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Literature summary for 3.4.24.80 extracted from

  • Koshikawa, N.; Mizushima, H.; Minegishi, T.; Iwamoto, R.; Mekada, E.; Seiki, M.
    Membrane type 1-matrix metalloproteinase cleaves off the NH2-terminal portion of heparin-binding epidermal growth factor and converts it into a heparin-independent growth factor (2010), Cancer Res., 70, 6093-6103.
    View publication on PubMed

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
70000
-
x * 70000, SDS-PAGE Mus musculus
70000
-
x * 70000, SDS-PAGE Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-
Mus musculus
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
MEF cell
-
Mus musculus
-
MKN-28 cell
-
Homo sapiens
-
MKN-7 cell
-
Homo sapiens
-
STKM-2 cell
-
Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
heparin-binding epidermal growth factor + H2O the enzyme removes the NH2-terminal 20 amino acids by cleaving between A-83LC Mus musculus ?
-
?
heparin-binding epidermal growth factor + H2O the enzyme removes the NH2-terminal 20 amino acids by cleaving between A-83LC Homo sapiens ?
-
?

Subunits

Subunits Comment Organism
? x * 70000, SDS-PAGE Mus musculus
? x * 70000, SDS-PAGE Homo sapiens

Synonyms

Synonyms Comment Organism
membrane type 1-matrix metalloproteinase
-
Mus musculus
membrane type 1-matrix metalloproteinase
-
Homo sapiens
MMP14
-
Mus musculus
MMP14
-
Homo sapiens
MT1-MMP
-
Mus musculus
MT1-MMP
-
Homo sapiens

General Information

General Information Comment Organism
physiological function the processing of heparin-binding epidermal growth factor by MT1-MMP converts the substrate into a heparin-independent growth factor with enhanced mitogenic activity, and thereby, expression of both proteins costimulates tumor cell growth in vitro and in vivo Mus musculus
physiological function the processing of heparin-binding epidermal growth factor by MT1-MMP converts the substrate into a heparin-independent growth factor with enhanced mitogenic activity, and thereby, expression of both proteins costimulates tumor cell growth in vitro and in vivo Homo sapiens