1yo0
From Proteopedia
| Line 1: | Line 1: | ||
[[Image:1yo0.gif|left|200px]] | [[Image:1yo0.gif|left|200px]] | ||
| - | + | <!-- | |
| - | + | The line below this paragraph, containing "STRUCTURE_1yo0", creates the "Structure Box" on the page. | |
| - | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
| - | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
| - | + | or leave the SCENE parameter empty for the default display. | |
| - | + | --> | |
| - | + | {{STRUCTURE_1yo0| PDB=1yo0 | SCENE= }} | |
| - | + | ||
| - | + | ||
| - | }} | + | |
'''Proton Transfer from His200 in Human Carbonic Anhydrase II''' | '''Proton Transfer from His200 in Human Carbonic Anhydrase II''' | ||
| Line 35: | Line 32: | ||
[[Category: Silverman, D N.]] | [[Category: Silverman, D N.]] | ||
[[Category: Tu, C.]] | [[Category: Tu, C.]] | ||
| - | [[Category: | + | [[Category: Human carbonic anhydrase]] |
| - | [[Category: | + | [[Category: Proton transfer]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 16:33:54 2008'' | |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
Revision as of 13:33, 3 May 2008
Proton Transfer from His200 in Human Carbonic Anhydrase II
Contents |
Overview
Human carbonic anhydrase II (HCA II) has a histidine at position 64 (His64) that donates a proton to the zinc-bound hydroxide in catalysis of the dehydration of bicarbonate. To examine the effect of the histidine location on proton shuttling, His64 was replaced with Ala and Thr200 replaced with histidine (H64A-T200H HCAII), effectively relocating the proton shuttle residue 2 A closer to the zinc-bound hydroxide compared to wild type HCA II. The crystal structure of H64A-T200H HCA II at 1.8 A resolution shows the side chain of His200 directly hydrogen-bonded with the zinc-bound solvent. Different proton transfer processes were observed at pH 6 and at pH 8 during the catalytic hydration-dehydration cycle, measured by mass spectrometry as the depletion of 18O from C18O2 by H64A-T200H HCA II. The process at pH 6.0 is attributed to proton transfer between the side chain of His200 and the zinc-bound hydroxide, in analogy with proton transfer involving His64 in wild-type HCA II. At pH 8.0 it is attributed to proton transfer between bicarbonate and the zinc-bound hydroxide, as supported by the dependence of the rate of proton transfer on bicarbonate concentration and on solvent hydrogen isotope effects. This study establishes that a histidine directly hydrogen-bonded to the zinc-bound hydroxide, can adopt the correct distance geometry to support proton transfer
Disease
Known disease associated with this structure: Osteopetrosis, autosomal recessive 3, with renal tubular acidosis OMIM:[611492]
About this Structure
1YO0 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Proton transfer in a Thr200His mutant of human carbonic anhydrase II., Bhatt D, Tu C, Fisher SZ, Hernandez Prada JA, McKenna R, Silverman DN, Proteins. 2005 Nov 1;61(2):239-45. PMID:16106378 Page seeded by OCA on Sat May 3 16:33:54 2008
