Structure of PDB 4pys Chain B Binding Site BS01

Receptor Information
>4pys Chain B (length=483) Species: 272559 (Bacteroides fragilis NCTC 9343) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GQIIMPTPGKIERADGRLRLQGKIRMYAEESPGSFIRLFYEKLVPESAVE
WCKEEVNSHISWKKDVTLPTEGYRIRVTPERIIVEAADDAGFIYAIQSLR
QWNTGEERGLIFPCVEITDFPRVKWRSFMLDSGRQYQKVSTIKKYIDMAS
MLKMNYFHWHLTEGLGWRIEIKRYPFLTRIGAFVGQGPEQQGFYSQEEVK
EIIGYAADRGITVVPEIDMPGHAEAALNAYPRLGCNVAVKVNIFCAGKDS
TLIFLKNVLDEVCRMFPSAYIHLGGDEAPKCPDCRSRIEKEKLSHDLQLW
FSARMADYLKQKGRKAIFWGDVIYKDYSLPDNVVIQWWNWRGHRDLALKN
AVRHNYPVICGTNYYTYLNFPLTPWKGYTQARTFDLEDVYLRNPSYRPRE
ENPLILGMSSALWTDDGVTESMIDRRVFPRILALAEQMWHSGNPENFDEF
YGKVLSKQLWFEQQGYSFGPALKEDAGTNYKWD
Ligand information
Ligand IDZN
InChIInChI=1S/Zn/q+2
InChIKeyPTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
FormulaZn
NameZINC ION
ChEMBLCHEMBL1236970
DrugBankDB14532
ZINC
PDB chain4pys Chain B Residue 601 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB4pys The crystal structure of beta-N-acetylhexosaminidase from Bacteroides fragilis NCTC 9343
Resolution1.822 Å
Binding residue
(original residue number in PDB)
C254 C272 C313 C316
Binding residue
(residue number reindexed from 1)
C235 C245 C281 C284
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) D303 E304
Catalytic site (residue number reindexed from 1) D276 E277
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:0030203 glycosaminoglycan metabolic process
Cellular Component
GO:0016020 membrane

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:4pys, PDBe:4pys, PDBj:4pys
PDBsum4pys
PubMed
UniProtD1JST6

[Back to BioLiP]