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InterPro: IPR000941 Enolase

Protein matchesHelp
UniProtKB
Matches:
2980 proteins
AccessionHelp IPR000941 Enolase
TypeHelp Family
SignaturesHelp
InterPro RelationshipsHelp
Contains IPR020809 Enolase, conserved site
IPR020810 Enolase, C-terminal
IPR020811 Enolase, N-terminal
GO Term annotationHelp
Process GO:0006096 glycolysis
Function GO:0000287 magnesium ion binding
GO:0004634 phosphopyruvate hydratase activity
Component GO:0000015 phosphopyruvate hydratase complex
InterPro annotation
BioMart Logo Entry Details in BioMart
AbstractHelp

Enolase (2-phospho-D-glycerate hydrolase) is an essential glycolytic enzyme that catalyses the interconversion of 2-phosphoglycerate and phosphoenolpyruvate [1, 2]. In vertebrates, there are 3 different, tissue-specific isoenzymes, designated alpha, beta and gamma. Alpha is present in most tissues, beta is localised in muscle tissue, and gamma is found only in nervous tissue. The functional enzyme exists as a dimer of any 2 isoforms. In immature organs and in adult liver, it is usually an alpha homodimer, in adult skeletal muscle, a beta homodimer, and in adult neurons, a gamma homodimer. In developing muscle, it is usually an alpha/beta heterodimer, and in the developing nervous system, an alpha/gamma heterodimer [3]. The tissue specific forms display minor kinetic differences. Tau-crystallin, one of the major lens proteins in some fish, reptiles and birds, has been shown [4] to be evolutionary related to enolase.

Neuron-specific enolase is released in a variety of neurological diseases, such as multiple sclerosis and after seizures or acute stroke. Several tumour cells have also been found positive for neuron-specific enolase. Beta-enolase deficiency is associated with glycogenosis type XIII defect.

Structural linksHelp
SCOP: c.1.11.1 , d.54.1.1
Database linksHelp
PDBe-motif: PS00164
Enzyme: EC:4.2.1.11
PROSITE doc: PDOC00148
PANDIT: PF00113 , PF03952
Blocks: IPB000941

Taxonomic coverageHelp

Overlapping InterPro entriesHelp
IPR000941 Numbers of overlapping proteins Average numbers of overlapping amino acids

Example proteinsHelp
P00924 Enolase 1

P06733 Alpha-enolase

P15007 Enolase

P17182 Alpha-enolase

Q27527 Enolase

More proteins


Example Proteins Key


InterPro entry accession number/name and structure databases Colour code
IPR020810 Enolase, C-terminal
IPR020811 Enolase, N-terminal
IPR000941 Enolase
IPR020809 Enolase, conserved site
SWISS-MODEL
PDB Chain
ModBase
SCOP Domain
CATH Domain

PublicationsHelp
1. Lal SK, Johnson S, Conway T, Kelley PM.
Characterization of a maize cDNA that complements an enolase-deficient mutant of Escherichia coli.
Plant Mol. Biol. 16 787-95 1991 [PubMed: 1859865]
http://dx.doi.org/10.1007/BF00015071
2. Peshavaria M, Day IN.
Molecular structure of the human muscle-specific enolase gene (ENO3).
Biochem. J. 275 ( Pt 2) 427-33 1991 [PubMed: 1840492]
http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=EBI&pubmedid=1840492
3. Segil N, Shrutkowski A, Dworkin MB, Dworkin-Rastl E.
Enolase isoenzymes in adult and developing Xenopus laevis and characterization of a cloned enolase sequence.
Biochem. J. 251 31-9 1988 [PubMed: 3390159]
http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=EBI&pubmedid=3390159
4. Wistow G, Piatigorsky J.
Recruitment of enzymes as lens structural proteins.
Science 236 1554-6 1987 [PubMed: 3589669]
http://www.sciencemag.org/cgi/content/abstract/236/4808/1554

Additional ReadingHelp
de A S Navarro MV, Gomes Dias SM, Mello LV, da Silva Giotto MT, Gavalda S, Blonski C, Garratt RC, Rigden DJ.
Structural flexibility in Trypanosoma brucei enolase revealed by X-ray crystallography and molecular dynamics.
FEBS J. 274 2007 5077-89 [PubMed: 17822439]
http://dx.doi.org/10.1111/j.1742-4658.2007.06027.x
Chandran V, Luisi BF.
Recognition of enolase in the Escherichia coli RNA degradosome.
J. Mol. Biol. 358 2006 8-15 [PubMed: 16516921]
http://dx.doi.org/10.1016/j.jmb.2006.02.012
Qin J, Chai G, Brewer JM, Lovelace LL, Lebioda L.
Fluoride inhibition of enolase: crystal structure and thermodynamics.
Biochemistry 45 2006 793-800 [PubMed: 16411755]
http://dx.doi.org/10.1021/bi051558s
Chai G, Brewer JM, Lovelace LL, Aoki T, Minor W, Lebioda L.
Expression, purification and the 1.8 angstroms resolution crystal structure of human neuron specific enolase.
J. Mol. Biol. 341 2004 1015-21 [PubMed: 15289101]
http://dx.doi.org/10.1016/j.jmb.2004.05.068
Sims PA, Menefee AL, Larsen TM, Mansoorabadi SO, Reed GH.
Structure and catalytic properties of an engineered heterodimer of enolase composed of one active and one inactive subunit.
J. Mol. Biol. 355 2006 422-31 [PubMed: 16309698]
http://dx.doi.org/10.1016/j.jmb.2005.10.050
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InterPro 23.1