Magnesium in PDB 3dg7: Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone
Protein crystallography data
The structure of Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone, PDB code: 3dg7
was solved by
A.A.Fedorov,
E.V.Fedorov,
A.Sakai,
J.A.Gerlt,
S.C.Almo,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
24.42 /
2.00
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
171.047,
124.265,
117.485,
90.00,
133.39,
90.00
|
R / Rfree (%)
|
18.8 /
20.3
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone
(pdb code 3dg7). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the
Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone, PDB code: 3dg7:
Jump to Magnesium binding site number:
1;
2;
3;
4;
Magnesium binding site 1 out
of 4 in 3dg7
Go back to
Magnesium Binding Sites List in 3dg7
Magnesium binding site 1 out
of 4 in the Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg2001
b:20.6
occ:1.00
|
OE2
|
A:GLU217
|
2.0
|
17.4
|
1.0
|
O
|
A:HOH2003
|
2.0
|
13.9
|
1.0
|
OD2
|
A:ASP191
|
2.1
|
16.6
|
1.0
|
O1
|
A:MUC1001
|
2.1
|
26.8
|
1.0
|
OD2
|
A:ASP242
|
2.2
|
16.2
|
1.0
|
O2
|
A:MUC1001
|
2.3
|
21.8
|
1.0
|
C1
|
A:MUC1001
|
2.5
|
27.1
|
1.0
|
CD
|
A:GLU217
|
3.0
|
17.3
|
1.0
|
CG
|
A:ASP191
|
3.1
|
16.6
|
1.0
|
CG
|
A:ASP242
|
3.3
|
13.7
|
1.0
|
NZ
|
A:LYS160
|
3.5
|
26.1
|
1.0
|
OD1
|
A:ASP191
|
3.5
|
16.0
|
1.0
|
CB
|
A:ASP242
|
3.6
|
12.7
|
1.0
|
CG
|
A:GLU217
|
3.7
|
15.6
|
1.0
|
O
|
A:HOH2072
|
3.7
|
17.6
|
1.0
|
OE1
|
A:GLU217
|
4.0
|
16.5
|
1.0
|
C2
|
A:MUC1001
|
4.0
|
27.9
|
1.0
|
NZ
|
A:LYS266
|
4.0
|
13.9
|
1.0
|
OE2
|
A:GLU243
|
4.1
|
20.7
|
1.0
|
O
|
A:HOH2176
|
4.2
|
31.6
|
1.0
|
ND2
|
A:ASN193
|
4.2
|
20.7
|
1.0
|
OD1
|
A:ASP242
|
4.4
|
15.6
|
1.0
|
CB
|
A:ASP191
|
4.4
|
15.9
|
1.0
|
NZ
|
A:LYS162
|
4.6
|
35.0
|
1.0
|
CE
|
A:LYS160
|
4.6
|
25.8
|
1.0
|
CE
|
A:LYS266
|
4.6
|
11.3
|
1.0
|
CB
|
A:GLU217
|
4.9
|
16.3
|
1.0
|
O
|
A:HOH2030
|
5.0
|
14.7
|
1.0
|
|
Magnesium binding site 2 out
of 4 in 3dg7
Go back to
Magnesium Binding Sites List in 3dg7
Magnesium binding site 2 out
of 4 in the Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg2002
b:20.4
occ:1.00
|
OE2
|
B:GLU217
|
2.0
|
18.1
|
1.0
|
OD2
|
B:ASP191
|
2.1
|
14.9
|
1.0
|
O1
|
B:MUC1002
|
2.1
|
24.2
|
1.0
|
O
|
B:HOH2085
|
2.1
|
16.4
|
1.0
|
OD2
|
B:ASP242
|
2.2
|
15.6
|
1.0
|
O2
|
B:MUC1002
|
2.4
|
19.6
|
1.0
|
C1
|
B:MUC1002
|
2.5
|
24.2
|
1.0
|
CD
|
B:GLU217
|
3.0
|
17.7
|
1.0
|
CG
|
B:ASP191
|
3.1
|
16.0
|
1.0
|
CG
|
B:ASP242
|
3.3
|
13.8
|
1.0
|
OD1
|
B:ASP191
|
3.5
|
15.1
|
1.0
|
NZ
|
B:LYS160
|
3.5
|
26.3
|
1.0
|
CB
|
B:ASP242
|
3.6
|
13.0
|
1.0
|
O
|
B:HOH2074
|
3.7
|
16.9
|
1.0
|
CG
|
B:GLU217
|
3.7
|
16.8
|
1.0
|
OE1
|
B:GLU217
|
4.0
|
16.8
|
1.0
|
NZ
|
B:LYS266
|
4.0
|
14.9
|
1.0
|
C2
|
B:MUC1002
|
4.0
|
25.6
|
1.0
|
OE2
|
B:GLU243
|
4.1
|
20.9
|
1.0
|
ND2
|
B:ASN193
|
4.2
|
21.7
|
1.0
|
O
|
B:HOH2191
|
4.2
|
28.9
|
1.0
|
OD1
|
B:ASP242
|
4.4
|
15.4
|
1.0
|
CB
|
B:ASP191
|
4.4
|
14.7
|
1.0
|
NZ
|
B:LYS162
|
4.5
|
34.2
|
1.0
|
CE
|
B:LYS160
|
4.6
|
25.7
|
1.0
|
CE
|
B:LYS266
|
4.6
|
12.1
|
1.0
|
CB
|
B:GLU217
|
4.9
|
16.0
|
1.0
|
O
|
B:HOH2023
|
5.0
|
17.2
|
1.0
|
|
Magnesium binding site 3 out
of 4 in 3dg7
Go back to
Magnesium Binding Sites List in 3dg7
Magnesium binding site 3 out
of 4 in the Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg2003
b:20.3
occ:1.00
|
OE2
|
C:GLU217
|
2.0
|
18.0
|
1.0
|
O1
|
C:MUC1003
|
2.1
|
24.4
|
1.0
|
OD2
|
C:ASP191
|
2.1
|
16.0
|
1.0
|
O
|
C:HOH2008
|
2.1
|
13.2
|
1.0
|
OD2
|
C:ASP242
|
2.2
|
16.4
|
1.0
|
O2
|
C:MUC1003
|
2.4
|
19.4
|
1.0
|
C1
|
C:MUC1003
|
2.5
|
24.2
|
1.0
|
CD
|
C:GLU217
|
3.0
|
16.9
|
1.0
|
CG
|
C:ASP191
|
3.1
|
15.6
|
1.0
|
CG
|
C:ASP242
|
3.3
|
14.3
|
1.0
|
OD1
|
C:ASP191
|
3.5
|
15.6
|
1.0
|
NZ
|
C:LYS160
|
3.5
|
26.8
|
1.0
|
O
|
C:HOH2114
|
3.6
|
16.7
|
1.0
|
CB
|
C:ASP242
|
3.6
|
13.5
|
1.0
|
CG
|
C:GLU217
|
3.7
|
16.1
|
1.0
|
OE1
|
C:GLU217
|
4.0
|
17.5
|
1.0
|
NZ
|
C:LYS266
|
4.0
|
15.9
|
1.0
|
C2
|
C:MUC1003
|
4.0
|
26.2
|
1.0
|
OE2
|
C:GLU243
|
4.1
|
20.6
|
1.0
|
O
|
C:HOH2167
|
4.1
|
25.6
|
1.0
|
ND2
|
C:ASN193
|
4.2
|
22.5
|
1.0
|
OD1
|
C:ASP242
|
4.4
|
15.3
|
1.0
|
CB
|
C:ASP191
|
4.4
|
14.9
|
1.0
|
NZ
|
C:LYS162
|
4.5
|
35.1
|
1.0
|
CE
|
C:LYS160
|
4.6
|
26.2
|
1.0
|
CE
|
C:LYS266
|
4.6
|
13.3
|
1.0
|
CB
|
C:GLU217
|
4.9
|
16.7
|
1.0
|
|
Magnesium binding site 4 out
of 4 in 3dg7
Go back to
Magnesium Binding Sites List in 3dg7
Magnesium binding site 4 out
of 4 in the Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Crystal Structure of Muconate Lactonizing Enzyme From Mucobacterium Smegmatis Complexed with Muconolactone within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg2004
b:19.6
occ:1.00
|
OE2
|
D:GLU217
|
2.0
|
16.4
|
1.0
|
O
|
D:HOH2013
|
2.0
|
14.1
|
1.0
|
OD2
|
D:ASP191
|
2.1
|
15.8
|
1.0
|
O1
|
D:MUC1004
|
2.1
|
25.4
|
1.0
|
OD2
|
D:ASP242
|
2.2
|
16.5
|
1.0
|
O2
|
D:MUC1004
|
2.4
|
20.3
|
1.0
|
C1
|
D:MUC1004
|
2.5
|
25.7
|
1.0
|
CD
|
D:GLU217
|
3.0
|
16.2
|
1.0
|
CG
|
D:ASP191
|
3.1
|
16.4
|
1.0
|
CG
|
D:ASP242
|
3.3
|
13.5
|
1.0
|
NZ
|
D:LYS160
|
3.5
|
25.4
|
1.0
|
OD1
|
D:ASP191
|
3.5
|
15.6
|
1.0
|
CB
|
D:ASP242
|
3.6
|
14.2
|
1.0
|
O
|
D:HOH2073
|
3.7
|
17.2
|
1.0
|
CG
|
D:GLU217
|
3.7
|
15.1
|
1.0
|
OE1
|
D:GLU217
|
4.0
|
16.8
|
1.0
|
NZ
|
D:LYS266
|
4.0
|
16.5
|
1.0
|
OE2
|
D:GLU243
|
4.1
|
21.7
|
1.0
|
C2
|
D:MUC1004
|
4.1
|
26.8
|
1.0
|
ND2
|
D:ASN193
|
4.2
|
22.3
|
1.0
|
O
|
D:HOH2162
|
4.3
|
28.2
|
1.0
|
OD1
|
D:ASP242
|
4.4
|
15.7
|
1.0
|
CB
|
D:ASP191
|
4.4
|
15.7
|
1.0
|
NZ
|
D:LYS162
|
4.6
|
34.4
|
1.0
|
CE
|
D:LYS160
|
4.6
|
25.4
|
1.0
|
CE
|
D:LYS266
|
4.6
|
14.4
|
1.0
|
CB
|
D:GLU217
|
4.9
|
15.9
|
1.0
|
|
Reference:
A.Sakai,
A.A.Fedorov,
E.V.Fedorov,
A.M.Schnoes,
M.E.Glasner,
S.Brown,
M.E.Rutter,
K.Bain,
S.Chang,
T.Gheyi,
J.M.Sauder,
S.K.Burley,
P.C.Babbitt,
S.C.Almo,
J.A.Gerlt.
Evolution of Enzymatic Activities in the Enolase Superfamily: Stereochemically Distinct Mechanisms in Two Families of Cis,Cis-Muconate Lactonizing Enzymes Biochemistry V. 48 1445 2009.
ISSN: ISSN 0006-2960
PubMed: 19220063
DOI: 10.1021/BI802277H
Page generated: Wed Aug 14 12:30:06 2024
|