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Magnesium in PDB 4zo6: Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose

Protein crystallography data

The structure of Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose, PDB code: 4zo6 was solved by M.Nakajima, R.Yoshida, A.Miyanaga, K.Abe, Y.Takahashi, N.Sugimoto, H.Toyoizumi, H.Nakai, M.Kitaoka, H.Taguchi, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 32.56 / 2.00
Space group I 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 89.790, 95.350, 215.376, 90.00, 96.30, 90.00
R / Rfree (%) 18.3 / 25.5

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose (pdb code 4zo6). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose, PDB code: 4zo6:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 4zo6

Go back to Magnesium Binding Sites List in 4zo6
Magnesium binding site 1 out of 2 in the Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg805

b:15.9
occ:1.00
O A:HOH1196 1.9 14.8 1.0
OD1 A:ASP648 2.0 14.4 1.0
O A:HOH1134 2.0 19.2 1.0
O A:HOH968 2.2 9.6 1.0
O A:THR650 2.2 11.5 1.0
O A:HOH1076 2.3 16.4 1.0
CG A:ASP648 3.1 13.9 1.0
C A:THR650 3.4 11.8 1.0
OD2 A:ASP648 3.4 13.5 1.0
N A:THR650 4.0 11.0 1.0
O A:PRO698 4.2 12.3 1.0
N A:ALA651 4.2 14.0 1.0
CA A:ALA651 4.2 12.7 1.0
O A:HOH1185 4.2 18.2 1.0
CA A:THR650 4.3 12.4 1.0
CB A:ALA651 4.3 11.9 1.0
O A:LEU700 4.3 10.4 1.0
NE2 A:HIS701 4.3 10.9 1.0
CB A:ASP648 4.4 12.7 1.0
CA A:GLY699 4.4 14.2 1.0
O A:GLU697 4.4 12.8 1.0
OE1 A:GLU697 4.6 12.7 1.0
N A:LEU700 4.6 12.7 1.0
N A:VAL649 4.6 12.6 1.0
C A:GLY699 4.7 13.3 1.0
CB A:GLU697 4.7 15.9 1.0
C A:PRO698 4.7 13.0 1.0
C A:ASP648 4.7 14.3 1.0
O A:HOH1080 4.7 11.9 1.0
CA A:ASP648 4.8 13.2 1.0
CE1 A:HIS701 4.8 11.1 1.0
CB A:THR650 4.8 12.5 1.0
N A:GLY699 4.8 12.3 1.0
CD2 A:HIS701 4.9 10.4 1.0

Magnesium binding site 2 out of 2 in 4zo6

Go back to Magnesium Binding Sites List in 4zo6
Magnesium binding site 2 out of 2 in the Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Crystal Structure of Mutant (D270A) Beta-Glucosidase From Listeria Innocua in Complex with Cellobiose within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg802

b:15.1
occ:1.00
OD1 B:ASP648 1.9 12.2 1.0
O B:HOH1220 2.1 10.4 1.0
O B:THR650 2.2 16.1 1.0
O B:HOH934 2.2 19.5 1.0
O B:HOH949 2.2 11.1 1.0
O B:HOH970 2.2 11.7 1.0
CG B:ASP648 2.9 11.8 1.0
OD2 B:ASP648 3.2 16.2 1.0
C B:THR650 3.3 13.8 1.0
N B:THR650 3.9 11.3 1.0
CB B:ALA651 4.2 9.3 1.0
CA B:THR650 4.2 12.4 1.0
O B:LEU700 4.2 12.0 1.0
CA B:ALA651 4.2 11.1 1.0
O B:PRO698 4.2 13.0 1.0
N B:ALA651 4.3 12.0 1.0
O B:HOH940 4.3 23.3 1.0
CB B:ASP648 4.3 12.1 1.0
O B:HOH1203 4.3 14.8 1.0
NE2 B:HIS701 4.3 13.1 1.0
O B:GLU697 4.5 15.0 1.0
CA B:GLY699 4.6 15.4 1.0
OE1 B:GLU697 4.6 14.5 1.0
N B:VAL649 4.6 13.3 1.0
C B:ASP648 4.6 13.3 1.0
CA B:ASP648 4.6 11.7 1.0
N B:LEU700 4.7 12.6 1.0
CB B:THR650 4.7 12.5 1.0
C B:GLY699 4.7 15.2 1.0
CD2 B:HIS701 4.8 11.5 1.0
C B:PRO698 4.8 16.2 1.0
O B:HOH974 4.8 12.4 1.0
CE1 B:HIS701 4.9 13.9 1.0
N B:GLY699 4.9 14.7 1.0
CB B:GLU697 4.9 16.2 1.0

Reference:

M.Nakajima, R.Yoshida, A.Miyanaga, K.Abe, Y.Takahashi, N.Sugimoto, H.Toyoizumi, H.Nakai, M.Kitaoka, H.Taguchi. Functional and Structural Analysis of A Beta-Glucosidase Involved in Beta-1,2-Glucan Metabolism in Listeria Innocua Plos One V. 11 48870 2016.
ISSN: ESSN 1932-6203
PubMed: 26886583
DOI: 10.1371/JOURNAL.PONE.0148870
Page generated: Sun Sep 29 00:05:31 2024

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