<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Wilke S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The family of lysosome-associated membrane proteins (LAMP) comprises the multifunctional, ubiquitous LAMP-1 and LAMP-2, and the cell type-specific proteins DC-LAMP (LAMP-3), BAD-LAMP (UNC-46, C20orf103) and macrosialin (CD68). LAMPs have been implicated in a multitude of cellular processes, including phagocytosis, autophagy, lipid transport and aging. LAMP-2 isoform A acts as a receptor in chaperone-mediated autophagy. LAMP-2 deficiency causes the fatal Danon disease. The abundant proteins LAMP-1 and LAMP-2 are major constituents of the glycoconjugate coat present on the inside of the lysosomal membrane, the 'lysosomal glycocalyx'. The LAMP family is characterized by a conserved domain of 150 to 200 amino acids with two disulfide bonds.&lt;h4>Results&lt;/h4>The crystal structu</pubmed_abstract><journal>BMC biology</journal><pagination>62</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3409847</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Crystal structure of the conserved domain of the DC lysosomal associated membrane protein: implications for the lysosomal glycocalyx.</pubmed_title><pmcid>PMC3409847</pmcid><pubmed_authors>Wilke S</pubmed_authors><pubmed_authors>Bussow K</pubmed_authors><pubmed_authors>Krausze J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystal structure of the conserved domain of the DC lysosomal associated membrane protein: implications for the lysosomal glycocalyx.</name><description>&lt;h4>Background&lt;/h4>The family of lysosome-associated membrane proteins (LAMP) comprises the multifunctional, ubiquitous LAMP-1 and LAMP-2, and the cell type-specific proteins DC-LAMP (LAMP-3), BAD-LAMP (UNC-46, C20orf103) and macrosialin (CD68). LAMPs have been implicated in a multitude of cellular processes, including phagocytosis, autophagy, lipid transport and aging. LAMP-2 isoform A acts as a receptor in chaperone-mediated autophagy. LAMP-2 deficiency causes the fatal Danon disease. The abundant proteins LAMP-1 and LAMP-2 are major constituents of the glycoconjugate coat present on the inside of the lysosomal membrane, the 'lysosomal glycocalyx'. The LAMP family is characterized by a conserved domain of 150 to 200 amino acids with two disulfide bonds.&lt;h4>Results&lt;/h4>The crystal structu</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Jul</publication><modification>2025-05-29T19:44:11.217Z</modification><creation>2025-05-29T19:44:11.217Z</creation></dates><accession>S-EPMC3409847</accession><cross_references><pubmed>22809326</pubmed><doi>10.1186/1741-7007-10-62</doi></cross_references></HashMap>