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 Dec 12 04:05:51 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