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抑咽侧体神经肽Allatotropin(free acid),H2N-Gly-Phe-Lys-Asn-Val-Glu-Met-Met-Thr-Ala-Arg-Gly-Phe-COOH,H2N-GFKNVEMMTARGF-OH,杭州专肽生物的产品

抑咽侧体神经肽Allatotropin(free acid)

编号:429573

CAS号:

单字母:H2N-GFKNVEMMTARGF-OH

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  • 编号:429573
    中文名称:抑咽侧体神经肽Allatotropin(free acid)
    英文名:Allatotropin(free acid)
    单字母:H2N-GFKNVEMMTARGF-OH
    三字母:H2N

    N端氨基

    -Gly

    甘氨酸

    -Phe

    苯丙氨酸

    -Lys

    赖氨酸

    -Asn

    天冬酰胺

    -Val

    缬氨酸

    -Glu

    谷氨酸

    -Met

    甲硫氨酸

    -Met

    甲硫氨酸

    -Thr

    苏氨酸

    -Ala

    丙氨酸

    -Arg

    精氨酸

    -Gly

    甘氨酸

    -Phe

    苯丙氨酸

    -OH

    C端羧基

    氨基酸个数:13
    分子式:C65H102N18O18S2
    平均分子量:1487.75
    精确分子量:1486.71
    等电点(PI):11.66
    pH=7.0时的净电荷数:1.98
    平均亲水性:-0.072727272727273
    疏水性值:-0.12
    消光系数:-
    标签:抑咽侧体神经肽(Allatostatin)   

  • Definition
    Allatostatins (ASTs) are pleiotropic neuropeptide hormones in insects and crustacean. There major function in the insect is the inhibition of juvenile hormone synthesis by the corpora allata and reduce their food intake1.

    Discovery
    The first identified ASTs were isolated from brain-retro cerebral complexes of the cockroach Diploptera punctata2.

    Classification
    ASTs encompass a group of three families determined by consensus sequences, the cockroach type representing the FGLa family, the cricket type representing the W(X)6 Wa family and the PISCF family 1.

    Structural Characteristics
    AST’s are 8-13 amino acids long, are amidated, and show sequence similarity, including a 3-amino acid sequence at the C-terminal end that is common to all four peptides. The peptide sequences are as follows: allatostatin-1, Ala-Pro-Ser-Gly-Ala-Gln-Arg-Leu-Tyr-Gly-Phe-Gly-Leu-NH2; allatostatin-2, Gly-Asp-Gly-Arg-Leu-Tyr-Ala-Phe-Gly-Leu-NH2; allatostatin-3, Gly-Gly-Ser-Leu-Tyr-Ser-Phe-Gly-Leu-NH2; and allatostatin-4, Asp-Arg-Leu-Tyr-Ser-Phe-Gly-Leu-NH23.

    Mode of action
    In mammalian cells, allatostatin bind to AST receptors to open G-protein coupled inward rectifying potassium channels, resulting in reduced membrane potential and input resistance4.

    References

     

    1.     Stay B and Tobe SS (2007). "The role of allatostatins in juvenile hormone synthesis in insects and crustaceans". Annu. Rev. Entomo., 52: 277–99.


    2.     Pratt GE, Farnsworth DE, Fok KF, Siegel NR, McCormack AL, Shabanowitz J, Hunt DF, Feyereisen R (1991). Identity of a second type of allatostatin from cockroach brains: an octadecapeptide amide with a tyrosine-rich address sequence. Proc Natl Acad Sci., 88(6): 2412–2416.


    3.     Woodhead AP, Stay B, Seidel SL, Khan MA, Tobe SS (1989). Primary structure of four allatostatins: neuropeptide inhibitors of juvenile hormone synthesis. Proc Natl Acad Sci., 86(15):5997-6001.


    4.     Tan EM, Yamaguchi Y, Horwitz GD, Gosgnach S, Lein ES, Goulding M, Albright TD, Callaway EM (2006). Selective and quickly reversible inactivation of mammalian neurons in vivo uses the Drosophila allatostatin receptor. Neuron, 1:57–170.

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