[1][5] Its main goal is to identify and cluster homodimeric and heterodimeric interfaces observed in multiple crystal forms of homologous proteins.
[6] A common interface in ProtCID indicates chain-chain or domain-domain interactions that occur in different crystal forms.
All protein sequences of known structure in the Protein Data Bank (PDB)[7] are assigned a ”Pfam chain architecture”, which denotes the ordered Pfam[8] assignments for that sequence, e.g. (Pkinase) or (Cyclin_N)_(Cyclin_C).
ProtCID provides an independent check on publicly available annotations of biological interactions for PDB entries.
ProtCID also contains interface clusters between protein domains and peptides, nucleic acids, and ligands.