Manganese in PDB 4raz: Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur
Protein crystallography data
The structure of Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur, PDB code: 4raz
was solved by
Z.Deng,
Q.Wang,
Z.Chen,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
50.00 /
1.90
|
Space group
|
I 2 2 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
79.595,
96.847,
119.874,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
20.3 /
22.7
|
Manganese Binding Sites:
The binding sites of Manganese atom in the Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur
(pdb code 4raz). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 4 binding sites of Manganese where determined in the
Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur, PDB code: 4raz:
Jump to Manganese binding site number:
1;
2;
3;
4;
Manganese binding site 1 out
of 4 in 4raz
Go back to
Manganese Binding Sites List in 4raz
Manganese binding site 1 out
of 4 in the Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn201
b:26.4
occ:1.00
|
OE1
|
A:GLU108
|
2.0
|
30.3
|
1.0
|
NE2
|
A:HIS87
|
2.2
|
32.4
|
1.0
|
NE2
|
A:HIS125
|
2.2
|
25.0
|
1.0
|
O
|
A:HOH395
|
2.3
|
23.2
|
1.0
|
OD1
|
A:ASP89
|
2.3
|
23.9
|
1.0
|
OD2
|
A:ASP89
|
2.4
|
24.8
|
1.0
|
CG
|
A:ASP89
|
2.7
|
27.0
|
1.0
|
CD
|
A:GLU108
|
3.0
|
30.3
|
1.0
|
CE1
|
A:HIS87
|
3.1
|
32.4
|
1.0
|
CE1
|
A:HIS125
|
3.1
|
26.6
|
1.0
|
CD2
|
A:HIS87
|
3.2
|
30.2
|
1.0
|
CD2
|
A:HIS125
|
3.3
|
24.3
|
1.0
|
OE2
|
A:GLU108
|
3.3
|
29.9
|
1.0
|
O
|
A:HOH315
|
3.7
|
29.1
|
1.0
|
CB
|
A:ASP89
|
4.2
|
25.0
|
1.0
|
O
|
A:HOH332
|
4.2
|
29.6
|
1.0
|
ND1
|
A:HIS87
|
4.3
|
29.6
|
1.0
|
ND1
|
A:HIS125
|
4.3
|
25.5
|
1.0
|
NE2
|
A:GLN111
|
4.3
|
26.1
|
1.0
|
CG
|
A:HIS87
|
4.3
|
31.0
|
1.0
|
CG
|
A:HIS125
|
4.4
|
25.7
|
1.0
|
CG
|
A:GLU108
|
4.4
|
31.9
|
1.0
|
O
|
A:HOH304
|
4.5
|
27.3
|
1.0
|
OE1
|
A:GLN111
|
4.5
|
27.3
|
1.0
|
CB
|
A:LEU127
|
4.8
|
22.2
|
1.0
|
N
|
A:ASP89
|
4.8
|
25.6
|
1.0
|
CD
|
A:GLN111
|
4.9
|
27.4
|
1.0
|
C
|
A:HIS88
|
4.9
|
26.8
|
1.0
|
CA
|
A:ASP89
|
4.9
|
24.2
|
1.0
|
O
|
A:HIS88
|
5.0
|
26.3
|
1.0
|
|
Manganese binding site 2 out
of 4 in 4raz
Go back to
Manganese Binding Sites List in 4raz
Manganese binding site 2 out
of 4 in the Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn202
b:29.3
occ:1.00
|
OE2
|
A:GLU101
|
2.2
|
32.3
|
1.0
|
NE2
|
A:HIS33
|
2.2
|
23.6
|
1.0
|
NE2
|
A:HIS90
|
2.2
|
26.6
|
1.0
|
NE2
|
A:HIS88
|
2.3
|
28.4
|
1.0
|
OE2
|
A:GLU81
|
2.3
|
31.8
|
1.0
|
OE1
|
A:GLU81
|
2.4
|
27.9
|
1.0
|
CD
|
A:GLU81
|
2.6
|
30.7
|
1.0
|
CD
|
A:GLU101
|
3.1
|
33.0
|
1.0
|
CD2
|
A:HIS88
|
3.1
|
28.2
|
1.0
|
CD2
|
A:HIS90
|
3.2
|
28.4
|
1.0
|
CE1
|
A:HIS33
|
3.2
|
24.1
|
1.0
|
CE1
|
A:HIS90
|
3.2
|
27.6
|
1.0
|
CD2
|
A:HIS33
|
3.2
|
23.8
|
1.0
|
CE1
|
A:HIS88
|
3.3
|
28.2
|
1.0
|
CG
|
A:GLU101
|
3.5
|
30.3
|
1.0
|
O
|
A:HOH301
|
4.1
|
34.8
|
1.0
|
CG
|
A:GLU81
|
4.1
|
29.6
|
1.0
|
OE1
|
A:GLU101
|
4.1
|
32.2
|
1.0
|
CG
|
A:HIS88
|
4.3
|
29.6
|
1.0
|
O
|
A:HOH391
|
4.3
|
47.5
|
1.0
|
ND1
|
A:HIS33
|
4.3
|
25.2
|
1.0
|
ND1
|
A:HIS88
|
4.4
|
30.4
|
1.0
|
ND1
|
A:HIS90
|
4.4
|
26.5
|
1.0
|
CG
|
A:HIS90
|
4.4
|
27.4
|
1.0
|
CG
|
A:HIS33
|
4.4
|
24.3
|
1.0
|
NE2
|
A:HIS71
|
4.5
|
35.9
|
1.0
|
CB
|
A:GLU81
|
4.7
|
26.9
|
1.0
|
CB
|
A:GLU101
|
4.7
|
28.5
|
1.0
|
O
|
A:HOH328
|
4.8
|
36.5
|
1.0
|
|
Manganese binding site 3 out
of 4 in 4raz
Go back to
Manganese Binding Sites List in 4raz
Manganese binding site 3 out
of 4 in the Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 3 of Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn201
b:26.0
occ:1.00
|
OE2
|
B:GLU108
|
2.1
|
26.6
|
1.0
|
NE2
|
B:HIS87
|
2.1
|
27.2
|
1.0
|
O
|
B:HOH394
|
2.2
|
24.0
|
1.0
|
NE2
|
B:HIS125
|
2.2
|
25.2
|
1.0
|
OD2
|
B:ASP89
|
2.4
|
25.7
|
1.0
|
OD1
|
B:ASP89
|
2.4
|
21.8
|
1.0
|
CG
|
B:ASP89
|
2.7
|
24.9
|
1.0
|
CD
|
B:GLU108
|
2.9
|
26.9
|
1.0
|
OE1
|
B:GLU108
|
3.0
|
27.5
|
1.0
|
CE1
|
B:HIS87
|
3.1
|
27.7
|
1.0
|
CE1
|
B:HIS125
|
3.1
|
24.9
|
1.0
|
CD2
|
B:HIS87
|
3.1
|
28.4
|
1.0
|
CD2
|
B:HIS125
|
3.3
|
23.4
|
1.0
|
O
|
B:HOH334
|
3.8
|
30.4
|
1.0
|
CB
|
B:ASP89
|
4.2
|
23.4
|
1.0
|
ND1
|
B:HIS87
|
4.2
|
28.6
|
1.0
|
O
|
B:HOH358
|
4.3
|
42.5
|
1.0
|
NE2
|
B:GLN111
|
4.3
|
24.5
|
1.0
|
ND1
|
B:HIS125
|
4.3
|
23.3
|
1.0
|
CG
|
B:HIS87
|
4.3
|
28.3
|
1.0
|
CG
|
B:GLU108
|
4.3
|
26.6
|
1.0
|
CG
|
B:HIS125
|
4.4
|
23.9
|
1.0
|
OE1
|
B:GLN111
|
4.5
|
27.8
|
1.0
|
O
|
B:HOH304
|
4.5
|
27.6
|
1.0
|
CB
|
B:LEU127
|
4.8
|
22.7
|
1.0
|
N
|
B:ASP89
|
4.8
|
24.1
|
1.0
|
CD
|
B:GLN111
|
4.8
|
24.9
|
1.0
|
C
|
B:HIS88
|
4.8
|
23.6
|
1.0
|
O
|
B:HIS88
|
4.9
|
23.3
|
1.0
|
CA
|
B:ASP89
|
4.9
|
22.5
|
1.0
|
|
Manganese binding site 4 out
of 4 in 4raz
Go back to
Manganese Binding Sites List in 4raz
Manganese binding site 4 out
of 4 in the Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 4 of Crystal Structure of Magnetospirillum Gryphiswaldense Msr-1 Holo-Fur within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn202
b:26.5
occ:1.00
|
OE2
|
B:GLU81
|
2.2
|
27.6
|
1.0
|
OE1
|
B:GLU101
|
2.2
|
30.3
|
1.0
|
NE2
|
B:HIS90
|
2.2
|
24.9
|
1.0
|
NE2
|
B:HIS88
|
2.2
|
23.3
|
1.0
|
NE2
|
B:HIS33
|
2.2
|
24.3
|
1.0
|
OE1
|
B:GLU81
|
2.3
|
28.4
|
1.0
|
CD
|
B:GLU81
|
2.5
|
29.1
|
1.0
|
CD
|
B:GLU101
|
3.2
|
29.0
|
1.0
|
CE1
|
B:HIS90
|
3.2
|
25.2
|
1.0
|
CE1
|
B:HIS88
|
3.2
|
24.8
|
1.0
|
CE1
|
B:HIS33
|
3.2
|
26.7
|
1.0
|
CD2
|
B:HIS88
|
3.2
|
25.4
|
1.0
|
CD2
|
B:HIS90
|
3.2
|
25.4
|
1.0
|
CD2
|
B:HIS33
|
3.3
|
27.7
|
1.0
|
CG
|
B:GLU101
|
3.5
|
27.8
|
1.0
|
O
|
B:HOH385
|
4.0
|
43.4
|
1.0
|
CG
|
B:GLU81
|
4.0
|
28.0
|
1.0
|
O
|
B:HOH377
|
4.2
|
42.9
|
1.0
|
OE2
|
B:GLU101
|
4.2
|
32.8
|
1.0
|
ND1
|
B:HIS88
|
4.3
|
27.0
|
1.0
|
ND1
|
B:HIS90
|
4.3
|
25.1
|
1.0
|
CG
|
B:HIS88
|
4.4
|
25.0
|
1.0
|
ND1
|
B:HIS33
|
4.4
|
26.8
|
1.0
|
CG
|
B:HIS90
|
4.4
|
24.0
|
1.0
|
CG
|
B:HIS33
|
4.4
|
27.1
|
1.0
|
NE2
|
B:HIS71
|
4.5
|
38.7
|
1.0
|
CB
|
B:GLU81
|
4.7
|
29.0
|
1.0
|
CB
|
B:GLU101
|
4.8
|
27.4
|
1.0
|
O
|
B:HOH345
|
4.8
|
41.1
|
1.0
|
|
Reference:
Z.Deng,
Q.Wang,
Z.Liu,
M.Zhang,
A.C.Machado,
T.P.Chiu,
C.Feng,
Q.Zhang,
L.Yu,
L.Qi,
J.Zheng,
X.Wang,
X.Huo,
X.Qi,
X.Li,
W.Wu,
R.Rohs,
Y.Li,
Z.Chen.
Mechanistic Insights Into Metal Ion Activation and Operator Recognition By the Ferric Uptake Regulator. Nat Commun V. 6 7642.
ISSN: ESSN 2041-1723
PubMed: 26134419
DOI: 10.1038/NCOMMS8642
Page generated: Sat Oct 5 21:08:44 2024
|