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Literature summary for 3.6.5.2 extracted from

  • Tsai, C.H.; Cheng, H.C.; Wang, Y.S.; Lin, P.; Jen, J.; Kuo, I.Y.; Chang, Y.H.; Liao, P.C.; Chen, R.H.; Yuan, W.C.; Hsu, H.S.; Yang, M.H.; Hsu, M.T.; Wu, C.Y.; Wang, Y.C.
    Small GTPase Rab37 targets tissue inhibitor of metalloproteinase 1 for exocytosis and thus suppresses tumour metastasis (2014), Nat. Commun., 5, 4804.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
additional information Rab proteins are members of the Ras superfamily of GTPases that switch between GDP-bound (inactive) and GTP-bound (active) forms Homo sapiens

Protein Variants

Protein Variants Comment Organism
additional information quantitative analyses of vesicular stomatitis virus ts045 G protein fused to green fluorescent protein exocytosis from endoplasmic reticulum through the Golgi to the PM22,23 in Rab37 knockdown (Rab37KD) or control COS1 cells Homo sapiens
Q89L site-directed mutagenesis, a GTP-bound active mutant Homo sapiens
T43N site-directed mutagenesis, a GDP-bound inactive mutant Homo sapiens

Inhibitors

Inhibitors Comment Organism Structure
additional information Rab proteins are members of the Ras superfamily of GTPases that switch between GDP-bound (inactive) and GTP-bound (active) forms Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
secretory vesicle colocalization with tissue inhibitor of metalloproteinase 1 (TIMP1) Homo sapiens 99503
-

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
GTP + H2O Homo sapiens
-
GDP + phosphate
-
?

Organism

Organism UniProt Comment Textmining
Homo sapiens Q96AX2
-
-

Source Tissue

Source Tissue Comment Organism Textmining
CL1-5 cell
-
Homo sapiens
-
lung cancer cell lung cancer patients with metastasis and poor survival show low hRAB37 protein expression coinciding with low TIMP1 in tumours, hRAB37 is downregulated mainly by promoter hypermethylation in lung cancer cells and patients, low mRNA expression of hRAB37 gene is associated with tumour metastasis in lung cancer patients Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
GTP + H2O
-
Homo sapiens GDP + phosphate
-
?

Synonyms

Synonyms Comment Organism
Rab37
-
Homo sapiens
small GTPase
-
Homo sapiens

Expression

Organism Comment Expression
Homo sapiens hRAB37 is downregulated mainly by promoter hypermethylation in lung cancer cells down

General Information

General Information Comment Organism
evolution Rab proteins are members of the Ras superfamily of GTPases that switch between GDP-bound (inactive) and GTP-bound (active) forms Homo sapiens
malfunction Dysfunction of hRAB37 or TIMP1 abrogates metastasis suppression Homo sapiens
physiological function Rab small GTPases are master regulators of membrane trafficking and guide vesicle targeting. Rab proteins transport cargo proteins to target membrane, organelle and cellular compartment to coordinate the cell membrane dynamics, cytoskeleton organization, signal transduction and membrane trafficking. Small GTPase Rab37 targets tissue inhibitor of metalloproteinase 1 (TIMP1) for exocytosis and thus suppresses tumour metastasis in a nucleotide-dependent manner. hRAB37 is involved in transportation of exocytotic vesicles and is involved in the exocytotic pathway of nascent secretory protein from the Golgi to the plasma membrane but not in the recycling endosome-mediated secretory pathway. Tissue inhibitor of metalloproteinase 1 is a secreted protein that inhibits MMPs and extracellular matrix turnover thereby decreasing cell motility. Rab-controlled trafficking pathways are altered during tumorigenesis. Tissue inhibitor of metalloproteinase 1 (TIMP1), a secreted glycoprotein that inhibits extracellular matrix turnover, is a cargo of hRAB37. hRAB37 regulates the exocytosis of TIMP1 in a nucleotide-dependent manner to inactivate matrix metalloproteinase 9 (MMP9) migration axis in vitro and in vivo Homo sapiens