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4LKO

Crystal structure of human DPP-IV in complex with BMS-744891

Summary for 4LKO
Entry DOI10.2210/pdb4lko/pdb
Related4JH0
DescriptorDipeptidyl peptidase 4, 3-(aminomethyl)-4-(2,4-dichlorophenyl)-6-(2-methoxyethyl)-2-methyl-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one (3 entities in total)
Functional Keywordsexopeptidase, beta barrel, alpha/beta hydrolase fold, hydrolase
Biological sourceHomo sapiens (human)
Cellular locationDipeptidyl peptidase 4 soluble form: Secreted. Cell membrane; Single-pass type II membrane protein: P27487
Total number of polymer chains2
Total formula weight169685.77
Authors
Klei, H.E. (deposition date: 2013-07-08, release date: 2013-09-04, Last modification date: 2024-04-03)
Primary citationDevasthale, P.,Wang, Y.,Wang, W.,Fevig, J.,Feng, J.,Wang, A.,Harrity, T.,Egan, D.,Morgan, N.,Cap, M.,Fura, A.,Klei, H.E.,Kish, K.,Weigelt, C.,Sun, L.,Levesque, P.,Moulin, F.,Li, Y.X.,Zahler, R.,Kirby, M.S.,Hamann, L.G.
Optimization of Activity, Selectivity, and Liability Profiles in 5-Oxopyrrolopyridine DPP4 Inhibitors Leading to Clinical Candidate (Sa)-2-(3-(Aminomethyl)-4-(2,4-dichlorophenyl)-2-methyl-5-oxo-5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)-N,N-dimethylacetamide (BMS-767778).
J.Med.Chem., 56:7343-7357, 2013
Cited by
PubMed: 23964740
DOI: 10.1021/jm4008906
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.43 Å)
Structure validation

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