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词条 TRIL (gene)
释义

  1. Function

  2. Protein sequence

  3. Homology

  4. Gene neighborhood

  5. References

  6. Further reading

{{Infobox_gene}}KIAA0644, also known as TRIL or TLR4 interactor with leucine rich repeats, is a protein that in humans is encoded by the KIAA0644 gene.[1]

Function

The exact function of KIAA0644 is not known. It is, however, a member of the leucine-rich repeat family of proteins, which are known to be involved in protein-protein interactions. This protein is known to interact with the TLR4 protein.

TRIL is a component of the TLR4 complex and is induced in a number of cell types by lipopolysaccharide (LPS).[2]

Protein sequence

The main isoform of the human protein is 811 amino long and is composed primarily of leucine (17%), alanine and arginine (~10%), and glycine (~ 8.5%) residues. The protein sequence is predicted to consists mostly of α-helices and a few β-sheet

Homology

KIAA0644 is conserved well among mammals but can be found in all chordates with lower sequence identities.

Gene neighborhood

The KIAA0644 gene is neighbors to mRNA-cAMP responsive element binding gene downstream and mRNA carboxypeptidase and serine carboxypeptidase gene upstream [3][4]

References

1. ^{{cite web | title = Entrez Gene: TRIL TLR4 interactor with leucine rich repeats| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&DbFrom=nuccore&Cmd=Link&LinkName=nuccore_gene&IdsFromResult=23271341| accessdate = 13 May 2010}}
2. ^{{cite journal |vauthors=Carpenter S, Carlson T, Dellacasagrande J, Garcia A, Gibbons S, Hertzog P, Lyons A, Lin LL, Lynch M, Monie T, Murphy C, Seidl KJ, Wells C, Dunne A, O'Neill LA | title = TRIL, a functional component of the TLR4 signaling complex, highly expressed in brain | journal = J. Immunol. | volume = 183 | issue = 6 | pages = 3989–95 |date=September 2009 | pmid = 19710467 | doi = 10.4049/jimmunol.0901518 | url = }}
3. ^{{cite web | title = NCBI Entrez| url = https://www.ncbi.nlm.nih.gov/nuccore/NC_000007.13?from=28992722&to=28998281&strand=true&report=graph| accessdate = 13 May 2010}}
4. ^{{cite journal |vauthors=Ishikawa K, Nagase T, Suyama M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O | title = Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro | journal = DNA Res. | volume = 5 | issue = 3 | pages = 169–76 |date=June 1998 | pmid = 9734811 | doi = 10.1093/dnares/5.3.169| url = }}

Further reading

{{refbegin | 2}}
  • {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2002 |pmid= 12477932 |pmc=139241 |doi= 10.1073/pnas.242603899 }}
  • {{cite journal |vauthors=Scherer SW, Cheung J, MacDonald JR, etal |title=Human Chromosome 7: DNA Sequence and Biology |journal=Science |volume=300 |issue= 5620 |pages= 767–72 |year= 2003 |pmid= 12690205 |pmc=2882961 |doi= 10.1126/science.1083423 }}
  • {{cite journal |vauthors=Büssow K, Cahill D, Nietfeld W, etal |title=A method for global protein expression and antibody screening on high-density filters of an arrayed cDNA library |journal=Nucleic Acids Res. |volume=26 |issue= 21 |pages= 5007–8 |year= 1998 |pmid= 9776767 |pmc=147919 |doi= 10.1093/nar/26.21.5007}}
  • {{cite journal |vauthors=Wheeler HE, Metter EJ, Tanaka T, etal |title=Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging |journal=PLoS Genet. |volume=5 |issue= 10 |pages= e1000685 |year= 2009 |pmid= 19834535 |pmc=2752811 |doi= 10.1371/journal.pgen.1000685 |editor1-last=Gibson |editor1-first=Greg }}
{{refend}}{{NLM content}}{{gene-7-stub}}
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