4civ
From Proteopedia
(Difference between revisions)
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- | + | {{STRUCTURE_4civ| PDB=4civ | SCENE= }} | |
+ | ===Crystal structure of Mycobacterium tuberculosis type 2 dehydroquinase in complex with (1R,4R,5R)-1,4,5-trihydroxy-3-hydroxymethylcyclohex-2-ene-1-carboxylic acid=== | ||
+ | {{ABSTRACT_PUBMED_24689821}} | ||
- | + | ==Function== | |
+ | [[http://www.uniprot.org/uniprot/AROQ_MYCTU AROQ_MYCTU]] Catalyzes a trans-dehydration via an enolate intermediate (By similarity).[HAMAP-Rule:MF_00169] | ||
- | + | ==About this Structure== | |
+ | [[4civ]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CIV OCA]. | ||
- | + | ==Reference== | |
+ | <ref group="xtra">PMID:024689821</ref><references group="xtra"/><references/> | ||
+ | [[Category: 3-dehydroquinate dehydratase]] | ||
+ | [[Category: Blanco, B.]] | ||
+ | [[Category: Gonzalez-Bello, C.]] | ||
+ | [[Category: Hawkins, A R.]] | ||
+ | [[Category: Lamb, H.]] | ||
+ | [[Category: Llamas-Saiz, A L.]] | ||
+ | [[Category: Otero, J M.]] | ||
+ | [[Category: Peon, A.]] | ||
+ | [[Category: Sedes, A.]] | ||
+ | [[Category: VanRaaij, M J.]] | ||
+ | [[Category: Bacterial protein]] | ||
+ | [[Category: Inhibitor]] | ||
+ | [[Category: Lyase]] | ||
+ | [[Category: Protein binding]] | ||
+ | [[Category: Shikimis acid pathway]] | ||
+ | [[Category: Substrate specificity]] |
Revision as of 09:42, 16 April 2014
Contents |
Crystal structure of Mycobacterium tuberculosis type 2 dehydroquinase in complex with (1R,4R,5R)-1,4,5-trihydroxy-3-hydroxymethylcyclohex-2-ene-1-carboxylic acid
Template:ABSTRACT PUBMED 24689821
Function
[AROQ_MYCTU] Catalyzes a trans-dehydration via an enolate intermediate (By similarity).[HAMAP-Rule:MF_00169]
About this Structure
4civ is a 1 chain structure. Full crystallographic information is available from OCA.
Reference
- Blanco B, Sedes A, Peon A, Otero JM, Raaij MJ, Thompson P, Hawkins AR, Gonzalez-Bello C. Exploring the Water-Binding Pocket of the Type II Dehydroquinase Enzyme in the Structure-Based Design of Inhibitors. J Med Chem. 2014 Apr 1. PMID:24689821 doi:http://dx.doi.org/10.1021/jm500175z