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Calcium in PDB 2e9b: Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose

Enzymatic activity of Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose

All present enzymatic activity of Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose:
3.2.1.41;

Protein crystallography data

The structure of Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose, PDB code: 2e9b was solved by B.Mikami, D.Malle, S.Utsumi, H.Iwamoto, Y.Katsuya, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 14.97 / 2.30
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 71.031, 129.178, 192.060, 90.00, 90.00, 90.00
R / Rfree (%) 19.4 / 24.2

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose (pdb code 2e9b). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose, PDB code: 2e9b:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 2e9b

Go back to Calcium Binding Sites List in 2e9b
Calcium binding site 1 out of 2 in the Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca741

b:38.6
occ:1.00
O A:HOH1121 2.3 27.8 1.0
O A:PHE276 2.4 25.4 1.0
O A:HOH1090 2.4 27.8 1.0
OD2 A:ASP275 2.4 23.1 1.0
OE2 A:GLU281 2.4 36.8 1.0
OE2 A:GLU301 2.4 26.1 1.0
CD A:GLU301 3.1 28.1 1.0
OE1 A:GLU301 3.1 28.2 1.0
CD A:GLU281 3.4 37.0 1.0
CG A:ASP275 3.4 22.5 1.0
C A:PHE276 3.5 25.1 1.0
N A:PHE276 3.8 21.0 1.0
CG A:GLU281 3.9 34.5 1.0
OD1 A:ASP275 3.9 20.1 1.0
O A:HOH848 4.2 23.9 1.0
CA A:PHE276 4.3 24.6 1.0
OE1 A:GLU281 4.3 39.8 1.0
N A:GLY302 4.4 24.2 1.0
CG A:GLU301 4.5 27.8 1.0
O A:VAL279 4.5 31.4 1.0
N A:ALA277 4.6 27.3 1.0
C A:ASP275 4.6 24.0 1.0
CB A:ASP275 4.7 22.5 1.0
CA A:ASP275 4.7 24.2 1.0
CD2 A:PHE276 4.8 24.9 1.0
CA A:ALA277 4.8 27.8 1.0
CA A:GLU301 4.9 25.3 1.0
CD1 A:LEU295 4.9 25.6 1.0
CG A:PHE276 5.0 25.2 1.0

Calcium binding site 2 out of 2 in 2e9b

Go back to Calcium Binding Sites List in 2e9b
Calcium binding site 2 out of 2 in the Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 Complexed with Maltose within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca742

b:38.7
occ:1.00
O B:HOH1208 2.3 29.3 1.0
OD2 B:ASP275 2.3 20.9 1.0
OE2 B:GLU281 2.4 37.6 1.0
O B:HOH1207 2.4 29.9 1.0
O B:PHE276 2.4 22.3 1.0
OE2 B:GLU301 2.5 25.7 1.0
CD B:GLU301 3.3 25.1 1.0
O B:HOH1273 3.3 32.4 1.0
CG B:ASP275 3.4 24.5 1.0
OE1 B:GLU301 3.4 26.9 1.0
CD B:GLU281 3.5 38.4 1.0
C B:PHE276 3.6 24.4 1.0
N B:PHE276 3.7 24.4 1.0
OD1 B:ASP275 3.9 26.1 1.0
CG B:GLU281 4.1 37.2 1.0
O B:HOH980 4.2 25.1 1.0
CA B:PHE276 4.3 23.8 1.0
N B:GLY302 4.5 27.6 1.0
OE1 B:GLU281 4.5 38.3 1.0
O B:VAL279 4.5 30.8 1.0
C B:ASP275 4.6 26.1 1.0
CB B:ASP275 4.7 24.9 1.0
N B:ALA277 4.7 25.7 1.0
CD2 B:PHE276 4.7 21.0 1.0
CA B:ASP275 4.7 25.2 1.0
CG B:GLU301 4.7 25.3 1.0
CD1 B:LEU295 4.9 31.0 1.0
CA B:ALA277 4.9 27.4 1.0
CG B:PHE276 5.0 22.6 1.0
CA B:GLU301 5.0 23.8 1.0
OD1 B:ASN188 5.0 27.4 1.0

Reference:

D.Malle, H.Iwamoto, Y.Katsuya, S.Utsumi, B.Mikami. Crystal Structure of Pullulanase Type I From Bacillus Subtilis Str. 168 in Complex with Maltose and Alpha-Cyclodextrin To Be Published.
Page generated: Tue Jul 8 05:17:57 2025

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