Atomistry » Calcium » PDB 8hfm-8if8 » 8i5o
Atomistry »
  Calcium »
    PDB 8hfm-8if8 »
      8i5o »

Calcium in PDB 8i5o: Crystal Structure of TXGH116 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum

Enzymatic activity of Crystal Structure of TXGH116 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum

All present enzymatic activity of Crystal Structure of TXGH116 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum:
3.2.1.21;

Protein crystallography data

The structure of Crystal Structure of TXGH116 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum, PDB code: 8i5o 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 / 2.30
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 178.199, 54.376, 83.378, 90, 90, 90
R / Rfree (%) 17.3 / 22.3

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of TXGH116 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum (pdb code 8i5o). 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 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum, PDB code: 8i5o:

Calcium binding site 1 out of 1 in 8i5o

Go back to Calcium Binding Sites List in 8i5o
Calcium binding site 1 out of 1 in the Crystal Structure of TXGH116 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum


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 D593A Acid/Base Mutant From Thermoanaerobacterium Xylanolyticum within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca1003

b:51.3
occ:1.00
 O A:ILE581 2.3 39.0 1.0
OD1 A:ASP583 2.3 49.0 1.0
OD1 A:ASP579 2.3 44.8 1.0
OD1 A:ASP577 2.5 63.5 1.0
OD1 A:ASP575 2.6 43.6 1.0
CG A:ASP583 3.1 49.2 1.0
CG A:ASP579 3.2 45.6 1.0
C A:ILE581 3.4 39.5 1.0
OD2 A:ASP583 3.5 52.9 1.0
OD2 A:ASP579 3.6 44.8 1.0
CG A:ASP575 3.7 44.5 1.0
CG A:ASP577 3.7 60.4 1.0
N A:ASP583 3.9 42.5 1.0
C A:PRO582 4.0 41.7 1.0
N A:ILE581 4.2 39.4 1.0
CA A:ASP583 4.2 44.7 1.0
CB A:ASP583 4.2 47.0 1.0
CA A:ILE581 4.2 39.5 1.0
OG1 A:THR600 4.2 39.7 1.0
OD2 A:ASP577 4.2 61.1 1.0
CA A:ASP575 4.2 47.2 1.0
CB A:ILE581 4.3 39.5 1.0
O A:PRO582 4.3 42.6 1.0
CB A:ASP575 4.4 45.9 1.0
N A:ASP579 4.4 49.4 1.0
N A:PRO582 4.4 40.7 1.0
CB A:ASP579 4.5 45.9 1.0
CA A:PRO582 4.5 41.0 1.0
N A:LYS576 4.5 54.2 1.0
OD2 A:ASP575 4.5 44.0 1.0
N A:ASP577 4.6 57.4 1.0
C A:ASP575 4.7 49.7 1.0
N A:ASN578 4.8 56.5 1.0
CA A:ASP579 4.9 46.6 1.0
CB A:ASP577 4.9 59.8 1.0
CG2 A:ILE581 4.9 39.7 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: Fri Jul 19 09:35:48 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy