1gvk

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 30: Line 30:
[[Category: serine protease]]
[[Category: serine protease]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 5 14:44:35 2007''
+
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 5 16:20:33 2007''

Revision as of 14:15, 5 November 2007


1gvk, resolution 0.945Å

Drag the structure with the mouse to rotate

PORCINE PANCREATIC ELASTASE ACYL ENZYME AT 0.95 A RESOLUTION

Overview

Kinetic analyses led to the discovery that N-acetylated tripeptides with, polar residues at P3 are inhibitors of porcine pancreatic elastase (PPE), that form unusually stable acyl-enzyme complexes. Peptides terminating in, a C-terminal carboxylate were more potent than those terminating in a, C-terminal amide, suggesting recognition by the oxy-anion hole is, important in binding. X-ray diffraction data were recorded to 0.95-A, resolution for an acyl-enzyme complex formed between PPE and, N-acetyl-Asn-Pro-Ile-CO2H at approximately pH 5. The accuracy of the, crystallographic coordinates allows structural issues concerning the, mechanism of serine proteases to be addressed. Significantly, the ester, bond of the acyl-enzyme showed a high level of planarity, suggesting, geometric strain of the ester link is not important during catalysis., Several hydrogen atoms could be clearly identified and were included, within the model. In keeping with a recent x-ray structure of subtilisin, at 0.78 A (1), limited electron density is visible consistent with the, putative location of a hydrogen atom approximately equidistant between the, histidine and aspartate residues of the catalytic triad. Comparison of, this high resolution crystal structure of the acyl-enzyme complex with, that of native elastase at 1.1 A (2) showed that binding of the N-terminal, part of the substrate can be accommodated with negligible structural, rearrangements. In contrast, comparison with structures obtained as part, of "time-resolved" studies on the reacting acyl-enzyme complex at >pH 7, (3) indicate small but significant structural differences, consistent with, the proposed synchronization of ester hydrolysis and substrate release.

About this Structure

1GVK is a Protein complex structure of sequences from Sus scrofa with CA, SO4 and ACE as ligands. Active as Pancreatic elastase, with EC number 3.4.21.36 Structure known Active Site: CA. Full crystallographic information is available from OCA.

Reference

X-ray structure of a serine protease acyl-enzyme complex at 0.95-A resolution., Katona G, Wilmouth RC, Wright PA, Berglund GI, Hajdu J, Neutze R, Schofield CJ, J Biol Chem. 2002 Jun 14;277(24):21962-70. Epub 2002 Mar 14. PMID:11896054

Page seeded by OCA on Mon Nov 5 16:20:33 2007

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools