Crystal structure of amino terminal domains of the NMDA receptor subunit GluN1 and GluN2A in the presence of EDTA. Determined by X-ray diffraction at 2.7 Å resolution. Released 14 Dec 2016.
Explore 5TQ0 in 3D Show helices and sheets RCSB PDB PDBe
5TQ0 contains 41 α-helices and 78 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 | 36-51 | 16 | |
| 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 | 163-168 | 6 | 2 |
| α-helix | 171-185 | 15 | |
| β-strand | 213-218 | 6 | 2 |
| α-helix | 226-234 | 9 | |
| β-strand | 239-243 | 5 | 2 |
| α-helix | 246-258 | 13 | |
| β-strand | 267-270 | 4 | 2 |
| α-helix | 273-275 | 3 | |
| α-helix | 278-282 | 5 | |
| α-helix | 283-284 | 2 | |
| β-strand | 288-292 | 5 | 2 |
| α-helix | 298-316 | 19 | |
| α-helix | 323-326 | 4 | |
| α-helix | 335-336 | 2 | |
| α-helix | 339-347 | 9 | |
| β-strand | 350-351 | 2 | 3 |
| β-strand | 359-361 | 3 | 3 |
| β-strand | 367-368 | 2 | 3 |
| β-strand | 372-378 | 7 | 2 |
| β-strand | 381-388 | 8 | 2 |
| β-strand | 393-394 | 2 | 2 |
| β-strand | 399-401 | 3 | 4 |
| β-strand | 407-409 | 3 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 35-40 | 6 | 5 |
| β-strand | 68-73 | 6 | 5 |
| α-helix | 79-91 | 13 | |
| β-strand | 97-101 | 5 | 5 |
| α-helix | 108-120 | 13 | |
| β-strand | 124-128 | 5 | 5 |
| α-helix | 129-132 | 4 | |
| α-helix | 137-139 | 3 | |
| β-strand | 144-146 | 3 | 5 |
| α-helix | 151-164 | 14 | |
| β-strand | 169-175 | 7 | 6 |
| α-helix | 180-193 | 14 | |
| β-strand | 199-200 | 2 | 6 |
| α-helix | 201-203 | 3 | |
| β-strand | 204-206 | 3 | 6 |
| α-helix | 213-219 | 7 | |
| β-strand | 226-230 | 5 | 6 |
| α-helix | 233-245 | 13 | |
| β-strand | 254-257 | 4 | 6 |
| α-helix | 259-262 | 4 | |
| α-helix | 273 | 1 | |
| β-strand | 277-280 | 4 | 6 |
| α-helix | 288-309 | 22 | |
| α-helix | 314-317 | 4 | |
| β-strand | 342-343 | 2 | 7 |
| β-strand | 346-347 | 2 | 7 |
| β-strand | 350 | 1 | 8 |
| β-strand | 356 | 1 | 8 |
| β-strand | 362-366 | 5 | 6 |
| β-strand | 372-377 | 6 | 6 |
| β-strand | 385 | 1 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-6 | 4 | 9 |
| β-strand | 10-12 | 3 | 10 |
| β-strand | 17-25 | 9 | 9 |
| β-strand | 33-40 | 8 | 10 |
| β-strand | 43-52 | 10 | 10 |
| β-strand | 58-60 | 3 | 10 |
| α-helix | 62-64 | 3 | |
| β-strand | 68-72 | 5 | 9 |
| β-strand | 78-84 | 7 | 9 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-99 | 8 | 10 |
| β-strand | 106-109 | 4 | 10 |
| β-strand | 113-117 | 5 | 10 |
| α-helix | 121-122 | 2 | |
| β-strand | 123 | 1 | 11 |
| β-strand | 126-130 | 5 | 12 |
| β-strand | 141-151 | 11 | 12 |
| β-strand | 152 | 1 | 11 |
| β-strand | 157-160 | 4 | 13 |
| β-strand | 165 | 1 | 13 |
| β-strand | 169-171 | 3 | 12 |
| α-helix | 172-174 | 3 | |
| β-strand | 175-176 | 2 | 12 |
| β-strand | 181-190 | 10 | 12 |
| β-strand | 200-205 | 6 | 13 |
| β-strand | 210-215 | 6 | 13 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-6 | 3 | 14 |
| β-strand | 10-13 | 4 | 15 |
| β-strand | 19-25 | 7 | 14 |
| β-strand | 33-38 | 6 | 15 |
| β-strand | 45-48 | 4 | 15 |
| β-strand | 62-67 | 6 | 14 |
| β-strand | 70-75 | 6 | 14 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-90 | 7 | 15 |
| α-helix | 96 | 1 | |
| β-strand | 98 | 1 | 15 |
| β-strand | 102-106 | 5 | 15 |
| β-strand | 111 | 1 | 16 |
| β-strand | 114-118 | 5 | 17 |
| α-helix | 119-121 | 3 | |
| β-strand | 130-139 | 10 | 17 |
| β-strand | 140 | 1 | 16 |
| β-strand | 145-150 | 6 | 18 |
| β-strand | 153-155 | 3 | 18 |
| β-strand | 159-163 | 5 | 17 |
| α-helix | 164-167 | 4 | |
| β-strand | 173-181 | 9 | 17 |
| α-helix | 183-186 | 4 | |
| β-strand | 191-197 | 7 | 18 |
| β-strand | 205-210 | 6 | 18 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| NMDA glutamate receptor subunit | A | protein | 391 | Xenopus laevis | A0A1L8F5J9 (AlphaFold model) |
| Glutamate receptor ionotropic, NMDA 2A | B | protein | 360 | Rattus norvegicus | Q00959 (AlphaFold model) |
| FAB, heavy chain | H | protein | 221 | Mus musculus | |
| FAB, light chain | L | protein | 214 | Mus musculus |
>5TQ0_1 NMDA glutamate receptor subunit (chains A) PKIVNIGAVLSTKKHEQIFREAVNQANKRHFTRKIQLQATSVTHRPNAIQMALSVCEDLI SSQVYAILVSHPPAPTDHLTPTPISYTAGFYRIPVIGLTTRMSIYSDKSIHLSFLRTVPP YSHQALVWFEMMRLFNWNHVILIVSDDHEGRAAQKKLETLLEGKESKSKKRNYENLDQLS YDNKRGPKADKVLQFEPGTKNLTALLLEAKELEARVIILSASEDDATAVYKSAAMLDMTG AGYVWLVGEREISGSALRYAPDGIIGLQLINGKNESAHISDAVAVVAQAIHELFEMENIT DPPRGCVGNTNIWKTGPLFKRVLMSSKYPDGVTGRIEFNEDGDRKFAQYSIMNLQNRKLV QVGIFNGSYIIQNDRKIIWPGGETEGTLVPR
>5TQ0_2 Glutamate receptor ionotropic, NMDA 2A (chains B) LNIAVLLGHSHDVTERELRNLWGPEQATGLPLDVNVVALLMNRTDPKSLITHVCDLMSGA RIHGLVFGDDTDQEAVAQMLDFISSQTFIPILGIHGGASMIMADKDPTSTFFQFGASIQQ QATVMLKIMQDYDWHVFSLVTTIFPGYRDFISFIKTTVDNSFVGWDMQNVITLDTSFEDA KTQVQLKKIHSSVILLYCSKDEAVLILSEARSLGLTGYDFFWIVPSLVSGNTELIPKEFP SGLISVSYDDWDYSLEARVRDGLGILTTAASSMLEKFSYIPEAKASCYGQAEKPETPLHT LHQFMVNVTWDGKDLSFTEEGYQVHPRLVVIVLNKDREWEKVGKWENQTLSLRHAVWPRY
>5TQ0_3 FAB, HEAVY CHAIN (chains H) EVKLVESGPELKKPGETVKISCKASGFTFTNYGMNWVKQAPGKGLKWMGWINIYTGEPTY ADDFKGRFAFSLETSASTAYLQINNLKNEDTATYFCARGYDYEGYFDYWGQGTTLTVSSA KTTPPSVYPLAPGSAAQTNSMVTLGCLVKGYFPEPVTVTWNSGSLSSGVHTFPAVLQSDL YTLSSSVTVPSSTWPSETVTCNVAHPASSTKVDKKIVPRDC
>5TQ0_4 FAB, LIGHT CHAIN (chains L) DIVMTQAPATLSVTPGDRVSLSCRASQSIADYLYWYQQKSHESPRLLLKYASQSISGIPS RFSGSGSGSDFTLTINSVEPEDVGMYYCQNGHSFPRTFGGGTKLEIKRADAAPTVSIFPP SSEQLAAGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTLT LTKDEYERHNSYTCEATHKTSTSPIVKSFNRNEC
| ID | Name | Formula | Copies |
|---|---|---|---|
| IPA | Isopropyl alcohol | C3 H8 O | 1 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 2 |
Water and common crystallization additives (SO4, GOL) are not listed.
Molecular Basis for Subtype Specificity and High-Affinity Zinc Inhibition in the GluN1-GluN2A NMDA Receptor Amino-Terminal Domain. Romero-Hernandez, A., Simorowski, N., Karakas, E. et al. Neuron (2016) 92:1324-1336. DOI 10.1016/j.neuron.2016.11.006 · 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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