Iron in PDB 5d08: Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
Enzymatic activity of Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
All present enzymatic activity of Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase:
1.17.99.6;
Protein crystallography data
The structure of Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase, PDB code: 5d08
was solved by
D.P.Dowling,
Z.D.Miles,
C.Kohrer,
V.Bandarian,
C.L.Drennan,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
46.41 /
1.75
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
84.301,
95.780,
111.175,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
16.7 /
19.6
|
Other elements in 5d08:
The structure of Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase 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 Selenomethionine-Labeled Epoxyqueuosine Reductase
(pdb code 5d08). 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 Selenomethionine-Labeled Epoxyqueuosine Reductase, PDB code: 5d08:
Jump to Iron binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Iron binding site 1 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 1 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe501
b:23.9
occ:1.00
|
FE1
|
A:SF4501
|
0.0
|
23.9
|
1.0
|
SG
|
A:CYS194
|
2.3
|
22.7
|
1.0
|
S2
|
A:SF4501
|
2.3
|
23.4
|
1.0
|
S3
|
A:SF4501
|
2.3
|
26.8
|
1.0
|
S4
|
A:SF4501
|
2.3
|
27.3
|
1.0
|
FE4
|
A:SF4501
|
2.7
|
27.3
|
1.0
|
FE2
|
A:SF4501
|
2.7
|
27.4
|
1.0
|
FE3
|
A:SF4501
|
2.7
|
25.3
|
1.0
|
CB
|
A:CYS194
|
3.2
|
24.6
|
1.0
|
N
|
A:CYS194
|
3.8
|
26.2
|
1.0
|
S1
|
A:SF4501
|
3.9
|
27.1
|
1.0
|
CA
|
A:CYS194
|
4.1
|
25.3
|
1.0
|
CB
|
A:LYS154
|
4.2
|
23.3
|
1.0
|
N
|
A:ASN155
|
4.3
|
21.4
|
1.0
|
CB
|
A:ASN155
|
4.5
|
16.9
|
1.0
|
ND2
|
A:ASN155
|
4.6
|
19.6
|
1.0
|
CG
|
A:ASN155
|
4.6
|
18.7
|
1.0
|
N
|
A:LYS193
|
4.7
|
29.5
|
1.0
|
SG
|
A:CYS191
|
4.7
|
30.2
|
1.0
|
SG
|
A:CYS188
|
4.8
|
25.4
|
1.0
|
C
|
A:LYS154
|
4.8
|
23.4
|
1.0
|
SG
|
A:CYS247
|
4.8
|
24.0
|
1.0
|
N
|
A:LYS154
|
4.9
|
23.7
|
1.0
|
CA
|
A:LYS154
|
4.9
|
24.2
|
1.0
|
C
|
A:LYS193
|
4.9
|
26.4
|
1.0
|
CA
|
A:ASN155
|
5.0
|
18.6
|
1.0
|
|
Iron binding site 2 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 2 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe501
b:27.4
occ:1.00
|
FE2
|
A:SF4501
|
0.0
|
27.4
|
1.0
|
SG
|
A:CYS191
|
2.3
|
30.2
|
1.0
|
S4
|
A:SF4501
|
2.3
|
27.3
|
1.0
|
S3
|
A:SF4501
|
2.3
|
26.8
|
1.0
|
S1
|
A:SF4501
|
2.3
|
27.1
|
1.0
|
FE3
|
A:SF4501
|
2.7
|
25.3
|
1.0
|
FE1
|
A:SF4501
|
2.7
|
23.9
|
1.0
|
FE4
|
A:SF4501
|
2.7
|
27.3
|
1.0
|
CB
|
A:CYS191
|
3.1
|
30.4
|
1.0
|
S2
|
A:SF4501
|
3.9
|
23.4
|
1.0
|
CD
|
A:PRO248
|
4.0
|
27.6
|
1.0
|
C
|
A:CYS191
|
4.2
|
29.6
|
1.0
|
N
|
A:LYS193
|
4.2
|
29.5
|
1.0
|
CA
|
A:CYS191
|
4.3
|
29.7
|
1.0
|
O
|
A:CYS191
|
4.4
|
29.7
|
1.0
|
CB
|
A:LYS193
|
4.5
|
27.5
|
1.0
|
N
|
A:THR192
|
4.5
|
31.9
|
1.0
|
CG
|
A:PRO248
|
4.7
|
30.7
|
1.0
|
SG
|
A:CYS194
|
4.7
|
22.7
|
1.0
|
N
|
A:CYS194
|
4.7
|
26.2
|
1.0
|
SG
|
A:CYS247
|
4.8
|
24.0
|
1.0
|
SG
|
A:CYS188
|
4.9
|
25.4
|
1.0
|
CA
|
A:LYS193
|
4.9
|
29.5
|
1.0
|
O
|
A:CYS188
|
4.9
|
37.2
|
1.0
|
CG
|
A:LYS193
|
4.9
|
31.7
|
1.0
|
C
|
A:THR192
|
5.0
|
27.4
|
1.0
|
|
Iron binding site 3 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 3 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe501
b:25.3
occ:1.00
|
FE3
|
A:SF4501
|
0.0
|
25.3
|
1.0
|
SG
|
A:CYS247
|
2.3
|
24.0
|
1.0
|
S4
|
A:SF4501
|
2.3
|
27.3
|
1.0
|
S1
|
A:SF4501
|
2.3
|
27.1
|
1.0
|
S2
|
A:SF4501
|
2.3
|
23.4
|
1.0
|
FE4
|
A:SF4501
|
2.7
|
27.3
|
1.0
|
FE2
|
A:SF4501
|
2.7
|
27.4
|
1.0
|
FE1
|
A:SF4501
|
2.7
|
23.9
|
1.0
|
CB
|
A:CYS247
|
3.2
|
21.6
|
1.0
|
CA
|
A:CYS247
|
3.8
|
23.8
|
1.0
|
S3
|
A:SF4501
|
3.9
|
26.8
|
1.0
|
CD
|
A:PRO248
|
3.9
|
27.6
|
1.0
|
O
|
A:HOH777
|
4.3
|
22.6
|
1.0
|
N
|
A:PRO248
|
4.4
|
26.8
|
1.0
|
C
|
A:CYS247
|
4.5
|
23.6
|
1.0
|
CD1
|
A:LEU249
|
4.5
|
32.4
|
1.0
|
ND2
|
A:ASN155
|
4.5
|
19.6
|
1.0
|
CG
|
A:LEU249
|
4.6
|
31.2
|
1.0
|
SG
|
A:CYS188
|
4.7
|
25.4
|
1.0
|
SG
|
A:CYS194
|
4.8
|
22.7
|
1.0
|
SG
|
A:CYS191
|
4.8
|
30.2
|
1.0
|
N
|
A:LEU249
|
4.9
|
28.9
|
1.0
|
N
|
A:CYS247
|
5.0
|
22.3
|
1.0
|
CB
|
A:LEU249
|
5.0
|
28.9
|
1.0
|
|
Iron binding site 4 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 4 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe501
b:27.3
occ:1.00
|
FE4
|
A:SF4501
|
0.0
|
27.3
|
1.0
|
S3
|
A:SF4501
|
2.3
|
26.8
|
1.0
|
S2
|
A:SF4501
|
2.3
|
23.4
|
1.0
|
SG
|
A:CYS188
|
2.3
|
25.4
|
1.0
|
S1
|
A:SF4501
|
2.3
|
27.1
|
1.0
|
FE3
|
A:SF4501
|
2.7
|
25.3
|
1.0
|
FE1
|
A:SF4501
|
2.7
|
23.9
|
1.0
|
FE2
|
A:SF4501
|
2.7
|
27.4
|
1.0
|
CB
|
A:CYS188
|
3.3
|
26.4
|
1.0
|
CA
|
A:CYS188
|
3.9
|
28.9
|
1.0
|
S4
|
A:SF4501
|
3.9
|
27.3
|
1.0
|
N
|
A:LYS154
|
4.3
|
23.7
|
1.0
|
CB
|
A:LYS154
|
4.3
|
23.3
|
1.0
|
CG
|
A:LYS154
|
4.4
|
26.4
|
1.0
|
CB
|
A:ALA153
|
4.4
|
22.0
|
1.0
|
CD1
|
A:LEU249
|
4.6
|
32.4
|
1.0
|
SG
|
A:CYS247
|
4.7
|
24.0
|
1.0
|
O
|
A:CYS188
|
4.7
|
37.2
|
1.0
|
SG
|
A:CYS194
|
4.8
|
22.7
|
1.0
|
SG
|
A:CYS191
|
4.8
|
30.2
|
1.0
|
CB
|
A:CYS191
|
4.8
|
30.4
|
1.0
|
CD
|
A:LYS154
|
4.8
|
28.7
|
1.0
|
C
|
A:CYS188
|
4.8
|
34.1
|
1.0
|
N
|
A:CYS188
|
4.9
|
30.4
|
1.0
|
CA
|
A:LYS154
|
4.9
|
24.2
|
1.0
|
|
Iron binding site 5 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 5 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe502
b:19.9
occ:1.00
|
FE1
|
A:SF4502
|
0.0
|
19.9
|
1.0
|
SG
|
A:CYS198
|
2.3
|
22.3
|
1.0
|
S4
|
A:SF4502
|
2.3
|
21.4
|
1.0
|
S2
|
A:SF4502
|
2.3
|
18.0
|
1.0
|
S3
|
A:SF4502
|
2.3
|
20.1
|
1.0
|
FE4
|
A:SF4502
|
2.7
|
18.2
|
1.0
|
FE2
|
A:SF4502
|
2.7
|
18.4
|
1.0
|
FE3
|
A:SF4502
|
2.8
|
17.8
|
1.0
|
CB
|
A:CYS198
|
3.3
|
17.0
|
1.0
|
CA
|
A:CYS198
|
3.9
|
20.5
|
1.0
|
S1
|
A:SF4502
|
3.9
|
18.6
|
1.0
|
CD
|
A:PRO199
|
3.9
|
26.1
|
1.0
|
CB
|
A:ALA202
|
4.5
|
18.8
|
1.0
|
N
|
A:PRO199
|
4.5
|
22.6
|
1.0
|
C
|
A:CYS198
|
4.6
|
23.8
|
1.0
|
OG1
|
A:THR200
|
4.6
|
22.8
|
1.0
|
SG
|
A:CYS243
|
4.8
|
19.4
|
1.0
|
SG
|
A:CYS214
|
4.9
|
16.9
|
1.0
|
SG
|
A:CYS240
|
4.9
|
19.2
|
1.0
|
CB
|
A:CYS243
|
4.9
|
18.3
|
1.0
|
CG
|
A:LEU203
|
4.9
|
19.3
|
1.0
|
CD1
|
A:LEU203
|
4.9
|
22.3
|
1.0
|
|
Iron binding site 6 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 6 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe502
b:18.4
occ:1.00
|
FE2
|
A:SF4502
|
0.0
|
18.4
|
1.0
|
S1
|
A:SF4502
|
2.3
|
18.6
|
1.0
|
SG
|
A:CYS243
|
2.3
|
19.4
|
1.0
|
S3
|
A:SF4502
|
2.3
|
20.1
|
1.0
|
S4
|
A:SF4502
|
2.3
|
21.4
|
1.0
|
FE3
|
A:SF4502
|
2.7
|
17.8
|
1.0
|
FE1
|
A:SF4502
|
2.7
|
19.9
|
1.0
|
FE4
|
A:SF4502
|
2.8
|
18.2
|
1.0
|
CB
|
A:CYS243
|
3.2
|
18.3
|
1.0
|
S2
|
A:SF4502
|
3.9
|
18.0
|
1.0
|
N45
|
A:B12503
|
3.9
|
19.3
|
1.0
|
N
|
A:CYS243
|
3.9
|
20.4
|
1.0
|
CA
|
A:CYS243
|
4.2
|
20.0
|
1.0
|
O
|
A:HOH718
|
4.2
|
23.2
|
1.0
|
C42
|
A:B12503
|
4.7
|
17.8
|
1.0
|
SG
|
A:CYS240
|
4.7
|
19.2
|
1.0
|
CD1
|
A:LEU203
|
4.8
|
22.3
|
1.0
|
C43
|
A:B12503
|
4.8
|
15.7
|
1.0
|
SG
|
A:CYS214
|
4.8
|
16.9
|
1.0
|
SG
|
A:CYS198
|
4.8
|
22.3
|
1.0
|
O
|
A:CYS240
|
5.0
|
17.7
|
1.0
|
|
Iron binding site 7 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 7 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe502
b:17.8
occ:1.00
|
FE3
|
A:SF4502
|
0.0
|
17.8
|
1.0
|
S4
|
A:SF4502
|
2.3
|
21.4
|
1.0
|
SG
|
A:CYS240
|
2.3
|
19.2
|
1.0
|
S2
|
A:SF4502
|
2.3
|
18.0
|
1.0
|
S1
|
A:SF4502
|
2.3
|
18.6
|
1.0
|
FE2
|
A:SF4502
|
2.7
|
18.4
|
1.0
|
FE4
|
A:SF4502
|
2.7
|
18.2
|
1.0
|
FE1
|
A:SF4502
|
2.8
|
19.9
|
1.0
|
CB
|
A:CYS240
|
3.2
|
15.6
|
1.0
|
S3
|
A:SF4502
|
3.9
|
20.1
|
1.0
|
CD
|
A:PRO199
|
4.3
|
26.1
|
1.0
|
C
|
A:CYS240
|
4.4
|
17.4
|
1.0
|
CA
|
A:CYS240
|
4.4
|
15.6
|
1.0
|
O
|
A:CYS240
|
4.5
|
17.7
|
1.0
|
CB
|
A:ILE215
|
4.5
|
21.0
|
1.0
|
CB
|
A:THR242
|
4.5
|
20.7
|
1.0
|
N
|
A:THR242
|
4.5
|
18.4
|
1.0
|
SG
|
A:CYS243
|
4.7
|
19.4
|
1.0
|
SG
|
A:CYS214
|
4.7
|
16.9
|
1.0
|
N
|
A:ILE215
|
4.8
|
16.7
|
1.0
|
N
|
A:CYS243
|
4.8
|
20.4
|
1.0
|
SG
|
A:CYS198
|
4.8
|
22.3
|
1.0
|
CG1
|
A:ILE215
|
4.8
|
25.5
|
1.0
|
OG1
|
A:THR242
|
4.9
|
20.1
|
1.0
|
N
|
A:ASP241
|
5.0
|
17.5
|
1.0
|
N
|
A:SER216
|
5.0
|
14.4
|
1.0
|
|
Iron binding site 8 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 8 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe502
b:18.2
occ:1.00
|
FE4
|
A:SF4502
|
0.0
|
18.2
|
1.0
|
S3
|
A:SF4502
|
2.3
|
20.1
|
1.0
|
S1
|
A:SF4502
|
2.3
|
18.6
|
1.0
|
S2
|
A:SF4502
|
2.3
|
18.0
|
1.0
|
SG
|
A:CYS214
|
2.3
|
16.9
|
1.0
|
FE1
|
A:SF4502
|
2.7
|
19.9
|
1.0
|
FE3
|
A:SF4502
|
2.7
|
17.8
|
1.0
|
FE2
|
A:SF4502
|
2.8
|
18.4
|
1.0
|
CB
|
A:CYS214
|
3.5
|
16.9
|
1.0
|
CA
|
A:CYS214
|
3.8
|
15.9
|
1.0
|
S4
|
A:SF4502
|
3.9
|
21.4
|
1.0
|
N
|
A:ILE215
|
4.0
|
16.7
|
1.0
|
C
|
A:CYS214
|
4.2
|
16.6
|
1.0
|
N
|
A:SER216
|
4.4
|
14.4
|
1.0
|
CD1
|
A:LEU209
|
4.5
|
19.3
|
1.0
|
C42
|
A:B12503
|
4.5
|
17.8
|
1.0
|
SG
|
A:CYS198
|
4.7
|
22.3
|
1.0
|
CB
|
A:ALA202
|
4.7
|
18.8
|
1.0
|
SG
|
A:CYS240
|
4.7
|
19.2
|
1.0
|
CB
|
A:SER216
|
4.8
|
14.4
|
1.0
|
N45
|
A:B12503
|
4.8
|
19.3
|
1.0
|
CB
|
A:CYS240
|
4.9
|
15.6
|
1.0
|
SG
|
A:CYS243
|
4.9
|
19.4
|
1.0
|
CA
|
A:ILE215
|
4.9
|
17.3
|
1.0
|
|
Iron binding site 9 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 9 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe501
b:25.7
occ:1.00
|
FE1
|
B:SF4501
|
0.0
|
25.7
|
1.0
|
SG
|
B:CYS194
|
2.3
|
24.5
|
1.0
|
S3
|
B:SF4501
|
2.3
|
27.9
|
1.0
|
S2
|
B:SF4501
|
2.3
|
25.2
|
1.0
|
S4
|
B:SF4501
|
2.3
|
28.9
|
1.0
|
FE4
|
B:SF4501
|
2.7
|
27.2
|
1.0
|
FE2
|
B:SF4501
|
2.7
|
30.5
|
1.0
|
FE3
|
B:SF4501
|
2.7
|
25.7
|
1.0
|
CB
|
B:CYS194
|
3.3
|
21.0
|
1.0
|
N
|
B:CYS194
|
3.8
|
25.4
|
1.0
|
S1
|
B:SF4501
|
3.9
|
29.0
|
1.0
|
CA
|
B:CYS194
|
4.2
|
23.6
|
1.0
|
CB
|
B:LYS154
|
4.2
|
24.8
|
1.0
|
N
|
B:ASN155
|
4.3
|
23.9
|
1.0
|
CB
|
B:ASN155
|
4.5
|
18.6
|
1.0
|
CG
|
B:ASN155
|
4.6
|
23.1
|
1.0
|
ND2
|
B:ASN155
|
4.6
|
22.4
|
1.0
|
N
|
B:LYS193
|
4.7
|
29.8
|
1.0
|
SG
|
B:CYS188
|
4.7
|
28.7
|
1.0
|
SG
|
B:CYS191
|
4.7
|
34.7
|
1.0
|
C
|
B:LYS154
|
4.8
|
23.4
|
1.0
|
N
|
B:LYS154
|
4.8
|
22.5
|
1.0
|
CA
|
B:LYS154
|
4.8
|
22.6
|
1.0
|
SG
|
B:CYS247
|
4.8
|
25.4
|
1.0
|
CA
|
B:ASN155
|
5.0
|
20.0
|
1.0
|
C
|
B:LYS193
|
5.0
|
26.4
|
1.0
|
|
Iron binding site 10 out
of 16 in 5d08
Go back to
Iron Binding Sites List in 5d08
Iron binding site 10 out
of 16 in the Crystal Structure of Selenomethionine-Labeled Epoxyqueuosine Reductase
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 Selenomethionine-Labeled Epoxyqueuosine Reductase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe501
b:30.5
occ:1.00
|
FE2
|
B:SF4501
|
0.0
|
30.5
|
1.0
|
S4
|
B:SF4501
|
2.3
|
28.9
|
1.0
|
SG
|
B:CYS191
|
2.3
|
34.7
|
1.0
|
S1
|
B:SF4501
|
2.3
|
29.0
|
1.0
|
S3
|
B:SF4501
|
2.3
|
27.9
|
1.0
|
FE3
|
B:SF4501
|
2.7
|
25.7
|
1.0
|
FE1
|
B:SF4501
|
2.7
|
25.7
|
1.0
|
FE4
|
B:SF4501
|
2.7
|
27.2
|
1.0
|
CB
|
B:CYS191
|
3.2
|
32.0
|
1.0
|
S2
|
B:SF4501
|
3.9
|
25.2
|
1.0
|
CD
|
B:PRO248
|
4.1
|
27.4
|
1.0
|
C
|
B:CYS191
|
4.2
|
32.7
|
1.0
|
N
|
B:LYS193
|
4.2
|
29.8
|
1.0
|
CA
|
B:CYS191
|
4.3
|
32.3
|
1.0
|
O
|
B:CYS191
|
4.4
|
32.2
|
1.0
|
N
|
B:THR192
|
4.4
|
35.1
|
1.0
|
CB
|
B:LYS193
|
4.5
|
29.2
|
1.0
|
SG
|
B:CYS194
|
4.7
|
24.5
|
1.0
|
SG
|
B:CYS247
|
4.8
|
25.4
|
1.0
|
CG
|
B:PRO248
|
4.8
|
30.1
|
1.0
|
N
|
B:CYS194
|
4.8
|
25.4
|
1.0
|
SG
|
B:CYS188
|
4.8
|
28.7
|
1.0
|
O
|
B:CYS188
|
4.8
|
33.5
|
1.0
|
CA
|
B:LYS193
|
4.9
|
30.4
|
1.0
|
CA
|
B:THR192
|
5.0
|
33.9
|
1.0
|
C
|
B:THR192
|
5.0
|
33.1
|
1.0
|
|
Reference:
D.P.Dowling,
Z.D.Miles,
C.Kohrer,
S.J.Maiocco,
S.J.Elliott,
V.Bandarian,
C.L.Drennan.
Molecular Basis of Cobalamin-Dependent Rna Modification. Nucleic Acids Res. V. 44 9965 2016.
ISSN: ESSN 1362-4962
PubMed: 27638883
DOI: 10.1093/NAR/GKW806
Page generated: Mon Aug 5 21:39:07 2024
|