0
|
CG
|
B:ASP107
|
3.0
|
27.8
|
1.0
|
OD1
|
B:ASP103
|
3.1
|
38.2
|
1.0
|
MG
|
B:MG4002
|
3.5
|
27.6
|
1.0
|
P2
|
B:1BY4001
|
3.5
|
35.6
|
1.0
|
OD1
|
B:ASP175
|
3.6
|
31.2
|
1.0
|
O5
|
B:1BY4001
|
3.9
|
28.1
|
1.0
|
NE2
|
B:GLN172
|
4.1
|
35.2
|
1.0
|
OE1
|
B:GLN172
|
4.1
|
33.6
|
1.0
|
CG
|
B:ASP175
|
4.1
|
27.9
|
1.0
|
O6
|
B:1BY4001
|
4.2
|
38.7
|
1.0
|
OD2
|
B:ASP175
|
4.2
|
26.4
|
1.0
|
CB
|
B:ASP103
|
4.4
|
27.2
|
1.0
|
CB
|
B:ASP107
|
4.5
|
31.0
|
1.0
|
CD
|
B:GLN172
|
4.5
|
33.3
|
1.0
|
O
|
B:HOH5288
|
4.7
|
42.8
|
1.0
|
C1
|
B:1BY4001
|
4.8
|
33.2
|
1.0
|
C4
|
B:1BY4001
|
4.9
|
25.5
|
1.0
|
O
|
B:ASP103
|
4.9
|
21.9
|
1.0
|
C2
|
B:1BY4001
|
4.9
|
36.4
|
1.0
|
NZ
|
B:LYS212
|
4.9
|
25.9
|
1.0
|
O
|
B:HOH5284
|
4.9
|
22.7
|
1.0
|
|
Reference:
J.Mao,
S.Mukherjee,
Y.Zhang,
R.Cao,
J.M.Sanders,
Y.Song,
Y.Zhang,
G.A.Meints,
Y.G.Gao,
D.Mukkamala,
M.P.Hudock,
E.Oldfield.
Solid-State uc(Nmr), Crystallographic, and Computational Investigation of Bisphosphonates and Farnesyl Diphosphate Synthase-Bisphosphonate Complexes. J.Am.Chem.Soc. V. 128 14485 2006.
ISSN: ISSN 0002-7863
PubMed: 17090032
DOI: 10.1021/JA061737C
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