1NCO
STRUCTURE OF THE ANTITUMOR PROTEIN-CHROMOPHORE COMPLEX NEOCARZINOSTATIN
Summary for 1NCO
| Entry DOI | 10.2210/pdb1nco/pdb |
| Descriptor | HOLO-NEOCARZINOSTATIN, (4R)-2-METHYLPENTANE-2,4-DIOL, NEOCARZINOSTATIN-CHROMOPHORE, ... (4 entities in total) |
| Functional Keywords | antibacterial and antitumor protein |
| Biological source | Streptomyces carzinostaticus |
| Total number of polymer chains | 2 |
| Total formula weight | 22977.92 |
| Authors | Kim, K.-H.,Kwon, B.-M.,Myers, A.G.,Rees, D.C. (deposition date: 1993-07-13, release date: 1993-10-31, Last modification date: 2024-10-09) |
| Primary citation | Kim, K.H.,Kwon, B.M.,Myers, A.G.,Rees, D.C. Crystal structure of neocarzinostatin, an antitumor protein-chromophore complex. Science, 262:1042-1046, 1993 Cited by PubMed Abstract: Structures of the protein-chromophore complex and the apoprotein form of neocarzinostatin were determined at 1.8 angstrom resolution. Neocarzinostatin is composed of a labile chromophore with DNA-cleaving activity and a stabilizing protein. The chromophore displays marked nonlinearity of the triple bonds and is bound noncovalently in a pocket formed by the two protein domains. The chromophore pi-face interacts with the phenyl ring edges of Phe52 and Phe78. The amino sugar and carbonate groups of the chromophore are solvent exposed, whereas the epoxide, acetylene groups, and carbon C-12, the site of nucleophilic thiol addition during chromophore activation, are unexposed. The position of the amino group of the chromophore carbohydrate relative to C-12 supports the idea that the amino group plays a role in thiol activation. PubMed: 8235619PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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