Pregled bibliografske jedinice broj: 992052
Human papillomaviruses and the specificity of PDZ domain targeting
Human papillomaviruses and the specificity of PDZ domain targeting // The FEBS Journal, 279 (2012), 19; 3530-3537 doi:10.1111/j.1742-4658.2012.08709.x (međunarodna recenzija, članak, ostalo)
CROSBI ID: 992052 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Human papillomaviruses and the specificity of PDZ domain targeting
Autori
Pim, David ; Bergant, Martina ; Boon, Siaw S. ; Ganti, Ketaki ; Kranjec, Christian ; Massimi, Paola ; Subbaiah, Vanitha K. ; Thomas, Miranda ; Tomaić, Vjekoslav ; Banks, Lawrence
Izvornik
The FEBS Journal (1742-464X) 279
(2012), 19;
3530-3537
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, ostalo
Ključne riječi
HPV E6, cervical cancer, PDZ
Sažetak
The human papillomavirus (HPV) E6 oncoprotein is fundamental to the ability of these viruses to induce human malignancy. A defining characteristic of the HPV E6 oncoproteins found in cancer‐causing HPV types is the presence of a PDZ binding motif at their extreme C‐terminus. Through this motif, E6 is able to interact with a large number of cellular proteins that contain PDZ domains. Many of these cellular proteins are involved in regulation of processes associated with the control of cell attachment, cell proliferation, cell polarity and cell signaling. How E6 targets multiple proteins containing the same recognition domain is still an open question. In this review, we highlight aspects of E6 function and biology that help to answer this question, and thereby provide insight into the role of these substrates during development of HPV‐induced malignancy.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE