1.14.13.172: salicylate 5-hydroxylase

This is an abbreviated version!
For detailed information about salicylate 5-hydroxylase, go to the full flat file.

Word Map on EC 1.14.13.172

1.14.13.172

gentisate

naphthalene

ralstonia

ferredoxin

putida

2-hydroxybenzoate

protocatechuate

naphthalene-degrading

polycyclic

maleylpyruvate

rieske-type

1,2-dihydroxynaphthalene

nonheme

2-chlorobenzoate

transposase

fumarylpyruvate

cis-dihydrodiol

marr-type

1-hydroxylase

rieske

ring-cleavage

incp-7

naphthalenivorans

salicylaldehyde

chlorocatechol

polaromonas

Reaction

Synonyms

nagG, NagGH, nagH, S5H, S5HR, SAL5H, SalABCD, SALD

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

1.14.13.172 salicylate 5-hydroxylase

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Results	in table
188	AA Sequence
1	Application
4	Cloned(Commentary)
11	Cofactor
1	Crystallization (Commentary)
2	General Information
6	KM Value [mM]
3	Metals/Ions
9	Molecular Weight [Da]
9	Natural Substrates/ Products (Substrates)
17	Organism
5	Pathway
8	PDB ID
1	Protein Variants
2	Purification (Commentary)
1	Reaction
12	Reference
2	Specific Activity [micromol/min/mg]
26	Substrates and Products (Substrate)
8	Subunits
25	Synonyms
1	Systematic Name
2	Turnover Number [1/s]

Reference

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Reference on EC 1.14.13.172 - salicylate 5-hydroxylase

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438959

Suemori, A.; Nakajima, K.; Kurane, R.; Nakamura, Y.

Physicochemical and immunochemical characterization of salicylate 5-hydroxylase, m-hydroxybenzoate 6-hydroxylase and p-hydroxybenzoate 3-hydroxylase from Rhodococcus erythropolis

Biotechnol. Lett.

1063-1068

1995

Rhodococcus erythropolis, Rhodococcus erythropolis S1

721398

Fang, T.; Zhou, N.Y.

Purification and characterization of salicylate 5-hydroxylase, a three-component monooxygenase from Ralstonia sp. strain U2

Appl. Microbiol. Biotechnol.

671-679

2014

Ralstonia sp. (O52379 and O52380), Ralstonia sp., Ralstonia sp. U2 (O52379 and O52380)

23624660

722496

Fuenmayor, S.L.; Wild, M.; Boyes, A.L.; Williams, P.A.

A gene cluster encoding steps in conversion of naphthalene to gentisate in Pseudomonas sp. strain U2

J. Bacteriol.

180

2522-2530

1998

Pseudomonas sp. (O52379 and O52380), Pseudomonas sp., Pseudomonas sp. U2 (O52379 and O52380)

9573207

722507

Zhou, N.Y.; Al-Dulayymi, J.; Baird, M.S.; Williams, P.A.

Salicylate 5-hydroxylase from Ralstonia sp. strain U2: a monooxygenase with close relationships to and shared electron transport proteins with naphthalene dioxygenase

J. Bacteriol.

184

1547-1555

2002

Ralstonia sp. (O52379 and O52380), Ralstonia sp., Ralstonia sp. U2 (O52379 and O52380)

11872705

743932

Sun, X.; Lin, Y.; Yuan, Q.; Yan, Y.

Precursor-directed biosynthesis of 5-hydroxytryptophan using metabolically engineered E. coli

ACS Synth. Biol.

554-558

2015

Cupriavidus necator (Q0KB56)

25275944

763976

Hou, Y.J.; Guo, Y.; Li, D.F.; Zhou, N.Y.

Structural and biochemical analysis reveals a distinct catalytic site of salicylate 5-monooxygenase NagGH from Rieske dioxygenases

Appl. Environ. Microbiol.

e01629

2021

Ralstonia sp. (O52378 and O52381 and O52379 and O52380), Ralstonia sp.

33452034

764170

Rogers, M.S.; Lipscomb, J.D.

Salicylate 5-hydroxylase intermediates in aromatic hydroxylation by a Rieske monooxygenase

Biochemistry

5305-5319

2019

Ralstonia sp. (O52378 and O52381 and O52379 and O52380)

31066545

764345

Sheng, H.; Jing, Y.; An, N.; Shen, X.; Sun, X.; Yan, Y.; Wang, J.; Yuan, Q.

Extending the shikimate pathway for microbial production of maleate from glycerol in engineered Escherichia coli

Biotechnol. Bioeng.

118

1840-1850

2021

Ralstonia sp. (O52379 and O52380)

33512000