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202739-41-1

202739-41-1 Structure

202739-41-1 Structure
IdentificationBack Directory
[Name]

H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA
[CAS]

202739-41-1
[Synonyms]

H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA
H-Trp-Phe-Tyr-Ser(PO3H2)-Pro-Arg-pNA trifluoroacetate salt
L-Argininamide, L-tryptophyl-L-phenylalanyl-L-tyrosyl-O-phosphono-L-seryl-L-prolyl-N-(4-nitrophenyl)- (9CI)
[Molecular Formula]

C49H59N12O13P
[MDL Number]

MFCD18633561
[MOL File]

202739-41-1.mol
[Molecular Weight]

1055.04
Chemical PropertiesBack Directory
[density ]

1.53±0.1 g/cm3(Predicted)
[storage temp. ]

-15°C
[pka]

1.80±0.10(Predicted)
[Sequence]

Trp-Phe-Tyr-{PO2}-Ser-Pro-Arg
Hazard InformationBack Directory
[Uses]

H-Trp-Phe-Tyr-Ser(PO3H2)-Pro-Arg-pNA is a chromogenic substrate for Pin1. Pin1 is an essential and conserved mitotic peptidyl-prolyl isomerase, and can recognize the phosphoserine-proline bonds present in mitotic phosphoproteins[1][2].
[References]

[1] M B Yaffe, et al. Sequence-specific and phosphorylation-dependent proline isomerization: a potential mitotic regulatory mechanism. Science. 1997 Dec 12;278(5345):1957-60. DOI:10.1126/science.278.5345.1957
[2] Kelly E Duncan, et al. Discovery and characterization of a nonphosphorylated cyclic peptide inhibitor of the peptidylprolyl isomerase, Pin1. J Med Chem. 2011 Jun 9;54(11):3854-65. DOI:10.1021/jm200156c
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