1.3.1.B13: polyprenol reductase (NADPH)
This is an abbreviated version!
For detailed information about polyprenol reductase (NADPH), go to the full flat file.
Word Map on EC 1.3.1.B13
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1.3.1.B13
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services
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violation
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reimbursement
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terminology
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bill
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lorentz
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medicare
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revisions
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sidereal
- 1.3.1.B13
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services
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violation
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reimbursement
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terminology
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bill
-
lorentz
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medicare
-
revisions
-
sidereal
Reaction
Synonyms
polyprenol reductase, polyprenol reductase 1, polyprenol reductase 2, polyprenol reductase2, PPRD1, PPRD2, SRD5A3
ECTree
1.3.1.B13 polyprenol reductase (NADPH)Advanced search results
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Engineering on EC 1.3.1.B13 - polyprenol reductase (NADPH)
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PROTEIN VARIANTS 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
H321L
site-directed mutagenesis, the mutant shows 47% of wild-type reductase activity
H336L
site-directed mutagenesis, the mutant shows 45% of wild-type reductase activity
H321L
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site-directed mutagenesis, the mutant shows 47% of wild-type reductase activity
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H336L
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site-directed mutagenesis, the mutant shows 45% of wild-type reductase activity
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additional information
additional information
PPRD2 mutants with His321 or His336, corresponding to His296 or His309 in human hSRD5A3, substituted by Leu are employed to complement the yeast dfg10DELTA mutant. Construction of two heterozygous T-DNA PPRD2 insertion lines, pprd2-1 (SALK_113221C) and pprd2-2 (SALK_006421), PPRD2 deficiency is lethal in Arabidopsis thaliana due to male sterility, PPRD2 knockout plants are not viable. For the pprd2 homozygous mutants, consistently with their Dol deficiency, defects in N-glycosylation are accompanied by degradation of some proteins, e.g., SKU5
additional information
PPRD2 mutants with His321 or His336, corresponding to His296 or His309 in human hSRD5A3, substituted by Leu are employed to complement the yeast dfg10DELTA mutant. Construction of two heterozygous T-DNA PPRD2 insertion lines, pprd2-1 (SALK_113221C) and pprd2-2 (SALK_006421), PPRD2 deficiency is lethal in Arabidopsis thaliana due to male sterility, PPRD2 knockout plants are not viable. For the pprd2 homozygous mutants, consistently with their Dol deficiency, defects in N-glycosylation are accompanied by degradation of some proteins, e.g., SKU5
additional information
-
PPRD2 mutants with His321 or His336, corresponding to His296 or His309 in human hSRD5A3, substituted by Leu are employed to complement the yeast dfg10DELTA mutant. Construction of two heterozygous T-DNA PPRD2 insertion lines, pprd2-1 (SALK_113221C) and pprd2-2 (SALK_006421), PPRD2 deficiency is lethal in Arabidopsis thaliana due to male sterility, PPRD2 knockout plants are not viable. For the pprd2 homozygous mutants, consistently with their Dol deficiency, defects in N-glycosylation are accompanied by degradation of some proteins, e.g., SKU5
additional information
total loss of activity of the putative C-terminally truncated PPRD1 proteins encoded by PPRD1-INT3 and PPRD1-INT4
additional information
total loss of activity of the putative C-terminally truncated PPRD1 proteins encoded by PPRD1-INT3 and PPRD1-INT4
additional information
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total loss of activity of the putative C-terminally truncated PPRD1 proteins encoded by PPRD1-INT3 and PPRD1-INT4
additional information
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total loss of activity of the putative C-terminally truncated PPRD1 proteins encoded by PPRD1-INT3 and PPRD1-INT4
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additional information
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PPRD2 mutants with His321 or His336, corresponding to His296 or His309 in human hSRD5A3, substituted by Leu are employed to complement the yeast dfg10DELTA mutant. Construction of two heterozygous T-DNA PPRD2 insertion lines, pprd2-1 (SALK_113221C) and pprd2-2 (SALK_006421), PPRD2 deficiency is lethal in Arabidopsis thaliana due to male sterility, PPRD2 knockout plants are not viable. For the pprd2 homozygous mutants, consistently with their Dol deficiency, defects in N-glycosylation are accompanied by degradation of some proteins, e.g., SKU5
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