Iron in PDB 3zh0: Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin
Protein crystallography data
The structure of Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin, PDB code: 3zh0
was solved by
C.Ciaccio,
A.Pesce,
G.R.Tundo,
L.Tilleman,
S.Dewilde,
L.Moens,
P.Ascenzi,
M.Bolognesi,
M.Nardini,
M.Coletta,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
91.93 /
2.00
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
80.670,
48.620,
92.030,
90.00,
92.61,
90.00
|
R / Rfree (%)
|
19.919 /
26.015
|
Iron Binding Sites:
The binding sites of Iron atom in the Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin
(pdb code 3zh0). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the
Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin, PDB code: 3zh0:
Jump to Iron binding site number:
1;
2;
3;
4;
Iron binding site 1 out
of 4 in 3zh0
Go back to
Iron Binding Sites List in 3zh0
Iron binding site 1 out
of 4 in the Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe200
b:7.8
occ:1.00
|
FE
|
A:HEM200
|
0.0
|
7.8
|
1.0
|
NA
|
A:HEM200
|
2.0
|
4.5
|
1.0
|
NC
|
A:HEM200
|
2.0
|
8.9
|
1.0
|
NB
|
A:HEM200
|
2.0
|
8.7
|
1.0
|
NE2
|
A:HIS120
|
2.0
|
7.6
|
1.0
|
O1
|
A:FMT201
|
2.1
|
15.0
|
1.0
|
ND
|
A:HEM200
|
2.1
|
8.5
|
1.0
|
C
|
A:FMT201
|
2.9
|
15.8
|
1.0
|
C4C
|
A:HEM200
|
3.0
|
8.3
|
1.0
|
C4A
|
A:HEM200
|
3.0
|
6.0
|
1.0
|
C1C
|
A:HEM200
|
3.0
|
7.5
|
1.0
|
C1A
|
A:HEM200
|
3.0
|
5.4
|
1.0
|
CE1
|
A:HIS120
|
3.0
|
7.8
|
1.0
|
CD2
|
A:HIS120
|
3.0
|
6.7
|
1.0
|
C1B
|
A:HEM200
|
3.0
|
6.3
|
1.0
|
C4B
|
A:HEM200
|
3.0
|
9.2
|
1.0
|
C4D
|
A:HEM200
|
3.0
|
8.2
|
1.0
|
C1D
|
A:HEM200
|
3.1
|
8.5
|
1.0
|
CHD
|
A:HEM200
|
3.3
|
6.7
|
1.0
|
CHB
|
A:HEM200
|
3.3
|
6.7
|
1.0
|
CHC
|
A:HEM200
|
3.4
|
7.9
|
1.0
|
CHA
|
A:HEM200
|
3.4
|
6.4
|
1.0
|
O2
|
A:FMT201
|
4.1
|
17.4
|
1.0
|
ND1
|
A:HIS120
|
4.1
|
7.7
|
1.0
|
CG
|
A:HIS120
|
4.2
|
5.6
|
1.0
|
C2A
|
A:HEM200
|
4.2
|
5.1
|
1.0
|
C2C
|
A:HEM200
|
4.2
|
8.3
|
1.0
|
C3A
|
A:HEM200
|
4.2
|
6.2
|
1.0
|
C3C
|
A:HEM200
|
4.2
|
7.3
|
1.0
|
C3D
|
A:HEM200
|
4.3
|
9.0
|
1.0
|
C2B
|
A:HEM200
|
4.3
|
6.9
|
1.0
|
C3B
|
A:HEM200
|
4.3
|
7.8
|
1.0
|
C2D
|
A:HEM200
|
4.3
|
7.8
|
1.0
|
|
Iron binding site 2 out
of 4 in 3zh0
Go back to
Iron Binding Sites List in 3zh0
Iron binding site 2 out
of 4 in the Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe200
b:7.9
occ:1.00
|
FE
|
B:HEM200
|
0.0
|
7.9
|
1.0
|
NA
|
B:HEM200
|
2.0
|
7.5
|
1.0
|
NC
|
B:HEM200
|
2.0
|
10.3
|
1.0
|
O1
|
B:FMT201
|
2.0
|
10.2
|
1.0
|
ND
|
B:HEM200
|
2.0
|
7.8
|
1.0
|
NB
|
B:HEM200
|
2.1
|
10.5
|
1.0
|
NE2
|
B:HIS120
|
2.1
|
9.6
|
1.0
|
C
|
B:FMT201
|
2.9
|
11.1
|
1.0
|
C4A
|
B:HEM200
|
3.0
|
9.6
|
1.0
|
C1A
|
B:HEM200
|
3.0
|
9.2
|
1.0
|
C4C
|
B:HEM200
|
3.0
|
9.3
|
1.0
|
C1D
|
B:HEM200
|
3.0
|
6.1
|
1.0
|
C4D
|
B:HEM200
|
3.0
|
7.4
|
1.0
|
C1C
|
B:HEM200
|
3.0
|
8.9
|
1.0
|
CD2
|
B:HIS120
|
3.0
|
8.1
|
1.0
|
C4B
|
B:HEM200
|
3.0
|
11.9
|
1.0
|
C1B
|
B:HEM200
|
3.1
|
9.0
|
1.0
|
CE1
|
B:HIS120
|
3.1
|
9.5
|
1.0
|
CHD
|
B:HEM200
|
3.3
|
6.8
|
1.0
|
CHC
|
B:HEM200
|
3.3
|
10.6
|
1.0
|
CHA
|
B:HEM200
|
3.3
|
6.1
|
1.0
|
CHB
|
B:HEM200
|
3.4
|
9.1
|
1.0
|
O2
|
B:FMT201
|
4.1
|
12.8
|
1.0
|
C3A
|
B:HEM200
|
4.2
|
8.5
|
1.0
|
C2A
|
B:HEM200
|
4.2
|
8.2
|
1.0
|
CG
|
B:HIS120
|
4.2
|
9.7
|
1.0
|
C3C
|
B:HEM200
|
4.2
|
8.0
|
1.0
|
C2C
|
B:HEM200
|
4.2
|
7.5
|
1.0
|
C3D
|
B:HEM200
|
4.2
|
6.4
|
1.0
|
ND1
|
B:HIS120
|
4.2
|
10.3
|
1.0
|
C2D
|
B:HEM200
|
4.2
|
6.9
|
1.0
|
C3B
|
B:HEM200
|
4.3
|
10.4
|
1.0
|
C2B
|
B:HEM200
|
4.3
|
10.2
|
1.0
|
|
Iron binding site 3 out
of 4 in 3zh0
Go back to
Iron Binding Sites List in 3zh0
Iron binding site 3 out
of 4 in the Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe200
b:8.8
occ:1.00
|
FE
|
C:HEM200
|
0.0
|
8.8
|
1.0
|
NA
|
C:HEM200
|
2.0
|
8.4
|
1.0
|
NC
|
C:HEM200
|
2.0
|
5.9
|
1.0
|
NB
|
C:HEM200
|
2.0
|
7.0
|
1.0
|
O1
|
C:FMT201
|
2.0
|
12.2
|
1.0
|
NE2
|
C:HIS120
|
2.1
|
8.7
|
1.0
|
ND
|
C:HEM200
|
2.1
|
7.1
|
1.0
|
C
|
C:FMT201
|
2.9
|
12.1
|
1.0
|
C4A
|
C:HEM200
|
2.9
|
8.3
|
1.0
|
CE1
|
C:HIS120
|
3.0
|
8.0
|
1.0
|
C1B
|
C:HEM200
|
3.0
|
7.8
|
1.0
|
C1A
|
C:HEM200
|
3.0
|
8.6
|
1.0
|
C4C
|
C:HEM200
|
3.0
|
7.4
|
1.0
|
C1D
|
C:HEM200
|
3.0
|
7.8
|
1.0
|
C1C
|
C:HEM200
|
3.0
|
6.1
|
1.0
|
C4B
|
C:HEM200
|
3.1
|
9.3
|
1.0
|
C4D
|
C:HEM200
|
3.1
|
9.6
|
1.0
|
CD2
|
C:HIS120
|
3.1
|
8.7
|
1.0
|
CHB
|
C:HEM200
|
3.3
|
6.1
|
1.0
|
CHD
|
C:HEM200
|
3.3
|
6.3
|
1.0
|
CHC
|
C:HEM200
|
3.4
|
5.7
|
1.0
|
CHA
|
C:HEM200
|
3.4
|
8.7
|
1.0
|
O2
|
C:FMT201
|
4.0
|
13.5
|
1.0
|
ND1
|
C:HIS120
|
4.1
|
8.9
|
1.0
|
C3A
|
C:HEM200
|
4.1
|
7.1
|
1.0
|
C2A
|
C:HEM200
|
4.2
|
8.4
|
1.0
|
C2B
|
C:HEM200
|
4.2
|
7.9
|
1.0
|
CG
|
C:HIS120
|
4.2
|
8.6
|
1.0
|
C2D
|
C:HEM200
|
4.3
|
6.8
|
1.0
|
C2C
|
C:HEM200
|
4.3
|
7.0
|
1.0
|
C3C
|
C:HEM200
|
4.3
|
4.5
|
1.0
|
C3B
|
C:HEM200
|
4.3
|
6.5
|
1.0
|
C3D
|
C:HEM200
|
4.3
|
7.6
|
1.0
|
|
Iron binding site 4 out
of 4 in 3zh0
Go back to
Iron Binding Sites List in 3zh0
Iron binding site 4 out
of 4 in the Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Fe200
b:7.2
occ:1.00
|
FE
|
D:HEM200
|
0.0
|
7.2
|
1.0
|
NA
|
D:HEM200
|
2.0
|
7.6
|
1.0
|
NB
|
D:HEM200
|
2.0
|
7.2
|
1.0
|
NC
|
D:HEM200
|
2.0
|
6.8
|
1.0
|
ND
|
D:HEM200
|
2.0
|
5.9
|
1.0
|
O1
|
D:FMT201
|
2.0
|
9.1
|
1.0
|
NE2
|
D:HIS120
|
2.1
|
7.2
|
1.0
|
C
|
D:FMT201
|
2.9
|
9.8
|
1.0
|
C4A
|
D:HEM200
|
3.0
|
8.8
|
1.0
|
C1B
|
D:HEM200
|
3.0
|
5.7
|
1.0
|
C1D
|
D:HEM200
|
3.0
|
5.0
|
1.0
|
CD2
|
D:HIS120
|
3.0
|
6.2
|
1.0
|
C1A
|
D:HEM200
|
3.0
|
9.3
|
1.0
|
C4D
|
D:HEM200
|
3.0
|
8.4
|
1.0
|
C4C
|
D:HEM200
|
3.0
|
7.1
|
1.0
|
C4B
|
D:HEM200
|
3.0
|
7.9
|
1.0
|
C1C
|
D:HEM200
|
3.1
|
5.7
|
1.0
|
CE1
|
D:HIS120
|
3.1
|
4.4
|
1.0
|
CHB
|
D:HEM200
|
3.3
|
6.0
|
1.0
|
CHD
|
D:HEM200
|
3.3
|
5.3
|
1.0
|
CHA
|
D:HEM200
|
3.4
|
9.7
|
1.0
|
CHC
|
D:HEM200
|
3.4
|
6.9
|
1.0
|
O2
|
D:FMT201
|
4.1
|
9.4
|
1.0
|
CG
|
D:HIS120
|
4.2
|
8.5
|
1.0
|
ND1
|
D:HIS120
|
4.2
|
7.1
|
1.0
|
C3A
|
D:HEM200
|
4.2
|
11.2
|
1.0
|
C2A
|
D:HEM200
|
4.2
|
7.1
|
1.0
|
C2B
|
D:HEM200
|
4.2
|
6.7
|
1.0
|
C2D
|
D:HEM200
|
4.2
|
6.5
|
1.0
|
C3D
|
D:HEM200
|
4.2
|
6.2
|
1.0
|
C3C
|
D:HEM200
|
4.2
|
2.9
|
1.0
|
C3B
|
D:HEM200
|
4.3
|
6.1
|
1.0
|
C2C
|
D:HEM200
|
4.3
|
5.0
|
1.0
|
|
Reference:
C.Ciaccio,
A.Pesce,
G.R.Tundo,
L.Tilleman,
L.Bertolacci,
S.Dewilde,
L.Moens,
P.Ascenzi,
M.Bolognesi,
M.Nardini,
M.Coletta.
Functional and Structural Role of the N-Terminal Extension in Methanosarcina Acetivorans Protoglobin. Biochim.Biophys.Acta V.1834 1813 2013.
ISSN: ISSN 0006-3002
PubMed: 23485914
DOI: 10.1016/J.BBAPAP.2013.02.026
Page generated: Sun Aug 4 23:07:34 2024
|