Magnesium in PDB 5z87: Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus
Protein crystallography data
The structure of Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus, PDB code: 5z87
was solved by
J.X.Li,
X.J.Hu,
Y.Zhao,
L.Li,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
43.32 /
2.30
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
86.640,
132.150,
194.560,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
16.2 /
21.2
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus
(pdb code 5z87). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 5 binding sites of Magnesium where determined in the
Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus, PDB code: 5z87:
Jump to Magnesium binding site number:
1;
2;
3;
4;
5;
Magnesium binding site 1 out
of 5 in 5z87
Go back to
Magnesium Binding Sites List in 5z87
Magnesium binding site 1 out
of 5 in the Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg802
b:13.2
occ:1.00
|
OG1
|
A:THR538
|
3.1
|
17.8
|
1.0
|
NH1
|
A:ARG583
|
3.2
|
19.5
|
1.0
|
O
|
A:HOH1213
|
3.4
|
24.4
|
1.0
|
NH1
|
A:ARG552
|
3.4
|
15.2
|
1.0
|
O
|
A:HOH1098
|
3.4
|
18.4
|
1.0
|
CD
|
A:ARG552
|
3.7
|
17.6
|
1.0
|
CB
|
A:THR538
|
3.7
|
17.9
|
1.0
|
CD2
|
A:LEU585
|
3.8
|
22.9
|
1.0
|
CA
|
A:GLY534
|
4.0
|
19.6
|
1.0
|
CG
|
A:ARG583
|
4.1
|
19.9
|
1.0
|
C
|
A:THR538
|
4.1
|
22.5
|
1.0
|
O
|
A:THR538
|
4.1
|
20.8
|
1.0
|
CD
|
A:ARG583
|
4.2
|
20.0
|
1.0
|
N
|
A:ALA539
|
4.3
|
20.2
|
1.0
|
CZ
|
A:ARG552
|
4.3
|
21.4
|
1.0
|
CZ
|
A:ARG583
|
4.4
|
24.6
|
1.0
|
NE
|
A:ARG552
|
4.4
|
19.6
|
1.0
|
CD1
|
A:LEU585
|
4.5
|
20.2
|
1.0
|
CB
|
A:ALA539
|
4.5
|
13.8
|
1.0
|
CA
|
A:THR538
|
4.5
|
24.9
|
1.0
|
CG
|
A:LEU585
|
4.6
|
19.0
|
1.0
|
NE
|
A:ARG583
|
4.8
|
20.5
|
1.0
|
N
|
A:GLY534
|
4.8
|
23.5
|
1.0
|
CG
|
A:ARG552
|
4.9
|
20.4
|
1.0
|
CA
|
A:ALA539
|
4.9
|
19.1
|
1.0
|
CG2
|
A:THR538
|
4.9
|
20.6
|
1.0
|
C
|
A:GLY534
|
4.9
|
21.3
|
1.0
|
N
|
A:ASN535
|
5.0
|
22.8
|
1.0
|
|
Magnesium binding site 2 out
of 5 in 5z87
Go back to
Magnesium Binding Sites List in 5z87
Magnesium binding site 2 out
of 5 in the Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg803
b:23.7
occ:1.00
|
OD1
|
A:ASP713
|
2.0
|
21.1
|
1.0
|
O
|
A:ILE715
|
2.1
|
24.6
|
1.0
|
O
|
A:HOH971
|
2.1
|
20.4
|
1.0
|
O
|
A:HOH967
|
2.1
|
22.2
|
1.0
|
O
|
A:HOH925
|
2.1
|
17.1
|
1.0
|
O
|
A:HOH999
|
2.2
|
24.1
|
1.0
|
CG
|
A:ASP713
|
3.0
|
22.6
|
1.0
|
C
|
A:ILE715
|
3.3
|
18.0
|
1.0
|
OD2
|
A:ASP713
|
3.3
|
22.8
|
1.0
|
N
|
A:ILE715
|
3.9
|
21.2
|
1.0
|
O
|
A:HOH1179
|
4.0
|
26.8
|
1.0
|
CA
|
A:ILE715
|
4.1
|
19.2
|
1.0
|
O
|
A:GLU765
|
4.1
|
23.1
|
1.0
|
O
|
A:PRO763
|
4.2
|
26.1
|
1.0
|
N
|
A:ALA716
|
4.3
|
19.0
|
1.0
|
O
|
A:HOH1107
|
4.3
|
26.5
|
1.0
|
O
|
A:GLU762
|
4.3
|
23.1
|
1.0
|
CB
|
A:ASP713
|
4.3
|
19.5
|
1.0
|
O
|
A:HOH1066
|
4.4
|
22.7
|
1.0
|
CA
|
A:ALA716
|
4.4
|
20.3
|
1.0
|
CB
|
A:ILE715
|
4.5
|
23.6
|
1.0
|
C
|
A:ASP713
|
4.5
|
20.1
|
1.0
|
N
|
A:SER714
|
4.6
|
19.2
|
1.0
|
C
|
A:GLY764
|
4.6
|
27.1
|
1.0
|
CA
|
A:GLY764
|
4.6
|
20.8
|
1.0
|
CB
|
A:ALA716
|
4.6
|
16.9
|
1.0
|
CA
|
A:ASP713
|
4.6
|
17.6
|
1.0
|
CD1
|
A:ILE766
|
4.7
|
18.3
|
1.0
|
CB
|
A:GLU762
|
4.7
|
23.3
|
1.0
|
N
|
A:GLU765
|
4.7
|
21.5
|
1.0
|
OE2
|
A:GLU762
|
4.7
|
23.7
|
1.0
|
C
|
A:PRO763
|
4.8
|
22.8
|
1.0
|
C
|
A:GLU762
|
4.9
|
23.6
|
1.0
|
O
|
A:GLY764
|
5.0
|
27.6
|
1.0
|
O
|
A:ASP713
|
5.0
|
20.3
|
1.0
|
C
|
A:SER714
|
5.0
|
24.3
|
1.0
|
|
Magnesium binding site 3 out
of 5 in 5z87
Go back to
Magnesium Binding Sites List in 5z87
Magnesium binding site 3 out
of 5 in the Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg804
b:43.9
occ:1.00
|
OD2
|
A:ASP292
|
2.8
|
28.1
|
1.0
|
O
|
A:HOH1248
|
3.0
|
27.5
|
1.0
|
CG
|
A:ASP292
|
3.7
|
26.0
|
1.0
|
OD1
|
A:ASP292
|
3.7
|
30.8
|
1.0
|
CD2
|
A:HIS294
|
3.9
|
24.0
|
1.0
|
O
|
A:HOH1237
|
4.2
|
20.1
|
1.0
|
CD2
|
A:LEU295
|
4.3
|
23.4
|
1.0
|
O
|
A:HOH1041
|
4.5
|
20.6
|
1.0
|
O
|
A:HOH1378
|
4.5
|
22.0
|
1.0
|
CD1
|
A:ILE284
|
4.7
|
15.6
|
1.0
|
CG
|
A:HIS294
|
4.8
|
26.0
|
1.0
|
CD1
|
A:LEU295
|
4.8
|
24.5
|
1.0
|
NE2
|
A:HIS294
|
4.8
|
29.7
|
1.0
|
O
|
A:HOH1297
|
4.8
|
36.1
|
1.0
|
CB
|
A:ILE284
|
4.9
|
20.3
|
1.0
|
CB
|
A:LEU295
|
4.9
|
27.5
|
1.0
|
CG
|
A:LEU295
|
4.9
|
38.9
|
1.0
|
CG2
|
A:ILE284
|
4.9
|
14.7
|
1.0
|
CB
|
A:HIS294
|
5.0
|
25.5
|
1.0
|
|
Magnesium binding site 4 out
of 5 in 5z87
Go back to
Magnesium Binding Sites List in 5z87
Magnesium binding site 4 out
of 5 in the Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg803
b:7.5
occ:1.00
|
OG1
|
B:THR538
|
3.1
|
19.2
|
1.0
|
NH1
|
B:ARG583
|
3.3
|
17.5
|
1.0
|
O
|
B:HOH1166
|
3.3
|
18.6
|
1.0
|
NH1
|
B:ARG552
|
3.5
|
14.7
|
1.0
|
O
|
B:HOH969
|
3.5
|
20.5
|
1.0
|
CD
|
B:ARG552
|
3.7
|
20.2
|
1.0
|
CD2
|
B:LEU585
|
3.8
|
18.3
|
1.0
|
CB
|
B:THR538
|
3.8
|
18.6
|
1.0
|
O
|
B:THR538
|
3.9
|
13.6
|
1.0
|
CG
|
B:ARG583
|
4.0
|
15.7
|
1.0
|
CA
|
B:GLY534
|
4.0
|
16.4
|
1.0
|
CD
|
B:ARG583
|
4.1
|
17.9
|
1.0
|
C
|
B:THR538
|
4.1
|
18.5
|
1.0
|
CZ
|
B:ARG552
|
4.3
|
20.2
|
1.0
|
N
|
B:ALA539
|
4.4
|
16.1
|
1.0
|
CZ
|
B:ARG583
|
4.4
|
19.1
|
1.0
|
NE
|
B:ARG552
|
4.4
|
15.9
|
1.0
|
CB
|
B:ALA539
|
4.4
|
16.9
|
1.0
|
CG
|
B:LEU585
|
4.5
|
15.8
|
1.0
|
CD1
|
B:LEU585
|
4.5
|
17.6
|
1.0
|
CA
|
B:THR538
|
4.6
|
18.5
|
1.0
|
NE
|
B:ARG583
|
4.7
|
22.8
|
1.0
|
N
|
B:GLY534
|
4.8
|
17.4
|
1.0
|
CG
|
B:ARG552
|
4.9
|
17.6
|
1.0
|
CA
|
B:ALA539
|
4.9
|
18.2
|
1.0
|
O
|
B:GLY533
|
4.9
|
16.5
|
1.0
|
C
|
B:GLY534
|
5.0
|
17.8
|
1.0
|
N
|
B:ASN535
|
5.0
|
15.6
|
1.0
|
|
Magnesium binding site 5 out
of 5 in 5z87
Go back to
Magnesium Binding Sites List in 5z87
Magnesium binding site 5 out
of 5 in the Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 5 of Structural of A Novel B-Glucosidase EMGH1 at 2.3 Angstrom From Erythrobacter Marinus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg804
b:24.5
occ:1.00
|
O
|
B:ILE715
|
2.0
|
23.4
|
1.0
|
O
|
B:HOH1015
|
2.0
|
21.7
|
1.0
|
O
|
B:HOH1054
|
2.1
|
28.6
|
1.0
|
OD1
|
B:ASP713
|
2.1
|
21.7
|
1.0
|
O
|
B:HOH948
|
2.2
|
18.3
|
1.0
|
O
|
B:HOH1022
|
2.2
|
22.1
|
1.0
|
CG
|
B:ASP713
|
3.1
|
19.3
|
1.0
|
C
|
B:ILE715
|
3.2
|
20.7
|
1.0
|
OD2
|
B:ASP713
|
3.4
|
20.4
|
1.0
|
N
|
B:ILE715
|
3.7
|
22.9
|
1.0
|
CA
|
B:ILE715
|
4.0
|
20.4
|
1.0
|
O
|
B:GLU765
|
4.1
|
27.7
|
1.0
|
N
|
B:ALA716
|
4.2
|
19.7
|
1.0
|
O
|
B:PRO763
|
4.2
|
28.5
|
1.0
|
O
|
B:HOH1278
|
4.3
|
22.3
|
1.0
|
O
|
B:HOH1067
|
4.3
|
23.6
|
1.0
|
CA
|
B:ALA716
|
4.3
|
21.0
|
1.0
|
O
|
B:GLU762
|
4.4
|
26.7
|
1.0
|
CB
|
B:ILE715
|
4.4
|
21.3
|
1.0
|
CB
|
B:ASP713
|
4.4
|
20.5
|
1.0
|
N
|
B:SER714
|
4.5
|
18.9
|
1.0
|
C
|
B:ASP713
|
4.5
|
20.8
|
1.0
|
O
|
B:HOH1079
|
4.6
|
21.7
|
1.0
|
CA
|
B:GLY764
|
4.6
|
21.0
|
1.0
|
OE2
|
B:GLU762
|
4.6
|
23.2
|
1.0
|
CB
|
B:ALA716
|
4.6
|
18.2
|
1.0
|
C
|
B:GLY764
|
4.7
|
22.9
|
1.0
|
CA
|
B:ASP713
|
4.7
|
19.2
|
1.0
|
N
|
B:GLU765
|
4.8
|
25.1
|
1.0
|
C
|
B:PRO763
|
4.8
|
26.9
|
1.0
|
CB
|
B:GLU762
|
4.9
|
21.4
|
1.0
|
O
|
B:ASP713
|
4.9
|
22.0
|
1.0
|
C
|
B:SER714
|
4.9
|
23.2
|
1.0
|
CD1
|
B:ILE766
|
4.9
|
24.0
|
1.0
|
|
Reference:
L.Li,
Y.Zhao,
X.J.Hu,
J.X.Li.
Structural and Biochemical Analysis of A Novel B-Glucosidase EMGH1 From Erythrobacter Marinus To Be Published.
Page generated: Mon Sep 30 11:46:49 2024
|