This page gives details of CPPsite entry with ID 1831 |
Primary information | |
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CPPsite ID | 1831 |
PEPTIDE SEQUENCE | GRKKRRQRRRPPQC |
PEPTIDE NAME | HIV-1 Tat (48-60) |
CHIRALITY | L |
LINEAR/CYCLIC | Linear |
SOURCE | Protein derived |
CATEGORY | Cationic |
SUB CELLULAR LOCALIZATION | Only punctate distribution (vesicles) |
N-TERMINAL MODIFICATION | Free |
C-TERMINAL MODIFICATION | Conjugation with Alexa 488 at glycyl cysteine sequence |
UPTAKE EFFICIENCY | Unknown |
PROPOSED UPTAKE MECHANISM | Endocytic pathway (Macropinocytosis) |
INVITRO/INVIVO | In vitro |
CELL LINE | CHO-K1, HeLa and Jurkat |
CARGO | Fluorophore (Alexa-488) |
PMID | 19707187 |
PATENT | US 20040132970 |
LENGTH | 14 |
Secondary Structure | CCTTCCCCCCSSCC |
SMILES | NCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CS)C=O |
Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |