Alanine racemase

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(New page: <StructureSection load='1l6g' size='350' side='right' caption='Structure of alanine racemase complex with PLP (PDB entry 1l6g)' scene=''> '''Alanine racemase''' (AR) catalyzes the ra...)
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<StructureSection load='1l6g' size='350' side='right' caption='Structure of alanine racemase dimer complex with phosphopyridoxyl-alanine (in magenta) (PDB entry [[1l6g]])' scene='55/551209/Cv/1'>
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<StructureSection load='1l6g' size='350' side='right' caption='Structure of alanine racemase complex with PLP (PDB entry [[1l6g]])' scene=''>
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== Function ==
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'''Alanine racemase''' (AR) catalyzes the racemization of L-alanine to D-alanine. AR uses pyridoxal-5’-phosphate (PLP) as a cofactor. PLP binds to a lysine residue of AR. AR participates in alanine and aspartate metabolism. The antibiotic D-cycloserine is an effective inhibitor of AR.
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'''Alanine racemase''' (AR) catalyzes the racemization of L-alanine to D-alanine. AR uses pyridoxal-5’-phosphate (PLP) as a cofactor. PLP binds to a lysine residue of AR. AR participates in alanine and aspartate metabolism. <ref name="Ad">PMID:11886871</ref>
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== 3D Structures of alanine racemase ==
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== Disease ==
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Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}
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The antibiotic D-cycloserine is an effective inhibitor of AR.
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[[3uw6]] – GsAR – ''Geobacillus stearothermophilus'' <BR />
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== Relevance ==
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===Alanine racemate complexes containing PLP===
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The D-alanine produced by AR is used for peptidoglycan biosynthesis. Peptidoglycans are found in cell walls of bacteria hence AR inhibitors are tested as antimicrobial drugs.
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[[1sft]] – GsAR + PLP <BR />
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== Structural highlights ==
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[[2sfp]] – GsAR + PLP + propionate inhibitor <BR />
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[[1l6f]], [[1l6g]] – GsAR + PLP-alanine <BR />
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AR uses 2 catalytic bases for the reaction: <scene name='55/551209/Cv/3'>Lys and Tyr</scene> from different monomers.<ref name="Ad">PMID:11886871</ref> Water molecules are shown as red spheres. <scene name='55/551209/Cv/5'>Whole active site</scene>.
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[[1xqk]] – GsAR (mutant) + PLP derivative <BR />
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[[1xql]] – GsAR (mutant) + PLP + pyridoxamine phosphate + pyridoxamine phosphate hydroxyisoxazole<BR />
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== 3D Structures of alanine racemase ==
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[[1vfh]] – SlAR + PLP – ''Streptomyces lavendulae'' <BR />
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[[Alanine racemase 3D structures]]
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[[1xfc]] – AR + PLP – ''Mycobacterium tuberculosis'' <BR />
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[[2dy3]] – AR + PLP – ''Corynebacterium glutamicum'' <BR />
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[[3ha1]] – BaAR + lysine-PLP <BR />
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[[3kw3]] – AR + lysine-PLP - ''Bartonella henselae''<BR />
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[[3s46]] – AR + lysine-PLP - ''Streptococcus pneumoniae''<BR />
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===Alanine racemate complexes not containing PLP===
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</StructureSection>
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[[1bd0]], [[1ftx]] – GsAR + alanine phosphonate <BR />
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== References ==
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[[1epv]], [[1niu]] – GsAR + cycloserine inhibitor <BR />
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<references/>
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[[1vfs]], [[1vft]] – SlAR + cycloserine inhibitor <BR />
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[[Category: Topic Page]]
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[[2dv8]], [[2vd9]] – BaAR + inhibitor – ''Bacillus anthracis'' <BR />
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Current revision

Structure of alanine racemase dimer complex with phosphopyridoxyl-alanine (in magenta) (PDB entry 1l6g)

Drag the structure with the mouse to rotate

References

  1. 1.0 1.1 Watanabe A, Yoshimura T, Mikami B, Hayashi H, Kagamiyama H, Esaki N. Reaction mechanism of alanine racemase from Bacillus stearothermophilus: x-ray crystallographic studies of the enzyme bound with N-(5'-phosphopyridoxyl)alanine. J Biol Chem. 2002 May 24;277(21):19166-72. Epub 2002 Mar 8. PMID:11886871 doi:10.1074/jbc.M201615200

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Michal Harel, Alexander Berchansky

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