1av5: Difference between revisions

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[[Category: protein kinase inhibitor]]
[[Category: protein kinase inhibitor]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 08:43:40 2007''
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 10:42:35 2007''

Revision as of 08:37, 30 October 2007

File:1av5.gif


1av5, resolution 2.0Å

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PKCI-SUBSTRATE ANALOG

Overview

The histidine triad (HIT) protein family is among the most ubiquitous and, highly conserved in nature, but a biological activity has not yet been, identified for any member of the HIT family. Fragile histidine triad, protein (FHIT) and protein kinase C interacting protein (PKCI) were used, in a structure-based approach to elucidate characteristics of in vivo, ligands and reactions. Crystallographic structures of apo, substrate, analog, pentacovalent transition-state analog, and product states of both, enzymes reveal a catalytic mechanism and define substrate characteristics, required for catalysis, thus unifying the HIT family as nucleotidyl, hydrolases, transferases, or both. The approach described here may be, useful in identifying structure-function relations between protein, families ... [(full description)]

About this Structure

1AV5 is a [Single protein] structure of sequence from [Homo sapiens] with AP2 as [ligand]. Structure known Active Sites: AVA, AVB, HNA and HNB. Full crystallographic information is available from [OCA].

Reference

Structure-based analysis of catalysis and substrate definition in the HIT protein family., Lima CD, Klein MG, Hendrickson WA, Science. 1997 Oct 10;278(5336):286-90. PMID:9323207

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