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2BM2

human beta-II tryptase in complex with 4-(3-Aminomethyl-phenyl)- piperidin-1-yl-(5-phenethyl- pyridin-3-yl)-methanone

Summary for 2BM2
Entry DOI10.2210/pdb2bm2/pdb
Related1A0L 1AAO
DescriptorHUMAN BETA2 TRYPTASE, 1-[3-(1-{[5-(2-PHENYLETHYL)PYRIDIN-3-YL]CARBONYL}PIPERIDIN-4-YL)PHENYL]METHANAMINE (3 entities in total)
Functional Keywordsserine protease inhibitor, glycoprotein, hydrolase, polymorphism, protease, serine protease
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains4
Total formula weight111563.82
Authors
Primary citationLevell, J.,Astles, P.,Eastwood, P.,Cairns, J.,Houille, O.,Aldous, S.,Merriman, G.,Whitley, B.,Pribish, J.,Czekaj, M.,Liang, G.,Maignan, S.,Guilloteau, J.-P.,Dupuy, A.,Davidson, J.,Harrison, T.,Morley, A.,Watson, S.,Fenton, G.,Mccarthy, C.,Romano, J.,Mathew, R.,Engers, D.,Gardyan, M.,Sides, K.,Kwong, J.,Tsay, J.,Rebello, S.,Shen, L.,Wang, J.,Luo, Y.,Giardino, O.,Lim, H.-K.,Smith, K.,Pauls, H.
Structure Based Design of 4-(3-Aminomethylphenyl) Piperidinyl-1-Amides: Novel, Potent, Selective, and Orally Bioavailable Inhibitors of Bii Tryptase
Bioorg.Med.Chem., 13:2859-, 2005
Cited by
PubMed: 15781396
DOI: 10.1016/J.BMC.2005.02.014
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

218500

數據於2024-04-17公開中

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