2XYS: Aplysia californica AChBP
Crystal structure of Aplysia californica AChBP in complex with strychnine. Determined by X-ray diffraction at 1.91 Å resolution. Released 23 Mar 2011.
- Method
- X-ray diffraction
- Resolution
- 1.91 Å
- Organism
- APLYSIA CALIFORNICA
- Chains
- 5
- Atoms
- 9,639
- Mol. weight
- 125.45 kDa
- Ligands
- SY9
- Released
- 23 Mar 2011
Explore 2XYS in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
2XYS contains 25 α-helices and 77 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: 5 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 2-12 | 11 | |
| α-helix | 16-18 | 3 | |
| β-strand | 27-42 | 16 | 1 |
| β-strand | 47-64 | 18 | 1 |
| α-helix | 67-69 | 3 | |
| β-strand | 75-79 | 5 | 1 |
| α-helix | 80-82 | 3 | |
| β-strand | 88-90 | 3 | 2 |
| β-strand | 93 | 1 | 1 |
| β-strand | 98-99 | 2 | 1 |
| β-strand | 104-108 | 5 | 1 |
| β-strand | 110-115 | 6 | 1 |
| β-strand | 118-124 | 7 | 1 |
| β-strand | 136-144 | 9 | 2 |
| β-strand | 152-155 | 4 | 1 |
| β-strand | 160 | 1 | 2 |
| α-helix | 161 | 1 | |
| β-strand | 162 | 1 | 1 |
| β-strand | 172-184 | 13 | 2 |
| β-strand | 193-204 | 12 | 2 |
Chain B: 6 helices, 17 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 2-12 | 11 | |
| α-helix | 16-18 | 3 | |
| β-strand | 22 | 1 | 3 |
| β-strand | 25 | 1 | 3 |
| β-strand | 27-42 | 16 | 4 |
| β-strand | 47-64 | 18 | 4 |
| α-helix | 67-69 | 3 | |
| β-strand | 75-79 | 5 | 4 |
| α-helix | 80-82 | 3 | |
| β-strand | 88-90 | 3 | 5 |
| β-strand | 93 | 1 | 4 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-99 | 2 | 4 |
| β-strand | 104-108 | 5 | 4 |
| β-strand | 110-115 | 6 | 4 |
| β-strand | 118-124 | 7 | 4 |
| β-strand | 136-144 | 9 | 5 |
| β-strand | 152-156 | 5 | 4 |
| β-strand | 160 | 1 | 5 |
| α-helix | 161 | 1 | |
| β-strand | 162 | 1 | 4 |
| β-strand | 172-184 | 13 | 5 |
| β-strand | 193-204 | 12 | 5 |
Chain C: 5 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 2-8 | 7 | |
| α-helix | 9-13 | 5 | |
| α-helix | 16-18 | 3 | |
| β-strand | 27-42 | 16 | 6 |
| β-strand | 47-64 | 18 | 6 |
| α-helix | 67-69 | 3 | |
| β-strand | 75-79 | 5 | 6 |
| α-helix | 80-82 | 3 | |
| β-strand | 88-90 | 3 | 7 |
| β-strand | 93 | 1 | 6 |
| β-strand | 98-99 | 2 | 6 |
| β-strand | 104-108 | 5 | 6 |
| β-strand | 110-115 | 6 | 6 |
| β-strand | 118-124 | 7 | 6 |
| β-strand | 136-144 | 9 | 7 |
| β-strand | 152-155 | 4 | 6 |
| β-strand | 160 | 1 | 7 |
| β-strand | 162 | 1 | 6 |
| β-strand | 172-184 | 13 | 7 |
| β-strand | 193-204 | 12 | 7 |
Chain D: 4 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 2-12 | 11 | |
| α-helix | 16-18 | 3 | |
| β-strand | 27-42 | 16 | 8 |
| β-strand | 47-64 | 18 | 8 |
| α-helix | 67-69 | 3 | |
| β-strand | 75-79 | 5 | 8 |
| α-helix | 80-82 | 3 | |
| β-strand | 88-90 | 3 | 9 |
| β-strand | 93 | 1 | 8 |
| β-strand | 98-99 | 2 | 8 |
| β-strand | 104-108 | 5 | 8 |
| β-strand | 110-115 | 6 | 8 |
| β-strand | 118-124 | 7 | 8 |
| β-strand | 136-144 | 9 | 9 |
| β-strand | 152-155 | 4 | 8 |
| β-strand | 160 | 1 | 9 |
| β-strand | 162 | 1 | 8 |
| β-strand | 172-184 | 13 | 9 |
| β-strand | 193-204 | 12 | 9 |
Chain E: 5 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 2-8 | 7 | |
| α-helix | 9-13 | 5 | |
| α-helix | 16-18 | 3 | |
| β-strand | 27-42 | 16 | 10 |
| β-strand | 47-64 | 18 | 10 |
| α-helix | 67-70 | 4 | |
| β-strand | 75-79 | 5 | 10 |
| α-helix | 80-82 | 3 | |
| β-strand | 88-90 | 3 | 11 |
| β-strand | 93 | 1 | 10 |
| β-strand | 98-99 | 2 | 10 |
| β-strand | 104-108 | 5 | 10 |
| β-strand | 110-115 | 6 | 10 |
| β-strand | 118-124 | 7 | 10 |
| β-strand | 136-144 | 9 | 11 |
| β-strand | 152-155 | 4 | 10 |
| β-strand | 160 | 1 | 11 |
| β-strand | 162 | 1 | 10 |
| β-strand | 172-184 | 13 | 11 |
| β-strand | 193-204 | 12 | 11 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Soluble acetylcholine receptor | A, B, C, D, E | protein | 217 | APLYSIA CALIFORNICA | Q8WSF8 (AlphaFold model) |
Sequence of entity 1 (A, B, C, D, E), FASTA
>2XYS_1 SOLUBLE ACETYLCHOLINE RECEPTOR (chains A, B, C, D, E)
QANLMRLKSDLFNRSPMYPGPTKDDPLTVTLGFTLQDIVKVDSSTNEVDLVYYEQQRWKL
NSLMWDPNEYGNITDFRTSAADIWTPDITAYSSTRPVQVLSPQIAVVTHDGSVMFIPAQR
LSFMCDPTGVDSEEGVTCAVKFGSWVYSGFEIDLKTDTDQVDLSSYYASSKYEILSATQT
RQVQHYSCCPEPYIDVNLVVKFRERRAGNGFFRNLFD
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| SY9 | Strychnine | C21 H22 N2 O2 | 6 |
Primary citation
A Structural and Mutagenic Blueprint for Molecular Recognition of Strychnine and D-Tubocurarine by Different Cys-Loop Receptors. Brams, M., Pandya, A., Kuzmin, D. et al. PLoS Biol (2011) 9:01034. DOI 10.1371/JOURNAL.PBIO.1001034 · PubMed
Other PDB entries of the same protein (UniProt Q8WSF8 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 6T9R 1.72 Å, Aplysia californica AChBP in complex with a cytisine derivative
- 2WN9 1.75 Å, Crystal structure of Aplysia ACHBP in complex with 4-0H-DMXBA
- 2PGZ 1.76 Å, Crystal structure of Cocaine bound to an ACh-Binding Protein
- 2WNJ 1.8 Å, Crystal structure of aplysia achbp in complex with dmxba
- 8QTL 1.85 Å, Aplysia californica acetylcholine-binding protein in complex with Spiroimine (-)-4 S
- 2Y7Y 1.9 Å, Aplysia californica achbp in apo state
- 4XHE 1.9 Å, Crystal Structure of A-AChBP in complex with pinnatoxin A
- 4ZK4 1.9 Å, Crystal structure of a chimeric acetylcholine binding protein from Aplysia californica…
- 5TVC 1.93 Å, Crystal structure of a chimeric acetylcholine binding protein from Aplysia californica…
- 3C84 1.94 Å, Crystal structure of a complex of AChBP from aplysia californica and the neonicotinoid…
- 2YMD 1.96 Å, Crystal structure of a mutant binding protein (5HTBP-AChBP) in complex with serotonin…
- 4WV9 2.0 Å, Crystal structure of acetylcholine binding protein (AChBP) from Aplysia Californica in…
Browse structure collections
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