Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation

10.1186/1471-2172-9-30

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Main Authors:	Tong, J.C, Sinha, A.A
Other Authors:	DEPT OF BIOCHEMISTRY
Format:	Article
Published:	2020
Subjects:	desmoglein 1 desmoglein 3 glycoprotein HLA DR antigen autoantibody epitope amino acid sequence article binding affinity controlled study disease course epitope mapping immunological technique immunopathology molecular docking molecular model nonhuman pemphigus vulgaris protein binding protein domain protein structure protein targeting screening sequence alignment sequence homology T lymphocyte biological model chemical structure chemistry comparative study computer simulation extracellular space genetics human immunology metabolism molecular genetics pathology pemphigus protein tertiary structure Amino Acid Sequence Autoantibodies Computer Simulation Desmoglein 1 Desmoglein 3 Epitopes, T-Lymphocyte Extracellular Space Humans Models, Immunological Models, Molecular Molecular Sequence Data Pemphigus Protein Structure, Tertiary
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/177970
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1779702023-09-13T21:11:37Z Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation Tong, J.C Sinha, A.A DEPT OF BIOCHEMISTRY desmoglein 1 desmoglein 3 glycoprotein HLA DR antigen autoantibody desmoglein 1 desmoglein 3 epitope amino acid sequence article binding affinity controlled study disease course epitope mapping immunological technique immunopathology molecular docking molecular model nonhuman pemphigus vulgaris protein binding protein domain protein structure protein targeting screening sequence alignment sequence homology T lymphocyte biological model chemical structure chemistry comparative study computer simulation extracellular space genetics human immunology metabolism molecular genetics pathology pemphigus protein tertiary structure Amino Acid Sequence Autoantibodies Computer Simulation Desmoglein 1 Desmoglein 3 Epitopes, T-Lymphocyte Extracellular Space Humans Models, Immunological Models, Molecular Molecular Sequence Data Pemphigus Protein Structure, Tertiary 10.1186/1471-2172-9-30 BMC Immunology 9 30 2020-10-20T04:42:16Z 2020-10-20T04:42:16Z 2008 Article Tong, J.C, Sinha, A.A (2008). Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation. BMC Immunology 9 : 30. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2172-9-30 14712172 https://scholarbank.nus.edu.sg/handle/10635/177970 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	desmoglein 1 desmoglein 3 glycoprotein HLA DR antigen autoantibody desmoglein 1 desmoglein 3 epitope amino acid sequence article binding affinity controlled study disease course epitope mapping immunological technique immunopathology molecular docking molecular model nonhuman pemphigus vulgaris protein binding protein domain protein structure protein targeting screening sequence alignment sequence homology T lymphocyte biological model chemical structure chemistry comparative study computer simulation extracellular space genetics human immunology metabolism molecular genetics pathology pemphigus protein tertiary structure Amino Acid Sequence Autoantibodies Computer Simulation Desmoglein 1 Desmoglein 3 Epitopes, T-Lymphocyte Extracellular Space Humans Models, Immunological Models, Molecular Molecular Sequence Data Pemphigus Protein Structure, Tertiary
spellingShingle	desmoglein 1 desmoglein 3 glycoprotein HLA DR antigen autoantibody desmoglein 1 desmoglein 3 epitope amino acid sequence article binding affinity controlled study disease course epitope mapping immunological technique immunopathology molecular docking molecular model nonhuman pemphigus vulgaris protein binding protein domain protein structure protein targeting screening sequence alignment sequence homology T lymphocyte biological model chemical structure chemistry comparative study computer simulation extracellular space genetics human immunology metabolism molecular genetics pathology pemphigus protein tertiary structure Amino Acid Sequence Autoantibodies Computer Simulation Desmoglein 1 Desmoglein 3 Epitopes, T-Lymphocyte Extracellular Space Humans Models, Immunological Models, Molecular Molecular Sequence Data Pemphigus Protein Structure, Tertiary Tong, J.C Sinha, A.A Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation
description	10.1186/1471-2172-9-30
author2	DEPT OF BIOCHEMISTRY
author_facet	DEPT OF BIOCHEMISTRY Tong, J.C Sinha, A.A
format	Article
author	Tong, J.C Sinha, A.A
author_sort	Tong, J.C
title	Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation
title_short	Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation
title_full	Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation
title_fullStr	Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation
title_full_unstemmed	Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation
title_sort	immunological hotspots analyzed by docking simulations: evidence for a general mechanism in pemphigus vulgaris pathology and transformation
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/177970
_version_	1779152120474238976

Immunological hotspots analyzed by docking simulations: Evidence for a general mechanism in pemphigus vulgaris pathology and transformation

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