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Calcium in PDB 3bai: Human Pancreatic Alpha Amylase with Bound Nitrate

Enzymatic activity of Human Pancreatic Alpha Amylase with Bound Nitrate

All present enzymatic activity of Human Pancreatic Alpha Amylase with Bound Nitrate:
3.2.1.1;

Protein crystallography data

The structure of Human Pancreatic Alpha Amylase with Bound Nitrate, PDB code: 3bai 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) 28.94 / 1.90
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 52.990, 69.110, 132.200, 90.00, 90.00, 90.00
R / Rfree (%) 16.9 / 20.8

Calcium Binding Sites:

The binding sites of Calcium atom in the Human Pancreatic Alpha Amylase with Bound Nitrate (pdb code 3bai). 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 Human Pancreatic Alpha Amylase with Bound Nitrate, PDB code: 3bai:

Calcium binding site 1 out of 1 in 3bai

Go back to Calcium Binding Sites List in 3bai
Calcium binding site 1 out of 1 in the Human Pancreatic Alpha Amylase with Bound Nitrate


Mono view


Stereo pair view

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

b:19.2
occ:1.00
OD1 A:ASN100 2.3 18.5 1.0
O A:ARG158 2.4 18.1 1.0
O A:HIS201 2.4 17.6 1.0
O A:HOH514 2.4 18.6 1.0
OD2 A:ASP167 2.5 18.0 1.0
O A:HOH521 2.5 22.2 1.0
OD1 A:ASP167 2.5 17.6 1.0
O A:HOH558 2.6 23.3 1.0
CG A:ASP167 2.8 17.8 1.0
CG A:ASN100 3.5 19.7 1.0
C A:ARG158 3.5 19.1 1.0
C A:HIS201 3.6 16.9 1.0
ND2 A:ASN100 4.0 16.5 1.0
CA A:ARG158 4.2 19.7 1.0
CB A:HIS201 4.3 18.2 1.0
O A:ASN100 4.3 18.3 1.0
CB A:ASP167 4.3 17.4 1.0
O A:HOH545 4.5 22.7 1.0
CA A:HIS201 4.5 16.5 1.0
O A:CYS160 4.5 20.4 1.0
N A:MET202 4.6 17.4 1.0
N A:ASP159 4.6 19.2 1.0
ND2 A:ASN137 4.6 18.5 1.0
CA A:MET202 4.6 16.9 1.0
CG A:MET202 4.7 17.9 1.0
O A:VAL157 4.7 20.1 1.0
O A:LEU168 4.7 16.4 1.0
CB A:ASN100 4.8 16.3 1.0
CA A:ASP159 4.8 21.1 1.0
O A:HOH510 4.9 18.7 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 08:12:34 2024

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