1.A.65.1.2 The SARS coronavirus pore-forming envelope (E) protein or protein 3a (76 aas; 1 TMS) forms a pentameric cation-selective pore (Torres et al. 2006; Scott and Griffin 2015) that binds amantadine (Torres et al., 2007). A single polar residue and distinct membrane topologies impact its function (Ruch and Machamer, 2012). The E protein ion channel (IC) activity is cation-specific and K+-selective and is specifically correlated with enhanced pulmonary damage, edema accumulation and death. Calcium ions together with pH modulated E protein pore charge and selectivity (Nieto-Torres et al. 2015). There is a single transmembrane domain in E, suggesting an allosteric
interaction between extramembrane and transmembrane domains (To et al. 2016).
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Accession Number: | Q19QW7 |
Protein Name: | E protein |
Length: | 76 |
Molecular Weight: | 8361.00 |
Species: | Human SARS coronavirus (SARS-CoV) [227859] |
Number of TMSs: | 1 |
Location1 / Topology2 / Orientation3: |
Membrane1 / Single-pass type I membrane protein2 |
Substrate |
ion, cation, potassium(1+) |
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Pfam: |
PF02723
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[1] “A Mouse-Adapted SARS-Coronavirus Causes Disease and Mortality in BALB/c Mice.” Roberts A. et.al. 17222058
[2] “The SR-rich motif in SARS-CoV nucleocapsid protein is important for virus replication.” Tylor S. et.al. 19370068
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1: MYSFVSEETG TLIVNSVLLF LAFVVFLLVT LAILTALRLC AYCCNIVNVS LVKPTVYVYS
61: RVKNLNSSEG VPDLLV