Calcium in PDB 3edj: Structural Base For Cyclodextrin Hydrolysis

All present enzymatic activity of Structural Base For Cyclodextrin Hydrolysis:
3.2.1.54;

The structure of Structural Base For Cyclodextrin Hydrolysis, PDB code: 3edj was solved by S.Buedenbender, G.E.Schulz, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	19.51 / 1.69
Space group	P 21 21 2
Cell size a, b, c (Å), α, β, γ (°)	106.464, 111.107, 106.793, 90.00, 90.00, 90.00
R / Rfree (%)	16.9 / 20.1

The binding sites of Calcium atom in the Structural Base For Cyclodextrin Hydrolysis (pdb code 3edj). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 4 binding sites of Calcium where determined in the Structural Base For Cyclodextrin Hydrolysis, PDB code: 3edj:
Jump to Calcium binding site number: 1; 2; 3; 4;

Calcium binding site 1 out of 4 in the Structural Base For Cyclodextrin Hydrolysis


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Structural Base For Cyclodextrin Hydrolysis within 5.0Å range: probe atom residue distance (Å) B Occ A:Ca602 b:13.2 occ:1.00 O A:TYR315 2.3 13.6 1.0 O A:HOH824 2.4 11.9 1.0 OG A:SER222 2.4 12.9 1.0 O A:THR270 2.4 11.3 1.0 OD1 A:ASP280 2.4 13.7 1.0 O A:HOH852 2.4 13.4 1.0 OD2 A:ASP280 2.5 13.7 1.0 CG A:ASP280 2.8 14.7 1.0 C A:THR270 3.3 12.1 1.0 C A:TYR315 3.5 13.4 1.0 CB A:SER222 3.6 12.2 1.0 O A:SER222 3.8 14.2 1.0 CA A:THR270 4.1 12.3 1.0 N A:LYS271 4.1 13.3 1.0 CA A:SER222 4.2 12.4 1.0 O A:HOH873 4.3 17.1 1.0 CB A:ASP280 4.3 13.1 1.0 C A:SER222 4.3 12.9 1.0 CB A:TYR315 4.3 12.5 1.0 CA A:LYS271 4.3 13.4 1.0 N A:SER316 4.4 12.6 1.0 CA A:TYR315 4.4 12.2 1.0 O A:GLY272 4.4 14.8 1.0 CA A:SER316 4.4 13.8 1.0 O A:HOH932 4.6 15.6 1.0 O A:PHE269 4.6 12.5 1.0 O A:LEU281 4.7 12.7 1.0 C A:LYS271 4.7 13.3 1.0 OD1 A:ASN241 4.8 19.3 1.0 OE1 A:GLN283 4.8 15.2 1.0 O A:LYS271 4.9 13.1 1.0 O A:HOH826 5.0 14.6 1.0 CB A:THR270 5.0 12.9 1.0

Calcium binding site 2 out of 4 in the Structural Base For Cyclodextrin Hydrolysis


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Structural Base For Cyclodextrin Hydrolysis within 5.0Å range: probe atom residue distance (Å) B Occ A:Ca603 b:16.9 occ:1.00 OD1 A:ASP125 2.3 18.8 1.0 OD1 A:ASP146 2.4 17.8 1.0 OD1 A:ASN124 2.4 18.5 1.0 O A:GLY144 2.5 15.6 1.0 O A:ASP121 2.5 21.6 1.0 OD1 A:ASN119 2.5 16.5 1.0 O A:HOH910 2.6 15.7 1.0 CG A:ASN119 3.4 18.0 1.0 CG A:ASP146 3.4 17.6 1.0 C A:ASP121 3.4 21.5 1.0 CG A:ASN124 3.5 18.4 1.0 C A:GLY144 3.5 15.7 1.0 CG A:ASP125 3.6 18.3 1.0 CB A:ASP146 3.9 16.2 1.0 ND2 A:ASN119 3.9 18.5 1.0 N A:ASP125 3.9 18.0 1.0 CA A:GLY144 4.0 15.9 1.0 CA A:PRO122 4.1 21.1 1.0 N A:PRO122 4.1 21.5 1.0 ND2 A:ASN124 4.2 19.3 1.0 N A:ASP121 4.2 20.6 1.0 CA A:ASP125 4.2 18.1 1.0 C A:ASN124 4.3 18.2 1.0 CA A:ASP121 4.3 21.6 1.0 OD2 A:ASP125 4.4 19.1 1.0 OD2 A:ASP146 4.4 15.9 1.0 O A:ARG194 4.4 15.1 1.0 CB A:ASN119 4.5 17.4 1.0 C A:PRO122 4.5 20.7 1.0 CB A:ASP125 4.5 18.5 1.0 N A:ASN124 4.5 18.6 1.0 CA A:ASN119 4.6 18.2 1.0 C A:GLY145 4.6 14.6 1.0 O A:GLY145 4.7 14.5 1.0 CB A:ASP121 4.7 22.2 1.0 O A:PRO122 4.7 20.1 1.0 N A:GLY145 4.7 14.3 1.0 CA A:ASN124 4.7 18.5 1.0 CB A:ASN124 4.7 18.6 1.0 N A:ASP146 4.7 15.7 1.0 O A:ASN124 4.8 18.6 1.0 C A:ASN119 4.8 18.9 1.0 N A:GLY120 4.9 18.5 1.0 CA A:ASP146 5.0 16.0 1.0 CA A:GLY145 5.0 14.4 1.0

Calcium binding site 3 out of 4 in the Structural Base For Cyclodextrin Hydrolysis


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 3 of Structural Base For Cyclodextrin Hydrolysis within 5.0Å range: probe atom residue distance (Å) B Occ B:Ca602 b:14.7 occ:1.00 O B:TYR315 2.3 13.2 1.0 O B:HOH1012 2.4 13.9 1.0 O B:HOH1061 2.4 13.3 1.0 OG B:SER222 2.4 13.9 1.0 O B:THR270 2.4 14.0 1.0 OD1 B:ASP280 2.5 13.9 1.0 OD2 B:ASP280 2.5 14.9 1.0 CG B:ASP280 2.8 15.0 1.0 C B:THR270 3.3 14.2 1.0 C B:TYR315 3.5 13.6 1.0 CB B:SER222 3.7 15.6 1.0 O B:SER222 3.9 14.8 1.0 CA B:THR270 4.1 14.3 1.0 N B:LYS271 4.2 14.6 1.0 O B:HOH1055 4.2 17.4 1.0 CA B:SER222 4.2 14.1 1.0 CB B:ASP280 4.3 14.5 1.0 CB B:TYR315 4.3 12.9 1.0 N B:SER316 4.4 13.4 1.0 CA B:LYS271 4.4 15.2 1.0 CA B:TYR315 4.4 13.2 1.0 O B:GLY272 4.4 14.7 1.0 CA B:SER316 4.4 13.5 1.0 C B:SER222 4.4 13.8 1.0 O B:PHE269 4.5 13.7 1.0 O B:LEU281 4.6 15.7 1.0 O B:HOH1151 4.7 16.7 1.0 C B:LYS271 4.7 14.7 1.0 OD1 B:ASN241 4.8 18.7 1.0 OE1 B:GLN283 4.8 19.8 1.0 O B:LYS271 4.9 15.0 1.0 CB B:THR270 5.0 14.2 1.0

Calcium binding site 4 out of 4 in the Structural Base For Cyclodextrin Hydrolysis


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 4 of Structural Base For Cyclodextrin Hydrolysis within 5.0Å range: probe atom residue distance (Å) B Occ B:Ca603 b:19.2 occ:1.00 OD1 B:ASP146 2.3 20.2 1.0 OD1 B:ASN124 2.4 19.9 1.0 OD1 B:ASP125 2.4 18.8 1.0 O B:ASP121 2.4 21.1 1.0 O B:GLY144 2.5 17.4 1.0 OD1 B:ASN119 2.5 18.5 1.0 O B:HOH1077 2.6 16.2 1.0 C B:ASP121 3.3 22.1 1.0 CG B:ASP146 3.4 19.4 1.0 CG B:ASN119 3.4 19.6 1.0 C B:GLY144 3.6 17.6 1.0 CG B:ASN124 3.6 22.1 1.0 CG B:ASP125 3.6 20.8 1.0 CB B:ASP146 3.9 18.2 1.0 ND2 B:ASN119 3.9 17.0 1.0 N B:ASP125 3.9 21.2 1.0 CA B:GLY144 4.1 17.1 1.0 N B:PRO122 4.1 22.1 1.0 CA B:PRO122 4.1 22.7 1.0 N B:ASP121 4.2 21.9 1.0 ND2 B:ASN124 4.2 21.1 1.0 CA B:ASP121 4.2 22.7 1.0 CA B:ASP125 4.3 20.6 1.0 C B:ASN124 4.3 21.4 1.0 O B:ARG194 4.4 19.4 1.0 OD2 B:ASP125 4.4 21.9 1.0 OD2 B:ASP146 4.4 19.0 1.0 C B:PRO122 4.5 22.6 1.0 CB B:ASN119 4.5 18.2 1.0 N B:ASN124 4.5 22.7 1.0 CB B:ASP125 4.5 20.5 1.0 CA B:ASN119 4.6 18.8 1.0 C B:GLY145 4.6 16.9 1.0 CB B:ASP121 4.6 23.1 1.0 O B:PRO122 4.7 22.9 1.0 O B:GLY145 4.7 17.0 1.0 N B:GLY145 4.7 17.1 1.0 CA B:ASN124 4.7 21.7 1.0 CB B:ASN124 4.7 21.7 1.0 O B:ASN124 4.7 20.9 1.0 N B:ASP146 4.8 16.6 1.0 C B:ASN119 4.9 19.3 1.0 CA B:GLY145 5.0 16.9 1.0 CA B:ASP146 5.0 16.9 1.0

S.Buedenbender, G.E.Schulz. Structural Base For Enzymatic Cyclodextrin Hydrolysis J.Mol.Biol. V. 385 606 2009.
ISSN: ISSN 0022-2836
PubMed: 19014948
DOI: 10.1016/J.JMB.2008.10.085