wwPDB validation report of PDB entry 2VIW

UROKINASE-TYPE PLASMINOGEN ACTIVATOR CHAIN B

UROKINASE-TYPE PLASMINOGEN ACTIVATOR, UPA, U-PLASMINOGEN ACTIVATOR

STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB- MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR

UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN INHIBITOR COMPLEX

CRYSTAL STRUCTURE OF HUMAN MICROUROKINASE IN COMPLEX WITH 2-AMINO-5-HYDROXY-BENZIMIDAZOLE

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

ENGINEERING INHIBITORS HIGHLY SELECTIVE FOR THE S1 SITES OFSER190 TRYPSIN-LIKE SERINE PROTEASE DRUG TARGETS

PLASMINOGEN ACTIVATOR (UROKINASE-TYPE, KRINGLE DOMAIN) (U-PA K) (NMR, MINIMIZED AVERAGE STRUCTURE)

DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTSAT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190UPA)

SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE

UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN-J435 COMPLEX

UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN- AMILORIDE COMPLEX

UROKINASE PLASMINOGEN ACTIVATOR B CHAIN-UKI- 1D COMPLEX

LMW U-PA STRUCTURE COMPLEXED WITH EGRCMK ( GLU-GLY-ARG CHLOROMETHYL KETONE)

ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATINGBINDING OF ACTIVE SITE- DIRECTED SERINE PROTEASE INHIBITORS

SUBSTITUTED 2-NAPHTHAMADINE INHIBITORS OF UROKINASE

UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN-JT464 COMPLEX

UROKINASE-TYPE PLASMINOGEN ACTIVATOR INHIBITOR COMPLEX WITHA 1-(7-SULPHOAMIDOISOQUINOLINYL) GUANIDINE

FRAGMENT-BASED DISCOVERY OF MEXILETINE DERIVATIVES AS ORALLY BIOAVAILABLE INHIBITORS OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR

ENGINEERED RESIDUE IN CHAIN A, MET 214 TO ILE ENGINEERED RESIDUE IN CHAIN A, CYS 299 TO SER

UROKINASE-TYPE PLASMINOGEN ACTIVATOR CHAIN B (E.C.3.4.21.73)

The largest off-origin peak in the Patterson function is 7.49% of the height of the origin peak. No significant pseudotranslation is detected.

20191225.v01 (using entries in the PDB archive December 25th 2019)

structure factor analysis and validation

geometric validation package for ligand chemistry in protein x-ray structures