1olp

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==Overview==
==Overview==
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Clostridium absonum phospholipase C (Caa) is a 42.7 kDa protein, which, shows 60% amino acid sequence identity with the Clostridium perfringens, phospholipase C, or alpha-toxin (Cpa), and has been isolated from patients, suffering from gas gangrene. We report the cloning and sequencing, purification, characterisation and crystal structure of the Caa enzyme., Caa had twice the phospholipid-hydrolysing (lecithinase) activity, 1.5, times the haemolytic activity and over seven times the activity towards, phosphatidylcholine-based liposomes when compared with Cpa. However, the, Caa enzyme had a lower activity than Cpa to the free (i.e. not in lipid, bilayer) substrate para-nitrophenylphosphorylcholine, towards, sphingomyelin-based liposomes and showed half the cytotoxicity. The lethal, dose (LD(50)) of Caa in mice was approximately twice that of Cpa. The, crystal structure of Caa shows that the 72-93 residue loop is in a, conformation different from those of previously determined open-form, alpha-toxin structures. This conformational change suggests a role for W84, in membrane binding and a possible route of entry into the active site, along a hydrophobic channel created by the re-arrangement of this loop., Overall, the properties of Caa are compatible with a role as a, virulence-determinant in gas gangrene caused by C.absonum.
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Clostridium absonum phospholipase C (Caa) is a 42.7 kDa protein, which shows 60% amino acid sequence identity with the Clostridium perfringens phospholipase C, or alpha-toxin (Cpa), and has been isolated from patients suffering from gas gangrene. We report the cloning and sequencing, purification, characterisation and crystal structure of the Caa enzyme. Caa had twice the phospholipid-hydrolysing (lecithinase) activity, 1.5 times the haemolytic activity and over seven times the activity towards phosphatidylcholine-based liposomes when compared with Cpa. However, the Caa enzyme had a lower activity than Cpa to the free (i.e. not in lipid bilayer) substrate para-nitrophenylphosphorylcholine, towards sphingomyelin-based liposomes and showed half the cytotoxicity. The lethal dose (LD(50)) of Caa in mice was approximately twice that of Cpa. The crystal structure of Caa shows that the 72-93 residue loop is in a conformation different from those of previously determined open-form alpha-toxin structures. This conformational change suggests a role for W84 in membrane binding and a possible route of entry into the active site along a hydrophobic channel created by the re-arrangement of this loop. Overall, the properties of Caa are compatible with a role as a virulence-determinant in gas gangrene caused by C.absonum.
==About this Structure==
==About this Structure==
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[[Category: Phospholipase C]]
[[Category: Phospholipase C]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Basak, A.K.]]
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[[Category: Basak, A K.]]
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[[Category: Briggs, D.C.]]
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[[Category: Briggs, D C.]]
[[Category: CA]]
[[Category: CA]]
[[Category: ZN]]
[[Category: ZN]]
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[[Category: zinc phospholipase c]]
[[Category: zinc phospholipase c]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 09:59:32 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:19:05 2008''

Revision as of 12:19, 21 February 2008


1olp, resolution 2.50Å

Drag the structure with the mouse to rotate

ALPHA TOXIN FROM CLOSTRIDIUM ABSONUM

Overview

Clostridium absonum phospholipase C (Caa) is a 42.7 kDa protein, which shows 60% amino acid sequence identity with the Clostridium perfringens phospholipase C, or alpha-toxin (Cpa), and has been isolated from patients suffering from gas gangrene. We report the cloning and sequencing, purification, characterisation and crystal structure of the Caa enzyme. Caa had twice the phospholipid-hydrolysing (lecithinase) activity, 1.5 times the haemolytic activity and over seven times the activity towards phosphatidylcholine-based liposomes when compared with Cpa. However, the Caa enzyme had a lower activity than Cpa to the free (i.e. not in lipid bilayer) substrate para-nitrophenylphosphorylcholine, towards sphingomyelin-based liposomes and showed half the cytotoxicity. The lethal dose (LD(50)) of Caa in mice was approximately twice that of Cpa. The crystal structure of Caa shows that the 72-93 residue loop is in a conformation different from those of previously determined open-form alpha-toxin structures. This conformational change suggests a role for W84 in membrane binding and a possible route of entry into the active site along a hydrophobic channel created by the re-arrangement of this loop. Overall, the properties of Caa are compatible with a role as a virulence-determinant in gas gangrene caused by C.absonum.

About this Structure

1OLP is a Single protein structure of sequence from Clostridium sardiniense with and as ligands. Active as Phospholipase C, with EC number 3.1.4.3 Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

Clostridium absonum alpha-toxin: new insights into clostridial phospholipase C substrate binding and specificity., Clark GC, Briggs DC, Karasawa T, Wang X, Cole AR, Maegawa T, Jayasekera PN, Naylor CE, Miller J, Moss DS, Nakamura S, Basak AK, Titball RW, J Mol Biol. 2003 Oct 31;333(4):759-69. PMID:14568535

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