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4KD5

substrate binding domain of putative molybdenum ABC transporter from Clostridium difficile

Summary for 4KD5
Entry DOI10.2210/pdb4kd5/pdb
DescriptorABC-type transport system, molybdenum-specific extracellular solute-binding protein, FORMIC ACID, 2-BUTANOL, ... (5 entities in total)
Functional Keywordsstructural genomics, niaid, national institute of allergy and infectious diseases, center for structural genomics of infectious diseases, csgid, alpha-beta-alpha fold, abc transporter, transport protein
Biological sourceClostridium difficile
Total number of polymer chains4
Total formula weight103482.85
Authors
Maltseva, N.,Kim, Y.,Grimshaw, S.,Anderson, W.F.,Joachimiak, A.,Center for Structural Genomics of Infectious Diseases (CSGID) (deposition date: 2013-04-24, release date: 2013-05-08, Last modification date: 2026-03-25)
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 (2.4999 Å)
Structure validation

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