Projects - Malaria |
Protein |
Description |
Statistics |
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Dihydrofolate reductase
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Dihydrofolate reductase (DHFR) has recently been suggested as a
drug target for Malaria and other parasitic diseases including
toxoplasmosis and cryptosporidiosis - see DDT (2005) 10.2 p121.
There have also been suggestions that DHFR drug resistance may be
a problem.
DHFR has been considered as a cancer target by some scientists.
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| Pictures | J Yuvaniyama et al Nat Struct Biol (2003) 10 p357 | last updated: 06:07 on 30-JAN-05 | ||||||||||||
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Hgprtase
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Hypoxanthine-Guanine Phosphoribosyltransferase (Hgprtase) is important as a source of
purine to Plasmodium falciparum (the parasite which causes Malaria). This is
because the parasite is unable to make its own purine. It has been suggested
that inhibiting this enzyme may be therapeutically valuable. This query is based
on a different crystal structure to 1d6n-q1.
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| Pictures | G K Balendiran et al, Protein Sci (1999) 8.5 p1023 | last updated: 12:07 on 23-SEP-05 | ||||||||||||
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Purine Phosphoribosyl transferase
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Plasmodium falciparum, the parasite associated with Malaria, has to salvage
purine from human cells because it cannot make it. Phosphoribosyl transferase (PRTase)
does so and is a recognised anti-malaria drug target.
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| Pictures | W Shi et al Biochemistry (1999) 38 p 9872 | last updated: 12:10 on 02-AUG-05 | ||||||||||||
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Rab6
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Rab6 is a RAS-like GTP binding protein which plays an important role in Plasmodium falciparum (the parasite that causes Malaria). A selective inhibitor for this GTP binding protein might have therapeutic potential for Malaria. This query gave higher than average number of hits and longer job times for some sample jobs. |
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| Pictures | D Chattopadhyay et al Acta Cryst D (2000) 56.8 p937-44. | last updated: 12:13 on 24-JUN-05 | ||||||||||||
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Hgprtase
|
Hypoxanthine-Guanine Phosphoribosyltransferase (Hgprtase) is important as a source of
purine to Plasmodium falciparum (the parasite which causes Malaria). This is
because the parasite is unable to make its own purine. It has been suggested
that inhibiting this enzyme may be therapeutically valuable.
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| Pictures | G K Balendiran et al, Protein Sci (1999) 8.5 p1023 | last updated: 00:09 on 22-JUL-05 | ||||||||||||
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Dihydrofolate reductase
|
Dihydrofolate reductase (DHFR) has recently been suggested as a
drug target for Malaria and other parasitic diseases including
toxoplasmosis and cryptosporidiosis - see DDT (2005) 10.2 p121.
There have also been suggestions that DHFR drug resistance may be
a problem.
DHFR has been considered as a cancer target by some scientists.
|
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| Pictures | J Yuvaniyama et al Nat Struct Biol (2003) 10 p357 | last updated: 18:15 on 03-APR-05 | ||||||||||||
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Plasmepsin 2
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Plasmodium falciparum (the parasite which causes Malaria) invades erythrocyte cells and consumes the host hemoglobin. Plasmepsin 2 plays a key role digesting the protein and has been recognised as a novel target for anti-malaria drugs. Inhibition of hemoglobin degradation lead to toxic concentrations and parasite death in culture. |
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| Pictures | O A Asojo et al Acta Cryst (2002) d58 p2001 | last updated: 12:22 on 07-DEC-04 | ||||||||||||
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Plasmepsin 2
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Plasmodium falciparum (the parasite which causes Malaria) invades erythrocyte cells and consumes the host hemoglobin. Plasmepsin 2 plays a key role digesting the protein and has been recognised as a novel target for anti-malaria drugs. Inhibition of hemoglobin degradation lead to toxic concentrations and parasite death in culture. This query is based on a different crystal structure to 1lee-q1. We expect jobs for this query to give typical numbers of hits in less time than typical jobs. |
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| Pictures | O A Asojo et al Acta Cryst (2002) d58 p2001 | last updated: 06:13 on 26-JUL-05 | ||||||||||||
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Plasmepsin IV
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Plasmodium falciparum (the parasite which causes Malaria) invades erythrocyte cells and consumes the host hemoglobin. Plasmepsin plays a key role digesting the protein and has been recognised as a novel target for anti-malaria drugs. Inhibition of hemoglobin degradation lead to toxic concentrations and parasite death in culture. This query is based on a different crystal structures to 1lf2-q1 and 1lee-q1. We expect jobs for this query to give more than typical numbers of hits in average times. |
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| Pictures | O A Asojo et al Acta Cryst (2002) d58 p2001 | last updated: 06:00 on 25-JAN-06 | ||||||||||||
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Trisephosphate isomerase
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This enzyme plays a crucial role in the energy cycle of Plasmodium falciparum (the parasite which causes Malaria) and certain other parasitic diseases such as Chagas Disease. Both of these diseases are rare in the Western world. This query gave average number of hits and below average job times for some sample jobs. |
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| Pictures | S Parthasarathy et al, Acta Cryst D (2002) 58.12 p1992-2000 | last updated: 18:17 on 29-MAR-05 | ||||||||||||
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Enoyl Reductase (ENR)
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In Plasmodium falciparum (the parasite which causes Malaria), Enoyl Reductase (ENR) plays a critical role creating long chain molecules known as fatty acids which are used in the synthesis of cell wall mycolic acids. Effective inhibition of this enzyme has been demonstrated to have therapeutic potential in the treatment of Malaria. Inhibiting Enoyl Reductase in Mycobacterium tuberculosis would also be effective against drug resistant strains of TB. |
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| Pictures | M R Kuo et al J Biol Chem (2003) 278.23 p20851-20859 | last updated: 00:00 on 24-JAN-06 | ||||||||||||
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Camodulin
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Plasmodium falciparum, the parasite associated with Malaria, has an obligate
calcium requirement for normal growth and invasion of host erythrocytes.
It has been shown that inhibiting Camodulin has therapeutic potential
in the treatment of Malaria. Selectivity for the parasite and side effects
may still be issues. This is an alternative query to 1xa5-q2 based on
a different crystal structure.
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| Pictures | V Harmat et al J Mol Biol (2000) 297 p747 | last updated: 12:14 on 13-JUN-05 | ||||||||||||
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Peptide deformylase
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Plasmodium falciparum is the parasite associated with Malaria. Peptide deformylase is a new antibiotic
target which may also be a useful target for new Malaria drugs.
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| Pictures | M A Robien et al Protein Sci (2004) 13 p1155 | last updated: 06:07 on 30-MAR-05 | ||||||||||||
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Camodulin
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Plasmodium falciparum, the parasite associated with Malaria, has an obligate
calcium requirement for normal growth and invasion of host erythrocytes.
It has been shown that inhibiting Camodulin has therapeutic potential
in the treatment of Malaria. Selectivity for the parasite and side effects
may still be issues.
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| Pictures | L W Scheibel et al Proc Nat Acad Sci (1987) 84.20 p7310-4 | last updated: 12:12 on 03-JUN-05 | ||||||||||||