Calcium in PDB 6ms3: Crystal Structure of the GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis

Protein crystallography data

The structure of Crystal Structure of the GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis, PDB code: 6ms3 was solved by L.M.Zanphorlin, M.A.B.Morais, J.A.Diogo, M.T.Murakami, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 48.23 / 1.95
Space group P 43
Cell size a, b, c (Å), α, β, γ (°) 82.126, 82.126, 173.236, 90.00, 90.00, 90.00
R / Rfree (%) 16.8 / 20.1

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of the GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis (pdb code 6ms3). 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 GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis, PDB code: 6ms3:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 6ms3

Go back to Calcium Binding Sites List in 6ms3
Calcium binding site 1 out of 2 in the Crystal Structure of the GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis


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 GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca601

b:32.5
occ:1.00
O A:GLY347 2.3 34.0 1.0
O A:ASP319 2.3 32.1 1.0
O A:ASP508 2.3 27.6 1.0
OD1 A:ASP319 2.3 40.7 1.0
OD1 A:ASP508 2.4 32.8 1.0
O A:HOH1001 2.4 35.3 1.0
C A:ASP508 3.3 28.6 1.0
C A:ASP319 3.3 31.6 1.0
CG A:ASP319 3.4 41.6 1.0
C A:GLY347 3.5 33.8 1.0
CG A:ASP508 3.5 33.0 1.0
CA A:ASP508 3.8 29.4 1.0
CA A:ASP319 3.9 32.6 1.0
CB A:ASP319 4.0 37.2 1.0
CA A:GLY347 4.1 33.4 1.0
CB A:ASP508 4.2 30.4 1.0
OD2 A:ASP319 4.4 44.5 1.0
N A:TRP509 4.4 27.6 1.0
N A:PHE320 4.5 30.1 1.0
OD2 A:ASP508 4.5 35.5 1.0
N A:TYR348 4.5 33.4 1.0
CB A:PHE320 4.7 30.1 1.0
CB A:TRP509 4.7 28.4 1.0
C A:PHE320 4.7 35.2 1.0
CA A:TRP509 4.8 26.9 1.0
O A:PHE320 4.8 36.2 1.0
CA A:PHE320 4.8 31.5 1.0
CA A:TYR348 4.9 32.4 1.0
CD1 A:TRP509 4.9 31.5 1.0

Calcium binding site 2 out of 2 in 6ms3

Go back to Calcium Binding Sites List in 6ms3
Calcium binding site 2 out of 2 in the Crystal Structure of the GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis


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 GH43 Protein Blxynb Mutant (K247S) From Bacillus Licheniformis within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca601

b:32.5
occ:1.00
O B:GLY347 2.2 33.5 1.0
OD1 B:ASP508 2.3 31.3 1.0
OD1 B:ASP319 2.3 40.3 1.0
O B:ASP319 2.3 32.3 1.0
O B:ASP508 2.4 28.5 1.0
O B:HOH997 2.4 31.5 1.0
C B:GLY347 3.3 33.3 1.0
CG B:ASP319 3.4 42.5 1.0
C B:ASP508 3.4 28.8 1.0
C B:ASP319 3.4 31.5 1.0
CG B:ASP508 3.5 31.2 1.0
CA B:GLY347 3.8 35.0 1.0
CA B:ASP508 3.9 29.2 1.0
O B:HOH972 3.9 55.4 1.0
CA B:ASP319 3.9 32.4 1.0
CB B:ASP319 4.0 38.3 1.0
CB B:ASP508 4.3 29.9 1.0
OD2 B:ASP319 4.3 46.4 1.0
OD2 B:ASP508 4.4 32.0 1.0
N B:TYR348 4.5 32.6 1.0
N B:TRP509 4.5 28.1 1.0
N B:PHE320 4.5 31.1 1.0
CB B:TRP509 4.7 28.3 1.0
O B:HOH810 4.7 46.9 1.0
CB B:PHE320 4.7 29.6 1.0
C B:PHE320 4.8 36.3 1.0
CA B:TYR348 4.9 31.4 1.0
CA B:TRP509 4.9 27.6 1.0
O B:PHE320 4.9 37.2 1.0
CA B:PHE320 4.9 32.0 1.0

Reference:

L.M.Zanphorlin, M.A.B.De Morais, J.A.Diogo, M.N.Domingues, F.H.M.De Souza, R.Ruller, M.T.Murakami. Structure-Guided Design Combined with Evolutionary Diversity Led to the Discovery of the Xylose-Releasing Exo-Xylanase Activity in the Glycoside Hydrolase Family 43. Biotechnol. Bioeng. V. 116 734 2019.
ISSN: ESSN 1097-0290
PubMed: 30556897
DOI: 10.1002/BIT.26899
Page generated: Sat Dec 12 07:10:19 2020

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy