2obv: Difference between revisions

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|PDB= 2obv |SIZE=350|CAPTION= <scene name='initialview01'>2obv</scene>, resolution 2.05&Aring;
|PDB= 2obv |SIZE=350|CAPTION= <scene name='initialview01'>2obv</scene>, resolution 2.05&Aring;
|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene> and <scene name='pdbligand=PG4:TETRAETHYLENE GLYCOL'>PG4</scene>
|LIGAND= <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=PG4:TETRAETHYLENE+GLYCOL'>PG4</scene>, <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/Methionine_adenosyltransferase Methionine adenosyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.6 2.5.1.6]  
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Methionine_adenosyltransferase Methionine adenosyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.6 2.5.1.6] </span>
|GENE= MAT1A, AMS1, MATA1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= MAT1A, AMS1, MATA1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|DOMAIN=
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2obv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2obv OCA], [http://www.ebi.ac.uk/pdbsum/2obv PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2obv RCSB]</span>
}}
}}


'''Crystal structure of the human S-adenosylmethionine synthetase 1 in complex with the product'''
'''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:[[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: Turnbull, A.]]
[[Category: Turnbull, A.]]
[[Category: Weigelt, J.]]
[[Category: Weigelt, J.]]
[[Category: NA]]
[[Category: PG4]]
[[Category: SAM]]
[[Category: sgc]]
[[Category: sgc]]
[[Category: structural genomic]]
[[Category: structural genomic]]
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[[Category: synthetase]]
[[Category: synthetase]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 17:57:38 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:15:32 2008''

Revision as of 01:15, 31 March 2008

File:2obv.gif


Drag the structure with the mouse to rotate
2obv, resolution 2.05Å
Ligands: NA, PG4, SAM
Gene: MAT1A, AMS1, MATA1 (Homo sapiens)
Activity: Methionine adenosyltransferase, with EC number 2.5.1.6
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Crystal structure of the human S-adenosylmethionine synthetase 1 in complex with the product


About this Structure

2OBV is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Mar 31 04:15:32 2008

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