Crystal structure of GluN1/GluN2A agonist-binding domains in complex with 7CKA and glutamate. Determined by X-ray diffraction at 2.05 Å resolution. Released 12 Mar 2025.
Explore 9DA9 in 3D Show helices and sheets RCSB PDB PDBe
9DA9 contains 34 α-helices and 41 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 |
|---|---|---|---|
| β-strand | 6-10 | 5 | 1 |
| β-strand | 13 | 1 | 2 |
| β-strand | 17 | 1 | 2 |
| β-strand | 18-21 | 4 | 1 |
| α-helix | 22-23 | 2 | |
| α-helix | 27-30 | 4 | |
| β-strand | 32 | 1 | 3 |
| α-helix | 37 | 1 | |
| β-strand | 38 | 1 | 3 |
| α-helix | 39-40 | 2 | |
| β-strand | 42-46 | 5 | 1 |
| β-strand | 59-64 | 6 | 1 |
| α-helix | 66-78 | 13 | |
| β-strand | 82-86 | 5 | 1 |
| β-strand | 95-97 | 3 | 4 |
| α-helix | 98 | 1 | |
| β-strand | 104-106 | 3 | 4 |
| α-helix | 108-114 | 7 | |
| β-strand | 120-121 | 2 | 1 |
| β-strand | 126 | 1 | 5 |
| α-helix | 129-132 | 4 | |
| β-strand | 135-137 | 3 | 1 |
| α-helix | 138 | 1 | |
| α-helix | 140 | 1 | |
| β-strand | 142-151 | 10 | 5 |
| α-helix | 162-165 | 4 | |
| β-strand | 168 | 1 | 6 |
| β-strand | 171 | 1 | 6 |
| β-strand | 173-174 | 2 | 5 |
| β-strand | 176 | 1 | 7 |
| α-helix | 180-187 | 8 | |
| α-helix | 189-191 | 3 | |
| α-helix | 192-199 | 8 | |
| β-strand | 203 | 1 | 7 |
| α-helix | 206-214 | 9 | |
| β-strand | 220-224 | 5 | 5 |
| α-helix | 225-234 | 10 | |
| β-strand | 238-250 | 13 | 5 |
| β-strand | 253-255 | 3 | 1 |
| α-helix | 261-273 | 13 | |
| α-helix | 276-284 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 8-13 | 6 | 8 |
| β-strand | 16 | 1 | 9 |
| β-strand | 20 | 1 | 9 |
| β-strand | 21-24 | 4 | 8 |
| α-helix | 25-26 | 2 | |
| β-strand | 37-44 | 8 | 8 |
| β-strand | 52-60 | 9 | 8 |
| α-helix | 62-73 | 12 | |
| β-strand | 77-82 | 6 | 8 |
| β-strand | 91-92 | 2 | 10 |
| β-strand | 95-96 | 2 | 10 |
| α-helix | 98-104 | 7 | |
| β-strand | 110-111 | 2 | 8 |
| β-strand | 116 | 1 | 11 |
| α-helix | 119-122 | 4 | |
| β-strand | 126-127 | 2 | 8 |
| α-helix | 128-130 | 3 | |
| β-strand | 132-141 | 10 | 11 |
| α-helix | 152-155 | 4 | |
| α-helix | 157-159 | 3 | |
| α-helix | 163-164 | 2 | |
| β-strand | 166-167 | 2 | 11 |
| α-helix | 173-181 | 9 | |
| α-helix | 183-189 | 7 | |
| α-helix | 190-192 | 3 | |
| α-helix | 197-205 | 9 | |
| β-strand | 211-215 | 5 | 11 |
| α-helix | 216-223 | 8 | |
| β-strand | 231-233 | 3 | 11 |
| α-helix | 234-237 | 4 | |
| β-strand | 240-245 | 6 | 11 |
| β-strand | 248-249 | 2 | 8 |
| α-helix | 256-268 | 13 | |
| α-helix | 271-280 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Glutamate receptor ionotropic, NMDA 1 | A | protein | 292 | Rattus norvegicus | P35439 (AlphaFold model) |
| Glutamate receptor ionotropic, NMDA 2A | B | protein | 283 | Rattus norvegicus | Q00959 (AlphaFold model) |
>9DA9_1 Glutamate receptor ionotropic, NMDA 1 (chains A) GMSTRLKIVTIHQEPFVYVKPTMSDGTCKEEFTVNGDPVKKVICTGPNDTSPGSPRHTVP QCCYGFCIDLLIKLARTMNFTYEVHLVADGKFGTQERVNNSNKKEWNGMMGELLSGQADM IVAPLTINNERAQYIEFSKPFKYQGLTILVKKGTRITGINDPRLRNPSDKFIYATVKQSS VDIYFRRQVELSTMYRHMEKHNYESAAEAIQAVRDNKLHAFIWDSAVLEFEASQKCDLVT TGELFFRSGFGIGMRKDSPWKQNVSLSILKSHENGFMEDLDKTWVRYQECDS
>9DA9_2 Glutamate receptor ionotropic, NMDA 2A (chains B) SDDNHLSIVTLEEAPFVIVEDIDPLTETCVRNTVPCRKFVKINNSTNEGMNVKKCCKGFC IDILKKLSRTVKFTYDLYLVTNGKHGKKVNNVWNGMIGEVVYQRAVMAVGSLTINEERSE VVDFSVPFVETGISVMVSRGTQVTGLSDKKFQRPHDYSPPFRFGTVPNGSTERNIRNNYP YMHQYMTRFNQRGVEDALVSLKTGKLDAFIYDAAVLNYKAGRDEGCKLVTIGSGYIFATT GYGIALQKGSPWKRQIDLALLQFVGDGEMEELETLWLTGICHN
A galactose-based auto-expression system improves T7-inducible protein production in Escherichia coli. Bosco, J., Gagliano, E., Boshae, K.L. et al. Sci Rep (2025) 15:8936-8936. DOI 10.1038/s41598-025-91954-5 · PubMed
Other PDB entries of the same protein (UniProt P35439 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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