Give sequences, structures, or both. Heavy and light chains can be entered as separate records; a single-chain Fv with two variable domains gives one row per domain.
Sequences
FASTA records, or one sequence per line. Up to 500 sequences of up to 1,000 residues; a sequence that is not a variable domain is reported as failed without stopping the others.
Structures
Up to 50 PDB or mmCIF files, for example designed antibody–antigen complexes. Every protein chain is annotated, and a table ties each residue number in the file to its position in every scheme. Only the first model is read.
Chain ids, separated by commas or spaces, applied to every structure. Leave empty to annotate all protein chains, including the antigen (which is reported as not an antibody).
Numbering schemes to report. Each scheme gets its own positions and CDR boundaries; T-cell receptor chains are numbered in IMGT only.
Advisory humanization lists framework positions where a chain differs from its nearest human germline, ranked by distance from the CDRs, with one candidate sequence per chain. A position that is a CDR in any scheme is never changed. It is a ranked list of possible edits, not a validated humanization predictor.
Numbering by ANARCI (Dunbar & Deane, 2016). Germline reference data: IMGT®, the international ImMunoGeneTics information system® (CC BY 4.0), snapshot of 2024-12-06; alleles added since are not called.