Structure of PDB 6coi Chain B Binding Site BS01
Receptor Information
>6coi Chain B (length=258) Species:
3702
(Arabidopsis thaliana) [
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MERKHHFVLVHNACHGAWIWYKLKPLLESAGHRVTAVELAASGIDPRPIQ
AVETVDEYSKPLIETLKSLPENEEVILVGFSFGGINIALAADIFPAKIKV
LVFLNAFLPDTTHVPSHVLDKLMEMFGGWGDTEFSSHETRNGTMSLLKMG
PKFMKARLYQNCPIEDYELAKMLHRQGSFFTEDLSKKEKFSEEGYGSVQR
VYVMSSEDKIIPCDFIRWMIDNFNVSKVYEIDGGDHMVMLSKPQKLFDSL
SAIATDYM
Ligand information
Ligand ID
HBX
InChI
InChI=1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H
InChIKey
HUMNYLRZRPPJDN-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
O=Cc1ccccc1
OpenEye OEToolkits 1.5.0
c1ccc(cc1)C=O
Formula
C7 H6 O
Name
benzaldehyde
ChEMBL
CHEMBL15972
DrugBank
ZINC
ZINC000000895145
PDB chain
6coi Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
6coi
AtHNL enantioselectivity mutants
Resolution
2.024 Å
Binding residue
(original residue number in PDB)
F107 L119 M123 W129 F179
Binding residue
(residue number reindexed from 1)
F107 L119 M123 W129 F179
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
N12 S81 F82 D208 H236 M237
Catalytic site (residue number reindexed from 1)
N12 S81 F82 D208 H236 M237
Enzyme Commision number
4.1.2.10
: (R)-mandelonitrile lyase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0016829
lyase activity
GO:0046593
mandelonitrile lyase activity
Biological Process
GO:0009611
response to wounding
GO:0016139
glycoside catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6coi
,
PDBe:6coi
,
PDBj:6coi
PDBsum
6coi
PubMed
UniProt
Q9LFT6
|HNL_ARATH Alpha-hydroxynitrile lyase (Gene Name=HNL)
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