Iron in PDB 9gcz: Xusb Lipoprotein Bound to Ferric Enterobactin
Protein crystallography data
The structure of Xusb Lipoprotein Bound to Ferric Enterobactin, PDB code: 9gcz
was solved by
A.Silale,
H.Mark,
A.Basle,
B.Van Den Berg,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
38.05 /
1.50
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
59.992,
48.18,
135.466,
90,
96.79,
90
|
R / Rfree (%)
|
20.4 /
24.4
|
Other elements in 9gcz:
The structure of Xusb Lipoprotein Bound to Ferric Enterobactin also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Xusb Lipoprotein Bound to Ferric Enterobactin
(pdb code 9gcz). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the
Xusb Lipoprotein Bound to Ferric Enterobactin, PDB code: 9gcz:
Jump to Iron binding site number:
1;
2;
Iron binding site 1 out
of 2 in 9gcz
Go back to
Iron Binding Sites List in 9gcz
Iron binding site 1 out
of 2 in the Xusb Lipoprotein Bound to Ferric Enterobactin
 Mono view
 Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Xusb Lipoprotein Bound to Ferric Enterobactin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe502
b:9.9
occ:1.00
|
O3
|
A:EB4503
|
2.0
|
11.8
|
1.0
|
O5
|
A:EB4503
|
2.1
|
11.4
|
1.0
|
O1
|
A:EB4503
|
2.1
|
10.1
|
1.0
|
O2
|
A:EB4503
|
2.1
|
11.6
|
1.0
|
O6
|
A:EB4503
|
2.1
|
12.1
|
1.0
|
O4
|
A:EB4503
|
2.1
|
10.2
|
1.0
|
C5
|
A:EB4503
|
2.9
|
9.8
|
1.0
|
C2
|
A:EB4503
|
2.9
|
9.5
|
1.0
|
C1
|
A:EB4503
|
2.9
|
12.8
|
1.0
|
C4
|
A:EB4503
|
2.9
|
12.5
|
1.0
|
C3
|
A:EB4503
|
2.9
|
10.4
|
1.0
|
C6
|
A:EB4503
|
2.9
|
11.6
|
1.0
|
CE2
|
A:TYR411
|
4.0
|
10.2
|
1.0
|
C8
|
A:EB4503
|
4.2
|
11.3
|
1.0
|
OH
|
A:TYR411
|
4.2
|
8.7
|
1.0
|
C17
|
A:EB4503
|
4.2
|
10.1
|
1.0
|
C7
|
A:EB4503
|
4.2
|
10.9
|
1.0
|
C16
|
A:EB4503
|
4.2
|
12.6
|
1.0
|
C18
|
A:EB4503
|
4.2
|
12.2
|
1.0
|
C9
|
A:EB4503
|
4.3
|
14.3
|
1.0
|
OG
|
A:SER121
|
4.3
|
9.3
|
1.0
|
CB
|
A:SER168
|
4.3
|
8.5
|
1.0
|
CB
|
A:ARG167
|
4.4
|
11.5
|
1.0
|
N
|
A:SER121
|
4.4
|
9.3
|
1.0
|
OG
|
A:SER168
|
4.4
|
9.2
|
1.0
|
CB
|
A:SER121
|
4.4
|
9.4
|
1.0
|
N
|
A:SER168
|
4.4
|
9.2
|
1.0
|
CB
|
A:ASN120
|
4.4
|
11.1
|
1.0
|
N1
|
A:EB4503
|
4.5
|
10.1
|
1.0
|
N2
|
A:EB4503
|
4.5
|
11.7
|
1.0
|
N3
|
A:EB4503
|
4.5
|
12.9
|
1.0
|
CZ
|
A:TYR411
|
4.6
|
9.9
|
1.0
|
CG
|
A:GLN413
|
4.6
|
10.6
|
1.0
|
CD
|
A:ARG167
|
4.8
|
13.0
|
1.0
|
C20
|
A:EB4503
|
4.9
|
12.0
|
1.0
|
C21
|
A:EB4503
|
4.9
|
14.3
|
1.0
|
C19
|
A:EB4503
|
4.9
|
13.7
|
1.0
|
CA
|
A:SER168
|
4.9
|
10.4
|
1.0
|
|
Iron binding site 2 out
of 2 in 9gcz
Go back to
Iron Binding Sites List in 9gcz
Iron binding site 2 out
of 2 in the Xusb Lipoprotein Bound to Ferric Enterobactin
 Mono view
 Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Xusb Lipoprotein Bound to Ferric Enterobactin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe502
b:13.2
occ:1.00
|
O1
|
B:EB4503
|
2.0
|
15.1
|
1.0
|
O6
|
B:EB4503
|
2.0
|
15.6
|
1.0
|
O3
|
B:EB4503
|
2.0
|
15.4
|
1.0
|
O5
|
B:EB4503
|
2.1
|
13.2
|
1.0
|
O4
|
B:EB4503
|
2.1
|
15.6
|
1.0
|
O2
|
B:EB4503
|
2.1
|
14.6
|
1.0
|
C6
|
B:EB4503
|
2.9
|
17.6
|
1.0
|
C3
|
B:EB4503
|
2.9
|
17.5
|
1.0
|
C5
|
B:EB4503
|
2.9
|
13.9
|
1.0
|
C2
|
B:EB4503
|
2.9
|
16.8
|
1.0
|
C1
|
B:EB4503
|
2.9
|
16.0
|
1.0
|
C4
|
B:EB4503
|
2.9
|
13.1
|
1.0
|
CE2
|
B:TYR411
|
3.9
|
14.6
|
1.0
|
CB
|
B:SER168
|
4.2
|
12.4
|
1.0
|
C8
|
B:EB4503
|
4.2
|
14.8
|
1.0
|
C9
|
B:EB4503
|
4.2
|
15.2
|
1.0
|
C18
|
B:EB4503
|
4.2
|
19.3
|
1.0
|
C17
|
B:EB4503
|
4.2
|
15.4
|
1.0
|
C16
|
B:EB4503
|
4.2
|
16.0
|
1.0
|
OH
|
B:TYR411
|
4.2
|
11.3
|
1.0
|
OG
|
B:SER168
|
4.2
|
12.8
|
1.0
|
OG
|
B:SER121
|
4.3
|
14.3
|
1.0
|
C7
|
B:EB4503
|
4.3
|
18.3
|
1.0
|
N
|
B:SER168
|
4.3
|
12.8
|
1.0
|
CB
|
B:ARG167
|
4.3
|
12.9
|
1.0
|
N
|
B:SER121
|
4.4
|
17.0
|
1.0
|
CB
|
B:ASN120
|
4.4
|
15.6
|
1.0
|
CB
|
B:SER121
|
4.5
|
13.8
|
1.0
|
N3
|
B:EB4503
|
4.5
|
18.2
|
1.0
|
N1
|
B:EB4503
|
4.5
|
15.2
|
1.0
|
CZ
|
B:TYR411
|
4.5
|
12.5
|
1.0
|
N2
|
B:EB4503
|
4.6
|
17.3
|
1.0
|
CG
|
B:GLN413
|
4.8
|
18.3
|
1.0
|
CD
|
B:ARG167
|
4.8
|
14.9
|
1.0
|
CA
|
B:SER168
|
4.8
|
10.8
|
1.0
|
CD2
|
B:TYR411
|
4.9
|
13.8
|
1.0
|
C19
|
B:EB4503
|
4.9
|
16.1
|
1.0
|
C21
|
B:EB4503
|
4.9
|
17.7
|
1.0
|
C20
|
B:EB4503
|
5.0
|
17.8
|
1.0
|
CG
|
B:ARG167
|
5.0
|
12.7
|
1.0
|
|
Reference:
A.Silale,
Y.L.Soo,
H.Mark,
A.Basle,
B.Van Den Berg.
Structural Basis of Iron Piracy By Human Gut Bacteroides To Be Published.
Page generated: Sat Aug 23 03:13:08 2025
|