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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：O95671 New Search
3PDB entries
4Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
O95671 2p5x N-acetylserotonin O-methyltransferase-like protein Author chain A Reference sequence 10–239 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
O95671 2p5x N-acetylserotonin O-methyltransferase-like protein Author chain B Reference sequence 10–239 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
O95671 2p5x N-acetylserotonin O-methyltransferase-like protein Author chain A Reference sequence 10–239 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
O95671 2p5x N-acetylserotonin O-methyltransferase-like protein Author chain B Reference sequence 10–239 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
O95671 6xi4 Probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein Author chain A Reference sequence 10–239 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O95671 6xi4 Probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein Author chain B Reference sequence 10–239 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O95671 6xi5 Probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein Author chain A Reference sequence 10–239 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O95671 6xi5 Probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein Author chain B Reference sequence 10–239 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.