Manganese in PDB 2glj: Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Protein crystallography data
The structure of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum, PDB code: 2glj
was solved by
T.Min,
L.Shapiro,
S.K.Burley,
New York Sgx Research Center Forstructural Genomics (Nysgxrc),
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
19.95 /
3.20
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
121.708,
129.680,
222.728,
89.88,
90.00,
116.68
|
R / Rfree (%)
|
25 /
29.7
|
Manganese Binding Sites:
Manganese binding site 1 out
of 48 in 2glj
Go back to
Manganese Binding Sites List in 2glj
Manganese binding site 1 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn6001
b:31.6
occ:1.00
|
OE1
|
A:GLU296
|
2.2
|
12.8
|
1.0
|
O
|
A:HOH6108
|
2.3
|
18.5
|
1.0
|
MN
|
A:MN6002
|
2.5
|
2.0
|
1.0
|
OE2
|
A:GLU296
|
2.7
|
14.3
|
1.0
|
CD
|
A:GLU296
|
2.7
|
15.3
|
1.0
|
NE2
|
A:HIS441
|
2.9
|
15.1
|
1.0
|
OD2
|
A:ASP265
|
3.0
|
16.4
|
1.0
|
O
|
A:HOH6078
|
3.4
|
27.5
|
1.0
|
OD1
|
A:ASP265
|
3.5
|
15.1
|
1.0
|
CE1
|
A:HIS441
|
3.5
|
16.1
|
1.0
|
CE
|
A:MSE440
|
3.6
|
33.1
|
1.0
|
CG
|
A:ASP265
|
3.6
|
17.8
|
1.0
|
OE2
|
A:GLU295
|
3.7
|
40.6
|
1.0
|
OE1
|
A:GLU295
|
3.7
|
38.6
|
1.0
|
OD1
|
A:ASP342
|
4.0
|
11.8
|
1.0
|
CD2
|
A:HIS441
|
4.1
|
15.8
|
1.0
|
CG
|
A:GLU296
|
4.1
|
16.4
|
1.0
|
CD
|
A:GLU295
|
4.2
|
37.8
|
1.0
|
NE2
|
A:HIS105
|
4.2
|
8.1
|
1.0
|
OD2
|
A:ASP342
|
4.5
|
11.0
|
1.0
|
NE2
|
D:HIS180
|
4.6
|
52.9
|
1.0
|
CE1
|
A:HIS105
|
4.7
|
6.7
|
1.0
|
CG
|
A:ASP342
|
4.7
|
13.1
|
1.0
|
ND1
|
A:HIS441
|
4.8
|
17.1
|
1.0
|
O
|
A:HOH6109
|
4.9
|
5.9
|
1.0
|
CE1
|
D:HIS180
|
4.9
|
52.7
|
1.0
|
|
Manganese binding site 2 out
of 48 in 2glj
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Manganese Binding Sites List in 2glj
Manganese binding site 2 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn6002
b:2.0
occ:1.00
|
NE2
|
A:HIS105
|
2.2
|
8.1
|
1.0
|
OD1
|
A:ASP342
|
2.2
|
11.8
|
1.0
|
OD2
|
A:ASP342
|
2.4
|
11.0
|
1.0
|
MN
|
A:MN6001
|
2.5
|
31.6
|
1.0
|
OD1
|
A:ASP265
|
2.5
|
15.1
|
1.0
|
CG
|
A:ASP342
|
2.6
|
13.1
|
1.0
|
CE1
|
A:HIS105
|
3.1
|
6.7
|
1.0
|
OE1
|
A:GLU296
|
3.2
|
12.8
|
1.0
|
CD2
|
A:HIS105
|
3.2
|
8.6
|
1.0
|
OE2
|
A:GLU295
|
3.3
|
40.6
|
1.0
|
OE1
|
A:GLU295
|
3.4
|
38.6
|
1.0
|
CG
|
A:ASP265
|
3.5
|
17.8
|
1.0
|
CD
|
A:GLU295
|
3.6
|
37.8
|
1.0
|
OD2
|
A:ASP265
|
3.7
|
16.4
|
1.0
|
CD
|
A:GLU296
|
3.9
|
15.3
|
1.0
|
O
|
A:HOH6078
|
4.0
|
27.5
|
1.0
|
CB
|
A:ASP266
|
4.1
|
26.9
|
1.0
|
CB
|
A:ASP342
|
4.2
|
16.4
|
1.0
|
ND1
|
A:HIS105
|
4.2
|
8.9
|
1.0
|
CG
|
A:HIS105
|
4.3
|
10.3
|
1.0
|
OE2
|
A:GLU296
|
4.5
|
14.3
|
1.0
|
O
|
A:HOH6108
|
4.5
|
18.5
|
1.0
|
CG2
|
A:VAL343
|
4.6
|
21.4
|
1.0
|
CG
|
A:ASP266
|
4.6
|
30.4
|
1.0
|
CG
|
A:GLU295
|
4.7
|
34.7
|
1.0
|
CG
|
A:GLU296
|
4.8
|
16.4
|
1.0
|
CB
|
A:ASP265
|
4.9
|
17.0
|
1.0
|
N
|
A:ASP266
|
5.0
|
23.6
|
1.0
|
C
|
A:ASP265
|
5.0
|
21.3
|
1.0
|
|
Manganese binding site 3 out
of 48 in 2glj
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Manganese Binding Sites List in 2glj
Manganese binding site 3 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 3 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn6003
b:31.9
occ:1.00
|
OE2
|
B:GLU296
|
2.3
|
12.3
|
1.0
|
OE1
|
B:GLU296
|
2.4
|
11.1
|
1.0
|
CD
|
B:GLU296
|
2.6
|
13.8
|
1.0
|
NE2
|
B:HIS441
|
2.6
|
15.9
|
1.0
|
CE1
|
B:HIS441
|
3.1
|
16.2
|
1.0
|
MN
|
B:MN6004
|
3.2
|
7.9
|
1.0
|
OD2
|
B:ASP265
|
3.3
|
19.8
|
1.0
|
O
|
K:HOH6155
|
3.4
|
0.3
|
1.0
|
CE
|
B:MSE440
|
3.5
|
29.0
|
1.0
|
CD2
|
B:HIS441
|
3.9
|
15.8
|
1.0
|
OE2
|
B:GLU295
|
3.9
|
42.2
|
1.0
|
OE1
|
B:GLU295
|
3.9
|
40.5
|
1.0
|
OD1
|
B:ASP265
|
4.0
|
18.4
|
1.0
|
CG
|
B:ASP265
|
4.1
|
18.5
|
1.0
|
CG
|
B:GLU296
|
4.1
|
15.9
|
1.0
|
NE2
|
K:HIS180
|
4.1
|
52.8
|
1.0
|
O
|
B:HOH6156
|
4.3
|
11.5
|
1.0
|
ND1
|
B:HIS441
|
4.3
|
15.3
|
1.0
|
CD
|
B:GLU295
|
4.4
|
39.1
|
1.0
|
CE1
|
K:HIS180
|
4.4
|
52.7
|
1.0
|
OD1
|
B:ASP342
|
4.5
|
15.2
|
1.0
|
O
|
B:HOH6044
|
4.7
|
0.9
|
1.0
|
CG
|
B:HIS441
|
4.8
|
14.9
|
1.0
|
NE2
|
B:HIS105
|
4.8
|
7.7
|
1.0
|
CB
|
B:GLU296
|
4.9
|
20.2
|
1.0
|
|
Manganese binding site 4 out
of 48 in 2glj
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Manganese Binding Sites List in 2glj
Manganese binding site 4 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 4 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn6004
b:7.9
occ:1.00
|
NE2
|
B:HIS105
|
2.2
|
7.7
|
1.0
|
OD1
|
B:ASP342
|
2.2
|
15.2
|
1.0
|
OD2
|
B:ASP342
|
2.3
|
15.8
|
1.0
|
OD1
|
B:ASP265
|
2.5
|
18.4
|
1.0
|
CG
|
B:ASP342
|
2.6
|
16.7
|
1.0
|
CE1
|
B:HIS105
|
3.1
|
7.5
|
1.0
|
CD2
|
B:HIS105
|
3.2
|
8.2
|
1.0
|
OE1
|
B:GLU296
|
3.2
|
11.1
|
1.0
|
MN
|
B:MN6003
|
3.2
|
31.9
|
1.0
|
CG
|
B:ASP265
|
3.4
|
18.5
|
1.0
|
OE2
|
B:GLU295
|
3.4
|
42.2
|
1.0
|
OE1
|
B:GLU295
|
3.5
|
40.5
|
1.0
|
OD2
|
B:ASP265
|
3.6
|
19.8
|
1.0
|
CD
|
B:GLU295
|
3.7
|
39.1
|
1.0
|
CB
|
B:ASP266
|
3.9
|
26.3
|
1.0
|
CD
|
B:GLU296
|
4.0
|
13.8
|
1.0
|
CB
|
B:ASP342
|
4.1
|
18.1
|
1.0
|
ND1
|
B:HIS105
|
4.2
|
7.7
|
1.0
|
CG
|
B:HIS105
|
4.3
|
8.1
|
1.0
|
OE2
|
B:GLU296
|
4.5
|
12.3
|
1.0
|
CG
|
B:ASP266
|
4.5
|
29.2
|
1.0
|
CG2
|
B:VAL343
|
4.6
|
22.6
|
1.0
|
CG
|
B:GLU295
|
4.8
|
35.0
|
1.0
|
CG
|
B:GLU296
|
4.8
|
15.9
|
1.0
|
CB
|
B:ASP265
|
4.9
|
17.8
|
1.0
|
N
|
B:ASP266
|
4.9
|
18.5
|
1.0
|
C
|
B:ASP265
|
4.9
|
17.6
|
1.0
|
CA
|
B:ASP342
|
4.9
|
19.4
|
1.0
|
OD1
|
B:ASP266
|
5.0
|
32.8
|
1.0
|
|
Manganese binding site 5 out
of 48 in 2glj
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Manganese Binding Sites List in 2glj
Manganese binding site 5 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 5 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn6005
b:44.2
occ:1.00
|
OE2
|
C:GLU296
|
2.3
|
14.2
|
1.0
|
OE1
|
C:GLU296
|
2.4
|
14.8
|
1.0
|
NE2
|
C:HIS441
|
2.6
|
16.8
|
1.0
|
CD
|
C:GLU296
|
2.6
|
16.2
|
1.0
|
MN
|
C:MN6006
|
2.9
|
6.8
|
1.0
|
CE1
|
C:HIS441
|
3.1
|
17.1
|
1.0
|
O
|
C:HOH6127
|
3.2
|
15.9
|
1.0
|
OD2
|
C:ASP265
|
3.3
|
15.3
|
1.0
|
CE
|
C:MSE440
|
3.4
|
30.7
|
1.0
|
CD2
|
C:HIS441
|
3.8
|
15.9
|
1.0
|
OE2
|
C:GLU295
|
3.9
|
42.5
|
1.0
|
OE1
|
C:GLU295
|
4.0
|
42.8
|
1.0
|
OD1
|
C:ASP265
|
4.0
|
15.0
|
1.0
|
CG
|
C:ASP265
|
4.0
|
16.1
|
1.0
|
CG
|
C:GLU296
|
4.1
|
17.7
|
1.0
|
ND1
|
C:HIS441
|
4.3
|
17.0
|
1.0
|
NE2
|
F:HIS180
|
4.4
|
55.6
|
1.0
|
CD
|
C:GLU295
|
4.4
|
37.8
|
1.0
|
O
|
C:HOH6084
|
4.4
|
0.3
|
1.0
|
OD1
|
C:ASP342
|
4.5
|
18.2
|
1.0
|
CE1
|
F:HIS180
|
4.7
|
55.8
|
1.0
|
NE2
|
C:HIS105
|
4.7
|
11.2
|
1.0
|
CG
|
C:HIS441
|
4.7
|
15.6
|
1.0
|
CB
|
C:GLU296
|
5.0
|
18.4
|
1.0
|
|
Manganese binding site 6 out
of 48 in 2glj
Go back to
Manganese Binding Sites List in 2glj
Manganese binding site 6 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 6 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn6006
b:6.8
occ:1.00
|
OD2
|
C:ASP342
|
2.3
|
16.7
|
1.0
|
OD1
|
C:ASP342
|
2.4
|
18.2
|
1.0
|
OD1
|
C:ASP265
|
2.4
|
15.0
|
1.0
|
NE2
|
C:HIS105
|
2.6
|
11.2
|
1.0
|
CG
|
C:ASP342
|
2.7
|
16.3
|
1.0
|
MN
|
C:MN6005
|
2.9
|
44.2
|
1.0
|
O
|
C:HOH6127
|
3.0
|
15.9
|
1.0
|
OE1
|
C:GLU296
|
3.1
|
14.8
|
1.0
|
CG
|
C:ASP265
|
3.2
|
16.1
|
1.0
|
OD2
|
C:ASP265
|
3.3
|
15.3
|
1.0
|
CE1
|
C:HIS105
|
3.4
|
11.6
|
1.0
|
CD2
|
C:HIS105
|
3.6
|
10.6
|
1.0
|
OE2
|
C:GLU295
|
3.7
|
42.5
|
1.0
|
OE1
|
C:GLU295
|
3.7
|
42.8
|
1.0
|
O
|
C:HOH6084
|
3.9
|
0.3
|
1.0
|
CD
|
C:GLU295
|
3.9
|
37.8
|
1.0
|
CD
|
C:GLU296
|
4.0
|
16.2
|
1.0
|
CB
|
C:ASP266
|
4.1
|
27.1
|
1.0
|
CB
|
C:ASP342
|
4.2
|
16.6
|
1.0
|
CG2
|
C:VAL343
|
4.3
|
21.4
|
1.0
|
OE2
|
C:GLU296
|
4.4
|
14.2
|
1.0
|
CE
|
C:MSE440
|
4.6
|
30.7
|
1.0
|
ND1
|
C:HIS105
|
4.6
|
11.0
|
1.0
|
CB
|
C:ASP265
|
4.7
|
16.1
|
1.0
|
CG
|
C:HIS105
|
4.7
|
11.7
|
1.0
|
NE2
|
C:HIS441
|
4.8
|
16.8
|
1.0
|
CG
|
C:ASP266
|
4.8
|
30.6
|
1.0
|
N
|
C:ASP266
|
4.8
|
21.4
|
1.0
|
C
|
C:ASP265
|
4.8
|
19.8
|
1.0
|
N
|
C:VAL343
|
4.9
|
20.4
|
1.0
|
CG
|
C:GLU296
|
4.9
|
17.7
|
1.0
|
|
Manganese binding site 7 out
of 48 in 2glj
Go back to
Manganese Binding Sites List in 2glj
Manganese binding site 7 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 7 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn6007
b:0.3
occ:1.00
|
OE1
|
D:GLU296
|
2.2
|
14.7
|
1.0
|
OE2
|
D:GLU296
|
2.2
|
16.6
|
1.0
|
CD
|
D:GLU296
|
2.5
|
17.7
|
1.0
|
NE2
|
D:HIS441
|
2.5
|
14.7
|
1.0
|
MN
|
D:MN6008
|
3.0
|
16.8
|
1.0
|
CE1
|
D:HIS441
|
3.0
|
16.0
|
1.0
|
OD2
|
D:ASP265
|
3.2
|
15.2
|
1.0
|
O
|
D:HOH6026
|
3.2
|
0.3
|
1.0
|
CE
|
D:MSE440
|
3.5
|
31.8
|
1.0
|
CD2
|
D:HIS441
|
3.8
|
15.9
|
1.0
|
OE2
|
D:GLU295
|
3.9
|
36.7
|
1.0
|
OD1
|
D:ASP265
|
3.9
|
15.8
|
1.0
|
CG
|
D:ASP265
|
3.9
|
15.1
|
1.0
|
OE1
|
D:GLU295
|
4.0
|
37.8
|
1.0
|
CG
|
D:GLU296
|
4.0
|
19.1
|
1.0
|
ND1
|
D:HIS441
|
4.3
|
16.0
|
1.0
|
CD
|
D:GLU295
|
4.4
|
36.2
|
1.0
|
NE2
|
A:HIS180
|
4.4
|
56.7
|
1.0
|
OD1
|
D:ASP342
|
4.6
|
13.6
|
1.0
|
NE2
|
D:HIS105
|
4.7
|
7.7
|
1.0
|
CG
|
D:HIS441
|
4.7
|
15.0
|
1.0
|
CE1
|
A:HIS180
|
4.7
|
56.5
|
1.0
|
CB
|
D:GLU296
|
4.8
|
20.7
|
1.0
|
CE1
|
D:HIS105
|
5.0
|
9.2
|
1.0
|
CA
|
D:GLU296
|
5.0
|
24.1
|
1.0
|
|
Manganese binding site 8 out
of 48 in 2glj
Go back to
Manganese Binding Sites List in 2glj
Manganese binding site 8 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 8 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn6008
b:16.8
occ:1.00
|
OD1
|
D:ASP265
|
2.3
|
15.8
|
1.0
|
OD2
|
D:ASP342
|
2.3
|
12.5
|
1.0
|
OD1
|
D:ASP342
|
2.3
|
13.6
|
1.0
|
NE2
|
D:HIS105
|
2.4
|
7.7
|
1.0
|
CG
|
D:ASP342
|
2.7
|
16.2
|
1.0
|
O
|
D:HOH6026
|
2.9
|
0.3
|
1.0
|
MN
|
D:MN6007
|
3.0
|
0.3
|
1.0
|
OE1
|
D:GLU296
|
3.1
|
14.7
|
1.0
|
CG
|
D:ASP265
|
3.2
|
15.1
|
1.0
|
CE1
|
D:HIS105
|
3.2
|
9.2
|
1.0
|
OD2
|
D:ASP265
|
3.3
|
15.2
|
1.0
|
CD2
|
D:HIS105
|
3.5
|
6.9
|
1.0
|
OE2
|
D:GLU295
|
3.6
|
36.7
|
1.0
|
OE1
|
D:GLU295
|
3.7
|
37.8
|
1.0
|
CD
|
D:GLU295
|
3.9
|
36.2
|
1.0
|
CD
|
D:GLU296
|
4.0
|
17.7
|
1.0
|
CB
|
D:ASP266
|
4.0
|
26.5
|
1.0
|
CB
|
D:ASP342
|
4.2
|
19.0
|
1.0
|
CG2
|
D:VAL343
|
4.3
|
15.5
|
1.0
|
ND1
|
D:HIS105
|
4.4
|
9.6
|
1.0
|
OE2
|
D:GLU296
|
4.5
|
16.6
|
1.0
|
CG
|
D:HIS105
|
4.6
|
8.3
|
1.0
|
CB
|
D:ASP265
|
4.6
|
17.1
|
1.0
|
CG
|
D:ASP266
|
4.7
|
29.6
|
1.0
|
CE
|
D:MSE440
|
4.7
|
31.8
|
1.0
|
N
|
D:ASP266
|
4.7
|
18.1
|
1.0
|
C
|
D:ASP265
|
4.8
|
17.2
|
1.0
|
NE2
|
D:HIS441
|
4.9
|
14.7
|
1.0
|
N
|
D:VAL343
|
4.9
|
20.5
|
1.0
|
CG
|
D:GLU296
|
4.9
|
19.1
|
1.0
|
O
|
D:ASP265
|
4.9
|
19.5
|
1.0
|
CA
|
D:ASP342
|
5.0
|
22.1
|
1.0
|
CA
|
D:ASP266
|
5.0
|
19.4
|
1.0
|
|
Manganese binding site 9 out
of 48 in 2glj
Go back to
Manganese Binding Sites List in 2glj
Manganese binding site 9 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 9 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Mn6009
b:35.9
occ:1.00
|
OE1
|
E:GLU296
|
2.3
|
9.2
|
1.0
|
O
|
E:HOH6203
|
2.4
|
33.8
|
1.0
|
NE2
|
E:HIS441
|
2.6
|
16.7
|
1.0
|
MN
|
E:MN6010
|
2.7
|
13.0
|
1.0
|
OE2
|
E:GLU296
|
2.7
|
12.2
|
1.0
|
CD
|
E:GLU296
|
2.8
|
13.1
|
1.0
|
OD2
|
E:ASP265
|
2.8
|
15.8
|
1.0
|
CE
|
E:MSE440
|
3.3
|
30.8
|
1.0
|
CE1
|
E:HIS441
|
3.3
|
17.3
|
1.0
|
OD1
|
E:ASP265
|
3.5
|
15.7
|
1.0
|
CG
|
E:ASP265
|
3.5
|
17.4
|
1.0
|
CD2
|
E:HIS441
|
3.8
|
16.6
|
1.0
|
O
|
E:HOH6144
|
3.9
|
42.4
|
1.0
|
OE2
|
E:GLU295
|
4.1
|
39.2
|
1.0
|
OE1
|
E:GLU295
|
4.1
|
37.3
|
1.0
|
OD1
|
E:ASP342
|
4.3
|
11.9
|
1.0
|
CG
|
E:GLU296
|
4.3
|
15.2
|
1.0
|
NE2
|
H:HIS180
|
4.3
|
49.5
|
1.0
|
NE2
|
E:HIS105
|
4.5
|
5.6
|
1.0
|
ND1
|
E:HIS441
|
4.5
|
17.3
|
1.0
|
CD
|
E:GLU295
|
4.5
|
37.2
|
1.0
|
OD2
|
E:ASP342
|
4.6
|
12.6
|
1.0
|
CE1
|
H:HIS180
|
4.7
|
50.0
|
1.0
|
CG
|
E:HIS441
|
4.8
|
16.1
|
1.0
|
CE1
|
E:HIS105
|
4.9
|
6.5
|
1.0
|
CG
|
E:ASP342
|
4.9
|
14.3
|
1.0
|
CB
|
E:ASP265
|
5.0
|
16.0
|
1.0
|
|
Manganese binding site 10 out
of 48 in 2glj
Go back to
Manganese Binding Sites List in 2glj
Manganese binding site 10 out
of 48 in the Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 10 of Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Mn6010
b:13.0
occ:1.00
|
OD1
|
E:ASP265
|
2.2
|
15.7
|
1.0
|
NE2
|
E:HIS105
|
2.3
|
5.6
|
1.0
|
OD2
|
E:ASP342
|
2.3
|
12.6
|
1.0
|
OD1
|
E:ASP342
|
2.5
|
11.9
|
1.0
|
MN
|
E:MN6009
|
2.7
|
35.9
|
1.0
|
CG
|
E:ASP342
|
2.7
|
14.3
|
1.0
|
OE1
|
E:GLU296
|
3.0
|
9.2
|
1.0
|
CE1
|
E:HIS105
|
3.1
|
6.5
|
1.0
|
CG
|
E:ASP265
|
3.1
|
17.4
|
1.0
|
OD2
|
E:ASP265
|
3.3
|
15.8
|
1.0
|
CD2
|
E:HIS105
|
3.4
|
6.0
|
1.0
|
OE2
|
E:GLU295
|
3.6
|
39.2
|
1.0
|
O
|
E:HOH6144
|
3.8
|
42.4
|
1.0
|
OE1
|
E:GLU295
|
3.8
|
37.3
|
1.0
|
O
|
E:HOH6203
|
3.9
|
33.8
|
1.0
|
CD
|
E:GLU296
|
3.9
|
13.1
|
1.0
|
CB
|
E:ASP266
|
3.9
|
25.0
|
1.0
|
CD
|
E:GLU295
|
3.9
|
37.2
|
1.0
|
CB
|
E:ASP342
|
4.3
|
16.1
|
1.0
|
ND1
|
E:HIS105
|
4.3
|
7.8
|
1.0
|
CG2
|
E:VAL343
|
4.3
|
21.1
|
1.0
|
OE2
|
E:GLU296
|
4.5
|
12.2
|
1.0
|
CG
|
E:HIS105
|
4.5
|
7.1
|
1.0
|
CB
|
E:ASP265
|
4.5
|
16.0
|
1.0
|
CG
|
E:ASP266
|
4.6
|
28.4
|
1.0
|
C
|
E:ASP265
|
4.7
|
19.2
|
1.0
|
N
|
E:ASP266
|
4.7
|
21.2
|
1.0
|
O
|
E:ASP265
|
4.8
|
17.5
|
1.0
|
CG
|
E:GLU296
|
4.8
|
15.2
|
1.0
|
CE
|
E:MSE440
|
4.8
|
30.8
|
1.0
|
NE2
|
E:HIS441
|
4.8
|
16.7
|
1.0
|
CA
|
E:ASP266
|
4.9
|
21.6
|
1.0
|
N
|
E:VAL343
|
4.9
|
20.5
|
1.0
|
|
Reference:
T.Min,
L.Shapiro.
Crystal Structure of Aminopeptidase I From Clostridium Acetobutylicum To Be Published.
Page generated: Sat Oct 5 14:11:02 2024
|