Structure of PDB 6oco Chain A Binding Site BS01
Receptor Information
>6oco Chain A (length=930) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
NQSVVVDFLLPTGVYLNFPVSRNANLSTIKQLLWHRAQYEPLFHMLSGPE
AYVFTCINQTAEQQELEDEQRRLCDVQPFLPVLRLVAREGDRVKKLINSQ
ISLLIGKGLHEFDSLCDPEVNDFRAKMCQFCEEAAARRQQLGWEAWLQYS
FPLQLEPLPNRALLVNVKFEGSEESFTFQVSTKDVPLALMACALRKKAVE
QPEDYTLQVNGRHEYLYGSYPLCQFQYICSCLHSGLTPHLTMVHSSSILA
MRDEQSLWSLEQPFRIELIQGSKVNADERMKLVVQAGLFHGNEMLCKTVS
SSEVSVCSEPVWKQRLEFDINICDLPRMARLCFALYAVIEKAKDCPIAWA
NLMLFDYKDQLKTGERCLYMWPSVPDEKGELLNPTGTVRSNPNTDSAAAL
LICLPEVAPHPVYYPALEKILELGRHTEEEQLQLREILERRYEHEKDLVW
KLRHEVQEHFPEALARLLLVTKWNKHEDVAQMLYLLCSWPELPVLSALEL
LDFSFPDCHVGSFAIKSLRKLTDDELFQYLLQLVQVLKYESYLDCELTKF
LLDRALANRKIGHFLFWHLRSEMHVPSVALRFGLILEAYCRGSTHHMKVL
MKQGEALSKLKALNDFVKLSSQKTPKPQTKELMHLCMRQEAYLEALSHLQ
SPLDPSTLLAEVCVEQCTFMDSKMKPLWIMYSNEEAGSGGSVGIIFKNGD
DLRQDMLTLQMIQLMDVLWKQEGLDLRMTPYGCLPTGDRTGLIEVVLRSD
TIANIQLNKDALLNWLKSKNPGEALDRAIEEFTLSCAGYCVATYVLGIGD
RHSDNIMIRESGQLFHIDFGHFLGNFERVPFILTYDFVHVIQQGKTNNSE
KFERFRGYCERAYTILRRHGLLFLHLFALMRAAGLPELSCSKDIQYLKDS
LALGKTEEEALKHFRVKFNEALRESWKTKV
Ligand information
Ligand ID
M5V
InChI
InChI=1S/C21H17ClN6/c22-16-4-1-5-17(7-16)27-12-19-8-18(27)13-28(19)21-15(9-23)11-25-20(26-21)14-3-2-6-24-10-14/h1-7,10-11,18-19H,8,12-13H2/t18-,19-/m0/s1
InChIKey
LYMCCCUAFBZMES-OALUTQOASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
c1cc(cc(c1)Cl)N2CC3CC2CN3c4c(cnc(n4)c5cccnc5)C#N
CACTVS 3.385
Clc1cccc(c1)N2C[CH]3C[CH]2CN3c4nc(ncc4C#N)c5cccnc5
CACTVS 3.385
Clc1cccc(c1)N2C[C@@H]3C[C@H]2CN3c4nc(ncc4C#N)c5cccnc5
OpenEye OEToolkits 2.0.7
c1cc(cc(c1)Cl)N2C[C@@H]3C[C@H]2CN3c4c(cnc(n4)c5cccnc5)C#N
ACDLabs 12.01
C1N(C2CC1N(C2)c3cc(ccc3)Cl)c5nc(c4cnccc4)ncc5C#N
Formula
C21 H17 Cl N6
Name
4-[(1S,4S)-5-(3-chlorophenyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-2-(pyridin-3-yl)pyrimidine-5-carbonitrile
ChEMBL
CHEMBL4648691
DrugBank
ZINC
PDB chain
6oco Chain A Residue 1101 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
6oco
Discovery and optimization of heteroaryl piperazines as potent and selective PI3K delta inhibitors.
Resolution
2.58 Å
Binding residue
(original residue number in PDB)
T750 M752 W760 V828 D832 M900 I910
Binding residue
(residue number reindexed from 1)
T668 M670 W678 V746 D750 M807 I817
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=6.32,IC50=474nM
Enzymatic activity
Enzyme Commision number
2.7.1.137
: phosphatidylinositol 3-kinase.
2.7.1.153
: phosphatidylinositol-4,5-bisphosphate 3-kinase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016303
1-phosphatidylinositol-3-kinase activity
GO:0035005
1-phosphatidylinositol-4-phosphate 3-kinase activity
GO:0046934
1-phosphatidylinositol-4,5-bisphosphate 3-kinase activity
Biological Process
GO:0001779
natural killer cell differentiation
GO:0001819
positive regulation of cytokine production
GO:0001938
positive regulation of endothelial cell proliferation
GO:0002250
adaptive immune response
GO:0002551
mast cell chemotaxis
GO:0002679
respiratory burst involved in defense response
GO:0006468
protein phosphorylation
GO:0006629
lipid metabolic process
GO:0006935
chemotaxis
GO:0006954
inflammatory response
GO:0006955
immune response
GO:0007165
signal transduction
GO:0010595
positive regulation of endothelial cell migration
GO:0010628
positive regulation of gene expression
GO:0010818
T cell chemotaxis
GO:0016310
phosphorylation
GO:0030101
natural killer cell activation
GO:0030154
cell differentiation
GO:0030183
B cell differentiation
GO:0030217
T cell differentiation
GO:0030335
positive regulation of cell migration
GO:0030593
neutrophil chemotaxis
GO:0033031
positive regulation of neutrophil apoptotic process
GO:0035747
natural killer cell chemotaxis
GO:0035754
B cell chemotaxis
GO:0036092
phosphatidylinositol-3-phosphate biosynthetic process
GO:0038084
vascular endothelial growth factor signaling pathway
GO:0042110
T cell activation
GO:0042113
B cell activation
GO:0043303
mast cell degranulation
GO:0043491
phosphatidylinositol 3-kinase/protein kinase B signal transduction
GO:0045087
innate immune response
GO:0045766
positive regulation of angiogenesis
GO:0046854
phosphatidylinositol phosphate biosynthetic process
GO:0048015
phosphatidylinositol-mediated signaling
GO:0050852
T cell receptor signaling pathway
GO:0050853
B cell receptor signaling pathway
GO:0060374
mast cell differentiation
GO:0072672
neutrophil extravasation
GO:1905278
positive regulation of epithelial tube formation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0005942
phosphatidylinositol 3-kinase complex
GO:0005943
phosphatidylinositol 3-kinase complex, class IA
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6oco
,
PDBe:6oco
,
PDBj:6oco
PDBsum
6oco
PubMed
31757666
UniProt
O00329
|PK3CD_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform (Gene Name=PIK3CD)
[
Back to BioLiP
]