Sialidase: Difference between revisions

From Proteopedia
Jump to navigationJump to search
Michal Harel (talk | contribs)
No edit summary
Michal Harel (talk | contribs)
No edit summary
Line 1: Line 1:
<StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''>
<StructureSection load='2w68' size='340' side='right' caption='Caption for this structure' scene=''>


== Function ==
== Function ==


'''Sialidase''' is a neuraminidase which cleaves terminal sialic acid from a variety of natural substances <ref>PMID:12374200</ref>. For '''Trans-sialidase''' see [[Neuraminidase]].  '''Anhydrosialidase''' catalyzes the elimination of sialyl group in N-acetylneuraminic acid glycosides to yield 2,7-anhydro-α-N-acetylneuraminate.
'''Sialidase''' is a neuraminidase which cleaves terminal sialic acid from a variety of natural substances <ref>PMID:12374200</ref>. The sialic acid-binding domain of sialidase is called CBD.  For '''Anhydrosialidase''' catalyzes the elimination of sialyl group in N-acetylneuraminic acid glycosides to yield 2,7-anhydro-α-N-acetylneuraminate. For '''Trans-sialidase''' see [[Neuraminidase]].  


== Disease ==
== Disease ==


== Relevance ==
== Relevance ==
''Trypanosoma cruzi'' trans-sialidase is a drug target agains Chagas Disease<ref>PMID:24144418</ref>.


== Structural highlights ==
== Structural highlights ==
Line 70: Line 68:
**[[1n1v]] – TrSal + neuraminic acid derivative <br />
**[[1n1v]] – TrSal + neuraminic acid derivative <br />
**[[1mz6]], [[1n1t]], [[2ags]] – TrSal + inhibitor  <br />
**[[1mz6]], [[1n1t]], [[2ags]] – TrSal + inhibitor  <br />
**[[1n1y]]– TrSal + sialic acid <br />
**[[1n1y]] – TrSal + sialic acid <br />
**[[2a75]], [[2fhr]] – TrSal + sialic acid derivative<br />
**[[2a75]], [[2fhr]] – TrSal + sialic acid derivative<br />
**[[1dim]], [[1dil]], [[2sil]], [[2sim]] – StSal + inhibitor  <br />  
**[[1dim]], [[1dil]], [[2sil]], [[2sim]] – StSal + inhibitor  <br />