ExplorEnz: EC 3.4.23.38

Your query returned 1 entry. Printable version

3.4.23.38

Accepted name:

plasmepsin I

Reaction:

Hydrolysis of the -Phe³³┼Leu- bond in the α-chain of hemoglobin, leading to denaturation of the molecule

Other name(s):

aspartic hemoglobinase I; PFAPG; malaria aspartic hemoglobinase

Comments:

Known from the malaria organism, Plasmodium. About 37 kDa. In peptidase family A1 (pepsin A family), closest to cathepsin D and renin in structure. Inhibited by pepstatin. Formerly included in EC 3.4.23.6

Links to other databases:

BRENDA, EXPASY, KEGG, MetaCyc, MEROPS, PDB, CAS registry number: 180189-87-1

References:

1.	Goldberg, D.E., Slater, A.F.G., Beavis, R., Chait, B., Cerami, A. and Henderson, G.B. Hemoglobin degradation in the human malaria pathogen Plasmodium falciparum: a catabolic pathway initiated by a specific aspartic protease. J. Exp. Med. 173 (1991) 961–969. [PMID: 2007860]
2.	Francis, S.E., Gluzman, I.Y., Oksman, A., Knickerbocker, A., Mueller, R., Bryant, M.L., Sherman, D.R., Russell, D.G. and Goldberg, D.E. Molecular characterization and inhibition of a Plasmodium falciparum aspartic hemoglobinase. EMBO J. 13 (1994) 306–317. [PMID: 8313875]
3.	Gluzman, I.Y., Francis, S.E., Oksman, A., Smith, C.E., Duffin, K.L. and Goldberg, D.E. Order and specificity of the Plasmodium falciparum hemoglobin degradation pathway. J. Clin. Invest. 93 (1994) 1602–1608. [DOI] [PMID: 8163662]

[EC 3.4.23.38 created 1995]