Structure of PDB 4zuq Chain A Binding Site BS02
Receptor Information
>4zuq Chain A (length=341) Species:
40837
(Mycoplana ramosa) [
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MRVIFSEDHKLRNAKTELYGGELVPPFEAPFRAEWILAAVKEAGFDDVVA
PARHGLETVLKVHDAGYLNFLETAWDRWKAAGYKGEAIATSFPVRRTSPR
IPTDIEGQIGYYCNAAETAISPGTWEAALSSMASAIDGADLIAAGHKAAF
SLCRPPGHHAGIDMFGGYCFINNAAVAAQRLLDKGAKKIAILDVDFHHGN
GTQDIFYERGDVFFASLHGDPAEAFPHFLGYAEETGKGAGAGTTANYPMG
RGTPYSVWGEALTDSLKRIAAFGAEAIVVSLGVDTFEQDPISFFKLTSPD
YITMGRTIAASGVPLLVVMEGGYGVPEIGLNVANVLKGVAG
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
4zuq Chain A Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
4zuq
Design, Synthesis, and Evaluation of Polyamine Deacetylase Inhibitors, and High-Resolution Crystal Structures of Their Complexes with Acetylpolyamine Amidohydrolase.
Resolution
1.22 Å
Binding residue
(original residue number in PDB)
D195 H197 D284
Binding residue
(residue number reindexed from 1)
D195 H197 D284
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.1.-
3.5.1.48
: acetylspermidine deacetylase.
3.5.1.62
: acetylputrescine deacetylase.
Gene Ontology
Molecular Function
GO:0004407
histone deacetylase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
GO:0047609
acetylputrescine deacetylase activity
GO:0047611
acetylspermidine deacetylase activity
Biological Process
GO:0006338
chromatin remodeling
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Molecular Function
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Biological Process
External links
PDB
RCSB:4zuq
,
PDBe:4zuq
,
PDBj:4zuq
PDBsum
4zuq
PubMed
26200446
UniProt
Q48935
|APAH_MYCRA Acetylpolyamine amidohydrolase (Gene Name=aphA)
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