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Literature summary for 3.4.21.B30 extracted from

  • Guzzo, A.; Lee, M.H.; Oda, K.; Walker, G.C.
    Analysis of the region between amino acids 30 and 42 of intact UmuD by a monocysteine approach (1996), J. Bacteriol., 178, 7295-7303.
    View publication on PubMedView publication on EuropePMC
Search for more literature for 3.4.21.B30

Cloned(Commentary)

Cloned (Comment) Organism
-
 Escherichia coli

Protein Variants

Protein Variants Comment Organism
A31C partial reduction in UV mutability Escherichia coli
D32C deficiencies in RecA-mediated cleavage as well as in UV mutagenesis, less than 30% of the wild-type activity Escherichia coli
E35C deficiencies in RecA-mediated cleavage as well as in UV mutagenesis, less than 30% of the wild-type activity Escherichia coli
I38C poor reaction with iodoacetate Escherichia coli
L40C less than 30% of the wild-type activity, although defective in UV mutagenesis and in vitro RecA-mediated cleavage, mutant is able to be cleaved efficiently by RecA in vivo Escherichia coli
R37C poor reaction with iodoacetate Escherichia coli
Y33C less than 30% of the wild-type activity, although defective in UV mutagenesis and in vitro RecA-mediated cleavage, mutant is able to be cleaved efficiently by RecA in vivo Escherichia coli

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Escherichia coli enzyme interacts with RecA ?
-
 ?

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
 Escherichia coli

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information enzyme interacts with RecA Escherichia coli ?
-
 ?