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1NJS

human GAR Tfase in complex with hydrolyzed form of 10-trifluoroacetyl-5,10-dideaza-acyclic-5,6,7,8-tetrahydrofolic acid

Summary for 1NJS
Entry DOI10.2210/pdb1njs/pdb
Related1MEJ 1MEN 1MEO
DescriptorPhosphoribosylglycinamide formyltransferase, PHOSPHATE ION, N-{4-[(1R)-4-[(2R,4R,5S)-2,4-DIAMINO-6-OXOHEXAHYDROPYRIMIDIN-5-YL]-1-(2,2,2-TRIFLUORO-1,1-DIHYDROXYETHYL)BUTYL]BENZOYL}-D-GLUTAMIC ACID, ... (4 entities in total)
Functional Keywordsprotein-cofactor analogue complex, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight46741.79
Authors
Zhang, Y.,Desharnais, J.,Marsilje, T.H.,Li, C.,Hedrick, M.P.,Gooljarsingh, L.T.,Tavassoli, A.,Benkovic, S.J.,Olson, A.J.,Boger, D.L.,Wilson, I.A. (deposition date: 2003-01-02, release date: 2003-06-10, Last modification date: 2023-08-16)
Primary citationZhang, Y.,Desharnais, J.,Marsilje, T.H.,Li, C.,Hedrick, M.P.,Gooljarsingh, L.T.,Tavassoli, A.,Benkovic, S.J.,Olson, A.J.,Boger, D.L.,Wilson, I.A.
Rational Design, Synthesis, Evaluation, and Crystal Structure of a Potent Inhibitor of Human GAR Tfase: 10-(Trifluoroacetyl)-5,10-dideazaacyclic-5,6,7,8-tetrahydrofolic Acid
Biochemistry, 42:6043-6056, 2003
Cited by
PubMed: 12755606
DOI: 10.1021/bi034219c
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.98 Å)
Structure validation

219140

數據於2024-05-01公開中

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