Zinc in PDB 7fir: The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Protein crystallography data
The structure of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose, PDB code: 7fir
was solved by
L.Dai,
Z.Chang,
J.Yang,
W.Liu,
Y.Yang,
C.-C.Chen,
L.Zhang,
J.Huang,
Y.Sun,
R.-T.Guo,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
36.29 /
2.20
|
Space group
|
I 4
|
Cell size a, b, c (Å), α, β, γ (°)
|
205.303,
205.303,
78.649,
90,
90,
90
|
R / Rfree (%)
|
17 /
20.6
|
Zinc Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
17;
Binding sites:
The binding sites of Zinc atom in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
(pdb code 7fir). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 17 binding sites of Zinc where determined in the
The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose, PDB code: 7fir:
Jump to Zinc binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Zinc binding site 1 out
of 17 in 7fir
Go back to
Zinc Binding Sites List in 7fir
Zinc binding site 1 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn502
b:33.2
occ:1.00
|
NE2
|
A:HIS194
|
2.1
|
22.7
|
1.0
|
O
|
B:HOH713
|
2.2
|
7.2
|
1.0
|
O
|
A:HOH859
|
2.3
|
23.6
|
1.0
|
OD2
|
B:ASP170
|
2.4
|
23.3
|
1.0
|
OD1
|
B:ASP170
|
2.5
|
20.2
|
1.0
|
CG
|
B:ASP170
|
2.8
|
20.4
|
1.0
|
CD2
|
A:HIS194
|
3.0
|
21.0
|
1.0
|
CE1
|
A:HIS194
|
3.1
|
21.4
|
1.0
|
CD
|
B:PRO169
|
3.7
|
21.8
|
1.0
|
CG
|
B:PRO169
|
4.1
|
24.5
|
1.0
|
ND1
|
A:HIS194
|
4.1
|
23.4
|
1.0
|
CG
|
A:HIS194
|
4.2
|
21.9
|
1.0
|
O
|
B:HOH507
|
4.2
|
20.3
|
1.0
|
CB
|
B:ASP170
|
4.2
|
19.8
|
1.0
|
OG
|
B:SER190
|
4.3
|
20.4
|
1.0
|
OG
|
A:SER193
|
4.6
|
27.1
|
1.0
|
CD1
|
B:ILE187
|
4.6
|
23.7
|
1.0
|
CB
|
B:SER190
|
4.7
|
18.1
|
1.0
|
CB
|
A:SER193
|
4.8
|
21.7
|
1.0
|
N
|
B:PRO169
|
4.9
|
20.3
|
1.0
|
CD
|
B:PRO191
|
4.9
|
19.5
|
1.0
|
N
|
B:ASP170
|
5.0
|
22.8
|
1.0
|
|
Zinc binding site 2 out
of 17 in 7fir
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Zinc Binding Sites List in 7fir
Zinc binding site 2 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn503
b:23.1
occ:1.00
|
OD2
|
A:ASP149
|
2.0
|
18.0
|
1.0
|
NE2
|
A:HIS219
|
2.1
|
16.0
|
1.0
|
O
|
A:HOH865
|
2.1
|
10.5
|
1.0
|
O
|
A:HOH774
|
2.3
|
6.5
|
1.0
|
CG
|
A:ASP149
|
2.8
|
19.8
|
1.0
|
OD1
|
A:ASP149
|
2.9
|
20.1
|
1.0
|
CE1
|
A:HIS219
|
3.1
|
17.3
|
1.0
|
CD2
|
A:HIS219
|
3.1
|
15.3
|
1.0
|
NH2
|
A:ARG166
|
3.8
|
25.1
|
1.0
|
CE2
|
A:PHE268
|
4.0
|
19.7
|
1.0
|
ND1
|
A:HIS219
|
4.2
|
16.9
|
1.0
|
CB
|
A:ASP149
|
4.2
|
15.2
|
1.0
|
CG
|
A:HIS219
|
4.2
|
17.0
|
1.0
|
CE2
|
A:TYR227
|
4.3
|
15.9
|
1.0
|
O
|
A:HOH843
|
4.3
|
25.0
|
1.0
|
CZ
|
A:ARG166
|
4.4
|
24.1
|
1.0
|
NH1
|
A:ARG166
|
4.5
|
17.9
|
1.0
|
CZ
|
A:PHE268
|
4.5
|
18.0
|
1.0
|
CA
|
A:GLY202
|
4.5
|
16.6
|
1.0
|
CD
|
A:LYS148
|
4.7
|
19.9
|
1.0
|
O
|
A:HOH787
|
4.8
|
22.7
|
1.0
|
OH
|
A:TYR227
|
4.8
|
22.4
|
1.0
|
N
|
A:GLY202
|
4.8
|
15.4
|
1.0
|
O
|
A:HOH692
|
4.9
|
18.9
|
1.0
|
|
Zinc binding site 3 out
of 17 in 7fir
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Zinc Binding Sites List in 7fir
Zinc binding site 3 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn504
b:30.4
occ:1.00
|
NE2
|
B:HIS194
|
2.0
|
20.6
|
1.0
|
OD2
|
A:ASP170
|
2.1
|
21.3
|
1.0
|
O
|
A:HOH847
|
2.2
|
8.5
|
1.0
|
O
|
B:HOH731
|
2.2
|
23.1
|
1.0
|
OD1
|
A:ASP170
|
2.7
|
19.0
|
1.0
|
CG
|
A:ASP170
|
2.8
|
19.1
|
1.0
|
CE1
|
B:HIS194
|
2.9
|
19.0
|
1.0
|
CD2
|
B:HIS194
|
3.0
|
19.9
|
1.0
|
CD
|
A:PRO169
|
3.7
|
19.2
|
1.0
|
CG
|
A:PRO169
|
4.0
|
21.8
|
1.0
|
ND1
|
B:HIS194
|
4.1
|
20.8
|
1.0
|
O
|
A:HOH684
|
4.1
|
19.2
|
1.0
|
CG
|
B:HIS194
|
4.1
|
22.3
|
1.0
|
OG
|
A:SER190
|
4.2
|
25.6
|
1.0
|
CB
|
A:ASP170
|
4.2
|
17.8
|
1.0
|
CD1
|
A:ILE187
|
4.5
|
16.0
|
1.0
|
OG
|
B:SER193
|
4.8
|
31.7
|
1.0
|
CB
|
B:SER193
|
4.8
|
26.9
|
1.0
|
N
|
A:ASP170
|
4.9
|
19.2
|
1.0
|
CB
|
A:SER190
|
4.9
|
19.1
|
1.0
|
N
|
A:PRO169
|
4.9
|
24.1
|
1.0
|
|
Zinc binding site 4 out
of 17 in 7fir
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Zinc Binding Sites List in 7fir
Zinc binding site 4 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn505
b:25.5
occ:1.00
|
OE2
|
A:GLU92
|
2.1
|
24.6
|
1.0
|
NE2
|
A:HIS139
|
2.1
|
22.6
|
1.0
|
SG
|
A:CYS126
|
2.2
|
18.3
|
1.0
|
O
|
A:HOH845
|
2.3
|
10.0
|
1.0
|
CD
|
A:GLU92
|
3.0
|
26.9
|
1.0
|
CE1
|
A:HIS139
|
3.1
|
24.5
|
1.0
|
CD2
|
A:HIS139
|
3.1
|
22.0
|
1.0
|
CB
|
A:CYS126
|
3.1
|
14.4
|
1.0
|
CG
|
A:GLU92
|
3.5
|
23.8
|
1.0
|
OH
|
A:TYR112
|
3.7
|
20.6
|
1.0
|
OE1
|
A:GLU92
|
4.0
|
25.9
|
1.0
|
ND1
|
A:HIS139
|
4.2
|
28.0
|
1.0
|
CG
|
A:HIS139
|
4.3
|
26.1
|
1.0
|
NH1
|
A:ARG124
|
4.4
|
30.6
|
1.0
|
CZ
|
A:TYR112
|
4.4
|
17.9
|
1.0
|
CE1
|
A:TYR112
|
4.4
|
16.7
|
1.0
|
CG1
|
A:ILE141
|
4.4
|
22.9
|
1.0
|
CA
|
A:CYS126
|
4.5
|
17.8
|
1.0
|
OE2
|
A:GLU88
|
4.6
|
43.1
|
1.0
|
O
|
A:ARG140
|
4.7
|
17.7
|
1.0
|
CD
|
A:GLU88
|
4.8
|
46.0
|
1.0
|
CA
|
A:GLY114
|
4.8
|
14.8
|
1.0
|
CG
|
A:GLU88
|
5.0
|
41.6
|
1.0
|
|
Zinc binding site 5 out
of 17 in 7fir
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Zinc Binding Sites List in 7fir
Zinc binding site 5 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 5 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn506
b:83.9
occ:1.00
|
O
|
A:HOH601
|
2.1
|
33.5
|
1.0
|
OE2
|
A:GLU248
|
2.7
|
43.5
|
1.0
|
NE2
|
D:HIS194
|
2.8
|
39.2
|
1.0
|
O
|
A:HOH604
|
2.8
|
31.0
|
1.0
|
O
|
A:HOH739
|
2.9
|
34.8
|
1.0
|
CE1
|
D:HIS194
|
3.2
|
40.4
|
1.0
|
CD
|
A:GLU248
|
3.4
|
41.8
|
1.0
|
OE1
|
A:GLU248
|
3.4
|
42.7
|
1.0
|
CD
|
A:PRO249
|
3.8
|
20.5
|
1.0
|
CD2
|
D:HIS194
|
3.9
|
33.9
|
1.0
|
OG
|
D:SER193
|
4.2
|
31.5
|
1.0
|
O
|
A:HOH836
|
4.3
|
26.4
|
1.0
|
ND1
|
D:HIS194
|
4.3
|
35.9
|
1.0
|
CG
|
A:PRO249
|
4.4
|
22.6
|
1.0
|
CB
|
D:SER193
|
4.4
|
27.1
|
1.0
|
CD1
|
A:TRP196
|
4.5
|
22.1
|
1.0
|
CG
|
D:HIS194
|
4.7
|
31.6
|
1.0
|
CG
|
A:GLU248
|
4.8
|
33.5
|
1.0
|
OE1
|
A:GLU252
|
4.8
|
32.9
|
1.0
|
O
|
D:HOH651
|
4.9
|
22.0
|
1.0
|
|
Zinc binding site 6 out
of 17 in 7fir
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Zinc Binding Sites List in 7fir
Zinc binding site 6 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 6 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn507
b:31.6
occ:1.00
|
NE2
|
A:HIS19
|
2.0
|
28.0
|
1.0
|
OD1
|
A:ASP81
|
2.0
|
19.1
|
1.0
|
O
|
A:HOH868
|
2.5
|
38.3
|
1.0
|
CE1
|
A:HIS19
|
3.0
|
22.7
|
1.0
|
CD2
|
A:HIS19
|
3.1
|
21.6
|
1.0
|
CG
|
A:ASP81
|
3.2
|
25.8
|
1.0
|
O
|
A:HOH807
|
3.6
|
44.8
|
1.0
|
CB
|
A:ASP81
|
3.8
|
27.5
|
1.0
|
CA
|
A:ASP81
|
3.9
|
19.0
|
1.0
|
ND1
|
A:HIS19
|
4.1
|
23.1
|
1.0
|
CG
|
A:HIS19
|
4.2
|
25.1
|
1.0
|
OD2
|
A:ASP81
|
4.3
|
27.4
|
1.0
|
O
|
A:ASP81
|
4.8
|
23.4
|
1.0
|
N
|
A:ASP81
|
4.8
|
22.4
|
1.0
|
C
|
A:ASP81
|
4.9
|
21.3
|
1.0
|
|
Zinc binding site 7 out
of 17 in 7fir
Go back to
Zinc Binding Sites List in 7fir
Zinc binding site 7 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 7 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn401
b:39.4
occ:1.00
|
OD1
|
B:ASP81
|
2.1
|
23.4
|
1.0
|
O
|
B:HOH758
|
2.3
|
34.5
|
1.0
|
NE2
|
B:HIS19
|
2.3
|
27.9
|
1.0
|
CD2
|
B:HIS19
|
3.2
|
26.7
|
1.0
|
CG
|
B:ASP81
|
3.2
|
21.5
|
1.0
|
CE1
|
B:HIS19
|
3.3
|
24.1
|
1.0
|
O
|
B:HOH773
|
3.7
|
39.8
|
1.0
|
OD2
|
B:ASP81
|
3.8
|
31.6
|
1.0
|
O
|
B:HOH700
|
4.1
|
44.1
|
1.0
|
CG
|
B:HIS19
|
4.4
|
27.8
|
1.0
|
ND1
|
B:HIS19
|
4.4
|
27.4
|
1.0
|
CB
|
B:ASP81
|
4.4
|
20.6
|
1.0
|
CA
|
B:ASP81
|
4.8
|
22.1
|
1.0
|
O
|
B:HOH735
|
4.9
|
39.4
|
1.0
|
|
Zinc binding site 8 out
of 17 in 7fir
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Zinc Binding Sites List in 7fir
Zinc binding site 8 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 8 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn402
b:33.9
occ:1.00
|
OE2
|
B:GLU92
|
2.2
|
30.2
|
1.0
|
NE2
|
B:HIS139
|
2.2
|
32.5
|
1.0
|
O
|
B:HOH741
|
2.3
|
11.6
|
1.0
|
SG
|
B:CYS126
|
2.3
|
25.6
|
1.0
|
CD2
|
B:HIS139
|
3.1
|
32.8
|
1.0
|
CB
|
B:CYS126
|
3.1
|
22.4
|
1.0
|
CD
|
B:GLU92
|
3.1
|
28.4
|
1.0
|
CE1
|
B:HIS139
|
3.2
|
30.5
|
1.0
|
CG
|
B:GLU92
|
3.5
|
27.8
|
1.0
|
OH
|
B:TYR112
|
3.7
|
24.2
|
1.0
|
OE1
|
B:GLU92
|
4.2
|
31.0
|
1.0
|
CG
|
B:HIS139
|
4.3
|
33.6
|
1.0
|
ND1
|
B:HIS139
|
4.3
|
35.7
|
1.0
|
CE1
|
B:TYR112
|
4.4
|
21.3
|
1.0
|
CZ
|
B:TYR112
|
4.4
|
25.1
|
1.0
|
CA
|
B:CYS126
|
4.4
|
22.8
|
1.0
|
CG1
|
B:ILE141
|
4.6
|
25.5
|
1.0
|
NH1
|
B:ARG124
|
4.8
|
38.2
|
1.0
|
O
|
B:ARG140
|
4.9
|
26.6
|
1.0
|
CA
|
B:GLY114
|
4.9
|
19.8
|
1.0
|
|
Zinc binding site 9 out
of 17 in 7fir
Go back to
Zinc Binding Sites List in 7fir
Zinc binding site 9 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 9 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn403
b:24.9
occ:1.00
|
OD2
|
B:ASP149
|
2.0
|
17.7
|
1.0
|
NE2
|
B:HIS219
|
2.1
|
17.8
|
1.0
|
O
|
B:HOH753
|
2.2
|
12.8
|
1.0
|
O
|
B:HOH656
|
2.2
|
8.2
|
1.0
|
CG
|
B:ASP149
|
2.8
|
17.7
|
1.0
|
OD1
|
B:ASP149
|
3.0
|
15.4
|
1.0
|
CE1
|
B:HIS219
|
3.0
|
20.0
|
1.0
|
CD2
|
B:HIS219
|
3.1
|
18.9
|
1.0
|
NH1
|
B:ARG166
|
3.7
|
24.9
|
1.0
|
CE2
|
B:PHE268
|
3.9
|
19.9
|
1.0
|
ND1
|
B:HIS219
|
4.1
|
17.8
|
1.0
|
CG
|
B:HIS219
|
4.2
|
15.8
|
1.0
|
CB
|
B:ASP149
|
4.2
|
13.6
|
1.0
|
O
|
B:HOH704
|
4.2
|
33.4
|
1.0
|
CZ
|
B:ARG166
|
4.3
|
21.8
|
1.0
|
NH2
|
B:ARG166
|
4.3
|
20.4
|
1.0
|
CZ
|
B:PHE268
|
4.3
|
17.4
|
1.0
|
CA
|
B:GLY202
|
4.4
|
18.5
|
1.0
|
CE2
|
B:TYR227
|
4.4
|
17.9
|
1.0
|
N
|
B:GLY202
|
4.7
|
19.4
|
1.0
|
O
|
B:HOH571
|
4.8
|
25.4
|
1.0
|
CD
|
B:LYS148
|
4.8
|
25.3
|
1.0
|
OH
|
B:TYR227
|
4.9
|
22.8
|
1.0
|
|
Zinc binding site 10 out
of 17 in 7fir
Go back to
Zinc Binding Sites List in 7fir
Zinc binding site 10 out
of 17 in the The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 10 of The Crystal Structure of Beta-1,2-Mannobiose Phosphorylase in Complex with 1,4-Mannobiose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn404
b:66.5
occ:1.00
|
CE1
|
C:HIS194
|
2.4
|
40.3
|
1.0
|
OE1
|
B:GLU248
|
2.5
|
46.0
|
1.0
|
OE2
|
B:GLU248
|
2.6
|
43.3
|
1.0
|
NE2
|
C:HIS194
|
2.7
|
44.6
|
1.0
|
CD
|
B:GLU248
|
2.8
|
42.1
|
1.0
|
O
|
C:HOH822
|
3.3
|
38.7
|
1.0
|
O
|
B:HOH697
|
3.5
|
25.9
|
1.0
|
ND1
|
C:HIS194
|
3.6
|
39.7
|
1.0
|
O
|
B:HOH502
|
3.7
|
43.5
|
1.0
|
CD2
|
C:HIS194
|
4.0
|
40.2
|
1.0
|
CG
|
B:GLU248
|
4.3
|
33.0
|
1.0
|
CD1
|
B:TRP196
|
4.4
|
24.5
|
1.0
|
CG
|
C:HIS194
|
4.4
|
38.3
|
1.0
|
CD
|
B:PRO249
|
4.5
|
19.5
|
1.0
|
O
|
C:HOH796
|
4.5
|
26.4
|
1.0
|
CA
|
B:GLU248
|
4.9
|
27.3
|
1.0
|
CB
|
B:GLU248
|
5.0
|
26.1
|
1.0
|
NZ
|
B:LYS247
|
5.0
|
47.3
|
1.0
|
|
Reference:
L.Dai,
Z.Chang,
J.Yang,
W.Liu,
Y.Yang,
C.C.Chen,
L.Zhang,
J.W.Huang,
Y.Sun,
R.T.Guo.
Structural Investigation of A Thermostable 1,2-Beta-Mannobiose Phosphorylase From Thermoanaerobacter Sp. X-514. Biochem.Biophys.Res.Commun. V. 579 54 2021.
ISSN: ESSN 1090-2104
PubMed: 34587555
DOI: 10.1016/J.BBRC.2021.09.046
Page generated: Tue Oct 29 20:22:48 2024
|