Structure of PDB 5emt Chain A Binding Site BS02
Receptor Information
>5emt Chain A (length=116) Species:
9606
(Homo sapiens) [
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ARPGGDTIFGKIIRKEIPAKIIFEDDRCLAFHDISPQAPTHFLVIPKKHI
SQISVAEDDDESLLGHLMIVGKKCAADLGLNKGYRMVVNEGSDGGQSVYH
VHLHVLGGRQMHWPPG
Ligand information
Ligand ID
CU
InChI
InChI=1S/Cu/q+2
InChIKey
JPVYNHNXODAKFH-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Cu+2]
CACTVS 3.341
[Cu++]
Formula
Cu
Name
COPPER (II) ION
ChEMBL
DrugBank
DB14552
ZINC
PDB chain
5emt Chain A Residue 203 [
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Receptor-Ligand Complex Structure
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PDB
5emt
Inhibition by divalent metal ions of human histidine triad nucleotide binding protein1 (hHint1), a regulator of opioid analgesia and neuropathic pain.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
H112 H114
Binding residue
(residue number reindexed from 1)
H102 H104
Annotation score
1
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
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Cellular Component
External links
PDB
RCSB:5emt
,
PDBe:5emt
,
PDBj:5emt
PDBsum
5emt
PubMed
28739258
UniProt
P49773
|HINT1_HUMAN Adenosine 5'-monophosphoramidase HINT1 (Gene Name=HINT1)
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