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3dyd
From Proteopedia
(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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| - | + | {{Seed}} | |
| + | [[Image:3dyd.png|left|200px]] | ||
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3dyd", creates the "Structure Box" on the page. | ||
| + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
| + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
| + | or leave the SCENE parameter empty for the default display. | ||
| + | --> | ||
| + | {{STRUCTURE_3dyd| PDB=3dyd | SCENE= }} | ||
| - | + | ===Human Tyrosine Aminotransferase=== | |
| - | Description: Human Tyrosine Aminotransferase | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | ==Disease== |
| + | Known disease associated with this structure: Tyrosinemia, type II OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276600 276600]] | ||
| + | |||
| + | ==About this Structure== | ||
| + | 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]. | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Tyrosine transaminase]] | ||
| + | [[Category: Andersson, J.]] | ||
| + | [[Category: Arrowsmith, C H.]] | ||
| + | [[Category: Berg, S Van Den.]] | ||
| + | [[Category: Berglund, H.]] | ||
| + | [[Category: Collins, R.]] | ||
| + | [[Category: Dahlgren, L G.]] | ||
| + | [[Category: Edwards, A M.]] | ||
| + | [[Category: Flodin, S.]] | ||
| + | [[Category: Flores, A.]] | ||
| + | [[Category: Graslund, S.]] | ||
| + | [[Category: Hammarstrom, M.]] | ||
| + | [[Category: Johansson, A.]] | ||
| + | [[Category: Johansson, I.]] | ||
| + | [[Category: Karlberg, T.]] | ||
| + | [[Category: Kotenyova, T.]] | ||
| + | [[Category: Lehtio, L.]] | ||
| + | [[Category: Moche, M.]] | ||
| + | [[Category: Nilsson, M E.]] | ||
| + | [[Category: Nordlund, P.]] | ||
| + | [[Category: Nyman, T.]] | ||
| + | [[Category: Olesen, K.]] | ||
| + | [[Category: Persson, C.]] | ||
| + | [[Category: SGC, Structural Genomics Consortium.]] | ||
| + | [[Category: Sagemark, J.]] | ||
| + | [[Category: Schuler, H.]] | ||
| + | [[Category: Thorsell, A G.]] | ||
| + | [[Category: Tresaugues, L.]] | ||
| + | [[Category: Weigelt, J.]] | ||
| + | [[Category: Welin, M.]] | ||
| + | [[Category: Wikstrom, M.]] | ||
| + | [[Category: Wisniewska, M.]] | ||
| + | [[Category: Aminotransferase]] | ||
| + | [[Category: Disease mutation]] | ||
| + | [[Category: Phenylalanine catabolism]] | ||
| + | [[Category: Plp]] | ||
| + | [[Category: Pyridoxal phosphate]] | ||
| + | [[Category: Sgc]] | ||
| + | [[Category: Structural genomic]] | ||
| + | [[Category: Structural genomics consortium]] | ||
| + | [[Category: Transferase]] | ||
| + | [[Category: Tyrosine]] | ||
| + | [[Category: Tyrosine catabolism]] | ||
| + | |||
| + | ''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
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
Categories: Homo sapiens | Tyrosine transaminase | Andersson, J. | Arrowsmith, C H. | Berg, S Van Den. | Berglund, H. | Collins, R. | Dahlgren, L G. | Edwards, A M. | Flodin, S. | Flores, A. | Graslund, S. | Hammarstrom, M. | Johansson, A. | Johansson, I. | Karlberg, T. | Kotenyova, T. | Lehtio, L. | Moche, M. | Nilsson, M E. | Nordlund, P. | Nyman, T. | Olesen, K. | Persson, C. | SGC, Structural Genomics Consortium. | Sagemark, J. | Schuler, H. | Thorsell, A G. | Tresaugues, L. | Weigelt, J. | Welin, M. | Wikstrom, M. | Wisniewska, M. | Aminotransferase | Disease mutation | Phenylalanine catabolism | Plp | Pyridoxal phosphate | Sgc | Structural genomic | Structural genomics consortium | Transferase | Tyrosine | Tyrosine catabolism
