Interaction of MCC2, a novel homologue of MCC tumor suppressor, with PDZ-domain Protein AIE-75

Gene

Volumn 267, Issue 1, 2001, Pages 101-110

  Ishikawa, Susumu ^a   Kobayashi, Ichiro ^b   Hamada, Jun Ichi ^a   Tada, Mitsuhiro ^a   Hirai, Atsuko ^a   Furuuchi, Keiji ^a   Takahashi, Yoko ^a   Ba, Yi ^a   Moriuchi, Tetsuya ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

Author keywords

AIE 75; MCC; MCC2; PDZ domain; Protein protein interaction; Tumor suppressor

Indexed keywords

AUTOIMMUNE ENTEROPATHY RELATED ANTIGEN; PROTEIN; PROTEIN MCC2; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CHROMOSOME 19P; CONTROLLED STUDY; GENE LOCATION; HUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN INTERACTION; PROTEIN PROTEIN INTERACTION; SEQUENCE HOMOLOGY; TUMOR SUPPRESSOR GENE; TWO HYBRID SYSTEM; USHER SYNDROME;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; BASE SEQUENCE; BINDING SITES; BLOTTING, NORTHERN; CARRIER PROTEINS; DNA, COMPLEMENTARY; FEMALE; GENE EXPRESSION; GENES; HUMANS; MOLECULAR SEQUENCE DATA; PROTEIN BINDING; PROTEINS; RNA, MESSENGER; SACCHAROMYCES CEREVISIAE; SEQUENCE ANALYSIS, DNA; TISSUE DISTRIBUTION; TUMOR CELLS, CULTURED; TUMOR SUPPRESSOR PROTEINS; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 0035804673     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(01)00378-X     Document Type: Article

References (26)

1. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
2. Colon cancer. Consider the coiled coil
3. Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains
4. A novel translocation (17;19) (p13;p13) in a patient with acute myelomonocytic leukemia
5. New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p
6. Suppression of the tumorigenicity of prostatic cancer cells by gene(s) located on human chromosome 19p13.1-13.2
7. Unexpected modes of PDZ domain scaffolding revealed by structure of nNOS-syntrophin complex
8. Cytoskeletal differences between stereocilia of the human sperm passageway and microvilli/stereocilia in other locations
9. Parallelization of a local similarity algorithm
10. The APC-hDLG complex negatively regulates cell cycle progression from the G0/G1 to S phase
11. Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast
12. Dimer formation by an N-terminal coiled coil in the APC protein
13. Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers
14. Identification of an autoimmune enteropathy-related 75-kDa antigen
15. Interaction of ion channels and receptors with PDZ domain proteins
16. Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene
17. Coiled coils: New structures and new functions
18. Association of protein-tyrosine phosphatase PTP-BAS with the transcription-factor-inhibitory protein IκBα through interaction between the PDZ1 domain and ankyrin repeats
19. MCC, a cytoplasmic protein that blocks cell cycle progression from the G0/G1 to S phase
20. Identification of a brain-specific APC homologue, APCL, and its interaction with beta-catenin
21. STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer
22. Characterization of human colon cancer antigens recognized by autologous antibodies
23. Isoforms of the human PDZ-73 protein exhibit differential tissue expression
24. Localization of MCC (mutated in colorectal cancer) in various tissues of mice and its involvement in cell differentiation
25. Recognition of unique carboxyl-terminal motifs by distinct PDZ domains
26. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C