2obv
From Proteopedia
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caption="2obv, resolution 2.05Å" /> | caption="2obv, resolution 2.05Å" /> | ||
'''Crystal structure of the human S-adenosylmethionine synthetase 1 in complex with the product'''<br /> | '''Crystal structure of the human S-adenosylmethionine synthetase 1 in complex with the product'''<br /> | ||
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| + | ==Disease== | ||
| + | Known diseases associated with this structure: Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250850 250850]], Methionine adenosyltransferase deficiency, autosomal recessive OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250850 250850]] | ||
==About this Structure== | ==About this Structure== | ||
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[[Category: Methionine adenosyltransferase]] | [[Category: Methionine adenosyltransferase]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
| - | [[Category: Arrowsmith, C | + | [[Category: Arrowsmith, C H.]] |
[[Category: Cooper, C.]] | [[Category: Cooper, C.]] | ||
| - | [[Category: Delft, F | + | [[Category: Delft, F Von.]] |
[[Category: Edwards, A.]] | [[Category: Edwards, A.]] | ||
[[Category: Hozjan, V.]] | [[Category: Hozjan, V.]] | ||
| - | [[Category: Kavanagh, K | + | [[Category: Kavanagh, K L.]] |
[[Category: Oppermann, U.]] | [[Category: Oppermann, U.]] | ||
| - | [[Category: Pilka, E | + | [[Category: Pilka, E S.]] |
| - | [[Category: SGC, Structural | + | [[Category: SGC, Structural Genomics Consortium.]] |
[[Category: Shafqat, N.]] | [[Category: Shafqat, N.]] | ||
[[Category: Sundstrom, M.]] | [[Category: Sundstrom, M.]] | ||
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[[Category: synthetase]] | [[Category: synthetase]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:16:40 2008'' |
Revision as of 16:16, 21 February 2008
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Crystal structure of the human S-adenosylmethionine synthetase 1 in complex with the product
Disease
Known diseases associated with this structure: Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency OMIM:[250850], Methionine adenosyltransferase deficiency, autosomal recessive OMIM:[250850]
About this Structure
2OBV is a Single protein structure of sequence from Homo sapiens with , and as ligands. Active as Methionine adenosyltransferase, with EC number 2.5.1.6 Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Feb 21 18:16:40 2008
Categories: Homo sapiens | Methionine adenosyltransferase | Single protein | Arrowsmith, C H. | Cooper, C. | Delft, F Von. | Edwards, A. | Hozjan, V. | Kavanagh, K L. | Oppermann, U. | Pilka, E S. | SGC, Structural Genomics Consortium. | Shafqat, N. | Sundstrom, M. | Turnbull, A. | Weigelt, J. | NA | PG4 | SAM | Sgc | Structural genomics | Structural genomics consortium | Synthetase
