← Back to search

Protein Structures and Oligomeric States

Enter a protein name, UniProt accession or PDB ID. Name searches ask you to confirm the protein identity before related structures are queried.

Current Protein Identity：Q13255 New Search
8PDB entries
10Biological assembly
20chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q13255 3ks9 Metabotropic glutamate receptor 1 Author chain A Reference sequence 28–518 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 3ks9 Metabotropic glutamate receptor 1 Author chain B Reference sequence 28–518 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 3ks9 Metabotropic glutamate receptor 1 Author chain A Reference sequence 28–518 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q13255 3ks9 Metabotropic glutamate receptor 1 Author chain B Reference sequence 28–518 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q13255 3ks9 Metabotropic glutamate receptor 1 Author chain A Reference sequence 28–518 3 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q13255 3ks9 Metabotropic glutamate receptor 1 Author chain B Reference sequence 28–518 3 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q13255 4or2 Soluble cytochrome b562, Metabotropic glutamate receptor 1 Author chain A Reference sequence 581–860 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 4or2 Soluble cytochrome b562, Metabotropic glutamate receptor 1 Author chain B Reference sequence 581–860 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 7dgd Metabotropic glutamate receptor 1 Author chain A Reference sequence 31–863 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 7dgd Metabotropic glutamate receptor 1 Author chain B Reference sequence 31–863 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 7dge Metabotropic glutamate receptor 1 Author chain A Reference sequence 31–863 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q13255 7dge Metabotropic glutamate receptor 1 Author chain B Reference sequence 31–863 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q13255 9wqm Metabotropic glutamate receptor 1 Author chain X Reference sequence 31–890 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q13255 9wqm Metabotropic glutamate receptor 1 Author chain Y Reference sequence 31–890 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q13255 9wqn Metabotropic glutamate receptor 1 Author chain X Reference sequence 31–890 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q13255 9wqn Metabotropic glutamate receptor 1 Author chain Y Reference sequence 31–890 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q13255 9wqo Metabotropic glutamate receptor 1 Author chain X Reference sequence 31–890 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 9wqo Metabotropic glutamate receptor 1 Author chain Y Reference sequence 31–890 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 9wqp Metabotropic glutamate receptor 1 Author chain X Reference sequence 31–890 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q13255 9wqp Metabotropic glutamate receptor 1 Author chain Y Reference sequence 31–890 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count

“Homomeric versus heteromeric classification follows protein identity; different constructs of the same UniProt entry still require comparison of reference-sequence ranges, mutations and missing segments. Assemblies marked for review remain visible but are not included in the highest-confidence candidate set.