Manganese in PDB 5nbc: Structure of Prokaryotic Transcription Factors
Protein crystallography data
The structure of Structure of Prokaryotic Transcription Factors, PDB code: 5nbc
was solved by
J.Perard,
P.Carpentier,
I.Michaud-Soret,
C.Cavazza,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
42.08 /
1.70
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
53.150,
90.000,
63.950,
90.00,
93.48,
90.00
|
R / Rfree (%)
|
21.5 /
24.4
|
Other elements in 5nbc:
The structure of Structure of Prokaryotic Transcription Factors also contains other interesting chemical elements:
Manganese Binding Sites:
The binding sites of Manganese atom in the Structure of Prokaryotic Transcription Factors
(pdb code 5nbc). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 4 binding sites of Manganese where determined in the
Structure of Prokaryotic Transcription Factors, PDB code: 5nbc:
Jump to Manganese binding site number:
1;
2;
3;
4;
Manganese binding site 1 out
of 4 in 5nbc
Go back to
Manganese Binding Sites List in 5nbc
Manganese binding site 1 out
of 4 in the Structure of Prokaryotic Transcription Factors
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of Structure of Prokaryotic Transcription Factors within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn201
b:18.9
occ:1.00
|
NE2
|
A:HIS90
|
2.2
|
15.3
|
1.0
|
OE2
|
A:GLU101
|
2.2
|
27.1
|
1.0
|
OE1
|
A:GLU81
|
2.3
|
21.8
|
1.0
|
NE2
|
A:HIS88
|
2.3
|
24.4
|
1.0
|
NE2
|
A:HIS33
|
2.3
|
16.6
|
1.0
|
OE2
|
A:GLU81
|
2.3
|
19.9
|
1.0
|
CD
|
A:GLU81
|
2.6
|
19.2
|
1.0
|
CD2
|
A:HIS88
|
3.1
|
21.8
|
1.0
|
CE1
|
A:HIS90
|
3.2
|
14.3
|
1.0
|
CD2
|
A:HIS90
|
3.2
|
16.9
|
1.0
|
CD
|
A:GLU101
|
3.2
|
22.4
|
1.0
|
CD2
|
A:HIS33
|
3.2
|
14.0
|
1.0
|
CE1
|
A:HIS33
|
3.3
|
20.6
|
1.0
|
CE1
|
A:HIS88
|
3.3
|
24.6
|
1.0
|
CG
|
A:GLU101
|
3.5
|
17.7
|
1.0
|
CG
|
A:GLU81
|
4.1
|
17.2
|
1.0
|
O
|
A:HOH361
|
4.3
|
31.6
|
1.0
|
ND1
|
A:HIS90
|
4.3
|
11.0
|
1.0
|
OE1
|
A:GLU101
|
4.3
|
22.0
|
1.0
|
CG
|
A:HIS88
|
4.3
|
24.1
|
1.0
|
CG
|
A:HIS90
|
4.3
|
15.6
|
1.0
|
ND1
|
A:HIS88
|
4.4
|
23.7
|
1.0
|
ND1
|
A:HIS33
|
4.4
|
18.1
|
1.0
|
CG
|
A:HIS33
|
4.4
|
20.0
|
1.0
|
CB
|
A:GLU81
|
4.7
|
18.2
|
1.0
|
CB
|
A:GLU101
|
4.9
|
16.7
|
1.0
|
|
Manganese binding site 2 out
of 4 in 5nbc
Go back to
Manganese Binding Sites List in 5nbc
Manganese binding site 2 out
of 4 in the Structure of Prokaryotic Transcription Factors
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of Structure of Prokaryotic Transcription Factors within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn201
b:19.6
occ:1.00
|
NE2
|
B:HIS90
|
2.2
|
15.3
|
1.0
|
OE2
|
B:GLU101
|
2.2
|
24.5
|
1.0
|
NE2
|
B:HIS88
|
2.2
|
17.9
|
1.0
|
OE2
|
B:GLU81
|
2.2
|
20.4
|
1.0
|
OE1
|
B:GLU81
|
2.2
|
20.6
|
1.0
|
NE2
|
B:HIS33
|
2.3
|
19.2
|
1.0
|
CD
|
B:GLU81
|
2.5
|
22.2
|
1.0
|
CE1
|
B:HIS90
|
3.1
|
13.6
|
1.0
|
CE1
|
B:HIS88
|
3.2
|
25.7
|
1.0
|
CD
|
B:GLU101
|
3.2
|
27.4
|
1.0
|
CD2
|
B:HIS90
|
3.2
|
14.5
|
1.0
|
CD2
|
B:HIS88
|
3.2
|
22.4
|
1.0
|
CD2
|
B:HIS33
|
3.3
|
21.4
|
1.0
|
CE1
|
B:HIS33
|
3.3
|
20.9
|
1.0
|
CG
|
B:GLU101
|
3.7
|
20.1
|
1.0
|
CG
|
B:GLU81
|
4.0
|
19.1
|
1.0
|
OE1
|
B:GLU101
|
4.2
|
28.2
|
1.0
|
ND1
|
B:HIS90
|
4.3
|
13.1
|
1.0
|
O
|
B:HOH311
|
4.3
|
32.8
|
1.0
|
ND1
|
B:HIS88
|
4.3
|
24.2
|
1.0
|
CG
|
B:HIS90
|
4.3
|
16.6
|
1.0
|
CG
|
B:HIS88
|
4.4
|
16.8
|
1.0
|
ND1
|
B:HIS33
|
4.4
|
22.4
|
1.0
|
CG
|
B:HIS33
|
4.4
|
19.7
|
1.0
|
O
|
B:HOH379
|
4.6
|
36.7
|
1.0
|
CB
|
B:GLU81
|
4.6
|
18.1
|
1.0
|
CB
|
B:GLU101
|
4.9
|
20.9
|
1.0
|
|
Manganese binding site 3 out
of 4 in 5nbc
Go back to
Manganese Binding Sites List in 5nbc
Manganese binding site 3 out
of 4 in the Structure of Prokaryotic Transcription Factors
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 3 of Structure of Prokaryotic Transcription Factors within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn201
b:17.8
occ:1.00
|
OE2
|
C:GLU101
|
2.1
|
21.9
|
1.0
|
NE2
|
C:HIS33
|
2.2
|
16.1
|
1.0
|
NE2
|
C:HIS90
|
2.3
|
16.6
|
1.0
|
NE2
|
C:HIS88
|
2.3
|
19.8
|
1.0
|
OE2
|
C:GLU81
|
2.3
|
16.8
|
1.0
|
OE1
|
C:GLU81
|
2.3
|
15.0
|
1.0
|
CD
|
C:GLU81
|
2.6
|
14.7
|
1.0
|
CD
|
C:GLU101
|
3.1
|
21.9
|
1.0
|
CE1
|
C:HIS33
|
3.1
|
21.8
|
1.0
|
CE1
|
C:HIS90
|
3.2
|
15.5
|
1.0
|
CD2
|
C:HIS88
|
3.2
|
19.5
|
1.0
|
CE1
|
C:HIS88
|
3.3
|
22.2
|
1.0
|
CD2
|
C:HIS33
|
3.3
|
13.0
|
1.0
|
CD2
|
C:HIS90
|
3.3
|
15.7
|
1.0
|
CG
|
C:GLU101
|
3.5
|
21.0
|
1.0
|
OE1
|
C:GLU101
|
4.1
|
27.3
|
1.0
|
CG
|
C:GLU81
|
4.1
|
15.1
|
1.0
|
ND1
|
C:HIS33
|
4.2
|
26.1
|
1.0
|
ND1
|
C:HIS90
|
4.3
|
15.6
|
1.0
|
CG
|
C:HIS33
|
4.4
|
18.1
|
1.0
|
ND1
|
C:HIS88
|
4.4
|
19.5
|
1.0
|
CG
|
C:HIS88
|
4.4
|
16.1
|
1.0
|
CG
|
C:HIS90
|
4.4
|
12.4
|
1.0
|
O
|
C:HOH381
|
4.6
|
44.3
|
1.0
|
O
|
C:HOH346
|
4.7
|
27.7
|
1.0
|
CB
|
C:GLU81
|
4.7
|
14.5
|
1.0
|
CB
|
C:GLU101
|
4.8
|
18.0
|
1.0
|
O
|
C:HOH395
|
4.8
|
41.1
|
1.0
|
O
|
C:HOH330
|
5.0
|
25.2
|
1.0
|
|
Manganese binding site 4 out
of 4 in 5nbc
Go back to
Manganese Binding Sites List in 5nbc
Manganese binding site 4 out
of 4 in the Structure of Prokaryotic Transcription Factors
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 4 of Structure of Prokaryotic Transcription Factors within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn201
b:15.2
occ:1.00
|
NE2
|
D:HIS88
|
2.1
|
18.6
|
1.0
|
NE2
|
D:HIS90
|
2.2
|
14.0
|
1.0
|
OE1
|
D:GLU101
|
2.2
|
18.3
|
1.0
|
OE1
|
D:GLU81
|
2.2
|
14.2
|
1.0
|
NE2
|
D:HIS33
|
2.3
|
15.9
|
1.0
|
OE2
|
D:GLU81
|
2.3
|
15.2
|
1.0
|
CD
|
D:GLU81
|
2.6
|
13.4
|
1.0
|
CE1
|
D:HIS88
|
3.1
|
19.0
|
1.0
|
CE1
|
D:HIS90
|
3.1
|
14.9
|
1.0
|
CD2
|
D:HIS88
|
3.1
|
13.6
|
1.0
|
CD
|
D:GLU101
|
3.2
|
21.1
|
1.0
|
CE1
|
D:HIS33
|
3.2
|
21.2
|
1.0
|
CD2
|
D:HIS90
|
3.2
|
12.0
|
1.0
|
CD2
|
D:HIS33
|
3.3
|
15.2
|
1.0
|
CG
|
D:GLU101
|
3.6
|
13.5
|
1.0
|
CG
|
D:GLU81
|
4.0
|
17.1
|
1.0
|
ND1
|
D:HIS88
|
4.2
|
23.6
|
1.0
|
OE2
|
D:GLU101
|
4.2
|
21.0
|
1.0
|
ND1
|
D:HIS90
|
4.2
|
14.6
|
1.0
|
CG
|
D:HIS88
|
4.3
|
16.1
|
1.0
|
ND1
|
D:HIS33
|
4.3
|
21.6
|
1.0
|
CG
|
D:HIS90
|
4.3
|
10.9
|
1.0
|
CG
|
D:HIS33
|
4.4
|
16.4
|
1.0
|
O
|
D:HOH332
|
4.6
|
23.5
|
1.0
|
CE
|
D:LYS32
|
4.6
|
19.7
|
1.0
|
CB
|
D:GLU81
|
4.7
|
10.1
|
1.0
|
CD
|
D:LYS32
|
4.8
|
20.8
|
1.0
|
CB
|
D:GLU101
|
4.9
|
10.8
|
1.0
|
CG
|
D:LYS32
|
5.0
|
23.0
|
1.0
|
O
|
D:HOH355
|
5.0
|
19.9
|
1.0
|
|
Reference:
J.Perard,
S.Nader,
M.Levert,
L.Arnaud,
P.Carpentier,
C.Siebert,
F.Blanquet,
C.Cavazza,
P.Renesto,
D.Schneider,
M.Maurin,
J.Coves,
S.Crouzy,
I.Michaud-Soret.
Structural and Functional Studies of the Metalloregulator Fur Identify A Promoter-Binding Mechanism and Its Role Infrancisella Tularensisvirulence. Commun Biol V. 1 93 2018.
ISSN: ESSN 2399-3642
PubMed: 30271974
DOI: 10.1038/S42003-018-0095-6
Page generated: Sun Oct 6 02:00:56 2024
|