3dyd | pdb_00003dyd
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
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
