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Ligand hexane

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Basic Ligand Information

Molecular Structure
Picture of hexane (click for magnification)
Molecular Formula
BRENDA Name
InChIKey
C6H14
hexane
VLKZOEOYAKHREP-UHFFFAOYSA-N
Synonyms:
GlcNAcbeta(1-4)Mur2Ac(oyl-L-Ala-gamma-D-Glu-L-Lys-D-Ala-D-Ala)-diphosphotetradecane, n-hexane

Roles as Enzyme Ligand

Substrate in Enzyme-catalyzed Reactions (5 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE
hexane + NADH + H+ + O2 = hexan-1-ol + NAD+ + H2O
show the reaction diagram
-
hexane + NAD(P)H + O2 = 1-hexanol + 2-hexanol + NAD(P)+ + H2O
show the reaction diagram
-
hexane + reduced ferreredoxin + O2 = hexan-2-ol + hexan-3-ol + oxidized ferredoxin + H2O
show the reaction diagram
-

Product in Enzyme-catalyzed Reactions (5 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE
UDP-N-acetylglucosamine + Mur2Ac(oyl-L-Ala-gamma-D-Glu-L-Lys-D-Ala-D-Ala)-diphosphotetradecane = UDP + GlcNAcbeta(1-4)Mur2Ac(oyl-L-Ala-gamma-D-Glu-L-Lys-D-Ala-D-Ala)-diphosphotetradecane
show the reaction diagram
-

Activator in Enzyme-catalyzed Reactions (29 results)

EC NUMBER
COMMENTARY
LITERATURE
ENZYME 3D STRUCTURE
significant increases in enzyme activity occurs after 25 h incubation at a concentration of 30%
-
activity retention is highest in the presence of hexane, reaction shows maximum conversion and enantiomeric excess of 96 and more than 99%, respectively in 15%, v/v hexane with 2-propanol as the cosubstrate
-
in asymmetric reduction by TeSADH in pure hexane, the organic solvent makes the process more efficient by allowing high concentrations of substrates to be used
-
92.1% increase of activity at 80% (v/v)
-
25%, activates to 106.13% of control
-
enzyme activity is highest at concentrations of hexane between 5% and 30%
-
enzyme activity is highest at concentrations of hexane between 5% and 30%
-
102.21% activity at 20% (v/v)
-
about 140% activity at 30% (v/v)
-
the addition of n-hexane markedly enhances the esterification activities on all the medium- and long-chain saturated fatty acids
-
53% activation of recombinant refolded enzyme at 10-30% v/v
-
hydrolysis activity is enhanced in the presence of non-acceptor type organic solvents such as hexane, cyclohexane, diethyl ether, and acetone
-
50%, 2fold higher activity compared to water as solvent
-
enhances enzyme activity
-
activates about 20% at 5-10% v/v, and 230% at 30% v/v
-
activates slightly at 15% v/v
-
1% (v/v), 1.1fold activation
-

Inhibitor in Enzyme-catalyzed Reactions (25 results)

EC NUMBER
COMMENTARY
LITERATURE
ENZYME 3D STRUCTURE
40% inhibition in buffer without NaCl, slight activation in buffer with 600 mM NaCl
-
about 80% residual activity at 2% (v/v)
-
enzyme activity is markedly reduced at concentrations of hexane below 5% and over 30%
-
enzyme activity is markedly reduced at concentrations of hexane below 5% and over 30%
-
0.1% (v/v)
-
the cross-linked enzyme aggregate shows about 20% residual activity after incubation in hexane for about 24 h
-
20%
-
about 90% residual activity at 1 mM
-
about 5% residual activity at 10% (w/v)
-
76.9% residual activity at 5% (v/v)
-
at 12.5% (v/v) remaining activity, 98.25%, and 25% (v/v) remaining activity, 92.22%
-

3D Structure of Enzyme-Ligand-Complex (PDB) (8 results)

Enzyme Kinetic Parameters

KM Value (1 result)

EC NUMBER
KM VALUE [MM]
KM VALUE MAXIMUM [MM]
COMMENTARY
LITERATURE

References & Links

Links to other databases for hexane

ChEBI
PubChem
ChEBI
PubChem