Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
1996-11-13
pubmed:abstractText
Plasmodium falciparum is the major causative agent of malaria, a disease of worldwide importance. Resistance to current drugs such as chloroquine and mefloquine is spreading at an alarming rate, and our antimalarial armamentarium is almost depleted. The malarial parasite encodes two homologous aspartic proteases, plasmepsins I and II, which are essential components of its hemoglobin-degradation pathway and are novel targets for antimalarial drug development. We have determined the crystal structure of recombinant plasmepsin II complexed with pepstatin A. This represents the first reported crystal structure of a protein from P. falciparum. The crystals contain molecules in two different conformations, revealing a remarkable degree of interdomain flexibility of the enzyme. The structure was used to design a series of selective low molecular weight compounds that inhibit both plasmepsin II and the growth of P. falciparum in culture.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-15275326, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-1939639, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-2106161, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-2194475, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-2217165, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-2493678, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-2676515, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-4912600, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-502865, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-6035483, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-7451499, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-7925966, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-8061223, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-8163662, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-8204609, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-8313875, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-8361993, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-8393577, http://linkedlifedata.com/resource/pubmed/commentcorrection/8816746-8540317
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
17
pubmed:volume
93
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
10034-9
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:8816746-Amino Acid Sequence, pubmed-meshheading:8816746-Animals, pubmed-meshheading:8816746-Aspartic Acid Endopeptidases, pubmed-meshheading:8816746-Cathepsin D, pubmed-meshheading:8816746-Cloning, Molecular, pubmed-meshheading:8816746-Conserved Sequence, pubmed-meshheading:8816746-Crystallography, X-Ray, pubmed-meshheading:8816746-Escherichia coli, pubmed-meshheading:8816746-Hemoglobins, pubmed-meshheading:8816746-Humans, pubmed-meshheading:8816746-Molecular Conformation, pubmed-meshheading:8816746-Molecular Sequence Data, pubmed-meshheading:8816746-Plasmodium falciparum, pubmed-meshheading:8816746-Protease Inhibitors, pubmed-meshheading:8816746-Protein Structure, Secondary, pubmed-meshheading:8816746-Protozoan Proteins, pubmed-meshheading:8816746-Recombinant Proteins, pubmed-meshheading:8816746-Sequence Homology, Amino Acid, pubmed-meshheading:8816746-Substrate Specificity
pubmed:year
1996
pubmed:articleTitle
Structure and inhibition of plasmepsin II, a hemoglobin-degrading enzyme from Plasmodium falciparum.
pubmed:affiliation
Structural Biochemistry Program, National Cancer Institute/SAIC, Frederick, MD 21702, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't