Structure of PDB 5sfp Chain D Binding Site BS02
Receptor Information
>5sfp Chain D (length=310) Species:
9606
(Homo sapiens) [
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LMQFTLPVRLCKEIELFHFDIGPFENMWPGIFVYMVHRSCGTSCFELEKL
CRFIMSVKKNYRRVPYHNWKHAVTVAHCMYAILQNNHTLFTDLERKGLLI
ACLCHDLDHRGFSNSYLQKFDHPLAALYSTSTMEQHHFSQTVSILQLEGH
NIFSTLSSSEYEQVLEIIRKAIIATDLALYFGNRKQLEEMYQTGSLNLNN
QSHRDRVIGLMMTACDLCSVTKLWPVTKLTANDIYAEFWAEGDEMKKLGI
QPIPMMDRDKKDEVPQGQLGFYNAVAIPCYTTLTQILPPTEPLLKACRDN
LSQWEKVIRG
Ligand information
Ligand ID
IO4
InChI
InChI=1S/C19H13ClN4O/c20-18-10-15(8-9-21-18)22-19(25)14-6-7-16-11-17(23-24(16)12-14)13-4-2-1-3-5-13/h1-12H,(H,21,22,25)
InChIKey
DPLIZFKHTDLAGO-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
Clc1nccc(c1)NC(=O)c1cn2nc(cc2cc1)c1ccccc1
CACTVS 3.385
Clc1cc(NC(=O)c2ccc3cc(nn3c2)c4ccccc4)ccn1
OpenEye OEToolkits 2.0.7
c1ccc(cc1)c2cc3ccc(cn3n2)C(=O)Nc4ccnc(c4)Cl
Formula
C19 H13 Cl N4 O
Name
(8S)-N-(2-chloropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine-6-carboxamide
ChEMBL
DrugBank
ZINC
PDB chain
5sfp Chain D Residue 803 [
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Receptor-Ligand Complex Structure
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PDB
5sfp
A high quality, industrial data set for binding affinity prediction: performance comparison in different early drug discovery scenarios.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
L675 Y693 P712 M713 E721 G725 Q726 F729
Binding residue
(residue number reindexed from 1)
L217 Y235 P254 M255 E263 G267 Q268 F271
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.4.17
: 3',5'-cyclic-nucleotide 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
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Molecular Function
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Biological Process
External links
PDB
RCSB:5sfp
,
PDBe:5sfp
,
PDBj:5sfp
PDBsum
5sfp
PubMed
36153472
UniProt
Q9Y233
|PDE10_HUMAN cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A (Gene Name=PDE10A)
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