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Literature summary extracted from

  • Zehner, S.; Kotzsch, A.; Bister, B.; Suessmuth, R.D.; Mendez, C.; Salas, J.A.; van Pee, K.H.
    A regioselective tryptophan 5-halogenase is involved in pyrroindomycin biosynthesis in Streptomyces rugosporus LL-42D005 (2005), Chem. Biol., 12, 445-452.
    View publication on PubMed

Cloned(Commentary)

EC Number Cloned (Comment) Organism
1.14.19.58 overexpression in Pseudomonas fluorescens BL915 DELTAORF1 Streptomyces rugosporus

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
1.14.19.58 0.15
-
L-tryptophan pH 7.2, 30°C Streptomyces rugosporus

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.14.19.58 L-tryptophan + FADH2 + Cl- + O2 + H+ Streptomyces rugosporus the enzyme is involved in the biosynthesis of the antibiotic pyrroindomycin B that contains an indole ring chlorinated in the 5 position 5-chloro-L-tryptophan + FAD + 2 H2O
-
?
1.14.19.58 L-tryptophan + FADH2 + Cl- + O2 + H+ Streptomyces rugosporus LL-42D005 the enzyme is involved in the biosynthesis of the antibiotic pyrroindomycin B that contains an indole ring chlorinated in the 5 position 5-chloro-L-tryptophan + FAD + 2 H2O
-
?

Organism

EC Number Organism UniProt Comment Textmining
1.14.19.58 Streptomyces rugosporus A4D0H5
-
-
1.14.19.58 Streptomyces rugosporus LL-42D005 A4D0H5
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
1.14.19.58
-
Streptomyces rugosporus

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.19.58 L-tryptophan + FADH2 + Br- + O2 + H+ brominating activity is about 75% of the chlorinating activity Streptomyces rugosporus 5-bromo-L-tryptophan + FAD + 2 H2O
-
?
1.14.19.58 L-tryptophan + FADH2 + Br- + O2 + H+ brominating activity is about 75% of the chlorinating activity Streptomyces rugosporus LL-42D005 5-bromo-L-tryptophan + FAD + 2 H2O
-
?
1.14.19.58 L-tryptophan + FADH2 + Cl- + O2 + H+
-
Streptomyces rugosporus 5-chloro-L-tryptophan + FAD + 2 H2O
-
?
1.14.19.58 L-tryptophan + FADH2 + Cl- + O2 + H+ the enzyme is involved in the biosynthesis of the antibiotic pyrroindomycin B that contains an indole ring chlorinated in the 5 position Streptomyces rugosporus 5-chloro-L-tryptophan + FAD + 2 H2O
-
?
1.14.19.58 L-tryptophan + FADH2 + Cl- + O2 + H+
-
Streptomyces rugosporus LL-42D005 5-chloro-L-tryptophan + FAD + 2 H2O
-
?
1.14.19.58 L-tryptophan + FADH2 + Cl- + O2 + H+ the enzyme is involved in the biosynthesis of the antibiotic pyrroindomycin B that contains an indole ring chlorinated in the 5 position Streptomyces rugosporus LL-42D005 5-chloro-L-tryptophan + FAD + 2 H2O
-
?

Synonyms

EC Number Synonyms Comment Organism
1.14.19.58 pyrH
-
Streptomyces rugosporus

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
1.14.19.58 30
-
assay at Streptomyces rugosporus

Turnover Number [1/s]

EC Number Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
1.14.19.58 0.00813
-
L-tryptophan pH 7.2, 30°C Streptomyces rugosporus

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
1.14.19.58 7.2
-
assay at Streptomyces rugosporus

General Information

EC Number General Information Comment Organism
1.14.19.58 malfunction a gene disruption mutant in the tryptophan 5-halogenase gene no longer produces the pyrroindomycin B, but still produces pyrroindomycin A, the nonhalogenated derivative Streptomyces rugosporus
1.14.19.58 physiological function the enzyme is involved in the biosynthesis of the antibiotic pyrroindomycin B that contains an indole ring chlorinated in the 5 position Streptomyces rugosporus

kcat/KM [mM/s]

EC Number kcat/KM Value [1/mMs-1] kcat/KM Value Maximum [1/mMs-1] Substrate Comment Organism Structure
1.14.19.58 0.0542
-
L-tryptophan pH 7.2, 30°C Streptomyces rugosporus