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This page gives details of CPPsite entry with ID 2957
Primary information
CPPsite ID2957
PEPTIDE SEQUENCEGWTLNSAGYLLGKINLKALAALAKKIL
PEPTIDE NAMETrans
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
N-TERMINAL MODIFICATIONConjugation with 5(6)-Carboxyfluorescein
C-TERMINAL MODIFICATIONFree
UPTAKE EFFICIENCYHigh
INVITRO/INVIVOIn vivo
In VIVO MODELAdult zebrafish
CARGOFluorophore (5-Carboxyfluorescein)
PMID25894337
PATENTUnknown
LENGTH27
Secondary StructureCCSHHHHTTTTTTTHHHHHHHHHHHHC
SMILESNCC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C=O)CC(C)C)[C@H](CC)C)CCCC[NH3])CCCC[NH3])C)CC(C)C)C)C)CC(C)C)C)CCCC[NH3])CC(C)C)CC(=O)N)[C@H](CC)C)CCCC[NH3])CC(C)C)CC(C)C)Cc1ccc(cc1)O)C)CO)CC(=O)N)CC(C)C)[C@H](O)C)Cc1c[nH]c2c1cccc2
Tertiary Structure
(Technique)		View in Jmol  OR Download Structure
  (Experimentally determined structure from PDB)