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Class of chemical compounds
D-Amino acids are amino acids where the stereogenic carbon alpha to the amino group has the D-configuration. For most naturally occurring amino acids
D-Amino_acid
Class of enzymes
D-amino-acid dehydrogenase (EC 1.4.99.1, transferred to 1.4.99.6) is a bacterial enzyme that catalyses the oxidation of D-amino acids into their corresponding
D-amino_acid_dehydrogenase
Enzyme
It is not present in plants or in bacteria which instead use D-amino acid dehydrogenase. DAAO in humans is a candidate susceptibility gene and together
D-amino_acid_oxidase
D-amino acid dehydrogenase (quinone) (EC 1.4.5.1, DadA) is an enzyme with systematic name D-amino acid:quinone oxidoreductase (deaminating). This enzyme
D-amino acid dehydrogenase (quinone)
D-amino_acid_dehydrogenase_(quinone)
Amino acid with a branched carbon chain
A branched-chain amino acid (BCAA) is an amino acid having an aliphatic side-chain with a branch (a central carbon atom bound to three or more carbon atoms)
Branched-chain_amino_acid
Amino acid and neurotransmitter
Glutamic acid (symbol Glu or E; known as glutamate in its anionic form) is an α-amino acid that is used by almost all living beings in the biosynthesis
Glutamic_acid
Interconnected biochemical reactions releasing energy
different pathways). In addition, the cycle provides precursors of certain amino acids, as well as the reducing agent NADH, which are used in other reactions
Citric_acid_cycle
Set of biochemical processes
Amino acid biosynthesis is the set of biochemical processes (metabolic pathways) by which the amino acids are produced. The substrates for these processes
Amino_acid_synthesis
Amino acids required in diet since they can not be synthesized in body
An essential amino acid, or indispensable amino acid, is an amino acid that cannot be synthesized from scratch by the organism fast enough to supply its
Essential_amino_acid
Amino acid
Aspartic acid (symbol Asp or D; known as aspartate in its anionic form), is an α-amino acid that is used in the biosynthesis of proteins. The L-isomer
Aspartic_acid
Protein family
dehydrogenase EC 1.1.99.5, Sarcosine oxidase beta subunit EC 1.5.3.1, D-amino-acid dehydrogenase EC 1.4.99.1, D-aspartate oxidase EC 1.4.3.1. D-amino
FAD dependent oxidoreductase family
FAD_dependent_oxidoreductase_family
Hexameric enzyme
metabolism of amino acids as a method of controlling insulin secretion and regulating blood glucose levels. Bovine liver glutamate dehydrogenase was found
Glutamate_dehydrogenase
Multienzyme complex
as well as the 2-oxoadipate dehydrogenase complex (OADHC), which plays a critical role in the degradation of the amino acids lysine, hydroxylysine, and
Branched-chain alpha-keto acid dehydrogenase complex
Branched-chain_alpha-keto_acid_dehydrogenase_complex
Sulfur-containing amino acid
amino acid in humans. Compared to other amino acids, methionine has particularly decisive biosynthetic roles. It is the precursor to the amino acid cysteine
Methionine
Amino acid
Lysine (symbol Lys or K) is an α-amino acid that is a precursor to many proteins. Lysine contains an α-amino group (which is in the protonated −NH+3 form
Lysine
Multienzyme complex
oxoglutarate dehydrogenase complex (OGDC), the 2-oxoadipate dehydrogenase complex (OADHC) and the branched-chain oxo-acid dehydrogenase complex (BCKDC)
Pyruvate dehydrogenase complex
Pyruvate_dehydrogenase_complex
Chemical compound
is an essential amino acid that is used in the biosynthesis of proteins. Leucine is an α-amino acid, meaning it contains an α-amino group (which is in
Leucine
Organic compound
L-malate, catalyzed by malate dehydrogenase, in the citric acid cycle. Malate is also oxidized by succinate dehydrogenase in a slow reaction with the initial
Oxaloacetic_acid
Main inhibitory neurotransmitter in the mammalian brain
dehydrogenase (ALDH) with γ-aminobutyraldehyde (GABAL) as a metabolic intermediate. GABA is also found in plants. It is the most abundant amino acid in
GABA
Biosynthetic pathway
protozoans, and plants for the biosynthesis of folates and aromatic amino acids (tryptophan, phenylalanine, and tyrosine). This pathway is not found
Shikimate_pathway
Amino acid
simplest stable amino acid, distinguished by having a single hydrogen atom as its side chain. As one of the 20 proteinogenic amino acids, glycine is a fundamental
Glycine
Class of enzymes
citric acid cycle to carry out cellular respiration. To distinguish between this enzyme and the PDC, it is systematically called pyruvate dehydrogenase (acetyl-transferring)
Pyruvate_dehydrogenase
Simplest of the alpha-keto acids
amino acid alanine and can be converted into ethanol or lactic acid via fermentation. Pyruvic acid supplies energy to cells through the citric acid cycle
Pyruvic_acid
Class of enzymes
Aromatic L-amino acid decarboxylase (AADC or AAAD), also known as DOPA decarboxylase (DDC), tryptophan decarboxylase, and 5-hydroxytryptophan decarboxylase
Aromatic L-amino acid decarboxylase
Aromatic_L-amino_acid_decarboxylase
Α-amino acid that is used in the biosynthesis of proteins
or α-alanine, is an α-amino acid that is used in the biosynthesis of proteins. It contains an amine group and a carboxylic acid group, both attached to
Alanine
Amino acid
Threonine (symbol Thr or T) is an amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated −NH+
Threonine
Chemical compound
3-dehydroshikimic acid by the enzyme 3-dehydroquinate dehydratase, which is reduced to shikimic acid by the enzyme shikimate dehydrogenase, which uses nicotinamide
Shikimic_acid
Type of biochemical process
biochemical processes responsible for the synthesis of proteins and amino acids (anabolism), and the breakdown of proteins by catabolism. The steps of
Protein_metabolism
Amino acid
/ˈsɪəriːn/ (symbol Ser or S) is an α-amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated −NH+
Serine
Chemical compound
fatty acids (e.g., butyrate), β-hydroxy β-methylbutyrate, and ketogenic amino acids through a series of reactions that metabolize these compounds into acetoacetate
Β-Hydroxybutyric_acid
Chemical compound
intermediates in the metabolic pathway for L-leucine. Leucine is an essential amino acid, and its degradation is critical for many biological duties. α-KIC is
Α-Ketoisocaproic_acid
Chemical compound
(beta-alanine) is a naturally occurring beta amino acid. Beta amino acids are amino acids in which the amino group is attached to the β-carbon atom (i.e
Β-Alanine
Proteinogenic amino acid
Cysteine (/ˈsɪstɪiːn/; symbol Cys or C) is a semiessential proteinogenic amino acid with the formula HS−CH2−CH(NH2)−COOH. The thiol side chain in cysteine
Cysteine
Aminosulfonic acid
non-proteinogenic amino sulfonic acid widely distributed in mammalian tissues and organs. Structurally, by containing a sulfonic acid group instead of
Taurine
Chemical compound
Valine (symbol Val or V) is an α-amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated −NH3+
Valine
Enzyme
Birnbaum D (1986). "Purification and properties of D-aromatic lactate dehydrogenase an enzyme involved in the catabolism of the aromatic amino acids of Candida
Aromatic_2-oxoacid_reductase
Chemical compound
action". Amino Acids. 40 (4): 1015–1025. doi:10.1007/s00726-010-0678-0. PMID 20607321. S2CID 11120110. HMB is a metabolite of the amino acid leucine (Van
Β-Hydroxy β-methylbutyric acid
Β-Hydroxy_β-methylbutyric_acid
Chemical compound
(symbol His or H) is an essential amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated –NH3+
Histidine
Class of enzymes
L-lactate dehydrogenase. Other LDHs act on D-lactate and/or are dependent on cytochrome c: D-lactate dehydrogenase (cytochrome) and L-lactate dehydrogenase (cytochrome)
Lactate_dehydrogenase
Chemical compound
amino acid can scavenge up to four molecules of HClO. Consistent with this, it has been proposed that sulfhydryl groups of sulfur-containing amino acids
Hypochlorous_acid
Medical condition
Medium-chain acyl-CoA dehydrogenase deficiency (MCAD deficiency or MCADD) is a disorder of fatty acid oxidation that impairs the body's ability to break
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency
Enzyme involved in the production of energy by cells
Glucose-6-phosphate dehydrogenase (G6PD or G6PDH) (EC 1.1.1.49) is a cytosolic enzyme that catalyzes the chemical reaction: Glucose 6-phosphonic acid + NADP+
Glucose-6-phosphate dehydrogenase
Glucose-6-phosphate_dehydrogenase
Dicarboxylic acid
intermediate being converted into fumarate by the enzyme succinate dehydrogenase in complex 2 of the electron transport chain which is involved in making
Succinic_acid
Process of fatty acid breakdown
long-chain fatty acid is dehydrogenated to create a trans double bond between C2 and C3. This is catalyzed by acyl CoA dehydrogenase to produce trans-delta
Beta_oxidation
Membrane transport proteins
An amino acid transporter is a membrane transport protein that transports amino acids. They are mainly of the solute carrier family. There are several
Amino_acid_transporter
Chemical compound
is an organic acid classed as a proteinogenic amino acid (used in the biosynthesis of proteins), although it does not contain the amino group -NH 2 but
Proline
Autosomal recessive metabolic disorder
body's ability to metabolize amino acids due to a deficiency in the activity of the branched-chain alpha-ketoacid dehydrogenase (BCKAD) complex. It particularly
Maple_syrup_urine_disease
Protein-coding gene in the species Homo sapiens
Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric
Aldehyde dehydrogenase 6 family, member A1
Aldehyde_dehydrogenase_6_family,_member_A1
Chemical compound
alcohol, it causes "Coprinus syndrome". It inhibits the enzyme aldehyde dehydrogenase, which is involved in the metabolism of alcohol. This inhibition leads
Coprine
(S)-2-amino-3-ketobutyric acid + coenzyme A The two substrates of this enzyme are glycine and acetyl-CoA. Its products are (S)-2-amino-3-ketobutyric acid
Glycine_C-acetyltransferase
Metabolic process
occurring in cells involves the amino acid glutamate, which can be oxidatively deaminated by the enzyme glutamate dehydrogenase (GDH), using NAD or NADP as
Oxidative_deamination
Chemical compound
either GHB dehydrogenase (ADH) or GHB transhydrogenase. SSA is further oxidized by succinic semialdehyde dehydrogenase (SSADH) to succinic acid, which enters
Γ-Hydroxybutyric_acid
Class of enzymes
part of many metabolic pathways, including the citric acid cycle. Other malate dehydrogenases, which have other EC numbers and catalyze other reactions
Malate_dehydrogenase
Biochemical process in which fatty acids are derived from acetyl-CoA and NADPH
reactions catalyzed by isocitrate dehydrogenase and alpha-ketoglutarate dehydrogenase. Thus each turn of the citric acid cycle oxidizes an acetyl-CoA unit
Fatty_acid_synthesis
Protein family
members of this family are proteins of about 250 to 300 amino acid residues. Most dehydrogenases possess at least 2 domains, the first binding the coenzyme
Short-chain_dehydrogenase
Metabolic pathway
oxidation of fatty acids and catabolism of amino acids and choline, as it accepts electrons from multiple acetyl-CoA dehydrogenases. In plants, ETF-Q oxidoreductase
Oxidative_phosphorylation
Codon that marks the end of a protein-coding sequence
protein. Most codons in messenger RNA correspond to the addition of an amino acid to a growing polypeptide chain, which may ultimately become a protein;
Stop_codon
American biochemist
Massachusetts Institute of Technology (1979) with a thesis on D-amino acid dehydrogenase evolution, supervised by Christopher T. Walsh. From 1980 to 1982
Paula_J._Olsiewski
Process where substrates are converted into more complex products in living organisms
for incorporating nitrogen onto the α-carbon of amino acids involves the enzyme glutamate dehydrogenase (GDH). GDH is able to transfer ammonia onto 2-oxoglutarate
Biosynthesis
Metabolic enzyme PHGDH
Phosphoglycerate dehydrogenase (PHGDH) is an enzyme that catalyzes two individual chemical reactions. 3-phosphoglyceric acid + NAD+ H+ H+
Phosphoglycerate dehydrogenase
Phosphoglycerate_dehydrogenase
Series of interconnected biochemical reactions
4-phosphate (E4P), used in the synthesis of aromatic amino acids in non-mammals. Aromatic amino acids, in turn, are precursors for many biosynthetic pathways
Pentose_phosphate_pathway
Class of enzymes
2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD). Substrates include steroids, neurosteroids, fatty acids, bile acids, isoleucine, and xenobiotics.
17β-Hydroxysteroid dehydrogenase
17β-Hydroxysteroid_dehydrogenase
Group of enzymes
dehydrogenases (EC 1.2.1.3) are a group of enzymes that catalyse the oxidation of aldehydes. They convert aldehydes (R–C(=O)–H) to carboxylic acids (R–C(=O)–O–H)
Aldehyde_dehydrogenase
Selenium-containing amino acid
or U, in older publications also as Se-Cys) is the 21st proteinogenic amino acid. Selenoproteins contain selenocysteine residues. Selenocysteine is an
Selenocysteine
Set of chemical reactions in organisms
cycle. Amino acids also contribute to cellular energy metabolism by providing a carbon source for entry into the citric acid cycle (tricarboxylic acid cycle)
Metabolism
Chemical compound
These include its being a component of metabolic pathways that: make amino acids and in the process regulate the cellular levels of carbon, nitrogen,
Α-Ketoglutaric_acid
Enzyme
which encode 517 amino acid residues. Except for the signal NH2-terminal peptide, which is absent in the mature enzyme, the amino acid sequence deduced
ALDH2
Compound active in mitochondria
water-soluble zwitterion with relatively low toxicity. Derived from amino acids, carnitine was first extracted from meat extracts in 1905, leading to
Carnitine
Class of enzymes
are conserved as well as the amino acids. Therefore, the active sites amongst most prokaryotic isocitrate dehydrogenase enzymes should be conserved as
Isocitrate_dehydrogenase
Group of dehydrogenase enzymes
oligomeric enzymes that had its amino acid sequence and three-dimensional structure determined. In early 1960, the alcohol dehydrogenase (ADH) gene was discovered
Alcohol_dehydrogenase
One of four stable isomers of butanediol
Butane-1,4-diol is rapidly converted into GHB acid by the enzymes alcohol dehydrogenase and aldehyde dehydrogenase, and differing levels of these enzymes may
1,4-Butanediol
Medical condition
occurs when the amino acid proline is not broken down properly by the enzymes proline oxidase or pyrroline-5-carboxylate dehydrogenase, causing a buildup
Hyperprolinemia
Metabolic processes for energy production
alcohol dehydrogenase. Hitting the wall (muscle fatigue due to glycogen depletion) Second wind (increased ATP synthesis primarily from free fatty acids) van
Bioenergetic_systems
Class of enzymes
4-diaminopentanoate dehydrogenase (EC 1.4.1.12) is an enzyme that catalyzes the chemical reaction 2,4-diaminopentanoic acid + NAD+ H2O H+ H2O H+ 2-amino-4-oxopentanoic
2,4-diaminopentanoate dehydrogenase
2,4-diaminopentanoate_dehydrogenase
Chemical compound
L-glutamate-5-semialdehyde + NADP+ In most eukaryotes, GSA is synthesised from the amino acid glutamate by the bifunctional enzyme 1-pyrroline-5-carboxylate synthase
1-Pyrroline-5-carboxylic_acid
Aminotransferase enzyme
Branched-chain amino acid aminotransferase (BCAT), also known as branched-chain amino acid transaminase, is an aminotransferase enzyme (EC 2.6.1.42) which
Branched-chain amino acid aminotransferase
Branched-chain_amino_acid_aminotransferase
Chemical compound
metabolic intermediate formed during the catabolism of the branched-chain amino acid, leucine. It is a short-chain acyl-CoA thioester that plays a key role
Isovaleryl-CoA
Medical condition
symptomatic GA1-affected children. Glutaryl-CoA dehydrogenase participates in the degradation of the amino acids, specifically lysine, hydroxylysine and tryptophan
Glutaric_aciduria_type_1
Chemical compound
hydroxyproline dehydrogenase (PRODH2) pathway results in the production of glycine, glyoxylate, glycolate, and oxalate, while the L-amino-acid oxidase pathway
Hydroxyproline
Class of enzymes
3-dehydrogenase (EC 1.1.1.103) is an enzyme that catalyzes the chemical reaction L-threonine + NAD+ H+ H+ (S)-2-amino-3-ketobutyric acid + NADH
L-threonine_3-dehydrogenase
Chemical compound
alcohol dehydrogenase. Degradation of branched-chain ketogenic amino acids such as valine, leucine, and isoleucine occurs. These amino acids are converted
Acetyl-CoA
Protein-coding gene in the species Homo sapiens
of the pyruvate, α-ketoglutarate, α-adipate and branched-chain amino acid-dehydrogenase complexes and the glycine cleavage system, all in the mitochondrial
Dihydrolipoamide dehydrogenase
Dihydrolipoamide_dehydrogenase
Class of enzymes
D-aminopropanol dehydrogenase, D-aminopropanol dehydrogenase, 1-amino-2-propanol dehydrogenase, 2,3-butanediol dehydrogenase, D-1-amino-2-propanol dehydrogenase, (R)-diacetyl
(R,R)-butanediol dehydrogenase
(R,R)-butanediol_dehydrogenase
Chemical compound
Kynurenic acid (KYNA or KYN) is a product of the normal metabolism of amino acid L-tryptophan. It has been shown that kynurenic acid possesses neuroactive
Kynurenic_acid
Chemical compound
Hypoglycin A is a naturally occurring amino acid derivative found in the unripened fruit of the ackee tree (Blighia sapida) and in the seeds of the box
Hypoglycin_A
Amino-acid-synthesizing enzyme in fungi, plants and prokaryota
enzymology, aspartate-semialdehyde dehydrogenase (EC 1.2.1.11) is an enzyme that is very important in the biosynthesis of amino acids in prokaryotes, fungi, and
Aspartate-semialdehyde dehydrogenase
Aspartate-semialdehyde_dehydrogenase
Chemical compound
enzymes to synthesize: Both L- and D-HPG are used in the vancomycin class of antibiotics. Tyrosine, a similar amino acid, differs by a methylene group (CH2)
4-Hydroxyphenylglycine
Set of biochemical reactions
place primarily in the liver and, to a lesser extent, in the kidneys. Amino acid catabolism results in waste ammonia. All animals need a way to excrete
Urea_cycle
Mammalian protein found in humans
dehydrogenase deficiency have been identified. Many of these mutations switch an amino acid building block in the ACADM enzyme. The most common amino
ACADM
Mammalian protein found in humans
inhibition of 11beta-hydroxysteroid dehydrogenase 1 by 18alpha-glycyrrhetinic acid but not 18beta-glycyrrhetinic acid". The Journal of Steroid Biochemistry
11β-Hydroxysteroid dehydrogenase type 1
11β-Hydroxysteroid_dehydrogenase_type_1
Medical condition
of D-BP[6]. Amino acid changes in the catalytic domains or those in contact with substrate or cofactors were the main cause of these variations of D-BP
D-bifunctional protein deficiency
D-bifunctional_protein_deficiency
Sulfoacetaldehyde dehydrogenase (EC 1.2.1.73, SafD) is an enzyme with systematic name 2-sulfoacetaldehyde:NAD+ oxidoreductase. This enzyme catalyses the
Sulfoacetaldehyde dehydrogenase
Sulfoacetaldehyde_dehydrogenase
Protein-coding gene in the species Homo sapiens
which enters the citric acid cycle and is converted to ATP. The mature protein encoded by the PDK4 gene contains 294 amino acids in its sequence. To form
PDK4
Medical condition
Congenital errors of amino acid metabolism are inherited metabolic disorders that impair the synthesis and degradation of amino acids. This means that the
Congenital disorders of amino acid metabolism
Congenital_disorders_of_amino_acid_metabolism
Autosomal recessive metabolic disorder
Branched-chain keto acid dehydrogenase kinase deficiency (BCKDK deficiency) is a disease resulting from mutations of the BCKDK gene. Patients with BCKDK
Branched-chain keto acid dehydrogenase kinase deficiency
Branched-chain_keto_acid_dehydrogenase_kinase_deficiency
Enzyme
properties. They are monomeric soluble proteins consisting of about 320 amino acid residues with molecular weights about 34±37 kilodaltons; although these
3α-Hydroxysteroid dehydrogenase
3α-Hydroxysteroid_dehydrogenase
(glutamine + -lysis) is a series of biochemical reactions by which the amino acid glutamine is lysed to glutamate, aspartate, CO2, pyruvate, lactate, alanine
Glutaminolysis
production needs also many amino acids in the culture media therefore nitrogen source concentration has a key. Hyaluronic acid Streptococcus zooepidemicus
Microbial hyaluronic acid production
Microbial_hyaluronic_acid_production
Protein-coding gene in the species Homo sapiens
short-chain dehydrogenase domain that contains a characteristic 3-layer (αβα) sandwich known as a Rossmann fold. The human enzyme contains 327 amino acids and
HSD17B1
Molecule produced by a living organism
acid. They are also known as fatty acids Amino acids contain both amino and carboxylic acid functional groups. (In biochemistry, the term amino acid is
Biomolecule
D AMINO-ACID-DEHYDROGENASE
D AMINO-ACID-DEHYDROGENASE
Girl/Female
British, Chilean, English, German, Indonesian
Horse Lover
Boy/Male
Arabic, Australian, Farsi, German, Indian, Kannada, Muslim, Pashtun, Punjabi, Sikh, Sindhi
Worshipper of Allah; Spark of Fire; Worshipper of God
Male
English
Pet form of English Ace, ACIE means "number one."
Female
Hebrew
Variant spelling of Hebrew Amina, AMINE means "faithful, trusted."
Male
Hungarian
Hungarian name ÃRPÃD means "seed."
Boy/Male
Arabic
Certain; Strong; Firm
Boy/Male
Greek Latin
Lover of Galatea.
Male
Hungarian
Hungarian name derived from Latin Alfredus, ALFRÉD means "elf counsel."
Boy/Male
Arabic, Muslim
Loving; Sweet; Cute
Boy/Male
Arabic, Muslim
Restore
Female
Hebrew
(×Ö·×žÖ´×™× Ö¸×”) Hebrew name AMINA means "faithful, trusted." Compare with another form of Amina.
Male
Hungarian
Hungarian form of German Konrad, KONRÃD means "bold counsel."
Boy/Male
Thai
Sun.
Boy/Male
Arabic
Great
Female
Finnish
Finnish myth name from the epic poem Kalevala, AINO means "the only one."
Male
English
Anglicized form of Hebrew Adiynow, ADINO means "soft, delicate" or "his ornament." In the bible, this is the name of one of King David's warriors.
Boy/Male
Arabic, Farsi, Hindu, Indian, Muslim
Support; Leader; Chief; A Great Man; Amin
Female
Irish
Pet form of Irish Gaelic BrÃghid, BRÃD means "exalted one."
Boy/Male
Muslim Arabic
Worshipper. Adorer.
Boy/Male
Indian
Worshipper of God
D AMINO-ACID-DEHYDROGENASE
D AMINO-ACID-DEHYDROGENASE
Boy/Male
Indian
Powerful
Boy/Male
Tamil
Kanahiya | கநாஹியாÂ
Lord Krishna
Boy/Male
Hindu
Pure, Eternally pure
Boy/Male
Hindu, Indian
Jeweled
Girl/Female
African, American, Australian, British, Christian, English, Hebrew
God is My Judge; Feminine Variant of Daniel
Boy/Male
Indian
The himalayas
Boy/Male
Arabic
Sword of the Kingdom
Girl/Female
Bengali, Hindu, Indian, Kannada
Prince of Living
Boy/Male
Hindu
The Moon, Intelligent, Collection
Boy/Male
Indian, Sanskrit
Ornamented with Jewels
D AMINO-ACID-DEHYDROGENASE
D AMINO-ACID-DEHYDROGENASE
D AMINO-ACID-DEHYDROGENASE
D AMINO-ACID-DEHYDROGENASE
D AMINO-ACID-DEHYDROGENASE
a.
Pertaining to, or designating, an amido acid related to lactic acid, and called also amido-propionic acid.
a.
Sharp and harsh, or bitter and not, to the taste; pungent; as, acrid salts.
a.
Having a taste compounded of saltness and acidity; both salt and acid.
v. t.
An aid-de-camp, so called by abbreviation; as, a general's aid.
n.
See Groundnut (d).
n.
An amido compound with only one amido group.
a.
Caustic; bitter; bitterly irritating; as, acrid temper, mind, writing.
a.
Pertaining to, or designating, an organic amido acid, which is regarded as a derivative of lactic acid and urea.
a.
Sour, sharp, or biting to the taste; tart; having the taste of vinegar: as, acid fruits or liquors. Also fig.: Sour-tempered.
n.
A basic compound containing one amido group; as, methyl amine is a monamine.
a.
Pertaining to, or designating, an acid, CH2O2(CO2H)2, obtained from amido malonic acid.
n.
Any compound containing two amido groups united with one or more acid or negative radicals, -- as distinguished from a diamine. Cf. Amido acid, under Amido, and Acid amide, under Amide.
n.
An amine containing three amido groups.
n.
An acid elevator, as a tube through which acid is forced to some height in a sulphuric acid manufactory.
a.
Of or pertaining to an acid; as, acid reaction.
a.
Causing heat and irritation; corrosive; as, acrid secretions.
n.
A white crystalline substance, C9H6N.OH, of acid properties derived from one of the amido cinnamic acids.