Calcium in PDB 1m34: Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Enzymatic activity of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
All present enzymatic activity of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate:
1.18.6.1;
Protein crystallography data
The structure of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate, PDB code: 1m34
was solved by
B.Schmid,
O.Einsle,
H.-J.Chiu,
A.Willing,
M.Yoshida,
J.B.Howard,
D.C.Rees,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.00 /
2.30
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
326.100,
75.800,
312.200,
90.00,
102.60,
90.00
|
R / Rfree (%)
|
20 /
23.6
|
Other elements in 1m34:
The structure of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
(pdb code 1m34). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 4 binding sites of Calcium where determined in the
Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate, PDB code: 1m34:
Jump to Calcium binding site number:
1;
2;
3;
4;
Calcium binding site 1 out
of 4 in 1m34
Go back to
Calcium Binding Sites List in 1m34
Calcium binding site 1 out
of 4 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 1 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ca2299
b:34.3
occ:1.00
|
OE2
|
D:GLU109
|
2.2
|
41.3
|
1.0
|
OD2
|
B:ASP357
|
2.2
|
28.1
|
1.0
|
OD2
|
B:ASP353
|
2.3
|
32.4
|
1.0
|
O
|
D:ARG108
|
2.3
|
33.6
|
1.0
|
O
|
B:HOH2477
|
2.5
|
34.3
|
1.0
|
OD1
|
B:ASP353
|
2.9
|
34.2
|
1.0
|
CG
|
B:ASP353
|
2.9
|
33.8
|
1.0
|
CG
|
B:ASP357
|
3.1
|
29.9
|
1.0
|
CD
|
D:GLU109
|
3.2
|
41.7
|
1.0
|
OD1
|
B:ASP357
|
3.3
|
28.8
|
1.0
|
C
|
D:ARG108
|
3.5
|
34.5
|
1.0
|
CG
|
D:GLU109
|
3.6
|
40.8
|
1.0
|
CD1
|
C:PHE429
|
4.0
|
30.0
|
1.0
|
CA
|
D:GLU109
|
4.1
|
36.0
|
1.0
|
NZ
|
C:LYS433
|
4.1
|
40.4
|
1.0
|
N
|
D:GLU109
|
4.2
|
34.9
|
1.0
|
O
|
D:HOH2461
|
4.2
|
48.7
|
1.0
|
OE1
|
D:GLU109
|
4.3
|
43.1
|
1.0
|
CB
|
B:ASP353
|
4.4
|
32.8
|
1.0
|
CB
|
D:GLU109
|
4.4
|
38.0
|
1.0
|
CB
|
B:ASP357
|
4.5
|
29.7
|
1.0
|
O
|
B:ASP353
|
4.6
|
32.8
|
1.0
|
CE1
|
C:PHE429
|
4.6
|
29.4
|
1.0
|
O
|
D:PHE107
|
4.6
|
29.7
|
1.0
|
CB
|
D:ARG108
|
4.6
|
35.0
|
1.0
|
CG
|
C:PHE429
|
4.6
|
31.9
|
1.0
|
CE
|
C:LYS433
|
4.6
|
40.5
|
1.0
|
CA
|
D:ARG108
|
4.7
|
34.1
|
1.0
|
O
|
B:HOH2452
|
4.8
|
42.4
|
1.0
|
CB
|
C:PHE429
|
4.9
|
31.7
|
1.0
|
C
|
B:ASP353
|
4.9
|
32.8
|
1.0
|
O
|
D:HOH2347
|
4.9
|
30.8
|
1.0
|
|
Calcium binding site 2 out
of 4 in 1m34
Go back to
Calcium Binding Sites List in 1m34
Calcium binding site 2 out
of 4 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 2 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Ca2099
b:61.4
occ:1.00
|
OD2
|
D:ASP357
|
2.1
|
35.7
|
1.0
|
OE2
|
B:GLU109
|
2.1
|
45.4
|
1.0
|
OD2
|
D:ASP353
|
2.2
|
26.3
|
1.0
|
O
|
B:ARG108
|
2.4
|
34.0
|
1.0
|
O
|
D:HOH2469
|
2.5
|
30.9
|
1.0
|
CG
|
D:ASP353
|
3.0
|
25.7
|
1.0
|
CG
|
D:ASP357
|
3.1
|
34.6
|
1.0
|
OD1
|
D:ASP353
|
3.1
|
25.5
|
1.0
|
CD
|
B:GLU109
|
3.3
|
44.4
|
1.0
|
OD1
|
D:ASP357
|
3.4
|
38.9
|
1.0
|
C
|
B:ARG108
|
3.6
|
31.8
|
1.0
|
CG
|
B:GLU109
|
3.9
|
41.4
|
1.0
|
NZ
|
A:LYS433
|
4.1
|
30.8
|
1.0
|
CA
|
B:GLU109
|
4.2
|
32.4
|
1.0
|
OE1
|
B:GLU109
|
4.3
|
46.2
|
1.0
|
O
|
D:HOH2442
|
4.3
|
44.0
|
1.0
|
N
|
B:GLU109
|
4.3
|
32.7
|
1.0
|
CD1
|
A:PHE429
|
4.3
|
28.1
|
1.0
|
O
|
B:PHE107
|
4.4
|
25.5
|
1.0
|
CB
|
D:ASP357
|
4.4
|
33.6
|
1.0
|
CB
|
D:ASP353
|
4.5
|
20.5
|
1.0
|
CB
|
B:ARG108
|
4.5
|
30.7
|
1.0
|
O
|
D:ASP353
|
4.6
|
21.6
|
1.0
|
CB
|
B:GLU109
|
4.6
|
35.2
|
1.0
|
CA
|
B:ARG108
|
4.6
|
31.1
|
1.0
|
CE
|
A:LYS433
|
4.7
|
32.4
|
1.0
|
CE1
|
A:PHE429
|
4.7
|
29.2
|
1.0
|
C
|
D:ASP353
|
4.8
|
21.9
|
1.0
|
O
|
B:HOH2405
|
4.9
|
37.3
|
1.0
|
CG
|
A:PHE429
|
5.0
|
27.4
|
1.0
|
|
Calcium binding site 3 out
of 4 in 1m34
Go back to
Calcium Binding Sites List in 1m34
Calcium binding site 3 out
of 4 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 3 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
J:Ca4299
b:56.4
occ:1.00
|
OD2
|
J:ASP357
|
2.0
|
37.2
|
1.0
|
OE2
|
L:GLU109
|
2.1
|
44.5
|
1.0
|
O
|
L:ARG108
|
2.2
|
27.4
|
1.0
|
OD2
|
J:ASP353
|
2.3
|
33.9
|
1.0
|
O
|
J:HOH4506
|
2.6
|
35.1
|
1.0
|
CG
|
J:ASP357
|
3.1
|
36.2
|
1.0
|
CD
|
L:GLU109
|
3.1
|
42.2
|
1.0
|
CG
|
J:ASP353
|
3.2
|
31.6
|
1.0
|
C
|
L:ARG108
|
3.4
|
29.8
|
1.0
|
OD1
|
J:ASP353
|
3.4
|
34.6
|
1.0
|
OD1
|
J:ASP357
|
3.4
|
38.9
|
1.0
|
CG
|
L:GLU109
|
3.6
|
40.0
|
1.0
|
O
|
L:PHE107
|
4.1
|
24.8
|
1.0
|
N
|
L:GLU109
|
4.2
|
30.4
|
1.0
|
CA
|
L:GLU109
|
4.2
|
31.9
|
1.0
|
CB
|
L:ARG108
|
4.2
|
33.1
|
1.0
|
OE1
|
L:GLU109
|
4.2
|
43.1
|
1.0
|
CD1
|
K:PHE429
|
4.2
|
28.1
|
1.0
|
CA
|
L:ARG108
|
4.4
|
30.1
|
1.0
|
CB
|
J:ASP357
|
4.4
|
33.8
|
1.0
|
O
|
J:HOH4478
|
4.4
|
44.9
|
1.0
|
CB
|
L:GLU109
|
4.5
|
34.1
|
1.0
|
CE1
|
K:PHE429
|
4.6
|
29.9
|
1.0
|
NZ
|
K:LYS433
|
4.6
|
29.1
|
1.0
|
O
|
J:ASP353
|
4.6
|
23.8
|
1.0
|
CB
|
J:ASP353
|
4.6
|
28.9
|
1.0
|
O
|
L:HOH4383
|
4.7
|
35.9
|
1.0
|
O
|
L:HOH4382
|
4.8
|
35.8
|
1.0
|
C
|
J:ASP353
|
4.9
|
23.6
|
1.0
|
CG
|
K:PHE429
|
5.0
|
29.1
|
1.0
|
|
Calcium binding site 4 out
of 4 in 1m34
Go back to
Calcium Binding Sites List in 1m34
Calcium binding site 4 out
of 4 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 4 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
L:Ca4099
b:53.2
occ:1.00
|
OE2
|
J:GLU109
|
2.1
|
37.9
|
1.0
|
OD2
|
L:ASP357
|
2.1
|
31.8
|
1.0
|
O
|
J:ARG108
|
2.2
|
27.3
|
1.0
|
OD2
|
L:ASP353
|
2.4
|
32.7
|
1.0
|
O
|
J:HOH4505
|
2.5
|
36.3
|
1.0
|
CG
|
L:ASP357
|
3.1
|
29.1
|
1.0
|
CG
|
L:ASP353
|
3.2
|
31.1
|
1.0
|
CD
|
J:GLU109
|
3.2
|
39.6
|
1.0
|
OD1
|
L:ASP353
|
3.3
|
31.6
|
1.0
|
C
|
J:ARG108
|
3.4
|
27.5
|
1.0
|
OD1
|
L:ASP357
|
3.4
|
32.4
|
1.0
|
CG
|
J:GLU109
|
3.7
|
37.2
|
1.0
|
CA
|
J:GLU109
|
4.1
|
29.7
|
1.0
|
N
|
J:GLU109
|
4.1
|
28.1
|
1.0
|
CD1
|
I:PHE429
|
4.2
|
27.0
|
1.0
|
OE1
|
J:GLU109
|
4.2
|
39.1
|
1.0
|
CB
|
J:ARG108
|
4.3
|
28.1
|
1.0
|
O
|
J:PHE107
|
4.4
|
25.6
|
1.0
|
CB
|
L:ASP357
|
4.5
|
26.1
|
1.0
|
CA
|
J:ARG108
|
4.5
|
27.1
|
1.0
|
CB
|
J:GLU109
|
4.5
|
31.9
|
1.0
|
NZ
|
I:LYS433
|
4.5
|
28.6
|
1.0
|
O
|
L:ASP353
|
4.6
|
26.1
|
1.0
|
CB
|
L:ASP353
|
4.6
|
29.1
|
1.0
|
CE1
|
I:PHE429
|
4.7
|
28.4
|
1.0
|
CG
|
I:PHE429
|
4.8
|
28.0
|
1.0
|
CE
|
I:LYS433
|
4.8
|
33.5
|
1.0
|
C
|
L:ASP353
|
5.0
|
27.9
|
1.0
|
|
Reference:
B.Schmid,
O.Einsle,
H.-J.Chiu,
A.Willing,
M.Yoshida,
J.B.Howard,
D.C.Rees.
Biochemical and Structural Characterization of the Crosslinked Complex of Nitrogenase: Comparison to the Adp-ALF4 Stabilized Structure Biochemistry V. 41 15557 2002.
ISSN: ISSN 0006-2960
PubMed: 12501184
DOI: 10.1021/BI026642B
Page generated: Thu Jul 11 12:14:30 2024
|