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HUMAN:CRCM

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Contents

Species (Taxon ID) Homo sapiens (Human). (9606)
Gene Name(s) MCC
Protein Name(s) Colorectal mutant cancer protein

Protein MCC

External Links
UniProt P23508
EMBL M62397
AC008536
AC010431
AC079465
AC093208
AC106750
AC126917
CH471086
CH471086
BC009279
BC018919
AK128596
IPI IPI00011957
IPI00443415
PIR A38434
RefSeq NP_001078846.1
NP_002378.1
UniGene Hs.593171
ProteinModelPortal P23508
DIP DIP-27599N
IntAct P23508
MINT MINT-1161194
STRING P23508
PhosphoSite P23508
DMDM 117424
PRIDE P23508
Ensembl ENST00000302475
GeneID 4163
KEGG hsa:4163
UCSC uc003kqj.2
CTD 4163
GeneCards GC05M112388
H-InvDB HIX0020315
HGNC HGNC:6935
HPA HPA037391
MIM 159350
neXtProt NX_P23508
PharmGKB PA30679
eggNOG prNOG15810
HOGENOM HBG357807
HOVERGEN HBG004762
OMA CADAASP
OrthoDB EOG4ZS92H
NextBio 16402
ArrayExpress P23508
Bgee P23508
CleanEx HS_MCC
Genevestigator P23508
GermOnline ENSG00000171444
GO GO:0005737
GO:0005634
GO:0005886
GO:0005515
GO:0004872
GO:0090090
GO:0010633
GO:0050680
GO:0016055
InterPro IPR019536
Pfam PF10506

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0004872

receptor activity

PMID:1848370[1]

TAS: Traceable Author Statement

F

Seeded From UniProt

GO:0005515

protein binding

PMID:18591935[2]

IPI: Inferred from Physical Interaction

UniProtKB:P35222

F

Seeded From UniProt

GO:0005515

protein binding

PMID:19555689[3]

IPI: Inferred from Physical Interaction

UniProtKB:O14745

F

Seeded From UniProt

GO:0005515

protein binding

PMID:19555689[3]

IPI: Inferred from Physical Interaction

UniProtKB:P15311

F

Seeded From UniProt

GO:0005515

protein binding

PMID:19555689[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q14160

F

Seeded From UniProt

GO:0005515

protein binding

PMID:19555689[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q15599

F

Seeded From UniProt

GO:0005515

protein binding

PMID:19555689[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q96L92

F

Seeded From UniProt

GO:0005515

protein binding

PMID:21988832[4]

IPI: Inferred from Physical Interaction

UniProtKB:P29084

F

Seeded From UniProt

GO:0005634

nucleus

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0539

C

Seeded From UniProt

GO:0005634

nucleus

GO_REF:0000023

IEA: Inferred from Electronic Annotation

SP_SL:SL-0191

C

Seeded From UniProt

GO:0005634

nucleus

PMID:18591935[2]

IDA: Inferred from Direct Assay

C

Seeded From UniProt

GO:0005737

cytoplasm

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0963

C

Seeded From UniProt

GO:0005737

cytoplasm

GO_REF:0000023

IEA: Inferred from Electronic Annotation

SP_SL:SL-0086

C

Seeded From UniProt

GO:0005737

cytoplasm

PMID:18029348[5]

IDA: Inferred from Direct Assay

C

Seeded From UniProt

GO:0005737

cytoplasm

PMID:18591935[2]

IDA: Inferred from Direct Assay

C

Seeded From UniProt

GO:0005886

plasma membrane

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-1003

C

Seeded From UniProt

GO:0005886

plasma membrane

GO_REF:0000023

IEA: Inferred from Electronic Annotation

SP_SL:SL-0039

C

Seeded From UniProt

GO:0005886

plasma membrane

PMID:19555689[3]

IDA: Inferred from Direct Assay

C

Seeded From UniProt

GO:0007165

signal transduction

PMID:1848370[1]

TAS: Traceable Author Statement

P

Seeded From UniProt

GO:0010633

negative regulation of epithelial cell migration

PMID:19555689[3]

IMP: Inferred from Mutant Phenotype

P

Seeded From UniProt

GO:0016020

membrane

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0472

C

Seeded From UniProt

GO:0016055

Wnt receptor signaling pathway

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0879

P

Seeded From UniProt

GO:0050680

negative regulation of epithelial cell proliferation

PMID:18591935[2]

IDA: Inferred from Direct Assay

P

Seeded From UniProt

GO:0090090

negative regulation of canonical Wnt receptor signaling pathway

PMID:18591935[2]

IDA: Inferred from Direct Assay

P

Seeded From UniProt

GO:0005737

cytoplasm

PMID:18591935[2]

IDA: Inferred from Direct Assay

C

Figure 1c showed Western Blot Analysis was used to confirm localization of the MCC protein to the cytoplasm.

complete

GO:0005634

nucleus

PMID:18591935[2]

IDA: Inferred from Direct Assay

C

Figure 1c showed the use of Western Blot Analysis to confirm MCC protein localization in the nucleus of cells.

complete

GO:0051726

regulation of cell cycle

PMID:18591935[2]

IDA: Inferred from Direct Assay

P

Figure 4C and 4D shows that MCC regulates the cell cycle by suppressing the DNA-binding activity of β-catenin/TCF/LEF in the nucleus through Western Blot Analysis. This is also confirmed in the section of the text "MCC interacts with β-catenin, blocks β-catenin/TCF/LEF DNA binding, and can affect endogenous β-catenin localization/levels".

complete

GO:0045184

establishment of protein localization

PMID:18591935[2]

IDA: Inferred from Direct Assay

P

The section of the text "MCC interacts with β-catenin, blocks β-catenin/TCF/LEF DNA binding, and can affect endogenous β-catenin localization/levels" confirms that MCC relocalizes the β-catenin to the cytoplasm. The results are further confirmed through Western Blot Analysis in Figure 4.

complete

GO:0030308

negative regulation of cell growth

PMID:18591935[2]

IDA: Inferred from Direct Assay

P

Immunofluorescence was used and confirmed in Figure 6A/B to show that MCC is responsible for the suppression of basal cell growth.

complete

Notes

References

See Help:References for how to manage references in GONUTS.

  1. 1.0 1.1 Kinzler KW et al. (1991) Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers. Science 251: 1366-70 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 2.9 Fukuyama R et al. (2008) Mutated in colorectal cancer, a putative tumor suppressor for serrated colorectal cancer, selectively represses beta-catenin-dependent transcription. Oncogene 27: 6044-55 PubMed GONUTS page
  3. 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Arnaud C et al. (2009) MCC, a new interacting protein for Scrib, is required for cell migration in epithelial cells. FEBS Lett 583: 2326-32 PubMed GONUTS page
  4. Wang J et al. (2011) Toward an understanding of the protein interaction network of the human liver. Mol Syst Biol 7: 536 PubMed GONUTS page
  5. Barbe L et al. (2008) Toward a confocal subcellular atlas of the human proteome. Mol Cell Proteomics 7: 499-508 PubMed GONUTS page
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