Structure of PDB 1sqd Chain A Binding Site BS01
Receptor Information
>1sqd Chain A (length=373) Species:
3702
(Arabidopsis thaliana) [
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KNPKSDKFKVKRFHHIEFWCGDATNVARRFSWGLGMRFSAKSDLSTGNMV
HASYLLTSGDLRFLFTAPYSPSLSAGEIKPTTTASIPSFDHGSCRSFFSS
HGLGVRAVAIEVEDAESAFSISVANGAIPSSPPIVLNEAVTIAEVKLYGD
VVLRYVSYKAEFLPGFERVEDASSFPLDYGIRRLDHAVGNVPELGPALTY
VAGFTGFHQFAEFTSGLNSAVLASNDEMVLLPINEPVHGKSQIQTYLEHN
EGAGLQHLALMSEDIFRTLREMRKRSSIGGFDFMPSPPPTYYQNLKKRVG
DVLSDDQIKECEELGILVDRDDQGTLLQIFTKPLGDRPTIFIEIIQRVGC
MMYQSGGCGGFGKGNFSELFKSI
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
1sqd Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1sqd
Structural basis for herbicidal inhibitor selectivity revealed by comparison of crystal structures of plant and Mammalian 4-hydroxyphenylpyruvate dioxygenases
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
H205 H287 E373
Binding residue
(residue number reindexed from 1)
H186 H257 E343
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.13.11.27
: 4-hydroxyphenylpyruvate dioxygenase.
Gene Ontology
Molecular Function
GO:0003868
4-hydroxyphenylpyruvate dioxygenase activity
GO:0005506
iron ion binding
GO:0016701
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0006559
L-phenylalanine catabolic process
GO:0006572
tyrosine catabolic process
GO:0009072
aromatic amino acid metabolic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1sqd
,
PDBe:1sqd
,
PDBj:1sqd
PDBsum
1sqd
PubMed
15301540
UniProt
P93836
|HPPD_ARATH 4-hydroxyphenylpyruvate dioxygenase (Gene Name=HPD)
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