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TargetNeuropeptide Y receptor type 2
LigandBDBM50197021
Substrate/Competitorn/a
Meas. Tech.ChEMBL_453177 (CHEMBL902327)
Ki 6±n/a nM
Citation DeCarr, LB; Buckholz, TM; Coish, PD; Fathi, Z; Fisk, SE; Mays, MR; O'Connor, SJ; Lumb, KJ Identification of selective neuropeptide Y2 peptide agonists. Bioorg Med Chem Lett17:538-41 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuropeptide Y receptor type 2
Name:Neuropeptide Y receptor type 2
Synonyms:NPY-Y2 | NPY-Y2 receptor | NPY2-R | NPY2R | NPY2R_HUMAN | Neuropeptide Y receptor type 2 | Y2 receptor | neuropeptide Y receptor Y2
Type:Enzyme Catalytic Domain
Mol. Mass.:42734.65
Organism:Homo sapiens (Human)
Description:NPY-Y2 NPY2R HUMAN::P49146
Residue:381
Sequence:
MGPIGAEADENQTVEEMKVEQYGPQTTPRGELVPDPEPELIDSTKLIEVQVVLILAYCSI
ILLGVIGNSLVIHVVIKFKSMRTVTNFFIANLAVADLLVNTLCLPFTLTYTLMGEWKMGP
VLCHLVPYAQGLAVQVSTITLTVIALDRHRCIVYHLESKISKRISFLIIGLAWGISALLA
SPLAIFREYSLIEIIPDFEIVACTEKWPGEEKSIYGTVYSLSSLLILYVLPLGIISFSYT
RIWSKLKNHVSPGAANDHYHQRRQKTTKMLVCVVVVFAVSWLPLHAFQLAVDIDSQVLDL
KEYKLIFTVFHIIAMCSTFANPLLYGWMNSNYRKAFLSAFRCEQRLDAIHSEVSVTFKAK
KNLEVRKNSGPNDSFTEATNV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50197021
n/a
NameBDBM50197021
Synonyms:(2S)-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoyl-2-(4-hydroxyphenyl)ethyl]carbamoyl}butyl]-2-[(2S)-5-carbamimidamido-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-5-carbamimidamido-2-(phenylformamido)pentanamido]-3-(1H-imidazol-5-yl)propanamido]-3-(4-hydroxyphenyl)propanamido]-4-methylpentanamido]-3-carbamoylpropanamido]-4-methylpentanamido]-3-methylbutanamido]-3-hydroxybutanamido]pentanamido]pentanediamide | CHEMBL437290
TypeSmall organic molecule
Emp. Form.C79H120N26O18
Mol. Mass.1721.9615
SMILESCC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccccc1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |wU:73.75,74.78,4.4,91.93,20.28,58.60,111.113,wD:66.68,8.17,30.39,80.82,50.52,100.102,(12.08,-14.52,;12.08,-16.06,;13.42,-16.83,;10.75,-16.83,;10.75,-18.37,;9.41,-19.13,;8.08,-18.36,;8.08,-16.82,;6.75,-19.13,;6.75,-20.67,;8.08,-21.44,;9.41,-20.67,;10.75,-21.44,;10.75,-22.98,;12.06,-23.74,;9.41,-23.75,;8.08,-22.98,;5.41,-18.36,;4.09,-19.14,;4.09,-20.68,;2.76,-18.37,;2.76,-16.83,;4.09,-16.06,;5.49,-16.69,;6.53,-15.54,;5.76,-14.21,;4.25,-14.53,;1.42,-19.13,;.08,-18.36,;.08,-16.82,;-1.25,-19.13,;-1.25,-20.67,;.08,-21.44,;.08,-22.98,;1.42,-23.75,;1.43,-25.29,;.08,-26.06,;2.74,-26.06,;-2.58,-18.37,;-3.91,-19.15,;-3.9,-20.69,;-5.24,-18.39,;-5.24,-16.85,;-6.57,-16.08,;-7.91,-16.85,;-7.9,-18.4,;-6.57,-19.16,;12.08,-19.14,;12.08,-20.68,;13.41,-18.36,;14.74,-19.13,;14.74,-20.67,;16.07,-21.44,;17.4,-20.66,;16.07,-22.98,;16.07,-18.36,;16.07,-16.82,;17.4,-19.13,;18.74,-18.36,;18.74,-16.82,;20.07,-16.05,;20.07,-14.51,;21.41,-16.82,;20.07,-19.13,;20.07,-20.67,;21.4,-18.36,;22.73,-19.13,;22.73,-20.67,;24.06,-21.44,;21.4,-21.44,;24.06,-18.36,;24.06,-16.82,;25.4,-19.13,;26.73,-18.36,;26.73,-16.82,;25.4,-16.05,;28.06,-16.04,;28.06,-19.13,;28.06,-20.67,;29.39,-18.35,;30.72,-19.13,;30.72,-20.67,;32.05,-21.44,;32.05,-22.98,;33.39,-23.74,;33.39,-25.28,;32.05,-26.04,;34.73,-26.04,;32.05,-18.36,;32.05,-16.82,;33.39,-19.12,;34.73,-18.36,;34.73,-16.82,;36.05,-16.05,;36.05,-14.51,;34.72,-13.73,;37.39,-13.74,;36.05,-19.13,;36.05,-20.67,;37.39,-18.36,;38.72,-19.13,;38.72,-20.67,;40.05,-21.44,;40.05,-22.98,;41.38,-23.74,;41.38,-25.28,;40.05,-26.05,;42.72,-26.05,;40.05,-18.36,;40.05,-16.82,;41.38,-19.13,;42.72,-18.36,;42.72,-16.82,;44.05,-16.05,;45.38,-16.82,;46.72,-16.05,;46.72,-14.51,;48.05,-13.74,;45.38,-13.74,;44.05,-14.51,;44.05,-19.13,;45.38,-18.36,;44.05,-20.67,)|
Structure
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