Cryo-EM structure of D1R in complex with de novo designed negative allosteric GEM targeting TM5/6/7. Determined by electron microscopy at 2.77 Å resolution. Released 4 Mar 2026.
Explore 9LLG in 3D Show helices and sheets RCSB PDB PDBe
9LLG contains 24 α-helices and 2 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 13-42 | 30 | |
| α-helix | 46-77 | 32 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 21-50 | 30 | |
| α-helix | 52-55 | 4 | |
| α-helix | 60-72 | 13 | |
| α-helix | 73-77 | 5 | |
| α-helix | 78-87 | 10 | |
| α-helix | 97-126 | 30 | |
| α-helix | 128-134 | 7 | |
| α-helix | 137-160 | 24 | |
| β-strand | 165 | 1 | 1 |
| α-helix | 189 | 1 | |
| β-strand | 190 | 1 | 1 |
| α-helix | 191 | 1 | |
| α-helix | 192-199 | 8 | |
| α-helix | 200-204 | 5 | |
| α-helix | 205-1243 | 39 | |
| α-helix | 1248-1266 | 19 | |
| α-helix | 1286-1305 | 20 | |
| α-helix | 1309-1334 | 26 | |
| α-helix | 1335-1339 | 5 | |
| α-helix | 1340-294 | 26 | |
| α-helix | 295-297 | 3 | |
| α-helix | 310-321 | 12 | |
| α-helix | 323-331 | 9 | |
| α-helix | 335-345 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| D(1A) dopamine receptor,Soluble cytochrome b562 | R | protein | 516 | Homo sapiens, Escherichia coli | P21728 (AlphaFold model) |
| De novo designed negative allosteric GPCR exoframe modulator targeting TM5/6/7 | M | protein | 95 | Homo sapiens |
>9LLG_1 D(1A) dopamine receptor,Soluble cytochrome b562 (chains R) RTLNTSAMDGTGLVVERDFSVRILTACFLSLLILSTLLGNTLVCAAVIRFRHLRSKVTNF FVISLAVSDLLVAVLVMPWKAVAEIAGFWPFGSFCNIWVAFDIMCSTASILNLCVISVDR YWAISSPFRYERKMTPKAAFILISVAWTLSVLISFIPVQLSWHKAKPTSPSDGNATSLAE TIDNCDSSLSRTYAISSSVISFYIPVAIMIVTYTRIYRILKKELDALNDNWETLNDNLKV IEKADNAAQVKDALTKMRAAALDAQKATPPKLEDKSPDSPEMKDFRHGFDILVGQIDDAL KLANEGKVKEAQAAAEQLKTTRDAILKPFIEELKELKGKPFLIDAVIMGVFVCCWLPFFI LNCILPFCGSGETQPFCIDSNTFDVFVWFGWANSSLNPIIYAFNADFRKAFSTLLGCYRL CPATNNAIETVSINNNGAAMFSSHHEPRGSISKECNLVYLIPHAVGSSEDLKKEEAAGIA RPLEKLSPALSVILDYDTDVSLEKIQPITQNGQHPT
>9LLG_2 De novo designed negative allosteric GPCR exoframe modulator targeting TM5/6/7 (chains M) PSPVPPPPPPLPIWKILLIIGTILYIVVFLYISIFLYRLLKTFVPKEERKKWFKFLGILF LIFLILLIYFVVYVIRVLFPPPPPPSPGPPPPPPP
| ID | Name | Formula | Copies |
|---|---|---|---|
| PLM | Palmitic acid | C16 H32 O2 | 1 |
| A1EKL | Flupentixol | C23 H25 F3 N2 O S | 1 |
| CLR | Cholesterol | C27 H46 O | 2 |
GPCR exoframe modulator. Cheng, S., Guo, J., Zhou, Y. et al. To be published.
Other PDB entries of the same protein (UniProt P21728 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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