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1GHX

A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE

Summary for 1GHX
Entry DOI10.2210/pdb1ghx/pdb
Related1C5N
DescriptorTHROMBIN, ACETYL HIRUDIN, ZINC ION, ... (8 entities in total)
Functional Keywordsthree-centered, very short hydrogen bond, oxyanion hole water, shift of pka of his57, structure-based drug design, specificity, urokinase, trypsin, thrombin, zn+2-mediated inhibition, blood clotting, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (human)
More
Cellular locationSecreted, extracellular space: P00734 P00734
Secreted: P28504
Total number of polymer chains3
Total formula weight35563.87
Authors
Katz, B.A.,Elrod, K.,Luong, C.,Rice, M.,Mackman, R.L.,Sprengeler, P.A.,Spencer, J.,Hatayte, J.,Janc, J.,Link, J.,Litvak, J.,Rai, R.,Rice, K.,Sideris, S.,Verner, E.,Young, W. (deposition date: 2001-01-22, release date: 2002-01-22, Last modification date: 2023-12-27)
Primary citationKatz, B.A.,Elrod, K.,Luong, C.,Rice, M.J.,Mackman, R.L.,Sprengeler, P.A.,Spencer, J.,Hataye, J.,Janc, J.,Link, J.,Litvak, J.,Rai, R.,Rice, K.,Sideris, S.,Verner, E.,Young, W.
A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site.
J.Mol.Biol., 307:1451-1486, 2001
Cited by
PubMed: 11292354
DOI: 10.1006/jmbi.2001.4516
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.65 Å)
Structure validation

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