Structure of PDB 7vi7 Chain B Binding Site BS02

Receptor Information
>7vi7 Chain B (length=339) Species: 349741 (Akkermansia muciniphila ATCC BAA-835) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MLPALIGISGHEVGAEEEAAIRRLQPAGFILFSRNIDSVEQVRGLTESLR
KLCLHHPVIAVDQEGGRVVRTASLGLNLPSPASLARLGSVGGIVELGAVT
ALALRYLGVNLNFAPVLDICHDPNALPGRCWGDNAQDVISRGGVYASNLR
RGGVQSCGKHFPGMGRALADPHFSLPVIGLDERELFKTDLLPFLALCPAL
SSIMSAHIMLPQIDPDYPATLSERVIRGLLRDRLGFRGVVFTDDLCMGAI
TTQYSPDDAAFLSLKAGCDLPLICHDPLPWLDGLASRQESLNAYDRWDSF
KRVEKLSDSLCFPFPEKASLWDSCLRRAEALCRLEEDGR
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain7vi7 Chain B Residue 503 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB7vi7 Functional and structural characterization of a GH3 beta-N-acetylhexosaminidase from Akkermansia muciniphila involved in mucin degradation
Resolution2.0 Å
Binding residue
(original residue number in PDB)
D37 S73
Binding residue
(residue number reindexed from 1)
D37 S73
Annotation score4
Enzymatic activity
Enzyme Commision number 3.2.1.52: beta-N-acetylhexosaminidase.
Gene Ontology
Molecular Function
GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0004563 beta-N-acetylhexosaminidase activity
GO:0016798 hydrolase activity, acting on glycosyl bonds
GO:0046872 metal ion binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0009254 peptidoglycan turnover

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Molecular Function

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Biological Process
External links
PDB RCSB:7vi7, PDBe:7vi7, PDBj:7vi7
PDBsum7vi7
PubMed
UniProtB2UPP0

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