Magnesium in PDB 3rit: Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys
Protein crystallography data
The structure of Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys, PDB code: 3rit
was solved by
T.Lukk,
A.Sakai,
L.Song,
J.A.Gerlt,
S.K.Nair,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
19.87 /
2.70
|
Space group
|
I 21 3 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
275.320,
275.320,
275.320,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
17.5 /
22.2
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys
(pdb code 3rit). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 5 binding sites of Magnesium where determined in the
Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys, PDB code: 3rit:
Jump to Magnesium binding site number:
1;
2;
3;
4;
5;
Magnesium binding site 1 out
of 5 in 3rit
Go back to
Magnesium Binding Sites List in 3rit
Magnesium binding site 1 out
of 5 in the Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys
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 Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg365
b:38.4
occ:1.00
|
OE2
|
A:GLU216
|
2.7
|
37.5
|
1.0
|
OD1
|
A:ASP190
|
3.0
|
33.5
|
1.0
|
OD2
|
A:ASP241
|
3.0
|
30.4
|
1.0
|
OD2
|
A:ASP190
|
3.0
|
31.7
|
1.0
|
OE1
|
A:GLU242
|
3.1
|
29.3
|
1.0
|
O
|
A:DLY364
|
3.1
|
43.1
|
1.0
|
OXT
|
A:DLY364
|
3.2
|
55.8
|
1.0
|
CD
|
A:GLU216
|
3.3
|
31.5
|
1.0
|
CG
|
A:ASP190
|
3.3
|
33.5
|
1.0
|
CB
|
A:ASP241
|
3.4
|
26.0
|
1.0
|
CG
|
A:GLU216
|
3.4
|
25.3
|
1.0
|
OE2
|
A:GLU242
|
3.6
|
46.1
|
1.0
|
CG
|
A:ASP241
|
3.6
|
28.1
|
1.0
|
C
|
A:DLY364
|
3.6
|
61.1
|
1.0
|
CD
|
A:GLU242
|
3.7
|
37.1
|
1.0
|
OD1
|
A:ASN192
|
3.9
|
50.7
|
1.0
|
CB
|
A:GLN217
|
3.9
|
23.6
|
1.0
|
OE1
|
A:GLU216
|
4.2
|
35.5
|
1.0
|
CG
|
A:ASN192
|
4.3
|
47.0
|
1.0
|
CB
|
A:GLU216
|
4.3
|
23.3
|
1.0
|
O
|
A:GLU216
|
4.5
|
24.5
|
1.0
|
ND2
|
A:ASN192
|
4.6
|
42.3
|
1.0
|
C
|
A:GLU216
|
4.6
|
24.1
|
1.0
|
CB
|
A:ASP190
|
4.7
|
29.9
|
1.0
|
CG
|
A:GLN217
|
4.7
|
23.3
|
1.0
|
CA
|
A:ASN192
|
4.7
|
30.3
|
1.0
|
OD1
|
A:ASP241
|
4.8
|
27.3
|
1.0
|
CA
|
A:ASP241
|
4.8
|
27.7
|
1.0
|
N
|
A:GLN217
|
4.9
|
23.1
|
1.0
|
|
Magnesium binding site 2 out
of 5 in 3rit
Go back to
Magnesium Binding Sites List in 3rit
Magnesium binding site 2 out
of 5 in the Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys
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 Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg363
b:45.7
occ:1.00
|
OD1
|
B:ASP190
|
2.9
|
33.2
|
1.0
|
OE2
|
B:GLU216
|
2.9
|
37.7
|
1.0
|
OE1
|
B:GLU242
|
3.0
|
31.5
|
1.0
|
O
|
B:DLY362
|
3.1
|
47.8
|
1.0
|
OD2
|
B:ASP241
|
3.1
|
34.8
|
1.0
|
OD2
|
B:ASP190
|
3.2
|
34.3
|
1.0
|
OXT
|
B:DLY362
|
3.3
|
61.6
|
1.0
|
CG
|
B:ASP190
|
3.4
|
36.5
|
1.0
|
C
|
B:DLY362
|
3.6
|
64.2
|
1.0
|
CB
|
B:ASP241
|
3.7
|
27.4
|
1.0
|
OD1
|
B:ASN192
|
3.7
|
54.7
|
1.0
|
OE2
|
B:GLU242
|
3.7
|
52.2
|
1.0
|
CD
|
B:GLU216
|
3.7
|
34.7
|
1.0
|
CD
|
B:GLU242
|
3.7
|
42.2
|
1.0
|
CG
|
B:ASP241
|
3.8
|
32.9
|
1.0
|
CG
|
B:GLU216
|
3.9
|
27.5
|
1.0
|
CB
|
B:GLN217
|
4.0
|
20.8
|
1.0
|
CG
|
B:ASN192
|
4.0
|
54.0
|
1.0
|
ND2
|
B:ASN192
|
4.4
|
44.1
|
1.0
|
CA
|
B:ASN192
|
4.4
|
29.4
|
1.0
|
O
|
B:GLU216
|
4.5
|
28.1
|
1.0
|
CB
|
B:GLU216
|
4.6
|
21.5
|
1.0
|
CB
|
B:ASN192
|
4.6
|
38.1
|
1.0
|
OE1
|
B:GLU216
|
4.7
|
33.1
|
1.0
|
CG
|
B:GLN217
|
4.7
|
23.6
|
1.0
|
CB
|
B:ASP190
|
4.8
|
25.6
|
1.0
|
C
|
B:GLU216
|
4.8
|
28.9
|
1.0
|
N
|
B:ASN192
|
4.8
|
29.6
|
1.0
|
|
Magnesium binding site 3 out
of 5 in 3rit
Go back to
Magnesium Binding Sites List in 3rit
Magnesium binding site 3 out
of 5 in the Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys
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 Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg363
b:39.1
occ:1.00
|
OE2
|
C:GLU216
|
2.9
|
34.5
|
1.0
|
OE1
|
C:GLU242
|
2.9
|
40.5
|
1.0
|
OD2
|
C:ASP190
|
2.9
|
35.4
|
1.0
|
OD2
|
C:ASP241
|
3.0
|
35.0
|
1.0
|
OD1
|
C:ASP190
|
3.0
|
37.2
|
1.0
|
O
|
C:DLY362
|
3.1
|
51.0
|
1.0
|
OXT
|
C:DLY362
|
3.2
|
61.4
|
1.0
|
CG
|
C:ASP190
|
3.3
|
37.5
|
1.0
|
CB
|
C:ASP241
|
3.4
|
30.1
|
1.0
|
CD
|
C:GLU216
|
3.5
|
36.3
|
1.0
|
CG
|
C:ASP241
|
3.6
|
30.3
|
1.0
|
CG
|
C:GLU216
|
3.6
|
29.1
|
1.0
|
C
|
C:DLY362
|
3.6
|
65.1
|
1.0
|
CD
|
C:GLU242
|
3.8
|
42.9
|
1.0
|
CB
|
C:GLN217
|
3.9
|
24.8
|
1.0
|
ND2
|
C:ASN192
|
3.9
|
50.7
|
1.0
|
OE2
|
C:GLU242
|
4.0
|
46.8
|
1.0
|
O
|
C:GLU216
|
4.3
|
30.8
|
1.0
|
CG
|
C:ASN192
|
4.4
|
54.7
|
1.0
|
CB
|
C:GLU216
|
4.4
|
24.0
|
1.0
|
OE1
|
C:GLU216
|
4.4
|
34.1
|
1.0
|
C
|
C:GLU216
|
4.6
|
31.1
|
1.0
|
CA
|
C:ASN192
|
4.6
|
34.8
|
1.0
|
CB
|
C:ASP190
|
4.7
|
31.0
|
1.0
|
OD1
|
C:ASP241
|
4.7
|
33.7
|
1.0
|
CG
|
C:GLN217
|
4.7
|
24.8
|
1.0
|
CA
|
C:ASP241
|
4.9
|
28.1
|
1.0
|
CB
|
C:ASN192
|
4.9
|
41.2
|
1.0
|
N
|
C:GLN217
|
4.9
|
26.6
|
1.0
|
OD1
|
C:ASN192
|
4.9
|
53.6
|
1.0
|
N
|
C:ASN192
|
5.0
|
33.6
|
1.0
|
|
Magnesium binding site 4 out
of 5 in 3rit
Go back to
Magnesium Binding Sites List in 3rit
Magnesium binding site 4 out
of 5 in the Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys
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 Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg365
b:52.1
occ:1.00
|
OD1
|
D:ASP190
|
2.6
|
47.6
|
1.0
|
OXT
|
D:DLY364
|
2.9
|
60.3
|
1.0
|
OD2
|
D:ASP190
|
2.9
|
46.1
|
1.0
|
OE2
|
D:GLU216
|
3.0
|
45.7
|
1.0
|
CG
|
D:ASP190
|
3.1
|
44.5
|
1.0
|
OD2
|
D:ASP241
|
3.1
|
42.5
|
1.0
|
OE1
|
D:GLU242
|
3.2
|
46.0
|
1.0
|
ND2
|
D:ASN192
|
3.4
|
59.4
|
1.0
|
CG
|
D:GLU216
|
3.5
|
38.0
|
1.0
|
CD
|
D:GLU216
|
3.5
|
46.2
|
1.0
|
O
|
D:DLY364
|
3.6
|
59.3
|
1.0
|
C
|
D:DLY364
|
3.6
|
64.8
|
1.0
|
CB
|
D:ASP241
|
3.7
|
44.5
|
1.0
|
CB
|
D:GLN217
|
3.9
|
29.0
|
1.0
|
OE2
|
D:GLU242
|
3.9
|
57.2
|
1.0
|
CG
|
D:ASP241
|
3.9
|
44.1
|
1.0
|
CD
|
D:GLU242
|
4.0
|
52.5
|
1.0
|
CG
|
D:ASN192
|
4.0
|
62.1
|
1.0
|
O
|
D:GLU216
|
4.2
|
35.8
|
1.0
|
CA
|
D:ASN192
|
4.3
|
40.6
|
1.0
|
CB
|
D:GLU216
|
4.4
|
30.3
|
1.0
|
CB
|
D:ASP190
|
4.5
|
36.8
|
1.0
|
C
|
D:GLU216
|
4.5
|
33.0
|
1.0
|
CB
|
D:ASN192
|
4.6
|
47.1
|
1.0
|
OE1
|
D:GLU216
|
4.6
|
44.6
|
1.0
|
OD1
|
D:ASN192
|
4.6
|
62.3
|
1.0
|
CG
|
D:GLN217
|
4.7
|
31.1
|
1.0
|
N
|
D:ASN192
|
4.7
|
41.5
|
1.0
|
N
|
D:GLN217
|
4.9
|
31.0
|
1.0
|
CA
|
D:GLN217
|
5.0
|
31.2
|
1.0
|
|
Magnesium binding site 5 out
of 5 in 3rit
Go back to
Magnesium Binding Sites List in 3rit
Magnesium binding site 5 out
of 5 in the Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 5 of Crystal Structure of Dipeptide Epimerase From Methylococcus Capsulatus Complexed with Mg and Dipeptide L-Arg-D-Lys within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Mg364
b:60.8
occ:1.00
|
OE2
|
E:GLU216
|
2.7
|
58.0
|
1.0
|
OD2
|
E:ASP241
|
2.7
|
58.0
|
1.0
|
OXT
|
E:DLY363
|
2.9
|
77.1
|
1.0
|
O
|
E:DLY363
|
2.9
|
73.5
|
1.0
|
OD1
|
E:ASP190
|
3.1
|
53.7
|
1.0
|
OD2
|
E:ASP190
|
3.1
|
61.4
|
1.0
|
C
|
E:DLY363
|
3.3
|
83.0
|
1.0
|
OE1
|
E:GLU242
|
3.4
|
57.6
|
1.0
|
CG
|
E:ASP190
|
3.4
|
58.2
|
1.0
|
OE2
|
E:GLU242
|
3.5
|
66.6
|
1.0
|
CG
|
E:ASP241
|
3.6
|
53.5
|
1.0
|
CD
|
E:GLU216
|
3.6
|
58.7
|
1.0
|
CB
|
E:ASP241
|
3.6
|
46.7
|
1.0
|
CG
|
E:GLU216
|
3.8
|
46.6
|
1.0
|
OD1
|
E:ASN192
|
3.8
|
72.8
|
1.0
|
CD
|
E:GLU242
|
3.8
|
62.2
|
1.0
|
CG
|
E:ASN192
|
4.3
|
71.5
|
1.0
|
CB
|
E:GLN217
|
4.3
|
41.0
|
1.0
|
CB
|
E:GLU216
|
4.6
|
41.8
|
1.0
|
OE1
|
E:GLU216
|
4.7
|
60.2
|
1.0
|
O
|
E:GLU216
|
4.7
|
52.8
|
1.0
|
CA
|
E:ASN192
|
4.8
|
57.3
|
1.0
|
OD1
|
E:ASP241
|
4.8
|
55.2
|
1.0
|
CB
|
E:ASP190
|
4.8
|
52.3
|
1.0
|
ND2
|
E:ASN192
|
4.8
|
66.7
|
1.0
|
CA
|
E:DLY363
|
4.8
|
82.8
|
1.0
|
NZ
|
E:LYS160
|
4.8
|
68.2
|
1.0
|
CB
|
E:ASN192
|
4.9
|
62.8
|
1.0
|
C
|
E:GLU216
|
5.0
|
52.4
|
1.0
|
|
Reference:
T.Lukk,
A.Sakai,
C.Kalyanaraman,
S.D.Brown,
H.J.Imker,
L.Song,
A.A.Fedorov,
E.V.Fedorov,
R.Toro,
B.Hillerich,
R.Seidel,
Y.Patskovsky,
M.W.Vetting,
S.K.Nair,
P.C.Babbitt,
S.C.Almo,
J.A.Gerlt,
M.P.Jacobson.
Homology Models Guide Discovery of Diverse Enzyme Specificities Among Dipeptide Epimerases in the Enolase Superfamily. Proc.Natl.Acad.Sci.Usa V. 109 4122 2012.
ISSN: ISSN 0027-8424
PubMed: 22392983
DOI: 10.1073/PNAS.1112081109
Page generated: Thu Aug 15 10:29:59 2024
|