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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：A0A9X4KGN5 New Search
6PDB entries
6Biological assembly
7chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
A0A9X4KGN5 8tu9 ;Enhanced green fluorescent protein,Heparan-alpha-glucosaminide N-acetyltransferase,Isoform 2 of Heparan-alpha-glucosaminide N-acetyltransferase ; Author chain A Reference sequence 9–251 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
A0A9X4KGN5 8tu9 ;Enhanced green fluorescent protein,Heparan-alpha-glucosaminide N-acetyltransferase,Isoform 2 of Heparan-alpha-glucosaminide N-acetyltransferase ; Author chain B Reference sequence 9–251 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
A0A9X4KGN5 8vdo Green fluorescent protein,Talin-1 Author chain A Reference sequence 8–246 1 Insufficient information Monomer Protein 1 monomeric （1） Consistent with protein count
A0A9X4KGN5 9boy Glycine receptor subunit beta,Green fluorescent protein Author chain E Reference sequence 9–248 1 Insufficient information Heteromer Protein 5 pentameric （5） Consistent with protein count
A0A9X4KGN5 9boz Glycine receptor subunit beta,Green fluorescent protein Author chain E Reference sequence 9–248 1 Insufficient information Heteromer Protein 5 pentameric （5） Consistent with protein count
A0A9X4KGN5 9bp0 Glycine receptor subunit beta,Green fluorescent protein Author chain E Reference sequence 9–248 1 Insufficient information Heteromer Protein 5 pentameric （5） Consistent with protein count
A0A9X4KGN5 9bp7 Glycine receptor subunit beta,Green fluorescent protein Author chain E Reference sequence 9–248 1 Insufficient information Heteromer Protein 5 pentameric （5） 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.