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2Q3C

2.1 A Resolution Crystal Structure of O-Acetylserine Sulfhydrylase (OASS) Holoenzyme From MYCOBACTERIUM TUBERCULOSIS in Complex with the Inhibitory Peptide DFSI

Summary for 2Q3C
Entry DOI10.2210/pdb2q3c/pdb
Related2Q3B 2Q3D
DescriptorCysteine synthase A, DFSI inhibitory peptide, (4S)-2-METHYL-2,4-PENTANEDIOL, ... (4 entities in total)
Functional Keywordsmycobacterium tuberculosis, pyridoxal-5'-phosphate, sulphur metabolism, cysteine biosynthesis, sat, peptide-inhibitor, transferase
Biological sourceMycobacterium tuberculosis
More
Total number of polymer chains2
Total formula weight33894.69
Authors
Schneider, G.,Schnell, R. (deposition date: 2007-05-30, release date: 2007-06-12, Last modification date: 2023-11-15)
Primary citationSchnell, R.,Oehlmann, W.,Singh, M.,Schneider, G.
Structural Insights into Catalysis and Inhibition of O-Acetylserine Sulfhydrylase from Mycobacterium tuberculosis: CRYSTAL STRUCTURES OF THE ENZYME {alpha}-AMINOACRYLATE INTERMEDIATE AND AN ENZYME-INHIBITOR COMPLEX.
J.Biol.Chem., 282:23473-23481, 2007
Cited by
PubMed: 17567578
DOI: 10.1074/jbc.M703518200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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