Structure of PDB 1mxd Chain A Binding Site BS08
Receptor Information
>1mxd Chain A (length=435) Species:
2262
(Pyrococcus woesei) [
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AKYLELEEGGVIMQAFYWDVPGGGIWWDHIRSKIPEWYEAGISAIWLPPP
SKGMSGGYSMGYDPYDYFDLGEYYQKGTVETRFGSKEELVRLIQTAHAYG
IKVIADVVINHRAGGDLEWNPFVGDYTWTDFSKVASGKYTANYLDFHPNE
LHCCDEGTFGGFPDICHHKEWDQYWLWKSNESYAAYLRSIGFDGWRFDYV
KGYGAWVVRDWLNWWGGWAVGEYWDTNVDALLSWAYESGAKVFDFPLYYK
MDEAFDNNNIPALVYALQNGQTVVSRDPFKAVTFVANHDTDIIWNKYPAY
AFILTYEGQPVIFYRDFEEWLNKDKLINLIWIHDHLAGGSTTIVYYDNDE
LIFVRNGDSRRPGLITYINLSPNWVGRWVYVPKFAGACIHEYTGNLGGWV
DKRVDSSGWVYLEAPPHDPANGYYGYSVWSYCGVG
Ligand information
Ligand ID
GLC
InChI
InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
InChIKey
WQZGKKKJIJFFOK-DVKNGEFBSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(C1C(C(C(C(O1)O)O)O)O)O
OpenEye OEToolkits 1.5.0
C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O)O
CACTVS 3.341
OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
CACTVS 3.341
OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
ACDLabs 10.04
OC1C(O)C(OC(O)C1O)CO
Formula
C6 H12 O6
Name
alpha-D-glucopyranose;
alpha-D-glucose;
D-glucose;
glucose
ChEMBL
CHEMBL423707
DrugBank
ZINC
ZINC000003861213
PDB chain
1mxd Chain E Residue 2 [
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Receptor-Ligand Complex Structure
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PDB
1mxd
Differential Regulation of a Hyperthermophilic alpha-Amylase with a Novel (Ca,Zn) Two-metal Center by Zinc
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
K201 W224
Binding residue
(residue number reindexed from 1)
K201 W224
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D198 E222 D289
Catalytic site (residue number reindexed from 1)
D198 E222 D289
Enzyme Commision number
3.2.1.1
: alpha-amylase.
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
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
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1mxd
,
PDBe:1mxd
,
PDBj:1mxd
PDBsum
1mxd
PubMed
12482867
UniProt
Q7LYT7
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