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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：O75027 New Search
4PDB entries
4Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
O75027 23pg Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain A Reference sequence 71–752 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O75027 23pg Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain B Reference sequence 71–752 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O75027 23ph Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain A Reference sequence 71–752 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O75027 23ph Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain B Reference sequence 71–752 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O75027 23pi Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain A Reference sequence 71–752 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O75027 23pi Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain B Reference sequence 71–752 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O75027 7vgf Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain A Reference sequence 72–751 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O75027 7vgf Iron-sulfur clusters transporter ABCB7, mitochondrial Author chain B Reference sequence 72–751 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.