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BIRD: 10 results
PRD_001074
PRD_001074
Name:Thiocillin GE2270 analogue NVP-LDI028
Formula:C55 H64 N13 O10 S6
Definition date:2012-12-12
Last modified:2012-12-12
PRD_001073
PRD_001073
Name:Thiocillin GE2270 analogue NVP-LDK733
Formula:C55 H64 N13 O11 S6
Definition date:2012-12-12
Last modified:2012-12-12
PRD_001072
PRD_001072
Name:Thiocillin GE2270 analogue NVP-LFF571
Formula:C60 H72 N13 O13 S6
Definition date:2012-12-12
Last modified:2012-12-12
PRD_000901
PRD_000901
Name:thiomuracin A derivative
Formula:C53 H54 N13 O9 S6
Definition date:2012-12-26
Last modified:2023-11-03
PRD_000760
PRD_000760
Name:THIOPEPTIDE THIOSTREPTON OXIDIZED AT CA-CB BOND OF RESIDUE 9
Formula:C69 H79 N18 O17 S5
Description:THIOSTREPTON IS A HETEROCYCLIC THIOPEPTIDE, CONSISTING OF FOUR THIAZOLES ONE THIOZOLINE ONE PIPERIDEINE RINGS. A MODIFIED QUINOLINE LINKED TO MAIN-CHAIN RESIDUE 1 AND SIDE-CHAIN OF RESIDUE 12. IN THIS ENTRY RESIDUE 9 WAS CHEMICALLY MODIFIED: THE CA-CB BOND WAS OXIDIZED FROM SINGLE TO DOUBLE. RESIDUE 17 (HET DHA) WAS DELETED.
Definition date:2012-12-12
Last modified:2023-09-20
PRD_000759
PRD_000759
Name:THIOPEPTIDE THIOSTREPTON WITH EPIMER FORM OF RESIDUE 9
Formula:C69 H81 N18 O17 S5
Description:THIOSTREPTON IS A HETEROCYCLIC THIOPEPTIDE, CONSISTING OF FOUR THIAZOLES ONE THIOZOLINE ONE PIPERIDEINE RINGS. A MODIFIED QUINOLINE, RESIDUE 0, IS LINKED TO MAIN-CHAIN RESIDUE 1 AND SIDE-CHAIN OF RESIDUE 12. IN THIS ENTRY RESIDUE 9 WAS CHEMICALLY MODIFIED FROM D-CYS TO L-CYS AND RESIDUE 17 (HET DHA) WAS DELETED.
Definition date:2012-12-12
Last modified:2023-09-20
PRD_000758
PRD_000758
Name:THIOPEPTIDE THIOSTREPTON REDUCED AT N-CA BOND OF RESIDUE 14
Formula:C72 H86 N19 O18 S5
Description:THIOSTREPTON IS A HETEROCYCLIC THIOPEPTIDE, CONSISTING OF FOUR THIAZOLES, ONE THIOZOLINE, ONE PIPERIDEINE RINGS. A MODIFIED QUINOLINE, RESIDUE 0, IS LINKED TO MAIN-CHAIN RESIDUE 1 AND SIDE-CHAIN OF RESIDUE 12. IN THIS ENTRY RESIDUE 14 WAS CHEMICALLY MODIFIED TO HAVE A SINGLE BOND N-CA.
Definition date:2012-12-12
Last modified:2023-09-20
PRD_000225
PRD_000225
Name:GE2270a
Formula:C56 H58 N15 O10 S6
Description:GEA2270A IS A THIOPEPTIDE CONSISTING OF ONE PYRIDINE, ONE OXAZOLE AND FIVE THIAZOLE RINGS. THE OBSERVED C-TERMINAL AMINO GROUP NH2(15) IS LIKELY TO BE A POST-TRANSLATIONAL DECARBOXYLATED REMNANT OF A SER C-TERMINAL RESIDUE.
Definition date:2012-12-12
Last modified:2023-09-20
PRD_000223
PRD_000223
Name:THIOSTREPTON
Formula:C72 H84 N19 O18 S5
Description:Thiostrepton is a hetrocyclic thiopeptide belonging to the thiocillin family, consisting of four thiazole, one thiozoline and one piperideine rings. A modified quinoline linked to main-chain residue 1 and side-chain of residue 12. Post translational maturation of thiazole and oxazole containing antibiotics involves the enzymic condensation of a Cys or Ser with the alpha-carbonyl of the preceding amino acid to form a thioether or ether bond, then dehydration to form a double bond with the alpha-amino nitrogen. Thiazoline or oxazoline ring are dehydrogenated to form thiazole or oxazole rings. the pyridinyl involves the cross-linking of a Ser and a Cys-Ser pair usually separated by 7 or 8 residues along the peptide chain. The Ser residues are dehydrated to didehydroalanines, then bonded between their beta carbons. The alpha carbonyl of the Cys condenses with alpha carbon of the first Ser to form a pyridinyl ring. The ring may be mutiply dehydrogenated to form a pyridine ring with loss of the amino nitrogen of the first Ser. The amidation of Ser-17 probably does not occur by the same mechanism, oxidative cleavage of glycine, as in eukaryotes.
Definition date:2012-12-12
Last modified:2023-09-20
PRD_000221
PRD_000221
Name:Nosiheptide
Formula:C51 H46 N13 O11 S6
Description:NOSIHEPTIDE IS A HETROCYCLIC THIOPEPTIDE, CONSISTING OF FIVE THIAZOLES AND ONE 3-HYDROXYPYRIDINE RINGS. A MODIFIED INDOLE RING NO1(14) IS LINKED VIA THE SIDE CHAINS OF 3-HYDROXY 3GL(6) AND CYS(8). THE OBSERVED C-TERMINAL AMINO GROUP NH2(13) IS LIKELY TO BE A POST-TRANSLATIONAL DECARBOXYLATED REMNANT OF A SER C-TERMINAL RESIDUE
Definition date:2012-12-12
Last modified:2023-09-20

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