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4R0I

CRYSTAL STRUCTURE of MATRIPTASE in COMPLEX WITH INHIBITOR

Summary for 4R0I
Entry DOI10.2210/pdb4r0i/pdb
DescriptorSuppressor of tumorigenicity 14 protein, SERINE PROTEASE, MATRIPTASE, MEMBRANE-TYPE SERINE PROTEASE 1, MT-SP1, 3-({(2S)-3-[4-(2-aminoethyl)piperidin-1-yl]-2-[(naphthalen-2-ylsulfonyl)amino]-3-oxopropyl}oxy)benzenecarboximidamide, ... (4 entities in total)
Functional Keywordshydrolase, matriptase, complex structure, trypsin-like serine proteinase fold, protease, small molecule inhibitor
Biological sourceHomo sapiens (human)
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Cellular locationMembrane ; Single-pass type II membrane protein : Q9Y5Y6 Q9Y5Y6
Total number of polymer chains2
Total formula weight27435.96
Authors
Rao, K.N.,Ashok, K.N.,Chakshusmathi, G.,Rajeev, G.,Subramanya, H. (deposition date: 2014-07-31, release date: 2015-02-11, Last modification date: 2023-11-08)
Primary citationGoswami, R.,Wohlfahrt, G.,Mukherjee, S.,Ghadiyaram, C.,Nagaraj, J.,Satyam, L.K.,Subbarao, K.,Gopinath, S.,Krishnamurthy, N.R.,Subramanya, H.S.,Ramachandra, M.
Discovery of O-(3-carbamimidoylphenyl)-l-serine amides as matriptase inhibitors using a fragment-linking approach
Bioorg.Med.Chem.Lett., 25:616-620, 2015
Cited by
PubMed: 25556099
DOI: 10.1016/j.bmcl.2014.12.008
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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