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ACS12 | Probable aminotransferase ACS12; Probable aminotransferase. Does not have 1-aminocyclopropane- 1-carboxylate synthase (ACS) activity, suggesting that it is not involved in ethylene biosynthesis. (495 aa) | ||||
F8N16.11 | 60S ribosomal protein L16-like, mitochondrial; Component of the large subunit of mitochondrial ribosome. Belongs to the universal ribosomal protein uL16 family. (291 aa) | ||||
SHM7 | Serine hydroxymethyltransferase 7; Catalyzes the interconversion of serine and glycine. Belongs to the SHMT family. (598 aa) | ||||
F20O9.100 | Probable aminotransferase TAT1; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (449 aa) | ||||
AGT1 | Serine--glyoxylate aminotransferase; Photorespiratory enzyme that catalyzes transamination reactions with multiple substrates, including asparagine. Function exclusively as a catabolic enzyme in Asn metabolism. Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. (401 aa) | ||||
BIO3-BIO1 | Bifunctional dethiobiotin synthetase/7,8-diamino-pelargonic acid aminotransferase, mitochondrial; Bifunctional enzyme that catalyzes two different reactions involved in the biotin biosynthesis. Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor; In the C-terminal section; belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. BioA subfamily. (833 aa) | ||||
ACS4 | 1-aminocyclopropane-1-carboxylate synthase 4; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene. (474 aa) | ||||
HISN6A | Histidinol-phosphate aminotransferase 1, chloroplastic. (417 aa) | ||||
ALAAT1 | Alanine aminotransferase 1, mitochondrial; Major alanine aminotransferase in roots. (543 aa) | ||||
F4JF53_ARATH | Pyridoxal phosphate (PLP)-dependent transferases superfamily protein. (350 aa) | ||||
TAR1 | Tryptophan aminotransferase-related protein 1; Probably involved in auxin production. TAA1, TAR1 and TAR2 are required for proper embryo patterning. Belongs to the alliinase family. (388 aa) | ||||
ACS10 | Probable aminotransferase ACS10; Probable aminotransferase. Does not have 1-aminocyclopropane- 1-carboxylate synthase (ACS) activity, suggesting that it is not involved in ethylene biosynthesis. (557 aa) | ||||
SHM6 | Serine hydroxymethyltransferase 6; Catalyzes the interconversion of serine and glycine. Belongs to the SHMT family. (599 aa) | ||||
ALAAT2 | Alanine aminotransferase 2, mitochondrial; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. Alanine aminotransferase subfamily. (540 aa) | ||||
THA2 | Probable low-specificity L-threonine aldolase 2; Threonine aldolase involved in threonine degradation to glycine. May play a role in the removal of L-allo-threonine. (355 aa) | ||||
GSA2 | Glutamate-1-semialdehyde 2,1-aminomutase 2, chloroplastic; Transaminase converting glutamate 1-semialdehyde (GSA) to 5- aminolevulinate (ALA). Involved in the biosynthesis of tetrapyrroles. (472 aa) | ||||
ACS5 | 1-aminocyclopropane-1-carboxylate synthase 5; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene. (470 aa) | ||||
ACS1 | 1-aminocyclopropane-1-carboxylate synthase-like protein 1; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (488 aa) | ||||
NIFS1 | Cysteine desulfurase, mitochondrial; Catalyzes the removal of elemental sulfur from cysteine to produce alanine. Supplies the inorganic sulfur for iron-sulfur (Fe-S) clusters. (453 aa) | ||||
DELTA-OAT | Ornithine aminotransferase, mitochondrial; Mediates degradation of arginine for nitrogen recycling. Plays a role in non-host disease resistance by regulating pyrroline-5- carboxylate metabolism-induced hypersensitive response. (475 aa) | ||||
TAT7 | Probable aminotransferase TAT2; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (414 aa) | ||||
K8A10.2 | Pyridoxal phosphate (PLP)-dependent transferases superfamily protein. (870 aa) | ||||
TAR3 | Tryptophan aminotransferase-related protein 3; Probable aminotransferase. (457 aa) | ||||
T5M16.26 | Pyridoxal phosphate (PLP)-dependent transferases superfamily protein. (440 aa) | ||||
CGS2 | Probable cystathionine gamma-synthase 2; Catalyzes the first committed step of methionine (Met) biosynthesis. Catalyzes the formation of L-cystathionine from homoserine esters and L-cysteine, via a gamma-replacement reaction. Belongs to the trans-sulfuration enzymes family. (412 aa) | ||||
ABA3 | Molybdenum cofactor sulfurase; Sulfurates the molybdenum cofactor. Sulfation of molybdenum is essential for xanthine dehydrogenase (XDH) and aldehyde oxidase (ADO) enzymes in which molybdenum cofactor is liganded by 1 oxygen and 1 sulfur atom in active form. Modulates cold stress- and osmotic stress-responsive gene expression by acting as key regulator of abscisic acid (ABA) biosynthesis. Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. MOCOS subfamily. (819 aa) | ||||
DPL1 | Sphingosine-1-phosphate lyase; Cleaves phosphorylated sphingoid bases (PSBs), such as sphingosine-1-phosphate, into fatty aldehydes and phosphoethanolamine. May play a minor role in maintenance of sphingolipid metabolism during normal plant development and growth, but be required for maintaining sphingoid long chain bases (LCB) and their phosphorylated derivatives (LCB-P) levels when sphingolipid metabolism is perturbed. May play a role in dehydration stress. (544 aa) | ||||
PSAT1 | Phosphoserine aminotransferase 1, chloroplastic; Involved in the plastidial phosphorylated pathway of serine biosynthesis (PPSB). Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine; Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. SerC subfamily. (430 aa) | ||||
SHM3 | Serine hydroxymethyltransferase 3, chloroplastic; Catalyzes the interconversion of serine and glycine and directs the hydroxymethyl moiety of serine into the metabolic network of H4PteGlu(n)-bound one-carbon units; Belongs to the SHMT family. (529 aa) | ||||
LCB1 | Long chain base biosynthesis protein 1; Serine palmitoyltransferase (SPT). The heterodimer formed with LCB2 constitutes the catalytic core. Involved in the regulation of the programmed cell death (PCD) signaling pathway. Plays an important role during male gametogenesis and embryogenesis. (482 aa) | ||||
POP2 | Gamma-aminobutyrate transaminase POP2, mitochondrial; Transaminase that degrades gamma-amino butyric acid (GABA) and uses pyruvate or glyoxylate as amino-group acceptor, but not 2- oxoglutarate. The pyruvate-dependent activity is reversible while the glyoxylate-dependent activity is irreversible. Cannot use beta-alanine, ornithine, acetylornithine, serine, glycine, asparagine, glutamine, glutamate, valine, leucine, isoleucine, methionine, phenylalanine, histidine, lysine, arginine, aspartate, threonine, tyrosine, tryptophan, proline, or cysteine as amino donors. Modulates steady- state [...] (504 aa) | ||||
SHM2 | Serine hydroxymethyltransferase 2, mitochondrial; Functions outside the photorespiratory pathway in catalyzing the interconversion of serine and glycine. Belongs to the SHMT family. (517 aa) | ||||
GLDP1 | Glycine dehydrogenase (decarboxylating) 1, mitochondrial; The glycine decarboxylase (GDC) or glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha- amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein (By similarity). (1037 aa) | ||||
AGT3 | Alanine--glyoxylate aminotransferase 2 homolog 2, mitochondrial. (477 aa) | ||||
TAR2 | Tryptophan aminotransferase-related protein 2; Involved in auxin production. Both TAA1 and TAR2 are required for maintaining proper auxin levels in roots, while TAA1, TAR1 and TAR2 are required for proper embryo patterning. Involved in the maintenance of the root stem cell niches. (440 aa) | ||||
AGT2 | Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial; Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. (476 aa) | ||||
DAP | LL-diaminopimelate aminotransferase, chloroplastic; Required for lysine biosynthesis. Catalyzes the direct conversion of tetrahydrodipicolinate to LL-diaminopimelate, a reaction that requires three enzymes in E.coli. Not active with meso- diaminopimelate, lysine or ornithine as substrates. Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. LL-diaminopimelate aminotransferase subfamily. (461 aa) | ||||
TAR4 | Tryptophan aminotransferase-related protein 4; Probable aminotransferase. (463 aa) | ||||
GGAT1 | Glutamate--glyoxylate aminotransferase 1; Catalyzes the glutamate:glyoxylate (GGT or GGAT), alanine:glyoxylate (AGT), alanine:2-oxoglutarate (AKT) and glutamate:pyruvate (GPT) aminotransferase reactions in peroxisomes. Required for abscisic acid (ABA)- and stress-mediated responses in an H(2)O(2)-dependent manner. Functions as a photorespiratory aminotransferase that modulates amino acid content during photorespiration (GGAT activity); promotes serine, glycine and citrulline metabolism in response to light. (481 aa) | ||||
LCB2a | Long chain base biosynthesis protein 2a; Serine palmitoyltransferase (SPT). The heterodimer formed with LCB1 constitutes the catalytic core. Involved in the regulation of the programmed cell death (PCD) signaling pathway. Plays an important role during male gametogenesis and embryogenesis. Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. (489 aa) | ||||
MMT1 | Methionine S-methyltransferase; Catalyzes the S-methylmethionine (SMM) biosynthesis from adenosyl-L-homocysteine (AdoMet) and methionine. SMM biosynthesis (by MMT1) and degradation (by HMT-1, HMT-2 and HMT-3) constitute the SMM cycle in plants, which is probably required to achieve short term control of AdoMet level. Also able to catalyze the selenium- methylmethionine (SeMM) from AdoMet and selenium-methionine (SeMet). May play a role in phoem sulfur transport; such function is however not essential. (1071 aa) | ||||
TAT | Tyrosine aminotransferase; Transaminase involved in tyrosine breakdown. Converts tyrosine to p-hydroxyphenylpyruvate. Can catalyze the reverse reaction, using L-glutamate in vitro. Can convert phenylalanine to phenylpyruvate and catalyze the reverse reaction in vitro. Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (420 aa) | ||||
TYRDC | Probable tyrosine decarboxylase 2; Belongs to the group II decarboxylase family. (545 aa) | ||||
ACS9 | 1-aminocyclopropane-1-carboxylate synthase 9; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (470 aa) | ||||
LCB2b | Long chain base biosynthesis protein 2b; Serine palmitoyltransferase (SPT). The heterodimer formed with LCB1 constitutes the catalytic core. Plays an important role during male gametogenesis and embryogenesis. (489 aa) | ||||
WIN1 | Acetylornithine aminotransferase, chloroplastic/mitochondrial; Involved in the biosynthesis of citrulline (By similarity). Essential gene that modulates defense response to pathogenic bacteria, conferring susceptibility and repressing salicylic acid (SA) accumulation; Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. (457 aa) | ||||
SDC-2 | Serine decarboxylase; Catalyzes the biosynthesis of ethanolamine from serine. Highly specific for L-serine and does not attack D-serine, L- phosphoserine, phosphatidylserine, L-histidine L-glutamate L-tyrosine or L-tryptophan. Decarboxylation of free serine is the major source of ethanolamine production in plants and ethanolamine metabolism is crucial for the synthesis of choline, phosphatidylethanolamine (PE) and phosphatidylcholine (PC), and thus for plant growth. (482 aa) | ||||
GGAT2 | Glutamate--glyoxylate aminotransferase 2; Catalyzes the Glu:glyoxylate aminotransferase (GGT), Ala:glyoxylate aminotransferase (AGT), Ala:2-oxoglutarate aminotransferase (AKT) and Glu:pyruvate aminotransferase (GPT) reactions in peroxisomes; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. Alanine aminotransferase subfamily. (481 aa) | ||||
TAA1 | L-tryptophan--pyruvate aminotransferase 1; L-tryptophan aminotransferase involved in auxin (IAA) biosynthesis. Can convert L-tryptophan and pyruvate to indole-3-pyruvic acid (IPA) and alanine. Catalyzes the first step in IPA branch of the auxin biosynthetic pathway. Required for auxin production to initiate multiple change in growth in response to environmental and developmental cues. It is also active with phenylalanine, tyrosine, leucine, alanine, methionine and glutamine. Both TAA1 and TAR2 are required for maintaining proper auxin levels in roots, while TAA1, TAR1 and TAR2 are requ [...] (391 aa) | ||||
ACS11 | 1-aminocyclopropane-1-carboxylate synthase 11; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (460 aa) | ||||
ACS6 | 1-aminocyclopropane-1-carboxylate synthase 6; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene. Involved in bacterial flagellin-induced ethylene production. Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (495 aa) | ||||
MGL | Methionine gamma-lyase; Catalyzes the degradation of L-methionine to alpha- ketobutyrate, methanethiol and ammonia. Exhibits a high activity toward L-methionine, L-ethionine, L-homocysteine and seleno-L-methionine, but not L-cysteine. Involved in an alternative cysteine biosynthesis pathway to the reverse trans-sulfuration pathway (methionine->homocysteine->cystathionine->cysteine) in which methanethiol is an intermediate. Mediates also an alternative isoleucine biosynthesis pathway in which 2-ketobutyrate is an intermediate. (441 aa) | ||||
PSAT2 | Phosphoserine aminotransferase 2, chloroplastic; Involved in the plastidial phosphorylated pathway of serine biosynthesis (PPSB). Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine; Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. SerC subfamily. (422 aa) | ||||
PAT | Bifunctional aspartate aminotransferase and glutamate/aspartate-prephenate aminotransferase; Prokaryotic-type aspartate aminotransferase. Has also a prenate transaminase activity. Involved in the aromatic amino acids biosynthesis pathway via the arogenate route. Required for the transamination of prephenate into arogenate. Required for early development of the embryo. (475 aa) | ||||
SUR1 | S-alkyl-thiohydroximate lyase SUR1; C-S lyase involved in glucosinolate biosynthesis. Converts S- (alkylacetohydroximoyl)-L-cysteine to thiohydroximate. Functions in auxin homeostasis. Probably required for glucosinolate activation in response to pathogens; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (462 aa) | ||||
TAT3 | Probable aminotransferase TAT3; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (445 aa) | ||||
PYD4 | Alanine--glyoxylate aminotransferase 2 homolog 3, mitochondrial; Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. (481 aa) | ||||
ACS7 | 1-aminocyclopropane-1-carboxylate synthase 7; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene. (447 aa) | ||||
CORI3 | Cystine lyase CORI3; Possesses cystine lyase activity in vitro. Does not possess tyrosine aminotransferase, alanine aminotransferase, aspartate aminotransferase and tryptophan aminotransferase activities. Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (422 aa) | ||||
SHM5 | Serine hydroxymethyltransferase 5; Catalyzes the interconversion of serine and glycine. Belongs to the SHMT family. (470 aa) | ||||
SHM4 | Serine hydroxymethyltransferase 4; Catalyzes the interconversion of serine and glycine. (471 aa) | ||||
ACS2 | 1-aminocyclopropane-1-carboxylate synthase 2; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (496 aa) | ||||
CGS1 | Cystathionine gamma-synthase 1, chloroplastic; Catalyzes the first committed step of methionine (Met) biosynthesis. Catalyzes the formation of L-cystathionine from homoserine esters and L-cysteine, via a gamma-replacement reaction. Substrate preference for cystathionine synthesis is O-phospho-L- homoserine (OPH) > O(4)-succinyl-L-homoserine (OSH) >> O-acetyl-L- homoserine (OAH). Is able, at extremely low rate, to catalyze a gamma- elimination of OPH in the absence of cysteine to produce inorganic phosphate (Pi), 2-oxobutanoate and ammonia. (563 aa) | ||||
CBL | Cystathionine beta-lyase, chloroplastic; Belongs to the trans-sulfuration enzymes family. (464 aa) | ||||
F20O9.90 | Tyrosine transaminase family protein. (447 aa) | ||||
ASP4 | Aspartate aminotransferase, cytoplasmic isozyme 2; Important for the metabolism of amino acids and Krebs-cycle related organic acids. In plants, it is involved in nitrogen metabolism and in aspects of carbon and energy metabolism. (403 aa) | ||||
ASP2 | Aspartate aminotransferase, cytoplasmic isozyme 1; Important for the metabolism of amino acids and Krebs-cycle related organic acids. Involved in plant nitrogen metabolism of Asp and Asp-derived amino acids and in the synthesis of Asp/Asn for seed storage. May be involved in the assessment of the pyridoxal phosphate levels in the cell. (405 aa) | ||||
ASP3 | Aspartate aminotransferase 3, chloroplastic; Amino acid aminotransferase important for the metabolism of amino acids and Krebs-cycle related organic acids. No activity with D- Asp or D-Ala as amino donors. In plants, it is involved in nitrogen metabolism and in aspects of carbon and energy metabolism. Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (449 aa) | ||||
ASP1 | Aspartate aminotransferase, mitochondrial; Amino acid aminotransferase important for the metabolism of amino acids and Krebs-cycle related organic acids. No activity with D- Asp or D-Ala as amino donors. In plants, it is involved in nitrogen metabolism and in aspects of carbon and energy metabolism. (430 aa) | ||||
ASP5 | Aspartate aminotransferase, chloroplastic; Amino acid aminotransferase important for the metabolism of amino acids and Krebs-cycle related organic acids. No activity with D- Asp or D-Ala as amino donors. In plants, it is involved in nitrogen metabolism and in aspects of carbon and energy metabolism. Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (453 aa) | ||||
GSA1 | Glutamate-1-semialdehyde 2,1-aminomutase 1, chloroplastic; Transaminase converting glutamate 1-semialdehyde (GSA) to 5- aminolevulinate (ALA). Involved in the biosynthesis of tetrapyrroles. (474 aa) | ||||
HISN6B | Histidinol-phosphate aminotransferase 2, chloroplastic; Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily. (417 aa) | ||||
F7H19.160 | Molybdenum cofactor sulfurase-like protein. (559 aa) | ||||
GLDP2 | Glycine dehydrogenase (decarboxylating) 2, mitochondrial; The glycine decarboxylase (GDC) or glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha- amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein (By similarity). (1044 aa) | ||||
BIOF | 8-amino-7-oxononanoate synthase; Catalyzes the decarboxylative condensation of pimeloyl-[acyl- carrier protein] and L-alanine to produce 8-amino-7-oxononanoate (AON), [acyl-carrier protein], and carbon dioxide. Required for the biosynthesis of D-biotin that prevents light-mediated cell death and modulates defense gene expression, probably by avoiding hydrogen peroxide H(2)O(2) accumulation ; Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. BioF subfamily. (476 aa) | ||||
SHM1 | Serine hydroxymethyltransferase 1, mitochondrial; Functions in the photorespiratory pathway in catalyzing the interconversion of serine and glycine. Involved in controlling cell damage caused by abiotic stress, such as high light and salt and the hypersensitive defense response of plants. Belongs to the SHMT family. (517 aa) | ||||
ACS8 | 1-aminocyclopropane-1-carboxylate synthase 8; 1-aminocyclopropane-1-carboxylate synthase (ACS) enzymes catalyze the conversion of S-adenosyl-L-methionine (SAM) into 1- aminocyclopropane-1-carboxylate (ACC), a direct precursor of ethylene. (469 aa) | ||||
ALD1 | Aminotransferase ALD1, chloroplastic; Aminotransferase involved in local and systemic acquired resistance (SAR) to the bacterial pathogen P.syringae. Required for salicylic acid (SA) and camalexin accumulation upon pathogen infection. Possesses aminotransferase activity in vitro and may generate amino- acid-derived defense signals in vivo. May be involved in ethylene- induced senescence signaling. Involved in the biosynthesis of pipecolate (Pip), a metabolite that orchestrates defense amplification, positive regulation of SA biosynthesis, and priming to guarantee effective local resist [...] (456 aa) | ||||
NFS2 | Cysteine desulfurase 1, chloroplastic; Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L-selenocystine to produce L-alanine. Supplies the inorganic sulfur for iron-sulfur (Fe-S) clusters. Required for the maturation of all plastidic Fe-S proteins and, thus, essential for plant growth. Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. (463 aa) | ||||
F9D16.60 | Probable aminotransferase TAT4. (424 aa) | ||||
ELI5 | Tyrosine decarboxylase 1. (490 aa) | ||||
THA1 | Probable low-specificity L-threonine aldolase 1; Threonine aldolase involved in threonine degradation to glycine. May play a role in the removal of L-allo-threonine. (358 aa) |