Laminin subunit alpha-1 explained

Laminin subunit alpha-1 is a protein that in humans is encoded by the LAMA1 gene.[1] [2]

Interactions

Laminin, alpha 1 has been shown to interact with FBLN2.[3] [4]

Role in pathology

Mutations of the LAMA1 gene cause the Poretti–Boltshauser syndrome.

Further reading

Notes and References

  1. Nagayoshi T, Mattei MG, Passage E, Knowlton R, Chu ML, Uitto J . Human laminin A chain (LAMA) gene: chromosomal mapping to locus 18p11.3 . Genomics . 5 . 4 . 932–5 . January 1990 . 2591971 . 10.1016/0888-7543(89)90136-5 .
  2. Web site: Entrez Gene: LAMA1 laminin, alpha 1.
  3. Utani . A . Nomizu M . Yamada Y . January 1997 . Fibulin-2 binds to the short arms of laminin-5 and laminin-1 via conserved amino acid sequences . J. Biol. Chem. . 272 . 5 . 2814–20 . 0021-9258. 9006922 . 10.1074/jbc.272.5.2814 . 24800195 . free .
  4. Talts . J F . Sasaki T . Miosge N . Göhring W . Mann K . Mayne R . Timpl R . November 2000 . Structural and functional analysis of the recombinant G domain of the laminin alpha4 chain and its proteolytic processing in tissues . J. Biol. Chem. . 275 . 45 . 35192–9 . 0021-9258. 10934193 . 10.1074/jbc.M003261200 . 36521395 . free .