Iron in PDB 1jro: Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Enzymatic activity of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
All present enzymatic activity of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus:
1.1.1.204;
Protein crystallography data
The structure of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus, PDB code: 1jro
was solved by
J.J.Truglio,
K.Theis,
S.Leimkuhler,
R.Rappa,
K.V.Rajagopalan,
C.Kisker,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
50.00 /
2.70
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
92.875,
141.053,
158.113,
109.53,
105.83,
101.33
|
R / Rfree (%)
|
21.3 /
25.2
|
Other elements in 1jro:
The structure of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus also contains other interesting chemical elements:
Iron Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
16;
Binding sites:
The binding sites of Iron atom in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
(pdb code 1jro). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 16 binding sites of Iron where determined in the
Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus, PDB code: 1jro:
Jump to Iron binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Iron binding site 1 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 1 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe3001
b:13.5
occ:1.00
|
FE1
|
A:FES3001
|
0.0
|
13.5
|
1.0
|
SG
|
A:CYS103
|
2.1
|
10.9
|
1.0
|
SG
|
A:CYS136
|
2.1
|
18.9
|
1.0
|
S2
|
A:FES3001
|
2.2
|
7.2
|
1.0
|
S1
|
A:FES3001
|
2.2
|
12.1
|
1.0
|
FE2
|
A:FES3001
|
2.8
|
15.4
|
1.0
|
CB
|
A:CYS103
|
3.3
|
15.2
|
1.0
|
CB
|
A:CYS136
|
3.4
|
21.2
|
1.0
|
N
|
A:CYS103
|
3.6
|
16.0
|
1.0
|
CA
|
A:CYS103
|
3.9
|
15.1
|
1.0
|
N
|
A:GLY104
|
4.1
|
15.3
|
1.0
|
N
|
A:CYS136
|
4.2
|
21.4
|
1.0
|
SG
|
A:CYS134
|
4.3
|
19.8
|
1.0
|
C
|
A:CYS103
|
4.4
|
14.8
|
1.0
|
CA
|
A:CYS136
|
4.4
|
20.4
|
1.0
|
SG
|
A:CYS106
|
4.5
|
20.0
|
1.0
|
N
|
A:PHE105
|
4.5
|
16.7
|
1.0
|
C
|
A:GLN102
|
4.8
|
17.5
|
1.0
|
N
|
A:ARG135
|
4.9
|
22.8
|
1.0
|
N
|
A:CYS106
|
4.9
|
15.3
|
1.0
|
|
Iron binding site 2 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 2 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe3001
b:15.4
occ:1.00
|
FE2
|
A:FES3001
|
0.0
|
15.4
|
1.0
|
S1
|
A:FES3001
|
2.1
|
12.1
|
1.0
|
S2
|
A:FES3001
|
2.1
|
7.2
|
1.0
|
SG
|
A:CYS106
|
2.2
|
20.0
|
1.0
|
SG
|
A:CYS134
|
2.2
|
19.8
|
1.0
|
FE1
|
A:FES3001
|
2.8
|
13.5
|
1.0
|
CB
|
A:CYS134
|
3.2
|
20.8
|
1.0
|
CB
|
A:CYS106
|
3.5
|
16.2
|
1.0
|
CA
|
A:CYS134
|
3.7
|
21.2
|
1.0
|
N
|
A:CYS106
|
4.3
|
15.3
|
1.0
|
SG
|
A:CYS136
|
4.3
|
18.9
|
1.0
|
N
|
A:ARG135
|
4.3
|
22.8
|
1.0
|
C
|
A:CYS134
|
4.4
|
22.4
|
1.0
|
N
|
A:CYS136
|
4.4
|
21.4
|
1.0
|
CA
|
A:CYS106
|
4.4
|
16.3
|
1.0
|
CB
|
A:CYS136
|
4.5
|
21.2
|
1.0
|
SG
|
A:CYS103
|
4.6
|
10.9
|
1.0
|
CG2
|
A:THR137
|
4.7
|
19.9
|
1.0
|
C
|
A:CYS106
|
4.9
|
17.0
|
1.0
|
O
|
A:LEU133
|
5.0
|
20.9
|
1.0
|
N
|
A:CYS134
|
5.0
|
21.4
|
1.0
|
|
Iron binding site 3 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 3 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe3002
b:24.4
occ:1.00
|
FE1
|
A:FES3002
|
0.0
|
24.4
|
1.0
|
S1
|
A:FES3002
|
2.2
|
19.0
|
1.0
|
S2
|
A:FES3002
|
2.2
|
15.4
|
1.0
|
SG
|
A:CYS63
|
2.3
|
27.4
|
1.0
|
SG
|
A:CYS47
|
2.3
|
22.3
|
1.0
|
FE2
|
A:FES3002
|
2.9
|
22.7
|
1.0
|
CB
|
A:CYS63
|
3.2
|
30.4
|
1.0
|
CB
|
A:CYS47
|
3.5
|
21.2
|
1.0
|
N
|
A:CYS47
|
4.3
|
19.7
|
1.0
|
N
|
A:CYS63
|
4.3
|
29.0
|
1.0
|
SG
|
A:CYS39
|
4.3
|
23.5
|
1.0
|
CA
|
A:CYS63
|
4.4
|
29.7
|
1.0
|
N
|
A:ASN40
|
4.4
|
26.9
|
1.0
|
N
|
A:GLY42
|
4.4
|
32.0
|
1.0
|
CB
|
A:ASN61
|
4.4
|
26.4
|
1.0
|
CA
|
A:ASN40
|
4.5
|
28.1
|
1.0
|
CA
|
A:CYS47
|
4.5
|
20.9
|
1.0
|
SG
|
A:CYS44
|
4.5
|
26.5
|
1.0
|
CA
|
A:GLY42
|
4.7
|
30.7
|
1.0
|
N
|
A:GLU41
|
4.7
|
30.8
|
1.0
|
OD1
|
A:ASN61
|
4.8
|
35.4
|
1.0
|
N
|
A:GLY45
|
4.9
|
23.6
|
1.0
|
N
|
A:ALA46
|
5.0
|
19.4
|
1.0
|
C
|
A:ASN40
|
5.0
|
29.3
|
1.0
|
|
Iron binding site 4 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 4 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe3002
b:22.7
occ:1.00
|
FE2
|
A:FES3002
|
0.0
|
22.7
|
1.0
|
SG
|
A:CYS44
|
2.0
|
26.5
|
1.0
|
S2
|
A:FES3002
|
2.2
|
15.4
|
1.0
|
S1
|
A:FES3002
|
2.2
|
19.0
|
1.0
|
SG
|
A:CYS39
|
2.3
|
23.5
|
1.0
|
FE1
|
A:FES3002
|
2.9
|
24.4
|
1.0
|
N
|
A:CYS44
|
3.2
|
29.4
|
1.0
|
N
|
A:CYS39
|
3.2
|
23.3
|
1.0
|
CB
|
A:CYS44
|
3.2
|
26.9
|
1.0
|
CA
|
A:CYS44
|
3.6
|
27.8
|
1.0
|
CB
|
A:CYS39
|
3.6
|
24.7
|
1.0
|
N
|
A:ASN40
|
3.8
|
26.9
|
1.0
|
CA
|
A:CYS39
|
3.9
|
24.3
|
1.0
|
C
|
A:GLY38
|
3.9
|
24.3
|
1.0
|
N
|
A:GLY45
|
3.9
|
23.6
|
1.0
|
C
|
A:CYS44
|
4.1
|
26.0
|
1.0
|
N
|
A:GLY38
|
4.1
|
25.2
|
1.0
|
CA
|
A:GLY38
|
4.2
|
23.8
|
1.0
|
N
|
A:ALA46
|
4.3
|
19.4
|
1.0
|
C
|
A:CYS39
|
4.3
|
25.5
|
1.0
|
C
|
A:ASP43
|
4.4
|
31.2
|
1.0
|
SG
|
A:CYS63
|
4.6
|
27.4
|
1.0
|
N
|
A:ASP43
|
4.6
|
31.0
|
1.0
|
N
|
A:GLY42
|
4.6
|
32.0
|
1.0
|
N
|
A:GLU41
|
4.7
|
30.8
|
1.0
|
SG
|
A:CYS47
|
4.7
|
22.3
|
1.0
|
CA
|
A:ASN40
|
4.8
|
28.1
|
1.0
|
O
|
A:GLY38
|
4.8
|
25.3
|
1.0
|
C
|
A:GLY42
|
4.9
|
30.6
|
1.0
|
CB
|
A:ALA46
|
5.0
|
17.5
|
1.0
|
|
Iron binding site 5 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 5 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 5 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe3001
b:9.7
occ:1.00
|
FE1
|
C:FES3001
|
0.0
|
9.7
|
1.0
|
SG
|
C:CYS136
|
2.1
|
14.2
|
1.0
|
S1
|
C:FES3001
|
2.1
|
8.2
|
1.0
|
SG
|
C:CYS103
|
2.1
|
12.7
|
1.0
|
S2
|
C:FES3001
|
2.2
|
10.0
|
1.0
|
FE2
|
C:FES3001
|
2.8
|
10.1
|
1.0
|
CB
|
C:CYS103
|
3.1
|
10.8
|
1.0
|
N
|
C:CYS103
|
3.4
|
11.7
|
1.0
|
CB
|
C:CYS136
|
3.4
|
12.0
|
1.0
|
O
|
D:HOH3027
|
3.5
|
3.7
|
1.0
|
CA
|
C:CYS103
|
3.7
|
11.1
|
1.0
|
N
|
C:GLY104
|
4.0
|
14.2
|
1.0
|
N
|
C:CYS136
|
4.2
|
14.4
|
1.0
|
C
|
C:CYS103
|
4.2
|
11.4
|
1.0
|
CA
|
C:CYS136
|
4.4
|
13.3
|
1.0
|
SG
|
C:CYS106
|
4.4
|
11.7
|
1.0
|
SG
|
C:CYS134
|
4.5
|
10.2
|
1.0
|
N
|
C:PHE105
|
4.5
|
12.5
|
1.0
|
C
|
C:GLN102
|
4.6
|
12.8
|
1.0
|
N
|
C:ARG135
|
5.0
|
13.8
|
1.0
|
N
|
C:GLN102
|
5.0
|
13.5
|
1.0
|
N
|
C:CYS106
|
5.0
|
12.2
|
1.0
|
|
Iron binding site 6 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 6 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 6 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe3001
b:10.1
occ:1.00
|
FE2
|
C:FES3001
|
0.0
|
10.1
|
1.0
|
S2
|
C:FES3001
|
2.1
|
10.0
|
1.0
|
S1
|
C:FES3001
|
2.2
|
8.2
|
1.0
|
SG
|
C:CYS134
|
2.2
|
10.2
|
1.0
|
SG
|
C:CYS106
|
2.2
|
11.7
|
1.0
|
FE1
|
C:FES3001
|
2.8
|
9.7
|
1.0
|
CB
|
C:CYS134
|
3.2
|
14.1
|
1.0
|
CB
|
C:CYS106
|
3.5
|
9.3
|
1.0
|
CA
|
C:CYS134
|
3.6
|
13.3
|
1.0
|
N
|
C:ARG135
|
4.1
|
13.8
|
1.0
|
N
|
C:CYS136
|
4.1
|
14.4
|
1.0
|
SG
|
C:CYS136
|
4.1
|
14.2
|
1.0
|
C
|
C:CYS134
|
4.2
|
13.6
|
1.0
|
CB
|
C:CYS136
|
4.4
|
12.0
|
1.0
|
N
|
C:CYS106
|
4.4
|
12.2
|
1.0
|
CA
|
C:CYS106
|
4.6
|
11.1
|
1.0
|
SG
|
C:CYS103
|
4.6
|
12.7
|
1.0
|
CA
|
C:CYS136
|
4.8
|
13.3
|
1.0
|
O
|
C:HOH3012
|
4.8
|
12.5
|
1.0
|
CG2
|
C:THR137
|
4.8
|
2.6
|
1.0
|
N
|
C:THR137
|
4.9
|
10.6
|
1.0
|
O
|
C:LEU133
|
4.9
|
15.8
|
1.0
|
N
|
C:CYS134
|
5.0
|
14.4
|
1.0
|
|
Iron binding site 7 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 7 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 7 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe3002
b:14.8
occ:1.00
|
FE1
|
C:FES3002
|
0.0
|
14.8
|
1.0
|
S2
|
C:FES3002
|
2.2
|
16.9
|
1.0
|
S1
|
C:FES3002
|
2.3
|
15.6
|
1.0
|
SG
|
C:CYS47
|
2.3
|
12.5
|
1.0
|
SG
|
C:CYS63
|
2.5
|
15.2
|
1.0
|
FE2
|
C:FES3002
|
2.8
|
15.2
|
1.0
|
CB
|
C:CYS63
|
3.5
|
19.5
|
1.0
|
CB
|
C:CYS47
|
3.6
|
14.9
|
1.0
|
SG
|
C:CYS39
|
4.2
|
16.5
|
1.0
|
N
|
C:CYS47
|
4.3
|
15.5
|
1.0
|
N
|
C:GLY42
|
4.3
|
26.0
|
1.0
|
N
|
C:ASN40
|
4.3
|
21.4
|
1.0
|
CB
|
C:ASN61
|
4.5
|
16.9
|
1.0
|
N
|
C:CYS63
|
4.5
|
18.6
|
1.0
|
CA
|
C:CYS47
|
4.5
|
14.4
|
1.0
|
SG
|
C:CYS44
|
4.6
|
13.8
|
1.0
|
CA
|
C:ASN40
|
4.6
|
23.5
|
1.0
|
CA
|
C:GLY42
|
4.6
|
24.6
|
1.0
|
CA
|
C:CYS63
|
4.6
|
20.2
|
1.0
|
OD1
|
C:ASN61
|
4.6
|
25.9
|
1.0
|
N
|
C:GLU41
|
4.6
|
25.2
|
1.0
|
N
|
C:GLY45
|
4.8
|
16.7
|
1.0
|
CG
|
C:ASN61
|
4.8
|
19.9
|
1.0
|
N
|
C:ALA46
|
4.8
|
15.6
|
1.0
|
C
|
C:ASN40
|
5.0
|
24.6
|
1.0
|
|
Iron binding site 8 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 8 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 8 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe3002
b:15.2
occ:1.00
|
FE2
|
C:FES3002
|
0.0
|
15.2
|
1.0
|
S2
|
C:FES3002
|
2.1
|
16.9
|
1.0
|
SG
|
C:CYS39
|
2.2
|
16.5
|
1.0
|
SG
|
C:CYS44
|
2.2
|
13.8
|
1.0
|
S1
|
C:FES3002
|
2.2
|
15.6
|
1.0
|
FE1
|
C:FES3002
|
2.8
|
14.8
|
1.0
|
N
|
C:CYS39
|
3.2
|
19.7
|
1.0
|
N
|
C:CYS44
|
3.3
|
21.5
|
1.0
|
CB
|
C:CYS39
|
3.3
|
17.9
|
1.0
|
CB
|
C:CYS44
|
3.3
|
18.6
|
1.0
|
CA
|
C:CYS44
|
3.7
|
19.7
|
1.0
|
N
|
C:ASN40
|
3.7
|
21.4
|
1.0
|
CA
|
C:CYS39
|
3.7
|
18.5
|
1.0
|
C
|
C:GLY38
|
3.8
|
22.0
|
1.0
|
N
|
C:GLY45
|
4.0
|
16.7
|
1.0
|
N
|
C:GLY38
|
4.1
|
22.0
|
1.0
|
CA
|
C:GLY38
|
4.1
|
21.6
|
1.0
|
C
|
C:CYS44
|
4.2
|
18.9
|
1.0
|
C
|
C:CYS39
|
4.2
|
19.2
|
1.0
|
N
|
C:ALA46
|
4.3
|
15.6
|
1.0
|
C
|
C:ASP43
|
4.5
|
24.8
|
1.0
|
N
|
C:GLU41
|
4.6
|
25.2
|
1.0
|
N
|
C:GLY42
|
4.6
|
26.0
|
1.0
|
N
|
C:ASP43
|
4.7
|
25.4
|
1.0
|
O
|
C:GLY38
|
4.7
|
23.2
|
1.0
|
CA
|
C:ASN40
|
4.8
|
23.5
|
1.0
|
SG
|
C:CYS47
|
4.8
|
12.5
|
1.0
|
CB
|
C:ALA46
|
4.8
|
13.6
|
1.0
|
SG
|
C:CYS63
|
4.8
|
15.2
|
1.0
|
C
|
C:GLY42
|
4.9
|
25.7
|
1.0
|
|
Iron binding site 9 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 9 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 9 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Fe3001
b:18.4
occ:1.00
|
FE1
|
E:FES3001
|
0.0
|
18.4
|
1.0
|
SG
|
E:CYS103
|
2.1
|
17.3
|
1.0
|
S2
|
E:FES3001
|
2.2
|
19.4
|
1.0
|
SG
|
E:CYS136
|
2.2
|
22.4
|
1.0
|
S1
|
E:FES3001
|
2.2
|
22.1
|
1.0
|
FE2
|
E:FES3001
|
2.6
|
16.8
|
1.0
|
CB
|
E:CYS136
|
3.1
|
22.0
|
1.0
|
CB
|
E:CYS103
|
3.1
|
21.8
|
1.0
|
N
|
E:CYS103
|
3.4
|
22.1
|
1.0
|
CA
|
E:CYS103
|
3.7
|
21.9
|
1.0
|
N
|
E:CYS136
|
4.0
|
21.6
|
1.0
|
SG
|
E:CYS134
|
4.1
|
20.7
|
1.0
|
N
|
E:GLY104
|
4.1
|
23.0
|
1.0
|
CA
|
E:CYS136
|
4.2
|
21.4
|
1.0
|
C
|
E:CYS103
|
4.3
|
22.4
|
1.0
|
SG
|
E:CYS106
|
4.4
|
19.2
|
1.0
|
C
|
E:GLN102
|
4.6
|
22.8
|
1.0
|
N
|
E:PHE105
|
4.7
|
24.4
|
1.0
|
N
|
E:ARG135
|
4.7
|
19.2
|
1.0
|
N
|
E:CYS106
|
4.9
|
22.2
|
1.0
|
CB
|
E:GLN102
|
5.0
|
21.8
|
1.0
|
|
Iron binding site 10 out
of 16 in 1jro
Go back to
Iron Binding Sites List in 1jro
Iron binding site 10 out
of 16 in the Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 10 of Crystal Structure of Xanthine Dehydrogenase From Rhodobacter Capsulatus within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Fe3001
b:16.8
occ:1.00
|
FE2
|
E:FES3001
|
0.0
|
16.8
|
1.0
|
SG
|
E:CYS106
|
2.1
|
19.2
|
1.0
|
S2
|
E:FES3001
|
2.1
|
19.4
|
1.0
|
SG
|
E:CYS134
|
2.1
|
20.7
|
1.0
|
S1
|
E:FES3001
|
2.2
|
22.1
|
1.0
|
FE1
|
E:FES3001
|
2.6
|
18.4
|
1.0
|
CB
|
E:CYS134
|
3.3
|
20.6
|
1.0
|
CB
|
E:CYS106
|
3.5
|
22.7
|
1.0
|
CA
|
E:CYS134
|
4.0
|
20.9
|
1.0
|
N
|
E:CYS106
|
4.1
|
22.2
|
1.0
|
CB
|
E:CYS136
|
4.1
|
22.0
|
1.0
|
SG
|
E:CYS136
|
4.3
|
22.4
|
1.0
|
SG
|
E:CYS103
|
4.3
|
17.3
|
1.0
|
CA
|
E:CYS106
|
4.4
|
22.1
|
1.0
|
N
|
E:ARG135
|
4.5
|
19.2
|
1.0
|
N
|
E:CYS136
|
4.5
|
21.6
|
1.0
|
C
|
E:CYS134
|
4.6
|
20.2
|
1.0
|
CG2
|
E:THR137
|
4.8
|
13.3
|
1.0
|
N
|
E:GLY104
|
4.9
|
23.0
|
1.0
|
CA
|
E:CYS136
|
4.9
|
21.4
|
1.0
|
N
|
E:THR107
|
4.9
|
25.2
|
1.0
|
N
|
E:CYS103
|
4.9
|
22.1
|
1.0
|
|
Reference:
J.J.Truglio,
K.Theis,
S.Leimkuhler,
R.Rappa,
K.V.Rajagopalan,
C.Kisker.
Crystal Structures of the Active and Alloxanthine-Inhibited Forms of Xanthine Dehydrogenase From Rhodobacter Capsulatus Structure V. 10 115 2002.
ISSN: ISSN 0969-2126
PubMed: 11796116
DOI: 10.1016/S0969-2126(01)00697-9
Page generated: Sat Aug 3 08:38:29 2024
|