Structure of PDB 7xaa Chain A Binding Site BS02
Receptor Information
>7xaa Chain A (length=326) Species:
9606
(Homo sapiens) [
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TEQEDVLAKELEDVNKWGLHVFRIAELSGNRPLTVIMHTIFQERDLLKTF
KIPVDTLITYLMTLEDHYHADVAYHNNIHAADVVQSTHVLLSTPALEAVF
TDLEILAAIFASAIHDVDHPGVSNQFLINTNSELALMYNDSSVLENHHLA
VGFKLLQEENCDIFQNLTKKQRQSLRKMVIDIVLATDMSKHMNLLADLKT
MVETKKVTSSGVLLLDNYSDRIQVLQNMVHCADLSNPTKPLQLYRQWTDR
IMEEFFRQGDRERERGMEISPMCDKHNASVEKSQVGFIDYIVHPLWETWA
DLVHPDAQDILDTLEDNREWYQSTIP
Ligand information
Ligand ID
AQL
InChI
InChI=1S/C30H29NO6/c1-17(2)6-7-20-25-23(14-21(32)28(20)34-5)36-24-15-22-19(8-11-30(3,4)37-22)29(26(24)27(25)33)35-16-18-9-12-31-13-10-18/h6,8-15,32H,7,16H2,1-5H3
InChIKey
REKLCXXJHWMMFP-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
COc1c(O)cc2Oc3cc4OC(C)(C)C=Cc4c(OCc5ccncc5)c3C(=O)c2c1CC=C(C)C
OpenEye OEToolkits 2.0.7
CC(=CCc1c2c(cc(c1OC)O)Oc3cc4c(c(c3C2=O)OCc5ccncc5)C=CC(O4)(C)C)C
Formula
C30 H29 N O6
Name
8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-9-oxidanyl-5-(pyridin-4-ylmethoxy)pyrano[3,2-b]xanthen-6-one
ChEMBL
DrugBank
ZINC
PDB chain
7xaa Chain A Residue 603 [
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Receptor-Ligand Complex Structure
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PDB
7xaa
Discovery of novel PDE4 inhibitors targeting the M-pocket from natural mangostanin with improved safety for the treatment of Inflammatory Bowel Diseases.
Resolution
2.10041 Å
Binding residue
(original residue number in PDB)
M273 P322 I336 M357 F372
Binding residue
(residue number reindexed from 1)
M188 P237 I251 M272 F287
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.4.53
: 3',5'-cyclic-AMP phosphodiesterase.
Gene Ontology
Molecular Function
GO:0004114
3',5'-cyclic-nucleotide phosphodiesterase activity
GO:0008081
phosphoric diester hydrolase activity
Biological Process
GO:0007165
signal transduction
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:7xaa
,
PDBe:7xaa
,
PDBj:7xaa
PDBsum
7xaa
PubMed
35985255
UniProt
Q08499
|PDE4D_HUMAN 3',5'-cyclic-AMP phosphodiesterase 4D (Gene Name=PDE4D)
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