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7RLR

Crystal Structure of K83A Mutant of Class D beta-lactamase from Clostridium difficile 630

Summary for 7RLR
Entry DOI10.2210/pdb7rlr/pdb
DescriptorBeta-lactamase, CHLORIDE ION, ACETATE ION, ... (6 entities in total)
Functional Keywordsstructural genomics, center for structural genomics of infectious diseases, csgid, blad, hydrolase
Biological sourceClostridioides difficile (Peptoclostridium difficile)
Total number of polymer chains4
Total formula weight117458.95
Authors
Minasov, G.,Shuvalova, L.,Dubrovska, I.,Rosas-Lemus, M.,Jedrzejczak, R.,Satchell, K.J.F.,Center for Structural Genomics of Infectious Diseases (CSGID) (deposition date: 2021-07-26, release date: 2021-08-11, Last modification date: 2026-02-11)
Primary citationRosas-Lemus, M.,Dey, S.,Minasov, G.,Tan, K.,Anderson, S.M.,Brunzelle, J.,Nocadello, S.,Shabalin, I.,Filippova, E.,Halavaty, A.,Kim, Y.,Maltseva, N.,Osipiuk, J.,Minor, W.,Joachimiak, A.,Savchenko, A.,Anderson, W.F.,Satchell, K.J.F.
A high-throughput structural system biology approach to increase structure representation of proteins from Clostridioides difficile.
Microbiol Resour Announc, 12:e0050723-e0050723, 2023
Cited by
PubMed Abstract: causes life-threatening gastrointestinal infections. It is a high-risk pathogen due to a lack of effective treatments, antimicrobial resistance, and a poorly conserved genomic core. Herein, we report 30 X-ray structures from a structure genomics pipeline spanning 13 years, representing 10.2% of the X-ray structures for this important pathogen.
PubMed: 37747257
DOI: 10.1128/MRA.00507-23
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.88 Å)
Structure validation

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