Structure of PDB 3a9y Chain B Binding Site BS02
Receptor Information
>3a9y Chain B (length=400) Species:
10116
(Rattus norvegicus) [
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RKVYMDYNATTPLEPEVIQAVTEAMKEAWGNPSSSYVAGRKAKDIINTAR
ASLAKMIGGKPQDIIFTSGGTESNNLVIHSTVRCFHEQQTRPHFITCTVE
HDSIRLPLEHLVEDQVAEVTFVPVSKVNGQVEVEDILAAVRPTTCLVTIM
LANNETGVIMPISEISRRIKALNQIRAASGLPRVLVHTDAAQALGKRRVD
VEDLGVDFLTIVGHKFYGPRIGALYVRGVGKLTPLYPMLFGGGQERNFRP
GTENTPMIAGLGKAADLVSENCETYEAHMRDIRDYLEERLEAEFGKRIHL
NSRFPGVERLPNTCNFSIQGSQLRGYMVLAQCQTLLASVGASCHSDHEDR
PSPVLLSCGIPVDVARNAVRLSVGRSTTRAEVDLIVQDLKQAVNQLEGPV
Ligand information
Ligand ID
PLP
InChI
InChI=1S/C8H10NO6P/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14/h2-3,11H,4H2,1H3,(H2,12,13,14)
InChIKey
NGVDGCNFYWLIFO-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(C=O)c1O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)C=O)O
ACDLabs 10.04
O=P(O)(O)OCc1cnc(c(O)c1C=O)C
Formula
C8 H10 N O6 P
Name
PYRIDOXAL-5'-PHOSPHATE;
VITAMIN B6 Phosphate
ChEMBL
CHEMBL82202
DrugBank
DB00114
ZINC
ZINC000001532514
PDB chain
3a9y Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
3a9y
Reaction mechanism and molecular basis for selenium/sulfur discrimination of selenocysteine lyase.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
G87 T88 H133 D221 A223 Q224 H246 K247
Binding residue
(residue number reindexed from 1)
G70 T71 H101 D189 A191 Q192 H214 K215
Annotation score
1
Enzymatic activity
Enzyme Commision number
4.4.1.16
: selenocysteine lyase.
Gene Ontology
Molecular Function
GO:0009000
selenocysteine lyase activity
GO:0016597
amino acid binding
GO:0016740
transferase activity
GO:0016829
lyase activity
GO:0042803
protein homodimerization activity
GO:0070279
vitamin B6 binding
Biological Process
GO:0001887
selenium compound metabolic process
GO:0006629
lipid metabolic process
GO:0016261
selenocysteine catabolic process
GO:0032868
response to insulin
GO:1900408
negative regulation of cellular response to oxidative stress
Cellular Component
GO:0005737
cytoplasm
GO:0005794
Golgi apparatus
GO:0005829
cytosol
GO:1902494
catalytic complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3a9y
,
PDBe:3a9y
,
PDBj:3a9y
PDBsum
3a9y
PubMed
20164179
UniProt
Q68FT9
|SCLY_RAT Selenocysteine lyase (Gene Name=Scly)
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