Calcium binding rigidifies the C2 domain and the intradomain interaction of GIVA phospholipase A2 as revealed by hydrogen/deuterium exchange mass spectrometry (Q39646620)

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scientific article published on 21 January 2008

Language	Label	Description	Also known as
English	Calcium binding rigidifies the C2 domain and the intradomain interaction of GIVA phospholipase A2 as revealed by hydrogen/deuterium exchange mass spectrometry	scientific article published on 21 January 2008

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scholarly article

1 reference

Europe PubMed Central

13 September 2017

Calcium binding rigidifies the C2 domain and the intradomain interaction of GIVA phospholipase A2 as revealed by hydrogen/deuterium exchange mass spectrometry (English)

1 reference

Europe PubMed Central

13 September 2017

object named as

John E Burke

2

0 references

Edward A. Dennis

object named as

Edward A Dennis

8

0 references

author name string

Yuan-Hao Hsu

1

1 reference

Europe PubMed Central

13 September 2017

Daren L Stephens

3

1 reference

Europe PubMed Central

13 September 2017

Raymond A Deems

4

1 reference

Europe PubMed Central

13 September 2017

Sheng Li

5

1 reference

Europe PubMed Central

13 September 2017

Kyle M Asmus

6

1 reference

Europe PubMed Central

13 September 2017

Virgil L Woods

7

1 reference

Europe PubMed Central

13 September 2017

language of work or name

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publication date

21 January 2008

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Europe PubMed Central

13 September 2017

number of pages

8

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inferred from page(s)

Journal of Biological Chemistry

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Europe PubMed Central

13 September 2017

283

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Europe PubMed Central

13 September 2017

15

1 reference

Europe PubMed Central

13 September 2017

9820-9827

1 reference

Europe PubMed Central

13 September 2017

Mechanism of specific membrane targeting by C2 domains: localized pools of target lipids enhance Ca2+ affinity

1 reference

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The phospholipase A2 superfamily and its group numbering system

1 reference

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An examination of dynamics crosstalk between SH2 and SH3 domains by hydrogen/deuterium exchange and mass spectrometry

1 reference

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Distinguishing phospholipase A2 types in biological samples by employing group-specific assays in the presence of inhibitors

1 reference

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X-ray reflectivity studies of cPLA2{alpha}-C2 domains adsorbed onto Langmuir monolayers of SOPC

1 reference

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Spinal phospholipase A2 in inflammatory hyperalgesia: role of group IVA cPLA2

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Investigating protein structure and dynamics by hydrogen exchange MS.

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Changes in protein conformational mobility upon activation of extracellular regulated protein kinase-2 as detected by hydrogen exchange

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Specific physiological roles of cytosolic phospholipase A(2) as defined by gene knockouts

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Role of phosphorylation sites and the C2 domain in regulation of cytosolic phospholipase A2.

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Crystal structure of human cytosolic phospholipase A2 reveals a novel topology and catalytic mechanism

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Identification of protein-protein interfaces by decreased amide proton solvent accessibility

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Solution structure and membrane interactions of the C2 domain of cytosolic phospholipase A2

1 reference

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Crystal structure of a calcium-phospholipid binding domain from cytosolic phospholipase A2

1 reference

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p38 mitogen-activated protein kinase phosphorylates cytosolic phospholipase A2 (cPLA2) in thrombin-stimulated platelets. Evidence that proline-directed phosphorylation is not required for mobilization of arachidonic acid by cPLA2

1 reference

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cPLA2 is phosphorylated and activated by MAP kinase

1 reference

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Primary structure effects on peptide group hydrogen exchange

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Delineation of two functionally distinct domains of cytosolic phospholipase A2, a regulatory Ca(2+)-dependent lipid-binding domain and a Ca(2+)-independent catalytic domain

1 reference

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Cloning and recombinant expression of phospholipase A2 present in rheumatoid arthritic synovial fluid

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A novel arachidonic acid-selective cytosolic PLA2 contains a Ca(2+)-dependent translocation domain with homology to PKC and GAP

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Specificity of expression and effects of eicosanoid mediators in normal physiology and human diseases.

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14 September 2017

Recent insights into the structure, function and biology of cPLA2.

1 reference

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14 September 2017

Roles of catalytic domain residues in interfacial binding and activation of group IV cytosolic phospholipase A2.

1 reference

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25 September 2017

Group-specific assays that distinguish between the four major types of mammalian phospholipase A2.

1 reference

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Translocation of the 85-kDa phospholipase A2 from cytosol to the nuclear envelope in rat basophilic leukemia cells stimulated with calcium ionophore or IgE/antigen

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PAS domain allostery and light-induced conformational changes in photoactive yellow protein upon I2 intermediate formation, probed with enhanced hydrogen/deuterium exchange mass spectrometry

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A structure-function study of the C2 domain of cytosolic phospholipase A2. Identification of essential calcium ligands and hydrophobic membrane binding residues.

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Group IV cytosolic phospholipase A2 binds with high affinity and specificity to phosphatidylinositol 4,5-bisphosphate resulting in dramatic increases in activity.

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A calcium-dependent mechanism for associating a soluble arachidonoyl-hydrolyzing phospholipase A2 with membrane in the macrophage cell line RAW 264.7.

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The Ca2(+)-sensitive cytosolic phospholipase A2 is a 100-kDa protein in human monoblast U937 cells

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Ceramide-1-phosphate binds group IVA cytosolic phospholipase a2 via a novel site in the C2 domain

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Ceramide 1-phosphate acts as a positive allosteric activator of group IVA cytosolic phospholipase A2 alpha and enhances the interaction of the enzyme with phosphatidylcholine.

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Ca2+-signaling cycle of a membrane-docking C2 domain

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https://pubmed.ncbi.nlm.nih.gov/18211893

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A cytosolic phospholipase in human neutrophils that hydrolyzes arachidonoyl-containing phosphatidylcholine

1 reference

https://pubmed.ncbi.nlm.nih.gov/18211893

12 December 2020

based on heuristic

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Identifiers

10.1074/JBC.M708143200

1 reference

Europe PubMed Central

13 September 2017

1 reference

Europe PubMed Central

13 September 2017

1 reference

Europe PubMed Central

13 September 2017

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