2dik

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[[Image:2dik.jpg|left|200px]]<br /><applet load="2dik" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:2dik.jpg|left|200px]]
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caption="2dik, resolution 2.5&Aring;" />
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'''R337A MUTANT OF PYRUVATE PHOSPHATE DIKINASE'''<br />
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{{Structure
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|PDB= 2dik |SIZE=350|CAPTION= <scene name='initialview01'>2dik</scene>, resolution 2.5&Aring;
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|SITE=
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|LIGAND= <scene name='pdbligand=SO4:SULFATE ION'>SO4</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/Pyruvate,_phosphate_dikinase Pyruvate, phosphate dikinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.9.1 2.7.9.1]
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|GENE= PPDK ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1512 Clostridium symbiosum])
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}}
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'''R337A MUTANT OF PYRUVATE PHOSPHATE DIKINASE'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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2DIK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Clostridium_symbiosum Clostridium symbiosum] with <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. This structure supersedes the now removed PDB entry 1BUK. Active as [http://en.wikipedia.org/wiki/Pyruvate,_phosphate_dikinase Pyruvate, phosphate dikinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.9.1 2.7.9.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2DIK OCA].
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2DIK is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Clostridium_symbiosum Clostridium symbiosum]. This structure supersedes the now removed PDB entry 1BUK. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2DIK OCA].
==Reference==
==Reference==
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Location of the phosphate binding site within Clostridium symbiosum pyruvate phosphate dikinase., McGuire M, Huang K, Kapadia G, Herzberg O, Dunaway-Mariano D, Biochemistry. 1998 Sep 29;37(39):13463-74. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9753432 9753432]
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Location of the phosphate binding site within Clostridium symbiosum pyruvate phosphate dikinase., McGuire M, Huang K, Kapadia G, Herzberg O, Dunaway-Mariano D, Biochemistry. 1998 Sep 29;37(39):13463-74. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9753432 9753432]
[[Category: Clostridium symbiosum]]
[[Category: Clostridium symbiosum]]
[[Category: Pyruvate, phosphate dikinase]]
[[Category: Pyruvate, phosphate dikinase]]
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[[Category: phosphotransferase]]
[[Category: phosphotransferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:59:11 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:27:34 2008''

Revision as of 14:27, 20 March 2008


PDB ID 2dik

Drag the structure with the mouse to rotate
, resolution 2.5Å
Ligands:
Gene: PPDK (Clostridium symbiosum)
Activity: Pyruvate, phosphate dikinase, with EC number 2.7.9.1
Coordinates: save as pdb, mmCIF, xml



R337A MUTANT OF PYRUVATE PHOSPHATE DIKINASE


Overview

Pyruvate phosphate dikinase (PPDK) catalyzes the interconversion of ATP, Pi, and pyruvate with AMP, PPi, and PEP in three partial reactions: (1) E + ATP --> E.ATP --> E-PP.AMP, (2) E-PP.AMP + Pi --> E-PP.AMP.Pi --> E-P.AMP.PPi, and (3) E-P + pyruvate --> E-P.pyruvate --> E.PEP. The Clostridium symbiosum PPDK structure consists of N-terminal, central, and C-terminal domains. The N-terminal and central domains catalyze partial reactions 1 and 2 whereas the C-terminal and central domains catalyze partial reaction 3. The goal of the present work is to determine where on the N-terminal domain catalysis of partial reactions 1 and 2 occurs and, in particular, where the Pi binding site is located. Computer modeling studies implicated Arg337 as a key residue for Pi binding. This role was tested by site-directed mutagenesis. The R337A PPDK was shown to be impaired in catalysis of the forward (kcat 300-fold lower) and reverse (kcat 30-fold lower) full reactions. Time courses for the single turnover reactions were measured to show that catalysis of partial reaction 1 is 5-fold slower in the mutant, catalysis of the second partial reaction is 140-fold slower in the mutant, and catalysis of the third partial reaction is unaffected. With the exception of the mutation site, the crystal structure of the R337A PPDK closely resembles the structure of the wild-type protein. Thus, the altered kinetic properties observed for this mutant are attributed solely to the elimination of the interaction between substrate and the guanidinium group of the Arg337 side chain. On the basis of these findings we propose that the Pi binding site is located within the crevice of the PPDK N-terminal domain, at a site that is flanked by the ATP beta-P and the Mg2+ cofactor.

About this Structure

2DIK is a Single protein structure of sequence from Clostridium symbiosum. This structure supersedes the now removed PDB entry 1BUK. Full crystallographic information is available from OCA.

Reference

Location of the phosphate binding site within Clostridium symbiosum pyruvate phosphate dikinase., McGuire M, Huang K, Kapadia G, Herzberg O, Dunaway-Mariano D, Biochemistry. 1998 Sep 29;37(39):13463-74. PMID:9753432

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