Iron in PDB 2fwt: Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides
Protein crystallography data
The structure of Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides, PDB code: 2fwt
was solved by
D.Leys,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.00 /
1.85
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
72.790,
72.790,
51.484,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
15 /
19.3
|
Iron Binding Sites:
The binding sites of Iron atom in the Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides
(pdb code 2fwt). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the
Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides, PDB code: 2fwt:
Jump to Iron binding site number:
1;
2;
Iron binding site 1 out
of 2 in 2fwt
Go back to
Iron Binding Sites List in 2fwt
Iron binding site 1 out
of 2 in the Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides
 Mono view
 Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe803
b:16.6
occ:1.00
|
FE
|
A:HEC803
|
0.0
|
16.6
|
1.0
|
NE2
|
A:HIS128
|
2.0
|
17.8
|
1.0
|
NE2
|
A:HIS106
|
2.0
|
16.0
|
1.0
|
ND
|
A:HEC803
|
2.0
|
16.8
|
1.0
|
NA
|
A:HEC803
|
2.0
|
16.4
|
1.0
|
NC
|
A:HEC803
|
2.0
|
17.1
|
1.0
|
NB
|
A:HEC803
|
2.0
|
15.8
|
1.0
|
CE1
|
A:HIS128
|
2.9
|
20.7
|
1.0
|
CD2
|
A:HIS106
|
3.0
|
16.3
|
1.0
|
CE1
|
A:HIS106
|
3.0
|
15.1
|
1.0
|
C1D
|
A:HEC803
|
3.0
|
17.7
|
1.0
|
CD2
|
A:HIS128
|
3.0
|
19.9
|
1.0
|
C4D
|
A:HEC803
|
3.0
|
17.9
|
1.0
|
C1A
|
A:HEC803
|
3.0
|
16.3
|
1.0
|
C4A
|
A:HEC803
|
3.0
|
17.0
|
1.0
|
C1C
|
A:HEC803
|
3.0
|
17.2
|
1.0
|
C1B
|
A:HEC803
|
3.1
|
16.9
|
1.0
|
C4B
|
A:HEC803
|
3.1
|
16.0
|
1.0
|
C4C
|
A:HEC803
|
3.1
|
16.5
|
1.0
|
CHA
|
A:HEC803
|
3.4
|
18.0
|
1.0
|
CHD
|
A:HEC803
|
3.4
|
17.1
|
1.0
|
CHB
|
A:HEC803
|
3.4
|
17.0
|
1.0
|
CHC
|
A:HEC803
|
3.4
|
16.1
|
1.0
|
ND1
|
A:HIS128
|
4.1
|
21.1
|
1.0
|
ND1
|
A:HIS106
|
4.1
|
15.9
|
1.0
|
CG
|
A:HIS106
|
4.1
|
15.8
|
1.0
|
CG
|
A:HIS128
|
4.1
|
20.8
|
1.0
|
C2A
|
A:HEC803
|
4.2
|
18.0
|
1.0
|
C3A
|
A:HEC803
|
4.2
|
17.6
|
1.0
|
C2C
|
A:HEC803
|
4.3
|
17.3
|
1.0
|
C2D
|
A:HEC803
|
4.3
|
19.4
|
1.0
|
C2B
|
A:HEC803
|
4.3
|
15.7
|
1.0
|
C3D
|
A:HEC803
|
4.3
|
20.1
|
1.0
|
C3B
|
A:HEC803
|
4.3
|
16.3
|
1.0
|
C3C
|
A:HEC803
|
4.3
|
17.8
|
1.0
|
CE1
|
A:PHE102
|
5.0
|
16.4
|
1.0
|
|
Iron binding site 2 out
of 2 in 2fwt
Go back to
Iron Binding Sites List in 2fwt
Iron binding site 2 out
of 2 in the Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides
 Mono view
 Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Crystal Structure of Dhc Purified From Rhodobacter Sphaeroides within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe805
b:17.2
occ:1.00
|
FE
|
A:HEC805
|
0.0
|
17.2
|
1.0
|
NE2
|
A:HIS51
|
2.0
|
16.3
|
1.0
|
NE2
|
A:HIS28
|
2.0
|
16.8
|
1.0
|
ND
|
A:HEC805
|
2.0
|
16.8
|
1.0
|
NA
|
A:HEC805
|
2.0
|
15.7
|
1.0
|
NC
|
A:HEC805
|
2.0
|
19.0
|
1.0
|
NB
|
A:HEC805
|
2.0
|
16.2
|
1.0
|
CD2
|
A:HIS51
|
2.9
|
17.1
|
1.0
|
CD2
|
A:HIS28
|
3.0
|
17.2
|
1.0
|
CE1
|
A:HIS28
|
3.0
|
16.5
|
1.0
|
CE1
|
A:HIS51
|
3.0
|
15.6
|
1.0
|
C1A
|
A:HEC805
|
3.0
|
15.1
|
1.0
|
C4D
|
A:HEC805
|
3.0
|
17.0
|
1.0
|
C1D
|
A:HEC805
|
3.0
|
17.3
|
1.0
|
C1C
|
A:HEC805
|
3.0
|
19.2
|
1.0
|
C4B
|
A:HEC805
|
3.0
|
14.6
|
1.0
|
C4C
|
A:HEC805
|
3.1
|
19.0
|
1.0
|
C4A
|
A:HEC805
|
3.1
|
15.2
|
1.0
|
C1B
|
A:HEC805
|
3.1
|
14.7
|
1.0
|
CHA
|
A:HEC805
|
3.4
|
15.7
|
1.0
|
CHC
|
A:HEC805
|
3.4
|
17.2
|
1.0
|
CHD
|
A:HEC805
|
3.4
|
17.4
|
1.0
|
CHB
|
A:HEC805
|
3.4
|
15.7
|
1.0
|
CG
|
A:HIS51
|
4.1
|
18.1
|
1.0
|
ND1
|
A:HIS51
|
4.1
|
16.4
|
1.0
|
ND1
|
A:HIS28
|
4.1
|
17.2
|
1.0
|
CG
|
A:HIS28
|
4.1
|
19.1
|
1.0
|
C3B
|
A:HEC805
|
4.3
|
14.9
|
1.0
|
C2A
|
A:HEC805
|
4.3
|
14.6
|
1.0
|
C2C
|
A:HEC805
|
4.3
|
20.6
|
1.0
|
C2D
|
A:HEC805
|
4.3
|
17.1
|
1.0
|
C3A
|
A:HEC805
|
4.3
|
14.8
|
1.0
|
C2B
|
A:HEC805
|
4.3
|
14.4
|
1.0
|
C3C
|
A:HEC805
|
4.3
|
21.2
|
1.0
|
C3D
|
A:HEC805
|
4.3
|
17.7
|
1.0
|
O
|
A:HOH816
|
4.6
|
19.8
|
1.0
|
CD1
|
A:PHE52
|
4.7
|
19.6
|
1.0
|
CE1
|
A:PHE52
|
4.9
|
19.0
|
1.0
|
|
Reference:
H.R.Gibson,
C.G.Mowat,
C.S.Miles,
B.R.Li,
D.Leys,
G.A.Reid,
S.K.Chapman.
Structural and Functional Studies on Dhc, the Diheme Cytochrome C From Rhodobacter Sphaeroides, and Its Interaction with Shp, the Sphaeroides Heme Protein Biochemistry V. 45 6363 2006.
ISSN: ISSN 0006-2960
PubMed: 16700547
DOI: 10.1021/BI060288Q
Page generated: Sat Aug 3 21:42:47 2024
|