Reaction Details |
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Target | Neuronal acetylcholine receptor subunit alpha-2 |
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Ligand | BDBM50220147 |
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Substrate/Competitor | n/a |
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Ki | >10000±n/a nM |
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Comments | PDSP_2967 |
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Citation | Shi, Q; Savage, JE; Hufeisen, SJ; Rauser, L; Grajkowska, E; Ernsberger, P; Wroblewski, JT; Nadeau, JH; Roth, BL L-homocysteine sulfinic acid and other acidic homocysteine derivatives are potent and selective metabotropic glutamate receptor agonists. J Pharmacol Exp Ther305:131-42 (2003) [PubMed] Article |
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More Info.: | Get all data from this article |
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Neuronal acetylcholine receptor subunit alpha-2 |
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Name: | Neuronal acetylcholine receptor subunit alpha-2 |
Synonyms: | ACHA2_HUMAN | CHRNA2 | Neuronal acetylcholine receptor; alpha2/beta2 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 59759.69 |
Organism: | Homo sapiens (Human) |
Description: | Cholinergic, Nicotinic Alpha2Beta2 0 HUMAN::Q15822 |
Residue: | 529 |
Sequence: | MGPSCPVFLSFTKLSLWWLLLTPAGGEEAKRPPPRAPGDPLSSPSPTALPQGGSHTETED
RLFKHLFRGYNRWARPVPNTSDVVIVRFGLSIAQLIDVDEKNQMMTTNVWLKQEWSDYKL
RWNPTDFGNITSLRVPSEMIWIPDIVLYNNADGEFAVTHMTKAHLFSTGTVHWVPPAIYK
SSCSIDVTFFPFDQQNCKMKFGSWTYDKAKIDLEQMEQTVDLKDYWESGEWAIVNATGTY
NSKKYDCCAEIYPDVTYAFVIRRLPLFYTINLIIPCLLISCLTVLVFYLPSDCGEKITLC
ISVLLSLTVFLLLITEIIPSTSLVIPLIGEYLLFTMIFVTLSIVITVFVLNVHHRSPSTH
TMPHWVRGALLGCVPRWLLMNRPPPPVELCHPLRLKLSPSYHWLESNVDAEEREVVVEEE
DRWACAGHVAPSVGTLCSHGHLHSGASGPKAEALLQEGELLLSPHMQKALEGVHYIADHL
RSEDADSSVKEDWKYVAMVIDRIFLWLFIIVCFLGTIGLFLPPFLAGMI
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BDBM50220147 |
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n/a |
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Name | BDBM50220147 |
Synonyms: | (S)-2-amino-4-sulfobutanoic acid | CHEMBL230951 | L-2-amino-4-sulfobutyric acid | L-Homocysteate | L-homocysteic acid |
Type | Small organic molecule |
Emp. Form. | C4H9NO5S |
Mol. Mass. | 183.183 |
SMILES | N[C@@H](CCS(O)(=O)=O)C(O)=O |r| |
Structure |
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