Structure of PDB 4izw Chain A Binding Site BS02
Receptor Information
>4izw Chain A (length=262) Species:
501897
(Nesterenkonia sp. 10004) [
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GLVPRGSHMRIALMQHTARPLDPQHNLDLIDDAAARASEQGAQLLLTPLL
FGFGYVPSQICAQVSAEQVDAARSRLRGIARDRGIALVWSLPGPEGPEQR
GITAELADEHGEVLASYQKVQLYGPEEKAAFVPGEQPPPVLSWGGRQLSL
LVCYDVEFPEMVRAAAARGAQLVLVPTALAGDETSVPGILLPARAVENGI
TLAYANHCGPEGGLVFDGGSVVVGPAGQPLGELGVEPGLLVVDLPDADYL
QDRRAELHRNWL
Ligand information
Ligand ID
FTM
InChI
InChI=1S/C2H4FNO/c3-1-2(4)5/h1H2,(H2,4,5)
InChIKey
FVTWJXMFYOXOKK-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
FCC(=O)N
OpenEye OEToolkits 1.7.6
C(C(=O)N)F
CACTVS 3.370
NC(=O)CF
Formula
C2 H4 F N O
Name
2-fluoroacetamide
ChEMBL
CHEMBL160811
DrugBank
ZINC
ZINC000005177774
PDB chain
4izw Chain A Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
4izw
Covalent modifications of the active site cysteine occur as a result of mutating the glutamate of the catalytic triad in the amidase from Nesterenkonia sp.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
Y47 A170
Binding residue
(residue number reindexed from 1)
Y55 A178
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.1.4
: amidase.
Gene Ontology
Molecular Function
GO:0004040
amidase activity
GO:0016787
hydrolase activity
GO:0043864
indoleacetamide hydrolase activity
GO:0050126
N-carbamoylputrescine amidase activity
Biological Process
GO:0033388
putrescine biosynthetic process from arginine
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Molecular Function
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Biological Process
External links
PDB
RCSB:4izw
,
PDBe:4izw
,
PDBj:4izw
PDBsum
4izw
PubMed
UniProt
D0VWZ1
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