Structure of PDB 5nna Chain C Binding Site BS01

Receptor Information
>5nna Chain C (length=257) Species: 187304 (Roseibium aggregatum) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
ASSLNQLVSGLASGAVRIVDLTHTLDPDFPVIVLPPEFGQCARFRMEEIS
AYDHRGPAWKWHNISMSEHTGTHFDAPSHWISGKDVPNGSVDEIPAEAFV
GPVVVIDCSKGAAENDDFELTPEIIAGWESEHGRIPEDAWVLMRTDWSKR
RGADYLNMRADGPHSPGPTPEAIRFLIEERNIRGFGTETVGTDAGQGAHY
VPPYPAHYLLHGAGKYGLQCLANLDQLPATGAVLIAAPLKIKNGTGSPLR
VLAMVTE
Ligand information
Ligand IDBZM
InChIInChI=1S/C14H12O2/c15-14(13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h1-10H,11H2
InChIKeySESFRYSPDFLNCH-UHFFFAOYSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0c1ccc(cc1)COC(=O)c2ccccc2
ACDLabs 10.04
CACTVS 3.341
O=C(OCc1ccccc1)c2ccccc2
FormulaC14 H12 O2
NameBENZOIC ACID PHENYLMETHYLESTER
ChEMBLCHEMBL1239
DrugBankDB00676
ZINCZINC000000001021
PDB chain5nna Chain C Residue 301 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB5nna A fundamental catalytic difference between zinc and manganese dependent enzymes revealed in a bacterial isatin hydrolase.
Resolution1.5 Å
Binding residue
(original residue number in PDB)
I32 L34 W80 P163 V190 G191 D193 Y204 H207
Binding residue
(residue number reindexed from 1)
I32 L34 W80 P163 V190 G191 D193 Y204 H207
Annotation score1
Enzymatic activity
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0004061 arylformamidase activity
GO:0046872 metal ion binding
Biological Process
GO:0019441 tryptophan catabolic process to kynurenine

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Molecular Function

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Biological Process
External links
PDB RCSB:5nna, PDBe:5nna, PDBj:5nna
PDBsum5nna
PubMed30166577
UniProtA0P0F0

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