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3dyd
From Proteopedia
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
