Heterodimer of the GluN1b-GluN2B NMDA receptor amino-terminal domains bound to allosteric inhibitor 93-115. Determined by X-ray diffraction at 2.67 Å resolution. Released 30 Jan 2019.
Explore 6E7W in 3D Show helices and sheets RCSB PDB PDBe
6E7W contains 68 α-helices and 70 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 |
|---|---|---|---|
| β-strand | 25-33 | 9 | 1 |
| α-helix | 36-52 | 17 | |
| β-strand | 58-66 | 9 | 1 |
| α-helix | 67-68 | 2 | |
| α-helix | 71-77 | 7 | |
| α-helix | 78-82 | 5 | |
| α-helix | 83-85 | 3 | |
| β-strand | 87-92 | 6 | 1 |
| α-helix | 105-113 | 9 | |
| β-strand | 118-120 | 3 | 1 |
| α-helix | 126-129 | 4 | |
| β-strand | 137-139 | 3 | 1 |
| α-helix | 144-147 | 4 | |
| α-helix | 148-157 | 10 | |
| β-strand | 162-168 | 7 | 2 |
| α-helix | 171-184 | 14 | |
| β-strand | 211-218 | 8 | 2 |
| α-helix | 226-233 | 8 | |
| β-strand | 239-243 | 5 | 2 |
| α-helix | 246-258 | 13 | |
| β-strand | 267-269 | 3 | 2 |
| α-helix | 273-275 | 3 | |
| α-helix | 277-280 | 4 | |
| α-helix | 283-284 | 2 | |
| β-strand | 288-292 | 5 | 2 |
| α-helix | 298-316 | 19 | |
| α-helix | 322-326 | 5 | |
| α-helix | 339-347 | 9 | |
| β-strand | 351-354 | 4 | 3 |
| β-strand | 357-359 | 3 | 3 |
| β-strand | 360-361 | 2 | 4 |
| α-helix | 366 | 1 | |
| β-strand | 367-368 | 2 | 4 |
| β-strand | 372-378 | 7 | 2 |
| β-strand | 381-388 | 8 | 2 |
| β-strand | 393-395 | 3 | 2 |
| α-helix | 399-400 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 34-42 | 9 | 5 |
| α-helix | 47-52 | 6 | |
| β-strand | 65-73 | 9 | 5 |
| α-helix | 78-90 | 13 | |
| β-strand | 94-100 | 7 | 5 |
| α-helix | 107-118 | 12 | |
| β-strand | 123-127 | 5 | 5 |
| α-helix | 128-131 | 4 | |
| α-helix | 133-134 | 2 | |
| β-strand | 143-145 | 3 | 5 |
| α-helix | 150-163 | 14 | |
| β-strand | 168-173 | 6 | 6 |
| α-helix | 179-191 | 13 | |
| β-strand | 198-204 | 7 | 6 |
| α-helix | 215-220 | 6 | |
| β-strand | 227-231 | 5 | 6 |
| α-helix | 234-246 | 13 | |
| β-strand | 255-258 | 4 | 6 |
| α-helix | 260-263 | 4 | |
| α-helix | 274 | 1 | |
| β-strand | 278-281 | 4 | 6 |
| α-helix | 289-311 | 23 | |
| α-helix | 315-318 | 4 | |
| α-helix | 327-330 | 4 | |
| α-helix | 336-339 | 4 | |
| β-strand | 343-344 | 2 | 7 |
| β-strand | 347-348 | 2 | 7 |
| β-strand | 351 | 1 | 8 |
| β-strand | 356 | 1 | 5 |
| β-strand | 357 | 1 | 8 |
| β-strand | 362-367 | 6 | 6 |
| β-strand | 373-380 | 8 | 6 |
| β-strand | 383-386 | 4 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 25-33 | 9 | 9 |
| α-helix | 36-52 | 17 | |
| β-strand | 58-66 | 9 | 9 |
| α-helix | 71-77 | 7 | |
| α-helix | 78-82 | 5 | |
| α-helix | 83-85 | 3 | |
| β-strand | 87-92 | 6 | 9 |
| α-helix | 93-96 | 4 | |
| α-helix | 105-114 | 10 | |
| β-strand | 118-120 | 3 | 9 |
| α-helix | 126-129 | 4 | |
| β-strand | 137-139 | 3 | 9 |
| α-helix | 144-147 | 4 | |
| α-helix | 148-157 | 10 | |
| β-strand | 162-168 | 7 | 10 |
| α-helix | 171-184 | 14 | |
| β-strand | 211-218 | 8 | 10 |
| α-helix | 226-234 | 9 | |
| β-strand | 239-243 | 5 | 10 |
| α-helix | 246-258 | 13 | |
| β-strand | 267-269 | 3 | 10 |
| α-helix | 273-275 | 3 | |
| α-helix | 278-282 | 5 | |
| α-helix | 284 | 1 | |
| β-strand | 288-292 | 5 | 10 |
| α-helix | 298-317 | 20 | |
| α-helix | 322-326 | 5 | |
| α-helix | 339-347 | 9 | |
| β-strand | 351-354 | 4 | 11 |
| β-strand | 357-359 | 3 | 11 |
| β-strand | 360-361 | 2 | 12 |
| α-helix | 366 | 1 | |
| β-strand | 367-368 | 2 | 12 |
| β-strand | 372-378 | 7 | 10 |
| β-strand | 381-388 | 8 | 10 |
| β-strand | 393-395 | 3 | 10 |
| α-helix | 399-400 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 34-42 | 9 | 13 |
| α-helix | 47-51 | 5 | |
| α-helix | 56-59 | 4 | |
| β-strand | 65-73 | 9 | 13 |
| α-helix | 78-90 | 13 | |
| β-strand | 94-100 | 7 | 13 |
| α-helix | 107-119 | 13 | |
| β-strand | 123-127 | 5 | 13 |
| α-helix | 128-131 | 4 | |
| β-strand | 143-145 | 3 | 13 |
| α-helix | 150-163 | 14 | |
| β-strand | 168-173 | 6 | 14 |
| α-helix | 179-191 | 13 | |
| β-strand | 198-204 | 7 | 14 |
| α-helix | 215-220 | 6 | |
| β-strand | 227-231 | 5 | 14 |
| α-helix | 234-246 | 13 | |
| β-strand | 255-258 | 4 | 14 |
| α-helix | 260-263 | 4 | |
| α-helix | 274 | 1 | |
| β-strand | 278-281 | 4 | 14 |
| α-helix | 289-311 | 23 | |
| α-helix | 336-339 | 4 | |
| β-strand | 343 | 1 | 15 |
| β-strand | 348 | 1 | 15 |
| β-strand | 351 | 1 | 16 |
| β-strand | 356 | 1 | 13 |
| β-strand | 357 | 1 | 16 |
| β-strand | 362-367 | 6 | 14 |
| β-strand | 373-380 | 8 | 14 |
| β-strand | 383-386 | 4 | 14 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Glutamate receptor ionotropic, NMDA 1 | A, C | protein | 385 | Xenopus laevis | A0A1L8F5J9 (AlphaFold model) |
| Glutamate receptor ionotropic, NMDA 2B | B, D | protein | 363 | Rattus norvegicus | Q00960 (AlphaFold model) |
>6E7W_1 Glutamate receptor ionotropic, NMDA 1 (chains A, C) DPKIVNIGAVLSTKKHEQIFREAVNQANKRHFTRKIQLQATSVTHRPNAIQMALSVCEDL ISSQVYAILVSHPPAPTDHLTPTPISYTAGFYRIPVIGLTTRMSIYSDKSIHLSFLRTVP PYSHQALVWFEMMRLFNWNHVILIVSDDHEGRAAQKKLETLLEGKESKSKKRNYENLDQL SYDNKRGPKADKVLQFEPGTKNLTALLLEAKELEARVIILSASEDDATAVYKSAAMLDMT GAGYVWLVGEREISGSALRYAPDGIIGLQLINGKNESAHISDAVAVVAQAIHELFEMENI TDPPRGCVGNTNIWKTGPLFKRVLMSSKYPDGVTGRIEFNEDGDRKFAQYSIMNLQNRKL VQVGIFNGSYIIQNDRKIIWPGGET
>6E7W_2 Glutamate receptor ionotropic, NMDA 2B (chains B, D) PPSIGIAVILVGTSDEVAIKDAHEKDDFHHLSVVPRVELVAMNETDPKSIITRICDLMSD RKIQGVVFADDTDQEAIAQILDFISAQTLTPILGIHGGSSMIMADKDESSMFFQFGPSIE QQASVMLNIMEEYDWYIFSIVTTYFPGYQDFVNKIRSTIENSFVGWELEEVLLLDMSLDD GDSKIQNQLKKLQSPIILLYCTKEEATYIFEVANSVGLTGYGYTWIVPSLVAGDTDTVPS EFPTGLISVSYDEWDYGLPARVRDGIAIITTAASDMLSEHSFIPEPKSSCYNTHEKRIYQ SNMLNRYLINVTFEGRDLSFSEDGYQMHPKLVIILLNKERKWERVGKWKDKSLQMKYYVW PRM
| ID | Name | Formula | Copies |
|---|---|---|---|
| HXM | N-{4-[(2S)-3-{[2-(3,4-dichlorophenyl)ethyl](propan-2-yl)amino}-2-hydroxypropoxy… | C21 H28 Cl2 N2 O4 S | 2 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 8 |
Water and common crystallization additives (CL, NA) are not listed.
Structural elements of a pH-sensitive inhibitor binding site in NMDA receptors. Regan, M.C., Furukawa, H. Nat Commun (2019) 10:321.
Other PDB entries of the same protein (UniProt A0A1L8F5J9 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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