Structure of PDB 4v06 Chain B Binding Site BS01
Receptor Information
>4v06 Chain B (length=341) Species:
9606
(Homo sapiens) [
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DVPWFPRKISELDKCSHRVLMYGSELDADHPGFKDNVYRQRRKYFVDVAM
GYKYGQPIPRVEYTEEETKTWGVVFRELSKLYPTHACREYLKNFPLLTKY
CGYREDNVPQLEDVSMFLKERSGFTVRPVAGYLSPRDFLAGLAYRVFHCT
QYIRHGSDPLYTPEPDTCHELLGHVPLLADPKFAQFSQEIGLASLGASDE
DVQKLATCYFFTIEFGLCKQEGQLRAYGAGLLSSIGELKHALSDKACVKA
FDPKTTCLQECLITTFQEAYFVSESFEEAKEKMRDFAKSITRPFSVYFNP
YTQSIEILKDTRSIENVVQDLRSDLNTVCDALNKMNQYLGI
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
4v06 Chain B Residue 1491 [
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Receptor-Ligand Complex Structure
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PDB
4v06
Crystal Structure of Human Tryptophane Hydroxylase 2 (Tph2), Catalytic Domain
Resolution
2.63 Å
Binding residue
(original residue number in PDB)
H318 H323 E363
Binding residue
(residue number reindexed from 1)
H169 H174 E214
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H318 H323 E363 S382
Catalytic site (residue number reindexed from 1)
H169 H174 E214 S233
Enzyme Commision number
1.14.16.4
: tryptophan 5-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:4v06
,
PDBe:4v06
,
PDBj:4v06
PDBsum
4v06
PubMed
UniProt
Q8IWU9
|TPH2_HUMAN Tryptophan 5-hydroxylase 2 (Gene Name=TPH2)
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