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3N5E

Crystal Structure of human thymidylate synthase bound to a peptide inhibitor

Summary for 3N5E
Entry DOI10.2210/pdb3n5e/pdb
Related3N5G
Related PRD IDPRD_000970
DescriptorThymidylate synthase, Synthetic peptide LR, SULFATE ION, ... (5 entities in total)
Functional Keywordspeptide inhibitor, protein-peptide complex, interface inhibitor, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
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Cellular locationNucleus: P04818 P04818
Total number of polymer chains3
Total formula weight75962.80
Authors
Pozzi, C.,Cardinale, D.,Guaitoli, G.,Tondi, D.,Luciani, R.,Myllykallio, H.,Ferrari, S.,Costi, M.P.,Mangani, S. (deposition date: 2010-05-25, release date: 2011-06-08, Last modification date: 2023-09-06)
Primary citationCardinale, D.,Guaitoli, G.,Tondi, D.,Luciani, R.,Henrich, S.,Salo-Ahen, O.M.,Ferrari, S.,Marverti, G.,Guerrieri, D.,Ligabue, A.,Frassineti, C.,Pozzi, C.,Mangani, S.,Fessas, D.,Guerrini, R.,Ponterini, G.,Wade, R.C.,Costi, M.P.
Protein-protein interface-binding peptides inhibit the cancer therapy target human thymidylate synthase.
Proc.Natl.Acad.Sci.USA, 108:E542-E549, 2011
Cited by
PubMed: 21795601
DOI: 10.1073/pnas.1104829108
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.26 Å)
Structure validation

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