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1mlv

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(New page: 200px<br /><applet load="1mlv" size="450" color="white" frame="true" align="right" spinBox="true" caption="1mlv, resolution 2.60&Aring;" /> '''Structure and Cataly...)
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[[Image:1mlv.gif|left|200px]]<br /><applet load="1mlv" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1mlv, resolution 2.60&Aring;" />
caption="1mlv, resolution 2.60&Aring;" />
'''Structure and Catalytic Mechanism of a SET Domain Protein Methyltransferase'''<br />
'''Structure and Catalytic Mechanism of a SET Domain Protein Methyltransferase'''<br />
==Overview==
==Overview==
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Protein lysine methylation by SET domain enzymes regulates chromatin, structure, gene silencing, transcriptional activation, plant metabolism, and other processes. The 2.6 A resolution structure of Rubisco large, subunit methyltransferase in a pseudo-bisubstrate complex with, S-adenosylhomocysteine and a HEPES ion reveals an all-beta architecture, for the SET domain embedded within a larger alpha-helical enzyme fold., Conserved regions of the SET domain bind S-adenosylmethionine and, substrate lysine at two sites connected by a pore. We propose that methyl, transfer is catalyzed by a conserved Tyr at a narrow pore connecting the, sites. The cofactor enters by a "back door" on the opposite side of the, enzyme from substrate, promoting highly specific protein recognition and, allowing addition of multiple methyl groups.
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Protein lysine methylation by SET domain enzymes regulates chromatin structure, gene silencing, transcriptional activation, plant metabolism, and other processes. The 2.6 A resolution structure of Rubisco large subunit methyltransferase in a pseudo-bisubstrate complex with S-adenosylhomocysteine and a HEPES ion reveals an all-beta architecture for the SET domain embedded within a larger alpha-helical enzyme fold. Conserved regions of the SET domain bind S-adenosylmethionine and substrate lysine at two sites connected by a pore. We propose that methyl transfer is catalyzed by a conserved Tyr at a narrow pore connecting the sites. The cofactor enters by a "back door" on the opposite side of the enzyme from substrate, promoting highly specific protein recognition and allowing addition of multiple methyl groups.
==About this Structure==
==About this Structure==
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1MLV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pisum_sativum Pisum sativum] with SAH and EPE as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/[Ribulose-bisphosphate_carboxylase]-lysine_N-methyltransferase [Ribulose-bisphosphate carboxylase]-lysine N-methyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.1.1.127 2.1.1.127] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1MLV OCA].
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1MLV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pisum_sativum Pisum sativum] with <scene name='pdbligand=SAH:'>SAH</scene> and <scene name='pdbligand=EPE:'>EPE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/[Ribulose-bisphosphate_carboxylase]-lysine_N-methyltransferase [Ribulose-bisphosphate carboxylase]-lysine N-methyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.1.1.127 2.1.1.127] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MLV OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: [Ribulose-bisphosphate carboxylase]-lysine N-methyltransferase]]
[[Category: [Ribulose-bisphosphate carboxylase]-lysine N-methyltransferase]]
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[[Category: Beach, B.M.]]
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[[Category: Beach, B M.]]
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[[Category: Dirk, L.M.A.]]
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[[Category: Dirk, L M.A.]]
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[[Category: Houtz, R.L.]]
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[[Category: Houtz, R L.]]
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[[Category: Hurley, J.H.]]
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[[Category: Hurley, J H.]]
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[[Category: Trievel, R.C.]]
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[[Category: Trievel, R C.]]
[[Category: EPE]]
[[Category: EPE]]
[[Category: SAH]]
[[Category: SAH]]
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[[Category: set domain]]
[[Category: set domain]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 21:31:00 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:56:31 2008''

Revision as of 11:56, 21 February 2008


1mlv, resolution 2.60Å

Drag the structure with the mouse to rotate

Structure and Catalytic Mechanism of a SET Domain Protein Methyltransferase

Overview

Protein lysine methylation by SET domain enzymes regulates chromatin structure, gene silencing, transcriptional activation, plant metabolism, and other processes. The 2.6 A resolution structure of Rubisco large subunit methyltransferase in a pseudo-bisubstrate complex with S-adenosylhomocysteine and a HEPES ion reveals an all-beta architecture for the SET domain embedded within a larger alpha-helical enzyme fold. Conserved regions of the SET domain bind S-adenosylmethionine and substrate lysine at two sites connected by a pore. We propose that methyl transfer is catalyzed by a conserved Tyr at a narrow pore connecting the sites. The cofactor enters by a "back door" on the opposite side of the enzyme from substrate, promoting highly specific protein recognition and allowing addition of multiple methyl groups.

About this Structure

1MLV is a Single protein structure of sequence from Pisum sativum with and as ligands. Active as [Ribulose-bisphosphate_carboxylase-lysine_N-methyltransferase [Ribulose-bisphosphate carboxylase]-lysine N-methyltransferase], with EC number 2.1.1.127 Full crystallographic information is available from OCA.

Reference

Structure and catalytic mechanism of a SET domain protein methyltransferase., Trievel RC, Beach BM, Dirk LM, Houtz RL, Hurley JH, Cell. 2002 Oct 4;111(1):91-103. PMID:12372303[[Category: [Ribulose-bisphosphate carboxylase]-lysine N-methyltransferase]]

Page seeded by OCA on Thu Feb 21 13:56:31 2008

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