Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

1POZ

SOLUTION STRUCTURE OF THE HYALURONAN BINDING DOMAIN OF HUMAN CD44

Summary for 1POZ
Entry DOI10.2210/pdb1poz/pdb
Related1o7b 1o7c
NMR InformationBMRB: 6093
DescriptorCD44 antigen (1 entity in total)
Functional Keywordshyaluronan-binding domain, carbohydrate-binding domain, link module, cell adhesion, glycoprotein
Biological sourceHomo sapiens (human)
Cellular locationMembrane; Single-pass type I membrane protein: Q16208
Total number of polymer chains1
Total formula weight17601.49
Authors
Teriete, P.,Banerji, S.,Blundell, C.D.,Kahmann, J.D.,Pickford, A.R.,Wright, A.J.,Campbell, I.D.,Jackson, D.G.,Day, A.J. (deposition date: 2003-06-16, release date: 2004-03-16, Last modification date: 2024-10-30)
Primary citationTeriete, P.,Banerji, S.,Noble, M.,Blundell, C.D.,Wright, A.J.,Pickford, A.R.,Lowe, E.,Mahoney, D.J.,Tammi, M.I.,Kahmann, J.D.,Campbell, I.D.,Day, A.J.,Jackson, D.G.
Structure of the Regulatory Hyaluronan Binding Domain in the Inflammatory Leukocyte Homing Receptor CD44.
Mol.Cell, 13:483-496, 2004
Cited by
PubMed Abstract: Adhesive interactions involving CD44, the cell surface receptor for hyaluronan, underlie fundamental processes such as inflammatory leukocyte homing and tumor metastasis. Regulation of such events is critical and appears to be effected by changes in CD44 N-glycosylation that switch the receptor "on" or "off" under appropriate circumstances. How altered glycosylation influences binding of hyaluronan to the lectin-like Link module in CD44 is unclear, although evidence suggests additional flanking sequences peculiar to CD44 may be involved. Here we show using X-ray crystallography and NMR spectroscopy that these sequences form a lobular extension to the Link module, creating an enlarged HA binding domain and a formerly unidentified protein fold. Moreover, the disposition of key N-glycosylation sites reveals how specific sugar chains could alter both the affinity and avidity of CD44 HA binding. Our results provide the necessary structural framework for understanding the diverse functions of CD44 and developing novel therapeutic strategies.
PubMed: 14992719
DOI: 10.1016/S1097-2765(04)00080-2
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

226707

건을2024-10-30부터공개중

PDB statisticsPDBj update infoContact PDBjnumon