Iron in PDB 3qzm: Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme
Protein crystallography data
The structure of Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme, PDB code: 3qzm
was solved by
J.C.Grigg,
C.X.Mao,
M.E.P.Murphy,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
55.66 /
1.25
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
52.490,
51.760,
55.690,
90.00,
91.94,
90.00
|
R / Rfree (%)
|
13.9 /
16.4
|
Iron Binding Sites:
The binding sites of Iron atom in the Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme
(pdb code 3qzm). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the
Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme, PDB code: 3qzm:
Jump to Iron binding site number:
1;
2;
Iron binding site 1 out
of 2 in 3qzm
Go back to
Iron Binding Sites List in 3qzm
Iron binding site 1 out
of 2 in the Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe200
b:9.8
occ:1.00
|
FE
|
A:HEM200
|
0.0
|
9.8
|
1.0
|
ND
|
A:HEM200
|
2.0
|
14.8
|
0.5
|
NC
|
A:HEM200
|
2.0
|
9.4
|
0.5
|
NC
|
A:HEM200
|
2.0
|
10.3
|
0.5
|
NA
|
A:HEM200
|
2.1
|
10.5
|
0.5
|
NB
|
A:HEM200
|
2.1
|
10.0
|
0.5
|
OH
|
A:TYR166
|
2.1
|
9.9
|
1.0
|
NA
|
A:HEM200
|
2.1
|
6.0
|
0.5
|
ND
|
A:HEM200
|
2.1
|
6.2
|
0.5
|
NB
|
A:HEM200
|
2.1
|
6.4
|
0.5
|
C4D
|
A:HEM200
|
3.0
|
14.0
|
0.5
|
C1D
|
A:HEM200
|
3.0
|
14.6
|
0.5
|
C1C
|
A:HEM200
|
3.0
|
10.3
|
0.5
|
C1C
|
A:HEM200
|
3.1
|
9.2
|
0.5
|
C4C
|
A:HEM200
|
3.1
|
11.4
|
0.5
|
C4C
|
A:HEM200
|
3.1
|
8.0
|
0.5
|
C1A
|
A:HEM200
|
3.1
|
10.6
|
0.5
|
C4B
|
A:HEM200
|
3.1
|
10.2
|
0.5
|
C1D
|
A:HEM200
|
3.1
|
6.6
|
0.5
|
C1B
|
A:HEM200
|
3.1
|
7.8
|
0.5
|
C4A
|
A:HEM200
|
3.1
|
7.0
|
0.5
|
C4D
|
A:HEM200
|
3.1
|
6.0
|
0.5
|
C4B
|
A:HEM200
|
3.1
|
7.5
|
0.5
|
CZ
|
A:TYR166
|
3.1
|
9.0
|
1.0
|
C1A
|
A:HEM200
|
3.1
|
6.5
|
0.5
|
C1B
|
A:HEM200
|
3.1
|
5.9
|
0.5
|
C4A
|
A:HEM200
|
3.1
|
7.5
|
0.5
|
CHA
|
A:HEM200
|
3.4
|
14.0
|
0.5
|
CHC
|
A:HEM200
|
3.4
|
10.1
|
0.5
|
CHD
|
A:HEM200
|
3.4
|
12.8
|
0.5
|
CHD
|
A:HEM200
|
3.4
|
6.5
|
0.5
|
CHC
|
A:HEM200
|
3.4
|
8.2
|
0.5
|
CHA
|
A:HEM200
|
3.5
|
6.4
|
0.5
|
CHB
|
A:HEM200
|
3.5
|
8.0
|
0.5
|
CHB
|
A:HEM200
|
3.5
|
5.9
|
0.5
|
CE2
|
A:TYR166
|
3.7
|
9.3
|
1.0
|
OH
|
A:TYR170
|
3.9
|
9.2
|
1.0
|
CE1
|
A:TYR166
|
4.1
|
8.7
|
1.0
|
C3D
|
A:HEM200
|
4.2
|
16.0
|
0.5
|
C2D
|
A:HEM200
|
4.2
|
15.0
|
0.5
|
C2C
|
A:HEM200
|
4.3
|
10.2
|
0.5
|
C3C
|
A:HEM200
|
4.3
|
10.3
|
0.5
|
C2C
|
A:HEM200
|
4.3
|
8.9
|
0.5
|
C2D
|
A:HEM200
|
4.3
|
7.2
|
0.5
|
C2A
|
A:HEM200
|
4.3
|
9.6
|
0.5
|
C3A
|
A:HEM200
|
4.3
|
6.8
|
0.5
|
C2B
|
A:HEM200
|
4.3
|
8.8
|
0.5
|
C3B
|
A:HEM200
|
4.3
|
9.8
|
0.5
|
C3C
|
A:HEM200
|
4.3
|
7.8
|
0.5
|
C3D
|
A:HEM200
|
4.3
|
7.5
|
0.5
|
C3B
|
A:HEM200
|
4.3
|
8.1
|
0.5
|
C2B
|
A:HEM200
|
4.3
|
6.2
|
0.5
|
C2A
|
A:HEM200
|
4.3
|
8.8
|
0.5
|
C3A
|
A:HEM200
|
4.3
|
8.1
|
0.5
|
CE2
|
A:TYR170
|
4.4
|
8.2
|
1.0
|
CZ
|
A:TYR170
|
4.5
|
7.8
|
1.0
|
CB
|
A:ALA83
|
4.6
|
8.6
|
1.0
|
CD2
|
A:TYR166
|
4.9
|
8.8
|
1.0
|
|
Iron binding site 2 out
of 2 in 3qzm
Go back to
Iron Binding Sites List in 3qzm
Iron binding site 2 out
of 2 in the Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Staphylococcus Aureus Isda Neat Domain H83A Variant in Complex with Heme within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe201
b:9.5
occ:1.00
|
FE
|
B:HEM201
|
0.0
|
9.5
|
1.0
|
NC
|
B:HEM201
|
2.0
|
10.1
|
0.5
|
NC
|
B:HEM201
|
2.0
|
11.3
|
0.5
|
NA
|
B:HEM201
|
2.0
|
9.1
|
0.5
|
NB
|
B:HEM201
|
2.0
|
9.5
|
0.5
|
ND
|
B:HEM201
|
2.1
|
7.3
|
0.5
|
OH
|
B:TYR166
|
2.1
|
9.0
|
1.0
|
ND
|
B:HEM201
|
2.1
|
14.0
|
0.5
|
NA
|
B:HEM201
|
2.1
|
6.5
|
0.5
|
NB
|
B:HEM201
|
2.1
|
5.6
|
0.5
|
C1C
|
B:HEM201
|
3.0
|
9.1
|
0.5
|
C1D
|
B:HEM201
|
3.0
|
13.2
|
0.5
|
C4C
|
B:HEM201
|
3.1
|
11.2
|
0.5
|
C4B
|
B:HEM201
|
3.1
|
8.9
|
0.5
|
C1C
|
B:HEM201
|
3.1
|
8.8
|
0.5
|
C4D
|
B:HEM201
|
3.1
|
12.9
|
0.5
|
C4A
|
B:HEM201
|
3.1
|
5.8
|
0.5
|
C4D
|
B:HEM201
|
3.1
|
6.8
|
0.5
|
C4C
|
B:HEM201
|
3.1
|
8.2
|
0.5
|
C1B
|
B:HEM201
|
3.1
|
7.3
|
0.5
|
C1A
|
B:HEM201
|
3.1
|
6.2
|
0.5
|
C1A
|
B:HEM201
|
3.1
|
8.7
|
0.5
|
C1D
|
B:HEM201
|
3.1
|
7.5
|
0.5
|
C1B
|
B:HEM201
|
3.1
|
5.5
|
0.5
|
CZ
|
B:TYR166
|
3.1
|
8.1
|
1.0
|
C4B
|
B:HEM201
|
3.1
|
6.5
|
0.5
|
C4A
|
B:HEM201
|
3.1
|
7.0
|
0.5
|
CHC
|
B:HEM201
|
3.4
|
9.7
|
0.5
|
CHD
|
B:HEM201
|
3.4
|
12.8
|
0.5
|
CHA
|
B:HEM201
|
3.4
|
5.7
|
0.5
|
CHB
|
B:HEM201
|
3.4
|
5.8
|
0.5
|
CHA
|
B:HEM201
|
3.5
|
12.2
|
0.5
|
CHC
|
B:HEM201
|
3.5
|
6.9
|
0.5
|
CHD
|
B:HEM201
|
3.5
|
7.6
|
0.5
|
CHB
|
B:HEM201
|
3.5
|
8.2
|
0.5
|
CE2
|
B:TYR166
|
3.7
|
8.8
|
1.0
|
OH
|
B:TYR170
|
3.9
|
9.1
|
1.0
|
CE1
|
B:TYR166
|
4.1
|
8.9
|
1.0
|
C2C
|
B:HEM201
|
4.2
|
9.3
|
0.5
|
C2D
|
B:HEM201
|
4.3
|
13.9
|
0.5
|
C3C
|
B:HEM201
|
4.3
|
11.4
|
0.5
|
C3D
|
B:HEM201
|
4.3
|
15.1
|
0.5
|
C2C
|
B:HEM201
|
4.3
|
10.0
|
0.5
|
C3B
|
B:HEM201
|
4.3
|
9.2
|
0.5
|
C3C
|
B:HEM201
|
4.3
|
9.7
|
0.5
|
C2B
|
B:HEM201
|
4.3
|
7.8
|
0.5
|
C3A
|
B:HEM201
|
4.3
|
5.8
|
0.5
|
C2A
|
B:HEM201
|
4.3
|
8.1
|
0.5
|
C3D
|
B:HEM201
|
4.3
|
8.8
|
0.5
|
C2D
|
B:HEM201
|
4.3
|
8.5
|
0.5
|
C3A
|
B:HEM201
|
4.3
|
8.4
|
0.5
|
C2A
|
B:HEM201
|
4.3
|
8.4
|
0.5
|
C3B
|
B:HEM201
|
4.3
|
7.3
|
0.5
|
C2B
|
B:HEM201
|
4.3
|
5.9
|
0.5
|
CE2
|
B:TYR170
|
4.3
|
8.2
|
1.0
|
CZ
|
B:TYR170
|
4.5
|
7.9
|
1.0
|
CB
|
B:ALA83
|
4.6
|
8.9
|
1.0
|
CD2
|
B:TYR166
|
5.0
|
8.7
|
1.0
|
|
Reference:
J.C.Grigg,
C.X.Mao,
M.E.Murphy.
Iron-Coordinating Tyrosine Is A Key Determinant of Neat Domain Heme Transfer. J.Mol.Biol. V. 413 684 2011.
ISSN: ISSN 0022-2836
PubMed: 21893067
DOI: 10.1016/J.JMB.2011.08.047
Page generated: Sun Aug 4 18:59:45 2024
|