Structure of PDB 6n7y Chain F Binding Site BS02
Receptor Information
>6n7y Chain F (length=336) Species:
9606
(Homo sapiens) [
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YAQEKQDFVQHFSQIVRVLTEGHPEIGDAIARLKEVLEYNAIGGKYNRGL
TVVVAFRELVEPRKQDADSLQRAWTVGWCVELLQAFFLVADDIMDSSLTR
RGQICWYQKPGVGLDAINDANLLEACIYRLLKLYCREQPYYLNLIELFLQ
SSYQTEIGQTLDLLTAPNVDLVRFTEKRYKSIVKYKTAFYSFYLPIAAAM
YMAGIDGEKEHANAKKILLEMGEFFQIQDDYLDLFGDPSVTGKIGTDIQD
NKCSWLVVQCLQRATPEQYQILKENYGQKEAEKVARVKALYEELDLPAVF
LQYEEDSYSHIMALIEQYAAPLPPAVFLGLARKIYK
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
6n7y Chain F Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
6n7y
Chirality-Driven Mode of Binding of alpha-Aminophosphonic Acid-Based Allosteric Inhibitors of the Human Farnesyl Pyrophosphate Synthase (hFPPS).
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
Q96 R113
Binding residue
(residue number reindexed from 1)
Q84 R101
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K57 F98 D103 D107 R112 D174 K200 F239 D243 D244
Catalytic site (residue number reindexed from 1)
K45 F86 D91 D95 R100 D162 K186 F225 D229 D230
Enzyme Commision number
2.5.1.1
: dimethylallyltranstransferase.
2.5.1.10
: (2E,6E)-farnesyl diphosphate synthase.
Gene Ontology
Molecular Function
GO:0004659
prenyltransferase activity
GO:0016765
transferase activity, transferring alkyl or aryl (other than methyl) groups
Biological Process
GO:0008299
isoprenoid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6n7y
,
PDBe:6n7y
,
PDBj:6n7y
PDBsum
6n7y
PubMed
31577901
UniProt
P14324
|FPPS_HUMAN Farnesyl pyrophosphate synthase (Gene Name=FDPS)
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