Aluminium 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:
Aluminium Binding Sites:
The binding sites of Aluminium 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 Aluminium atom.
In total 8 binding sites of Aluminium where determined in the
Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate, PDB code: 1m34:
Jump to Aluminium binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
Aluminium binding site 1 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 1 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al 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
|
E:Al3093
b:38.5
occ:1.00
|
AL
|
E:ALF3093
|
0.0
|
38.5
|
1.0
|
F2
|
E:ALF3093
|
1.7
|
33.4
|
1.0
|
F1
|
E:ALF3093
|
1.8
|
38.9
|
1.0
|
F4
|
E:ALF3093
|
1.8
|
38.2
|
1.0
|
F3
|
E:ALF3093
|
1.8
|
40.4
|
1.0
|
O
|
E:HOH3130
|
2.1
|
34.1
|
1.0
|
O1B
|
E:ADP3091
|
3.0
|
38.9
|
1.0
|
MG
|
E:MG3092
|
3.7
|
35.6
|
1.0
|
N
|
E:GLY12
|
3.8
|
27.4
|
1.0
|
PB
|
E:ADP3091
|
3.8
|
33.1
|
1.0
|
N
|
E:GLY128
|
3.9
|
38.4
|
1.0
|
O3B
|
E:ADP3091
|
3.9
|
30.9
|
1.0
|
NZ
|
E:LYS15
|
4.1
|
32.1
|
1.0
|
NZ
|
F:LYS10
|
4.1
|
22.9
|
1.0
|
OD2
|
E:ASP39
|
4.2
|
40.0
|
1.0
|
OD1
|
F:ASP129
|
4.3
|
35.3
|
1.0
|
O2B
|
E:ADP3091
|
4.4
|
31.9
|
1.0
|
O
|
E:HOH3131
|
4.4
|
46.2
|
1.0
|
CA
|
E:GLY11
|
4.4
|
25.6
|
1.0
|
OD2
|
F:ASP129
|
4.5
|
40.4
|
1.0
|
CA
|
E:GLY12
|
4.5
|
29.7
|
1.0
|
CA
|
E:LEU127
|
4.6
|
38.2
|
1.0
|
C
|
E:GLY11
|
4.6
|
26.2
|
1.0
|
CA
|
E:GLY128
|
4.6
|
38.2
|
1.0
|
C
|
E:LEU127
|
4.6
|
39.1
|
1.0
|
CE
|
F:LYS10
|
4.7
|
22.9
|
1.0
|
O
|
E:HOH3132
|
4.8
|
31.4
|
1.0
|
O
|
E:HOH3133
|
4.8
|
38.6
|
1.0
|
NZ
|
E:LYS41
|
4.8
|
50.6
|
1.0
|
CG
|
F:ASP129
|
4.8
|
38.8
|
1.0
|
CB
|
E:LEU127
|
4.9
|
38.8
|
1.0
|
|
Aluminium binding site 2 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 2 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al 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
|
F:Al3193
b:41.3
occ:1.00
|
AL
|
F:ALF3193
|
0.0
|
41.3
|
1.0
|
F2
|
F:ALF3193
|
1.8
|
40.5
|
1.0
|
F1
|
F:ALF3193
|
1.8
|
42.5
|
1.0
|
F4
|
F:ALF3193
|
1.8
|
40.1
|
1.0
|
F3
|
F:ALF3193
|
1.8
|
46.8
|
1.0
|
O
|
E:HOH3134
|
2.1
|
39.0
|
1.0
|
O1B
|
F:ADP3191
|
3.0
|
32.0
|
1.0
|
MG
|
F:MG3192
|
3.7
|
31.0
|
1.0
|
PB
|
F:ADP3191
|
3.7
|
28.1
|
1.0
|
N
|
F:GLY12
|
3.8
|
22.7
|
1.0
|
N
|
F:GLY128
|
4.0
|
35.4
|
1.0
|
O3B
|
F:ADP3191
|
4.0
|
31.3
|
1.0
|
NZ
|
E:LYS10
|
4.1
|
33.5
|
1.0
|
NZ
|
F:LYS15
|
4.1
|
34.4
|
1.0
|
O2B
|
F:ADP3191
|
4.1
|
28.9
|
1.0
|
OD1
|
E:ASP129
|
4.2
|
49.7
|
1.0
|
OD2
|
F:ASP39
|
4.2
|
38.1
|
1.0
|
O
|
F:HOH3196
|
4.4
|
25.9
|
1.0
|
CA
|
F:GLY12
|
4.4
|
25.0
|
1.0
|
OD2
|
E:ASP129
|
4.5
|
50.4
|
1.0
|
NZ
|
F:LYS41
|
4.6
|
46.6
|
1.0
|
CA
|
F:GLY128
|
4.6
|
36.3
|
1.0
|
CA
|
F:GLY11
|
4.7
|
25.3
|
1.0
|
CA
|
F:LEU127
|
4.7
|
35.8
|
1.0
|
O
|
F:HOH3197
|
4.7
|
27.0
|
1.0
|
C
|
F:GLY11
|
4.7
|
24.1
|
1.0
|
C
|
F:LEU127
|
4.8
|
35.4
|
1.0
|
CE
|
E:LYS10
|
4.8
|
31.1
|
1.0
|
O
|
F:HOH3198
|
4.8
|
41.2
|
1.0
|
CG
|
E:ASP129
|
4.8
|
49.2
|
1.0
|
CB
|
F:LEU127
|
4.9
|
35.3
|
1.0
|
|
Aluminium binding site 3 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 3 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al 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
|
G:Al3293
b:45.0
occ:1.00
|
AL
|
G:ALF3293
|
0.0
|
45.0
|
1.0
|
F1
|
G:ALF3293
|
1.7
|
47.3
|
1.0
|
F2
|
G:ALF3293
|
1.8
|
44.9
|
1.0
|
F4
|
G:ALF3293
|
1.8
|
44.3
|
1.0
|
F3
|
G:ALF3293
|
1.8
|
47.1
|
1.0
|
O
|
G:HOH3345
|
2.1
|
43.7
|
1.0
|
O1B
|
G:ADP3291
|
3.0
|
39.4
|
1.0
|
N
|
G:GLY12
|
3.6
|
33.8
|
1.0
|
MG
|
G:MG3292
|
3.7
|
48.6
|
1.0
|
PB
|
G:ADP3291
|
3.8
|
31.6
|
1.0
|
O3B
|
G:ADP3291
|
3.8
|
33.6
|
1.0
|
N
|
G:GLY128
|
4.0
|
37.5
|
1.0
|
NZ
|
G:LYS15
|
4.0
|
29.4
|
1.0
|
OD1
|
H:ASP129
|
4.2
|
49.1
|
1.0
|
NZ
|
H:LYS10
|
4.2
|
33.1
|
1.0
|
CA
|
G:GLY12
|
4.3
|
33.1
|
1.0
|
OD2
|
G:ASP39
|
4.3
|
35.4
|
1.0
|
OD2
|
H:ASP129
|
4.4
|
48.9
|
1.0
|
CA
|
G:GLY11
|
4.5
|
34.3
|
1.0
|
C
|
G:GLY11
|
4.5
|
34.0
|
1.0
|
O2B
|
G:ADP3291
|
4.6
|
37.2
|
1.0
|
NZ
|
G:LYS41
|
4.6
|
44.8
|
1.0
|
O
|
G:HOH3346
|
4.6
|
27.1
|
1.0
|
CE
|
H:LYS10
|
4.6
|
33.0
|
1.0
|
CA
|
G:GLY128
|
4.6
|
39.1
|
1.0
|
O
|
G:HOH3347
|
4.7
|
26.4
|
1.0
|
CG
|
H:ASP129
|
4.7
|
48.8
|
1.0
|
CA
|
G:LEU127
|
4.8
|
39.4
|
1.0
|
O
|
G:HOH3348
|
4.8
|
42.7
|
1.0
|
C
|
G:LEU127
|
4.9
|
38.1
|
1.0
|
|
Aluminium binding site 4 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 4 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al 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
|
H:Al3393
b:36.0
occ:1.00
|
AL
|
H:ALF3393
|
0.0
|
36.0
|
1.0
|
F1
|
H:ALF3393
|
1.8
|
36.7
|
1.0
|
F2
|
H:ALF3393
|
1.8
|
35.5
|
1.0
|
F4
|
H:ALF3393
|
1.8
|
35.3
|
1.0
|
F3
|
H:ALF3393
|
1.8
|
36.8
|
1.0
|
O
|
G:HOH3349
|
2.1
|
34.9
|
1.0
|
O1B
|
H:ADP3391
|
3.0
|
43.9
|
1.0
|
O3B
|
H:ADP3391
|
3.5
|
39.8
|
1.0
|
N
|
H:GLY12
|
3.7
|
32.5
|
1.0
|
PB
|
H:ADP3391
|
3.8
|
37.9
|
1.0
|
MG
|
H:MG3392
|
3.8
|
41.6
|
1.0
|
N
|
H:GLY128
|
4.0
|
39.3
|
1.0
|
NZ
|
G:LYS10
|
4.1
|
32.8
|
1.0
|
OD1
|
G:ASP129
|
4.1
|
45.7
|
1.0
|
NZ
|
H:LYS15
|
4.2
|
37.9
|
1.0
|
OD2
|
H:ASP39
|
4.3
|
39.9
|
1.0
|
OD2
|
G:ASP129
|
4.3
|
42.0
|
1.0
|
CA
|
H:GLY12
|
4.4
|
34.0
|
1.0
|
CA
|
H:GLY11
|
4.5
|
31.1
|
1.0
|
C
|
H:GLY11
|
4.6
|
31.6
|
1.0
|
O
|
H:HOH3418
|
4.6
|
41.3
|
1.0
|
CA
|
H:GLY128
|
4.6
|
39.3
|
1.0
|
NZ
|
H:LYS41
|
4.7
|
54.4
|
1.0
|
CG
|
G:ASP129
|
4.7
|
43.8
|
1.0
|
O
|
H:HOH3417
|
4.7
|
31.6
|
1.0
|
CA
|
H:LEU127
|
4.8
|
39.1
|
1.0
|
CE
|
G:LYS10
|
4.8
|
35.9
|
1.0
|
O3A
|
H:ADP3391
|
4.8
|
37.2
|
1.0
|
C
|
H:LEU127
|
4.9
|
39.1
|
1.0
|
O2B
|
H:ADP3391
|
4.9
|
43.4
|
1.0
|
|
Aluminium binding site 5 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 5 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al binding
site number 5 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
M:Al5093
b:42.4
occ:1.00
|
AL
|
M:ALF5093
|
0.0
|
42.4
|
1.0
|
F1
|
M:ALF5093
|
1.8
|
42.9
|
1.0
|
F2
|
M:ALF5093
|
1.8
|
44.3
|
1.0
|
F4
|
M:ALF5093
|
1.8
|
42.2
|
1.0
|
F3
|
M:ALF5093
|
1.8
|
42.6
|
1.0
|
O
|
M:HOH5151
|
2.1
|
42.6
|
1.0
|
O1B
|
M:ADP5091
|
3.0
|
34.9
|
1.0
|
MG
|
M:MG5092
|
3.7
|
30.8
|
1.0
|
PB
|
M:ADP5091
|
3.7
|
29.3
|
1.0
|
N
|
M:GLY12
|
3.8
|
27.5
|
1.0
|
O2B
|
M:ADP5091
|
3.9
|
30.8
|
1.0
|
N
|
M:GLY128
|
4.0
|
32.6
|
1.0
|
OD1
|
N:ASP129
|
4.1
|
43.1
|
1.0
|
NZ
|
N:LYS10
|
4.1
|
24.2
|
1.0
|
NZ
|
M:LYS15
|
4.2
|
22.2
|
1.0
|
O3B
|
M:ADP5091
|
4.2
|
34.0
|
1.0
|
OD2
|
M:ASP39
|
4.2
|
42.4
|
1.0
|
O
|
N:HOH5202
|
4.3
|
29.2
|
1.0
|
O
|
M:HOH5152
|
4.3
|
26.1
|
1.0
|
O
|
M:HOH5154
|
4.5
|
48.4
|
1.0
|
CA
|
M:GLY12
|
4.5
|
26.9
|
1.0
|
NZ
|
M:LYS41
|
4.6
|
56.1
|
1.0
|
CA
|
M:GLY11
|
4.6
|
27.4
|
1.0
|
CE
|
N:LYS10
|
4.6
|
23.4
|
1.0
|
O
|
M:HOH5153
|
4.7
|
26.1
|
1.0
|
CA
|
M:LEU127
|
4.7
|
32.6
|
1.0
|
C
|
M:GLY11
|
4.7
|
28.3
|
1.0
|
CA
|
M:GLY128
|
4.7
|
32.4
|
1.0
|
C
|
M:LEU127
|
4.8
|
32.6
|
1.0
|
OD2
|
N:ASP129
|
4.8
|
46.7
|
1.0
|
CG
|
N:ASP129
|
4.9
|
45.2
|
1.0
|
CB
|
M:LEU127
|
4.9
|
30.7
|
1.0
|
|
Aluminium binding site 6 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 6 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al binding
site number 6 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
N:Al5193
b:36.6
occ:1.00
|
AL
|
N:ALF5193
|
0.0
|
36.6
|
1.0
|
F2
|
N:ALF5193
|
1.8
|
36.1
|
1.0
|
F1
|
N:ALF5193
|
1.8
|
40.1
|
1.0
|
F4
|
N:ALF5193
|
1.8
|
39.3
|
1.0
|
F3
|
N:ALF5193
|
1.8
|
38.6
|
1.0
|
O
|
M:HOH5155
|
2.1
|
36.3
|
1.0
|
O1B
|
N:ADP5191
|
2.9
|
33.1
|
1.0
|
PB
|
N:ADP5191
|
3.7
|
25.7
|
1.0
|
MG
|
N:MG5192
|
3.7
|
35.0
|
1.0
|
N
|
N:GLY12
|
3.8
|
24.2
|
1.0
|
NZ
|
N:LYS15
|
3.9
|
29.1
|
1.0
|
N
|
N:GLY128
|
3.9
|
35.7
|
1.0
|
O3B
|
N:ADP5191
|
3.9
|
27.1
|
1.0
|
NZ
|
M:LYS10
|
4.0
|
24.6
|
1.0
|
O
|
M:HOH5102
|
4.2
|
30.7
|
1.0
|
OD2
|
M:ASP129
|
4.2
|
39.6
|
1.0
|
O
|
N:HOH5232
|
4.2
|
28.4
|
1.0
|
OD2
|
N:ASP39
|
4.3
|
37.0
|
1.0
|
O2B
|
N:ADP5191
|
4.3
|
27.1
|
1.0
|
OD1
|
M:ASP129
|
4.3
|
40.7
|
1.0
|
CA
|
N:GLY12
|
4.5
|
24.5
|
1.0
|
CA
|
N:GLY11
|
4.5
|
24.6
|
1.0
|
CA
|
N:GLY128
|
4.5
|
36.7
|
1.0
|
O
|
N:HOH5233
|
4.6
|
30.3
|
1.0
|
C
|
N:GLY11
|
4.6
|
24.1
|
1.0
|
O
|
N:HOH5234
|
4.7
|
41.0
|
1.0
|
CG
|
M:ASP129
|
4.7
|
40.1
|
1.0
|
CA
|
N:LEU127
|
4.7
|
37.3
|
1.0
|
C
|
N:LEU127
|
4.8
|
36.4
|
1.0
|
NZ
|
N:LYS41
|
4.8
|
51.0
|
1.0
|
CE
|
M:LYS10
|
4.9
|
25.9
|
1.0
|
|
Aluminium binding site 7 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 7 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al binding
site number 7 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
O:Al5293
b:50.7
occ:1.00
|
AL
|
O:ALF5293
|
0.0
|
50.7
|
1.0
|
F2
|
O:ALF5293
|
1.8
|
49.2
|
1.0
|
F1
|
O:ALF5293
|
1.8
|
52.5
|
1.0
|
F4
|
O:ALF5293
|
1.8
|
49.4
|
1.0
|
F3
|
O:ALF5293
|
1.8
|
52.9
|
1.0
|
O
|
O:HOH5294
|
2.1
|
50.5
|
1.0
|
O1B
|
O:ADP5291
|
3.0
|
42.7
|
1.0
|
MG
|
O:MG5292
|
3.7
|
41.8
|
1.0
|
N
|
O:GLY12
|
3.8
|
37.9
|
1.0
|
PB
|
O:ADP5291
|
3.8
|
37.8
|
1.0
|
N
|
O:GLY128
|
3.9
|
44.9
|
1.0
|
NZ
|
P:LYS10
|
3.9
|
42.3
|
1.0
|
O3B
|
O:ADP5291
|
4.0
|
37.0
|
1.0
|
OD2
|
P:ASP129
|
4.0
|
53.0
|
1.0
|
OD2
|
O:ASP39
|
4.3
|
46.2
|
1.0
|
OD1
|
P:ASP129
|
4.3
|
54.6
|
1.0
|
O2B
|
O:ADP5291
|
4.4
|
37.1
|
1.0
|
NZ
|
O:LYS15
|
4.4
|
36.8
|
1.0
|
O
|
O:HOH5296
|
4.4
|
41.5
|
1.0
|
CA
|
O:GLY11
|
4.4
|
37.6
|
1.0
|
NZ
|
O:LYS41
|
4.5
|
52.6
|
1.0
|
CA
|
O:GLY128
|
4.6
|
46.4
|
1.0
|
CE
|
P:LYS10
|
4.6
|
40.3
|
1.0
|
CA
|
O:GLY12
|
4.6
|
39.1
|
1.0
|
CA
|
O:LEU127
|
4.6
|
43.2
|
1.0
|
C
|
O:GLY11
|
4.6
|
37.8
|
1.0
|
CG
|
P:ASP129
|
4.6
|
53.6
|
1.0
|
C
|
O:LEU127
|
4.7
|
44.1
|
1.0
|
CB
|
O:LEU127
|
4.9
|
42.5
|
1.0
|
O
|
O:HOH5298
|
4.9
|
42.9
|
1.0
|
O
|
O:HOH5297
|
4.9
|
39.4
|
1.0
|
CE
|
O:LYS41
|
5.0
|
52.2
|
1.0
|
|
Aluminium binding site 8 out
of 8 in 1m34
Go back to
Aluminium Binding Sites List in 1m34
Aluminium binding site 8 out
of 8 in the Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate
Mono view
Stereo pair view
|
A full contact list of Aluminium with other atoms in the Al binding
site number 8 of Nitrogenase Complex From Azotobacter Vinelandii Stabilized By Adp- Tetrafluoroaluminate within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
P:Al5393
b:48.5
occ:1.00
|
AL
|
P:ALF5393
|
0.0
|
48.5
|
1.0
|
F1
|
P:ALF5393
|
1.8
|
48.7
|
1.0
|
F2
|
P:ALF5393
|
1.8
|
47.3
|
1.0
|
F4
|
P:ALF5393
|
1.8
|
44.6
|
1.0
|
F3
|
P:ALF5393
|
1.8
|
48.4
|
1.0
|
O
|
O:HOH5394
|
2.1
|
46.6
|
1.0
|
O1B
|
P:ADP5391
|
3.1
|
46.4
|
1.0
|
N
|
P:GLY12
|
3.6
|
34.6
|
1.0
|
O3B
|
P:ADP5391
|
3.6
|
41.4
|
1.0
|
MG
|
P:MG5392
|
3.7
|
42.6
|
1.0
|
PB
|
P:ADP5391
|
3.8
|
40.7
|
1.0
|
OD1
|
O:ASP129
|
3.9
|
59.2
|
1.0
|
N
|
P:GLY128
|
4.0
|
44.3
|
1.0
|
NZ
|
P:LYS15
|
4.1
|
38.7
|
1.0
|
CA
|
P:GLY12
|
4.3
|
34.8
|
1.0
|
OD2
|
P:ASP39
|
4.3
|
47.5
|
1.0
|
NZ
|
O:LYS10
|
4.4
|
39.7
|
1.0
|
CA
|
P:GLY11
|
4.5
|
35.6
|
1.0
|
OD2
|
O:ASP129
|
4.5
|
57.0
|
1.0
|
C
|
P:GLY11
|
4.5
|
36.1
|
1.0
|
CE
|
O:LYS10
|
4.6
|
38.8
|
1.0
|
CG
|
O:ASP129
|
4.6
|
57.2
|
1.0
|
CA
|
P:GLY128
|
4.7
|
46.3
|
1.0
|
NZ
|
P:LYS41
|
4.7
|
52.7
|
1.0
|
O2B
|
P:ADP5391
|
4.7
|
41.9
|
1.0
|
O
|
P:HOH5396
|
4.8
|
34.8
|
1.0
|
O
|
P:HOH5397
|
4.9
|
57.9
|
1.0
|
CA
|
P:LEU127
|
4.9
|
43.5
|
1.0
|
C
|
P:LEU127
|
5.0
|
44.0
|
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: Wed Jul 10 09:23:37 2024
|