Cloning and characterization of heat shock protein DnaJ homologues from Plasmodium falciparum and comparison with ring infected erythrocyte surface antigen1Note: Nucleotide sequence data reported in this paper is available in the DDJB data bases under the accession number D85686.1

[1]  K. Wüthrich,et al.  NMR structure of the J-domain and the Gly/Phe-rich region of the Escherichia coli DnaJ chaperone. , 1996, Journal of molecular biology.

[2]  M. Douglas,et al.  A Conserved HPD Sequence of the J-domain Is Necessary for YDJ1 Stimulation of Hsp70 ATPase Activity at a Site Distinct from Substrate Binding (*) , 1996, The Journal of Biological Chemistry.

[3]  W. Neupert,et al.  Role of the mitochondrial DnaJ homologue, Mdj1p, in the prevention of heat‐induced protein aggregation , 1996, FEBS letters.

[4]  K. Arndt,et al.  Transcriptional Regulation of the Yeast DnaJ Homologue SIS1(*) , 1996, The Journal of Biological Chemistry.

[5]  F. Hartl,et al.  A zinc finger‐like domain of the molecular chaperone DnaJ is involved in binding to denatured protein substrates. , 1996, The EMBO journal.

[6]  C. Georgopoulos,et al.  The Conserved G/F Motif of the DnaJ Chaperone Is Necessary for the Activation of the Substrate Binding Properties of the DnaK Chaperone (*) , 1995, The Journal of Biological Chemistry.

[7]  A. Scherf,et al.  Karyotype analysis of virulent Plasmodium falciparum strains propagated in Saimiri sciureus: strain adaptation leads to deletion of the RESA gene , 1995, Infection and immunity.

[8]  K. Wüthrich,et al.  NMR structure determination of the Escherichia coli DnaJ molecular chaperone: secondary structure and backbone fold of the N-terminal region (residues 2-108) containing the highly conserved J domain. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[9]  M. Foley,et al.  Plasmodium falciparum: mapping the membrane-binding domain in the ring-infected erythrocyte surface antigen. , 1994, Experimental parasitology.

[10]  W. Neupert,et al.  XDJ1, a gene encoding a novel non-essential DnaJ homologue from Saccharomyces cerevisiae. , 1994, Gene.

[11]  Mukai Hideyuki,et al.  Isolation and characterization of CAJ1, a novel yeast homolog of dnaJ , 1994 .

[12]  J. Inselburg,et al.  Establishing a physical map of chromosome No. 4 of Plasmodium falciparum. , 1994, Molecular and biochemical parasitology.

[13]  B. Barrell,et al.  Mdj1p, a novel chaperone of the DnaJ family, is involved in mitochondrial biogenesis and protein folding , 1994, Cell.

[14]  T. Langer,et al.  DnaJ-like proteins: molecular chaperones and specific regulators of Hsp70. , 1994, Trends in biochemical sciences.

[15]  C. Georgopoulos,et al.  The NH2-terminal 108 amino acids of the Escherichia coli DnaJ protein stimulate the ATPase activity of DnaK and are sufficient for lambda replication. , 1994, The Journal of biological chemistry.

[16]  T. Mizuno,et al.  An analogue of the DnaJ molecular chaperone in Escherichia coli. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[17]  G. Reddy,et al.  Gene sequence tags from Plasmodium falciparum genomic DNA fragments prepared by the "genease" activity of mung bean nuclease. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[18]  T. Fandeur,et al.  The RESA-2 gene of Plasmodium falciparum is transcribed in several independent isolates , 1993, Infection and immunity.

[19]  O. Mercereau‐Puijalon,et al.  The virulent Saimiri-adapted Palo Alto strain of Plasmodium falciparum does not express the ring-infected erythrocyte surface antigen. , 1993, Molecular and biochemical parasitology.

[20]  P. Silver,et al.  Eukaryotic DnaJ homologs and the specificity of Hsp70 activity , 1993, Cell.

[21]  K. Arndt,et al.  The yeast SIS1 protein, a DnaJ homolog, is required for the initiation of translation , 1993, Cell.

[22]  D. Cyr,et al.  Eukaryotic homologues of Escherichia coli dnaJ: a diverse protein family that functions with hsp70 stress proteins. , 1993, Molecular biology of the cell.

[23]  D. Cyr,et al.  Regulation of Hsp70 function by a eukaryotic DnaJ homolog. , 1992, The Journal of biological chemistry.

[24]  A. Rich,et al.  Zuotin, a putative Z‐DNA binding protein in Saccharomyces cerevisiae. , 1992, The EMBO journal.

[25]  A. Cowman,et al.  Cloning and analysis of the RESA-2 gene: a DNA homologue of the ring-infected erythrocyte surface antigen gene of Plasmodium falciparum. , 1992, Molecular and biochemical parasitology.

[26]  C. Sander,et al.  A module of the DnaJ heat shock proteins found in malaria parasites. , 1992, Trends in biochemical sciences.

[27]  Nirbhay Kumar,et al.  Induction and localization of Plasmodium falciparum stress proteins related to the heat shock protein 70 family. , 1991, Molecular and biochemical parasitology.

[28]  A. Caplan,et al.  Characterization of YDJ1: a yeast homologue of the bacterial dnaJ protein , 1991, The Journal of cell biology.

[29]  K. Arndt,et al.  Characterization of SIS1, a Saccharomyces cerevisiae homologue of bacterial dnaJ proteins , 1991, The Journal of cell biology.

[30]  R. Udomsangpetch,et al.  Plasmodium falciparum: analysis of the interaction of antigen Pf155/RESA with the erythrocyte membrane. , 1991, Experimental parasitology.

[31]  M. Foley,et al.  The ring-infected erythrocyte surface antigen of Plasmodium falciparum associates with spectrin in the erythrocyte membrane. , 1991, Molecular and biochemical parasitology.

[32]  P. Silver,et al.  A homologue of the bacterial heat-shock gene DnaJ that alters protein sorting in yeast , 1991, Nature.

[33]  A. Sjölander,et al.  Pf155/RESA antigen is localized in dense granules of Plasmodium falciparum merozoites. , 1990, Experimental parasitology.

[34]  W. B. Li,et al.  Plasmodium falciparum: analysis of chromosomes separated by contour-clamped homogenous electric fields. , 1990, Experimental parasitology.

[35]  J. Ravetch,et al.  A and T homopolymeric stretches mediate a DNA inversion in Plasmodium falciparum which results in loss of gene expression , 1990, Molecular and cellular biology.

[36]  R. Schekman,et al.  Multiple genes are required for proper insertion of secretory proteins into the endoplasmic reticulum in yeast , 1989, The Journal of cell biology.

[37]  P. Silver,et al.  A yeast gene important for protein assembly into the endoplasmic reticulum and the nucleus has homology to DnaJ, an Escherichia coli heat shock protein , 1989, The Journal of cell biology.

[38]  A. Cowman,et al.  Expression of the RESA gene in Plasmodium falciparum isolate FCR3 is prevented by a subtelomeric deletion , 1989, Molecular and cellular biology.

[39]  F. Hartl,et al.  Molecular chaperone functions of heat-shock proteins. , 1993, Annual review of biochemistry.

[40]  M. Foley,et al.  The ring-infected erythrocyte surface antigen protein of Plasmodium falciparum is phosphorylated upon association with the host cell membrane. , 1990, Molecular and biochemical parasitology.

[41]  S. Lindquist,et al.  The heat-shock proteins. , 1988, Annual review of genetics.

[42]  S. Lindquist The heat-shock response. , 1986, Annual review of biochemistry.