Crystal structure of amino terminal domains of the NMDA receptor subunit GluN1 and GluN2B in complex with ifenprodil. Determined by X-ray diffraction at 2.6 Å resolution. Released 15 Jun 2011.
Explore 3QEL in 3D Show helices and sheets RCSB PDB PDBe
3QEL contains 67 α-helices and 69 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 | 24 | 1 | |
| 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 | 105-114 | 10 | |
| β-strand | 118-120 | 3 | 1 |
| α-helix | 126-129 | 4 | |
| β-strand | 137-139 | 3 | 1 |
| α-helix | 144-146 | 3 | |
| α-helix | 147-157 | 11 | |
| 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 | 278-281 | 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 | 350-354 | 5 | 3 |
| β-strand | 357-361 | 5 | 3 |
| β-strand | 366 | 1 | 1 |
| β-strand | 367-368 | 2 | 3 |
| 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 | 4 |
| α-helix | 47-50 | 4 | |
| β-strand | 65-73 | 9 | 4 |
| α-helix | 78-91 | 14 | |
| β-strand | 94-101 | 8 | 4 |
| α-helix | 107-119 | 13 | |
| β-strand | 123-127 | 5 | 4 |
| α-helix | 128-131 | 4 | |
| β-strand | 143-145 | 3 | 4 |
| α-helix | 150-163 | 14 | |
| β-strand | 168-174 | 7 | 5 |
| α-helix | 179-191 | 13 | |
| β-strand | 198-205 | 8 | 5 |
| α-helix | 215-220 | 6 | |
| β-strand | 227-231 | 5 | 5 |
| α-helix | 234-245 | 12 | |
| β-strand | 255-258 | 4 | 5 |
| α-helix | 260-263 | 4 | |
| α-helix | 274 | 1 | |
| β-strand | 278-279 | 2 | 5 |
| β-strand | 282 | 1 | 5 |
| α-helix | 289-308 | 20 | |
| α-helix | 327-330 | 4 | |
| α-helix | 336-339 | 4 | |
| β-strand | 343-344 | 2 | 6 |
| β-strand | 347-348 | 2 | 6 |
| β-strand | 351 | 1 | 7 |
| β-strand | 357 | 1 | 7 |
| β-strand | 362-367 | 6 | 5 |
| β-strand | 373-379 | 7 | 5 |
| β-strand | 384-386 | 3 | 5 |
| α-helix | 391-392 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 25-33 | 9 | 8 |
| α-helix | 36-52 | 17 | |
| β-strand | 58-66 | 9 | 8 |
| α-helix | 71-77 | 7 | |
| α-helix | 78-82 | 5 | |
| α-helix | 83-85 | 3 | |
| β-strand | 87-92 | 6 | 8 |
| α-helix | 105-114 | 10 | |
| β-strand | 118-120 | 3 | 8 |
| α-helix | 126-129 | 4 | |
| β-strand | 137-139 | 3 | 8 |
| α-helix | 144-147 | 4 | |
| α-helix | 148-157 | 10 | |
| β-strand | 162-168 | 7 | 9 |
| α-helix | 171-183 | 13 | |
| β-strand | 211-218 | 8 | 9 |
| α-helix | 226-234 | 9 | |
| β-strand | 239-243 | 5 | 9 |
| α-helix | 246-258 | 13 | |
| β-strand | 267-270 | 4 | 9 |
| α-helix | 273-275 | 3 | |
| α-helix | 278-282 | 5 | |
| α-helix | 283-284 | 2 | |
| β-strand | 288-292 | 5 | 9 |
| α-helix | 298-316 | 19 | |
| α-helix | 324-326 | 3 | |
| α-helix | 339-347 | 9 | |
| β-strand | 351-354 | 4 | 10 |
| β-strand | 357-359 | 3 | 10 |
| β-strand | 360-361 | 2 | 11 |
| β-strand | 366 | 1 | 8 |
| β-strand | 367-368 | 2 | 11 |
| β-strand | 372-378 | 7 | 9 |
| β-strand | 381-388 | 8 | 9 |
| β-strand | 393-395 | 3 | 9 |
| α-helix | 399-400 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 34-42 | 9 | 12 |
| α-helix | 47-50 | 4 | |
| β-strand | 65-73 | 9 | 12 |
| α-helix | 78-89 | 12 | |
| β-strand | 94-100 | 7 | 12 |
| α-helix | 107-119 | 13 | |
| β-strand | 123-127 | 5 | 12 |
| α-helix | 128-131 | 4 | |
| β-strand | 143-145 | 3 | 12 |
| α-helix | 150-163 | 14 | |
| β-strand | 168-174 | 7 | 13 |
| α-helix | 179-192 | 14 | |
| β-strand | 198-205 | 8 | 13 |
| α-helix | 215-220 | 6 | |
| β-strand | 227-231 | 5 | 13 |
| α-helix | 234-246 | 13 | |
| β-strand | 255-258 | 4 | 13 |
| α-helix | 260-263 | 4 | |
| α-helix | 274 | 1 | |
| β-strand | 278-282 | 5 | 13 |
| α-helix | 289-300 | 12 | |
| α-helix | 304-311 | 8 | |
| α-helix | 315-317 | 3 | |
| α-helix | 336-339 | 4 | |
| β-strand | 351 | 1 | 14 |
| β-strand | 356 | 1 | 12 |
| β-strand | 357 | 1 | 14 |
| β-strand | 362-367 | 6 | 13 |
| β-strand | 373-378 | 6 | 13 |
| β-strand | 385-386 | 2 | 13 |
| α-helix | 391-393 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| NMDA glutamate receptor subunit | A, C | protein | 383 | Xenopus laevis | A0A1L8F5J9 (AlphaFold model) |
| Glutamate [NMDA] receptor subunit epsilon-2 | B, D | protein | 364 | Rattus norvegicus | Q00960 (AlphaFold model) |
>3QEL_1 NMDA glutamate receptor subunit (chains A, C) DPKIVNIGAVLSTKKHEQIFREAVNQANKRHFTRKIQLQATSVTHRPNAIQMALSVCEDL ISSQVYAILVSHPPAPTDHLTPTPISYTAGFYRIPVIGLTTRMSIYSDKSIHLSFLRTVP PYSHQALVWFEMMRLFNWNHVILIVSDDHEGRAAQKKLETLLEGKESKSKKRNYENLDQL SYDNKRGPKADKVLQFEPGTKNLTALLLEAKELEARVIILSASEDDATAVYKSAAMLDMT GAGYVWLVGEREISGSALRYAPDGIIGLQLINGKNESAHISDAVAVVAQAIHELFEMENI TDPPRGCVGNTNIWKTGPLFKRVLMSSKYPDGVTGRIEFNEDGDRKFAQYSIMNLQNRKL VQVGIFNGSYIIQNDRKIIWPGG
>3QEL_2 Glutamate [NMDA] receptor subunit epsilon-2 (chains B, D) SPPSIGIAVILVGTSDEVAIKDAHEKDDFHHLSVVPRVELVAMNETDPKSIITRICDLMS DRKIQGVVFADDTDQEAIAQILDFISAQTLTPILGIHGGSSMIMADKDESSMFFQFGPSI EQQASVMLNIMEEYDWYIFSIVTTYFPGYQDFVNKIRSTIENSFVGWELEEVLLLDMSLD DGDSKIQNQLKKLQSPIILLYCTKEEATYIFEVANSVGLTGYGYTWIVPSLVAGDTDTVP SEFPTGLISVSYDEWDYGLPARVRDGIAIITTAASDMLSEHSFIPEPKSSCYNTHEKRIY QSNMLNRYLINVTFEGRDLSFSEDGYQMHPKLVIILLNKERKWERVGKWKDKSLQMKYYV WPRM
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 6 |
| QEL | 4-[(1R,2S)-2-(4-benzylpiperidin-1-yl)-1-hydroxypropyl]phenol | C21 H27 N O2 | 2 |
Water and common crystallization additives (NA) are not listed.
Subunit arrangement and phenylethanolamine binding in GluN1/GluN2B NMDA receptors. Karakas, E., Simorowski, N., Furukawa, H. Nature (2011) 475:249-253. DOI 10.1038/nature10180 · PubMed
Other PDB entries of the same protein (UniProt A0A1L8F5J9 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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