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Ligand N-benzyloxycarbonyl-3-aminopropanal

Basic Ligand Information

Molecular Structure

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Roles as Enzyme Ligand

Substrate in Enzyme-catalyzed Reactions (6 results)

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Show Substrate (6 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

2.1.2.1

D-alanine + benzyl (3-oxopropyl)carbamate + H2O = (3S)-N6-[(benzyloxy)carbonyl]-3-hydroxy-2-methyl-L-lysine + (2S,3R)-2-amino-6-[[(benzyloxy)carbonyl]amino]-3-hydroxy-2-methylhexanoic acid

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2.1.2.1

D-serine + benzyl (3-oxopropyl)carbamate + H2O = (3S)-N6-[(benzyloxy)carbonyl]-3-hydroxy-2-(hydroxymethyl)-L-lysine + (3R)-N6-[(benzyloxy)carbonyl]-3-hydroxy-2-(hydroxymethyl)-L-lysine

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2.1.2.1

glycine + benzyl (3-oxopropyl)carbamate + H2O = (2S,3S)-2-amino-6-[[(benzyloxy)carbonyl]amino]-3-hydroxyhexanoic acid + (2S,3R)-2-amino-6-[[(benzyloxy)carbonyl]amino]-3-hydroxyhexanoic acid

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4.1.2.48

N-benzyloxycarbonyl-3-aminopropanal + glycine = (2S,3R)-2-amino-5-(benzyloxycarbonylamino)-3-hydroxypentanoic acid

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4.1.2.48

N-benzyloxycarbonyl-3-aminopropanal + glycine = (2S,3S)-2-amino-5-(benzyloxycarbonylamino)-3-hydroxypentanoic acid

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2.1.2.1

3 entries

4.1.2.48

2 entries

4.1.2.53

benzyl (3-oxopropyl)carbamate + 2-oxopropanoate = (3R)-5-[[(benzyloxy)carbonyl]amino]-3-hydroxypentanoate + (3S)-5-[[(benzyloxy)carbonyl]amino]-3-hydroxypentanoate

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Product in Enzyme-catalyzed Reactions (2 results)

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EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.11.1.10

N-Cbz-3-amino-1-propanol + H2O2 = N-Cbz-3-aminopropanal + H2O

0

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1.11.1.10

N-Cbz-3-amino-1-propanol + tert-butyl hydroperoxide = N-Cbz-3-aminopropanal + H2O + ?

0

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1.11.1.10

2 entries

Enzyme Kinetic Parameters

References & Links

Literature References (3)

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Show Reference (3 entries)

BRENDA REFERENCE ID

PUBMED ID

TITLE

YEAR

AUTHORS

JOURNAL

VOLUME

PAGES

691804

18384024

Serine hydroxymethyl transferase from Streptococcus thermophilus and L-threonine aldolase from Escherichia coli as stereocomplementary biocatalysts for the synthesis of beta-hydroxy-alpha,omega-diamino acid derivatives

2008

Gutierrez, M.L.; Garrabou, X.; Agosta, E.; Servi, S.; Parella, T.; Joglar, J.; Clapes, P.

Chemistry

14

4647-4656

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2-Keto-3-deoxy-L-rhamnonate aldolase (YfaU) as catalyst in aldol additions of pyruvate to amino aldehyde derivatives

2017

Hernandez, K.; Gomez, A.; Joglar, J.; Bujons, J.; Parella, T.; Clapes, P.

Adv. Synth. Catal.

359

2090-2100

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25611820

Engineered L-serine hydroxymethyltransferase from Streptococcus thermophilus for the synthesis of alpha,alpha-dialkyl-alpha-amino acids

2015

Hernandez, K.; Zelen, I.; Petrillo, G.; Uson, I.; Wandtke, C.M.; Bujons, J.; Joglar, J.; Parella, T.; Clapes, P.

Angew. Chem. Int. Ed. Engl.

54

3013-3017

Links to other databases for N-benzyloxycarbonyl-3-aminopropanal

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Show Links (1 entry)

ChEBI

PubChem

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