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PDBsum entry 2ea3

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Hydrolase PDB id
2ea3
Contents
Protein chain
183 a.a.
Ligands
SO4 ×3
Waters ×58

References listed in PDB file
Key reference
Title Structure determination and analysis of a bacterial chymotrypsin from cellulomonas bogoriensis.
Authors A.Shaw, M.L.Saldajeno, M.A.Kolkman, B.E.Jones, R.Bott.
Ref. Acta Crystallogr Sect F Struct Biol Cryst Commun, 2007, 63, 266-269. [DOI no: 10.1107/S1744309107008937]
PubMed id 17401191
Abstract
The crystal structure of a secreted chymotrypsin from the alkaliphile Cellulomonas bogoriensis has been determined using data to 1.78 A resolution and refined to a crystallographic R factor of 0.167. The crystal structure reveals a large P1 substrate-specificity pocket, as expected for chymotrypsins. The structure is compared with close structural homologues. This comparison does not reveal clear reasons for the alkali tolerance of the enzyme, but the greater compactness of the structure and lowered hydrogen bonding may play a role.
Figure 1.
(a) Crystals of cellulomonadin. (b) 2F [o] [minus sign] F [c] electron density of cellulomonadin around the catalytic triad, contoured at 1[sigma]. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 April 1; 63(Pt 4): 266–269. Published online 2007 March 23. doi: 10.1107/S1744309107008937. Copyright [copyright] International Union of Crystallography 2007
Figure 2.
Structure of cellulomonadin. (a) Topology diagram of cellulomonadin. [beta]-Sheets are shown as blue arrows pointing in the direction from the N-terminal to the C-terminal ends. [alpha]-Helices are shown as red cylinders. Connections between secondary-structure elements are shown as black line arrows. (b) Tertiary structure of cellulomonadin. The catalytic triad residues His32, Asp56 and Ser137 are shown as ball-and-stick representations. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 April 1; 63(Pt 4): 266–269. Published online 2007 March 23. doi: 10.1107/S1744309107008937. Copyright [copyright] International Union of Crystallography 2007
The above figures are reprinted from an Open Access publication published by the IUCr: Acta Crystallogr Sect F Struct Biol Cryst Commun (2007, 63, 266-269) copyright 2007.
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