← 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：P0AC81 New Search
5PDB entries
5Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P0AC81 1f9z GLYOXALASE I Author chain A Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1f9z GLYOXALASE I Author chain B Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa5 GLYOXALASE I Author chain A Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa5 GLYOXALASE I Author chain B Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa6 GLYOXALASE I Author chain A Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa6 GLYOXALASE I Author chain B Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa7 GLYOXALASE I Author chain A Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa7 GLYOXALASE I Author chain B Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa8 GLYOXALASE I Author chain A Reference sequence 1–135 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P0AC81 1fa8 GLYOXALASE I Author chain B Reference sequence 1–135 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.