immunum
Fast antibody and T-cell receptor numbering, in your browser.
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Flank
FR1
CDR1
FR2
CDR2
FR3
CDR3
FR4
Sequence
How to read the result
- Sequence: your whole input, coloured by the region each residue falls in: FR1 to FR4 and CDR1 to CDR3. Hover over a stretch to see its domain and region.
- Flank: grey residues outside every domain. A domain's prefix holds the residues before it, back to the previous domain or the start of the sequence (a leader, or the linker of an scFv); the last domain's postfix holds the residues after it. See Prefix and postfix.
- Query: the residues of your input that the domain's alignment covers, counted from 1 and
inclusive. The APIs report the same range 0-based, as
queryStart/queryEnd(query_start/query_endin Python and the CLI). - Confidence: how well the domain aligns to the chain it was assigned, from 0 to 1. A domain below the minimum confidence isn't numbered. See Confidence.
- Numbering: one box per numbered residue, with its position in the chosen scheme above it.
A position with a letter, such as
111A, is an insertion: a residue the scheme has no plain number for. In IMGT CDR3 insertions grow from the middle, so111Afollows111and112Acomes before112; Kabat, Chothia and Martin append them after the number (100,100A,100B). Positions missing from the run, such as IMGT10in the IGH example, are gaps: the sequence has no residue there. - Compare schemes: per domain, where each scheme puts the FR/CDR boundaries for that chain and which residues each scheme calls CDRs. Only IMGT numbers TCR chains.
- Copy link: a URL holding the sequence and settings; opening it numbers the sequence again.
Downloads use the columns and keys of the CLI's
immunum number --all-domainsoutput, and the JSON adds each domain's segments.