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Ligand p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose

Basic Ligand Information

Molecular Structure

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Roles as Enzyme Ligand

Substrate in Enzyme-catalyzed Reactions (9 results)

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Show Substrate (9 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

2.3.1.79

acetyl-CoA + 4-nitrophenyl alpha-D-maltoside = CoA + 4-nitrophenyl 4-O-(6-O-acetyl-alpha-D-glucopyranosyl)-alpha-D-glucopyranoside

487512

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2.4.1.19

p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + glycosyl acceptor = p-nitrophenyl-D-glucose + p-nitrophenyl-alpha-1,4-glucopyranosyl-D-glucose + ?

488843

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3.2.1.1

4-nitrophenyl alpha-D-maltoside + H2O = 4-nitrophenol + alpha-D-maltose

666839

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3.2.1.1

4-nitrophenyl-alpha-D-maltoside + H2O = 4-nitrophenol + maltose

704143

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3.2.1.1

p-nitrophenyl alpha-D-maltoside + H2O = p-nitrophenol + maltose

393379, 393448, 393388

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3.2.1.1

3 entries

3.2.1.177

4-nitrophenyl alpha-maltoside + H2O = 4-nitrophenyl alpha-D-glucoside + D-glucose

715446

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3.2.1.2

4-nitrophenyl alpha-maltopyranoside + H2O = 4-nitrophenol + alpha-maltopyranose

721339

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3.2.1.20

4-nitrophenyl alpha-D-glucopyranosyl-1,4-alpha-D-glucopyranoside + H2O = 4-nitrophenol + alpha-D-glucose

665788

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3.2.1.20

p-nitrophenyl-alpha-D-maltoside + H2O = p-nitrophenol + alpha-D-maltose

698521

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3.2.1.20

2 entries

Product in Enzyme-catalyzed Reactions (10 results)

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Show Product (10 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

2.4.1.19

p-nitrophenyl-(glucose)5 + glycosyl acceptor = p-nitrophenyl alpha-D-glucoside + p-nitrophenyl 4-O-alpha-D-glucopyranosyl-alpha-D-glucopyranoside + p-nitrophenyl-(alpha-1,4-D-glucopyranosyl)2-D-glucose + p-nitrophenyl-(alpha-1,4-D-glucopyranosyl)3-D-glucose

488843

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2.4.1.19

p-nitrophenyl-(glucose)6 + glycosyl acceptor = p-nitrophenyl alpha-D-glucoside + p-nitrophenyl 4-O-alpha-D-glucopyranosyl-alpha-D-glucopyranoside + p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)3-D-glucose + ?

488843

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2.4.1.19

4,6-benzylidene-alpha-D-4-nitrophenylmaltoheptaose + D-glucose = 4,6-benzylidene-maltopentaose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose

0

-

2.4.1.19

p-nitrophenyl-(alpha-1,4-glucopyranosyl)3-D-glucose + glycosyl acceptor = p-nitrophenyl alpha-D-glucoside + p-nitrophenyl-alpha-1,4-glucopyranosyl-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + ?

488843

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2.4.1.19

p-nitrophenyl-(alpha-1,4-glucopyranosyl)7-D-glucose + glycosyl acceptor = p-nitrophenyl-glucose + p-nitrophenyl-alpha-1,4-glucopyranosyl-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)3-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)4-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)5-D-glucose + ?

488843

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2.4.1.19

p-nitrophenyl-(glucose)6 + glycosyl acceptor = p-nitrophenyl alpha-D-glucoside + p-nitrophenyl 4-O-alpha-D-glucopyranosyl-alpha-D-glucopyranoside + p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)3-D-glucose + ?

488843

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2.4.1.19

p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + glycosyl acceptor = p-nitrophenyl-D-glucose + p-nitrophenyl-alpha-1,4-glucopyranosyl-D-glucose + ?

488843

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2.4.1.19

p-nitrophenyl-(alpha-1,4-glucopyranosyl)3-D-glucose + glycosyl acceptor = p-nitrophenyl alpha-D-glucoside + p-nitrophenyl-alpha-1,4-glucopyranosyl-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + ?

488843

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2.4.1.19

p-nitrophenyl-(alpha-1,4-glucopyranosyl)6-D-glucose + glycosyl acceptor = p-nitrophenyl-glucose + p-nitrophenyl-alpha-1,4-glucopyranosyl-D-glucose + p-nitrophenyl-(glucose)3 + p-nitrophenyl-(alpha-1,4-glucopyranosyl)3-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)4-D-glucose + ?

488843

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2.4.1.19

p-nitrophenyl-(alpha-1,4-glucopyranosyl)7-D-glucose + glycosyl acceptor = p-nitrophenyl-glucose + p-nitrophenyl-alpha-1,4-glucopyranosyl-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)3-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)4-D-glucose + p-nitrophenyl-(alpha-1,4-glucopyranosyl)5-D-glucose + ?

488843

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2.4.1.19

10 entries

Enzyme Kinetic Parameters

k_cat Value (Turnover Number) (5 results)

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Show Turnover Number (5 entries)

EC NUMBER

TURNOVER NUMBER [1/S]

TURNOVER NUMBER MAXIMUM [1/S]

COMMENTARY

LITERATURE

2.4.1.19

1.66

-

E 192

488843

3.2.1.1

0.0494

-

isozyme PPA-I, at pH 6.9 and 30°C

704143

3.2.1.1

0.0497

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isozyme PPA-II, at pH 6.9 and 30°C

704143

3.2.1.1

2 entries

3.2.1.2

962

-

pH 7.0, 90°C

721339

3.2.1.20

75.9

-

pH 5.8, 34°C

665788

K_M Value (4 results)

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Show KM Value (4 entries)

EC NUMBER

KM VALUE [MM]

KM VALUE MAXIMUM [MM]

COMMENTARY

LITERATURE

3.2.1.1

4.48

-

isozyme PPA-I, at pH 6.9 and 30°C

704143

3.2.1.1

4.63

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isozyme PPA-II, at pH 6.9 and 30°C

704143

3.2.1.1

2 entries

3.2.1.2

0.0827

-

pH 7.0, 90°C

721339

3.2.1.20

2.06

-

pH 5.8, 34°C

665788

References & Links

Literature References (11)

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Show Reference (11 entries)

BRENDA REFERENCE ID

PUBMED ID

TITLE

YEAR

AUTHORS

JOURNAL

VOLUME

PAGES

393379

16347662

Production and characterization of raw-potato-starch-digesting alpha-amylase from Bacillus subtilis 65

1988

Hayashida, S.; Teramoto, Y.; Inoue, T.

Appl. Environ. Microbiol.

54

1516-1522

393388

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A Bacillus acidocaldarius alpha-amylase that is highly stable to heat under acidic conditions

1986

Kanno, M.

Agric. Biol. Chem.

50

23-31

393448

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Purification and properties of the raw strach-degrading alpha-amylase of Bacillus sp. IMD 434

1999

Hamilton, L.M.; Kelly, C.T.; Fogarty, W.M.

Biotechnol. Lett.

21

111-115

487512

12731863

The structure and specificity of Escherichia coli maltose acetyltransferase give new insight into the LacA family of acyltransferases

2003

Lo Leggio, L.; Dal Degan, F.; Poulsen, P.; Moeller Andersen, S.; Larsen, S.

Biochemistry

42

5225-5235

488843

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Cyclomaltodextrin glucanotransferase from Bacillus circulans E 192. II. Action Patterns

1992

Bovetto, L.J.; Villette, J.R.; Fontaine, I.F.; Sicard, P.J.; Bouquelet, S.J.L.

Biotechnol. Appl. Biochem.

15

59-68

665788

16290308

Hydrolyses and transglycosylations performed by purified alpha-D-glucosidase of the marine mollusc Aplysia fasciata

2006

Andreotti, G.; Giordano, A.; Tramice, A.; Mollo, E.; Trincone, A.

J. Biotechnol.

122

274-284

666839

15517985

Crystal structure of the pig pancreatic alpha-amylase complexed with rho-nitrophenyl-alpha-D-maltoside-flexibility in the active site

2004

Zhuo, H.; Payan, F.; Qian, M.

Protein J.

23

379-387

698521

18171380

Chaperone mediated solubilization of 69-kDa recombinant maltodextrin glucosidase in Escherichia coli

2008

Paul, S.; Chaudhuri, T. K.

J. Appl. Microbiol.

104

35-41

704143

19807164

Kinetic analysis and mechanism on the inhibition of chlorogenic acid and its components against porcine pancreas alpha-amylase isozymes I and II

2009

Narita, Y.; Inouye, K.

J. Agric. Food Chem.

57

9218-9225

715446

10801892

Identification and molecular characterization of the first alpha-xylosidase from an archaeon

2000

Moracci, M.; Cobucci Ponzano, B.; Trincone, A.; Fusco, S.; De Rosa, M.; van Der Oost, J.; Sensen, C.W.; Charlebois, R.L.; Rossi, M.

J. Biol. Chem.

275

22082-22089

721339

18156337

Functional-genomics-based identification and characterization of open reading frames encoding alpha-glucoside-processing enzymes in the hyperthermophilic archaeon Pyrococcus furiosus

2008

Comfort, D.A.; Chou, C.J.; Conners, S.B.; VanFossen, A.L.; Kelly, R.M.

Appl. Environ. Microbiol.

74

1281-1283

Links to other databases for p-nitrophenyl-(alpha-1,4-glucopyranosyl)2-D-glucose

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Show Links (1 entry)

ChEBI

PubChem

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