Hemolysin: Difference between revisions

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{{STRUCTURE_3k55|  PDB=3k55  | SIZE=400| SCENE= |right|CAPTION=β-hemolysin, [[3k55]] }}
<StructureSection load='7ahl' size='350' side='right' caption='α-hemolysin heptamer (PDB code [[7ahl]]).' scene=''>
== Function ==
'''Hemolysin''' (HL) is exotoxin from bacteria which causes lysis of red blood cells<ref>PMID:20110774</ref>.
*'''alpha-hemolysin''' is a transmembrane pore-forming heptameric molecule<ref>PMID:8943190</ref>.  See details for in [[Pore forming toxin, α-hemolysin]]
*'''delta-hemolysin''' is a 26 amino acid peptide from the bacterium ''Staphylococcus'' exhibiting antimicrobial activity against'' Legionerlla'' <ref>PMID:19150639</ref>.


'''Hemolysin''' (HL) is exotoxin from bacteria which causes lysis of red blood cells.  See details for α-hemolysin in [[Pore forming toxin, α-hemolysin]].  For toxins in Proteopdia see [[Toxins]].
See details of hemolysin E in [[Molecular Playground/ClyA]].


{{TOC limit|limit=2}}
For toxins in Proteopdia see [[Toxins]].


== 3D Structures of hemolysin ==
== Relevance ==
HL acts as a virulence factor in the pathogenesis of invasive infections<ref>PMID:12564994</ref>.


''Updated December 2011''
==3D Printed Physical Model of Hemolysin==


===α-hemolysin===
Shown below is a 3D printed physical model of Hemolysin. The model is shown in alpha carbon backbone format with each chain colored uniquely.


[[3anz]], [[7ahl]] – SaHL-α – S''taphylococcus aureus''<br />
[[Image:hemolysin1_centerForBioMolecularModeling.jpg|550px]]
A full page devoted to exploring [[7ahl]] is found here [[Pore_forming_toxin,_α-hemolsyin]].<br/>
[[Image:hemolysin2_centerForBioMolecularModeling.jpg|550px]]
[[3m2l]], [[3m4d]] - SaHL-α (mutant)<br />
[[3m3r]], [[3m4e]] - SaHL-α (mutant) + β-cyclodextrin


===β-hemolysin===
====The MSOE Center for BioMolecular Modeling====


[[3k55]] – SaHL-β)<br />
[[Image:CbmUniversityLogo.jpg | left | 150px]]
[[3i5v]] - SaHL-β residues 35-330)<br />
[[3i41]] - SaHL-β residues 35-330 (mutant)<br />
[[3i46]], [[3i48]] - SaHL-β residues 35-330 (mutant)<br /> + metal ion


===γ-hemolysin===
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].


[[2qk7]] – SaHL-γ (mutant)<br />
== 3D Structures of hemolysin ==
[[3b07]] - SaHL-γ
 
===δ-hemolysin===
 
[[2kam]] – SaHL-δ - NMR


===Hemolysin===
[[Hemolysin 3D structures]]


[[3o44]] – VcHL residues 161-741 – ''Vibrio cholerae''<br />
</StructureSection>
[[1xez]] – VcHL (mutant)<br />
[[3a57]] – HL 2 – ''Vibrio parahaemolyticus''<br />
[[3hvn]] – HL (mutant) – ''Streptococcus suis''<br />
[[3fy3]] – HL A residues 30-265 – ''Proteus mirabilis''<br />
[[2wcd]] – EcHL E residues 2-303 – ''Escherichia coli''<br />
[[1qoy]] - EcHL E (mutant)<br />
[[1mt0]] – EcHL B ATP-binding domain<br />
[[2oai]], [[2r8d]] – HL corc_hlyc domain – ''Xylella fastidiosa''<br />
[[2r2z]] – HL residues 346-435 – ''Enterococcus faecalis''


== References ==
<references/>
[[Category:Topic Page]]
[[Category:Topic Page]]

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

Wayne Decatur, Alexander Berchansky, Michal Harel, Mark Hoelzer