Magnesium in PDB 6lga: Bombyx Mori GH13 Sucrose Hydrolase

Protein crystallography data

The structure of Bombyx Mori GH13 Sucrose Hydrolase, PDB code: 6lga was solved by T.Miyazaki, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 48.91 / 1.85
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 65.880, 145.684, 153.796, 90.00, 90.00, 90.00
R / Rfree (%) 15.7 / 18.6

Other elements in 6lga:

The structure of Bombyx Mori GH13 Sucrose Hydrolase also contains other interesting chemical elements:

Calcium (Ca) 2 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Bombyx Mori GH13 Sucrose Hydrolase (pdb code 6lga). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 3 binding sites of Magnesium where determined in the Bombyx Mori GH13 Sucrose Hydrolase, PDB code: 6lga:
Jump to Magnesium binding site number: 1; 2; 3;

Magnesium binding site 1 out of 3 in 6lga

Go back to Magnesium Binding Sites List in 6lga
Magnesium binding site 1 out of 3 in the Bombyx Mori GH13 Sucrose Hydrolase


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Bombyx Mori GH13 Sucrose Hydrolase within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg701

b:18.1
occ:1.00
OD1 A:ASP63 2.1 20.4 1.0
O A:HOH817 2.1 23.9 1.0
OD1 A:ASP65 2.1 25.5 1.0
OD1 A:ASP67 2.1 22.4 1.0
O A:ILE69 2.2 20.8 1.0
OD2 A:ASP71 2.2 18.6 1.0
CG A:ASP67 3.0 22.9 1.0
CG A:ASP63 3.2 19.7 1.0
CG A:ASP65 3.2 28.4 1.0
C A:ILE69 3.3 21.1 1.0
CG A:ASP71 3.4 18.9 1.0
OD2 A:ASP67 3.4 23.4 1.0
OD2 A:ASP65 3.7 34.3 1.0
CB A:ASP71 3.9 18.8 1.0
CB A:ASP63 3.9 20.4 1.0
OD2 A:ASP63 4.0 20.8 1.0
N A:ILE69 4.0 20.3 1.0
CA A:ILE69 4.0 21.4 1.0
CA A:ASP63 4.1 20.6 1.0
N A:ASP65 4.1 22.5 1.0
CB A:ILE69 4.2 21.6 1.0
N A:SER64 4.2 21.7 1.0
CB A:ASP67 4.4 22.8 1.0
N A:ASP67 4.4 22.3 1.0
N A:GLY70 4.4 20.8 1.0
C A:GLY70 4.4 18.7 1.0
CB A:ASP65 4.4 25.1 1.0
OD1 A:ASP71 4.5 19.3 1.0
O A:HOH895 4.5 42.4 1.0
C A:ASP63 4.5 21.8 1.0
N A:ASP71 4.6 18.2 1.0
O A:GLY70 4.6 18.8 1.0
O A:GLU116 4.6 23.5 1.0
CA A:ASP65 4.6 23.8 1.0
CA A:GLY70 4.7 19.3 1.0
N A:GLY66 4.7 22.4 1.0
C A:ASP65 4.7 23.8 1.0
CG2 A:ILE69 4.7 22.3 1.0
CA A:ASP67 4.8 22.1 1.0
N A:GLY68 4.9 20.9 1.0
CA A:ASP71 4.9 18.8 1.0

Magnesium binding site 2 out of 3 in 6lga

Go back to Magnesium Binding Sites List in 6lga
Magnesium binding site 2 out of 3 in the Bombyx Mori GH13 Sucrose Hydrolase


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Bombyx Mori GH13 Sucrose Hydrolase within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg703

b:18.1
occ:1.00
O A:HOH1295 2.1 15.2 1.0
O B:HOH882 2.1 15.6 1.0
O A:HOH874 2.1 15.7 1.0
O A:HOH1307 2.1 15.5 1.0
O B:HOH861 2.1 15.9 1.0
O B:HOH1303 2.2 16.4 1.0
NE2 A:HIS564 4.0 19.7 1.0
NE2 B:HIS564 4.1 17.7 1.0
OD2 A:ASP523 4.1 18.7 1.0
OD1 A:ASP523 4.1 18.1 1.0
OD1 B:ASP523 4.2 18.0 1.0
O B:HOH1352 4.2 20.8 1.0
OD2 B:ASP523 4.2 17.5 1.0
O A:HOH1329 4.2 22.8 1.0
O B:HOH1353 4.2 25.1 1.0
O A:HOH1377 4.3 20.9 1.0
O A:HOH1359 4.3 15.8 1.0
O B:HOH1361 4.3 14.7 1.0
O A:HOH1358 4.3 22.5 1.0
O B:HOH1328 4.4 20.4 1.0
CG A:ASP523 4.5 17.9 1.0
O B:HOH1212 4.5 19.5 1.0
CG B:ASP523 4.5 17.7 1.0
CE1 A:HIS564 4.6 22.9 1.0
O A:HOH1235 4.6 17.7 1.0
CE1 B:HIS564 4.7 19.4 1.0

Magnesium binding site 3 out of 3 in 6lga

Go back to Magnesium Binding Sites List in 6lga
Magnesium binding site 3 out of 3 in the Bombyx Mori GH13 Sucrose Hydrolase


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 3 of Bombyx Mori GH13 Sucrose Hydrolase within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg701

b:20.6
occ:1.00
OD1 B:ASP65 2.1 25.2 1.0
OD2 B:ASP71 2.1 22.0 1.0
O B:ILE69 2.1 20.2 1.0
OD1 B:ASP63 2.2 22.3 1.0
O B:HOH979 2.2 21.5 1.0
OD1 B:ASP67 2.3 22.7 1.0
CG B:ASP67 3.1 25.1 1.0
CG B:ASP65 3.2 31.1 1.0
CG B:ASP63 3.2 23.5 1.0
CG B:ASP71 3.3 21.7 1.0
C B:ILE69 3.3 20.9 1.0
OD2 B:ASP67 3.5 22.9 1.0
OD2 B:ASP65 3.6 37.8 1.0
CB B:ASP71 3.8 20.2 1.0
CB B:ASP63 3.9 23.5 1.0
CA B:ASP63 4.0 22.8 1.0
N B:ILE69 4.0 23.6 1.0
OD2 B:ASP63 4.0 23.2 1.0
CA B:ILE69 4.1 22.0 1.0
N B:ASP65 4.1 26.8 1.0
N B:SER64 4.1 23.7 1.0
CB B:ILE69 4.3 22.8 1.0
OD1 B:ASP71 4.3 21.9 1.0
C B:GLY70 4.4 19.5 1.0
N B:GLY70 4.4 20.6 1.0
CB B:ASP65 4.4 27.8 1.0
CB B:ASP67 4.4 26.4 1.0
C B:ASP63 4.4 23.9 1.0
N B:ASP67 4.4 25.9 1.0
O B:GLY70 4.5 19.3 1.0
N B:ASP71 4.6 20.2 1.0
CA B:ASP65 4.6 28.0 1.0
CA B:GLY70 4.6 20.0 1.0
C B:ASP65 4.7 30.0 1.0
O B:GLU116 4.7 21.2 1.0
N B:GLY66 4.8 28.8 1.0
CG2 B:ILE69 4.8 22.3 1.0
CA B:ASP67 4.8 25.1 1.0
CA B:ASP71 4.8 19.9 1.0
N B:GLY68 4.9 24.4 1.0

Reference:

T.Miyazaki, E.Y.Park. Structure-Function Analysis of Silkworm Sucrose Hydrolase Uncovers the Mechanism of Substrate Specificity in GH13 Subfamily 17EXO-Alpha-Glucosidases. J.Biol.Chem. 2020.
ISSN: ESSN 1083-351X
PubMed: 32381508
DOI: 10.1074/JBC.RA120.013595
Page generated: Mon Dec 14 23:12:55 2020

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