Home > Name List By l > L-Aspartic acid,L-alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-arginyl-L-a-aspartyl-L-prol...

CAS No 137181-56-7 , L-Aspartic acid,L-alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-arginyl-L-a-aspartyl-L-prolyl-L-prolyl-L-lysyl-L-methionyl-L-glutaminyl-L-threonyl-

  • Name: L-Aspartic acid,L-alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-arginyl-L-a-aspartyl-L-prolyl-L-prolyl-L-lysyl-L-methionyl-L-glutaminyl-L-threonyl-
  • Synonyms: 1270:PN: US20090175821 SEQID: 1557 claimed protein; Systemin (peptide);Systemin; 134: PN: US20030119021 SEQID:132 unclaimed sequence; 252: PN: WO0069900 SEQID: 1557 unclaimed sequence; Systemin (tomato clone pSYS1);L-Aspartic acid,L-alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-arginyl-L-a-aspartyl-L-prolyl-L-prolyl-L-lysyl-L-methionyl-L-glutaminyl-L-threonyl-;
  • CAS Registry Number:
  • Molecular Weight: 2010.28
  • InChI: InChI=1/C85H144N26O28S/c1-43(2)65(106-67(121)44(3)89)77(131)100-49(25-27-61(91)115)71(125)104-55(41-112)75(129)101-52(19-8-11-32-88)79(133)109-35-14-22-58(109)81(135)108-34-13-21-57(108)76(130)105-56(42-113)74(128)98-47(18-7-10-31-87)69(123)97-48(20-12-33-95-85(93)94)70(124)102-53(39-63(117)118)80(134)110-36-15-23-59(110)82(136)111-37-16-24-60(111)84(138)139-83(137)54(40-64(119)120)103-78(132)66(45(4)114)107-73(127)50(26-28-62(92)116)99-72(126)51(29-38-140-5)96-68(122)46(90)17-6-9-30-86/h43-60,65-66,112-114H,6-42,86-90H2,1-5H3,(H2,91,115)(H2,92,116)(H,96,122)(H,97,123)(H,98,128)(H,99,126)(H,100,131)(H,101,129)(H,102,124)(H,103,132)(H,104,125)(H,105,130)(H,106,121)(H,107,127)(H,117,118)(H,119,120)(H4,93,94,95)/t44-,45+,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,60-,65-,66-/m0/s1
  • Molecular Formula: C85H144 N26 O28 S
  • Molecular Structure:CAS No:137181-56-7 L-Aspartic acid,L-alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-arginyl-L-a-aspartyl-L-prolyl-L-prolyl-L-lysyl-L-methionyl-L-glutaminyl-L-threonyl-

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137181-56-7 L-Aspartic acid,L-alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-arginyl-L-a-aspartyl-L-prolyl-L-prolyl-L-lysyl-L-methionyl-L-glutaminyl-L-threonyl-

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137181-56-7 SYSTEMIN

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References of L-Aspartic acid,L-alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-arginyl-L-a-aspartyl-L-prolyl-L-prolyl-L-lysyl-L-methionyl-L-glutaminyl-L-threonyl-
Title: Systemin
CAS Registry Number: 137181-56-7
CAS Name: L-Alanyl-L-valyl-L-glutaminyl-L-seryl-L-lysyl-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-argininyl-L-a-aspartyl-L-prolyl-L-prolyl-L-lysyl-L-methionyl-L-glutaminyl-L-threonyl-L-aspartic acid
Literature References: First known polypeptide signal in plants. Systemically induces plant defenses in response to wounding of leaves by insects or pathogens. Proline-rich palindromic structure. Identification of activity: C. A. Ryan, Plant Physiol. 54, 328 (1974). Isolation from tomato leaves and characterization: G. Pearce et al., Science 253, 895 (1991). Purification by capillary electrophoresis: P. Mucha et al., J. Chromatogr. A 734, 410 (1996). Proton NMR assignments: D. J. Russell et al., J. Protein Chem. 11, 265 (1992). Structure-activity: T. Meindl et al., Plant Cell 10, 1561 (1998). Tertiary structure and mechanism of action: T. Specht et al., Plants Proteins Eur. Crops 1998, 41. Review: C. A. Ryan, G. Pearce, Annu. Rev. Cell Dev. Biol. 14, 1-17 (1998).
Properties: Insol in lipid solvents.
Use: Wound hormone in plants.