1.14.13.2: 4-hydroxybenzoate 3-monooxygenase

This is an abbreviated version!
For detailed information about 4-hydroxybenzoate 3-monooxygenase, go to the full flat file.

Reaction

Synonyms

4-HBA 3-hydroxylase, 4-HBA 3-monooxygenase, 4-HBA-3-hydroxylase, 4-HBMO, 4-hydroxybenzoate 3-hydroxylase, 4-hydroxybenzoate 3-monooxygenase, 4-hydroxybenzoate hydroxylase, 4-hydroxybenzoate monooxygenase, 4-hydroxybenzoic hydroxylase, 4HBA 3-hydroxylase, An_PhhA, BxeA2040, FAD-dependent 4-hydroxybenzoate hydroxylase, fungal 4-hydroxybenzoate 3-hydroxylase, HBH, m-hydroxybenzoate hydroxylase, MobA, NADPH-dependent 4-HBA hydroxylase, ncgl1032, oxygenase, 4-hydroxybenzoate 3-mono-, p-hydroxybenzoate hydroxylase, p-hydroxybenzoate-3-hydroxylase, p-hydroxybenzoic acid hydrolase, p-hydroxybenzoic acid hydroxylase, p-hydroxybenzoic hydroxylase, PaPobA, para-hydroxybenzoate hydroxylase, PHBAD, PHBH, PHBHase, PHBHCn2, phhA, PobA, pobACg, POHBase, Reut_B4006

ECTree

     1 Oxidoreductases

         1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen

             1.14.13 With NADH or NADPH as one donor, and incorporation of one atom of oxygen into the other donor

                1.14.13.2 4-hydroxybenzoate 3-monooxygenase

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Results	in table
8	Activating Compound
4541	AA Sequence
5	Application
1	CAS Registry Number
22	Cloned(Commentary)
96	Cofactor
17	Crystallization (Commentary)
6	Expression
43	General Information
7	General Stability
88	Inhibitors
17	kcat/KM [mM/s]
13	Ki Value [mM]
88	KM Value [mM]
1	Metals/Ions
27	Molecular Weight [Da]
57	Natural Substrates/ Products (Substrates)
170	Organism
14	Pathway
37	PDB ID
17	pH Optimum
1	pH Range
4	pH Stability
147	Protein Variants
19	Purification (Commentary)
14	Reaction
3	Reaction Type
115	Reference
16	Specific Activity [micromol/min/mg]
5	Storage Stability
208	Substrates and Products (Substrate)
32	Subunits
145	Synonyms
1	Systematic Name
6	Temperature Optimum [°C]
19	Temperature Stability [°C]
53	Turnover Number [1/s]

Application

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Application on EC 1.14.13.2 - 4-hydroxybenzoate 3-monooxygenase

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APPLICATION

ORGANISM

UNIPROT

COMMENTARY

LITERATURE

analysis

Pseudomonas sp.

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a bienzyme-based Clark electrode is developed for the interference-free determination of L-glutamate. This sensor is based on the specific dehydrogenation by L-glutamate dehydrogenase (EC 1.4.1.3) in combination with p-hydroxybenzoate hydroxylase (EC 1.14.13.2). The enzymes are entrapped by a poly(carbamoyl) sulfonate hydrogel on a Teflon membrane

690069

degradation

2 entries

drug development

2 entries

degradation

Diaporthe liquidambaris

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in soil conditions, Phomopsis liquidambari effectively decomposes 99% of the available 4-hydroxybenzoic acid within 48 h. 4-Hydroxybenzoic acid hydroxylase activity is present in a high level early at 20 h, followed by 3,4-dihydroxybenzoic acid decarboxylase which reaches its highest relative activity at 24 h, and finally catechol 1,2-dioxygenase exhibits peak activity at 32 h

724101

degradation

Diaporthe liquidambaris B3

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in soil conditions, Phomopsis liquidambari effectively decomposes 99% of the available 4-hydroxybenzoic acid within 48 h. 4-Hydroxybenzoic acid hydroxylase activity is present in a high level early at 20 h, followed by 3,4-dihydroxybenzoic acid decarboxylase which reaches its highest relative activity at 24 h, and finally catechol 1,2-dioxygenase exhibits peak activity at 32 h

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drug development

Pseudomonas putida

Q88H28

p-hydroxybenzoate hydroxylase (PobA) from Pseudomonas putida is a possible drug target to combat tetracycline resistance, in complex with flavin adenine dinucleotide (FAD)

763846

drug development

Pseudomonas putida KT-2440

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p-hydroxybenzoate hydroxylase (PobA) from Pseudomonas putida is a possible drug target to combat tetracycline resistance, in complex with flavin adenine dinucleotide (FAD)

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