Zinc in PDB 5uag: Escherichia Coli Rna Polymerase Mutant - Rpob D516V
Enzymatic activity of Escherichia Coli Rna Polymerase Mutant - Rpob D516V
All present enzymatic activity of Escherichia Coli Rna Polymerase Mutant - Rpob D516V:
2.7.7.6;
Protein crystallography data
The structure of Escherichia Coli Rna Polymerase Mutant - Rpob D516V, PDB code: 5uag
was solved by
V.Molodtsov,
N.T.Scharf,
M.A.Stefan,
G.A.Garcia,
K.S.Murakami,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
29.99 /
3.40
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
184.826,
205.043,
307.347,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
27.7 /
31.1
|
Other elements in 5uag:
The structure of Escherichia Coli Rna Polymerase Mutant - Rpob D516V also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Escherichia Coli Rna Polymerase Mutant - Rpob D516V
(pdb code 5uag). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 4 binding sites of Zinc where determined in the
Escherichia Coli Rna Polymerase Mutant - Rpob D516V, PDB code: 5uag:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 5uag
Go back to
Zinc Binding Sites List in 5uag
Zinc binding site 1 out
of 4 in the Escherichia Coli Rna Polymerase Mutant - Rpob D516V
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Escherichia Coli Rna Polymerase Mutant - Rpob D516V within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Zn2003
b:0.1
occ:1.00
|
SG
|
D:CYS70
|
2.1
|
0.7
|
1.0
|
SG
|
D:CYS72
|
2.1
|
0.8
|
1.0
|
SG
|
D:CYS85
|
2.3
|
0.6
|
1.0
|
SG
|
D:CYS88
|
2.4
|
0.1
|
1.0
|
CB
|
D:CYS72
|
2.7
|
1.0
|
1.0
|
CB
|
D:CYS85
|
3.0
|
0.1
|
1.0
|
N
|
D:CYS72
|
3.1
|
0.7
|
1.0
|
CA
|
D:CYS72
|
3.4
|
0.4
|
1.0
|
O
|
D:CYS88
|
3.7
|
0.3
|
1.0
|
N
|
D:CYS88
|
3.7
|
0.9
|
1.0
|
CB
|
D:CYS70
|
3.8
|
0.3
|
1.0
|
CB
|
D:CYS88
|
4.0
|
0.0
|
1.0
|
N
|
D:GLY73
|
4.0
|
0.7
|
1.0
|
C
|
D:CYS72
|
4.2
|
0.1
|
1.0
|
CB
|
D:LYS87
|
4.2
|
0.9
|
1.0
|
N
|
D:LEU71
|
4.2
|
0.2
|
1.0
|
C
|
D:LEU71
|
4.3
|
0.9
|
1.0
|
CA
|
D:CYS88
|
4.3
|
0.2
|
1.0
|
N
|
D:LYS74
|
4.5
|
0.1
|
1.0
|
C
|
D:CYS88
|
4.5
|
0.4
|
1.0
|
CA
|
D:CYS85
|
4.5
|
0.2
|
1.0
|
C
|
D:CYS70
|
4.6
|
0.6
|
1.0
|
CB
|
D:LYS74
|
4.7
|
0.8
|
1.0
|
CA
|
D:LEU71
|
4.7
|
0.5
|
1.0
|
C
|
D:LYS87
|
4.8
|
0.7
|
1.0
|
CA
|
D:CYS70
|
4.8
|
0.2
|
1.0
|
CA
|
D:LYS87
|
4.8
|
0.3
|
1.0
|
N
|
D:LYS87
|
4.9
|
0.9
|
1.0
|
C
|
D:CYS85
|
5.0
|
0.0
|
1.0
|
|
Zinc binding site 2 out
of 4 in 5uag
Go back to
Zinc Binding Sites List in 5uag
Zinc binding site 2 out
of 4 in the Escherichia Coli Rna Polymerase Mutant - Rpob D516V
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Escherichia Coli Rna Polymerase Mutant - Rpob D516V within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Zn2004
b:0.1
occ:1.00
|
SG
|
D:CYS888
|
2.2
|
0.4
|
1.0
|
SG
|
D:CYS898
|
2.2
|
0.7
|
1.0
|
SG
|
D:CYS814
|
2.3
|
0.6
|
1.0
|
CA
|
D:CYS888
|
2.3
|
0.5
|
1.0
|
CB
|
D:CYS888
|
2.3
|
0.5
|
1.0
|
SG
|
D:CYS895
|
2.4
|
0.8
|
1.0
|
N
|
D:ASP889
|
3.0
|
0.8
|
1.0
|
C
|
D:CYS888
|
3.0
|
0.5
|
1.0
|
CB
|
D:CYS898
|
3.0
|
0.5
|
1.0
|
CB
|
D:CYS814
|
3.4
|
0.6
|
1.0
|
N
|
D:CYS888
|
3.6
|
0.2
|
1.0
|
CB
|
D:CYS895
|
3.7
|
1.0
|
1.0
|
NH2
|
D:ARG883
|
4.1
|
0.2
|
1.0
|
CG2
|
D:THR816
|
4.1
|
0.0
|
1.0
|
O
|
D:CYS888
|
4.2
|
0.8
|
1.0
|
N
|
D:THR890
|
4.3
|
0.7
|
1.0
|
CA
|
D:ASP889
|
4.3
|
0.2
|
1.0
|
C
|
D:SER887
|
4.4
|
0.9
|
1.0
|
CA
|
D:CYS898
|
4.4
|
0.5
|
1.0
|
O
|
D:SER887
|
4.4
|
0.4
|
1.0
|
N
|
D:CYS895
|
4.4
|
0.2
|
1.0
|
CA
|
D:CYS814
|
4.6
|
0.6
|
1.0
|
N
|
D:CYS898
|
4.6
|
0.4
|
1.0
|
CA
|
D:CYS895
|
4.6
|
0.7
|
1.0
|
N
|
D:CYS814
|
4.7
|
0.4
|
1.0
|
O
|
D:SER884
|
4.8
|
0.8
|
1.0
|
C
|
D:ASP889
|
4.9
|
0.4
|
1.0
|
CB
|
D:ASP889
|
4.9
|
0.0
|
1.0
|
O
|
D:CYS895
|
4.9
|
0.7
|
1.0
|
CZ
|
D:ARG883
|
5.0
|
0.8
|
1.0
|
NE
|
D:ARG883
|
5.0
|
0.5
|
1.0
|
|
Zinc binding site 3 out
of 4 in 5uag
Go back to
Zinc Binding Sites List in 5uag
Zinc binding site 3 out
of 4 in the Escherichia Coli Rna Polymerase Mutant - Rpob D516V
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Escherichia Coli Rna Polymerase Mutant - Rpob D516V within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
J:Zn2002
b:0.0
occ:1.00
|
SG
|
J:CYS70
|
2.1
|
0.4
|
1.0
|
SG
|
J:CYS85
|
2.2
|
0.3
|
1.0
|
SG
|
J:CYS72
|
2.3
|
0.5
|
1.0
|
CB
|
J:CYS85
|
2.4
|
0.5
|
1.0
|
SG
|
J:CYS88
|
2.5
|
0.2
|
1.0
|
CB
|
J:CYS72
|
3.1
|
0.6
|
1.0
|
O
|
J:CYS88
|
3.4
|
1.0
|
1.0
|
N
|
J:CYS72
|
3.7
|
0.4
|
1.0
|
N
|
J:CYS88
|
3.7
|
0.4
|
1.0
|
CB
|
J:CYS70
|
3.8
|
0.7
|
1.0
|
CA
|
J:CYS85
|
3.9
|
0.2
|
1.0
|
CA
|
J:CYS72
|
4.0
|
0.5
|
1.0
|
CB
|
J:CYS88
|
4.0
|
0.3
|
1.0
|
CA
|
J:CYS88
|
4.2
|
0.4
|
1.0
|
C
|
J:CYS88
|
4.2
|
0.5
|
1.0
|
CB
|
J:LYS87
|
4.3
|
0.3
|
1.0
|
C
|
J:CYS85
|
4.5
|
0.5
|
1.0
|
N
|
J:LEU71
|
4.5
|
0.6
|
1.0
|
N
|
J:GLY73
|
4.6
|
0.9
|
1.0
|
C
|
J:CYS72
|
4.7
|
0.8
|
1.0
|
C
|
J:LYS87
|
4.7
|
0.2
|
1.0
|
N
|
J:CYS85
|
4.7
|
0.3
|
1.0
|
N
|
J:LYS87
|
4.8
|
0.0
|
1.0
|
CA
|
J:LYS87
|
4.8
|
0.1
|
1.0
|
C
|
J:LEU71
|
4.8
|
0.6
|
1.0
|
CA
|
J:CYS70
|
4.9
|
0.3
|
1.0
|
O
|
J:CYS85
|
4.9
|
0.2
|
1.0
|
N
|
J:LYS74
|
4.9
|
0.6
|
1.0
|
CB
|
J:LYS74
|
4.9
|
0.2
|
1.0
|
C
|
J:CYS70
|
4.9
|
0.6
|
1.0
|
CB
|
J:VAL90
|
5.0
|
0.0
|
1.0
|
|
Zinc binding site 4 out
of 4 in 5uag
Go back to
Zinc Binding Sites List in 5uag
Zinc binding site 4 out
of 4 in the Escherichia Coli Rna Polymerase Mutant - Rpob D516V
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of Escherichia Coli Rna Polymerase Mutant - Rpob D516V within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
J:Zn2003
b:0.1
occ:1.00
|
SG
|
J:CYS895
|
2.0
|
0.8
|
1.0
|
SG
|
J:CYS898
|
2.1
|
0.6
|
1.0
|
SG
|
J:CYS814
|
2.1
|
0.9
|
1.0
|
SG
|
J:CYS888
|
2.2
|
0.8
|
1.0
|
CB
|
J:CYS898
|
2.8
|
0.4
|
1.0
|
CB
|
J:CYS888
|
3.0
|
0.0
|
1.0
|
CB
|
J:CYS814
|
3.2
|
0.3
|
1.0
|
CB
|
J:CYS895
|
3.3
|
0.3
|
1.0
|
CA
|
J:CYS888
|
3.5
|
0.5
|
1.0
|
NH2
|
J:ARG883
|
3.8
|
0.4
|
1.0
|
N
|
J:ASP889
|
3.9
|
0.9
|
1.0
|
CA
|
J:CYS898
|
3.9
|
0.9
|
1.0
|
N
|
J:CYS898
|
4.0
|
0.9
|
1.0
|
N
|
J:CYS814
|
4.1
|
0.3
|
1.0
|
C
|
J:CYS888
|
4.1
|
0.0
|
1.0
|
CA
|
J:CYS814
|
4.3
|
0.2
|
1.0
|
N
|
J:CYS895
|
4.3
|
0.8
|
1.0
|
CA
|
J:CYS895
|
4.3
|
0.9
|
1.0
|
CG2
|
J:THR816
|
4.3
|
0.9
|
1.0
|
OG1
|
J:THR890
|
4.4
|
0.6
|
1.0
|
N
|
J:THR890
|
4.5
|
0.3
|
1.0
|
O
|
J:CYS895
|
4.6
|
0.5
|
1.0
|
CZ
|
J:ARG883
|
4.7
|
0.8
|
1.0
|
N
|
J:CYS888
|
4.7
|
0.6
|
1.0
|
C
|
J:CYS895
|
4.8
|
0.5
|
1.0
|
CB
|
J:THR890
|
4.8
|
0.5
|
1.0
|
NE
|
J:ARG883
|
4.9
|
0.4
|
1.0
|
|
Reference:
V.Molodtsov,
N.T.Scharf,
M.A.Stefan,
G.A.Garcia,
K.S.Murakami.
Structural Basis For Rifamycin Resistance of Bacterial Rna Polymerase By the Three Most Clinically Important Rpob Mutations Found in Mycobacterium Tuberculosis. Mol. Microbiol. V. 103 1034 2017.
ISSN: ESSN 1365-2958
PubMed: 28009073
DOI: 10.1111/MMI.13606
Page generated: Mon Oct 28 09:15:06 2024
|