Welcome to the GenomeWeb Antibody, MHC and Immunological proteins Search for:

Databases

Programs

Resources

Groups

Associations and Committees

Miscellaneous

Detailed information on the above options

MHC binding peptides - MHCPEP
MHCPEP is a curated database of peptide sequences known to bind MHC molecules. Each entry contains the source protein (when known), an estimate of binding affinity and critical anchor residues (if identified), and is fully referenced.

ImMunoGeneTics database
IMGT, the international ImMunoGeneTics database, is a high-quality integrated database specialising in Immunoglobulins (Ig), T cell receptors (TcR) and Major Histocompatibility Complex (MHC) molecules of all vertebrate species, created in 1989 by Marie-Paule Lefranc (Universiti Montpellier II, CNRS). IMGT, a European project since 1992, works in close collaboration with EBI. At present, IMGT includes two databases: IMGT/LIGM-DB, a comprehensive database of Ig and TcR from human and other vertebrates, with translation for fully annotated sequences, and IMGT/HLA-DB, a database of the human MHC referred to as HLA (Human Leucocyte Antigens). The IMGT server provides a common access to all Immunogenetics data.

Kabat Database of sequences of immunological interest
Immunoglobulins, T-cell receptors and MHC.

V BASE - human germline variable region sequences
V BASE is a comprehensive directory of all human germline variable region sequences compiled from over a thousand published sequences, including those in the current releases of the Genbank and EMBL data libraries.

HLA Peptide Binding Predictions
This ranks potential 8-mer, 9-mer, or 10-mer peptides based on a predicted half-time of dissociation to HLA class I molecules. The analysis is based on coefficient tables deduced from the published literature by Dr. Kenneth Parker

EpiMatrix MHC-Binding Prediction
A site providing MHC-binding predictions for researchers working on vaccines and therapeutics for HIV and a range of other pathogens.

NetChop - prediction of proteasomal cleavages

The Antibody Resource Page
This is devoted to bringing together the vast number of resources about antibodies on the net. It includes links to educational websites, links to on-line companies (more than 30) that sell antibodies and antibody-related products, links to antibody-related databases, essays on antibody-related topics, and more.

Recombinant Antibody Page by Stefan Dubel
Descriptions of recombinant antibodies and some useful links.

A resource on Immunoglobulins
Based on Janice Kuby's Immunology Text Book.

Antibodies - Structure and Sequence
This page attempts to summarise useful information on antibody structure and sequence. It provides a query interface to the Kabat antibody sequence data, general information on antibodies and crystal structures and links to other antibody-related information.

Humanization by Design
Humanisation (also called Reshaping or CDR-grafting) is a technique for reducing the immunogenicity of monoclonal antibodies (mAbs) from xenogeneic sources (commonly rodent) and for improving their activation of the human immune system.

• Text Search of Selected Humanised Antibodies from the Literature
• Sequence Search of Selected Humanised Antibodies from the Literature
• Design Issues
• Historical Perspective
• Useful Links
• Brief Introduction to Antibody Structure

HLA Informatics Group

• HLA Sequence Data
• HLA Nomenclature Information
• HLA Nomenclature Updates

Therapeutic Immunology Group (TIG)

• Index of TIG related pages
• The Therapeutic Antibody Centre
• An intoduction to antibodies in therapy
• Making monoclonal antibodies in large amounts
• Immunology Glossary
• Use of TIG FACSCans and FACSort (including 4 colour analysis)

Therapeutic Antibody Centre

• The Therapeutic Antibody Centre at Work
• An intoduction to antibodies in therapy
• Current TAC projects

Immuno-Recognition & Targetting Group
Mainly concerned with the immunological interactions of antibodies and mucin, a tumour associated antigen.

The aim of the research carried out here, is to investigate possible treatment and diagnostic options of cancer utilising the properties of antibodies and antibody fragments.

British Society for Histocompatibility and Immunogenetics (BSHI)
BSHI is a non profit making, non political society. It is essentially a forum for discussion and refinement of scientific and technical innovations, as well as personnel training and communication between H & I labs throughout the country.

Interests of BSHI labs include Tissue typing (Matching donor and recipient for solid organ and bone marrow transplantation and blood transfusion:- the Histocompatibility bit), the study of genetic polymorphisms of immune system components (the Immunogenetics bit) and the aetiopathogenesis of autoimmune diseases. The common denominator being MHC:- The Major Histocompatibility Complex, which is expressed on cells throughout the body.

Mike's Part II Pathology Home Page

• Images of Immunoglobulin Molecules. Basic IgG structure.
• Some models of human IgG1. Differences in human IgG isotype and allotype.
• IgG functions. Functional sites on the IgG molecule (complement and Fc receptor).

Mike's Immunoglobulin Structure/Function Home Page

• Images of Immunoglobulin Molecules.
• Some models of human IgG1
• IgG functions
• Humanising or reshaping antibodies for therapeutic use.

CDR-H3 classification
The main limitation in antibody modeling is the lack of information to predict the structure of the H3 loop that, among the six loops that constitute the antigen binding site, is thought to play a major role in determining the wide range of antibody specificity. In order to assess the existence of rules relating the H3 conformation to the amino acid sequence, we analyzed all available structures of the immunoglobulin H3 loops.

The identification of key-residues determining the mainchain conformation of H3 loops led us to define "canonical structures" for the ten residues proximal to the framework of H3 loops of any length and, for loops with a specific torso structure, for the entire loop; on the basis of these rules, the H3 structure can be predicted by amino acid sequence alone.

This new information, combined with the previously defined canonical structures for the other five hypervariable loops, is an important step toward the prediction of the complete immunoglobulin antigen-binding site.

Modelling antibody antigen interactions
A description of modelling and docking an antibody to Ferritin by Manuela Helmer-Citterich, Ermanna Rovida, Alessandra Luzzago and Anna Tramontano as part of the IRBM Biocomputing course.

Antibodies and therapy
An introduction to the promise and problems of the therapeutic use of antibodies.