Manganese in PDB 6l9i: Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
Protein crystallography data
The structure of Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex, PDB code: 6l9i
was solved by
F.Wu,
L.K.Cheng,
C.Y.Wang,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
48.00 /
2.79
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
92.957,
122.842,
115.223,
90,
92.48,
90
|
R / Rfree (%)
|
19.7 /
22.9
|
Manganese Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
12;
Binding sites:
The binding sites of Manganese atom in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
(pdb code 6l9i). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 12 binding sites of Manganese where determined in the
Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex, PDB code: 6l9i:
Jump to Manganese binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Manganese binding site 1 out
of 12 in 6l9i
Go back to
Manganese Binding Sites List in 6l9i
Manganese binding site 1 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn402
b:31.0
occ:1.00
|
OE2
|
A:GLU101
|
1.7
|
35.7
|
1.0
|
O1
|
A:FMT401
|
2.0
|
31.1
|
1.0
|
C
|
A:FMT401
|
2.2
|
41.7
|
1.0
|
NE2
|
A:HIS140
|
2.3
|
15.5
|
1.0
|
NE2
|
A:HIS95
|
2.3
|
29.3
|
1.0
|
NE2
|
A:HIS97
|
2.6
|
29.5
|
1.0
|
CD
|
A:GLU101
|
2.9
|
32.2
|
1.0
|
CE1
|
A:HIS140
|
3.2
|
17.4
|
1.0
|
CE1
|
A:HIS95
|
3.2
|
23.9
|
1.0
|
CD2
|
A:HIS140
|
3.3
|
16.1
|
1.0
|
CD2
|
A:HIS95
|
3.3
|
20.8
|
1.0
|
O2
|
A:FMT401
|
3.3
|
41.7
|
1.0
|
CD2
|
A:HIS97
|
3.5
|
17.7
|
1.0
|
OE1
|
A:GLU101
|
3.6
|
33.8
|
1.0
|
CE1
|
A:HIS97
|
3.6
|
37.9
|
1.0
|
CG
|
A:GLU101
|
4.1
|
25.1
|
1.0
|
ND1
|
A:HIS140
|
4.3
|
18.1
|
1.0
|
ND1
|
A:HIS95
|
4.4
|
25.0
|
1.0
|
CG
|
A:HIS140
|
4.4
|
19.6
|
1.0
|
CE2
|
A:PHE155
|
4.4
|
24.7
|
1.0
|
CG
|
A:HIS95
|
4.4
|
23.9
|
1.0
|
CZ
|
A:PHE155
|
4.6
|
27.1
|
1.0
|
CG
|
A:HIS97
|
4.7
|
22.3
|
1.0
|
ND1
|
A:HIS97
|
4.7
|
39.0
|
1.0
|
CB
|
A:GLU101
|
4.7
|
24.3
|
1.0
|
OE2
|
A:GLU162
|
4.8
|
34.6
|
1.0
|
|
Manganese binding site 2 out
of 12 in 6l9i
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Manganese Binding Sites List in 6l9i
Manganese binding site 2 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn403
b:32.8
occ:1.00
|
NE2
|
A:HIS273
|
2.2
|
37.7
|
1.0
|
NE2
|
A:HIS275
|
2.2
|
27.6
|
1.0
|
NE2
|
A:HIS319
|
2.4
|
34.1
|
1.0
|
OE1
|
A:GLU280
|
2.4
|
37.4
|
1.0
|
OE2
|
A:GLU333
|
2.9
|
53.0
|
1.0
|
CE1
|
A:HIS273
|
3.1
|
33.6
|
1.0
|
CE1
|
A:HIS275
|
3.2
|
24.8
|
1.0
|
CD2
|
A:HIS275
|
3.2
|
22.6
|
1.0
|
CD
|
A:GLU280
|
3.2
|
34.6
|
1.0
|
CD2
|
A:HIS273
|
3.3
|
30.0
|
1.0
|
CD2
|
A:HIS319
|
3.3
|
28.2
|
1.0
|
CE1
|
A:HIS319
|
3.3
|
28.9
|
1.0
|
CD
|
A:GLU333
|
3.4
|
44.3
|
1.0
|
OE2
|
A:GLU280
|
3.4
|
32.2
|
1.0
|
OE1
|
A:GLU333
|
3.5
|
46.9
|
1.0
|
NH2
|
A:ARG270
|
4.2
|
47.8
|
1.0
|
ND1
|
A:HIS273
|
4.2
|
28.5
|
1.0
|
ND1
|
A:HIS275
|
4.3
|
23.2
|
1.0
|
CG
|
A:HIS273
|
4.3
|
27.8
|
1.0
|
CG
|
A:HIS275
|
4.3
|
21.1
|
1.0
|
CG
|
A:HIS319
|
4.4
|
27.6
|
1.0
|
ND1
|
A:HIS319
|
4.4
|
24.1
|
1.0
|
CG
|
A:GLU333
|
4.5
|
27.5
|
1.0
|
CZ
|
A:ARG270
|
4.6
|
54.8
|
1.0
|
CG
|
A:GLU280
|
4.6
|
20.6
|
1.0
|
NE
|
A:ARG270
|
4.8
|
50.8
|
1.0
|
CD1
|
A:ILE321
|
4.9
|
33.8
|
1.0
|
|
Manganese binding site 3 out
of 12 in 6l9i
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Manganese Binding Sites List in 6l9i
Manganese binding site 3 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn402
b:23.9
occ:1.00
|
OE2
|
B:GLU101
|
1.6
|
28.5
|
1.0
|
NE2
|
B:HIS95
|
2.1
|
26.9
|
1.0
|
NE2
|
B:HIS140
|
2.3
|
17.6
|
1.0
|
C
|
B:FMT401
|
2.4
|
35.5
|
1.0
|
O1
|
B:FMT401
|
2.6
|
18.9
|
1.0
|
NE2
|
B:HIS97
|
2.7
|
22.1
|
1.0
|
CD
|
B:GLU101
|
2.9
|
28.2
|
1.0
|
CE1
|
B:HIS95
|
2.9
|
24.9
|
1.0
|
CD2
|
B:HIS95
|
3.1
|
18.4
|
1.0
|
CE1
|
B:HIS140
|
3.2
|
18.1
|
1.0
|
CD2
|
B:HIS140
|
3.4
|
17.2
|
1.0
|
CD2
|
B:HIS97
|
3.4
|
13.0
|
1.0
|
O2
|
B:FMT401
|
3.6
|
33.7
|
1.0
|
OE1
|
B:GLU101
|
3.7
|
25.9
|
1.0
|
CG
|
B:GLU101
|
3.8
|
24.3
|
1.0
|
CE1
|
B:HIS97
|
3.8
|
30.7
|
1.0
|
ND1
|
B:HIS95
|
4.1
|
20.0
|
1.0
|
CG
|
B:HIS95
|
4.2
|
19.6
|
1.0
|
ND1
|
B:HIS140
|
4.4
|
17.9
|
1.0
|
CG
|
B:HIS140
|
4.5
|
19.6
|
1.0
|
CE1
|
B:PHE155
|
4.5
|
19.9
|
1.0
|
CZ
|
B:PHE155
|
4.6
|
22.2
|
1.0
|
CG
|
B:HIS97
|
4.6
|
21.1
|
1.0
|
ND1
|
B:HIS97
|
4.8
|
34.7
|
1.0
|
CB
|
B:GLU101
|
4.9
|
24.6
|
1.0
|
|
Manganese binding site 4 out
of 12 in 6l9i
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Manganese Binding Sites List in 6l9i
Manganese binding site 4 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn403
b:36.5
occ:1.00
|
NE2
|
B:HIS275
|
2.2
|
24.6
|
1.0
|
OE1
|
B:GLU280
|
2.2
|
31.3
|
1.0
|
NE2
|
B:HIS273
|
2.4
|
22.2
|
1.0
|
NE2
|
B:HIS319
|
2.5
|
20.4
|
1.0
|
OE2
|
B:GLU333
|
2.7
|
47.4
|
1.0
|
CD
|
B:GLU280
|
3.0
|
30.2
|
1.0
|
CD2
|
B:HIS275
|
3.1
|
23.6
|
1.0
|
OE2
|
B:GLU280
|
3.1
|
25.7
|
1.0
|
CE1
|
B:HIS275
|
3.2
|
27.3
|
1.0
|
CE1
|
B:HIS273
|
3.2
|
26.0
|
1.0
|
CE1
|
B:HIS319
|
3.4
|
18.2
|
1.0
|
CD2
|
B:HIS273
|
3.4
|
25.2
|
1.0
|
CD
|
B:GLU333
|
3.5
|
46.7
|
1.0
|
CD2
|
B:HIS319
|
3.5
|
19.8
|
1.0
|
OE1
|
B:GLU333
|
3.9
|
37.9
|
1.0
|
CG
|
B:HIS275
|
4.2
|
24.4
|
1.0
|
ND1
|
B:HIS275
|
4.3
|
27.4
|
1.0
|
ND1
|
B:HIS273
|
4.4
|
26.5
|
1.0
|
CG
|
B:GLU280
|
4.4
|
21.4
|
1.0
|
CG
|
B:HIS273
|
4.5
|
26.1
|
1.0
|
ND1
|
B:HIS319
|
4.5
|
16.6
|
1.0
|
CG
|
B:GLU333
|
4.5
|
27.9
|
1.0
|
CG
|
B:HIS319
|
4.6
|
19.4
|
1.0
|
NH2
|
B:ARG270
|
4.7
|
49.5
|
1.0
|
CB
|
B:GLU280
|
4.9
|
21.2
|
1.0
|
|
Manganese binding site 5 out
of 12 in 6l9i
Go back to
Manganese Binding Sites List in 6l9i
Manganese binding site 5 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn402
b:41.2
occ:1.00
|
NE2
|
C:HIS95
|
1.9
|
43.0
|
1.0
|
OE2
|
C:GLU101
|
2.0
|
43.3
|
1.0
|
NE2
|
C:HIS140
|
2.2
|
35.1
|
1.0
|
O1
|
C:FMT401
|
2.3
|
46.2
|
1.0
|
CE1
|
C:HIS97
|
2.6
|
35.3
|
1.0
|
CD2
|
C:HIS95
|
2.7
|
27.9
|
1.0
|
CE1
|
C:HIS140
|
3.0
|
32.5
|
1.0
|
CE1
|
C:HIS95
|
3.0
|
34.7
|
1.0
|
C
|
C:FMT401
|
3.0
|
50.9
|
1.0
|
CD
|
C:GLU101
|
3.3
|
44.1
|
1.0
|
ND1
|
C:HIS97
|
3.3
|
31.2
|
1.0
|
CD2
|
C:HIS140
|
3.3
|
38.1
|
1.0
|
NE2
|
C:HIS97
|
3.8
|
42.6
|
1.0
|
CG
|
C:HIS95
|
3.9
|
30.9
|
1.0
|
ND1
|
C:HIS95
|
4.0
|
29.8
|
1.0
|
OE1
|
C:GLU101
|
4.1
|
52.2
|
1.0
|
ND1
|
C:HIS140
|
4.1
|
34.9
|
1.0
|
CG
|
C:GLU101
|
4.2
|
35.6
|
1.0
|
O2
|
C:FMT401
|
4.2
|
50.9
|
1.0
|
CG
|
C:HIS140
|
4.4
|
33.4
|
1.0
|
CG
|
C:HIS97
|
4.6
|
29.8
|
1.0
|
CE2
|
C:PHE155
|
4.6
|
35.6
|
1.0
|
CZ
|
C:PHE155
|
4.7
|
33.1
|
1.0
|
CD2
|
C:HIS97
|
4.8
|
36.6
|
1.0
|
OE1
|
C:GLU162
|
4.9
|
44.7
|
1.0
|
CB
|
C:GLU101
|
4.9
|
36.3
|
1.0
|
|
Manganese binding site 6 out
of 12 in 6l9i
Go back to
Manganese Binding Sites List in 6l9i
Manganese binding site 6 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn403
b:39.1
occ:1.00
|
NE2
|
C:HIS319
|
2.1
|
32.2
|
1.0
|
NE2
|
C:HIS275
|
2.1
|
35.7
|
1.0
|
OE2
|
C:GLU333
|
2.2
|
40.2
|
1.0
|
OE1
|
C:GLU280
|
2.2
|
41.5
|
1.0
|
NE2
|
C:HIS273
|
2.3
|
32.8
|
1.0
|
CE1
|
C:HIS273
|
2.9
|
28.5
|
1.0
|
CE1
|
C:HIS319
|
2.9
|
27.4
|
1.0
|
CD2
|
C:HIS275
|
3.1
|
30.3
|
1.0
|
CE1
|
C:HIS275
|
3.1
|
32.2
|
1.0
|
CD
|
C:GLU280
|
3.2
|
36.7
|
1.0
|
CD2
|
C:HIS319
|
3.2
|
32.1
|
1.0
|
OE2
|
C:GLU280
|
3.4
|
29.8
|
1.0
|
CD
|
C:GLU333
|
3.4
|
41.8
|
1.0
|
CD2
|
C:HIS273
|
3.5
|
29.4
|
1.0
|
OE1
|
C:GLU333
|
4.0
|
41.3
|
1.0
|
ND1
|
C:HIS273
|
4.1
|
22.9
|
1.0
|
ND1
|
C:HIS319
|
4.1
|
31.0
|
1.0
|
ND1
|
C:HIS275
|
4.2
|
23.0
|
1.0
|
CG
|
C:HIS275
|
4.3
|
19.6
|
1.0
|
CG
|
C:HIS319
|
4.3
|
28.6
|
1.0
|
CG
|
C:HIS273
|
4.4
|
28.5
|
1.0
|
CG
|
C:GLU333
|
4.5
|
32.6
|
1.0
|
NH2
|
C:ARG270
|
4.6
|
41.2
|
1.0
|
CG
|
C:GLU280
|
4.6
|
29.7
|
1.0
|
CD1
|
C:ILE321
|
4.9
|
31.5
|
1.0
|
CZ
|
C:ARG270
|
4.9
|
45.2
|
1.0
|
CB
|
C:GLU333
|
5.0
|
27.5
|
1.0
|
|
Manganese binding site 7 out
of 12 in 6l9i
Go back to
Manganese Binding Sites List in 6l9i
Manganese binding site 7 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn402
b:28.5
occ:1.00
|
OE2
|
D:GLU101
|
1.8
|
32.1
|
1.0
|
NE2
|
D:HIS95
|
2.0
|
26.0
|
1.0
|
O1
|
D:FMT401
|
2.3
|
40.2
|
1.0
|
NE2
|
D:HIS140
|
2.3
|
25.6
|
1.0
|
NE2
|
D:HIS97
|
2.6
|
35.7
|
1.0
|
CE1
|
D:HIS95
|
2.9
|
27.3
|
1.0
|
CD2
|
D:HIS95
|
3.0
|
22.3
|
1.0
|
C
|
D:FMT401
|
3.0
|
46.7
|
1.0
|
CD
|
D:GLU101
|
3.0
|
31.0
|
1.0
|
CE1
|
D:HIS140
|
3.2
|
23.2
|
1.0
|
CD2
|
D:HIS97
|
3.3
|
31.7
|
1.0
|
CD2
|
D:HIS140
|
3.4
|
29.8
|
1.0
|
OE1
|
D:GLU101
|
3.7
|
28.1
|
1.0
|
CE1
|
D:HIS97
|
3.8
|
55.5
|
1.0
|
ND1
|
D:HIS95
|
4.0
|
27.4
|
1.0
|
CG
|
D:GLU101
|
4.1
|
30.2
|
1.0
|
CG
|
D:HIS95
|
4.1
|
20.8
|
1.0
|
O2
|
D:FMT401
|
4.2
|
46.6
|
1.0
|
ND1
|
D:HIS140
|
4.4
|
26.0
|
1.0
|
CG
|
D:HIS140
|
4.5
|
28.1
|
1.0
|
CE2
|
D:PHE155
|
4.5
|
25.1
|
1.0
|
CG
|
D:HIS97
|
4.5
|
30.7
|
1.0
|
CZ
|
D:PHE155
|
4.6
|
28.4
|
1.0
|
ND1
|
D:HIS97
|
4.8
|
54.9
|
1.0
|
CB
|
D:GLU101
|
4.9
|
25.4
|
1.0
|
|
Manganese binding site 8 out
of 12 in 6l9i
Go back to
Manganese Binding Sites List in 6l9i
Manganese binding site 8 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn403
b:44.0
occ:1.00
|
NE2
|
D:HIS319
|
2.2
|
36.0
|
1.0
|
OE1
|
D:GLU280
|
2.2
|
41.4
|
1.0
|
NE2
|
D:HIS275
|
2.3
|
33.9
|
1.0
|
NE2
|
D:HIS273
|
2.4
|
38.7
|
1.0
|
OE2
|
D:GLU333
|
2.9
|
50.3
|
1.0
|
CD
|
D:GLU280
|
3.0
|
39.9
|
1.0
|
CE1
|
D:HIS273
|
3.1
|
39.2
|
1.0
|
CE1
|
D:HIS319
|
3.1
|
35.7
|
1.0
|
CD2
|
D:HIS275
|
3.2
|
38.7
|
1.0
|
CD2
|
D:HIS319
|
3.2
|
35.0
|
1.0
|
OE2
|
D:GLU280
|
3.2
|
38.9
|
1.0
|
CE1
|
D:HIS275
|
3.3
|
31.6
|
1.0
|
CD
|
D:GLU333
|
3.4
|
47.6
|
1.0
|
CD2
|
D:HIS273
|
3.5
|
42.0
|
1.0
|
OE1
|
D:GLU333
|
3.6
|
43.3
|
1.0
|
NH2
|
D:ARG270
|
4.1
|
46.6
|
1.0
|
ND1
|
D:HIS319
|
4.2
|
35.7
|
1.0
|
ND1
|
D:HIS273
|
4.2
|
40.2
|
1.0
|
CG
|
D:GLU280
|
4.3
|
32.0
|
1.0
|
CG
|
D:HIS319
|
4.3
|
36.2
|
1.0
|
CG
|
D:HIS275
|
4.3
|
34.9
|
1.0
|
ND1
|
D:HIS275
|
4.4
|
33.7
|
1.0
|
CG
|
D:HIS273
|
4.5
|
38.6
|
1.0
|
CG
|
D:GLU333
|
4.6
|
36.7
|
1.0
|
CZ
|
D:ARG270
|
4.7
|
59.8
|
1.0
|
NE
|
D:ARG270
|
4.9
|
55.3
|
1.0
|
CB
|
D:GLU280
|
4.9
|
29.0
|
1.0
|
CB
|
D:GLU333
|
5.0
|
32.7
|
1.0
|
|
Manganese binding site 9 out
of 12 in 6l9i
Go back to
Manganese Binding Sites List in 6l9i
Manganese binding site 9 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Mn402
b:28.8
occ:1.00
|
OE2
|
E:GLU101
|
1.7
|
29.9
|
1.0
|
O1
|
E:FMT401
|
2.0
|
66.0
|
1.0
|
NE2
|
E:HIS95
|
2.1
|
27.9
|
1.0
|
NE2
|
E:HIS140
|
2.2
|
30.8
|
1.0
|
NE2
|
E:HIS97
|
2.3
|
29.9
|
1.0
|
CE1
|
E:HIS95
|
2.9
|
28.0
|
1.0
|
CE1
|
E:HIS140
|
2.9
|
27.0
|
1.0
|
C
|
E:FMT401
|
2.9
|
74.2
|
1.0
|
CD
|
E:GLU101
|
3.0
|
25.8
|
1.0
|
CD2
|
E:HIS95
|
3.1
|
24.5
|
1.0
|
CE1
|
E:HIS97
|
3.2
|
27.5
|
1.0
|
CD2
|
E:HIS97
|
3.3
|
23.3
|
1.0
|
CD2
|
E:HIS140
|
3.4
|
30.7
|
1.0
|
CG
|
E:GLU101
|
3.8
|
28.3
|
1.0
|
OE1
|
E:GLU101
|
3.9
|
27.9
|
1.0
|
O2
|
E:FMT401
|
3.9
|
68.8
|
1.0
|
ND1
|
E:HIS95
|
4.1
|
25.3
|
1.0
|
ND1
|
E:HIS140
|
4.2
|
32.0
|
1.0
|
CG
|
E:HIS95
|
4.2
|
23.9
|
1.0
|
ND1
|
E:HIS97
|
4.4
|
30.0
|
1.0
|
CG
|
E:HIS140
|
4.4
|
31.1
|
1.0
|
CG
|
E:HIS97
|
4.4
|
28.2
|
1.0
|
CE2
|
E:PHE155
|
4.5
|
21.3
|
1.0
|
CZ
|
E:PHE155
|
4.5
|
27.9
|
1.0
|
CB
|
E:GLU101
|
4.9
|
29.2
|
1.0
|
|
Manganese binding site 10 out
of 12 in 6l9i
Go back to
Manganese Binding Sites List in 6l9i
Manganese binding site 10 out
of 12 in the Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex
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 Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Mn403
b:49.8
occ:1.00
|
NE2
|
E:HIS275
|
2.1
|
35.2
|
1.0
|
NE2
|
E:HIS273
|
2.4
|
34.5
|
1.0
|
NE2
|
E:HIS319
|
2.5
|
35.7
|
1.0
|
OE2
|
E:GLU333
|
2.6
|
55.0
|
1.0
|
OE1
|
E:GLU280
|
2.6
|
43.5
|
1.0
|
CD2
|
E:HIS275
|
3.0
|
30.7
|
1.0
|
CE1
|
E:HIS273
|
3.1
|
38.1
|
1.0
|
CD
|
E:GLU280
|
3.1
|
41.3
|
1.0
|
CE1
|
E:HIS275
|
3.1
|
31.1
|
1.0
|
OE2
|
E:GLU280
|
3.1
|
38.6
|
1.0
|
CD
|
E:GLU333
|
3.4
|
47.6
|
1.0
|
CE1
|
E:HIS319
|
3.4
|
35.2
|
1.0
|
CD2
|
E:HIS319
|
3.5
|
28.7
|
1.0
|
CD2
|
E:HIS273
|
3.5
|
40.0
|
1.0
|
OE1
|
E:GLU333
|
3.8
|
44.5
|
1.0
|
CG
|
E:HIS275
|
4.2
|
27.7
|
1.0
|
ND1
|
E:HIS275
|
4.2
|
28.4
|
1.0
|
ND1
|
E:HIS273
|
4.3
|
38.3
|
1.0
|
CG
|
E:GLU280
|
4.4
|
31.4
|
1.0
|
NH2
|
E:ARG270
|
4.4
|
59.0
|
1.0
|
CG
|
E:GLU333
|
4.4
|
37.3
|
1.0
|
CG
|
E:HIS273
|
4.5
|
39.7
|
1.0
|
ND1
|
E:HIS319
|
4.6
|
30.5
|
1.0
|
CG
|
E:HIS319
|
4.7
|
31.5
|
1.0
|
CZ
|
E:ARG270
|
4.8
|
62.2
|
1.0
|
CZ
|
E:PHE335
|
4.9
|
27.2
|
1.0
|
CB
|
E:GLU333
|
4.9
|
33.2
|
1.0
|
|
Reference:
F.Wu,
L.K.Cheng,
C.Y.Wang.
Crystal Structure of Lactobacillus Farciminis Oxalate Decarboxylase Formate Complex To Be Published.
Page generated: Sun Oct 6 05:22:23 2024
|