Magnesium in PDB 2d32: Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
Enzymatic activity of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
All present enzymatic activity of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase:
6.3.2.2;
Protein crystallography data
The structure of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase, PDB code: 2d32
was solved by
T.Hibi,
M.Nakayama,
H.Nii,
Y.Kurokawa,
H.Katano,
J.Oda,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
40.00 /
2.40
|
Space group
|
H 3
|
Cell size a, b, c (Å), α, β, γ (°)
|
325.530,
325.530,
105.003,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
16.8 /
19.8
|
Magnesium Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
13;
Binding sites:
The binding sites of Magnesium atom in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
(pdb code 2d32). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 13 binding sites of Magnesium where determined in the
Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase, PDB code: 2d32:
Jump to Magnesium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Magnesium binding site 1 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 1 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
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 Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg1522
b:38.5
occ:1.00
|
OE1
|
A:GLU1519
|
2.2
|
50.1
|
1.0
|
O
|
A:HOH1727
|
2.2
|
32.8
|
1.0
|
OE2
|
A:GLU29
|
2.2
|
37.1
|
1.0
|
OD1
|
A:ASP60
|
2.3
|
34.6
|
1.0
|
OE1
|
A:GLU67
|
2.3
|
41.5
|
1.0
|
O1G
|
A:ANP1521
|
3.1
|
58.3
|
1.0
|
CD
|
A:GLU67
|
3.2
|
39.0
|
1.0
|
CD
|
A:GLU1519
|
3.3
|
48.9
|
1.0
|
CG
|
A:ASP60
|
3.3
|
34.0
|
1.0
|
CD
|
A:GLU29
|
3.3
|
33.8
|
1.0
|
OE2
|
A:GLU67
|
3.6
|
42.4
|
1.0
|
CG
|
A:GLU1519
|
3.7
|
47.0
|
1.0
|
CG
|
A:GLU29
|
3.8
|
30.7
|
1.0
|
N
|
A:CYS1520
|
3.9
|
36.7
|
1.0
|
CB
|
A:ASP60
|
3.9
|
30.9
|
1.0
|
OD2
|
A:ASP60
|
4.1
|
33.3
|
1.0
|
O
|
A:HOH1764
|
4.3
|
35.4
|
1.0
|
CE1
|
A:HIS150
|
4.3
|
35.2
|
1.0
|
OE1
|
A:GLU29
|
4.3
|
35.9
|
1.0
|
OE2
|
A:GLU1519
|
4.4
|
49.2
|
1.0
|
O
|
A:HOH1664
|
4.4
|
40.5
|
1.0
|
PG
|
A:ANP1521
|
4.4
|
58.1
|
1.0
|
MG
|
A:MG1524
|
4.4
|
42.2
|
1.0
|
CG
|
A:GLU67
|
4.4
|
33.0
|
1.0
|
CB
|
A:GLU1519
|
4.5
|
46.5
|
1.0
|
O3G
|
A:ANP1521
|
4.6
|
58.8
|
1.0
|
OE1
|
A:GLU27
|
4.7
|
38.2
|
1.0
|
ND1
|
A:HIS150
|
4.8
|
34.0
|
1.0
|
CA
|
A:ASP60
|
4.9
|
30.2
|
1.0
|
CB
|
A:GLU67
|
5.0
|
26.5
|
1.0
|
|
Magnesium binding site 2 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 2 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
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 Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg1523
b:49.0
occ:1.00
|
OE2
|
A:GLU328
|
1.9
|
41.9
|
1.0
|
O3G
|
A:ANP1521
|
2.0
|
58.8
|
1.0
|
OE2
|
A:GLU27
|
2.2
|
39.9
|
1.0
|
O1B
|
A:ANP1521
|
2.2
|
51.2
|
1.0
|
OE1
|
A:GLU27
|
2.3
|
38.2
|
1.0
|
CD
|
A:GLU27
|
2.5
|
36.7
|
1.0
|
ND1
|
A:HIS150
|
2.7
|
34.0
|
1.0
|
CD
|
A:GLU328
|
3.1
|
39.3
|
1.0
|
PG
|
A:ANP1521
|
3.3
|
58.1
|
1.0
|
PB
|
A:ANP1521
|
3.5
|
53.8
|
1.0
|
CE1
|
A:HIS150
|
3.6
|
35.2
|
1.0
|
CG
|
A:HIS150
|
3.6
|
33.0
|
1.0
|
N3B
|
A:ANP1521
|
3.8
|
54.7
|
1.0
|
CB
|
A:HIS150
|
3.9
|
29.6
|
1.0
|
OE1
|
A:GLU328
|
3.9
|
41.0
|
1.0
|
O1G
|
A:ANP1521
|
3.9
|
58.3
|
1.0
|
MG
|
A:MG1524
|
3.9
|
42.2
|
1.0
|
CG
|
A:GLU27
|
4.0
|
33.2
|
1.0
|
O
|
A:HOH1752
|
4.1
|
40.1
|
1.0
|
NH1
|
A:ARG330
|
4.1
|
43.2
|
1.0
|
CG
|
A:GLU328
|
4.1
|
36.2
|
1.0
|
O
|
A:HOH1727
|
4.2
|
32.8
|
1.0
|
O2G
|
A:ANP1521
|
4.5
|
58.3
|
1.0
|
CB
|
A:GLU27
|
4.6
|
28.7
|
1.0
|
O2A
|
A:ANP1521
|
4.7
|
45.7
|
1.0
|
O5'
|
A:ANP1521
|
4.7
|
43.1
|
1.0
|
O3A
|
A:ANP1521
|
4.7
|
48.8
|
1.0
|
O2B
|
A:ANP1521
|
4.7
|
55.2
|
1.0
|
NE2
|
A:HIS150
|
4.7
|
34.1
|
1.0
|
OD1
|
A:ASN152
|
4.8
|
30.1
|
1.0
|
CD2
|
A:HIS150
|
4.8
|
34.2
|
1.0
|
ND2
|
A:ASN152
|
4.9
|
30.1
|
1.0
|
|
Magnesium binding site 3 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 3 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
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 Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg1524
b:42.2
occ:1.00
|
O2A
|
A:ANP1521
|
2.1
|
45.7
|
1.0
|
OE2
|
A:GLU67
|
2.2
|
42.4
|
1.0
|
OE1
|
A:GLU27
|
2.3
|
38.2
|
1.0
|
O
|
A:HOH1768
|
2.4
|
36.4
|
1.0
|
O1G
|
A:ANP1521
|
2.5
|
58.3
|
1.0
|
N3B
|
A:ANP1521
|
2.9
|
54.7
|
1.0
|
PG
|
A:ANP1521
|
3.1
|
58.1
|
1.0
|
CD
|
A:GLU67
|
3.3
|
39.0
|
1.0
|
CD
|
A:GLU27
|
3.4
|
36.7
|
1.0
|
PA
|
A:ANP1521
|
3.5
|
46.5
|
1.0
|
O3G
|
A:ANP1521
|
3.6
|
58.8
|
1.0
|
PB
|
A:ANP1521
|
3.7
|
53.8
|
1.0
|
O1B
|
A:ANP1521
|
3.8
|
51.2
|
1.0
|
O3A
|
A:ANP1521
|
3.9
|
48.8
|
1.0
|
OE1
|
A:GLU67
|
3.9
|
41.5
|
1.0
|
MG
|
A:MG1523
|
3.9
|
49.0
|
1.0
|
CD1
|
A:ILE69
|
3.9
|
30.0
|
1.0
|
CG
|
A:GLU27
|
4.1
|
33.2
|
1.0
|
O
|
A:HOH1727
|
4.1
|
32.8
|
1.0
|
O5'
|
A:ANP1521
|
4.2
|
43.1
|
1.0
|
OE2
|
A:GLU27
|
4.3
|
39.9
|
1.0
|
CG1
|
A:ILE69
|
4.3
|
29.1
|
1.0
|
MG
|
A:MG1522
|
4.4
|
38.5
|
1.0
|
O
|
A:HOH1664
|
4.5
|
40.5
|
1.0
|
O2G
|
A:ANP1521
|
4.5
|
58.3
|
1.0
|
CG
|
A:GLU67
|
4.5
|
33.0
|
1.0
|
CB
|
A:GLU27
|
4.6
|
28.7
|
1.0
|
O1A
|
A:ANP1521
|
4.7
|
47.0
|
1.0
|
|
Magnesium binding site 4 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 4 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
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 Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg1525
b:40.5
occ:1.00
|
OD2
|
A:ASP444
|
2.3
|
28.1
|
1.0
|
O
|
A:HOH1708
|
2.3
|
26.4
|
1.0
|
OD1
|
A:ASN442
|
2.3
|
30.4
|
1.0
|
O
|
A:HOH1837
|
2.4
|
30.0
|
1.0
|
O
|
A:HOH1579
|
2.6
|
37.7
|
1.0
|
CG
|
A:ASN442
|
3.2
|
29.5
|
1.0
|
CG
|
A:ASP444
|
3.3
|
27.2
|
1.0
|
ND2
|
A:ASN442
|
3.4
|
28.8
|
1.0
|
CB
|
A:ASP444
|
3.6
|
23.6
|
1.0
|
O
|
A:HOH1863
|
3.6
|
40.0
|
1.0
|
O
|
A:HOH1756
|
4.0
|
38.1
|
1.0
|
N
|
A:ASP444
|
4.4
|
24.5
|
1.0
|
OD1
|
A:ASP444
|
4.5
|
26.0
|
1.0
|
CB
|
A:ASN442
|
4.5
|
29.1
|
1.0
|
O
|
A:HOH1761
|
4.6
|
38.8
|
1.0
|
CA
|
A:ASP444
|
4.6
|
24.4
|
1.0
|
O
|
A:HOH1789
|
4.6
|
37.6
|
1.0
|
CA
|
A:ASN442
|
4.8
|
29.7
|
1.0
|
CD
|
A:PRO443
|
4.9
|
26.4
|
1.0
|
|
Magnesium binding site 5 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 5 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
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 Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg2522
b:45.1
occ:1.00
|
OE1
|
B:GLU2519
|
2.0
|
45.5
|
1.0
|
O
|
B:HOH2568
|
2.0
|
34.7
|
1.0
|
OE1
|
B:GLU67
|
2.2
|
49.7
|
1.0
|
OD1
|
B:ASP60
|
2.2
|
45.0
|
1.0
|
OE2
|
B:GLU29
|
2.4
|
45.5
|
1.0
|
CD
|
B:GLU2519
|
3.2
|
47.3
|
1.0
|
CD
|
B:GLU67
|
3.2
|
48.8
|
1.0
|
O1G
|
B:ANP2521
|
3.2
|
64.1
|
1.0
|
CG
|
B:ASP60
|
3.2
|
44.7
|
1.0
|
CD
|
B:GLU29
|
3.5
|
44.1
|
1.0
|
OE2
|
B:GLU67
|
3.7
|
54.1
|
1.0
|
CG
|
B:GLU29
|
3.9
|
40.8
|
1.0
|
CG
|
B:GLU2519
|
3.9
|
48.0
|
1.0
|
CB
|
B:ASP60
|
4.0
|
43.8
|
1.0
|
N
|
B:CYS2520
|
4.1
|
52.9
|
1.0
|
OE2
|
B:GLU2519
|
4.1
|
48.6
|
1.0
|
OD2
|
B:ASP60
|
4.1
|
44.8
|
1.0
|
MG
|
B:MG2524
|
4.2
|
76.4
|
1.0
|
O
|
B:HOH2592
|
4.3
|
39.8
|
1.0
|
CG
|
B:GLU67
|
4.4
|
46.5
|
1.0
|
CB
|
B:GLU2519
|
4.4
|
48.4
|
1.0
|
PG
|
B:ANP2521
|
4.5
|
65.1
|
1.0
|
CE1
|
B:HIS150
|
4.5
|
37.9
|
1.0
|
OE1
|
B:GLU29
|
4.6
|
45.5
|
1.0
|
OE1
|
B:GLU27
|
4.6
|
49.8
|
1.0
|
O3G
|
B:ANP2521
|
4.9
|
65.6
|
1.0
|
CA
|
B:ASP60
|
4.9
|
43.9
|
1.0
|
ND1
|
B:HIS150
|
4.9
|
37.6
|
1.0
|
CB
|
B:GLU67
|
5.0
|
43.0
|
1.0
|
|
Magnesium binding site 6 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 6 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 6 of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg2523
b:49.4
occ:1.00
|
OE2
|
B:GLU328
|
2.0
|
43.2
|
1.0
|
OE1
|
B:GLU27
|
2.0
|
49.8
|
1.0
|
OE2
|
B:GLU27
|
2.1
|
49.0
|
1.0
|
O3G
|
B:ANP2521
|
2.3
|
65.6
|
1.0
|
CD
|
B:GLU27
|
2.3
|
47.4
|
1.0
|
ND1
|
B:HIS150
|
2.6
|
37.6
|
1.0
|
O1B
|
B:ANP2521
|
2.7
|
62.7
|
1.0
|
CD
|
B:GLU328
|
3.1
|
40.8
|
1.0
|
PG
|
B:ANP2521
|
3.5
|
65.1
|
1.0
|
CE1
|
B:HIS150
|
3.5
|
37.9
|
1.0
|
CG
|
B:HIS150
|
3.5
|
37.0
|
1.0
|
CB
|
B:HIS150
|
3.7
|
36.5
|
1.0
|
CG
|
B:GLU27
|
3.8
|
45.0
|
1.0
|
O1G
|
B:ANP2521
|
3.8
|
64.1
|
1.0
|
O
|
B:HOH2568
|
3.8
|
34.7
|
1.0
|
MG
|
B:MG2524
|
3.8
|
76.4
|
1.0
|
OE1
|
B:GLU328
|
3.9
|
41.3
|
1.0
|
PB
|
B:ANP2521
|
4.0
|
63.5
|
1.0
|
CG
|
B:GLU328
|
4.1
|
39.9
|
1.0
|
N3B
|
B:ANP2521
|
4.1
|
63.5
|
1.0
|
O
|
B:HOH2610
|
4.1
|
45.9
|
1.0
|
O
|
B:HOH2575
|
4.1
|
37.0
|
1.0
|
CB
|
B:GLU27
|
4.3
|
40.6
|
1.0
|
O2A
|
B:ANP2521
|
4.5
|
60.6
|
1.0
|
NE2
|
B:HIS150
|
4.7
|
38.7
|
1.0
|
CD2
|
B:HIS150
|
4.7
|
38.5
|
1.0
|
O2G
|
B:ANP2521
|
4.8
|
64.6
|
1.0
|
NH1
|
B:ARG330
|
4.8
|
36.1
|
1.0
|
OD1
|
B:ASN152
|
4.9
|
39.1
|
1.0
|
OE1
|
B:GLU2519
|
4.9
|
45.5
|
1.0
|
|
Magnesium binding site 7 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 7 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 7 of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg2524
b:76.4
occ:1.00
|
OE2
|
B:GLU67
|
2.0
|
54.1
|
1.0
|
O2A
|
B:ANP2521
|
2.1
|
60.6
|
1.0
|
O1G
|
B:ANP2521
|
2.2
|
64.1
|
1.0
|
OE1
|
B:GLU27
|
2.4
|
49.8
|
1.0
|
N3B
|
B:ANP2521
|
3.0
|
63.5
|
1.0
|
PG
|
B:ANP2521
|
3.1
|
65.1
|
1.0
|
CD
|
B:GLU67
|
3.2
|
48.8
|
1.0
|
CD
|
B:GLU27
|
3.3
|
47.4
|
1.0
|
PA
|
B:ANP2521
|
3.5
|
60.2
|
1.0
|
O3G
|
B:ANP2521
|
3.7
|
65.6
|
1.0
|
OE1
|
B:GLU67
|
3.7
|
49.7
|
1.0
|
MG
|
B:MG2523
|
3.8
|
49.4
|
1.0
|
CD1
|
B:ILE69
|
3.8
|
43.9
|
1.0
|
O1B
|
B:ANP2521
|
3.9
|
62.7
|
1.0
|
PB
|
B:ANP2521
|
3.9
|
63.5
|
1.0
|
O
|
B:HOH2568
|
3.9
|
34.7
|
1.0
|
CG
|
B:GLU27
|
4.1
|
45.0
|
1.0
|
O3A
|
B:ANP2521
|
4.1
|
61.5
|
1.0
|
OE2
|
B:GLU27
|
4.1
|
49.0
|
1.0
|
MG
|
B:MG2522
|
4.2
|
45.1
|
1.0
|
CG1
|
B:ILE69
|
4.3
|
41.8
|
1.0
|
CG
|
B:GLU67
|
4.3
|
46.5
|
1.0
|
O5'
|
B:ANP2521
|
4.4
|
56.4
|
1.0
|
O2G
|
B:ANP2521
|
4.4
|
64.6
|
1.0
|
O1A
|
B:ANP2521
|
4.6
|
59.9
|
1.0
|
CB
|
B:GLU27
|
4.6
|
40.6
|
1.0
|
|
Magnesium binding site 8 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 8 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 8 of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg3522
b:52.2
occ:1.00
|
O
|
C:HOH3594
|
2.2
|
45.5
|
1.0
|
OE1
|
C:GLU3519
|
2.3
|
59.0
|
1.0
|
OE2
|
C:GLU29
|
2.3
|
51.9
|
1.0
|
OD1
|
C:ASP60
|
2.3
|
53.2
|
1.0
|
OE1
|
C:GLU67
|
2.3
|
55.6
|
1.0
|
CD
|
C:GLU67
|
3.0
|
54.6
|
1.0
|
OE2
|
C:GLU67
|
3.2
|
56.4
|
1.0
|
CG
|
C:ASP60
|
3.3
|
54.8
|
1.0
|
O1G
|
C:ANP3521
|
3.3
|
71.8
|
1.0
|
CD
|
C:GLU3519
|
3.4
|
58.8
|
1.0
|
CD
|
C:GLU29
|
3.4
|
50.7
|
1.0
|
CG
|
C:GLU3519
|
3.8
|
58.4
|
1.0
|
CG
|
C:GLU29
|
3.9
|
48.6
|
1.0
|
CB
|
C:ASP60
|
4.0
|
54.9
|
1.0
|
OD2
|
C:ASP60
|
4.1
|
54.4
|
1.0
|
O
|
C:HOH3601
|
4.2
|
45.4
|
1.0
|
N
|
C:CYS3520
|
4.2
|
58.8
|
1.0
|
CG
|
C:GLU67
|
4.3
|
52.7
|
1.0
|
MG
|
C:MG3524
|
4.4
|
67.8
|
1.0
|
OE2
|
C:GLU3519
|
4.4
|
59.2
|
1.0
|
OE1
|
C:GLU29
|
4.5
|
49.8
|
1.0
|
CB
|
C:GLU3519
|
4.6
|
57.9
|
1.0
|
PG
|
C:ANP3521
|
4.6
|
72.8
|
1.0
|
CE1
|
C:HIS150
|
4.6
|
44.9
|
1.0
|
OE1
|
C:GLU27
|
4.7
|
50.4
|
1.0
|
CA
|
C:ASP60
|
4.9
|
55.0
|
1.0
|
ND1
|
C:HIS150
|
4.9
|
45.0
|
1.0
|
CB
|
C:GLU67
|
4.9
|
51.3
|
1.0
|
CA
|
C:CYS3520
|
4.9
|
60.4
|
1.0
|
O2G
|
C:ANP3521
|
5.0
|
71.9
|
1.0
|
|
Magnesium binding site 9 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 9 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 9 of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg3523
b:58.5
occ:1.00
|
OE2
|
C:GLU328
|
2.0
|
46.9
|
1.0
|
OE1
|
C:GLU27
|
2.2
|
50.4
|
1.0
|
OE2
|
C:GLU27
|
2.2
|
51.9
|
1.0
|
O3G
|
C:ANP3521
|
2.3
|
72.5
|
1.0
|
CD
|
C:GLU27
|
2.4
|
50.3
|
1.0
|
ND1
|
C:HIS150
|
2.7
|
45.0
|
1.0
|
O1B
|
C:ANP3521
|
2.8
|
71.5
|
1.0
|
CD
|
C:GLU328
|
3.2
|
45.7
|
1.0
|
PG
|
C:ANP3521
|
3.3
|
72.8
|
1.0
|
O1G
|
C:ANP3521
|
3.4
|
71.8
|
1.0
|
O
|
C:HOH3594
|
3.5
|
45.5
|
1.0
|
CG
|
C:HIS150
|
3.5
|
45.2
|
1.0
|
CB
|
C:HIS150
|
3.6
|
43.8
|
1.0
|
CE1
|
C:HIS150
|
3.7
|
44.9
|
1.0
|
CG
|
C:GLU27
|
3.9
|
48.2
|
1.0
|
OE1
|
C:GLU328
|
3.9
|
46.3
|
1.0
|
PB
|
C:ANP3521
|
4.0
|
72.2
|
1.0
|
N3B
|
C:ANP3521
|
4.1
|
71.7
|
1.0
|
CG
|
C:GLU328
|
4.2
|
43.7
|
1.0
|
MG
|
C:MG3524
|
4.2
|
67.8
|
1.0
|
CB
|
C:GLU27
|
4.4
|
46.3
|
1.0
|
O
|
C:HOH3600
|
4.4
|
55.5
|
1.0
|
NH1
|
C:ARG330
|
4.6
|
36.3
|
1.0
|
O2G
|
C:ANP3521
|
4.7
|
71.9
|
1.0
|
CD2
|
C:HIS150
|
4.7
|
45.6
|
1.0
|
NE2
|
C:HIS150
|
4.8
|
46.0
|
1.0
|
OE1
|
C:GLU3519
|
4.8
|
59.0
|
1.0
|
OD1
|
C:ASN152
|
4.9
|
43.8
|
1.0
|
OE2
|
C:GLU67
|
4.9
|
56.4
|
1.0
|
O2A
|
C:ANP3521
|
4.9
|
69.8
|
1.0
|
ND2
|
C:ASN152
|
5.0
|
43.2
|
1.0
|
|
Magnesium binding site 10 out
of 13 in 2d32
Go back to
Magnesium Binding Sites List in 2d32
Magnesium binding site 10 out
of 13 in the Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 10 of Crystal Structure of Michaelis Complex of Gamma- Glutamylcysteine Synthetase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg3524
b:67.8
occ:1.00
|
OE2
|
C:GLU67
|
2.1
|
56.4
|
1.0
|
O1G
|
C:ANP3521
|
2.3
|
71.8
|
1.0
|
O2A
|
C:ANP3521
|
2.3
|
69.8
|
1.0
|
OE1
|
C:GLU27
|
2.6
|
50.4
|
1.0
|
N3B
|
C:ANP3521
|
3.1
|
71.7
|
1.0
|
PG
|
C:ANP3521
|
3.3
|
72.8
|
1.0
|
CD
|
C:GLU67
|
3.3
|
54.6
|
1.0
|
CD
|
C:GLU27
|
3.6
|
50.3
|
1.0
|
PA
|
C:ANP3521
|
3.7
|
70.5
|
1.0
|
CD1
|
C:ILE69
|
3.7
|
51.9
|
1.0
|
O
|
C:HOH3594
|
4.0
|
45.5
|
1.0
|
OE1
|
C:GLU67
|
4.0
|
55.6
|
1.0
|
CG1
|
C:ILE69
|
4.0
|
49.9
|
1.0
|
PB
|
C:ANP3521
|
4.1
|
72.2
|
1.0
|
O3G
|
C:ANP3521
|
4.1
|
72.5
|
1.0
|
O1B
|
C:ANP3521
|
4.1
|
71.5
|
1.0
|
MG
|
C:MG3523
|
4.2
|
58.5
|
1.0
|
CG
|
C:GLU27
|
4.2
|
48.2
|
1.0
|
O3A
|
C:ANP3521
|
4.2
|
71.2
|
1.0
|
CG
|
C:GLU67
|
4.3
|
52.7
|
1.0
|
O2G
|
C:ANP3521
|
4.4
|
71.9
|
1.0
|
MG
|
C:MG3522
|
4.4
|
52.2
|
1.0
|
O5'
|
C:ANP3521
|
4.5
|
66.5
|
1.0
|
OE2
|
C:GLU27
|
4.6
|
51.9
|
1.0
|
CB
|
C:GLU27
|
4.7
|
46.3
|
1.0
|
O1A
|
C:ANP3521
|
4.9
|
70.9
|
1.0
|
|
Reference:
T.Hibi,
M.Nakayama,
H.Nii,
Y.Kurokawa,
H.Katano,
J.Oda.
Structural Basis of Efficient Coupling Peptide Ligation and Atp Hydrolysis By Gamma-Gluatamylcysteine Synthetase To Be Published.
Page generated: Tue Aug 13 22:25:07 2024
|