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High homologous

The cause of Wilson disease was also revealed in 1993, when it was reported that a variety of mutations in a gene encoding a copper-binding P-type ATPase were responsible. The gene is estimated to encode a protein of 1411 amino acids, which is highly homologous to the product of the gene affected in Menkes disease. In a manner not yet fully explained, a nonfunctional ATPase causes defective excretion of copper into the bile, a reduction of incorporation of copper into... [Pg.588]

The most extensively investigated HNL structures are those from H. brasiliensis (HbHNL)" " and M. esculenta (MeHNL)," which are highly homologous (76% identity). For MeHNL, the crystal structure of the wild-type enzyme complexed with acetone has been reported in 2001 (Fig. 1)." ... [Pg.151]

The PE2 isoform has been purified and fully sequenced (Markovic and Joumval 1986). Using this sequence data Ray et al (1988) succeeded in isolating a clone fi om a tomato fruit cDNA library. The predicted amino acid sequence fi om this clone had high homology to the actual amino acid sequence determined for PE2 but was not identical. Subsequent screening of the tomato... [Pg.351]

The dihydrofolate reductase enzyme (DHFR) is involved in one-carbon metabolism and is required for the survival of prokaryotic and eukaryotic cells. The enzyme catalyzes the reduction of dihydrofolate to tetrahydrofolate, which is required for the biosynthesis of serine, methionine, purines, and thymidylate. The mouse dihydrofolate reductase (mDHFR) is a small (21 kD), monomeric enzyme that is highly homologous to the E. coli enzyme (29% identify) (Pelletier et al., 1998). The three-dimensional structure of DHFR indicates that it is comprised of three structural fragments F[l], F[2] andF[3] (Gegg etal., 1997). [Pg.69]

A human cDNA highly homologous to the transferrin receptor, has been identified and reported to encode a protein, designated TfR2, which binds diferrictransferrin and mediates iron uptake of transferrin-bound iron (Kawabata etal., 1999). A mouse orthologue of human TfR2 has been found independently (Fleming etal.,... [Pg.159]


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