3dyd

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(New page: '''Unreleased structure''' The entry 3dyd is ON HOLD Authors: Karlberg, T., Moche, M., Andersson, J., Arrowsmith, C.H., Berglund, H., Collins, R., Dahlgren, L.G., Edwards, A.M., Flodin,...)
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'''Unreleased structure'''
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{{Seed}}
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[[Image:3dyd.png|left|200px]]
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The entry 3dyd is ON HOLD
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{{STRUCTURE_3dyd| PDB=3dyd | SCENE= }}
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Authors: Karlberg, T., Moche, M., Andersson, J., Arrowsmith, C.H., Berglund, H., Collins, R., Dahlgren, L.G., Edwards, A.M., Flodin, S., Flores, A., Graslund, S., Hammarstrom, M., Johansson, A., Johansson, I., Kotenyova, T., Lehtio, L., Nilsson, M.E., Nordlund, P.
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===Human Tyrosine Aminotransferase===
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Description: Human Tyrosine Aminotransferase
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 6 12:31:57 2008''
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==Disease==
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Known disease associated with this structure: Tyrosinemia, type II OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276600 276600]]
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==About this Structure==
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3DYD is a 2 chains structure of sequences 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=3DYD OCA].
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[[Category: Homo sapiens]]
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[[Category: Tyrosine transaminase]]
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[[Category: Andersson, J.]]
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[[Category: Arrowsmith, C H.]]
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[[Category: Berg, S Van Den.]]
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[[Category: Berglund, H.]]
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[[Category: Collins, R.]]
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[[Category: Dahlgren, L G.]]
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[[Category: Edwards, A M.]]
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[[Category: Flodin, S.]]
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[[Category: Flores, A.]]
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[[Category: Graslund, S.]]
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[[Category: Hammarstrom, M.]]
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[[Category: Johansson, A.]]
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[[Category: Johansson, I.]]
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[[Category: Karlberg, T.]]
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[[Category: Kotenyova, T.]]
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[[Category: Lehtio, L.]]
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[[Category: Moche, M.]]
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[[Category: Nilsson, M E.]]
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[[Category: Nordlund, P.]]
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[[Category: Nyman, T.]]
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[[Category: Olesen, K.]]
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[[Category: Persson, C.]]
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[[Category: SGC, Structural Genomics Consortium.]]
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[[Category: Sagemark, J.]]
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[[Category: Schuler, H.]]
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[[Category: Thorsell, A G.]]
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[[Category: Tresaugues, L.]]
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[[Category: Weigelt, J.]]
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[[Category: Welin, M.]]
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[[Category: Wikstrom, M.]]
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[[Category: Wisniewska, M.]]
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[[Category: Aminotransferase]]
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[[Category: Disease mutation]]
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[[Category: Phenylalanine catabolism]]
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[[Category: Plp]]
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[[Category: Pyridoxal phosphate]]
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[[Category: Sgc]]
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[[Category: Structural genomic]]
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[[Category: Structural genomics consortium]]
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[[Category: Transferase]]
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[[Category: Tyrosine]]
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[[Category: Tyrosine catabolism]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 06:08:41 2009''

Revision as of 04:08, 18 February 2009

Image:3dyd.png

Template:STRUCTURE 3dyd

Human Tyrosine Aminotransferase

Disease

Known disease associated with this structure: Tyrosinemia, type II OMIM:[276600]

About this Structure

3DYD is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Wed Feb 18 06:08:41 2009

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/3dyd"
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