Structure of PDB 7lvy Chain A Binding Site BS03

Receptor Information
>7lvy Chain A (length=431) Species: 32264 (Tetranychus urticae) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
LYDPFMKIFFIPMDAFGHVNACIGLARMLSEFEHQCIFAVPKRWCKPIEE
YNFKVEIVKDPTVPDDQDLQKKNGDFVNRYSHTLSKTPREQFIELLIPSI
NRDIHYAKIIDGQIPTILESIDPDLIIIDFYVTLPSVVNSGKPWIHLTSC
NPLNLYAGPNVPPSCFGLSIDTDPDTVISYKQFIAESMKDVKSDFDEWLV
SKGVKPEPFAISKSSPYLNVYSFPSDLDYSEFGPVPDKCFRLDHMVRLVQ
EDPLGFDEKFFDRPGKKILFSLGSMGAADVELMKRLVGILGKSKHLFIVS
KGLFHDKYELPENMIGAKFLNQMAILPRVDLVIHHGGNNTFVESLYFGKP
SIVLPLFGDQHDNGRRAEDKKIGRSFRPHHVTEDELLMAIDELLNDKELN
NRVLKIGENIRNSKSIDDFNKKIEEIIKVHK
Ligand information
Ligand IDBGC
InChIInChI=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
InChIKeyWQZGKKKJIJFFOK-VFUOTHLCSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.7.6C(C1C(C(C(C(O1)O)O)O)O)O
CACTVS 3.370OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
CACTVS 3.370OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
OpenEye OEToolkits 1.7.6C([C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)O)O)O)O
ACDLabs 12.01OC1C(O)C(OC(O)C1O)CO
FormulaC6 H12 O6
Namebeta-D-glucopyranose;
beta-D-glucose;
D-glucose;
glucose
ChEMBLCHEMBL1614854
DrugBankDB02379
ZINCZINC000003833800
PDB chain7lvy Chain A Residue 503 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB7lvy Crystal Structure of Tetur04g02350
Resolution1.85 Å
Binding residue
(original residue number in PDB)		Y126 G332 N333 D354 Q355
Binding residue
(residue number reindexed from 1)		Y131 G337 N338 D359 Q360
Annotation score4
Enzymatic activity
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0000166 nucleotide binding
GO:0008194 UDP-glycosyltransferase activity
GO:0016740 transferase activity
GO:0016758 hexosyltransferase activity

View graph for
Molecular Function
External links
PDB RCSB:7lvy, PDBe:7lvy, PDBj:7lvy
PDBsum7lvy
PubMed
UniProtT1K1R5

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