2d1i
From Proteopedia
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- | [[Image:2d1i.gif|left|200px]] | + | [[Image:2d1i.gif|left|200px]] |
- | + | ||
- | '''Structure of human Atg4b''' | + | {{Structure |
+ | |PDB= 2d1i |SIZE=350|CAPTION= <scene name='initialview01'>2d1i</scene>, resolution 2.00Å | ||
+ | |SITE= | ||
+ | |LIGAND= | ||
+ | |ACTIVITY= | ||
+ | |GENE= | ||
+ | }} | ||
+ | |||
+ | '''Structure of human Atg4b''' | ||
+ | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
- | 2D1I is a [ | + | 2D1I is a [[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== | ||
- | 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:[http:// | + | 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:[http://www.ncbi.nlm.nih.gov/pubmed/16325851 16325851] |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: cysteine protease]] | [[Category: cysteine protease]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:22:14 2008'' |
Revision as of 14:22, 20 March 2008
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, resolution 2.00Å | |||||||
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Coordinates: | save as pdb, mmCIF, xml |
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
Page seeded by OCA on Thu Mar 20 16:22:14 2008
Categories: Homo sapiens | Single protein | Komatsu, M. | Kominami, E. | Kumanomidou, T. | Mizushima, T. | Sou, Y S. | Suzuki, A. | Tanaka, K. | Tanida, I. | Ueno, T. | Yamane, T. | Apg | Atg | Autophagy | Cysteine protease