Skip to main content
. Author manuscript; available in PMC: 2013 Sep 1.
Published in final edited form as: Neurochem Int. 2011 Dec 17;61(4):601–609. doi: 10.1016/j.neuint.2011.11.016

Table 1.

Comparison of amino acid sequences for human and rat NMDA receptor subunits.

Signal peptide
# of residues
ATD
# of residues
ABD
# of residues
TMD
# of residues
CTD
# of residues
Total subunit
# of residues
non-
identical
total non-
identical
total non-
identical
total non-
identical
total non-
identical
total non-
identical
total
GluN1 3 20 3 376 1 286 0 106 0 150 7 938
GluN2A 4 27 14 377 2 275 0 158 49 627 69 1464
GluN2B 2 28 1 376 2 276 0 158 18 646 23 1484
GluN2C 14 19 28 395 6 276 3 158 111 388 162 1236
GluN2D 0 25 15 402 0 277 0 158 44 474 59 1336

NMDA receptor subunits consist of the extracellular amino-terminal domain (ATD), the agonist binding domain (ABD), the transmembrane domain (TMD), and the intracellular carboxyl-terminal domain (CTD). Insertion or deletions in human subunits compared to rat subunits are also categorized as non-identical positions. ATD includes the ATD-S1 linker, and TMD is M1M2M3 including pre-M1 and intracellular loops. The ABD is S1 and S2 as well as S1-M1, M3-S2, and S2-M4 linkers. The amino acid sequences of all rat ionotropic glutamate receptor subunits were aligned using the ClustalW algorithm and the regions for each of the NMDA receptor subunits were determined based on GluA2 in this global alignment. In GluA2, the regions were defined as amino acids 1–397 (signal peptide and ATD), 398–414 (ATD-S1 linker), 415–527 (S1), 528–534 (S1-M1 linker), 535–647 (M1M2M3), 648–652 (M3-S2 linker), 653–794 (S2), 795–809 (S2-M4 linker), 810–833 (M4) and 834–884 (CTD). Signal peptides were predicted using the SignalP 3.0 server (Bendtsen et al., 2004). The GenBank IDs for amino acid sequences of human subunits used in the alignment are listed in Materials and Methods. NP_015566.1, NP_000824.1, NP_000825.2, NP_000826.1 (and NP_000826.2), and NP_000827.1 were used in the alignment for rat GluN1, GluN2A, GluN2B, GluN2C, and GluN2D, respectively.