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Volumn 325, Issue 5945, 2009, Pages 1230-1234

A Sulfilimine Bond Identified in Collagen IV

Author keywords

[No Author keywords available]

Indexed keywords

CELL SURFACE RECEPTOR; COLLAGEN TYPE 4; HYDROXYLYSINE; METHIONINE; NITROGEN DERIVATIVE; SULFILIMINE; SULFOXIDE; SULFUR DERIVATIVE; UNCLASSIFIED DRUG;

EID: 69949177973     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1176811     Document Type: Article
Times cited : (198)

References (34)
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    • Materials and methods are available as supporting material on Science Online
    • Materials and methods are available as supporting material on Science Online.
  • 31
    • 69949150147 scopus 로고    scopus 로고
    • Single-letter abbreviations for the amino acid residues are as follows: A, Ala; C, Cys; D, Asp; E, Glu; F, Phe; G, Gly; H, His; I, Ile; K, Lys; L, Leu; M, Met; N, Asn; P, Pro; Q, Gln; R, Arg; S, Ser; T, Thr; V, Val; W, Trp; X, any amino acid; and Y, Tyr.
    • Single-letter abbreviations for the amino acid residues are as follows: A, Ala; C, Cys; D, Asp; E, Glu; F, Phe; G, Gly; H, His; I, Ile; K, Lys; L, Leu; M, Met; N, Asn; P, Pro; Q, Gln; R, Arg; S, Ser; T, Thr; V, Val; W, Trp; X, any amino acid; and Y, Tyr.
  • 34
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    • We thank D. Liebler for facilitating the initial contact with T. D. Veenstra from SAIC-Frederick, Incorporated, and C. Bolm (Aachen University, Germany) for helpful discussions. The technical assistance of P. Todd and M. Rati is greatly appreciated. We would also like to thank S. Hill and H. McDonald, from the Proteomics Laboratory at the Mass Spectrometry Research Center of Vanderbilt University, for their assistance with the Orbitrap-LTQ (Therme Electron, San Jose, CA) instrument. This work was supported in part by NIH grants DK065123 and DK18381 (to B.G.H.), DC007416 (C.R.S.), and GM059380 (P.E.D.); the W. M. Keck Foundation (K.B.S.); and the Skaggs Institute for Chemical Biology (K.B.S.). R.V. and B.G.H. have filed a provisional patent (1 June 2009) on the potential enzyme system that catalyses the sutfilimine bond formation and that may be involved in pathophysiological processes.
    • We thank D. Liebler for facilitating the initial contact with T. D. Veenstra from SAIC-Frederick, Incorporated, and C. Bolm (Aachen University, Germany) for helpful discussions. The technical assistance of P. Todd and M. Rati is greatly appreciated. We would also like to thank S. Hill and H. McDonald, from the Proteomics Laboratory at the Mass Spectrometry Research Center of Vanderbilt University, for their assistance with the Orbitrap-LTQ (Therme Electron, San Jose, CA) instrument. This work was supported in part by NIH grants DK065123 and DK18381 (to B.G.H.), DC007416 (C.R.S.), and GM059380 (P.E.D.); the W. M. Keck Foundation (K.B.S.); and the Skaggs Institute for Chemical Biology (K.B.S.). R.V. and B.G.H. have filed a provisional patent (1 June 2009) on the potential enzyme system that catalyses the sutfilimine bond formation and that may be involved in pathophysiological processes.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.