Structure of PDB 7vb3 Chain D Binding Site BS02
Receptor Information
>7vb3 Chain D (length=408) Species:
4006
(Linum usitatissimum) [
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GVITCKAIMLKEAKLPGMSYADTVQIIDIQVDPPQNVELRVKMLCASVCR
TDILTIEGFMAPTQFPKINGHEGVGIIESMGPDTKNFKVGDVIVAPTLGE
CQTCSSCRSGRTNFCQNYGANESALEPDGTSRFSYIDSDGKKKLLYYKLG
CSTWTQYMVVDSNYATKLNEIAPELPPPHGSILSCAFATGYGAVWLDAAV
QEGDSVAIFGVGSVGISAVIAAKELKAKQIIVVDRNEYKLKMAMELGATH
CINSEKLPEGVTPSQAVRKLTPKEVGVDASIESSGYDVFMNEAMKAAIHG
KAKTVITGEGIYENDRIFFDFKDFLFGGNVVGNVTGRVRIHSDFPGLLRK
AQEPVIRAGMDKILGYDAATMKCKYEVDIREGTPALLKALEEVENVDCVK
LVIKLNDY
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
7vb3 Chain D Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
7vb3
Structural characterization of Linum usitatissimum hydroxynitrile lyase: A new cyanohydrin decomposition mechanism involving a cyano-zinc complex.
Resolution
1.48 Å
Binding residue
(original residue number in PDB)
C115 C118 C121 C129
Binding residue
(residue number reindexed from 1)
C101 C104 C107 C115
Annotation score
1
Enzymatic activity
Enzyme Commision number
4.1.2.46
: aliphatic (R)-hydroxynitrile lyase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0016829
lyase activity
GO:0046872
metal ion binding
GO:0051903
S-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity
GO:0052919
aliphatic (R)-hydroxynitrile lyase activity
Biological Process
GO:0046294
formaldehyde catabolic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7vb3
,
PDBe:7vb3
,
PDBj:7vb3
PDBsum
7vb3
PubMed
35101448
UniProt
P93243
|AHNL_LINUS Aliphatic (R)-hydroxynitrile lyase
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