2d1i

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(New page: 200px<br /> <applet load="2d1i" size="450" color="white" frame="true" align="right" spinBox="true" caption="2d1i, resolution 2.00&Aring;" /> '''Structure of human ...)
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'''Structure of human Atg4b'''<br />
'''Structure of human Atg4b'''<br />
==Overview==
==Overview==
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Autophagy is an evolutionarily conserved pathway in which the cytoplasm, and organelles are engulfed within double-membrane vesicles, termed, autophagosomes, for the turnover and recycling of these cellular, constituents. The yeast Atg8 and its human orthologs, such as LC3 and, GABARAP, have a unique feature as they conjugate covalently to, phospholipids, differing from ubiquitin and other ubiquitin-like modifiers, that attach only to protein substrates. The lipidated Atg8 and LC3, localize to autophagosomal membranes and play indispensable roles for, maturation of autophagosomes. Upon completion of autophagosome formation, some populations of lipidated Atg8 and LC3 are delipidated for recycling., Atg4b, a specific protease for LC3 and GABARAP, catalyzes the processing, reaction of LC3 and GABARAP precursors to mature forms and de-conjugating, reaction of the modifiers from phospholipids. Atg4b is a unique enzyme, whose primary structure differs from that of any other proteases that, function as processing and/or de-conjugating enzymes of ubiquitin and, ubiquitin-like modifiers. However, the tertiary structures of the, substrates considerably resemble that of ubiquitin except for the, N-terminal additional domain. Here we determined the crystal structure of, human Atg4b by X-ray crystallography at 2.0 A resolution, and show that, Atg4b is a cysteine protease whose active catalytic triad site consists of, Cys74, His280 and Asp278. The structure is comprised of a left lobe and a, small right lobe, designated the "protease domain" and the "auxiliary, domain", respectively. Whereas the protease domain structure of Atg4b, matches that of papain superfamily cysteine proteinases, the auxiliary, domain contains a unique structure with yet-unknown function. We propose, that the R229 and W142 residues in Atg4b are specifically essential for, recognition of substrates and catalysis of both precursor processing and, de-conjugation of phospholipids.
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Autophagy is an evolutionarily conserved pathway in which the cytoplasm and organelles are engulfed within double-membrane vesicles, termed autophagosomes, for the turnover and recycling of these cellular constituents. The yeast Atg8 and its human orthologs, such as LC3 and GABARAP, have a unique feature as they conjugate covalently to phospholipids, differing from ubiquitin and other ubiquitin-like modifiers that attach only to protein substrates. The lipidated Atg8 and LC3 localize to autophagosomal membranes and play indispensable roles for maturation of autophagosomes. Upon completion of autophagosome formation, some populations of lipidated Atg8 and LC3 are delipidated for recycling. Atg4b, a specific protease for LC3 and GABARAP, catalyzes the processing reaction of LC3 and GABARAP precursors to mature forms and de-conjugating reaction of the modifiers from phospholipids. Atg4b is a unique enzyme whose primary structure differs from that of any other proteases that function as processing and/or de-conjugating enzymes of ubiquitin and ubiquitin-like modifiers. However, the tertiary structures of the substrates considerably resemble that of ubiquitin except for the N-terminal additional domain. Here we determined the crystal structure of human Atg4b by X-ray crystallography at 2.0 A resolution, and show that Atg4b is a cysteine protease whose active catalytic triad site consists of Cys74, His280 and Asp278. The structure is comprised of a left lobe and a small right lobe, designated the "protease domain" and the "auxiliary domain", respectively. Whereas the protease domain structure of Atg4b matches that of papain superfamily cysteine proteinases, the auxiliary domain contains a unique structure with yet-unknown function. We propose that the R229 and W142 residues in Atg4b are specifically essential for recognition of substrates and catalysis of both precursor processing and de-conjugation of phospholipids.
==About this Structure==
==About this Structure==
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2D1I is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2D1I OCA].
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2D1I is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2D1I OCA].
==Reference==
==Reference==
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[[Category: Kumanomidou, T.]]
[[Category: Kumanomidou, T.]]
[[Category: Mizushima, T.]]
[[Category: Mizushima, T.]]
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[[Category: Sou, Y.S.]]
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[[Category: Sou, Y S.]]
[[Category: Suzuki, A.]]
[[Category: Suzuki, A.]]
[[Category: Tanaka, K.]]
[[Category: Tanaka, K.]]
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[[Category: cysteine protease]]
[[Category: cysteine protease]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 21:25:18 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:54:27 2008''

Revision as of 14:54, 21 February 2008


2d1i, resolution 2.00Å

Drag the structure with the mouse to rotate

Structure of human Atg4b

Overview

Autophagy is an evolutionarily conserved pathway in which the cytoplasm and organelles are engulfed within double-membrane vesicles, termed autophagosomes, for the turnover and recycling of these cellular constituents. The yeast Atg8 and its human orthologs, such as LC3 and GABARAP, have a unique feature as they conjugate covalently to phospholipids, differing from ubiquitin and other ubiquitin-like modifiers that attach only to protein substrates. The lipidated Atg8 and LC3 localize to autophagosomal membranes and play indispensable roles for maturation of autophagosomes. Upon completion of autophagosome formation, some populations of lipidated Atg8 and LC3 are delipidated for recycling. Atg4b, a specific protease for LC3 and GABARAP, catalyzes the processing reaction of LC3 and GABARAP precursors to mature forms and de-conjugating reaction of the modifiers from phospholipids. Atg4b is a unique enzyme whose primary structure differs from that of any other proteases that function as processing and/or de-conjugating enzymes of ubiquitin and ubiquitin-like modifiers. However, the tertiary structures of the substrates considerably resemble that of ubiquitin except for the N-terminal additional domain. Here we determined the crystal structure of human Atg4b by X-ray crystallography at 2.0 A resolution, and show that Atg4b is a cysteine protease whose active catalytic triad site consists of Cys74, His280 and Asp278. The structure is comprised of a left lobe and a small right lobe, designated the "protease domain" and the "auxiliary domain", respectively. Whereas the protease domain structure of Atg4b matches that of papain superfamily cysteine proteinases, the auxiliary domain contains a unique structure with yet-unknown function. We propose that the R229 and W142 residues in Atg4b are specifically essential for recognition of substrates and catalysis of both precursor processing and de-conjugation of phospholipids.

About this Structure

2D1I is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

The crystal structure of human Atg4b, a processing and de-conjugating enzyme for autophagosome-forming modifiers., Kumanomidou T, Mizushima T, Komatsu M, Suzuki A, Tanida I, Sou YS, Ueno T, Kominami E, Tanaka K, Yamane T, J Mol Biol. 2006 Jan 27;355(4):612-8. Epub 2005 Nov 28. PMID:16325851

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