Iron in PDB 3ozz: Structure of A Cytochrome B5 Core-Swap Mutant
Protein crystallography data
The structure of Structure of A Cytochrome B5 Core-Swap Mutant, PDB code: 3ozz
was solved by
S.Terzyan,
S.Parthasarathy,
X.C.Zhang,
D.Benson,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
50.00 /
1.70
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
110.669,
30.654,
23.553,
90.00,
95.65,
90.00
|
R / Rfree (%)
|
17.6 /
22.9
|
Iron Binding Sites:
The binding sites of Iron atom in the Structure of A Cytochrome B5 Core-Swap Mutant
(pdb code 3ozz). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the
Structure of A Cytochrome B5 Core-Swap Mutant, PDB code: 3ozz:
Jump to Iron binding site number:
1;
2;
Iron binding site 1 out
of 2 in 3ozz
Go back to
Iron Binding Sites List in 3ozz
Iron binding site 1 out
of 2 in the Structure of A Cytochrome B5 Core-Swap Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Structure of A Cytochrome B5 Core-Swap Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe201
b:12.9
occ:0.50
|
FE
|
B:HEM201
|
0.0
|
12.9
|
0.5
|
FE
|
B:HEM201
|
0.2
|
14.6
|
0.5
|
NC
|
B:HEM201
|
1.9
|
13.7
|
0.5
|
ND
|
B:HEM201
|
1.9
|
13.9
|
0.5
|
NB
|
B:HEM201
|
1.9
|
13.2
|
0.5
|
ND
|
B:HEM201
|
2.0
|
14.1
|
0.5
|
NA
|
B:HEM201
|
2.0
|
11.3
|
0.5
|
NC
|
B:HEM201
|
2.0
|
13.5
|
0.5
|
NE2
|
B:HIS39
|
2.0
|
14.7
|
1.0
|
NB
|
B:HEM201
|
2.1
|
13.6
|
0.5
|
NA
|
B:HEM201
|
2.1
|
15.8
|
0.5
|
NE2
|
B:HIS63
|
2.1
|
12.2
|
1.0
|
C1D
|
B:HEM201
|
2.9
|
13.9
|
0.5
|
C4C
|
B:HEM201
|
2.9
|
11.3
|
0.5
|
C1B
|
B:HEM201
|
3.0
|
10.2
|
0.5
|
CE1
|
B:HIS39
|
3.0
|
13.8
|
1.0
|
CD2
|
B:HIS39
|
3.0
|
16.1
|
1.0
|
C4A
|
B:HEM201
|
3.0
|
11.0
|
0.5
|
C1C
|
B:HEM201
|
3.0
|
13.1
|
0.5
|
C4D
|
B:HEM201
|
3.0
|
14.2
|
0.5
|
C1A
|
B:HEM201
|
3.0
|
10.8
|
0.5
|
C4D
|
B:HEM201
|
3.0
|
14.8
|
0.5
|
C1D
|
B:HEM201
|
3.0
|
14.7
|
0.5
|
C4B
|
B:HEM201
|
3.1
|
13.2
|
0.5
|
CD2
|
B:HIS63
|
3.1
|
11.1
|
1.0
|
C4C
|
B:HEM201
|
3.1
|
13.9
|
0.5
|
C1C
|
B:HEM201
|
3.1
|
12.8
|
0.5
|
CE1
|
B:HIS63
|
3.1
|
10.0
|
1.0
|
C4B
|
B:HEM201
|
3.1
|
13.0
|
0.5
|
C1B
|
B:HEM201
|
3.1
|
14.5
|
0.5
|
C1A
|
B:HEM201
|
3.1
|
16.5
|
0.5
|
C4A
|
B:HEM201
|
3.2
|
15.8
|
0.5
|
CHD
|
B:HEM201
|
3.3
|
12.4
|
0.5
|
CHB
|
B:HEM201
|
3.4
|
10.6
|
0.5
|
CHA
|
B:HEM201
|
3.4
|
13.6
|
0.5
|
CHD
|
B:HEM201
|
3.4
|
14.9
|
0.5
|
CHC
|
B:HEM201
|
3.5
|
13.6
|
0.5
|
CHC
|
B:HEM201
|
3.5
|
12.9
|
0.5
|
CHA
|
B:HEM201
|
3.5
|
16.0
|
0.5
|
CHB
|
B:HEM201
|
3.5
|
15.1
|
0.5
|
ND1
|
B:HIS39
|
4.1
|
14.4
|
1.0
|
CG
|
B:HIS39
|
4.1
|
14.1
|
1.0
|
C2D
|
B:HEM201
|
4.2
|
13.9
|
0.5
|
ND1
|
B:HIS63
|
4.2
|
10.4
|
1.0
|
C3C
|
B:HEM201
|
4.2
|
10.7
|
0.5
|
C2B
|
B:HEM201
|
4.2
|
11.2
|
0.5
|
CG
|
B:HIS63
|
4.2
|
13.3
|
1.0
|
C3A
|
B:HEM201
|
4.2
|
9.8
|
0.5
|
C2A
|
B:HEM201
|
4.2
|
9.9
|
0.5
|
C2C
|
B:HEM201
|
4.2
|
11.5
|
0.5
|
C3D
|
B:HEM201
|
4.2
|
14.5
|
0.5
|
C2D
|
B:HEM201
|
4.3
|
15.6
|
0.5
|
C3B
|
B:HEM201
|
4.3
|
12.5
|
0.5
|
C3D
|
B:HEM201
|
4.3
|
15.1
|
0.5
|
C2C
|
B:HEM201
|
4.3
|
14.2
|
0.5
|
C3C
|
B:HEM201
|
4.3
|
15.5
|
0.5
|
C2B
|
B:HEM201
|
4.3
|
15.3
|
0.5
|
C2A
|
B:HEM201
|
4.4
|
16.7
|
0.5
|
C3A
|
B:HEM201
|
4.4
|
17.0
|
0.5
|
C3B
|
B:HEM201
|
4.4
|
13.9
|
0.5
|
N
|
B:GLY41
|
5.0
|
15.5
|
1.0
|
|
Iron binding site 2 out
of 2 in 3ozz
Go back to
Iron Binding Sites List in 3ozz
Iron binding site 2 out
of 2 in the Structure of A Cytochrome B5 Core-Swap Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Structure of A Cytochrome B5 Core-Swap Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe201
b:14.6
occ:0.50
|
FE
|
B:HEM201
|
0.0
|
14.6
|
0.5
|
FE
|
B:HEM201
|
0.2
|
12.9
|
0.5
|
ND
|
B:HEM201
|
1.8
|
14.1
|
0.5
|
NC
|
B:HEM201
|
1.9
|
13.5
|
0.5
|
NB
|
B:HEM201
|
2.0
|
13.6
|
0.5
|
NA
|
B:HEM201
|
2.0
|
15.8
|
0.5
|
ND
|
B:HEM201
|
2.0
|
13.9
|
0.5
|
NC
|
B:HEM201
|
2.0
|
13.7
|
0.5
|
NE2
|
B:HIS39
|
2.0
|
14.7
|
1.0
|
NA
|
B:HEM201
|
2.1
|
11.3
|
0.5
|
NB
|
B:HEM201
|
2.1
|
13.2
|
0.5
|
NE2
|
B:HIS63
|
2.1
|
12.2
|
1.0
|
C1D
|
B:HEM201
|
2.9
|
14.7
|
0.5
|
CE1
|
B:HIS39
|
2.9
|
13.8
|
1.0
|
C4C
|
B:HEM201
|
2.9
|
13.9
|
0.5
|
C4D
|
B:HEM201
|
3.0
|
14.8
|
0.5
|
C1B
|
B:HEM201
|
3.0
|
14.5
|
0.5
|
C4A
|
B:HEM201
|
3.0
|
15.8
|
0.5
|
C1D
|
B:HEM201
|
3.0
|
13.9
|
0.5
|
CE1
|
B:HIS63
|
3.0
|
10.0
|
1.0
|
C1C
|
B:HEM201
|
3.0
|
12.8
|
0.5
|
C4D
|
B:HEM201
|
3.1
|
14.2
|
0.5
|
CD2
|
B:HIS39
|
3.1
|
16.1
|
1.0
|
C1A
|
B:HEM201
|
3.1
|
16.5
|
0.5
|
C4B
|
B:HEM201
|
3.1
|
13.0
|
0.5
|
C1A
|
B:HEM201
|
3.1
|
10.8
|
0.5
|
C4C
|
B:HEM201
|
3.1
|
11.3
|
0.5
|
C1C
|
B:HEM201
|
3.1
|
13.1
|
0.5
|
CD2
|
B:HIS63
|
3.1
|
11.1
|
1.0
|
C1B
|
B:HEM201
|
3.1
|
10.2
|
0.5
|
C4A
|
B:HEM201
|
3.1
|
11.0
|
0.5
|
C4B
|
B:HEM201
|
3.1
|
13.2
|
0.5
|
CHD
|
B:HEM201
|
3.3
|
14.9
|
0.5
|
CHB
|
B:HEM201
|
3.4
|
15.1
|
0.5
|
CHA
|
B:HEM201
|
3.4
|
13.6
|
0.5
|
CHD
|
B:HEM201
|
3.4
|
12.4
|
0.5
|
CHA
|
B:HEM201
|
3.5
|
16.0
|
0.5
|
CHC
|
B:HEM201
|
3.5
|
12.9
|
0.5
|
CHC
|
B:HEM201
|
3.5
|
13.6
|
0.5
|
CHB
|
B:HEM201
|
3.5
|
10.6
|
0.5
|
ND1
|
B:HIS39
|
4.1
|
14.4
|
1.0
|
C2D
|
B:HEM201
|
4.1
|
15.6
|
0.5
|
CG
|
B:HIS39
|
4.2
|
14.1
|
1.0
|
ND1
|
B:HIS63
|
4.2
|
10.4
|
1.0
|
C3D
|
B:HEM201
|
4.2
|
15.1
|
0.5
|
C2B
|
B:HEM201
|
4.2
|
15.3
|
0.5
|
C3C
|
B:HEM201
|
4.2
|
15.5
|
0.5
|
C3A
|
B:HEM201
|
4.2
|
17.0
|
0.5
|
C2C
|
B:HEM201
|
4.2
|
14.2
|
0.5
|
C2A
|
B:HEM201
|
4.2
|
16.7
|
0.5
|
CG
|
B:HIS63
|
4.2
|
13.3
|
1.0
|
C2A
|
B:HEM201
|
4.3
|
9.9
|
0.5
|
C2D
|
B:HEM201
|
4.3
|
13.9
|
0.5
|
C3B
|
B:HEM201
|
4.3
|
13.9
|
0.5
|
C3D
|
B:HEM201
|
4.3
|
14.5
|
0.5
|
C2C
|
B:HEM201
|
4.3
|
11.5
|
0.5
|
C3A
|
B:HEM201
|
4.3
|
9.8
|
0.5
|
C3C
|
B:HEM201
|
4.3
|
10.7
|
0.5
|
C2B
|
B:HEM201
|
4.4
|
11.2
|
0.5
|
C3B
|
B:HEM201
|
4.4
|
12.5
|
0.5
|
N
|
B:GLY41
|
4.9
|
15.5
|
1.0
|
|
Reference:
S.Parthasarathy,
S.Terzyan,
X.C.Zhang,
D.Benson.
Structure of A Cytochrome B5 Core-Swap Mutant To Be Published.
Page generated: Sun Aug 4 17:21:32 2024
|