Manganese in PDB 6k1f: Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
Enzymatic activity of Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
All present enzymatic activity of Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.:
5.3.1.25;
Protein crystallography data
The structure of Crystal Structure of the L-Fucose Isomerase From Raoultella Sp., PDB code: 6k1f
was solved by
I.J.Kim,
D.H.Kim,
K.H.Nam,
K.H.Kim,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
50.01 /
2.50
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
113.987,
127.611,
257.298,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
17.7 /
23.3
|
Manganese Binding Sites:
The binding sites of Manganese atom in the Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
(pdb code 6k1f). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 6 binding sites of Manganese where determined in the
Crystal Structure of the L-Fucose Isomerase From Raoultella Sp., PDB code: 6k1f:
Jump to Manganese binding site number:
1;
2;
3;
4;
5;
6;
Manganese binding site 1 out
of 6 in 6k1f
Go back to
Manganese Binding Sites List in 6k1f
Manganese binding site 1 out
of 6 in the Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
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 the L-Fucose Isomerase From Raoultella Sp. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn601
b:68.3
occ:1.00
|
NE2
|
A:HIS528
|
2.5
|
40.8
|
1.0
|
OE1
|
A:GLU337
|
2.7
|
50.4
|
1.0
|
OD1
|
A:ASP361
|
2.8
|
51.7
|
1.0
|
OG
|
A:SER393
|
3.2
|
38.7
|
1.0
|
CD2
|
A:HIS528
|
3.4
|
36.7
|
1.0
|
CE1
|
A:HIS528
|
3.4
|
37.1
|
1.0
|
OD2
|
A:ASP361
|
3.5
|
42.5
|
1.0
|
CG
|
A:ASP361
|
3.5
|
42.9
|
1.0
|
CD
|
A:GLU337
|
3.5
|
46.5
|
1.0
|
OE2
|
A:GLU337
|
3.7
|
47.5
|
1.0
|
CB
|
A:SER393
|
4.1
|
39.6
|
1.0
|
OD1
|
A:ASN392
|
4.2
|
40.4
|
1.0
|
ND2
|
A:ASN527
|
4.4
|
38.2
|
1.0
|
ND1
|
A:HIS528
|
4.6
|
34.0
|
1.0
|
CG
|
A:HIS528
|
4.6
|
33.8
|
1.0
|
N
|
A:SER393
|
4.8
|
35.7
|
1.0
|
CG
|
A:GLU337
|
4.9
|
43.8
|
1.0
|
CB
|
A:ASP361
|
5.0
|
40.2
|
1.0
|
|
Manganese binding site 2 out
of 6 in 6k1f
Go back to
Manganese Binding Sites List in 6k1f
Manganese binding site 2 out
of 6 in the Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
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 the L-Fucose Isomerase From Raoultella Sp. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn601
b:72.0
occ:1.00
|
NE2
|
B:HIS528
|
2.6
|
48.6
|
1.0
|
OE1
|
B:GLU337
|
2.7
|
48.2
|
1.0
|
OD1
|
B:ASP361
|
2.8
|
56.8
|
1.0
|
O
|
B:HOH721
|
2.8
|
32.8
|
1.0
|
ND2
|
B:ASN527
|
3.3
|
33.9
|
1.0
|
CE1
|
B:HIS528
|
3.4
|
42.5
|
1.0
|
CD
|
B:GLU337
|
3.5
|
36.5
|
1.0
|
OE2
|
B:GLU337
|
3.5
|
36.7
|
1.0
|
CD2
|
B:HIS528
|
3.6
|
41.5
|
1.0
|
CG
|
B:ASP361
|
3.8
|
46.1
|
1.0
|
OD2
|
B:ASP361
|
4.0
|
53.6
|
1.0
|
CG
|
B:ASN527
|
4.5
|
34.1
|
1.0
|
ND1
|
B:HIS528
|
4.6
|
40.3
|
1.0
|
CD1
|
B:ILE187
|
4.7
|
32.8
|
1.0
|
CG
|
B:HIS528
|
4.7
|
38.5
|
1.0
|
CH2
|
A:TRP90
|
4.7
|
33.6
|
1.0
|
CZ2
|
A:TRP90
|
4.8
|
34.5
|
1.0
|
OG
|
B:SER393
|
4.8
|
40.4
|
1.0
|
|
Manganese binding site 3 out
of 6 in 6k1f
Go back to
Manganese Binding Sites List in 6k1f
Manganese binding site 3 out
of 6 in the Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
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 the L-Fucose Isomerase From Raoultella Sp. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn601
b:67.4
occ:1.00
|
NE2
|
C:HIS528
|
2.5
|
44.9
|
1.0
|
OE1
|
C:GLU337
|
2.7
|
46.3
|
1.0
|
OD1
|
C:ASP361
|
2.7
|
53.1
|
1.0
|
O
|
C:HOH844
|
2.9
|
25.1
|
1.0
|
CD
|
C:GLU337
|
3.3
|
40.7
|
1.0
|
OE2
|
C:GLU337
|
3.3
|
40.3
|
1.0
|
CD2
|
C:HIS528
|
3.3
|
40.7
|
1.0
|
OG
|
C:SER393
|
3.3
|
32.0
|
1.0
|
CE1
|
C:HIS528
|
3.4
|
42.5
|
1.0
|
CG
|
C:ASP361
|
3.5
|
44.5
|
1.0
|
OD2
|
C:ASP361
|
3.7
|
50.7
|
1.0
|
OD1
|
C:ASN392
|
3.8
|
31.3
|
1.0
|
CB
|
C:SER393
|
4.1
|
33.0
|
1.0
|
CG
|
C:HIS528
|
4.4
|
38.2
|
1.0
|
ND1
|
C:HIS528
|
4.5
|
38.5
|
1.0
|
ND2
|
C:ASN527
|
4.5
|
33.0
|
1.0
|
N
|
C:SER393
|
4.6
|
33.3
|
1.0
|
CG
|
C:GLU337
|
4.7
|
35.5
|
1.0
|
CE1
|
C:PHE359
|
4.7
|
25.8
|
1.0
|
CG2
|
C:THR336
|
4.7
|
26.7
|
1.0
|
CB
|
C:ASP361
|
4.8
|
41.3
|
1.0
|
|
Manganese binding site 4 out
of 6 in 6k1f
Go back to
Manganese Binding Sites List in 6k1f
Manganese binding site 4 out
of 6 in the Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
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 the L-Fucose Isomerase From Raoultella Sp. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn601
b:66.2
occ:1.00
|
NE2
|
D:HIS528
|
2.5
|
33.9
|
1.0
|
OE1
|
D:GLU337
|
2.7
|
38.0
|
1.0
|
OD1
|
D:ASP361
|
2.8
|
54.0
|
1.0
|
ND2
|
D:ASN527
|
3.1
|
22.8
|
1.0
|
O
|
D:HOH891
|
3.1
|
30.4
|
1.0
|
CE1
|
D:HIS528
|
3.4
|
29.5
|
1.0
|
CD2
|
D:HIS528
|
3.5
|
29.8
|
1.0
|
CD
|
D:GLU337
|
3.6
|
29.7
|
1.0
|
CG
|
D:ASP361
|
3.7
|
41.6
|
1.0
|
OE2
|
D:GLU337
|
3.7
|
31.0
|
1.0
|
OD2
|
D:ASP361
|
3.8
|
47.3
|
1.0
|
CG
|
D:ASN527
|
4.4
|
22.9
|
1.0
|
OG
|
D:SER393
|
4.4
|
34.0
|
1.0
|
ND1
|
D:HIS528
|
4.6
|
27.0
|
1.0
|
CG
|
D:HIS528
|
4.6
|
27.0
|
1.0
|
CH2
|
F:TRP90
|
4.7
|
23.5
|
1.0
|
CD1
|
D:ILE187
|
4.7
|
24.8
|
1.0
|
CZ2
|
F:TRP90
|
4.8
|
23.0
|
1.0
|
CZ3
|
F:TRP90
|
4.9
|
23.8
|
1.0
|
|
Manganese binding site 5 out
of 6 in 6k1f
Go back to
Manganese Binding Sites List in 6k1f
Manganese binding site 5 out
of 6 in the Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
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 the L-Fucose Isomerase From Raoultella Sp. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Mn601
b:75.3
occ:1.00
|
NE2
|
E:HIS528
|
2.5
|
51.0
|
1.0
|
OE1
|
E:GLU337
|
2.7
|
55.7
|
1.0
|
OD1
|
E:ASP361
|
2.8
|
51.9
|
1.0
|
O
|
E:HOH796
|
3.1
|
25.4
|
1.0
|
CE1
|
E:HIS528
|
3.3
|
47.6
|
1.0
|
OE2
|
E:GLU337
|
3.3
|
52.4
|
1.0
|
ND2
|
E:ASN527
|
3.3
|
36.1
|
1.0
|
CD
|
E:GLU337
|
3.4
|
52.3
|
1.0
|
CG
|
E:ASP361
|
3.6
|
44.6
|
1.0
|
CD2
|
E:HIS528
|
3.7
|
45.3
|
1.0
|
OD2
|
E:ASP361
|
3.7
|
50.7
|
1.0
|
ND1
|
E:HIS528
|
4.5
|
42.9
|
1.0
|
CD1
|
E:ILE187
|
4.5
|
36.4
|
1.0
|
CG
|
E:ASN527
|
4.6
|
36.0
|
1.0
|
CG
|
E:HIS528
|
4.7
|
39.6
|
1.0
|
CH2
|
D:TRP90
|
4.8
|
37.1
|
1.0
|
CZ2
|
D:TRP90
|
4.8
|
35.7
|
1.0
|
CG
|
E:GLU337
|
4.9
|
48.4
|
1.0
|
|
Manganese binding site 6 out
of 6 in 6k1f
Go back to
Manganese Binding Sites List in 6k1f
Manganese binding site 6 out
of 6 in the Crystal Structure of the L-Fucose Isomerase From Raoultella Sp.
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 the L-Fucose Isomerase From Raoultella Sp. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
F:Mn601
b:74.0
occ:1.00
|
NE2
|
F:HIS528
|
2.5
|
44.1
|
1.0
|
OE1
|
F:GLU337
|
2.7
|
42.4
|
1.0
|
OD1
|
F:ASP361
|
2.8
|
58.5
|
1.0
|
OE2
|
F:GLU337
|
2.9
|
40.0
|
1.0
|
CD
|
F:GLU337
|
3.1
|
37.0
|
1.0
|
OD2
|
F:ASP361
|
3.4
|
56.9
|
1.0
|
CE1
|
F:HIS528
|
3.4
|
40.6
|
1.0
|
CG
|
F:ASP361
|
3.5
|
49.2
|
1.0
|
CD2
|
F:HIS528
|
3.6
|
40.0
|
1.0
|
OG
|
F:SER393
|
3.7
|
33.8
|
1.0
|
ND2
|
F:ASN527
|
4.1
|
34.8
|
1.0
|
CB
|
F:SER393
|
4.5
|
34.0
|
1.0
|
ND1
|
F:HIS528
|
4.6
|
37.3
|
1.0
|
CG
|
F:GLU337
|
4.6
|
33.3
|
1.0
|
CG
|
F:HIS528
|
4.7
|
37.5
|
1.0
|
CD1
|
F:ILE187
|
4.9
|
27.4
|
1.0
|
OD1
|
F:ASN392
|
4.9
|
35.1
|
1.0
|
CB
|
F:ASP361
|
4.9
|
43.2
|
1.0
|
|
Reference:
I.J.Kim,
D.H.Kim,
K.H.Nam,
K.H.Kim.
Crystal Structure of the L-Fucose Isomerase From Raoultella Sp. To Be Published.
Page generated: Sun Oct 6 05:13:26 2024
|