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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：P37330 New Search
6PDB entries
8Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P37330 1d8c MALATE SYNTHASE G Author chain A Reference sequence 1–722 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 1p7t Malate synthase G Author chain A Reference sequence 1–722 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 1p7t Malate synthase G Author chain B Reference sequence 1–722 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 1y8b Malate synthase G Author chain A Reference sequence 1–722 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 2jqx Malate synthase G Author chain A Reference sequence 1–723 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 7yqm Malate synthase G Author chain A Reference sequence 1–723 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 7yqn Malate synthase G Author chain A Reference sequence 1–723 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 7yqn Malate synthase G Author chain B Reference sequence 1–723 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 7yqn Malate synthase G Author chain A Reference sequence 1–723 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P37330 7yqn Malate synthase G Author chain B Reference sequence 1–723 2 Protein monomer Monomer Protein 1 monomeric （1） 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.