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1oas

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(New page: 200px<br /><applet load="1oas" size="450" color="white" frame="true" align="right" spinBox="true" caption="1oas, resolution 2.200&Aring;" /> '''O-ACETYLSERINE SULF...)
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caption="1oas, resolution 2.200&Aring;" />
'''O-ACETYLSERINE SULFHYDRYLASE FROM SALMONELLA TYPHIMURIUM'''<br />
'''O-ACETYLSERINE SULFHYDRYLASE FROM SALMONELLA TYPHIMURIUM'''<br />
==Overview==
==Overview==
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The last step in cysteine biosynthesis in enteric bacteria is catalyzed by, the pyridoxal 5'-phosphate-dependent enzyme O-acetylserine sulfhydrylase., Here we report the crystal structure at 2.2 A resolution of the A-isozyme, of O-acetylserine sulfhydrylase isolated from Salmonella typhimurium., O-acetylserine sulfhydrylase shares the same fold with tryptophan, synthase-beta from Salmonella typhimurium but the sequence identity level, is below 20%. There are some major structural differences: the loops, providing the interface to the alpha-subunit in tryptophan synthase-beta, and two surface helices of tryptophan synthase-beta are missing in, O-acetylserine sulfhydrylase. The hydrophobic channel for indole transport, from the alpha to the beta active site of tryptophan synthase-beta is, not, unexpectedly, also absent in O-acetylserine sulfhydrylase. The dimer, interface, on the other hand, is more or less conserved in the two, enzymes. The active site cleft of O-acetylserine sulfhydrylase is wider, and therefore more exposed to the solvent. A possible binding site for the, substrate O-acetylserine is discussed.
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The last step in cysteine biosynthesis in enteric bacteria is catalyzed by the pyridoxal 5'-phosphate-dependent enzyme O-acetylserine sulfhydrylase. Here we report the crystal structure at 2.2 A resolution of the A-isozyme of O-acetylserine sulfhydrylase isolated from Salmonella typhimurium. O-acetylserine sulfhydrylase shares the same fold with tryptophan synthase-beta from Salmonella typhimurium but the sequence identity level is below 20%. There are some major structural differences: the loops providing the interface to the alpha-subunit in tryptophan synthase-beta and two surface helices of tryptophan synthase-beta are missing in O-acetylserine sulfhydrylase. The hydrophobic channel for indole transport from the alpha to the beta active site of tryptophan synthase-beta is, not unexpectedly, also absent in O-acetylserine sulfhydrylase. The dimer interface, on the other hand, is more or less conserved in the two enzymes. The active site cleft of O-acetylserine sulfhydrylase is wider and therefore more exposed to the solvent. A possible binding site for the substrate O-acetylserine is discussed.
==About this Structure==
==About this Structure==
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1OAS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Salmonella_typhimurium Salmonella typhimurium] with PLP as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Cysteine_synthase Cysteine synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.47 2.5.1.47] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OAS OCA].
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1OAS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Salmonella_typhimurium Salmonella typhimurium] with <scene name='pdbligand=PLP:'>PLP</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Cysteine_synthase Cysteine synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.47 2.5.1.47] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1OAS OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Burkhard, P.]]
[[Category: Burkhard, P.]]
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[[Category: Cook, P.F.]]
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[[Category: Cook, P F.]]
[[Category: Hohenester, E.]]
[[Category: Hohenester, E.]]
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[[Category: Jansonius, J.N.]]
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[[Category: Jansonius, J N.]]
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[[Category: Rao, G.S.J.]]
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[[Category: Rao, G S.J.]]
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[[Category: Schnackerz, K.D.]]
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[[Category: Schnackerz, K D.]]
[[Category: PLP]]
[[Category: PLP]]
[[Category: beta replacement enzyme]]
[[Category: beta replacement enzyme]]
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[[Category: plp dependent enzyme]]
[[Category: plp dependent enzyme]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 22:53:33 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:15:28 2008''

Revision as of 12:15, 21 February 2008


1oas, resolution 2.200Å

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O-ACETYLSERINE SULFHYDRYLASE FROM SALMONELLA TYPHIMURIUM

Overview

The last step in cysteine biosynthesis in enteric bacteria is catalyzed by the pyridoxal 5'-phosphate-dependent enzyme O-acetylserine sulfhydrylase. Here we report the crystal structure at 2.2 A resolution of the A-isozyme of O-acetylserine sulfhydrylase isolated from Salmonella typhimurium. O-acetylserine sulfhydrylase shares the same fold with tryptophan synthase-beta from Salmonella typhimurium but the sequence identity level is below 20%. There are some major structural differences: the loops providing the interface to the alpha-subunit in tryptophan synthase-beta and two surface helices of tryptophan synthase-beta are missing in O-acetylserine sulfhydrylase. The hydrophobic channel for indole transport from the alpha to the beta active site of tryptophan synthase-beta is, not unexpectedly, also absent in O-acetylserine sulfhydrylase. The dimer interface, on the other hand, is more or less conserved in the two enzymes. The active site cleft of O-acetylserine sulfhydrylase is wider and therefore more exposed to the solvent. A possible binding site for the substrate O-acetylserine is discussed.

About this Structure

1OAS is a Single protein structure of sequence from Salmonella typhimurium with as ligand. Active as Cysteine synthase, with EC number 2.5.1.47 Full crystallographic information is available from OCA.

Reference

Three-dimensional structure of O-acetylserine sulfhydrylase from Salmonella typhimurium., Burkhard P, Rao GS, Hohenester E, Schnackerz KD, Cook PF, Jansonius JN, J Mol Biol. 1998;283(1):121-33. PMID:9761678

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