5H8H: Human GluN1/GluN2A LBD

Structure of the human GluN1/GluN2A LBD in complex with GNE3419. Determined by X-ray diffraction at 2.23 Å resolution. Released 24 Feb 2016.

Method
X-ray diffraction
Resolution
2.23 Å
Organism
Homo sapiens
Chains
2
Atoms
4,601
Mol. weight
65.91 kDa
Ligands
GLU, CA, GLY, 5YC
Released
24 Feb 2016

Explore 5H8H in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5H8H contains 31 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.

Chain A: 16 helices, 18 β-strands

ElementResiduesLengthSheet
β-strand7-1261
β-strand1512
β-strand1912
β-strand20-2341
α-helix24-252
β-strand36-4381
β-strand51-5991
α-helix61-7313
β-strand76-8161
β-strand90-9123
β-strand94-9523
α-helix97-1037
β-strand109-11021
β-strand11514
α-helix118-1236
β-strand125-12621
β-strand131-140104
α-helix151-1544
α-helix156-1583
α-helix162-1632
β-strand165-16624
α-helix172-1809
α-helix182-1887
α-helix189-1913
α-helix196-2049
β-strand210-21454
α-helix215-2239
α-helix226-2283
β-strand230-23234
α-helix233-2364
β-strand239-24464
β-strand247-24821
α-helix255-26713
α-helix270-2789
Chain B: 15 helices, 23 β-strands
ElementResiduesLengthSheet
β-strand7-1155
β-strand1416
β-strand1816
β-strand19-2245
α-helix23-242
β-strand3317
α-helix381
β-strand3917
α-helix40-412
β-strand43-4865
β-strand59-6575
α-helix67-7913
β-strand83-8755
β-strand96-9838
β-strand105-10738
α-helix109-1168
β-strand121-12225
β-strand12719
α-helix130-1334
β-strand136-13835
β-strand143-152109
α-helix163-1664
β-strand169110
β-strand172110
β-strand174-17529
β-strand177111
α-helix181-1888
α-helix190-1923
α-helix193-1997
β-strand204111
α-helix207-2159
β-strand221-22559
α-helix226-23510
β-strand239-251139
β-strand254-25635
α-helix262-27413
α-helix277-2815
α-helix282-2865

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Glutamate receptor ionotropic, NMDA 2A,Glutamate receptor ionotropic, NMDA 2AAprotein285Homo sapiensQ12879 (AlphaFold model)
Glutamate receptor ionotropic, NMDA 1,Glutamate receptor ionotropic, NMDA 1Bprotein293Homo sapiensQ05586 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5H8H_1 Glutamate receptor ionotropic, NMDA 2A,Glutamate receptor ionotropic, NMDA 2A (chains A)
GSPDDNHLSIVTLEEAPFVIVEDIDPLTETCVRNTVPCRKFVKINNSTNEGMNVKKCCKG
FCIDILKKLSRTVKFTYDLYLVTNGKHGKKVNNVWNGMIGEVVYQRAVMAVGSLTINEER
SEVVDFSVPFVETGISVMVSRGTQVTGLSDKKFQRPHDYSPPFRFGTVPNGSTERNIRNN
YPYMHQYMTKFNQKGVEDALVSLKTGKLDAFIYDAAVLNYKAGRDEGCKLVTIGSGYIFA
TTGYGIALQKGSPWKRQIDLALLQFVGDGEMEELETLWLTGICHN
Sequence of entity 2 (B), FASTA
>5H8H_2 Glutamate receptor ionotropic, NMDA 1,Glutamate receptor ionotropic, NMDA 1 (chains B)
GSMSTRLKIVTIHQEPFVYVKPTLSDGTCKEEFTVNGDPVKKVICTGPNDTSPGSPRHTV
PQCCYGFCIDLLIKLARTMNFTYEVHLVADGKFGTQERVNNSNKKEWNGMMGELLSGQAD
MIVAPLTINNERAQYIEFSKPFKYQGLTILVKKGTRITGINDPRLRNPSDKFIYATVKQS
SVDIYFRRQVELSTMYRHMEKHNYESAAEAIQAVRDNKLHAFIWDSAVLEFEASQKCDLV
TTGELFFRSGFGIGMRKDSPWKQNVSLSILKSHENGFMEDLDKTWVRYQECDS

Ligands and cofactors

IDNameFormulaCopies
GLUGlutamic acidC5 H9 N O41
CACalcium ionCa1
GLYGlycineC2 H5 N O21
5YC7-[[ethyl(phenyl)amino]methyl]-2-methyl-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-oneC15 H16 N4 O S1

Water and common crystallization additives (ACT) are not listed.

Primary citation

Positive Allosteric Modulators of GluN2A-Containing NMDARs with Distinct Modes of Action and Impacts on Circuit Function. Hackos, D.H., Lupardus, P.J., Grand, T. et al. Neuron (2016) 89:983-999. DOI 10.1016/j.neuron.2016.01.016 · PubMed

Other PDB entries of the same protein (UniProt Q12879 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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