Structure of PDB 1amy Chain A Binding Site BS02
Receptor Information
>1amy Chain A (length=403) Species:
4513
(Hordeum vulgare) [
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QVLFQGFNWESWKHNGGWYNFLMGKVDDIAAAGITHVWLPPASQSVAEQG
YMPGRLYDLDASKYGNKAQLKSLIGALHGKGVKAIADIVINHRTAEHKDG
RGIYCIFEGGTPDARLDWGPHMICRDDRPYADGTGNPDTGADFGAAPDID
HLNLRVQKELVEWLNWLKADIGFDGWRFDFAKGYSADVAKIYIDRSEPSF
AVAEIWTSLAYGGDGKPNLNQDQHRQELVNWVDKVGGKGPATTFDFTTKG
ILNVAVEGELWRLRGTDGKAPGMIGWWPAKAVTFVDNHDTGSTQHMWPFP
SDRVMQGYAYILTHPGTPCIFYDHFFDWGLKEEIDRLVSVRTRHGIHNES
KLQIIEADADLYLAEIDGKVIVKLGPRYDVGNLIPGGFKVAAHGNDYAVW
EKI
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1amy Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
1amy
Crystal and molecular structure of barley alpha-amylase.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
E108 T111 P112 D113 D117
Binding residue
(residue number reindexed from 1)
E108 T111 P112 D113 D117
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D179 E204 D289
Catalytic site (residue number reindexed from 1)
D179 E204 D289
Enzyme Commision number
3.2.1.1
: alpha-amylase.
Gene Ontology
Molecular Function
GO:0004556
alpha-amylase activity
GO:0005509
calcium ion binding
GO:0016798
hydrolase activity, acting on glycosyl bonds
GO:0043169
cation binding
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0005983
starch catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1amy
,
PDBe:1amy
,
PDBj:1amy
PDBsum
1amy
PubMed
8196040
UniProt
P04063
|AMY2_HORVU Alpha-amylase type B isozyme (Gene Name=AMY1.2)
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