Magnesium in PDB 2xim: Arginine Residues As Stabilizing Elements in Proteins
Enzymatic activity of Arginine Residues As Stabilizing Elements in Proteins
All present enzymatic activity of Arginine Residues As Stabilizing Elements in Proteins:
5.3.1.5;
Protein crystallography data
The structure of Arginine Residues As Stabilizing Elements in Proteins, PDB code: 2xim
was solved by
N.T.Mrabet,
A.Van Denbroek,
I.Van Den Brande,
P.Stanssens,
Y.Laroche,
A.-M.Lambeir,
G.Matthyssens,
J.Jenkins,
M.Chiadmi,
H.Vantilbeurgh,
F.Rey,
J.Janin,
W.J.Quax,
I.Lasters,
M.Demaeyer,
S.J.Wodak,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
N/A /
2.30
|
Space group
|
P 32 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
143.450,
143.450,
231.500,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
n/a /
n/a
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Arginine Residues As Stabilizing Elements in Proteins
(pdb code 2xim). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 8 binding sites of Magnesium where determined in the
Arginine Residues As Stabilizing Elements in Proteins, PDB code: 2xim:
Jump to Magnesium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
Magnesium binding site 1 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 1 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg395
b:21.5
occ:1.00
|
OD2
|
A:ASP292
|
2.0
|
13.9
|
1.0
|
OD2
|
A:ASP245
|
2.0
|
14.1
|
1.0
|
OE1
|
A:GLU217
|
2.1
|
14.9
|
1.0
|
OE2
|
A:GLU181
|
2.1
|
15.6
|
1.0
|
O2
|
A:XYL397
|
2.3
|
20.2
|
1.0
|
O4
|
A:XYL397
|
2.4
|
22.0
|
1.0
|
CD
|
A:GLU181
|
3.0
|
14.8
|
1.0
|
CG
|
A:ASP292
|
3.1
|
13.2
|
1.0
|
CG
|
A:ASP245
|
3.2
|
15.2
|
1.0
|
CD
|
A:GLU217
|
3.3
|
14.7
|
1.0
|
OE1
|
A:GLU181
|
3.3
|
15.6
|
1.0
|
C4
|
A:XYL397
|
3.4
|
22.3
|
1.0
|
O3
|
A:XYL397
|
3.5
|
23.1
|
1.0
|
C2
|
A:XYL397
|
3.5
|
21.1
|
1.0
|
C3
|
A:XYL397
|
3.6
|
22.1
|
1.0
|
CB
|
A:ASP292
|
3.7
|
12.7
|
1.0
|
CB
|
A:ASP245
|
3.8
|
12.6
|
1.0
|
O
|
A:HOH453
|
4.0
|
17.6
|
1.0
|
OE2
|
A:GLU217
|
4.0
|
16.8
|
1.0
|
OD1
|
A:ASP292
|
4.1
|
13.5
|
1.0
|
OD1
|
A:ASP245
|
4.2
|
15.0
|
1.0
|
CG
|
A:GLU217
|
4.3
|
13.5
|
1.0
|
O
|
A:HOH528
|
4.3
|
32.0
|
1.0
|
CE1
|
A:HIS220
|
4.3
|
11.6
|
1.0
|
CG
|
A:GLU181
|
4.3
|
12.8
|
1.0
|
CB
|
A:GLU217
|
4.4
|
11.8
|
1.0
|
NE2
|
A:HIS220
|
4.6
|
12.2
|
1.0
|
C5
|
A:XYL397
|
4.7
|
21.1
|
1.0
|
C1
|
A:XYL397
|
4.7
|
20.6
|
1.0
|
ND2
|
A:ASN215
|
4.7
|
5.8
|
1.0
|
MG
|
A:MG396
|
5.0
|
45.3
|
1.0
|
|
Magnesium binding site 2 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 2 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg396
b:45.3
occ:1.00
|
O
|
A:HOH528
|
2.1
|
32.0
|
1.0
|
OE2
|
A:GLU217
|
2.5
|
16.8
|
1.0
|
OD2
|
A:ASP255
|
2.5
|
27.0
|
1.0
|
O1
|
A:XYL397
|
2.7
|
23.2
|
1.0
|
OD1
|
A:ASP255
|
2.8
|
23.7
|
1.0
|
NE2
|
A:HIS220
|
2.9
|
12.2
|
1.0
|
OD1
|
A:ASP257
|
3.0
|
20.3
|
1.0
|
CG
|
A:ASP255
|
3.0
|
22.8
|
1.0
|
O2
|
A:XYL397
|
3.5
|
20.2
|
1.0
|
CD
|
A:GLU217
|
3.5
|
14.7
|
1.0
|
C1
|
A:XYL397
|
3.6
|
20.6
|
1.0
|
CD2
|
A:HIS220
|
3.6
|
11.9
|
1.0
|
OD2
|
A:ASP257
|
3.7
|
21.5
|
1.0
|
CG
|
A:ASP257
|
3.7
|
18.3
|
1.0
|
CE1
|
A:HIS220
|
4.0
|
11.6
|
1.0
|
OE1
|
A:GLU217
|
4.0
|
14.9
|
1.0
|
NZ
|
A:LYS183
|
4.1
|
7.9
|
1.0
|
C2
|
A:XYL397
|
4.1
|
21.1
|
1.0
|
O
|
A:HOH560
|
4.3
|
44.4
|
1.0
|
CE
|
A:LYS183
|
4.4
|
6.1
|
1.0
|
ND2
|
A:ASN247
|
4.4
|
9.8
|
1.0
|
CB
|
A:ASP255
|
4.5
|
18.9
|
1.0
|
O
|
A:HOH557
|
4.8
|
50.9
|
1.0
|
CG
|
A:GLU217
|
4.8
|
13.5
|
1.0
|
CG
|
A:HIS220
|
4.8
|
10.8
|
1.0
|
O
|
A:HOH426
|
4.9
|
17.7
|
1.0
|
MG
|
A:MG395
|
5.0
|
21.5
|
1.0
|
OD2
|
A:ASP292
|
5.0
|
13.9
|
1.0
|
ND1
|
A:HIS220
|
5.0
|
12.6
|
1.0
|
|
Magnesium binding site 3 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 3 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg395
b:28.0
occ:1.00
|
OE1
|
B:GLU217
|
2.0
|
18.9
|
1.0
|
OE2
|
B:GLU181
|
2.1
|
18.0
|
1.0
|
OD2
|
B:ASP245
|
2.2
|
19.3
|
1.0
|
OD2
|
B:ASP292
|
2.2
|
15.2
|
1.0
|
O2
|
B:XYL397
|
2.3
|
28.4
|
1.0
|
O4
|
B:XYL397
|
2.5
|
27.4
|
1.0
|
CD
|
B:GLU181
|
3.0
|
17.6
|
1.0
|
CD
|
B:GLU217
|
3.2
|
17.1
|
1.0
|
CG
|
B:ASP245
|
3.3
|
16.6
|
1.0
|
OE1
|
B:GLU181
|
3.3
|
17.4
|
1.0
|
CG
|
B:ASP292
|
3.3
|
14.1
|
1.0
|
C2
|
B:XYL397
|
3.5
|
27.9
|
1.0
|
C4
|
B:XYL397
|
3.5
|
28.3
|
1.0
|
C3
|
B:XYL397
|
3.7
|
27.9
|
1.0
|
O3
|
B:XYL397
|
3.7
|
27.8
|
1.0
|
CB
|
B:ASP245
|
3.8
|
12.7
|
1.0
|
CB
|
B:ASP292
|
3.8
|
12.2
|
1.0
|
O
|
B:HOH459
|
3.9
|
16.8
|
1.0
|
OE2
|
B:GLU217
|
3.9
|
19.7
|
1.0
|
CE1
|
B:HIS220
|
4.1
|
14.4
|
1.0
|
CB
|
B:GLU217
|
4.1
|
13.5
|
1.0
|
CG
|
B:GLU217
|
4.1
|
15.4
|
1.0
|
OD1
|
B:ASP245
|
4.2
|
17.8
|
1.0
|
CG
|
B:GLU181
|
4.3
|
15.8
|
1.0
|
O
|
B:HOH534
|
4.3
|
33.8
|
1.0
|
OD1
|
B:ASP292
|
4.4
|
14.8
|
1.0
|
NE2
|
B:HIS220
|
4.5
|
14.7
|
1.0
|
C1
|
B:XYL397
|
4.7
|
26.7
|
1.0
|
ND2
|
B:ASN215
|
4.7
|
13.1
|
1.0
|
C5
|
B:XYL397
|
4.8
|
27.6
|
1.0
|
MG
|
B:MG396
|
4.8
|
41.2
|
1.0
|
O1
|
B:XYL397
|
4.9
|
24.0
|
1.0
|
ND1
|
B:HIS220
|
5.0
|
14.3
|
1.0
|
|
Magnesium binding site 4 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 4 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg396
b:41.2
occ:1.00
|
O
|
B:HOH534
|
2.0
|
33.8
|
1.0
|
OE2
|
B:GLU217
|
2.6
|
19.7
|
1.0
|
O1
|
B:XYL397
|
2.7
|
24.0
|
1.0
|
OD2
|
B:ASP255
|
2.7
|
27.3
|
1.0
|
NE2
|
B:HIS220
|
2.8
|
14.7
|
1.0
|
OD1
|
B:ASP255
|
2.9
|
23.9
|
1.0
|
OD1
|
B:ASP257
|
3.0
|
19.5
|
1.0
|
CG
|
B:ASP255
|
3.1
|
23.4
|
1.0
|
CD
|
B:GLU217
|
3.6
|
17.1
|
1.0
|
CD2
|
B:HIS220
|
3.6
|
12.9
|
1.0
|
O2
|
B:XYL397
|
3.6
|
28.4
|
1.0
|
OD2
|
B:ASP257
|
3.6
|
20.1
|
1.0
|
C1
|
B:XYL397
|
3.7
|
26.7
|
1.0
|
CG
|
B:ASP257
|
3.8
|
17.6
|
1.0
|
CE1
|
B:HIS220
|
3.8
|
14.4
|
1.0
|
OE1
|
B:GLU217
|
4.0
|
18.9
|
1.0
|
NZ
|
B:LYS183
|
4.0
|
10.8
|
1.0
|
C2
|
B:XYL397
|
4.3
|
27.9
|
1.0
|
CE
|
B:LYS183
|
4.3
|
10.3
|
1.0
|
ND2
|
B:ASN247
|
4.4
|
11.2
|
1.0
|
CB
|
B:ASP255
|
4.5
|
18.0
|
1.0
|
O
|
B:HOH563
|
4.6
|
52.7
|
1.0
|
CG
|
B:HIS220
|
4.8
|
13.0
|
1.0
|
MG
|
B:MG395
|
4.8
|
28.0
|
1.0
|
CG
|
B:GLU217
|
4.9
|
15.4
|
1.0
|
O
|
B:HOH431
|
4.9
|
20.5
|
1.0
|
ND1
|
B:HIS220
|
4.9
|
14.3
|
1.0
|
OD2
|
B:ASP292
|
4.9
|
15.2
|
1.0
|
|
Magnesium binding site 5 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 5 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 5 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg395
b:17.5
occ:1.00
|
OE1
|
C:GLU217
|
2.0
|
18.4
|
1.0
|
OD2
|
C:ASP245
|
2.0
|
17.0
|
1.0
|
OD2
|
C:ASP292
|
2.1
|
13.3
|
1.0
|
OE2
|
C:GLU181
|
2.1
|
17.5
|
1.0
|
O2
|
C:XYL397
|
2.3
|
23.3
|
1.0
|
O4
|
C:XYL397
|
2.4
|
20.5
|
1.0
|
CD
|
C:GLU181
|
3.0
|
15.8
|
1.0
|
CG
|
C:ASP245
|
3.2
|
13.8
|
1.0
|
CG
|
C:ASP292
|
3.2
|
14.2
|
1.0
|
CD
|
C:GLU217
|
3.2
|
16.6
|
1.0
|
OE1
|
C:GLU181
|
3.3
|
16.1
|
1.0
|
C4
|
C:XYL397
|
3.5
|
20.9
|
1.0
|
C2
|
C:XYL397
|
3.5
|
22.2
|
1.0
|
CB
|
C:ASP292
|
3.7
|
12.3
|
1.0
|
CB
|
C:ASP245
|
3.7
|
11.1
|
1.0
|
C3
|
C:XYL397
|
3.9
|
21.4
|
1.0
|
OE2
|
C:GLU217
|
4.0
|
18.7
|
1.0
|
O3
|
C:XYL397
|
4.0
|
21.7
|
1.0
|
O
|
C:HOH469
|
4.0
|
21.1
|
1.0
|
OD1
|
C:ASP245
|
4.1
|
13.6
|
1.0
|
CG
|
C:GLU217
|
4.1
|
13.3
|
1.0
|
O
|
C:HOH536
|
4.2
|
29.7
|
1.0
|
CB
|
C:GLU217
|
4.2
|
9.6
|
1.0
|
OD1
|
C:ASP292
|
4.2
|
13.8
|
1.0
|
CE1
|
C:HIS220
|
4.2
|
13.6
|
1.0
|
CG
|
C:GLU181
|
4.3
|
13.8
|
1.0
|
NE2
|
C:HIS220
|
4.5
|
12.7
|
1.0
|
ND2
|
C:ASN215
|
4.6
|
5.7
|
1.0
|
C1
|
C:XYL397
|
4.7
|
22.5
|
1.0
|
C5
|
C:XYL397
|
4.8
|
18.5
|
1.0
|
MG
|
C:MG396
|
5.0
|
39.1
|
1.0
|
|
Magnesium binding site 6 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 6 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 6 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg396
b:39.1
occ:1.00
|
O
|
C:HOH536
|
2.0
|
29.7
|
1.0
|
OD2
|
C:ASP255
|
2.3
|
25.3
|
1.0
|
OE2
|
C:GLU217
|
2.4
|
18.7
|
1.0
|
OD1
|
C:ASP257
|
2.7
|
16.7
|
1.0
|
OD1
|
C:ASP255
|
2.8
|
23.9
|
1.0
|
CG
|
C:ASP255
|
2.9
|
22.2
|
1.0
|
NE2
|
C:HIS220
|
3.0
|
12.7
|
1.0
|
O1
|
C:XYL397
|
3.0
|
21.8
|
1.0
|
CD
|
C:GLU217
|
3.5
|
16.6
|
1.0
|
CD2
|
C:HIS220
|
3.5
|
11.2
|
1.0
|
OD2
|
C:ASP257
|
3.5
|
19.5
|
1.0
|
CG
|
C:ASP257
|
3.6
|
16.3
|
1.0
|
C1
|
C:XYL397
|
3.8
|
22.5
|
1.0
|
O2
|
C:XYL397
|
3.8
|
23.3
|
1.0
|
OE1
|
C:GLU217
|
4.0
|
18.4
|
1.0
|
O
|
C:HOH575
|
4.0
|
75.9
|
1.0
|
CE1
|
C:HIS220
|
4.1
|
13.6
|
1.0
|
ND2
|
C:ASN247
|
4.2
|
9.0
|
1.0
|
NZ
|
C:LYS183
|
4.3
|
7.8
|
1.0
|
CB
|
C:ASP255
|
4.4
|
16.3
|
1.0
|
C2
|
C:XYL397
|
4.4
|
22.2
|
1.0
|
O
|
C:HOH441
|
4.6
|
19.1
|
1.0
|
CG
|
C:GLU217
|
4.8
|
13.3
|
1.0
|
CG
|
C:HIS220
|
4.8
|
11.0
|
1.0
|
CE
|
C:LYS183
|
4.8
|
6.8
|
1.0
|
MG
|
C:MG395
|
5.0
|
17.5
|
1.0
|
|
Magnesium binding site 7 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 7 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 7 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg395
b:16.7
occ:1.00
|
OD2
|
D:ASP292
|
2.0
|
12.9
|
1.0
|
OE2
|
D:GLU181
|
2.0
|
18.9
|
1.0
|
OE1
|
D:GLU217
|
2.1
|
14.9
|
1.0
|
OD2
|
D:ASP245
|
2.1
|
18.8
|
1.0
|
O2
|
D:XYL397
|
2.3
|
21.8
|
1.0
|
O4
|
D:XYL397
|
2.4
|
22.3
|
1.0
|
CD
|
D:GLU181
|
3.0
|
17.1
|
1.0
|
CG
|
D:ASP292
|
3.1
|
11.3
|
1.0
|
CG
|
D:ASP245
|
3.2
|
16.6
|
1.0
|
CD
|
D:GLU217
|
3.3
|
15.0
|
1.0
|
OE1
|
D:GLU181
|
3.3
|
17.1
|
1.0
|
C4
|
D:XYL397
|
3.5
|
22.4
|
1.0
|
C2
|
D:XYL397
|
3.6
|
21.6
|
1.0
|
O3
|
D:XYL397
|
3.6
|
22.2
|
1.0
|
CB
|
D:ASP245
|
3.7
|
15.1
|
1.0
|
CB
|
D:ASP292
|
3.7
|
10.4
|
1.0
|
C3
|
D:XYL397
|
3.8
|
22.4
|
1.0
|
O
|
D:HOH475
|
3.8
|
18.1
|
1.0
|
CG
|
D:GLU217
|
4.1
|
13.0
|
1.0
|
OD1
|
D:ASP292
|
4.1
|
10.9
|
1.0
|
CB
|
D:GLU217
|
4.1
|
11.7
|
1.0
|
OE2
|
D:GLU217
|
4.1
|
16.2
|
1.0
|
OD1
|
D:ASP245
|
4.2
|
15.8
|
1.0
|
CE1
|
D:HIS220
|
4.2
|
8.1
|
1.0
|
CG
|
D:GLU181
|
4.3
|
14.1
|
1.0
|
O
|
D:HOH540
|
4.4
|
31.6
|
1.0
|
C1
|
D:XYL397
|
4.6
|
21.5
|
1.0
|
ND2
|
D:ASN215
|
4.6
|
10.8
|
1.0
|
NE2
|
D:HIS220
|
4.6
|
8.1
|
1.0
|
MG
|
D:MG396
|
4.7
|
11.2
|
1.0
|
C5
|
D:XYL397
|
4.7
|
22.2
|
1.0
|
|
Magnesium binding site 8 out
of 8 in 2xim
Go back to
Magnesium Binding Sites List in 2xim
Magnesium binding site 8 out
of 8 in the Arginine Residues As Stabilizing Elements in Proteins
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 8 of Arginine Residues As Stabilizing Elements in Proteins within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg396
b:11.2
occ:1.00
|
O
|
D:HOH540
|
2.3
|
31.6
|
1.0
|
OE2
|
D:GLU217
|
2.3
|
16.2
|
1.0
|
O1
|
D:XYL397
|
2.5
|
19.6
|
1.0
|
OD2
|
D:ASP255
|
2.5
|
24.0
|
1.0
|
NE2
|
D:HIS220
|
2.7
|
8.1
|
1.0
|
OD1
|
D:ASP255
|
2.9
|
20.9
|
1.0
|
OD1
|
D:ASP257
|
3.0
|
21.2
|
1.0
|
CG
|
D:ASP255
|
3.2
|
20.6
|
1.0
|
C1
|
D:XYL397
|
3.2
|
21.5
|
1.0
|
CD
|
D:GLU217
|
3.2
|
15.0
|
1.0
|
O2
|
D:XYL397
|
3.4
|
21.8
|
1.0
|
CD2
|
D:HIS220
|
3.6
|
8.3
|
1.0
|
OE1
|
D:GLU217
|
3.6
|
14.9
|
1.0
|
CE1
|
D:HIS220
|
3.7
|
8.1
|
1.0
|
CG
|
D:ASP257
|
3.8
|
19.6
|
1.0
|
OD2
|
D:ASP257
|
3.8
|
22.2
|
1.0
|
O
|
D:HOH577
|
3.9
|
62.5
|
1.0
|
C2
|
D:XYL397
|
4.0
|
21.6
|
1.0
|
NZ
|
D:LYS183
|
4.4
|
10.2
|
1.0
|
ND2
|
D:ASN247
|
4.4
|
6.9
|
1.0
|
OD2
|
D:ASP292
|
4.6
|
12.9
|
1.0
|
CG
|
D:GLU217
|
4.6
|
13.0
|
1.0
|
CE
|
D:LYS183
|
4.6
|
8.3
|
1.0
|
CB
|
D:ASP255
|
4.6
|
16.0
|
1.0
|
MG
|
D:MG395
|
4.7
|
16.7
|
1.0
|
CG
|
D:HIS220
|
4.7
|
7.2
|
1.0
|
ND1
|
D:HIS220
|
4.8
|
7.3
|
1.0
|
O
|
D:HOH449
|
4.9
|
16.4
|
1.0
|
O3
|
D:XYL397
|
4.9
|
22.2
|
1.0
|
|
Reference:
N.T.Mrabet,
A.Van Den Broeck,
I.Van Den Brande,
P.Stanssens,
Y.Laroche,
A.M.Lambeir,
G.Matthijssens,
J.Jenkins,
M.Chiadmi,
H.Van Tilbeurgh,
F.Rey,
J.Janin,
W.J.Quax,
I.Lasters,
M.Demaeyer,
S.J.Wodak.
Arginine Residues As Stabilizing Elements in Proteins. Biochemistry V. 31 2239 1992.
ISSN: ISSN 0006-2960
PubMed: 1540579
DOI: 10.1021/BI00123A005
Page generated: Wed Aug 14 07:09:26 2024
|