Zinc in PDB 8oto: Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp
Enzymatic activity of Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp
All present enzymatic activity of Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp:
2.1.1.57;
Protein crystallography data
The structure of Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp, PDB code: 8oto
was solved by
V.Kremling,
J.Sprenger,
D.Oberthuer,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
42.07 /
1.80
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
167.86,
167.86,
51.592,
90,
90,
120
|
R / Rfree (%)
|
17.5 /
18.6
|
Other elements in 8oto:
The structure of Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp
(pdb code 8oto). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the
Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp, PDB code: 8oto:
Jump to Zinc binding site number:
1;
2;
Zinc binding site 1 out
of 2 in 8oto
Go back to
Zinc Binding Sites List in 8oto
Zinc binding site 1 out
of 2 in the Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn4402
b:34.6
occ:1.00
|
NE2
|
B:HIS4336
|
2.1
|
37.2
|
1.0
|
SG
|
B:CYS4343
|
2.2
|
35.2
|
1.0
|
SG
|
B:CYS4327
|
2.2
|
34.2
|
1.0
|
SG
|
B:CYS4330
|
2.3
|
36.3
|
1.0
|
H
|
B:CYS4330
|
3.0
|
39.7
|
1.0
|
CE1
|
B:HIS4336
|
3.0
|
37.1
|
1.0
|
HB3
|
B:CYS4327
|
3.1
|
40.0
|
1.0
|
CD2
|
B:HIS4336
|
3.1
|
39.5
|
1.0
|
HB2
|
B:CYS4343
|
3.1
|
50.3
|
1.0
|
CB
|
B:CYS4327
|
3.1
|
33.3
|
1.0
|
HE1
|
B:HIS4336
|
3.2
|
44.6
|
1.0
|
HD2
|
B:HIS4336
|
3.3
|
47.4
|
1.0
|
HB2
|
B:CYS4327
|
3.3
|
40.0
|
1.0
|
CB
|
B:CYS4343
|
3.3
|
41.9
|
1.0
|
HB2
|
B:CYS4330
|
3.4
|
37.6
|
1.0
|
CB
|
B:CYS4330
|
3.4
|
31.3
|
1.0
|
N
|
B:CYS4330
|
3.6
|
33.0
|
1.0
|
HB2
|
B:TYR4329
|
3.6
|
43.0
|
1.0
|
HB3
|
B:CYS4343
|
3.9
|
50.3
|
1.0
|
HB2
|
B:LYS4346
|
3.9
|
45.1
|
1.0
|
CA
|
B:CYS4330
|
4.0
|
30.9
|
1.0
|
ND1
|
B:HIS4336
|
4.1
|
37.6
|
1.0
|
O
|
B:HOH4555
|
4.2
|
45.8
|
1.0
|
HA
|
B:CYS4330
|
4.2
|
37.1
|
1.0
|
CG
|
B:HIS4336
|
4.2
|
45.2
|
1.0
|
HA
|
B:CYS4343
|
4.2
|
52.5
|
1.0
|
HB3
|
B:CYS4330
|
4.3
|
37.6
|
1.0
|
H
|
B:LYS4346
|
4.3
|
37.6
|
1.0
|
HB2
|
B:LEU4345
|
4.3
|
39.5
|
1.0
|
CA
|
B:CYS4343
|
4.4
|
43.8
|
1.0
|
HA
|
B:ALA4324
|
4.5
|
31.9
|
1.0
|
HD2
|
B:TYR4329
|
4.5
|
49.5
|
1.0
|
CB
|
B:TYR4329
|
4.6
|
35.8
|
1.0
|
CA
|
B:CYS4327
|
4.6
|
33.8
|
1.0
|
H
|
B:TYR4329
|
4.6
|
34.3
|
1.0
|
H
|
B:LEU4345
|
4.6
|
41.5
|
1.0
|
C
|
B:TYR4329
|
4.6
|
34.1
|
1.0
|
CB
|
B:LYS4346
|
4.9
|
37.6
|
1.0
|
HD12
|
B:LEU4345
|
4.9
|
46.3
|
1.0
|
HD1
|
B:HIS4336
|
4.9
|
45.1
|
1.0
|
HA
|
B:CYS4327
|
4.9
|
40.5
|
1.0
|
N
|
B:LYS4346
|
4.9
|
31.3
|
1.0
|
C
|
B:CYS4327
|
5.0
|
36.2
|
1.0
|
CA
|
B:TYR4329
|
5.0
|
33.7
|
1.0
|
HB3
|
B:TYR4329
|
5.0
|
43.0
|
1.0
|
N
|
B:TYR4329
|
5.0
|
28.6
|
1.0
|
|
Zinc binding site 2 out
of 2 in 8oto
Go back to
Zinc Binding Sites List in 8oto
Zinc binding site 2 out
of 2 in the Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Sars-Cov-2 NSP10-16 Methyltransferase in Complex with Amp within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn4403
b:50.6
occ:1.00
|
SG
|
B:CYS4381
|
2.3
|
49.5
|
1.0
|
SG
|
B:CYS4370
|
2.3
|
54.1
|
1.0
|
SG
|
B:CYS4373
|
2.4
|
45.2
|
1.0
|
SG
|
B:CYS4383
|
2.4
|
57.4
|
1.0
|
HB2
|
B:CYS4383
|
2.8
|
73.2
|
1.0
|
HB3
|
B:CYS4370
|
3.1
|
67.2
|
1.0
|
CB
|
B:CYS4370
|
3.1
|
56.0
|
1.0
|
HB2
|
B:CYS4370
|
3.1
|
67.2
|
1.0
|
CB
|
B:CYS4383
|
3.2
|
61.0
|
1.0
|
H
|
B:CYS4373
|
3.2
|
53.7
|
1.0
|
HB3
|
B:CYS4373
|
3.2
|
55.5
|
1.0
|
H
|
B:CYS4383
|
3.4
|
80.4
|
1.0
|
CB
|
B:CYS4373
|
3.4
|
46.2
|
1.0
|
HB2
|
B:CYS4381
|
3.4
|
60.5
|
1.0
|
CB
|
B:CYS4381
|
3.5
|
50.4
|
1.0
|
HB
|
B:VAL4372
|
3.6
|
68.5
|
1.0
|
HA
|
B:CYS4381
|
3.7
|
67.1
|
1.0
|
HZ2
|
B:LYS4377
|
3.8
|
99.0
|
1.0
|
O
|
B:HOH4550
|
3.9
|
50.8
|
1.0
|
HB3
|
B:CYS4383
|
3.9
|
73.2
|
1.0
|
N
|
B:CYS4373
|
3.9
|
44.7
|
1.0
|
N
|
B:CYS4383
|
4.0
|
67.0
|
1.0
|
O
|
B:HOH4569
|
4.1
|
57.8
|
1.0
|
CA
|
B:CYS4381
|
4.1
|
55.9
|
1.0
|
H
|
B:SER4382
|
4.2
|
63.1
|
1.0
|
HB2
|
B:CYS4373
|
4.2
|
55.5
|
1.0
|
CA
|
B:CYS4383
|
4.2
|
67.7
|
1.0
|
CA
|
B:CYS4373
|
4.2
|
48.9
|
1.0
|
HB3
|
B:CYS4381
|
4.3
|
60.5
|
1.0
|
HB2
|
B:MET4375
|
4.4
|
48.6
|
1.0
|
H
|
B:VAL4372
|
4.4
|
60.2
|
1.0
|
N
|
B:SER4382
|
4.5
|
52.6
|
1.0
|
HG12
|
B:VAL4372
|
4.5
|
61.7
|
1.0
|
HA
|
B:CYS4383
|
4.6
|
81.2
|
1.0
|
CA
|
B:CYS4370
|
4.6
|
48.9
|
1.0
|
CB
|
B:VAL4372
|
4.6
|
57.1
|
1.0
|
H
|
B:MET4375
|
4.6
|
52.0
|
1.0
|
C
|
B:CYS4381
|
4.6
|
51.9
|
1.0
|
HD3
|
B:LYS4377
|
4.7
|
78.5
|
1.0
|
NZ
|
B:LYS4377
|
4.7
|
82.5
|
1.0
|
HD2
|
B:LYS4377
|
4.8
|
78.5
|
1.0
|
H
|
B:GLY4374
|
4.8
|
61.4
|
1.0
|
HZ3
|
B:LYS4377
|
4.9
|
99.0
|
1.0
|
C
|
B:VAL4372
|
4.9
|
48.0
|
1.0
|
HA
|
B:CYS4370
|
4.9
|
58.6
|
1.0
|
C
|
B:CYS4373
|
5.0
|
49.3
|
1.0
|
|
Reference:
V.Kremling,
D.Oberthuer,
O.Yefanov,
M.Galchenkova,
P.Middendorf,
Y.Fernandez Garcia,
C.Ehrt,
S.Falke,
A.Kiene,
B.Klopprogge,
H.Chapman,
J.Sprenger.
Crystal Structures of Tubercidin and Adenosine Bound to the Active Site of the Sars-Cov-2 Methyltransferase NSP10-16 To Be Published.
Page generated: Thu Oct 31 08:56:58 2024
|