1e9c

Revision as of 19:22, 29 October 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="1e9c" size="450" color="white" frame="true" align="right" spinBox="true" caption="1e9c, resolution 1.6Å" /> '''MUTANT HUMAN THYMIDY...)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

MUTANT HUMAN THYMIDYLATE KINASE COMPLEXED WITH TMP AND APPNP

File:1e9c.gif


1e9c, resolution 1.6Å

Drag the structure with the mouse to rotate

OverviewOverview

The 60-fold reduced phosphorylation rate of azidothymidine (AZT), monophosphate (AZTMP), the partially activated AZT metabolite, by human, thymidylate kinase (TMPK) severely limits the efficacy of this anti-HIV, prodrug. Crystal structures of different TMPK nucleotide complexes, indicate that steric hindrance by the azido group of AZTMP prevents, formation of the catalytically active closed conformation of the P-loop of, TMPK. The F105Y mutant and a chimeric mutant that contains sequences of, the human and Escherichia coli enzyme phosphorylate AZTMP 20-fold faster, than the wild-type enzyme. The structural basis of the increased activity, is assigned to stabilization of the closed P-loop conformation.

About this StructureAbout this Structure

1E9C is a [Single protein] structure of sequence from [Homo sapiens] with MG, TMP and ADP as [ligands]. Active as [[1]], with EC number [2.7.4.9]. Full crystallographic information is available from [OCA].

ReferenceReference

Potentiating AZT activation: structures of wild-type and mutant human thymidylate kinase suggest reasons for the mutants' improved kinetics with the HIV prodrug metabolite AZTMP., Ostermann N, Lavie A, Padiyar S, Brundiers R, Veit T, Reinstein J, Goody RS, Konrad M, Schlichting I, J Mol Biol. 2000 Nov 17;304(1):43-53. PMID:11071809

Page seeded by OCA on Mon Oct 29 18:26:50 2007

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA