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1IT5

Solution structure of apo-type PLA2 from Streptomyces violaceruber A-2688.

Summary for 1IT5
Entry DOI10.2210/pdb1it5/pdb
Related1IT4
DescriptorPhospholipase A2 (1 entity in total)
Functional Keywordsprokaryotic pla2, hydrolase
Biological sourceStreptomyces violaceoruber
Total number of polymer chains1
Total formula weight13570.78
Authors
Sugiyama, M.,Ohtani, K.,Izuhara, M.,Koike, T. (deposition date: 2002-01-09, release date: 2002-09-04, Last modification date: 2024-11-20)
Primary citationSugiyama, M.,Ohtani, K.,Izuhara, M.,Koike, T.,Suzuki, K.,Imamura, S.,Misaki, H.
A novel prokaryotic phospholipase A2. Characterization, gene cloning, and solution structure.
J.Biol.Chem., 277:20051-20058, 2002
Cited by
PubMed Abstract: Until now, phospholipase A(2) (PLA(2); EC 3.1.14) has been found only from eukaryotic sources. In the present study, we found a secreted PLA(2), which is produced by a soil bacterium, Streptomyces violaceoruber A-2688, demonstrating that the enzyme is the first phospholipase A(2) identified in prokaryote. After characterization of the novel PLA(2), a gene encoding the enzyme was cloned, sequenced, and overexpressed using a Streptomyces host-vector system. The amino acid sequence showed that the prokaryotic PLA(2) has only four cysteines and less homology to the eukaryotic ones, which have 12-16 cysteines. The solution structures of the prokaryotic PLA(2), bound and unbound with calcium(II) ion, were determined by using the NMR technique and structure calculation. The overall structure of the S. violaceoruber PLA(2), which is composed of only five alpha-helices, is completely different from those of eukaryotic PLA(2)s, which consist of beta-sheets and alpha-helices. The structure of the calcium-binding domain is obviously distinct from that without the ion; the ligands for the calcium(II) ion are the two carboxylates of Asp(43) (monodentate) and Asp(65) (bidentate), the carbonyl oxygen of Leu(44), and three water molecules. A calcium-binding experiment showed that the calcium dissociation constant ( approximately 5 mm) for the prokaryotic PLA(2) is much larger than those of eukaryotic ones.
PubMed: 11897786
DOI: 10.1074/jbc.M200264200
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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数据于2025-06-18公开中

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