8CC6: Mouse serotonin 5-HT3A receptor
Mouse serotonin 5-HT3A receptor in complex with PZ-1922. Determined by electron microscopy at 3.2 Å resolution. Released 11 Oct 2023.
- Method
- Electron microscopy
- Resolution
- 3.2 Å
- Organism
- Mus musculus
- Chains
- 5
- Atoms
- 16,640
- Mol. weight
- 325.65 kDa
- Ligands
- U9L, NAG
- Released
- 11 Oct 2023
Explore 8CC6 in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
8CC6 contains 74 α-helices and 65 β-strands across 5 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.
Chain A: 15 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 11-20 | 10 | |
| β-strand | 37-52 | 16 | 1 |
| β-strand | 57-69 | 13 | 1 |
| α-helix | 77-79 | 3 | |
| β-strand | 85-89 | 5 | 1 |
| α-helix | 90-92 | 3 | |
| β-strand | 98-100 | 3 | 2 |
| β-strand | 103-105 | 3 | 1 |
| β-strand | 114-118 | 5 | 1 |
| β-strand | 122-134 | 13 | 1 |
| α-helix | 142-144 | 3 | |
| β-strand | 146-155 | 10 | 2 |
| β-strand | 163-167 | 5 | 1 |
| α-helix | 171-175 | 5 | |
| β-strand | 187-200 | 14 | 2 |
| β-strand | 206-218 | 13 | 2 |
| α-helix | 220-222 | 3 | |
| α-helix | 224-242 | 19 | |
| α-helix | 246-248 | 3 | |
| α-helix | 251-269 | 19 | |
| β-strand | 276 | 1 | 3 |
| β-strand | 279 | 1 | 3 |
| α-helix | 283-308 | 26 | |
| α-helix | 314-318 | 5 | |
| α-helix | 319-323 | 5 | |
| α-helix | 324-329 | 6 | |
| α-helix | 330-332 | 3 | |
| α-helix | 398-459 | 62 | |
Chain B: 15 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 11-20 | 10 | |
| β-strand | 37-52 | 16 | 4 |
| β-strand | 57-69 | 13 | 4 |
| α-helix | 77-80 | 4 | |
| β-strand | 85-89 | 5 | 4 |
| α-helix | 90-92 | 3 | |
| β-strand | 98-100 | 3 | 5 |
| β-strand | 103-105 | 3 | 4 |
| β-strand | 114-118 | 5 | 4 |
| β-strand | 122-134 | 13 | 4 |
| α-helix | 142-144 | 3 | |
| β-strand | 146-155 | 10 | 5 |
| β-strand | 163-167 | 5 | 4 |
| α-helix | 171-175 | 5 | |
| β-strand | 187-200 | 14 | 5 |
| β-strand | 206-218 | 13 | 5 |
| α-helix | 220-222 | 3 | |
| α-helix | 224-242 | 19 | |
| α-helix | 246-248 | 3 | |
| α-helix | 251-269 | 19 | |
| β-strand | 276 | 1 | 6 |
| β-strand | 279 | 1 | 6 |
| α-helix | 283-308 | 26 | |
| α-helix | 314-318 | 5 | |
| α-helix | 319-323 | 5 | |
| α-helix | 324-329 | 6 | |
| α-helix | 330-332 | 3 | |
| α-helix | 398-459 | 62 | |
Chain C: 15 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 11-20 | 10 | |
| α-helix | 36 | 1 | |
| β-strand | 37-52 | 16 | 7 |
| β-strand | 57-74 | 18 | 7 |
| α-helix | 77-79 | 3 | |
| β-strand | 85-89 | 5 | 7 |
| α-helix | 90-92 | 3 | |
| β-strand | 98-100 | 3 | 8 |
| β-strand | 103-106 | 4 | 7 |
| β-strand | 114-118 | 5 | 7 |
| β-strand | 120-134 | 15 | 7 |
| α-helix | 142-144 | 3 | |
| β-strand | 146-155 | 10 | 8 |
| β-strand | 163-167 | 5 | 7 |
| α-helix | 171-175 | 5 | |
| β-strand | 187-200 | 14 | 8 |
| β-strand | 206-218 | 13 | 8 |
| α-helix | 221-242 | 22 | |
| α-helix | 246-248 | 3 | |
| α-helix | 251-269 | 19 | |
| β-strand | 276 | 1 | 9 |
| β-strand | 279 | 1 | 9 |
| α-helix | 283-308 | 26 | |
| α-helix | 316-318 | 3 | |
| α-helix | 319-323 | 5 | |
| α-helix | 324-329 | 6 | |
| α-helix | 330-332 | 3 | |
| α-helix | 398-459 | 62 | |
Chain D: 14 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 11-20 | 10 | |
| β-strand | 37-52 | 16 | 10 |
| β-strand | 57-69 | 13 | 10 |
| α-helix | 77-80 | 4 | |
| β-strand | 85-89 | 5 | 10 |
| α-helix | 90-92 | 3 | |
| β-strand | 98-100 | 3 | 11 |
| β-strand | 103-105 | 3 | 10 |
| β-strand | 114-118 | 5 | 10 |
| β-strand | 122-134 | 13 | 10 |
| α-helix | 142-144 | 3 | |
| β-strand | 146-155 | 10 | 11 |
| β-strand | 163-167 | 5 | 10 |
| α-helix | 171-175 | 5 | |
| β-strand | 187-200 | 14 | 11 |
| β-strand | 206-218 | 13 | 11 |
| α-helix | 221-242 | 22 | |
| α-helix | 246-248 | 3 | |
| α-helix | 251-269 | 19 | |
| β-strand | 276 | 1 | 12 |
| β-strand | 279 | 1 | 12 |
| α-helix | 283-308 | 26 | |
| α-helix | 314-318 | 5 | |
| α-helix | 319-323 | 5 | |
| α-helix | 324-329 | 6 | |
| α-helix | 330-332 | 3 | |
| α-helix | 398-459 | 62 | |
Chain E: 15 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 11-20 | 10 | |
| β-strand | 37-52 | 16 | 13 |
| β-strand | 57-69 | 13 | 13 |
| α-helix | 77-79 | 3 | |
| β-strand | 85-89 | 5 | 13 |
| α-helix | 90-92 | 3 | |
| β-strand | 98-100 | 3 | 14 |
| β-strand | 103-105 | 3 | 13 |
| β-strand | 114-118 | 5 | 13 |
| β-strand | 122-134 | 13 | 13 |
| α-helix | 142-144 | 3 | |
| β-strand | 146-155 | 10 | 14 |
| β-strand | 163-167 | 5 | 13 |
| α-helix | 171-175 | 5 | |
| β-strand | 187-200 | 14 | 14 |
| β-strand | 206-218 | 13 | 14 |
| α-helix | 220-222 | 3 | |
| α-helix | 224-242 | 19 | |
| α-helix | 246-248 | 3 | |
| α-helix | 251-269 | 19 | |
| β-strand | 276 | 1 | 15 |
| β-strand | 279 | 1 | 15 |
| α-helix | 283-308 | 26 | |
| α-helix | 316-318 | 3 | |
| α-helix | 319-323 | 5 | |
| α-helix | 324-329 | 6 | |
| α-helix | 330-332 | 3 | |
| α-helix | 398-459 | 62 | |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| 5-hydroxytryptamine receptor 3A | A, B, C, D, E | protein | 566 | Mus musculus | P23979 (AlphaFold model) |
Sequence of entity 1 (A, B, C, D, E), FASTA
>8CC6_1 5-hydroxytryptamine receptor 3A (chains A, B, C, D, E)
MRLCIPQVLLALFLSMLTGPGEGSRRRWSHPQFEKGGGSGGGSGGGSWSHPQFEKGGGSG
GGSGGGSWSHPQFEKGGGSGGGSGGGSWSHPQFEKENLYFQGSGATQARDTTQPALLRLS
DHLLANYKKGVRPVRDWRKPTTVSIDVIMYAILNVDEKNQVLTTYIWYRQYWTDEFLQWT
PEDFDNVTKLSIPTDSIWVPDILINEFVDVGKSPNIPYVYVHHRGEVQNYKPLQLVTACS
LDIYNFPFDVQNCSLTFTSWLHTIQDINITLWRSPEEVRSDKSIFINQGEWELLEVFPQF
KEFSIDISNSYAEMKFYVIIRRRPLFYAVSLLLPSIFLMVVDIVGFCLPPDSGERVSFKI
TLLLGYSVFLIIVSDTLPATAIGTPLIGVYFVVCMALLVISLAETIFIVRLVHKQDLQRP
VPDWLRHLVLDRIAWILCLGEQPMAHRPPATFQANKTDDCSGSDLLPAMGNHCSHVGGPQ
DLEKTPRGRGSPLPPPREASLAVRGLLQELSSIRHFLEKRDEMREVARDWLRVGYVLDRL
LFRIYLLAVLAYSITLVTLWSIWHSS
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| U9L | 1-[(3-chlorophenyl)methyl]-4-piperazin-1-yl-pyrrolo[3,2-c]quinoline | C22 H21 Cl N4 | 5 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 5 |
Primary citation
Superiority of the Triple-Acting 5-HT 6 R/5-HT 3 R Antagonist and MAO-B Reversible Inhibitor PZ-1922 over 5-HT 6 R Antagonist Intepirdine in Alleviation of Cognitive Deficits in Rats. Grychowska, K., Lopez-Sanchez, U., Vitalis, M. et al. J Med Chem (2023) 66:14928-14947. DOI 10.1021/acs.jmedchem.3c01482 · PubMed
Other PDB entries of the same protein (UniProt P23979 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 8FRX 2.7 Å, Full-length mouse 5-HT3A receptor in complex with SMP100, pre-activated
- 8FRZ 2.75 Å, Full-length mouse 5-HT3A receptor in complex with serotonin, pre-activated
- 8FSB 2.75 Å, Full-length mouse 5-HT3A receptor in complex with serotonin, open-like
- 6Y5A 2.8 Å, Serotonin-bound 5-HT3A receptor in Salipro
- 6Y1Z 2.82 Å, Mouse serotonin 5HT3 receptor in complex with palonosetron
- 6NP0 2.92 Å, Cryo-EM structure of 5HT3A receptor in presence of granisetron
- 6W1J 2.92 Å, Cryo-EM structure of 5HT3A receptor in presence of Alosetron
- 8FRW 2.92 Å, Full-length mouse 5-HT3A receptor in complex with ALB148471, pre-activated
- 8CC7 3.0 Å, Mouse serotonin 5-HT3A receptor in complex with PZ-1939
- 8AW2 3.01 Å, Mouse serotonin 5-HT3A receptor in complex with vortioxetine
- 6W1M 3.06 Å, Cryo-EM structure of 5HT3A receptor in presence of Ondansetron
- 6Y5B 3.1 Å, 5-HT3A receptor in Salipro (apo, asymmetric)
Browse structure collections
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