1998
DOI: 10.1016/s0014-5793(98)01076-x
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Intestinal lactase‐phlorizin hydrolase (LPH): the two catalytic sites; the role of the pancreas in pro‐LPH maturation

Abstract: Brush border lactase-phlorizin hydrolase carries two catalytic sites. In the human enzyme lactase comprises Glu-1749, phlorizin hydrolase Glu-1273. The proteolytic processing of pro-lactase-phlorizin hydrolase by (rat) enterocytes stops two amino acid residues short of the N-terminus of`mature' final, brush border lactase-phlorizin hydrolase. Only these two amino acid residues are removed by luminal pancreatic protease(s), probably trypsin.z 1998 Federation of European Biochemical Societies.

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Cited by 54 publications
(63 citation statements)
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“…. (51). The enterocytes can, therefore, almost (but not quite) produce mature, brush-border LPH in the absence of trypsin.…”
Section: Furin Cleaves Human Prolactasementioning
confidence: 98%
“…. (51). The enterocytes can, therefore, almost (but not quite) produce mature, brush-border LPH in the absence of trypsin.…”
Section: Furin Cleaves Human Prolactasementioning
confidence: 98%
“…It harbors the lactase catalytic site at Glu 1749 (9,22) and acquires activity only when LPH dimerizes (35). Therefore, domain IV plays a role as a regulatory switch that triggers the dimerization of the LPH molecule, thus activating itself and elevating the phlorizin hydrolase activities in domain III.…”
Section: Discussionmentioning
confidence: 99%
“…It is devoid of sorting signals and catalytic activity and rich in cysteine and hydrophobic amino acid residues (9). LPH is cleaved in the trans-Golgi network by a trypsin-like protease (10 -13) at Arg 734 /Leu 735 generating LPH␤initial (160 kDa) (14 -16), whereby the profragment LPH␣ is ultimately degraded (17,18).…”
mentioning
confidence: 99%
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“…Активный фермент имеет 2 катали-тических участка. Лактазная активность связана с участ-ком Glu-1749, в то время как активность в отношении флоризина -с участком Glu-1273 [3].…”
unclassified