Zinc in PDB 4nei: ALG17C PL17 Family Alginate Lyase
Protein crystallography data
The structure of ALG17C PL17 Family Alginate Lyase, PDB code: 4nei
was solved by
D.S.Park,
S.K.Nair,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
25.00 /
1.85
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
85.530,
126.351,
87.631,
90.00,
111.51,
90.00
|
R / Rfree (%)
|
16.8 /
19.2
|
Zinc Binding Sites:
The binding sites of Zinc atom in the ALG17C PL17 Family Alginate Lyase
(pdb code 4nei). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the
ALG17C PL17 Family Alginate Lyase, PDB code: 4nei:
Jump to Zinc binding site number:
1;
2;
Zinc binding site 1 out
of 2 in 4nei
Go back to
Zinc Binding Sites List in 4nei
Zinc binding site 1 out
of 2 in the ALG17C PL17 Family Alginate Lyase
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of ALG17C PL17 Family Alginate Lyase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn800
b:19.9
occ:1.00
|
O
|
A:HOH1447
|
2.2
|
14.2
|
1.0
|
O
|
A:HOH919
|
2.2
|
14.4
|
1.0
|
NE2
|
A:HIS464
|
2.2
|
15.0
|
1.0
|
O
|
A:HOH933
|
2.2
|
13.7
|
1.0
|
ND1
|
A:HIS415
|
2.2
|
16.1
|
1.0
|
OD1
|
A:ASP433
|
2.3
|
15.0
|
1.0
|
CE1
|
A:HIS415
|
3.0
|
16.2
|
1.0
|
CD2
|
A:HIS464
|
3.0
|
14.8
|
1.0
|
CE1
|
A:HIS464
|
3.2
|
15.1
|
1.0
|
CG
|
A:ASP433
|
3.2
|
15.5
|
1.0
|
CG
|
A:HIS415
|
3.3
|
16.2
|
1.0
|
OD2
|
A:ASP433
|
3.4
|
15.4
|
1.0
|
CB
|
A:HIS415
|
3.8
|
16.5
|
1.0
|
O
|
A:HOH914
|
3.9
|
15.0
|
1.0
|
O
|
A:ALA458
|
4.0
|
17.4
|
1.0
|
N
|
A:ASN310
|
4.1
|
16.0
|
1.0
|
OD2
|
A:ASP417
|
4.1
|
17.3
|
1.0
|
NE2
|
A:HIS415
|
4.2
|
16.2
|
1.0
|
CG
|
A:HIS464
|
4.2
|
14.8
|
1.0
|
O
|
A:ASN310
|
4.3
|
15.8
|
1.0
|
ND1
|
A:HIS464
|
4.3
|
14.9
|
1.0
|
N
|
A:GLY435
|
4.3
|
15.2
|
1.0
|
O
|
A:GLY435
|
4.4
|
16.0
|
1.0
|
CD2
|
A:HIS415
|
4.4
|
16.4
|
1.0
|
O
|
A:PRO308
|
4.5
|
16.0
|
1.0
|
CA
|
A:ASN310
|
4.5
|
15.8
|
1.0
|
CB
|
A:ASP433
|
4.6
|
15.3
|
1.0
|
CA
|
A:GLY435
|
4.7
|
15.7
|
1.0
|
C
|
A:ASN310
|
4.7
|
16.0
|
1.0
|
N
|
A:TYR434
|
4.7
|
15.1
|
1.0
|
CA
|
A:ILE309
|
4.8
|
16.1
|
1.0
|
C
|
A:ILE309
|
4.8
|
16.0
|
1.0
|
C
|
A:GLY435
|
4.9
|
16.0
|
1.0
|
CG
|
A:ASP417
|
4.9
|
17.0
|
1.0
|
|
Zinc binding site 2 out
of 2 in 4nei
Go back to
Zinc Binding Sites List in 4nei
Zinc binding site 2 out
of 2 in the ALG17C PL17 Family Alginate Lyase
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of ALG17C PL17 Family Alginate Lyase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn800
b:18.0
occ:1.00
|
NE2
|
B:HIS464
|
2.1
|
14.1
|
1.0
|
O
|
B:HOH902
|
2.2
|
10.9
|
1.0
|
O
|
B:HOH906
|
2.2
|
12.5
|
1.0
|
O
|
B:HOH903
|
2.2
|
12.2
|
1.0
|
ND1
|
B:HIS415
|
2.2
|
14.1
|
1.0
|
OD1
|
B:ASP433
|
2.3
|
13.6
|
1.0
|
CE1
|
B:HIS415
|
3.0
|
14.2
|
1.0
|
CD2
|
B:HIS464
|
3.0
|
14.3
|
1.0
|
CG
|
B:ASP433
|
3.2
|
13.8
|
1.0
|
CE1
|
B:HIS464
|
3.2
|
14.4
|
1.0
|
CG
|
B:HIS415
|
3.4
|
14.4
|
1.0
|
OD2
|
B:ASP433
|
3.4
|
13.7
|
1.0
|
CB
|
B:HIS415
|
3.9
|
14.5
|
1.0
|
O
|
B:ALA458
|
4.0
|
14.4
|
1.0
|
O
|
B:HOH937
|
4.0
|
13.8
|
1.0
|
N
|
B:ASN310
|
4.1
|
14.5
|
1.0
|
NE2
|
B:HIS415
|
4.2
|
14.3
|
1.0
|
OD2
|
B:ASP417
|
4.2
|
16.9
|
1.0
|
CG
|
B:HIS464
|
4.2
|
14.3
|
1.0
|
ND1
|
B:HIS464
|
4.3
|
14.7
|
1.0
|
O
|
B:ASN310
|
4.3
|
14.8
|
1.0
|
O
|
B:GLY435
|
4.3
|
15.0
|
1.0
|
N
|
B:GLY435
|
4.3
|
14.5
|
1.0
|
CD2
|
B:HIS415
|
4.4
|
14.2
|
1.0
|
O
|
B:PRO308
|
4.4
|
14.4
|
1.0
|
CA
|
B:ASN310
|
4.6
|
14.7
|
1.0
|
CB
|
B:ASP433
|
4.6
|
13.8
|
1.0
|
N
|
B:TYR434
|
4.7
|
14.1
|
1.0
|
CA
|
B:GLY435
|
4.7
|
14.7
|
1.0
|
C
|
B:ASN310
|
4.7
|
14.9
|
1.0
|
CA
|
B:ILE309
|
4.8
|
14.1
|
1.0
|
C
|
B:ILE309
|
4.8
|
14.5
|
1.0
|
C
|
B:GLY435
|
4.9
|
14.9
|
1.0
|
CG
|
B:ASP417
|
4.9
|
16.9
|
1.0
|
|
Reference:
D.Park,
S.Jagtap,
S.K.Nair.
Structure of A PL17 Family Alginate Lyase Demonstrates Functional Similarities Among Exotype Depolymerases. J.Biol.Chem. V. 289 8645 2014.
ISSN: ISSN 0021-9258
PubMed: 24478312
DOI: 10.1074/JBC.M113.531111
Page generated: Sun Oct 27 03:06:15 2024
|