Structure of PDB 1xha Chain A Binding Site BS02
Receptor Information
>1xha Chain A (length=350) Species:
9913
(Bos taurus) [
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GNAAAAKKGSEQESVKEFLAKAKEDFLKKWENPAQNTAHLDQFERIKTLG
TGSFGRVMLVKHMETGNHYAMKILDKQKVVKLKEIEHTLNEKRILQAVNF
PFLVKLEFSFKDNSNLYMVMEYAPGGEMFSHLRRIGRFSEPHARFYAAQI
VLTFEYLHSLDLIYRDLKPENLMIDQQGYIQVTDFGLAKRVKGRTWTLCG
TPEYLAPEIILSKGYNKAVDWWALGVLIYEMAAGYPPFFADQPIQIYEKI
VSGKVRFPSHFSSDLKDLLRNLLQVDLTKRFGNLKNGVNDIKNHKWFATT
DWIAIYQRKVEAPFIPKFKGPGDTSNFDDYEEEEIRVSINEKCGKEFSEF
Ligand information
Ligand ID
R68
InChI
InChI=1S/C33H38FN5O4/c1-33(2)14-4-16-37-30(33)23-10-11-26(40)27(28(23)34)29(41)20-6-8-21(9-7-20)31(42)38-24-5-3-15-36-19-25(24)39-32(43)22-12-17-35-18-13-22/h6-13,17-18,24-25,30,36-37,40H,3-5,14-16,19H2,1-2H3,(H,38,42)(H,39,43)/t24-,25-,30+/m1/s1
InChIKey
LLDRWTNKJQFSDC-KQZWIPHESA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC1(CCCN[C@H]1c2ccc(c(c2F)C(=O)c3ccc(cc3)C(=O)N[C@@H]4CCCNC[C@H]4NC(=O)c5ccncc5)O)C
CACTVS 3.341
CC1(C)CCCN[CH]1c2ccc(O)c(c2F)C(=O)c3ccc(cc3)C(=O)N[CH]4CCCNC[CH]4NC(=O)c5ccncc5
CACTVS 3.341
CC1(C)CCCN[C@H]1c2ccc(O)c(c2F)C(=O)c3ccc(cc3)C(=O)N[C@@H]4CCCNC[C@H]4NC(=O)c5ccncc5
OpenEye OEToolkits 1.5.0
CC1(CCCNC1c2ccc(c(c2F)C(=O)c3ccc(cc3)C(=O)NC4CCCNCC4NC(=O)c5ccncc5)O)C
ACDLabs 10.04
O=C(c1ccncc1)NC5CNCCCC5NC(=O)c2ccc(cc2)C(=O)c3c(O)ccc(c3F)C4NCCCC4(C)C
Formula
C33 H38 F N5 O4
Name
N-{4-[(4-{3-[(2R)-3,3-DIMETHYLPIPERIDIN-2-YL]-2-FLUORO-6-HYDROXYBENZOYL}BENZOYL)AMINO]AZEPAN-3-YL}ISONICOTINAMIDE
ChEMBL
DrugBank
ZINC
ZINC000014948570
PDB chain
1xha Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
1xha
Design and crystal structures of protein kinase B-selective inhibitors in complex with protein kinase A and mutants
Resolution
2.46 Å
Binding residue
(original residue number in PDB)
G50 T51 G52 S53 F54 V57 A70 K72 L74 E84 E91 E170 N171 M173 T183 D184 G186 L187 F327
Binding residue
(residue number reindexed from 1)
G50 T51 G52 S53 F54 V57 A70 K72 L74 E84 E91 E170 N171 M173 T183 D184 G186 L187 F327
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D166 K168 E170 N171 D184 T201
Catalytic site (residue number reindexed from 1)
D166 K168 E170 N171 D184 T201
Enzyme Commision number
2.7.11.11
: cAMP-dependent protein kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004674
protein serine/threonine kinase activity
GO:0004679
AMP-activated protein kinase activity
GO:0004691
cAMP-dependent protein kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0019904
protein domain specific binding
GO:0034237
protein kinase A regulatory subunit binding
GO:0106310
protein serine kinase activity
Biological Process
GO:0001707
mesoderm formation
GO:0006468
protein phosphorylation
GO:0010737
protein kinase A signaling
GO:0016310
phosphorylation
GO:0018105
peptidyl-serine phosphorylation
GO:0034605
cellular response to heat
GO:1904262
negative regulation of TORC1 signaling
Cellular Component
GO:0001669
acrosomal vesicle
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0005952
cAMP-dependent protein kinase complex
GO:0031594
neuromuscular junction
GO:0036126
sperm flagellum
GO:0048471
perinuclear region of cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1xha
,
PDBe:1xha
,
PDBj:1xha
PDBsum
1xha
PubMed
15634010
UniProt
P00517
|KAPCA_BOVIN cAMP-dependent protein kinase catalytic subunit alpha (Gene Name=PRKACA)
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