Structure of PDB 2gnj Chain A Binding Site BS02
Receptor Information
>2gnj Chain A (length=337) Species:
9913
(Bos taurus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
SVKEFLAKAKEDFLKKWENPAQNTAHLDQFERIKTIGTGSFGRVMLVKHM
ETGNHYAMKILDKQKVVKLKQIEHTLNEKRILQAVNFPFLVKLEFSFKDN
SNLYMVMEYVPGGEMFSHLRRIGRFSEPHARFYAAQIVLTFEYLHSLDLI
YRDLKPENLLIDQQGYIKVADFGFAKRVKGRTWTLCGTPEYLAPEIILSK
GYNKAVDWWALGVLIYEMAAGYPPFFADQPIQIYEKIVSGKVRFPSHFSS
DLKDLLRNLLQVDLTKRFGNLKNGVNDIKNHKWFATTDWIAIYQRKVEAP
FIPKFKGPGDTSNFDDYEEEEIRVSINEKCGKEFSEF
Ligand information
Ligand ID
Y27
InChI
InChI=1S/C14H21N3O/c1-10(15)11-2-4-12(5-3-11)14(18)17-13-6-8-16-9-7-13/h6-12H,2-5,15H2,1H3,(H,16,17,18)/t10-,11-,12-/m1/s1
InChIKey
IYOZTVGMEWJPKR-IJLUTSLNSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C[C@H](C1CCC(CC1)C(=O)Nc2ccncc2)N
CACTVS 3.341
C[CH](N)[CH]1CC[CH](CC1)C(=O)Nc2ccncc2
OpenEye OEToolkits 1.5.0
CC(C1CCC(CC1)C(=O)Nc2ccncc2)N
ACDLabs 10.04
O=C(Nc1ccncc1)C2CCC(C(N)C)CC2
CACTVS 3.341
C[C@@H](N)[C@H]1CC[C@@H](CC1)C(=O)Nc2ccncc2
Formula
C14 H21 N3 O
Name
(R)-TRANS-4-(1-AMINOETHYL)-N-(4-PYRIDYL) CYCLOHEXANECARBOXAMIDE
ChEMBL
CHEMBL559147
DrugBank
DB08756
ZINC
PDB chain
2gnj Chain A Residue 501 [
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
2gnj
Structural analysis of protein kinase A mutants with Rho-kinase inhibitor specificity
Resolution
2.28 Å
Binding residue
(original residue number in PDB)
I49 T51 G52 S53 V57 A70 Y122 V123 N171 L173 D184 F327
Binding residue
(residue number reindexed from 1)
I36 T38 G39 S40 V44 A57 Y109 V110 N158 L160 D171 F314
Annotation score
1
Binding affinity
MOAD
: Ki=6uM
PDBbind-CN
: -logKd/Ki=5.22,IC50=6uM
BindingDB: IC50=42000nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D166 K168 E170 N171 D184 T201
Catalytic site (residue number reindexed from 1)
D153 K155 E157 N158 D171 T188
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
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2gnj
,
PDBe:2gnj
,
PDBj:2gnj
PDBsum
2gnj
PubMed
16699172
UniProt
P00517
|KAPCA_BOVIN cAMP-dependent protein kinase catalytic subunit alpha (Gene Name=PRKACA)
[
Back to BioLiP
]