Structure of PDB 6n3y Chain A Binding Site BS01
Receptor Information
>6n3y Chain A (length=115) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
RPGGDTIFGKIIRKEIPAKIIFEDDRCLAFHDISPQAPTHFLVIPKKHIS
QISVAEDDDESLLGHLMIVGKKCAADLGLNKGYRMVVNEGSDGGQSVYHV
HLHVLGGRQMHWPPG
Ligand information
Ligand ID
HHJ
InChI
InChI=1S/C21H23N7O6/c22-20-26-17-14(18(31)27-20)25-9-28(17)19-16(30)15(29)13(34-19)8-33-21(32)23-6-5-10-7-24-12-4-2-1-3-11(10)12/h1-4,7,9,13,15-16,19,24,29-30H,5-6,8H2,(H,23,32)(H3,22,26,27,31)/t13-,15-,16-,19-/m1/s1
InChIKey
WKHCFGWBMMFLHU-NVQRDWNXSA-N
SMILES
Software
SMILES
CACTVS 3.385
NC1=NC(=O)c2ncn([C@@H]3O[C@H](COC(=O)NCCc4c[nH]c5ccccc45)[C@@H](O)[C@H]3O)c2N1
OpenEye OEToolkits 1.9.2
c1ccc2c(c1)c(c[nH]2)CCNC(=O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4NC(=NC5=O)N)O)O
OpenEye OEToolkits 1.9.2
c1ccc2c(c1)c(c[nH]2)CCNC(=O)OCC3C(C(C(O3)n4cnc5c4NC(=NC5=O)N)O)O
ACDLabs 12.01
O=C5N=C(N)Nc1c5ncn1C2OC(C(O)C2O)COC(=O)NCCc4c3ccccc3nc4
CACTVS 3.385
NC1=NC(=O)c2ncn([CH]3O[CH](COC(=O)NCCc4c[nH]c5ccccc45)[CH](O)[CH]3O)c2N1
Formula
C21 H23 N7 O6
Name
5'-O-{[2-(1H-indol-3-yl)ethyl]carbamoyl}guanosine
ChEMBL
CHEMBL1934757
DrugBank
ZINC
ZINC000082158125
PDB chain
6n3y Chain A Residue 201 [
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
6n3y
Inhibition of HINT1 Modulates Spinal Nociception and NMDA Evoked Behavior in Mice.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
I18 F41 D43 I44 N99 G105 Q106 S107 H112 H114
Binding residue
(residue number reindexed from 1)
I7 F30 D32 I33 N88 G94 Q95 S96 H101 H103
Annotation score
1
Binding affinity
MOAD
: Kd=3.65uM
PDBbind-CN
: -logKd/Ki=5.44,Kd=3.65uM
Enzymatic activity
Enzyme Commision number
3.4.22.-
3.9.1.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003824
catalytic activity
GO:0005080
protein kinase C binding
GO:0005515
protein binding
GO:0008234
cysteine-type peptidase activity
GO:0016787
hydrolase activity
GO:0016929
deSUMOylase activity
GO:0043530
adenosine 5'-monophosphoramidase activity
Biological Process
GO:0006355
regulation of DNA-templated transcription
GO:0006508
proteolysis
GO:0006915
apoptotic process
GO:0007165
signal transduction
GO:0009154
purine ribonucleotide catabolic process
GO:0016926
protein desumoylation
GO:0050850
positive regulation of calcium-mediated signaling
GO:0072332
intrinsic apoptotic signaling pathway by p53 class mediator
Cellular Component
GO:0000118
histone deacetylase complex
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005856
cytoskeleton
GO:0005886
plasma membrane
GO:0070062
extracellular exosome
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6n3y
,
PDBe:6n3y
,
PDBj:6n3y
PDBsum
6n3y
PubMed
31503445
UniProt
P49773
|HINT1_HUMAN Adenosine 5'-monophosphoramidase HINT1 (Gene Name=HINT1)
[
Back to BioLiP
]