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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：C1CB04 New Search
2PDB entries
4Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
C1CB04 2ygl BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain A Reference sequence 66–413 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
C1CB04 2ygl BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain B Reference sequence 66–413 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
C1CB04 2ygl BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain A Reference sequence 66–413 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
C1CB04 2ygl BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain B Reference sequence 66–413 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
C1CB04 2ygm BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain A Reference sequence 66–413 1 Other combination Monomer Protein 1 其他 1 monomeric （1） Consistent with protein count
C1CB04 2ygm BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain B Reference sequence 66–413 1 Other combination Monomer Protein 1 其他 1 monomeric （1） Consistent with protein count
C1CB04 2ygm BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain A Reference sequence 66–413 2 Other combination Monomer Protein 1 其他 1 monomeric （1） Consistent with protein count
C1CB04 2ygm BLOOD GROUP A-AND B-CLEAVING ENDO-BETA-GALACTOSIDASE Author chain B Reference sequence 66–413 2 Other combination Monomer Protein 1 其他 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.