Structure of PDB 5k8o Chain G Binding Site BS01
Receptor Information
>5k8o Chain G (length=422) Species:
376
(Bradyrhizobium sp.) [
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SNDVAKVMKTLDGMREGLIQTAVELGSIEAPTGREGAAGDYVYEWMARNG
FGPERVGVFDDRFNVVGRLRGTGGGASLSFNSHLDTIMAREDTARFADAN
DRIYHEAWHEEGRIYGYSVVNCKGPMACWLIAAKALKEAGAALKGDVVLT
AVCGEIDCEPVDEFQGHDYLAEDIGARYAISHGAISDYALVAEATNFKPA
WVEAGKVFLKVTVFAGPSRYTPYVPRPVAALDSPNAIVRMAKLVEALEEW
ADNYEKRYTREYGGGTVVPKVAIGAIRGGVPYKIYRFPELCSIYMDIRLN
PDTNPLVVQREVEAVVSKLGLKAEVKPFLFRRGYEAQGIEPLQNALEVAH
REVVGRPTERPGSPECSMWRDTNPYNELGIPSLTYGCGGGAGGGNTYFLV
DDMLKAAKVYAMTAMDLCNRTP
Ligand information
Ligand ID
6R7
InChI
InChI=1S/C7H5NO5/c9-6-2-1-4(8(12)13)3-5(6)7(10)11/h1-3,9H,(H,10,11)
InChIKey
PPDRLQLKHRZIJC-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.5
c1cc(c(cc1[N+](=O)[O-])C(=O)O)O
CACTVS 3.385
OC(=O)c1cc(ccc1O)[N+]([O-])=O
Formula
C7 H5 N O5
Name
5-nitrosalicylic acid;
5-nitro-2-oxidanyl-benzoic acid
ChEMBL
CHEMBL1940317
DrugBank
ZINC
ZINC000001555337
PDB chain
5k8o Chain F Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
5k8o
Enzymatic hydrolysis by transition-metal-dependent nucleophilic aromatic substitution.
Resolution
2.893 Å
Binding residue
(original residue number in PDB)
Y223 Y288 R289
Binding residue
(residue number reindexed from 1)
Y220 Y285 R286
Annotation score
3
Enzymatic activity
Enzyme Commision number
3.5.99.8
: 5-nitroanthranilic acid aminohydrolase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:5k8o
,
PDBe:5k8o
,
PDBj:5k8o
PDBsum
5k8o
PubMed
27694799
UniProt
D3WZ85
|NAAA_BRASZ 5-nitroanthranilic acid aminohydrolase (Gene Name=naaA)
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