Atomistry » Calcium » PDB 3b1u-3biw » 3bak
Atomistry »
  Calcium »
    PDB 3b1u-3biw »
      3bak »

Calcium in PDB 3bak: N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate

Enzymatic activity of N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate

All present enzymatic activity of N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate:
3.2.1.1;

Protein crystallography data

The structure of N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate, PDB code: 3bak was solved by J.R.Fredriksen, R.Maurus, G.D.Brayer, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 17.14 / 1.90
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 52.439, 68.977, 131.318, 90.00, 90.00, 90.00
R / Rfree (%) 17.4 / 20.6

Calcium Binding Sites:

The binding sites of Calcium atom in the N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate (pdb code 3bak). 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 N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate, PDB code: 3bak:

Calcium binding site 1 out of 1 in 3bak

Go back to Calcium Binding Sites List in 3bak
Calcium binding site 1 out of 1 in the N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of N298S Mutant of Human Pancreatic Alpha-Amylase in Complex with Nitrate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca498

b:13.8
occ:1.00
OD1 A:ASN100 2.4 14.7 1.0
O A:HIS201 2.4 14.1 1.0
O A:ARG158 2.4 16.4 1.0
O A:HOH533 2.5 20.6 1.0
OD2 A:ASP167 2.5 15.9 1.0
O A:HOH762 2.5 18.2 1.0
OD1 A:ASP167 2.6 15.9 1.0
O A:HOH504 2.6 14.1 1.0
CG A:ASP167 2.9 16.0 1.0
CG A:ASN100 3.6 16.8 1.0
C A:ARG158 3.6 15.8 1.0
C A:HIS201 3.7 14.1 1.0
ND2 A:ASN100 4.1 15.0 1.0
CA A:ARG158 4.2 16.0 1.0
CB A:HIS201 4.3 16.1 1.0
CB A:ASP167 4.4 15.2 1.0
O A:ASN100 4.4 15.3 1.0
O A:HOH530 4.5 17.2 1.0
CA A:HIS201 4.5 14.6 1.0
ND2 A:ASN137 4.5 17.9 1.0
O A:CYS160 4.6 18.8 1.0
N A:MET202 4.6 13.8 1.0
N A:ASP159 4.6 16.8 1.0
CA A:MET202 4.7 14.0 1.0
O A:VAL157 4.8 17.0 1.0
O A:LEU168 4.8 15.3 1.0
CG A:MET202 4.8 14.7 1.0
CA A:ASP159 4.8 17.7 1.0
CB A:ASN100 4.9 14.0 1.0
O A:HOH515 5.0 16.4 1.0

Reference:

R.Maurus, A.Begum, L.K.Williams, J.R.Fredriksen, R.Zhang, S.G.Withers, G.D.Brayer. Alternative Catalytic Anions Differentially Modulate Human Alpha-Amylase Activity and Specificity Biochemistry V. 47 3332 2008.
ISSN: ISSN 0006-2960
PubMed: 18284212
DOI: 10.1021/BI701652T
Page generated: Sat Jul 13 08:13:19 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