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Calcium in PDB 4gia: Crystal Structure of the Mutb F164L Mutant From Crystals Soaked with Isomaltulose

Enzymatic activity of Crystal Structure of the Mutb F164L Mutant From Crystals Soaked with Isomaltulose

All present enzymatic activity of Crystal Structure of the Mutb F164L Mutant From Crystals Soaked with Isomaltulose:
5.4.11.99;

Protein crystallography data

The structure of Crystal Structure of the Mutb F164L Mutant From Crystals Soaked with Isomaltulose, PDB code: 4gia was solved by A.Lipski, R.Haser, N.Aghajari, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 14.95 / 2.01
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 64.100, 86.500, 118.600, 90.00, 97.70, 90.00
R / Rfree (%) 16.2 / 21.3

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of the Mutb F164L Mutant From Crystals Soaked with Isomaltulose (pdb code 4gia). 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 the Mutb F164L Mutant From Crystals Soaked with Isomaltulose, PDB code: 4gia:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 4gia

Go back to Calcium Binding Sites List in 4gia
Calcium binding site 1 out of 2 in the Crystal Structure of the Mutb F164L Mutant From Crystals Soaked with Isomaltulose


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 the Mutb F164L Mutant From Crystals Soaked with Isomaltulose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca7001

b:13.0
occ:1.00
O A:HOH7492 2.2 18.2 1.0
OD1 A:ASP22 2.4 13.3 1.0
O A:ILE28 2.4 12.3 1.0
OD2 A:ASP30 2.4 14.3 1.0
OD1 A:ASN24 2.5 17.7 1.0
OD1 A:ASP26 2.5 15.2 1.0
O A:HOH7478 2.5 28.5 1.0
CG A:ASP26 3.3 16.0 1.0
CG A:ASP22 3.3 14.0 1.0
CG A:ASP30 3.5 13.7 1.0
CG A:ASN24 3.5 18.4 1.0
OD2 A:ASP26 3.6 17.2 1.0
C A:ILE28 3.6 11.8 1.0
CB A:ASP30 3.9 12.9 1.0
OD2 A:ASP22 4.1 14.7 1.0
ND2 A:ASN24 4.2 18.2 1.0
CB A:ASP22 4.2 13.6 1.0
CA A:ASP22 4.2 14.1 1.0
N A:ASN24 4.2 16.5 1.0
N A:THR23 4.3 15.2 1.0
N A:ILE28 4.3 12.3 1.0
CA A:ILE28 4.3 11.8 1.0
O A:GLU75 4.4 15.6 1.0
C A:GLY29 4.4 11.1 1.0
O A:GLY29 4.5 11.3 1.0
CB A:ILE28 4.6 12.0 1.0
N A:GLY29 4.6 11.2 1.0
CB A:ASN24 4.6 17.1 1.0
OD1 A:ASP30 4.6 13.1 1.0
N A:ASP26 4.6 16.4 1.0
CB A:ASP26 4.6 16.1 1.0
N A:ASP30 4.7 12.1 1.0
CA A:GLY29 4.7 10.7 1.0
C A:ASP22 4.7 15.2 1.0
CA A:ASN24 4.8 17.7 1.0
O A:HOH7523 4.9 38.0 1.0
O A:HOH7373 4.9 35.4 1.0
CA A:ASP30 4.9 12.7 1.0
C A:ASN24 5.0 16.9 1.0

Calcium binding site 2 out of 2 in 4gia

Go back to Calcium Binding Sites List in 4gia
Calcium binding site 2 out of 2 in the Crystal Structure of the Mutb F164L Mutant From Crystals Soaked with Isomaltulose


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 the Mutb F164L Mutant From Crystals Soaked with Isomaltulose within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca601

b:14.8
occ:1.00
O B:HOH983 2.3 22.4 1.0
OD1 B:ASP22 2.4 13.4 1.0
O B:HOH948 2.4 17.6 1.0
O B:ILE28 2.4 12.7 1.0
OD1 B:ASN24 2.4 16.5 1.0
OD1 B:ASP26 2.4 16.7 1.0
OD2 B:ASP30 2.4 12.8 1.0
CG B:ASP26 3.3 17.2 1.0
CG B:ASP22 3.4 13.4 1.0
CG B:ASN24 3.4 18.4 1.0
CG B:ASP30 3.5 12.4 1.0
OD2 B:ASP26 3.6 17.7 1.0
C B:ILE28 3.6 12.9 1.0
CB B:ASP30 3.9 12.4 1.0
ND2 B:ASN24 4.0 19.0 1.0
OD2 B:ASP22 4.1 13.5 1.0
N B:ASN24 4.1 16.5 1.0
N B:THR23 4.2 15.8 1.0
CB B:ASP22 4.2 13.7 1.0
CA B:ASP22 4.3 14.4 1.0
N B:ILE28 4.3 13.2 1.0
C B:GLY29 4.4 11.3 1.0
CA B:ILE28 4.4 13.0 1.0
O B:GLU75 4.5 16.7 1.0
O B:GLY29 4.5 12.0 1.0
CB B:ASN24 4.5 17.3 1.0
CB B:ASP26 4.5 16.8 1.0
N B:ASP26 4.6 17.2 1.0
N B:GLY29 4.6 12.2 1.0
OD1 B:ASP30 4.6 12.2 1.0
N B:ASP30 4.6 11.8 1.0
CB B:ILE28 4.6 13.6 1.0
CA B:GLY29 4.7 11.3 1.0
C B:ASP22 4.7 15.1 1.0
CA B:ASN24 4.7 17.0 1.0
CA B:ASP30 4.9 12.2 1.0
C B:ASN24 4.9 17.4 1.0
O B:HOH1112 5.0 45.6 1.0
CA B:ASP26 5.0 15.9 1.0

Reference:

A.Lipski, H.Watzlawick, S.Ravaud, X.Robert, M.Rhimi, R.Haser, R.Mattes, N.Aghajari. Mutations Inducing An Active-Site Aperture in Rhizobium Sp. Sucrose Isomerase Confer Hydrolytic Activity Acta Crystallogr.,Sect.D V. 69 298 2013.
ISSN: ISSN 0907-4449
PubMed: 23385465
DOI: 10.1107/S0907444912045532
Page generated: Sat Dec 12 04:48:08 2020

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