Id |
Subject |
Object |
Predicate |
Lexical cue |
T251 |
0-4 |
Sentence |
denotes |
5.1. |
T252 |
5-57 |
Sentence |
denotes |
Evolutionary Origin and Classification of the CoV HE |
T253 |
58-159 |
Sentence |
denotes |
Certain viruses use glycoproteins such as HA, HE, S and HEF for host receptor binding or destruction. |
T254 |
160-284 |
Sentence |
denotes |
Coronaviridae, Orthomyxoviridae, Paramyxoviridae and Adenoviridae utilize SAs as binding molecules for attachment and entry. |
T255 |
285-341 |
Sentence |
denotes |
However, only limited human pathogens recognize O-Ac SA. |
T256 |
343-349 |
Sentence |
denotes |
5.1.1. |
T257 |
350-401 |
Sentence |
denotes |
Influenza Virus A and B Spike Proteins of HA and NA |
T258 |
402-479 |
Sentence |
denotes |
Influenza A and B viruses bear two spikes of receptor-binding HA and NA [45]. |
T259 |
481-487 |
Sentence |
denotes |
5.1.2. |
T260 |
488-512 |
Sentence |
denotes |
Influenza C virus HA-HEF |
T261 |
513-566 |
Sentence |
denotes |
HEF is indeed an ancient type of SA-O-acetylesterase. |
T262 |
567-675 |
Sentence |
denotes |
In contrast to A/B, the influenza C virus bears one spike with triple functions of HEF as a homotrimer [46]. |
T263 |
676-761 |
Sentence |
denotes |
Each HEF subunit bears two Neu5,9Ac2-binding sites and binds to the 9-O-acetyl group. |
T264 |
762-822 |
Sentence |
denotes |
In parallel, another modification of O-acetylation is found. |
T265 |
823-941 |
Sentence |
denotes |
Indeed, influenza C virus bears SA-O-acetylesterase [47], which converts 5-N-acetyl-9-O-NeuAc (Neu5,9Ac2) to 5-Neu5Ac. |
T266 |
942-1097 |
Sentence |
denotes |
The 9-O-acetyl SA is a unique determinant for the influenza C virus receptor and Neu5,9Ac2 is crucial for receptor activity, but not Neu5Gc or Neu5Ac [48]. |
T267 |
1098-1190 |
Sentence |
denotes |
Neu5,9Ac2 is an essential determinant for influenza virus C type-specific host cell tropism. |
T268 |
1191-1250 |
Sentence |
denotes |
NAs cleave the α-ketosidic linkages to the D-Gal or GalNAc. |
T269 |
1251-1318 |
Sentence |
denotes |
SA-O-acetylesterases cleave different O-acetyl linkages (Figure 5). |
T270 |
1319-1421 |
Sentence |
denotes |
The OH-group of Tyr224 and the guanidino group of Arg236 interact with the CH3CO-carbonyl oxygen [49]. |
T271 |
1422-1561 |
Sentence |
denotes |
HEF SA-O-acetylesterase is found in several enveloped (+) ssRNA viruses of influenza C virus and also in certain CoVs and toroviruses [47]. |
T272 |
1562-1740 |
Sentence |
denotes |
The CoVs are different from the orthomyxoviruses, which hold a segmented (−) ssRNA genome and are instead evolutionary linked to the family Coronaviridae, order Nidovirales [45]. |
T273 |
1742-1748 |
Sentence |
denotes |
5.1.3. |
T274 |
1749-1775 |
Sentence |
denotes |
CoV SA-O-Acetylesterase HE |
T275 |
1776-1864 |
Sentence |
denotes |
CoVs and toroviruses of the Coronaviridae family are specific for the O-Ac SA receptors. |
T276 |
1865-1931 |
Sentence |
denotes |
Their S and HE glycoproteins are similar to influenza C virus HEF. |
T277 |
1932-2089 |
Sentence |
denotes |
CoVs and all toroviruses bear HE gene form class I envelope membrane proteins of about 400 amino acid residues which bear 7 to 12 N-glycosylation sites [50]. |
T278 |
2090-2122 |
Sentence |
denotes |
HE multimer forms enter virions. |
T279 |
2123-2241 |
Sentence |
denotes |
Bovine CoV (BCoV) and HCoV-OC43, similar to influenza C virus, recognize Neu5,9Ac2 and bear SA-9-O-acetylesterase [8]. |
T280 |
2242-2276 |
Sentence |
denotes |
CoV HEs are all O-acetylesterases. |
T281 |
2277-2470 |
Sentence |
denotes |
The HE enzymes found in torovirus, CoV and influenza C virus are evolutionarily interspecies-mutated with about 30% homology by heterologous RNA recombination [51] and horizontal gene transfer. |
T282 |
2471-2534 |
Sentence |
denotes |
Therefore, viral HEs are diverse and widespread over evolution. |