Analysis of Host Cell Receptor GRP78 for Potential Natural Reservoirs of SARS-CoV-2

被引：0
|
作者：
I. Sirakov
D. Bakalov
R. Popova
I. Mitov
机构：
[1] Medical University of Sofia,Department of Medical Microbiology, Faculty of Medicine
[2] Medical University of Sofia,Department of Pathophysiology, Faculty of Medicine
[3] Gen Lab Ltd.,undefined
来源：
Journal of Epidemiology and Global Health | 2020年 / 10卷
关键词：
SARS-CoV-2; potential hosts; GRP78; protein receptor; COVID-19;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：198 / 200
页数：2
相关论文
共 50 条
  • [11] GRP78: A Multifunctional Receptor on the Cell Surface
    Gonzalez-Gronow, Mario
    Selim, Maria Angelica
    Papalas, John
    Pizzo, Salvatore V.
    ANTIOXIDANTS & REDOX SIGNALING, 2009, 11 (09) : 2299 - 2306
  • [12] Structural basis for the mechanism of interaction of SARS-CoV-2 B.1.640.2 variant RBD with the host receptors hACE2 and GRP78
    Shafiq, Athar
    Khalid, Ujala
    Abdur Rehman, Umar
    Abdullah Almuqri, Eman
    Mudassir, Maria
    Ahmad, Sajjad
    Khan, Muhammad Idrees
    Khan, Abbas
    Wei, Dong-Qing
    JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2024, 42 (04): : 2034 - 2042
  • [13] Structural-Dynamics and Binding Analysis of RBD from SARS-CoV-2 Variants of Concern (VOCs) and GRP78 Receptor Revealed Basis for Higher Infectivity
    Khan, Abbas
    Mohammad, Anwar
    Haq, Inamul
    Nasar, Mohammad
    Ahmad, Waqar
    Yousafi, Qudsia
    Suleman, Muhammad
    Ahmad, Sajjad
    Albutti, Aqel
    Khan, Taimoor
    Marafie, Sulaiman K.
    Alshawaf, Eman
    Ali, Syed Shujait
    Abubaker, Jehad
    Wei, Dong-Qing
    MICROORGANISMS, 2021, 9 (11)
  • [14] Targeting SARS-CoV-2 and host cell receptor interactions
    Lim, Siew Pheng
    ANTIVIRAL RESEARCH, 2023, 210
  • [15] AR12 (OSU-03012) suppresses GRP78 expression and inhibits SARS-CoV-2 replication
    Rayner, Jonathan O.
    Roberts, Rosemary A.
    Kim, Jin
    Poklepovic, Andrew
    Roberts, Jane L.
    Booth, Laurence
    Dent, Paul
    BIOCHEMICAL PHARMACOLOGY, 2020, 182
  • [16] Preliminary Virtual Screening Studies to Identify GRP78 Inhibitors Which May Interfere with SARS-CoV-2 Infection
    Palmeira, Andreia
    Sousa, Emilia
    Koseler, Aylin
    Sabirli, Ramazan
    Goren, Tarik
    Turkcuer, Ibrahim
    Kurt, Ozgur
    Pinto, Madalena M.
    Helena Vasconcelos, M.
    PHARMACEUTICALS, 2020, 13 (06) : 1 - 13
  • [17] Recognition through GRP78 is enhanced in the UK, South African, and Brazilian variants of SARS-CoV-2; An in silico perspective
    Ibrahim, Ibrahim M.
    Elfiky, Abdo A.
    Elgohary, Alaa M.
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2021, 562 : 89 - 93
  • [18] Identification of a druggable site on GRP78 at the GRP78-SARS-CoV-2 interface and virtual screening of compounds to disrupt that interface
    Lazou, Maria
    Hutton, Jonathan R.
    Chakravarty, Arijit
    Joseph-McCarthy, Diane
    JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 2024, 38 (01)
  • [19] Vulnerability of The Male Reproductive System to SARS-CoV-2 Invasion: Potential Role for The Endoplasmic Reticulum Chaperone Grp78/HSPA5/BiP
    Sadeghi, Niloofar
    Tavalaee, Marziyeh
    Shahverdi, Abdolhossein
    Sengupta, Pallav
    Leisegang, Kristian
    Saleh, Ramadan
    Agarwal, Ashok
    Nasr-Esfahani, Mohammad Hossein
    CELL JOURNAL, 2022, 24 (08) : 427 - 433
  • [20] Therapeutic potential of miRNAs targeting SARS-CoV-2 host cell receptor ACE2
    Bozgeyik, Ibrahim
    META GENE, 2021, 27
12345