2mj7

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'''Unreleased structure'''
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{{STRUCTURE_2mj7| PDB=2mj7 | SCENE= }}
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===Solution NMR structure of beta-adaptin appendage domain of human adaptor protein complex 4 subunit beta, Northeast Structural Genomics Consortium (NESG) Target HR8998C===
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The entry 2mj7 is ON HOLD
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==Disease==
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[[http://www.uniprot.org/uniprot/AP4B1_HUMAN AP4B1_HUMAN]] Severe intellectual deficit and progressive spastic paraplegia. The disease is caused by mutations affecting the gene represented in this entry.
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Authors: Eletsky, A., Rothshteyn, D.J., Pederson, K., Shastry, R., Maglaqui, M., Janjua, H., Xiao, R., Everett, J.K., Montelione, G.T., Prestegard, J.H., Szyperski, T., Northeast Structural Genomics Consortium (NESG)
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==Function==
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[[http://www.uniprot.org/uniprot/AP4B1_HUMAN AP4B1_HUMAN]] Subunit of novel type of clathrin- or non-clathrin-associated protein coat involved in targeting proteins from the trans-Golgi network (TGN) to the endosomal-lysosomal system.
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Description: Solution NMR structure of beta-adaptin appendage domain of human adaptor protein complex 4 subunit beta, Northeast Structural Genomics Consortium (NESG) Target HR8998C
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==About this Structure==
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[[2mj7]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MJ7 OCA].
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[[Category: Eletsky, A.]]
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[[Category: Everett, J K.]]
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[[Category: Janjua, H.]]
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[[Category: Maglaqui, M.]]
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[[Category: Montelione, G T.]]
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[[Category: NESG, Northeast Structural Genomics Consortium.]]
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[[Category: Pederson, K.]]
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[[Category: Prestegard, J H.]]
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[[Category: Rotshteyn, D J.]]
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[[Category: Shastry, R.]]
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[[Category: Szyperski, T.]]
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[[Category: Xiao, R.]]
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[[Category: Nesg]]
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[[Category: Northeast structural genomics consortium]]
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[[Category: Protein structure initiative]]
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[[Category: Psi-biology]]
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[[Category: Structural genomic]]
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[[Category: Transport protein]]

Revision as of 07:42, 29 January 2014

Template:STRUCTURE 2mj7

Contents

Solution NMR structure of beta-adaptin appendage domain of human adaptor protein complex 4 subunit beta, Northeast Structural Genomics Consortium (NESG) Target HR8998C

Disease

[AP4B1_HUMAN] Severe intellectual deficit and progressive spastic paraplegia. The disease is caused by mutations affecting the gene represented in this entry.

Function

[AP4B1_HUMAN] Subunit of novel type of clathrin- or non-clathrin-associated protein coat involved in targeting proteins from the trans-Golgi network (TGN) to the endosomal-lysosomal system.

About this Structure

2mj7 is a 1 chain structure. Full experimental information is available from OCA.

Proteopedia Page Contributors and Editors (what is this?)

OCA

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