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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：Q7TS98 New Search
7PDB entries
13Biological assembly
26chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q7TS98 1d5b chimeric OXY-COPE catalytic ANTIBODY AZ-28 (light chain) Author chain A Reference sequence 23–129 1 Insufficient information Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q7TS98 1d5b chimeric OXY-COPE catalytic ANTIBODY AZ-28 (light chain) Author chain L Reference sequence 23–129 1 Insufficient information Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q7TS98 1d5b chimeric OXY-COPE catalytic ANTIBODY AZ-28 (light chain) Author chain A Reference sequence 23–129 2 Insufficient information Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 1d5b chimeric OXY-COPE catalytic ANTIBODY AZ-28 (light chain) Author chain L Reference sequence 23–129 2 Insufficient information Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 1d5b chimeric OXY-COPE catalytic ANTIBODY AZ-28 (light chain) Author chain A Reference sequence 23–129 3 Insufficient information Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 1d5b chimeric OXY-COPE catalytic ANTIBODY AZ-28 (light chain) Author chain L Reference sequence 23–129 3 Insufficient information Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 1d5i CHIMERIC GERMLINE PRECURSOR OF OXY-COPE CATALYTIC ANTIBODY AZ-28 (LIGHT CHAIN) Author chain L Reference sequence 23–129 1 Insufficient information Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 1d6v CHIMERIC GERMLINE PRECURSOR OF OXY-COPE CATALYTIC ANTIBODY AZ-28 (LIGHT CHAIN) Author chain L Reference sequence 23–129 1 Insufficient information Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain H Reference sequence 130–234 1 Insufficient information Heteromer Protein 720 720-meric （720） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain J Reference sequence 130–234 1 Insufficient information Heteromer Protein 720 720-meric （720） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain L Reference sequence 130–234 1 Insufficient information Heteromer Protein 720 720-meric （720） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain H Reference sequence 130–234 2 Insufficient information Heteromer Protein 12 dodecameric （12） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain J Reference sequence 130–234 2 Insufficient information Heteromer Protein 12 dodecameric （12） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain L Reference sequence 130–234 2 Insufficient information Heteromer Protein 12 dodecameric （12） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain H Reference sequence 130–234 3 Insufficient information Heteromer Protein 60 60-meric （60） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain J Reference sequence 130–234 3 Insufficient information Heteromer Protein 60 60-meric （60） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain L Reference sequence 130–234 3 Insufficient information Heteromer Protein 60 60-meric （60） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain H Reference sequence 130–234 4 Insufficient information Heteromer Protein 72 72-meric （72） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain J Reference sequence 130–234 4 Insufficient information Heteromer Protein 72 72-meric （72） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain L Reference sequence 130–234 4 Insufficient information Heteromer Protein 72 72-meric （72） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain H Reference sequence 130–234 5 Insufficient information Heteromer Protein 12 dodecameric （12） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain J Reference sequence 130–234 5 Insufficient information Heteromer Protein 12 dodecameric （12） Consistent with protein count
Q7TS98 3j42 Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain chimera Author chain L Reference sequence 130–234 5 Insufficient information Heteromer Protein 12 dodecameric （12） Consistent with protein count
Q7TS98 4kvc Ig kappa chain V-V region MOPC 21, Anti-colorectal carcinoma light chain Author chain L Reference sequence 130–234 1 Insufficient information Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 5tr8 441D6 Fab Light chain Author chain L Reference sequence 132–234 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q7TS98 5vpl 4C1 - LIGHT CHAIN Author chain C Reference sequence 24–235 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） 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.