Structure of PDB 4pah Chain A Binding Site BS01
Receptor Information
>4pah Chain A (length=308) Species:
9606
(Homo sapiens) [
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TVPWFPRTIQELDRFANQILSYGAELDADHPGFKDPVYRARRKQFADIAY
NYRHGQPIPRVEYMEEEKKTWGTVFKTLKSLYKTHACYEYNHIFPLLEKY
CGFHEDNIPQLEDVSQFLQTCTGFRLRPVAGLLSSRDFLGGLAFRVFHCT
QYIRHGSKPMYTPEPDICHELLGHVPLFSDRSFAQFSQEIGLASLGAPDE
YIEKLATIYWFTVEFGLCKQGDSIKAYGAGLLSSFGELQYCLSEKPKLLP
LELEKTAIQNYTVTEFQPLYYVAESFNDAKEKVRNFAATIPRPFSVRYDP
YTQRIEVL
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
4pah Chain A Residue 425 [
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Receptor-Ligand Complex Structure
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PDB
4pah
Crystallographic analysis of the human phenylalanine hydroxylase catalytic domain with bound catechol inhibitors at 2.0 A resolution.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
H285 H290 E330
Binding residue
(residue number reindexed from 1)
H169 H174 E214
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H285 H290 E330 S349
Catalytic site (residue number reindexed from 1)
H169 H174 E214 S233
Enzyme Commision number
1.14.16.1
: phenylalanine 4-monooxygenase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0016714
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen
Biological Process
GO:0009072
aromatic amino acid metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:4pah
,
PDBe:4pah
,
PDBj:4pah
PDBsum
4pah
PubMed
9843368
UniProt
P00439
|PH4H_HUMAN Phenylalanine-4-hydroxylase (Gene Name=PAH)
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