Manganese in PDB 1de6: L-Rhamnose Isomerase
Enzymatic activity of L-Rhamnose Isomerase
All present enzymatic activity of L-Rhamnose Isomerase:
5.3.1.14;
Protein crystallography data
The structure of L-Rhamnose Isomerase, PDB code: 1de6
was solved by
I.P.Korndorfer,
W.D.Fessner,
B.W.Matthews,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
30.00 /
2.10
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
169.179,
162.439,
77.726,
90.00,
109.89,
90.00
|
R / Rfree (%)
|
n/a /
n/a
|
Other elements in 1de6:
The structure of L-Rhamnose Isomerase also contains other interesting chemical elements:
Manganese Binding Sites:
The binding sites of Manganese atom in the L-Rhamnose Isomerase
(pdb code 1de6). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 4 binding sites of Manganese where determined in the
L-Rhamnose Isomerase, PDB code: 1de6:
Jump to Manganese binding site number:
1;
2;
3;
4;
Manganese binding site 1 out
of 4 in 1de6
Go back to
Manganese Binding Sites List in 1de6
Manganese binding site 1 out
of 4 in the L-Rhamnose Isomerase
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of L-Rhamnose Isomerase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn451
b:59.0
occ:1.00
|
OD1
|
A:ASP302
|
2.3
|
38.5
|
1.0
|
O2
|
A:RNS1462
|
2.4
|
30.5
|
0.6
|
OD2
|
A:ASP302
|
2.6
|
44.9
|
1.0
|
NE2
|
A:HIS270
|
2.7
|
24.2
|
1.0
|
CG
|
A:ASP302
|
2.8
|
34.4
|
1.0
|
OD1
|
A:ASP304
|
3.0
|
54.4
|
1.0
|
OD2
|
A:ASP304
|
3.2
|
30.2
|
1.0
|
CD2
|
A:HIS270
|
3.3
|
19.5
|
1.0
|
CG
|
A:ASP304
|
3.5
|
35.6
|
1.0
|
C2
|
A:RNS1462
|
3.8
|
21.1
|
0.6
|
O4
|
A:RNS1462
|
3.8
|
36.3
|
0.6
|
CE1
|
A:HIS270
|
3.8
|
28.5
|
1.0
|
O1
|
A:RNS1462
|
3.9
|
27.8
|
0.6
|
OD1
|
A:ASP267
|
4.1
|
33.6
|
1.0
|
OD2
|
A:ASP334
|
4.1
|
24.7
|
1.0
|
OD2
|
A:ASP267
|
4.1
|
26.7
|
1.0
|
O
|
A:HOH1517
|
4.2
|
22.1
|
1.0
|
C1
|
A:RNS1462
|
4.2
|
19.6
|
0.6
|
CB
|
A:ASP302
|
4.3
|
22.0
|
1.0
|
CG
|
A:ASP267
|
4.3
|
18.9
|
1.0
|
CG
|
A:ASP334
|
4.3
|
25.2
|
1.0
|
OD1
|
A:ASP334
|
4.5
|
34.5
|
1.0
|
CG
|
A:HIS270
|
4.6
|
25.4
|
1.0
|
CZ
|
A:PHE336
|
4.6
|
80.3
|
1.0
|
OG
|
A:SER296
|
4.6
|
23.8
|
1.0
|
C3
|
A:RNS1462
|
4.7
|
17.3
|
0.6
|
ZN
|
A:ZN450
|
4.7
|
36.9
|
1.0
|
O
|
A:ASP302
|
4.7
|
31.7
|
1.0
|
O
|
A:ASP334
|
4.8
|
34.8
|
1.0
|
ND1
|
A:HIS270
|
4.8
|
35.3
|
1.0
|
NZ
|
A:LYS236
|
4.8
|
36.4
|
1.0
|
C4
|
A:RNS1462
|
4.8
|
10.0
|
0.6
|
CE
|
A:LYS236
|
4.9
|
21.9
|
1.0
|
|
Manganese binding site 2 out
of 4 in 1de6
Go back to
Manganese Binding Sites List in 1de6
Manganese binding site 2 out
of 4 in the L-Rhamnose Isomerase
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of L-Rhamnose Isomerase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn451
b:53.5
occ:1.00
|
OD1
|
B:ASP302
|
2.0
|
37.3
|
1.0
|
OD1
|
B:ASP304
|
2.4
|
50.4
|
1.0
|
OD2
|
B:ASP302
|
2.6
|
44.6
|
1.0
|
CG
|
B:ASP302
|
2.6
|
33.4
|
1.0
|
OD2
|
B:ASP304
|
2.9
|
26.4
|
1.0
|
NE2
|
B:HIS270
|
3.0
|
22.2
|
1.0
|
CG
|
B:ASP304
|
3.0
|
31.4
|
1.0
|
O1
|
B:RNS2462
|
3.1
|
39.9
|
0.5
|
CD2
|
B:HIS270
|
3.4
|
18.4
|
1.0
|
O2
|
B:RNS2462
|
3.5
|
40.8
|
0.5
|
O
|
B:HOH2533
|
4.0
|
21.2
|
1.0
|
CB
|
B:ASP302
|
4.1
|
22.7
|
1.0
|
O4
|
B:RNS2462
|
4.1
|
56.0
|
0.5
|
C1
|
B:RNS2462
|
4.1
|
29.0
|
0.5
|
CE1
|
B:HIS270
|
4.2
|
25.7
|
1.0
|
OD2
|
B:ASP267
|
4.3
|
22.6
|
1.0
|
O
|
B:ASP302
|
4.4
|
31.6
|
1.0
|
C2
|
B:RNS2462
|
4.4
|
22.4
|
0.5
|
OG
|
B:SER296
|
4.4
|
24.4
|
1.0
|
OD1
|
B:ASP267
|
4.5
|
32.1
|
1.0
|
CB
|
B:ASP304
|
4.5
|
20.7
|
1.0
|
CG
|
B:ASP267
|
4.6
|
16.4
|
1.0
|
CZ
|
B:PHE336
|
4.7
|
79.2
|
1.0
|
OD2
|
B:ASP334
|
4.7
|
21.5
|
1.0
|
C
|
B:ASP302
|
4.8
|
27.6
|
1.0
|
O
|
B:ASP334
|
4.8
|
29.9
|
1.0
|
CG
|
B:HIS270
|
4.8
|
26.8
|
1.0
|
CG
|
B:ASP334
|
4.8
|
25.0
|
1.0
|
CA
|
B:ASP302
|
4.8
|
26.2
|
1.0
|
N
|
B:ASP304
|
4.9
|
26.4
|
1.0
|
NZ
|
B:LYS236
|
4.9
|
36.3
|
1.0
|
O
|
B:HOH2505
|
4.9
|
41.4
|
1.0
|
OD1
|
B:ASP334
|
4.9
|
28.5
|
1.0
|
CA
|
B:ASP304
|
4.9
|
19.6
|
1.0
|
|
Manganese binding site 3 out
of 4 in 1de6
Go back to
Manganese Binding Sites List in 1de6
Manganese binding site 3 out
of 4 in the L-Rhamnose Isomerase
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 3 of L-Rhamnose Isomerase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn451
b:51.4
occ:1.00
|
OD1
|
C:ASP302
|
2.2
|
38.0
|
1.0
|
OD2
|
C:ASP302
|
2.4
|
42.8
|
1.0
|
CG
|
C:ASP302
|
2.7
|
31.1
|
1.0
|
NE2
|
C:HIS270
|
2.7
|
25.3
|
1.0
|
OD1
|
C:ASP304
|
2.9
|
51.2
|
1.0
|
O2
|
C:RNS3462
|
3.1
|
38.6
|
0.5
|
O1
|
C:RNS3462
|
3.1
|
26.9
|
0.5
|
OD2
|
C:ASP304
|
3.2
|
29.0
|
1.0
|
CD2
|
C:HIS270
|
3.3
|
17.7
|
1.0
|
CG
|
C:ASP304
|
3.4
|
31.7
|
1.0
|
CE1
|
C:HIS270
|
3.9
|
27.0
|
1.0
|
C1
|
C:RNS3462
|
3.9
|
14.0
|
0.5
|
O4
|
C:RNS3462
|
3.9
|
45.7
|
0.5
|
C2
|
C:RNS3462
|
4.1
|
21.6
|
0.5
|
OD2
|
C:ASP267
|
4.1
|
22.1
|
1.0
|
CB
|
C:ASP302
|
4.2
|
24.6
|
1.0
|
OD2
|
C:ASP334
|
4.3
|
23.6
|
1.0
|
OD1
|
C:ASP267
|
4.3
|
35.5
|
1.0
|
O
|
C:HOH3532
|
4.3
|
22.0
|
1.0
|
CG
|
C:ASP267
|
4.5
|
17.2
|
1.0
|
CZ
|
C:PHE336
|
4.6
|
78.5
|
1.0
|
CG
|
C:HIS270
|
4.6
|
25.6
|
1.0
|
CG
|
C:ASP334
|
4.6
|
23.5
|
1.0
|
OG
|
C:SER296
|
4.7
|
21.6
|
1.0
|
O
|
C:ASP302
|
4.7
|
33.2
|
1.0
|
O
|
C:ASP334
|
4.7
|
32.1
|
1.0
|
OD1
|
C:ASP334
|
4.8
|
31.4
|
1.0
|
NZ
|
C:LYS236
|
4.8
|
36.8
|
1.0
|
CE
|
C:LYS236
|
4.9
|
20.1
|
1.0
|
ND1
|
C:HIS270
|
4.9
|
36.1
|
1.0
|
CB
|
C:ASP304
|
4.9
|
18.2
|
1.0
|
ZN
|
C:ZN450
|
4.9
|
36.6
|
1.0
|
|
Manganese binding site 4 out
of 4 in 1de6
Go back to
Manganese Binding Sites List in 1de6
Manganese binding site 4 out
of 4 in the L-Rhamnose Isomerase
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 4 of L-Rhamnose Isomerase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn451
b:61.0
occ:1.00
|
OD1
|
D:ASP302
|
2.4
|
40.7
|
1.0
|
OD2
|
D:ASP302
|
2.4
|
45.5
|
1.0
|
CG
|
D:ASP302
|
2.7
|
37.0
|
1.0
|
NE2
|
D:HIS270
|
2.8
|
24.6
|
1.0
|
O2
|
D:RNS4462
|
2.9
|
29.2
|
0.5
|
O1
|
D:RNS4462
|
3.0
|
30.8
|
0.5
|
OD1
|
D:ASP304
|
3.0
|
54.9
|
1.0
|
OD2
|
D:ASP304
|
3.2
|
31.1
|
1.0
|
CD2
|
D:HIS270
|
3.4
|
22.1
|
1.0
|
CG
|
D:ASP304
|
3.5
|
35.9
|
1.0
|
O4
|
D:RNS4462
|
3.6
|
37.6
|
0.5
|
C1
|
D:RNS4462
|
3.7
|
23.2
|
0.5
|
C2
|
D:RNS4462
|
3.9
|
20.7
|
0.5
|
CE1
|
D:HIS270
|
4.0
|
29.9
|
1.0
|
OD2
|
D:ASP334
|
4.2
|
29.0
|
1.0
|
OD2
|
D:ASP267
|
4.2
|
25.2
|
1.0
|
CB
|
D:ASP302
|
4.3
|
26.4
|
1.0
|
OD1
|
D:ASP267
|
4.3
|
36.1
|
1.0
|
O
|
D:HOH4546
|
4.4
|
21.0
|
1.0
|
CG
|
D:ASP267
|
4.4
|
19.5
|
1.0
|
CG
|
D:ASP334
|
4.5
|
27.5
|
1.0
|
OD1
|
D:ASP334
|
4.6
|
34.7
|
1.0
|
O
|
D:ASP302
|
4.6
|
34.8
|
1.0
|
CZ
|
D:PHE336
|
4.6
|
82.2
|
1.0
|
CG
|
D:HIS270
|
4.7
|
28.4
|
1.0
|
OG
|
D:SER296
|
4.7
|
26.8
|
1.0
|
ZN
|
D:ZN450
|
4.7
|
41.8
|
1.0
|
CE
|
D:LYS236
|
4.8
|
25.2
|
1.0
|
C4
|
D:RNS4462
|
4.8
|
18.3
|
0.5
|
NZ
|
D:LYS236
|
4.8
|
40.4
|
1.0
|
C3
|
D:RNS4462
|
4.9
|
19.3
|
0.5
|
ND1
|
D:HIS270
|
5.0
|
37.5
|
1.0
|
|
Reference:
I.P.Korndorfer,
W.D.Fessner,
B.W.Matthews.
The Structure of Rhamnose Isomerase From Escherichia Coli and Its Relation with Xylose Isomerase Illustrates A Change Between Inter and Intra-Subunit Complementation During Evolution. J.Mol.Biol. V. 300 917 2000.
ISSN: ISSN 0022-2836
PubMed: 10891278
DOI: 10.1006/JMBI.2000.3896
Page generated: Sat Oct 5 10:06:19 2024
|