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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：P01999 New Search
5PDB entries
9Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P01999 8wix Hemoglobin subunit alpha Author chain A Reference sequence 1–142 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P01999 8wiy Hemoglobin subunit alpha Author chain A Reference sequence 1–142 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P01999 8wiz Hemoglobin subunit alpha Author chain A Reference sequence 1–142 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P01999 9vid Hemoglobin subunit alpha Author chain A Reference sequence 1–142 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P01999 9vid Hemoglobin subunit alpha Author chain A Reference sequence 1–142 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P01999 9vid Hemoglobin subunit alpha Author chain A Reference sequence 1–142 3 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P01999 9vie Hemoglobin subunit alpha Author chain A Reference sequence 1–142 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P01999 9vie Hemoglobin subunit alpha Author chain A Reference sequence 1–142 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P01999 9vie Hemoglobin subunit alpha Author chain A Reference sequence 1–142 3 Protein heterocomplex Heteromer 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.