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TargetBeta-arrestin-2
LigandBDBM50029150
Substrate/Competitorn/a
Ki 3235.93±n/a nM
CommentsPDSP_976
Citation Wong, DTThrelkeld, PGRobertson, DW Affinities of fluoxetine, its enantiomers, and other inhibitors of serotonin uptake for subtypes of serotonin receptors. Neuropsychopharmacology5:43-7 (1991) [PubMed]
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Beta-arrestin-2
Name:Beta-arrestin-2
Synonyms:5-HT2C | ARRB2 | ARRB2_BOVIN | Beta-arrestin-2 | HTR2C
Type:Enzyme Catalytic Domain
Mol. Mass.:47232.00
Organism:Beef
Description:5-HT2C HTR2C Beef::P32120
Residue:420
Sequence:
MGEKPGTRVFKKSSPNCKLTVYLGKRDFVDHLDKVDPVDGVVLVDPDYLKDRKVFVTLTC
AFRYGREDLDVLGLSFRKDLFIANYQAFPPTPNPPRPPTRLQERLLRKLGQHAHPFFFTI
PQNLPCSVTLQPGPEDTGKACGVDFEIRAFCAKSLEEKSHKRNSVRLVIRKVQFAPEKPG
PQPSAETTRHFLMSDRSLHLEASLDKELYYHGEPLNVNVHVTNNSTKTVKKIKVSVRQYA
DICLFSTAQYKCPVAQVEQDDQVSPSSTFCKVYTITPLLSNNREKRGLALDGKLKHEDTN
LASSTIVKEGANKEVLGILVSYRVKVKLVVSRGGDVSVELPFVLMHPKPHDHIALPRPQS
AATHPPTLLPSAVPETDAPVDTNLIEFETNYATDDDIVFEDFARLRLKGLKDEDYDDQFC
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  Blast E-value cutoff:
BDBM50029150
n/a
NameBDBM50029150
Synonyms:3-(2-Piperidin-4-yl-ethyl)-1H-indole | CHEMBL276520 | Indalpine
TypeSmall organic molecule
Emp. Form.C15H20N2
Mol. Mass.228.3327
SMILESC(Cc1c[nH]c2ccccc12)C1CCNCC1
Structure
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