Cadherin-like domains in α-dystroglycan, α/ε-sarcoglycan and yeast and bacterial proteins

Current Biology

Volumn 12, Issue 6, 2002, Pages

  Dickens, Nicholas J ^a   Beatson, Scott ^a   Ponting, Chris P ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIA (MICROORGANISMS);

AXL2 PROTEIN, S CEREVISIAE; BACTERIAL PROTEIN; CADHERIN; CYTOSKELETON PROTEIN; DAG1 PROTEIN, HUMAN; DYSTROGLYCAN; FUNGAL PROTEIN; MEMBRANE PROTEIN; SACCHAROMYCES CEREVISIAE PROTEIN; SARCOGLYCAN;

AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; HUMAN; LETTER; METABOLISM; MOLECULAR GENETICS; MUTATION; PROTEIN CONFORMATION; PROTEIN TERTIARY STRUCTURE; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; BACTERIAL PROTEINS; CADHERINS; CYTOSKELETAL PROTEINS; DYSTROGLYCANS; FUNGAL PROTEINS; HUMANS; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN CONFORMATION; PROTEIN STRUCTURE, TERTIARY; SACCHAROMYCES CEREVISIAE PROTEINS; SARCOGLYCANS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0036126711     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-9822(02)00748-0     Document Type: Note

References (18)

1. Selective deficiency of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
2. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin α2 deficiency and abnormal glycosylation of α-dystroglycan
3. Mutations in the laminin α 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy
4. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
5. Mutations in the gene encoding ε-sarcoglycan cause myoclonus-dystonia syndrome
6. The complexities of dystroglycan
7. Cadherins in embryonic and neural morphogenesis
8. Selection of axial growth sites in yeast requires Axl2p, a novel plasma membrane glycoprotein
9. O-glycosylation of Axl2/Bud10p by Pmt4p is required for its stability, localization, and function in daughter cells
10. Structural basis of calcium-induced E-cadherin rigidification and dimerization
11. Sequence analysis suggests the presence of an IG-like domain in the N-terminal region of α-dystroglycan which was crystallized after mutation of a protease susceptible site (Arg168→His)
12. Identification of the β-dystroglycan binding epitope within the C-terminal region of α-dystroglycan
13. The small leucine-rich repeat proteoglycan biglycan binds to α-dystroglycan and is upregulated in dystrophic muscle
14. CHROMA. Consensus-based colouring of multiple alignments for publication
15. Prediction of protein secondary structure at better than 70% accuracy
16. Improving the accuracy of PSI-BLAST protein database searches with composition-based statistics and other refinements
17. Accurate formula for P-values of gapped local sequence and profile alignments
18. Profile hidden Markov models