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6AK0

Solution NMR structure of a new lasso peptide specialicin

Summary for 6AK0
Entry DOI10.2210/pdb6ak0/pdb
DescriptorCYS-LEU-GLY-VAL-GLY-SER-CYS-VAL-ASP-PHE-ALA-GLY-CYS-GLY-TYR-ALA-VAL-VAL-CYS-PHE-DTR (1 entity in total)
Functional Keywordslasso peptide, streptomyces specialis, specialicin, unknown function
Biological sourceStreptomyces specialis
Total number of polymer chains1
Total formula weight2156.53
Authors
Hemmi, H.,Kodani, S.,Kaweewan, I.,Komaki, H. (deposition date: 2018-08-28, release date: 2018-12-05, Last modification date: 2024-11-06)
Primary citationKaweewan, I.,Hemmi, H.,Komaki, H.,Harada, S.,Kodani, S.
Isolation and structure determination of a new lasso peptide specialicin based on genome mining
Bioorg. Med. Chem., 26:6050-6055, 2018
Cited by
PubMed Abstract: Based on genome mining, a new lasso peptide specialicin was isolated from the extract of Streptomyces specialis. The structure of specialicin was established by ESI-MS and NMR analyses to be a lasso peptide with the length of 21 amino acids, containing an isopeptide bond and two disulfide bonds in the molecule. The stereochemistries of the constituent amino acids except for Trp were determined to be L and the stereochemistry of Trp at C-terminus was determined to be D. Three dimensional structure of specialicin was determined based on NOE experimental data, which indicated that specialicin possessed the similar conformational structure with siamycin I. Specialicin showed the antibacterial activity against Micrococcus luteus and the moderate anti-HIV activity against HIV-1 NL4-3. The biosynthetic gene cluster of specialicin was proposed from the genome sequence data of S. specialis.
PubMed: 30448257
DOI: 10.1016/j.bmc.2018.11.007
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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数据于2024-11-06公开中

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