TY - JOUR
T1 - Paratome
T2 - An online tool for systematic identification of antigen-binding regions in antibodies based on sequence or structure
AU - Kunik, Vered
AU - Ashkenazi, Shaul
AU - Ofran, Yanay
N1 - Funding Information:
Funding for open access charge: Research grant from the Israel Science Foundation [511].
PY - 2012/7
Y1 - 2012/7
N2 - Antibodies are capable of specifically recognizing and binding antigens. Identification of the antigen-binding site, commonly dubbed paratope, is of high importance both for medical and biological applications. To date, the identification of antigen-binding regions (ABRs) relies on tools for the identification of complementarity-determining regions (CDRs). However, we have shown that up to 22 of the residues that actually bind the antigen fall outside the traditionally defined CDRs. The Paratome web server predicts the ABRs of an antibody, given its amino acid sequence or 3D structure. It is based on a set of consensus regions derived from a structural alignment of a non-redundant set of all known antibody-antigen complexes. Given a query sequence or structure, the server identifies the regions in the query antibody that correspond to the consensus ABRs. An independent set of antibody-antigen complexes was used to test the server and it was shown to correctly identify at least 94 of the antigen-binding residues. The Paratome web server is freely available at http://www.ofranlab.org/paratome/.
AB - Antibodies are capable of specifically recognizing and binding antigens. Identification of the antigen-binding site, commonly dubbed paratope, is of high importance both for medical and biological applications. To date, the identification of antigen-binding regions (ABRs) relies on tools for the identification of complementarity-determining regions (CDRs). However, we have shown that up to 22 of the residues that actually bind the antigen fall outside the traditionally defined CDRs. The Paratome web server predicts the ABRs of an antibody, given its amino acid sequence or 3D structure. It is based on a set of consensus regions derived from a structural alignment of a non-redundant set of all known antibody-antigen complexes. Given a query sequence or structure, the server identifies the regions in the query antibody that correspond to the consensus ABRs. An independent set of antibody-antigen complexes was used to test the server and it was shown to correctly identify at least 94 of the antigen-binding residues. The Paratome web server is freely available at http://www.ofranlab.org/paratome/.
UR - http://www.scopus.com/inward/record.url?scp=84864465479&partnerID=8YFLogxK
U2 - 10.1093/nar/gks480
DO - 10.1093/nar/gks480
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C2 - 22675071
AN - SCOPUS:84864465479
SN - 0305-1048
VL - 40
SP - W521-W524
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - W1
ER -