5ptd
From Proteopedia
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| - | [[Image:5ptd.gif|left|200px]]<br /> | + | [[Image:5ptd.gif|left|200px]]<br /><applet load="5ptd" size="450" color="white" frame="true" align="right" spinBox="true" |
| - | <applet load="5ptd" size="450" color="white" frame="true" align="right" spinBox="true" | + | |
caption="5ptd, resolution 2.7Å" /> | caption="5ptd, resolution 2.7Å" /> | ||
'''PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C MUTANT H32A'''<br /> | '''PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C MUTANT H32A'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
| - | 5PTD is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_cereus Bacillus cereus]. Active as [http://en.wikipedia.org/wiki/Transferred_entry:_4.6.1.13 Transferred entry: 4.6.1.13], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.4.10 3.1.4.10] | + | 5PTD is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_cereus Bacillus cereus]. Active as [http://en.wikipedia.org/wiki/Transferred_entry:_4.6.1.13 Transferred entry: 4.6.1.13], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.4.10 3.1.4.10] Known structural/functional Site: <scene name='pdbsite=ACT:Active Site'>ACT</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=5PTD OCA]. |
==Reference== | ==Reference== | ||
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[[Category: phosphoric diester]] | [[Category: phosphoric diester]] | ||
| - | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 20:46:50 2007'' |
Revision as of 18:37, 18 December 2007
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PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C MUTANT H32A
Overview
The role of amino acid residues located in the active site pocket of, phosphatidylinositol-specific phospholipase C (PI-PLC) from Bacillus, cereus[Heinz, D. W., Ryan, M., Bullock, T., & Griffith, O. H. (1995) EMBO, J. 14, 3855-3863] was investigated by site-directed mutagenesis, kinetics, and crystal structure analysis. Twelve residues involved in catalysis and, substrate binding (His32, Arg69, His82, Gly83, Lys115, Glu117, Arg163, Trp178, Asp180, Asp198, Tyr200, and Asp274) were individually replaced by, 1-3 other amino acids, resulting in a total number of 21 mutants., Replacements in the mutants H32A, H32L, R69A, R69E, R69K, H82A, H82L, E117K, R163I, D198A, D198E, D198S, Y200S, and D274S caused essentially, complete inactivation of the enzyme. The remaining mutants (G83S, K115E, R163K, W178Y, D180S, Y200F, and D274N) exhibited reduced activities up to, 57% when compared with wild-type PI-PLC. Crystal structures determined at, a resolution ranging from 2.0 to 2.7 A for six mutants (H32A, H32L, R163K, D198E, D274N, and D274S) showed that significant changes were confined to, the site of the respective mutation without perturbation of the rest of, the structure. Only in mutant D198E do the side chains of two neighboring, arginine residues move across the inositol binding pocket toward the newly, introduced glutamic acid. An analysis of these structure-function, relationships provides new insight into the catalytic mechanism, and, suggests a molecular explanation of some of the substrate, stereospecificity and inhibitor binding data available for this enzyme.
About this Structure
5PTD is a Single protein structure of sequence from Bacillus cereus. Active as Transferred entry: 4.6.1.13, with EC number 3.1.4.10 Known structural/functional Site: . Full crystallographic information is available from OCA.
Reference
Probing the roles of active site residues in phosphatidylinositol-specific phospholipase C from Bacillus cereus by site-directed mutagenesis., Gassler CS, Ryan M, Liu T, Griffith OH, Heinz DW, Biochemistry. 1997 Oct 21;36(42):12802-13. PMID:9335537
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