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Literature summary for 2.4.1.18 extracted from

  • Jo, H.J.; Park, S.; Jeong, H.G.; Kim, J.W.; Park, J.T.
    Vibrio vulnificus glycogen branching enzyme preferentially transfers very short chains: N1 domain determines the chain length transferred (2015), FEBS Lett., 589, 1089-1094.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
additional information construction of domain-truncated (N1 and N) and N1-domain-swapped (with VvGBE N1 replacing the counter part of Escherichia coli GBE) mutants. The truncation mutants synthesize branched products with a greatly reduced proportion of short chains compared to the wild-type. The swapping mutant exhibit a branching pattern of the short chain region similar to that of the ewild-type enzyme Vibrio vulnificus

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Vibrio vulnificus the glycogen branching enzyme from Vibrio vulnificus transfers short side chains (DP 3-5) significantly greater than any other bacterial glycogen branching enzyme. The N1-domain of the enzyme has a crucial role in the determination of the branching pattern of glycogen, degrees of polymerization in enzyme reaction products compared to enzymes from other origin, overview ?
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additional information Vibrio vulnificus MO6-24/O the glycogen branching enzyme from Vibrio vulnificus transfers short side chains (DP 3-5) significantly greater than any other bacterial glycogen branching enzyme. The N1-domain of the enzyme has a crucial role in the determination of the branching pattern of glycogen, degrees of polymerization in enzyme reaction products compared to enzymes from other origin, overview ?
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Organism

Organism UniProt Comment Textmining
Vibrio vulnificus
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Vibrio vulnificus MO6-24/O
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information the glycogen branching enzyme from Vibrio vulnificus transfers short side chains (DP 3-5) significantly greater than any other bacterial glycogen branching enzyme. The N1-domain of the enzyme has a crucial role in the determination of the branching pattern of glycogen, degrees of polymerization in enzyme reaction products compared to enzymes from other origin, overview Vibrio vulnificus ?
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?
additional information the glycogen branching enzyme from Vibrio vulnificus transfers short side chains (DP 3-5) significantly greater than any other bacterial glycogen branching enzyme. The N1-domain of the enzyme has a crucial role in the determination of the branching pattern of glycogen, degrees of polymerization in enzyme reaction products compared to enzymes from other origin, overview Vibrio vulnificus MO6-24/O ?
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?

Synonyms

Synonyms Comment Organism
GBE
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Vibrio vulnificus
glycogen branching enzyme
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Vibrio vulnificus

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
30
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assay at Vibrio vulnificus

Temperature Range [°C]

Temperature Minimum [°C] Temperature Maximum [°C] Comment Organism
25 45 activity range, profile overview Vibrio vulnificus

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7.5
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assay at Vibrio vulnificus

pH Range

pH Minimum pH Maximum Comment Organism
5.5 8.5 active at Vibrio vulnificus

General Information

General Information Comment Organism
evolution the enzyme belongs to the glycoside hydrolase family 13, GH13. Phylogenetic analysis groups VvGBE with other Vibrio GBEs and closely related to GBEs of enteric bacteria. VvGBE and Escherichia coli GBE are type I bacterial GBEs and share 57% sequence similarity Vibrio vulnificus
additional information branching patterns of the truncation mutants and the swapping mutant. Branching patterns of VvGBE wild-type Vibrio vulnificus
physiological function glycogen is a major polysaccharide of energy reservoir in animals and microorganisms. It is a highly branched polysaccharide, in which glucose residues are linked by alpha-1,4 glycosidic bonds to from linear chains and at every 10 residues, other linear chains are linked by alpha-1,6-glycosidic bonds to form side chains. Formation of side chains in glycogen is catalyzed by glycogen branching enzyme (GBE) or branching enzyme (BE). GBE catalyzes formation of alpha-1,6-glycosidic linkage by cleaving alpha-1,4 linkages of substrate and transferring the non-reducing end of the chain to an acceptor Vibrio vulnificus