Structure of PDB 3nfz Chain A Binding Site BS01
Receptor Information
>3nfz Chain A (length=305) Species:
10090
(Mus musculus) [
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SREPLLRVAVTGGTHGNEMCGVYLARYWLQNPGELQRPSFSAMPVLANPA
ATAACCRYLDRDLNRSCTLTFLGSTATPDDPYEVKRARELNQLLGPKGTG
QAFDFTLDLHNTTANTGVCLISESNISFNLHLCHYLQRQNPGMPCRLFLY
EPAGTETFSVESISKNGICLAMGPQPQGVLRADLFSRMRALVASILDFIE
LFNQGMDLPAFEMDIYRNLGSVDFPRTADGDLAGTVHPQLQDHDFEPLRP
GEPIFKLFSGEDVLYEGDSIVYPVFINEAAYYEKHVAFLKSEKIRVTVPA
LLRLT
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
3nfz Chain A Residue 319 [
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Receptor-Ligand Complex Structure
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PDB
3nfz
Structures of aminoacylase 3 in complex with acetylated substrates.
Resolution
2.147 Å
Binding residue
(original residue number in PDB)
H21 E24 H116
Binding residue
(residue number reindexed from 1)
H15 E18 H110
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.1.114
: N-acyl-aromatic-L-amino acid amidohydrolase.
Gene Ontology
Molecular Function
GO:0004046
aminoacylase activity
GO:0005515
protein binding
GO:0016787
hydrolase activity
GO:0016788
hydrolase activity, acting on ester bonds
GO:0016811
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Cellular Component
GO:0005737
cytoplasm
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0016324
apical plasma membrane
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:3nfz
,
PDBe:3nfz
,
PDBj:3nfz
PDBsum
3nfz
PubMed
20921362
UniProt
Q91XE4
|ACY3_MOUSE N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming) (Gene Name=Acy3)
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