[Reconstruction of spatial structure of plant protein phosphatase type-1 and -2A in complex with okadaic acid]

Tsitol Genet. 2011 May-Jun;45(3):26-34.
[Article in Russian]

Abstract

The homology modeling, based on known temple structures of Homo sapiens protein phosphatase type-1 and -2A was implemented. The spatial structures of the human protein phosphatases and their plant homologs from Arabidopsis thaliana was predicted. The quality of models was confirmed by conformational analysis and root mean square deviations. The sites of okadaic acid binding in molecules of plant protein phosphatases (type-1 and -2A) were proved by the data of comparative analysis and molecular dynamics.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Arabidopsis / drug effects
  • Arabidopsis / enzymology
  • Arabidopsis Proteins / antagonists & inhibitors
  • Arabidopsis Proteins / chemistry*
  • Catalytic Domain
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Okadaic Acid / chemistry
  • Okadaic Acid / pharmacology*
  • Protein Binding
  • Protein Phosphatase 1 / antagonists & inhibitors
  • Protein Phosphatase 1 / chemistry*
  • Protein Phosphatase 2 / antagonists & inhibitors
  • Protein Phosphatase 2 / chemistry*
  • Sequence Alignment
  • Sequence Homology, Amino Acid

Substances

  • Arabidopsis Proteins
  • Enzyme Inhibitors
  • Okadaic Acid
  • Protein Phosphatase 1
  • Protein Phosphatase 2