Structure of PDB 3k4d Chain A Binding Site BS01

Receptor Information
>3k4d Chain A (length=596) Species: 83333 (Escherichia coli K-12) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
SHMLRPVETPTREIKKLDGLWAFSLDRENCGIDQRWWESALQESRAIAVP
GSFNDQFADADIRNYAGNVWYQREVFIPKGWAGQRIVLRFDAVTHYGKVW
VNNQEVMEHQGGYTPFEADVTPYVIAGKSVRITVCVNNELNWQTIPPGMV
ITDENGKKKQSYFHDFFNYAGIHRSVMLYTTPNTWVDDITVVTHVAQDCN
HASVDWQVVANGDVSVELRDADQQVVATGQGTSGTLQVVNPHLWQPGEGY
LYELCVTAKSQTECDIYPLRVGIRSVAVKGEQFLINHKPFYFTGFGRHED
ADLRGKGFDNVLMVHDHALMDWIGANSYRTSHYPYAEEMLDWADEHGIVV
IDETAAVGFNLSLGKPKELYSEEAVNGETQQAHLQAIKELIARDKNHPSV
VMWSIANEPDTRPQGAREYFAPLAEATRKLDPTRPITCVNVMFCDAHTDT
ISDLFDVLCLNRYYGWYVQSGDLETAEKVLEKELLAWQEKLHQPIIITEY
GVDTLAGLHSMYTDMWSEEYQCAWLDMYHRVFDRVSAVVGEQVWNFADFA
TSQGILRVGGNKKGIFTRDRKPKSAAFLLQKRWTGMNFGEKPQQGG
Ligand information
Ligand IDEVA
InChIInChI=1S/C6H9NO6/c8-2-1(6(12)13)7-5(11)4(10)3(2)9/h1-4,8-10H,(H,7,11)(H,12,13)/t1-,2+,3-,4+/m0/s1
InChIKeyYEWOHTVJCCDCCS-NTAGLIMJSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.7.0C1(C(C(NC(=O)C1O)C(=O)O)O)O
OpenEye OEToolkits 1.7.0[C@@H]1([C@@H]([C@H](NC(=O)[C@@H]1O)C(=O)O)O)O
CACTVS 3.352O[CH]1[CH](O)[CH](NC(=O)[CH]1O)C(O)=O
ACDLabs 11.02O=C(O)C1NC(=O)C(O)C(O)C1O
CACTVS 3.352O[C@H]1[C@H](O)[C@H](NC(=O)[C@@H]1O)C(O)=O
FormulaC6 H9 N O6
Name(2S,3R,4S,5R)-3,4,5-trihydroxy-6-oxopiperidine-2-carboxylic acid
ChEMBLCHEMBL1232598
DrugBank
ZINC
PDB chain3k4d Chain A Residue 604 [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]
PDB3k4d Alleviating cancer drug toxicity by inhibiting a bacterial enzyme.
Resolution2.393 Å
Binding residue
(original residue number in PDB)
D163 H330 E413 Y468 Y472 E504 W549 K568
Binding residue
(residue number reindexed from 1)
D165 H332 E408 Y463 Y467 E499 W544 K563
Annotation score1
Binding affinityMOAD: Ki=7750nM
PDBbind-CN: -logKd/Ki=5.11,Ki=7750nM
BindingDB: Ki=232nM
Enzymatic activity
Catalytic site (original residue number in PDB) D163 H296 H330 V355 F357 E413 Y468 E504 K568
Catalytic site (residue number reindexed from 1) D165 H298 H332 V357 F359 E408 Y463 E499 K563
Enzyme Commision number 3.2.1.31: beta-glucuronidase.
Gene Ontology
Molecular Function
GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0004566 beta-glucuronidase activity
GO:0016798 hydrolase activity, acting on glycosyl bonds
GO:0030246 carbohydrate binding
GO:0042802 identical protein binding
Biological Process
GO:0005975 carbohydrate metabolic process
Cellular Component
GO:0005829 cytosol
GO:0032991 protein-containing complex

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:3k4d, PDBe:3k4d, PDBj:3k4d
PDBsum3k4d
PubMed21051639
UniProtP05804|BGLR_ECOLI Beta-glucuronidase (Gene Name=uidA)

[Back to BioLiP]