Atomistry » Calcium » PDB 8hcj-8ic1 » 8i5t
Atomistry »
  Calcium »
    PDB 8hcj-8ic1 »
      8i5t »

Calcium in PDB 8i5t: Crystal Structure of TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose

Enzymatic activity of Crystal Structure of TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose

All present enzymatic activity of Crystal Structure of TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose:
3.2.1.21;

Protein crystallography data

The structure of Crystal Structure of TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose, PDB code: 8i5t was solved by S.Pengthaisong, J.R.Ketudat Cairns, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 30.00 / 1.50
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 177.712, 54.409, 83.168, 90, 90, 90
R / Rfree (%) 15.9 / 18.1

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose (pdb code 8i5t). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Crystal Structure of TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose, PDB code: 8i5t:

Calcium binding site 1 out of 1 in 8i5t

Go back to Calcium Binding Sites List in 8i5t
Calcium binding site 1 out of 1 in the Crystal Structure of TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose


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 TXGH116 D593N Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum with Cellobiose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca914

b:23.9
occ:1.00
 OD1 A:ASP579 2.3 22.9 1.0
OD1 A:ASP583 2.3 27.2 1.0
O A:ILE581 2.3 20.1 1.0
O A:HOH1114 2.4 23.6 1.0
OD1 A:ASP575 2.4 23.1 1.0
OD1 A:ASP577 2.5 33.2 1.0
O3 A:GOL911 3.0 45.9 1.0
CG A:ASP583 3.2 27.8 1.0
CG A:ASP579 3.2 24.4 1.0
CG A:ASP575 3.4 22.2 1.0
C A:ILE581 3.5 20.2 1.0
OD2 A:ASP583 3.5 33.4 1.0
OD2 A:ASP579 3.6 25.7 1.0
CG A:ASP577 3.6 35.7 1.0
CA A:ASP575 4.0 24.3 1.0
N A:ILE581 4.0 19.5 1.0
CB A:ASP575 4.2 23.5 1.0
N A:ASP583 4.2 21.7 1.0
CA A:ILE581 4.2 19.6 1.0
OD2 A:ASP577 4.2 37.5 1.0
C A:PRO582 4.2 21.8 1.0
N A:ASP579 4.2 27.1 1.0
N A:LYS576 4.3 30.5 1.0
C3 A:GOL911 4.3 45.5 1.0
CB A:ILE581 4.3 19.9 1.0
N A:ASP577 4.3 33.9 1.0
OD2 A:ASP575 4.3 23.2 1.0
CB A:ASP579 4.4 25.3 1.0
CB A:ASP583 4.4 25.5 1.0
C A:ASP575 4.5 26.5 1.0
CA A:ASP583 4.5 22.9 1.0
OG1 A:THR600 4.5 21.1 1.0
O A:PRO582 4.5 22.8 1.0
N A:PRO582 4.5 20.3 1.0
CA A:PRO582 4.6 20.4 1.0
N A:ASN578 4.7 32.6 1.0
CA A:ASP579 4.7 25.9 1.0
CB A:ASP577 4.8 35.1 1.0
N A:GLY580 4.8 21.5 1.0
CA A:ASP577 4.9 34.3 1.0
C A:ASP577 4.9 34.1 1.0
C A:ASP579 5.0 23.9 1.0

Reference:

S.Pengthaisong, B.Piniello, G.J.Davies, C.Rovira, J.R.K.Cairns. Reaction Mechanism of Glycoside Hydrolase Family 116 Utilizes Perpendicular Protonation Acs Catalysis 5850 2023.
ISSN: ESSN 2155-5435
DOI: 10.1021/ACSCATAL.3C00620
Page generated: Thu Jul 10 05:12:06 2025

Last articles

Fe in 8ZNS
Fe in 8ZK2
Fe in 8ZGP
Fe in 8ZGO
Fe in 8ZGH
Fe in 8ZGG
Fe in 8ZET
Fe in 8ZEH
Fe in 8ZGE
Fe in 8Z82
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy