CryoEM structure of Gq-coupled MRGPRX1 with ligand Compound-16. Determined by electron microscopy at 3.25 Å resolution. Released 2 Nov 2022.
Explore 8DWH in 3D Show helices and sheets RCSB PDB PDBe
8DWH contains 27 α-helices and 37 β-strands across 4 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 | 7-31 | 25 | |
| β-strand | 33-35 | 3 | 1 |
| β-strand | 38-40 | 3 | 2 |
| β-strand | 69 | 1 | 3 |
| β-strand | 72-76 | 5 | 1 |
| β-strand | 79-83 | 5 | 1 |
| β-strand | 86 | 1 | 3 |
| α-helix | 96-101 | 6 | |
| β-strand | 105-111 | 7 | 2 |
| α-helix | 118-130 | 13 | |
| α-helix | 132-134 | 3 | |
| β-strand | 138-144 | 7 | 2 |
| α-helix | 146-155 | 10 | |
| α-helix | 160-162 | 3 | |
| α-helix | 165-169 | 5 | |
| α-helix | 184-203 | 20 | |
| β-strand | 211-215 | 5 | 2 |
| α-helix | 223-242 | 20 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-22 | 19 | |
| α-helix | 30-33 | 4 | |
| β-strand | 47-51 | 5 | 4 |
| β-strand | 58-63 | 6 | 5 |
| β-strand | 69-74 | 6 | 5 |
| β-strand | 78-83 | 6 | 5 |
| β-strand | 89-94 | 6 | 5 |
| β-strand | 100-105 | 6 | 6 |
| β-strand | 111-116 | 6 | 6 |
| β-strand | 121-125 | 5 | 6 |
| β-strand | 135-139 | 5 | 6 |
| β-strand | 146-151 | 6 | 7 |
| β-strand | 156-161 | 6 | 7 |
| β-strand | 166-170 | 5 | 7 |
| β-strand | 175-180 | 6 | 7 |
| β-strand | 187-192 | 6 | 8 |
| β-strand | 198-203 | 6 | 8 |
| β-strand | 208-212 | 5 | 8 |
| β-strand | 218-222 | 5 | 8 |
| β-strand | 229-234 | 6 | 9 |
| β-strand | 240-245 | 6 | 9 |
| β-strand | 250-254 | 5 | 9 |
| β-strand | 260-264 | 5 | 9 |
| β-strand | 273-278 | 6 | 10 |
| β-strand | 284-289 | 6 | 10 |
| β-strand | 294-298 | 5 | 10 |
| β-strand | 306-308 | 3 | 10 |
| β-strand | 315-320 | 6 | 4 |
| β-strand | 327-331 | 5 | 4 |
| β-strand | 335-339 | 5 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 12-23 | 12 | |
| α-helix | 30-43 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 26-54 | 29 | |
| α-helix | 60-87 | 28 | |
| α-helix | 95-125 | 31 | |
| α-helix | 127-128 | 2 | |
| α-helix | 129-133 | 5 | |
| α-helix | 138-160 | 23 | |
| α-helix | 173-203 | 31 | |
| α-helix | 212-224 | 13 | |
| α-helix | 225-229 | 5 | |
| α-helix | 231-234 | 4 | |
| α-helix | 238-241 | 4 | |
| α-helix | 246-251 | 6 | |
| α-helix | 255-272 | 18 | |
| α-helix | 274-277 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Gs-mini-Gq chimera | B | protein | 246 | Homo sapiens | |
| Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 | C | protein | 345 | Homo sapiens | P62873 (AlphaFold model) |
| Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 | D | protein | 71 | Homo sapiens | P59768 (AlphaFold model) |
| Mas-related G-protein coupled receptor member X1 | R | protein | 323 | Homo sapiens | Q96LB2 (AlphaFold model) |
>8DWH_1 Gs-mini-Gq chimera (chains B) MGSTVSAEDKAAAERSKMIDKNLREDGEKARRTLRLLLLGADNSGKSTIVKQMRILHGGS GGSGGTSGIFETKFQVDKVNFHMFDVGGQRDERRKWIQCFNDVTAIIFVVDSSDYNRLQE ALNDFKSIWNNRWLRTISVILFLNKQDLLAEKVLAGKSKIEDYFPEFARYTTPEDATPEP GEDPRVTRAKYFIRKEFVDISTASGDGRHICYPHFTCAVDTENARRIFNDCKDIILQMNL REYNLV
>8DWH_2 Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 (chains C) GPGSSGSELDQLRQEAEQLKNQIRDARKACADATLSQITNNIDPVGRIQMRTRRTLRGHL AKIYAMHWGTDSRLLVSASQDGKLIIWDSYTTNKVHAIPLRSSWVMTCAYAPSGNYVACG GLDNICSIYNLKTREGNVRVSRELAGHTGYLSCCRFLDDNQIVTSSGDTTCALWDIETGQ QTTTFTGHTGDVMSLSLAPDTRLFVSGACDASAKLWDVREGMCRQTFTGHESDINAICFF PNGNAFATGSDDATCRLFDLRADQELMTYSHDNIICGITSVSFSKSGRLLLAGYDDFNCN VWDALKADRAGVLAGHDNRVSCLGVTDDGMAVATGSWDSFLKIWN
>8DWH_3 Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 (chains D) MASNNTASIAQARKLVEQLKMEANIDRIKVSKAAADLMAYCEAHAKEDPLLTPVPASENP FREKKFFCAIL
>8DWH_4 Mas-related G-protein coupled receptor member X1 (chains R) GPDPTISTLDTELTPINGTEETLCYKQTLSLTVLTCIVSLVGLTGNAVVLWLLGCRMRRN AFSIYILNLAAADFLFLSGRLIYSLLSFISIPHTISKILYPVMMFSYFAGLSFLSAVSTE RCLSVLWPIWYRCHRPTHLSAVVCVLLWALSLLRSILEWMLCGFLFSGADSAWCQTSDFI TVAWLIFLCVVLCGSSLVLLIRILCGSRKIPLTRLYVTILLTVLVFLLCGLPFGIQFFLF LWIHVDREVLFCHVHLVSIFLSALNSSANPIIYFFVGSFRQRQNRQNLKLVLQRALQDAS EVDEGGGQLPEEILELSGSRLEQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| U2U | N-{2-[(1-aminoisoquinolin-6-yl)oxy]-4-methylphenyl}-2-methoxybenzene-1-sulfonam… | C23 H21 N3 O4 S | 1 |
Ligand recognition and allosteric modulation of the human MRGPRX1 receptor. Liu, Y., Cao, C., Huang, X.P. et al. Nat Chem Biol (2023) 19:416-422. DOI 10.1038/s41589-022-01173-6 · PubMed
Other PDB entries of the same protein (UniProt P62873 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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