| Identification |
| HMDB Protein ID
| HMDBP13110 |
| Secondary Accession Numbers
| None |
| Name
| N-acetylglucosamine kinase 1 |
| Synonyms
|
- GlcNAc kinase 1
- Hexokinase 1
|
| Gene Name
| HXK1 |
| Protein Type
| Unknown |
| Biological Properties |
| General Function
| Not Available |
| Specific Function
| Component of the N-acetylglucosamine catabolic cascade that phosphorylates N-acetylglucosamine (GlcNAc), and allows the unique ability to utilise GlcNAc as carbon source. Converts GlcNAc to GlcNAc-6-P. Also able to phosphorylate glucose, glucosamine (GlcN), and mannose. Galactose, fructose, N-acetylmannosamine (ManNAc), mannosamine (ManN), galactosamine (GalN), and N-acetylgalactosamine (GalNAc) are not phosphorylated by HXK1. GlcNAc metabolism is closely associated with virulence and morphogenesis, and is involved in the cell wall synthesis. Acts both as a repressor and an activator of genes involved in maintaining cellular homeostasis. Contributes to white-opaque morphological transition and plays a role as a filamentation repressor. |
| Pathways
|
- Amino sugar and nucleotide sugar metabolism
- Biosynthesis of secondary metabolites
- Carbon metabolism
- Fructose and mannose metabolism
- Galactose metabolism
- glycolysis
- Glycolysis / Gluconeogenesis
- hexose metabolism
- Starch and sucrose metabolism
|
| Reactions
| Not Available |
| GO Classification
|
| Biological Process |
| glycolysis |
| pathogenesis |
| glucose 6-phosphate metabolic process |
| hexose metabolic process |
| cellular glucose homeostasis |
| cell wall organization |
| Cellular Component |
| cytosol |
| mitochondrion |
| nucleus |
| Molecular Function |
| ATP binding |
| glucose binding |
| fructokinase activity |
| glucokinase activity |
| mannokinase activity |
| N-acetylglucosamine kinase activity |
| glucosamine kinase activity |
|
| Cellular Location
|
Not Available
|
| Gene Properties |
| Chromosome Location
| Not Available |
| Locus
| Not Available |
| SNPs
| Not Available |
| Gene Sequence
|
Not Available
|
| Protein Properties |
| Number of Residues
| 493 |
| Molecular Weight
| 54822.32 |
| Theoretical pI
| 5.395 |
| Pfam Domain Function
|
|
| Signals
|
Not Available
|
|
Transmembrane Regions
|
Not Available
|
| Protein Sequence
|
Not Available
|
| External Links |
| GenBank ID Protein
| Not Available |
| UniProtKB/Swiss-Prot ID
| Q59RW5 |
| UniProtKB/Swiss-Prot Entry Name
| HXK1_CANAL |
| PDB IDs
|
Not Available |
| GenBank Gene ID
| Not Available |
| GeneCard ID
| Not Available |
| GenAtlas ID
| Not Available |
| HGNC ID
| Not Available |
| References |
| General References
| - Jones T, Federspiel NA, Chibana H, Dungan J, Kalman S, Magee BB, Newport G, Thorstenson YR, Agabian N, Magee PT, Davis RW, Scherer S: The diploid genome sequence of Candida albicans. Proc Natl Acad Sci U S A. 2004 May 11;101(19):7329-34. doi: 10.1073/pnas.0401648101. Epub 2004 May 3. [PubMed:15123810 ]
- van het Hoog M, Rast TJ, Martchenko M, Grindle S, Dignard D, Hogues H, Cuomo C, Berriman M, Scherer S, Magee BB, Whiteway M, Chibana H, Nantel A, Magee PT: Assembly of the Candida albicans genome into sixteen supercontigs aligned on the eight chromosomes. Genome Biol. 2007;8(4):R52. doi: 10.1186/gb-2007-8-4-r52. [PubMed:17419877 ]
- Muzzey D, Schwartz K, Weissman JS, Sherlock G: Assembly of a phased diploid Candida albicans genome facilitates allele-specific measurements and provides a simple model for repeat and indel structure. Genome Biol. 2013;14(9):R97. doi: 10.1186/gb-2013-14-9-r97. [PubMed:24025428 ]
- Kumar MJ, Jamaluddin MS, Natarajan K, Kaur D, Datta A: The inducible N-acetylglucosamine catabolic pathway gene cluster in Candida albicans: discrete N-acetylglucosamine-inducible factors interact at the promoter of NAG1. Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14218-23. doi: 10.1073/pnas.250452997. [PubMed:11114181 ]
- Yamada-Okabe T, Sakamori Y, Mio T, Yamada-Okabe H: Identification and characterization of the genes for N-acetylglucosamine kinase and N-acetylglucosamine-phosphate deacetylase in the pathogenic fungus Candida albicans. Eur J Biochem. 2001 Apr;268(8):2498-505. doi: 10.1046/j.1432-1327.2001.02135.x. [PubMed:11298769 ]
- Singh P, Ghosh S, Datta A: Attenuation of virulence and changes in morphology in Candida albicans by disruption of the N-acetylglucosamine catabolic pathway. Infect Immun. 2001 Dec;69(12):7898-903. doi: 10.1128/IAI.69.12.7898-7903.2001. [PubMed:11705974 ]
- Wendland J, Hellwig D, Walther A, Sickinger S, Shadkchan Y, Martin R, Bauer J, Osherov N, Tretiakov A, Saluz HP: Use of the Porcine Intestinal Epithelium (PIE)-Assay to analyze early stages of colonization by the human fungal pathogen Candida albicans. J Basic Microbiol. 2006;46(6):513-23. doi: 10.1002/jobm.200610167. [PubMed:17139615 ]
- Wendland J, Schaub Y, Walther A: N-acetylglucosamine utilization by Saccharomyces cerevisiae based on expression of Candida albicans NAG genes. Appl Environ Microbiol. 2009 Sep;75(18):5840-5. doi: 10.1128/AEM.00053-09. Epub 2009 Jul 31. [PubMed:19648376 ]
- Gunasekera A, Alvarez FJ, Douglas LM, Wang HX, Rosebrock AP, Konopka JB: Identification of GIG1, a GlcNAc-induced gene in Candida albicans needed for normal sensitivity to the chitin synthase inhibitor nikkomycin Z. Eukaryot Cell. 2010 Oct;9(10):1476-83. doi: 10.1128/EC.00178-10. Epub 2010 Jul 30. [PubMed:20675577 ]
- Naseem S, Gunasekera A, Araya E, Konopka JB: N-acetylglucosamine (GlcNAc) induction of hyphal morphogenesis and transcriptional responses in Candida albicans are not dependent on its metabolism. J Biol Chem. 2011 Aug 19;286(33):28671-28680. doi: 10.1074/jbc.M111.249854. Epub 2011 Jun 23. [PubMed:21700702 ]
- Rao KH, Ghosh S, Natarajan K, Datta A: N-acetylglucosamine kinase, HXK1 is involved in morphogenetic transition and metabolic gene expression in Candida albicans. PLoS One. 2013;8(1):e53638. doi: 10.1371/journal.pone.0053638. Epub 2013 Jan 14. [PubMed:23341961 ]
- Rao KH, Ruhela D, Ghosh S, Abdin MZ, Datta A: N-acetylglucosamine kinase, HXK1 contributes to white-opaque morphological transition in Candida albicans. Biochem Biophys Res Commun. 2014 Feb 28;445(1):138-44. doi: 10.1016/j.bbrc.2014.01.123. Epub 2014 Jan 31. [PubMed:24491547 ]
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