Zinc in PDB 5mcu: New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2)
Protein crystallography data
The structure of New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2), PDB code: 5mcu
was solved by
D.Golovenko,
H.Rozenberg,
Z.Shakked,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
42.90 /
1.70
|
Space group
|
P 21 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
109.133,
68.422,
69.422,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
16.9 /
20.1
|
Zinc Binding Sites:
The binding sites of Zinc atom in the New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2)
(pdb code 5mcu). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the
New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2), PDB code: 5mcu:
Jump to Zinc binding site number:
1;
2;
Zinc binding site 1 out
of 2 in 5mcu
Go back to
Zinc Binding Sites List in 5mcu
Zinc binding site 1 out
of 2 in the New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2)
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn301
b:14.2
occ:1.00
|
ND1
|
A:HIS179
|
2.0
|
14.3
|
1.0
|
SG
|
A:CYS176
|
2.3
|
13.0
|
1.0
|
SG
|
A:CYS242
|
2.4
|
13.6
|
1.0
|
SG
|
A:CYS238
|
2.4
|
14.5
|
1.0
|
HB3
|
A:CYS242
|
2.8
|
16.8
|
1.0
|
CE1
|
A:HIS179
|
2.9
|
14.9
|
1.0
|
HB2
|
A:HIS179
|
2.9
|
18.6
|
1.0
|
HE1
|
A:HIS179
|
3.0
|
17.9
|
1.0
|
HB3
|
A:CYS238
|
3.1
|
16.4
|
1.0
|
CG
|
A:HIS179
|
3.1
|
15.2
|
1.0
|
CB
|
A:CYS242
|
3.1
|
14.0
|
1.0
|
CB
|
A:CYS238
|
3.2
|
13.6
|
1.0
|
HB3
|
A:CYS176
|
3.3
|
15.7
|
1.0
|
H
|
A:CYS176
|
3.3
|
17.2
|
1.0
|
HA
|
A:CYS238
|
3.3
|
16.4
|
1.0
|
HB2
|
A:CYS242
|
3.4
|
16.8
|
1.0
|
CB
|
A:CYS176
|
3.4
|
13.1
|
1.0
|
CB
|
A:HIS179
|
3.5
|
15.5
|
1.0
|
H
|
A:HIS179
|
3.8
|
19.0
|
1.0
|
CA
|
A:CYS238
|
3.8
|
13.7
|
1.0
|
H
|
A:ASN239
|
3.9
|
15.1
|
1.0
|
NE2
|
A:HIS179
|
4.0
|
18.4
|
1.0
|
N
|
A:CYS176
|
4.1
|
14.4
|
1.0
|
HB3
|
A:HIS179
|
4.1
|
18.6
|
1.0
|
HB2
|
A:CYS238
|
4.1
|
16.4
|
1.0
|
CD2
|
A:HIS179
|
4.1
|
18.0
|
1.0
|
HB2
|
A:CYS176
|
4.2
|
15.7
|
1.0
|
CA
|
A:CYS176
|
4.3
|
12.8
|
1.0
|
N
|
A:HIS179
|
4.5
|
15.8
|
1.0
|
N
|
A:ASN239
|
4.5
|
12.6
|
1.0
|
CA
|
A:CYS242
|
4.5
|
14.5
|
1.0
|
HD11
|
A:LEU137
|
4.5
|
27.3
|
1.0
|
HD2
|
A:HIS178
|
4.5
|
26.5
|
1.0
|
HA
|
A:CYS242
|
4.6
|
17.4
|
1.0
|
CA
|
A:HIS179
|
4.6
|
16.2
|
1.0
|
O
|
A:HOH489
|
4.6
|
17.0
|
1.0
|
O
|
A:MET237
|
4.7
|
15.9
|
1.0
|
C
|
A:CYS238
|
4.7
|
14.8
|
1.0
|
HB3
|
A:HIS178
|
4.7
|
19.4
|
1.0
|
HE2
|
A:HIS179
|
4.8
|
22.1
|
1.0
|
HB3
|
A:ARG175
|
4.9
|
23.3
|
1.0
|
HA
|
A:ARG175
|
4.9
|
19.1
|
1.0
|
O
|
A:CYS176
|
5.0
|
14.8
|
1.0
|
N
|
A:CYS238
|
5.0
|
14.0
|
1.0
|
C
|
A:CYS176
|
5.0
|
13.5
|
1.0
|
|
Zinc binding site 2 out
of 2 in 5mcu
Go back to
Zinc Binding Sites List in 5mcu
Zinc binding site 2 out
of 2 in the New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2)
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins (Complex P53DBD-LHG2) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn301
b:13.9
occ:1.00
|
ND1
|
B:HIS179
|
2.0
|
13.2
|
1.0
|
SG
|
B:CYS242
|
2.2
|
14.4
|
1.0
|
SG
|
B:CYS238
|
2.3
|
14.8
|
1.0
|
SG
|
B:CYS176
|
2.3
|
12.3
|
1.0
|
HB2
|
B:HIS179
|
2.8
|
21.4
|
1.0
|
HB3
|
B:CYS242
|
2.9
|
20.9
|
1.0
|
CE1
|
B:HIS179
|
2.9
|
18.9
|
1.0
|
CG
|
B:HIS179
|
3.0
|
14.2
|
1.0
|
HE1
|
B:HIS179
|
3.1
|
22.6
|
1.0
|
CB
|
B:CYS242
|
3.1
|
17.4
|
1.0
|
HB3
|
B:CYS238
|
3.2
|
18.1
|
1.0
|
H
|
B:CYS176
|
3.3
|
15.1
|
1.0
|
HB3
|
B:CYS176
|
3.3
|
23.0
|
1.0
|
CB
|
B:CYS238
|
3.3
|
15.1
|
1.0
|
HA
|
B:CYS238
|
3.4
|
17.2
|
1.0
|
CB
|
B:HIS179
|
3.4
|
17.8
|
1.0
|
HB2
|
B:CYS242
|
3.4
|
20.9
|
1.0
|
CB
|
B:CYS176
|
3.5
|
19.2
|
1.0
|
H
|
B:HIS179
|
3.7
|
17.8
|
1.0
|
CA
|
B:CYS238
|
3.9
|
14.3
|
1.0
|
HB3
|
B:HIS179
|
4.0
|
21.4
|
1.0
|
H
|
B:ASN239
|
4.0
|
16.4
|
1.0
|
N
|
B:CYS176
|
4.0
|
12.6
|
1.0
|
NE2
|
B:HIS179
|
4.1
|
19.8
|
1.0
|
HB2
|
B:CYS238
|
4.1
|
18.1
|
1.0
|
CD2
|
B:HIS179
|
4.1
|
19.4
|
1.0
|
HB2
|
B:CYS176
|
4.2
|
23.0
|
1.0
|
CA
|
B:CYS176
|
4.3
|
12.4
|
1.0
|
N
|
B:HIS179
|
4.4
|
14.8
|
1.0
|
HD2
|
B:HIS178
|
4.5
|
25.1
|
1.0
|
HD11
|
B:LEU137
|
4.5
|
25.9
|
1.0
|
CA
|
B:HIS179
|
4.6
|
16.6
|
1.0
|
CA
|
B:CYS242
|
4.6
|
16.2
|
1.0
|
N
|
B:ASN239
|
4.6
|
13.7
|
1.0
|
O
|
B:HOH491
|
4.6
|
15.8
|
1.0
|
HB3
|
B:HIS178
|
4.6
|
17.5
|
1.0
|
HA
|
B:CYS242
|
4.7
|
19.4
|
1.0
|
O
|
B:MET237
|
4.7
|
15.4
|
1.0
|
C
|
B:CYS238
|
4.8
|
13.5
|
1.0
|
HB3
|
B:ARG175
|
4.8
|
25.1
|
1.0
|
O
|
B:CYS176
|
4.8
|
17.1
|
1.0
|
HE2
|
B:HIS179
|
4.8
|
23.8
|
1.0
|
HA
|
B:ARG175
|
4.9
|
19.4
|
1.0
|
C
|
B:CYS176
|
4.9
|
14.7
|
1.0
|
|
Reference:
D.Golovenko,
B.Brauning,
P.Vyas,
T.E.Haran,
H.Rozenberg,
Z.Shakked.
New Insights Into the Role of Dna Shape on Its Recognition By P53 Proteins. Structure V. 26 1237 2018.
ISSN: ISSN 1878-4186
PubMed: 30057026
DOI: 10.1016/J.STR.2018.06.006
Page generated: Sun Oct 27 22:06:13 2024
|