Page last updated: 2024-10-06

toluene degradation VI (anaerobic)

Proteins (18)

ProteinSynonymsTaxonomy
6-hydroxycyclohex-1-ene-1-carbonyl-CoA dehydrogenaseEC 1.1.1.368Thauera aromatica
Succinyl-CoA:(R)-benzylsuccinate CoA-transferase subunit BbsFEC 2.8.3.15Thauera aromatica
Succinyl-CoA:(R)-benzylsuccinate CoA-transferase subunit BbsEEC 2.8.3.15Thauera aromatica
Benzoyl-CoA reductase subunit CEC 1.3.7.8; 3-hydroxybenzoyl-CoA reductase subunit gamma; 1.3.99.n1Thauera aromatica
Benzoyl-CoA reductase subunit BEC 1.3.7.8; 3-hydroxybenzoyl-CoA reductase subunit beta; 1.3.99.n1Thauera aromatica
Benzoyl-CoA reductase subunit AEC 1.3.7.8; 3-hydroxybenzoyl-CoA reductase subunit alpha; 1.3.99.n1Thauera aromatica
Benzoyl-CoA reductase subunit DEC 1.3.7.8; 3-hydroxybenzoyl-CoA reductase subunit delta; 1.3.99.n1Thauera aromatica
(R)-benzylsuccinyl-CoA dehydrogenaseEC 1.3.8.3Thauera aromatica
Benzylsuccinate synthase gamma subunitEC 4.1.99.11Thauera aromatica
Benzylsuccinate synthase alpha subunitEC 4.1.99.11Thauera aromatica
Benzylsuccinate synthase beta subunitEC 4.1.99.11Thauera aromatica
Benzylsuccinate synthase gamma subunit
Putative benzoylsuccinyl-CoA thiolaseThauera aromatica
Beta subunit of benzylsuccinate synthase
BbsCThauera aromatica
Putative E-phenylitaconyl-CoA hydrataseThauera aromatica
Alpha subunit of benzylsuccinate synthase
BbsDThauera aromatica

Compounds (23)

CompoundDescription
hydronium ion
tolueneA widely used industrial solvent.
Succinate
NADH
benzyl alcoholA colorless liquid with a sharp burning taste and slight odor. It is used as a local anesthetic and to reduce pain associated with LIDOCAINE injection. Also, it is used in the manufacture of other benzyl compounds, as a pharmaceutic aid, and in perfumery and flavoring.
Carbon DioxideA colorless, odorless gas that can be formed by the body and is necessary for the respiration cycle of plants and animals.
ZincA metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.
Orthophosphate
fumaratesCompounds based on fumaric acid.
adenosine diphosphateAdenosine 5'-(trihydrogen diphosphate). An adenine nucleotide containing two phosphate groups esterified to the sugar moiety at the 5'-position.
MagnesiumA metallic element that has the atomic symbol Mg, atomic number 12, and atomic weight 24.31. It is important for the activity of many enzymes, especially those involved in OXIDATIVE PHOSPHORYLATION.
WaterA clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
succinyl-coenzyme A
nadA coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. It is found widely in nature and is involved in numerous enzymatic reactions in which it serves as an electron carrier by being alternately oxidized (NAD+) and reduced (NADH). (Dorland, 27th ed)
benzaldehydeRN given refers to parent cpd; structure
adenosine triphosphateAn adenine nucleotide containing three phosphate groups esterified to the sugar moiety. In addition to its crucial roles in metabolism adenosine triphosphate is a neurotransmitter.
Coenzyme A
acetoacetyl CoA
Acetyl Coenzyme AAcetyl CoA participates in the biosynthesis of fatty acids and sterols, in the oxidation of fatty acids and in the metabolism of many amino acids. It also acts as a biological acetylating agent.
glutaconyl-coenzyme A
benzoyl-coenzyme ARN given refers to unlabeled cpd
glutaryl-coenzyme A
Flavin-Adenine DinucleotideA condensation product of riboflavin and adenosine diphosphate. The coenzyme of various aerobic dehydrogenases, e.g., D-amino acid oxidase and L-amino acid oxidase. (Lehninger, Principles of Biochemistry, 1982, p972)