Pulmonary surfactant-associated protein B
From Wikipedia, the free encyclopedia
Surfactant, pulmonary-associated protein B
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Identifiers | |||||||||||
Symbol(s) | SFTPB; PSP-B; SFTB3; SFTP3; SP-B | ||||||||||
External IDs | OMIM: 178640 MGI: 109516 HomoloGene: 456 | ||||||||||
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RNA expression pattern | |||||||||||
Orthologs | |||||||||||
Human | Mouse | ||||||||||
Entrez | 6439 | 20388 | |||||||||
Ensembl | ENSG00000168878 | ENSMUSG00000056370 | |||||||||
Uniprot | P07988 | Q2M2M2 | |||||||||
Refseq | NM_000542 (mRNA) NP_000533 (protein) |
XM_974249 (mRNA) XP_979343 (protein) |
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Location | Chr 2: 85.74 - 85.75 Mb | Chr 6: 72.23 - 72.24 Mb | |||||||||
Pubmed search | [1] | [2] |
Surfactant, pulmonary-associated protein B, also known as SFTPB, is a human gene.[1]
Pulmonary surfactant-associated protein B' is a membrane protein which manufactures surfactant.
Humans and animals born with a congenital absence of SP-B suffer from intractable respiratory failure.
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[edit] See also
[edit] References
[edit] Further reading
- Pérez-Gil J (2002). "Lipid-protein interactions of hydrophobic proteins SP-B and SP-C in lung surfactant assembly and dynamics.". Pediatric pathology & molecular medicine 20 (6): 445–69. PMID 11699574.
- Johansson J, Curstedt T, Robertson B (2002). "Artificial surfactants based on analogues of SP-B and SP-C.". Pediatric pathology & molecular medicine 20 (6): 501–18. PMID 11699576.
- Nogee LM (2004). "Alterations in SP-B and SP-C expression in neonatal lung disease.". Annu. Rev. Physiol. 66: 601–23. doi: . PMID 14977415.
- Moore KJ, D'Amore-Bruno MA, Korfhagen TR, et al. (1992). "Chromosomal localization of three pulmonary surfactant protein genes in the mouse.". Genomics 12 (2): 388–93. PMID 1346779.
- Voorhout WF, Veenendaal T, Haagsman HP, et al. (1992). "Intracellular processing of pulmonary surfactant protein B in an endosomal/lysosomal compartment.". Am. J. Physiol. 263 (4 Pt 1): L479–86. PMID 1415726.
- Johansson J, Jörnvall H, Curstedt T (1992). "Human surfactant polypeptide SP-B. Disulfide bridges, C-terminal end, and peptide analysis of the airway form.". FEBS Lett. 301 (2): 165–7. PMID 1568474.
- Yu SH, Possmayer F (1992). "Effect of pulmonary surfactant protein B (SP-B) and calcium on phospholipid adsorption and squeeze-out of phosphatidylglycerol from binary phospholipid monolayers containing dipalmitoylphosphatidylcholine.". Biochim. Biophys. Acta 1126 (1): 26–34. PMID 1606172.
- Weaver TE, Whitsett JA (1989). "Processing of hydrophobic pulmonary surfactant protein B in rat type II cells.". Am. J. Physiol. 257 (2 Pt 1): L100–8. PMID 2475034.
- Pilot-Matias TJ, Kister SE, Fox JL, et al. (1989). "Structure and organization of the gene encoding human pulmonary surfactant proteolipid SP-B.". DNA 8 (2): 75–86. PMID 2924687.
- Glasser SW, Korfhagen TR, Weaver T, et al. (1987). "cDNA and deduced amino acid sequence of human pulmonary surfactant-associated proteolipid SPL(Phe).". Proc. Natl. Acad. Sci. U.S.A. 84 (12): 4007–11. PMID 3035561.
- Revak SD, Merritt TA, Degryse E, et al. (1988). "Use of human surfactant low molecular weight apoproteins in the reconstitution of surfactant biologic activity.". J. Clin. Invest. 81 (3): 826–33. PMID 3343343.
- Jacobs KA, Phelps DS, Steinbrink R, et al. (1987). "Isolation of a cDNA clone encoding a high molecular weight precursor to a 6-kDa pulmonary surfactant-associated protein.". J. Biol. Chem. 262 (20): 9808–11. PMID 3597440.
- Vamvakopoulos NC, Modi WS, Floros J (1994). "Mapping the human pulmonary surfactant-associated protein B gene (SFTP3) to chromosome 2p12-->p11.2.". Cytogenet. Cell Genet. 68 (1-2): 8–10. PMID 7956367.
- Nogee LM, Garnier G, Dietz HC, et al. (1994). "A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds.". J. Clin. Invest. 93 (4): 1860–3. PMID 8163685.
- Stuhrmann M, Bohnhorst B, Peters U, et al. (1999). "Prenatal diagnosis of congenital alveolar proteinosis (surfactant protein B deficiency).". Prenat. Diagn. 18 (9): 953–5. PMID 9793979.
- Wallot M, Wagenvoort C, deMello D, et al. (1999). "Congenital alveolar proteinosis caused by a novel mutation of the surfactant protein B gene and misalignment of lung vessels in consanguineous kindred infants.". Eur. J. Pediatr. 158 (6): 513–8. PMID 10378403.
- Tredano M, van Elburg RM, Kaspers AG, et al. (2000). "Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency.". Hum. Mutat. 14 (6): 502–9. doi: . PMID 10571948.
- Korimilli A, Gonzales LW, Guttentag SH (2000). "Intracellular localization of processing events in human surfactant protein B biosynthesis.". J. Biol. Chem. 275 (12): 8672–9. PMID 10722708.
- Gordon LM, Lee KY, Lipp MM, et al. (2000). "Conformational mapping of the N-terminal segment of surfactant protein B in lipid using 13C-enhanced Fourier transform infrared spectroscopy.". J. Pept. Res. 55 (4): 330–47. PMID 10798379.
- Lin Z, Pearson C, Chinchilli V, et al. (2001). "Polymorphisms of human SP-A, SP-B, and SP-D genes: association of SP-B Thr131Ile with ARDS.". Clin. Genet. 58 (3): 181–91. PMID 11076040.