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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：P43813 New Search
10PDB entries
10Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P43813 3bac DNA ligase Author chain A Reference sequence 73–336 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P43813 3pn1 DNA ligase Author chain A Reference sequence 1–318 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P43813 3uq8 DNA ligase Author chain A Reference sequence 3–324 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P43813 4uco DNA LIGASE Author chain A Reference sequence 1–324 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P43813 4ucr DNA LIGASE Author chain A Reference sequence 1–324 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P43813 4ucs DNA LIGASE Author chain A Reference sequence 1–324 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P43813 4uct DNA LIGASE Author chain A Reference sequence 1–324 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P43813 4ucu DNA LIGASE Author chain A Reference sequence 1–324 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P43813 4ucv DNA LIGASE Author chain A Reference sequence 1–324 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P43813 4ufz DNA LIGASE Author chain A Reference sequence 1–324 1 Protein monomer Monomer Protein 1 monomeric （1） 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.