Immunoglobulin superfamily proteins: Structure, mechanisms, and drug discovery

Biopolymers

Volumn 43, Issue 5, 1997, Pages 367-382

  Huang, Ziwei ^a   Li, Song ^a   Korngold, Robert ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

CD4; Computer screening; Drug discovery; Immunoglobulin superfamily; Mechanisms; MHC class II; Molecular data base; Nonpeptide organic inhibitors; Peptide inhibitors; Peptidomimetic modifications; Protein interactions; Structures; T cell activation

Indexed keywords

ASSOCIATION REACTIONS; BIOCOMPATIBILITY; CHEMICAL ACTIVATION; CHEMICAL BONDS; CHEMICAL MODIFICATION; DRUG PRODUCTS; IMMUNOLOGY; MATHEMATICAL MODELS; MOLECULAR STRUCTURE; OLIGOMERS; REACTION KINETICS;

DIMERIZATION; IMMUNOGLOBULIN; OLIGOMERIZATION; PEPTIDE INHIBITORS;

PROTEINS;

CD4 ANTIGEN; IMMUNOGLOBULIN; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; PROTEIN INHIBITOR; T LYMPHOCYTE RECEPTOR;

CELLULAR IMMUNITY; DIMERIZATION; DRUG DESIGN; IMMUNOTHERAPY; LIGAND BINDING; LYMPHOCYTE ACTIVATION; MOLECULAR DYNAMICS; OLIGOMERIZATION; PROTEIN INTERACTION; PROTEIN MODIFICATION; PROTEIN STRUCTURE; REVIEW; STRUCTURE ACTIVITY RELATION;

ANIMALS; ANTIGENS, CD4; DRUG DESIGN; HUMANS; IMMUNOGLOBULINS; LYMPHOCYTE ACTIVATION; MODELS, MOLECULAR; PROTEIN CONFORMATION; T-LYMPHOCYTES;

EID: 0031410504     PISSN: 00063525     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0282(1997)43:5<367::AID-BIP3>3.0.CO;2-T     Document Type: Article

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