5CNI: MGlu2 with Glutamate

mGlu2 with Glutamate. Determined by X-ray diffraction at 2.69 Å resolution. Released 9 Sept 2015.

Method
X-ray diffraction
Resolution
2.69 Å
Organism
Homo sapiens
Chains
2
Atoms
7,131
Mol. weight
112.72 kDa
Ligands
NAG, GLU
Released
9 Sept 2015

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

Secondary structure: helices and β-sheets

5CNI contains 40 α-helices and 36 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: 20 helices, 18 β-strands

ElementResiduesLengthSheet
β-strand26-2831
β-strand32-3871
β-strand41-4332
β-strand50-5342
α-helix55-606
α-helix61-7212
β-strand84-9071
α-helix95-10612
β-strand138-14031
α-helix145-15511
α-helix156-1583
β-strand162-16431
α-helix170-1734
β-strand181-18331
α-helix189-20113
β-strand206-21273
α-helix217-22913
β-strand234-24183
α-helix247-25812
β-strand265-26953
α-helix272-28413
β-strand290-29343
α-helix301-3044
α-helix308-3114
β-strand315-31953
α-helix325-3328
α-helix345-3539
α-helix378-39922
α-helix408-4103
α-helix415-4173
α-helix418-4225
α-helix423-4253
β-strand428-42924
α-helix4301
β-strand440-44124
β-strand452-46093
β-strand466-475103
β-strand478-48033
Chain B: 20 helices, 18 β-strands
ElementResiduesLengthSheet
β-strand26-2835
β-strand32-3875
β-strand41-4336
β-strand50-5346
α-helix55-606
α-helix61-7212
β-strand84-9075
α-helix95-10612
β-strand136-14055
α-helix145-15511
α-helix156-1583
β-strand162-16435
α-helix170-1734
β-strand181-18335
α-helix188-20114
β-strand206-21277
α-helix217-22913
β-strand234-24187
α-helix247-25812
β-strand265-26957
α-helix272-28413
β-strand290-29347
α-helix301-3044
α-helix308-3114
β-strand315-31957
α-helix325-3328
α-helix345-3528
α-helix378-39922
α-helix408-4103
α-helix415-4173
α-helix418-4225
α-helix423-4253
β-strand428-42928
α-helix430-4312
β-strand440-44128
β-strand452-46097
β-strand466-475107
β-strand47817

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Metabotropic glutamate receptor 2A, Bprotein503Homo sapiensQ14416 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5CNI_1 Metabotropic glutamate receptor 2 (chains A, B)
MALGSLLALLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEDCGPVNEHRG
IQRLEAMLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSR
HICPDGSYATHGDAPTAITGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRY
DYFARTVPPDFFQAKAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNISVATS
EKVGRAMSRAAFEGVVRALLQKPSARVAVLFTRSEDARELLAASQRLNASFTWVASDGWG
ALEEVVAGSEGAAEGAITIELASYPISDFASYFQSLDPWNNSRNPWFREFWEQRFRCSFR
QRDCAAHSLRAVPFEQESKIMFVVNAVYAMAHALHNMHRALCPNTTRLCDAMRPVNGRRL
YKDFVLNVKFDAPFRPADTHNEVRFDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGL
TLDTSLIPWASPSAGEGHHHHHH

Ligands and cofactors

IDNameFormulaCopies
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O64
GLUGlutamic acidC5 H9 N O42

Water and common crystallization additives (NA, CL) are not listed.

Primary citation

Synthesis and Pharmacological Characterization of C4-(Thiotriazolyl)-substituted-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylates. Identification of (1R,2S,4R,5R,6R)-2-Amino-4-(1H-1,2,4-triazol-3-ylsulfanyl)bicyclo[3.1.0]hexane-2,6-dicarboxylic Acid (LY2812223), a Highly Potent, Functionally…. Monn, J.A., Prieto, L., Taboada, L. et al. J Med Chem (2015) 58:7526-7548. DOI 10.1021/acs.jmedchem.5b01124 · PubMed

Other PDB entries of the same protein (UniProt Q14416 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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