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This page gives details of CPPsite entry with ID 3009
Primary information
CPPsite ID3009
PEPTIDE SEQUENCEMVTVLFRRLRIRRACGPPRVRV
PEPTIDE NAMEM918
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
C-TERMINAL MODIFICATIONAmidation
PROPOSED UPTAKE MECHANISMEndocytosis
INVITRO/INVIVOIn vitro
CELL LINEHeLa cells
CARGONucleic acid (SCO)
PMID0
PATENTUS 2014/0140929 A1
LENGTH22
Secondary StructureCHHHHSHHHHHHHHSSCSSSCC
SMILESN[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C)C(=O)N[C@@H](CS)C(=O)NCC(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C(C)C)C(=O)N
Tertiary Structure
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