 |
PDBsum entry 1g0f
|
|
|
|
 |
Contents |
 |
|
|
|
|
|
|
|
|
|
|
|
* Residue conservation analysis
|
|
|
|
 |
|
|
 |
 |
 |
 |
Enzyme class 2:
|
 |
E.C.4.2.1.1
- carbonic anhydrase.
|
|
 |
 |
 |
 |
 |
Reaction:
|
 |
hydrogencarbonate + H+ = CO2 + H2O
|
 |
 |
 |
 |
 |
hydrogencarbonate
|
+
|
H(+)
|
=
|
CO2
|
+
|
H2O
|
|
 |
 |
 |
 |
 |
 |
 |
 |
Cofactor:
|
 |
Zn(2+)
|
 |
 |
 |
 |
 |
Enzyme class 3:
|
 |
E.C.4.2.1.69
- cyanamide hydratase.
|
|
 |
 |
 |
 |
 |
Reaction:
|
 |
urea = cyanamide + H2O
|
 |
 |
 |
 |
 |
urea
|
=
|
cyanamide
|
+
|
H2O
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
Note, where more than one E.C. class is given (as above), each may
correspond to a different protein domain or, in the case of polyprotein
precursors, to a different mature protein.
|
|
 |
|
Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
|
|
| |
|
|
| |
|
DOI no:
|
Biochemistry
40:1741-1748
(2001)
|
|
PubMed id:
|
|
|
|
|
| |
|
Structural and kinetic analysis of the chemical rescue of the proton transfer function of carbonic anhydrase II.
|
|
D.Duda,
C.Tu,
M.Qian,
P.Laipis,
M.Agbandje-McKenna,
D.N.Silverman,
R.McKenna.
|
|
|
|
| |
ABSTRACT
|
|
|
| |
|
Histidine 64 in human carbonic anhydrase II (HCA II) functions in the catalytic
pathway of CO(2) hydration as a shuttle to transfer protons between the
zinc-bound water and bulk water. Catalysis of the exchange of (18)O between
CO(2) and water, measured by mass spectrometry, is dependent on this proton
transfer and was decreased more than 10-fold for H64A HCA II compared with
wild-type HCA II. The loss of catalytic activity of H64A HCA II could be rescued
by 4-methylimidazole (4-MI), an exogenous proton donor, in a saturable process
with a maximum activity of 40% of wild-type HCA II. The crystal structure of the
rescued complex at 1.6 A resolution shows 4-MI bound in the active-site cavity
of H64A HCA II, through pi stacking interactions with Trp 5 and H-bonding
interactions with water molecules. In this location, 4-MI is about 12 A from the
zinc and approximates the observed "out" position of His 64 in the structure of
the wild-type enzyme. 4-MI appears to compensate for the absence of His 64 and
rescues the catalytic activity of the H64A HCA II mutant. This result strongly
suggests that the out conformation of His 64 is effective in the transfer of
protons between the zinc-bound solvent molecule and solution.
|
|
|
|
|
|
|
 |
 |
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
Literature references that cite this PDB file's key reference
|
|
 |
| |
PubMed id
|
 |
Reference
|
 |
|
|
|
 |
H.M.Becker,
M.Klier,
C.Schüler,
R.McKenna,
and
J.W.Deitmer
(2011).
Intramolecular proton shuttle supports not only catalytic but also noncatalytic function of carbonic anhydrase II.
|
| |
Proc Natl Acad Sci U S A,
108,
3071-3076.
|
 |
|
|
|
|
 |
K.Dave,
A.Scozzafava,
D.Vullo,
C.T.Supuran,
and
M.A.Ilies
(2011).
Pyridinium derivatives of histamine are potent activators of cytosolic carbonic anhydrase isoforms I, II and VII.
|
| |
Org Biomol Chem,
9,
2790-2800.
|
 |
|
|
|
|
 |
K.Dave,
M.A.Ilies,
A.Scozzafava,
C.Temperini,
D.Vullo,
and
C.T.Supuran
(2011).
An inhibitor-like binding mode of a carbonic anhydrase activator within the active site of isoform II.
|
| |
Bioorg Med Chem Lett,
21,
2764-2768.
|
 |
|
|
|
|
 |
C.M.Maupin,
and
G.A.Voth
(2010).
Proton transport in carbonic anhydrase: Insights from molecular simulation.
|
| |
Biochim Biophys Acta,
1804,
332-341.
|
 |
|
|
|
|
 |
C.M.Maupin,
J.Zheng,
C.Tu,
R.McKenna,
D.N.Silverman,
and
G.A.Voth
(2009).
Effect of active-site mutation at Asn67 on the proton transfer mechanism of human carbonic anhydrase II.
|
| |
Biochemistry,
48,
7996-8005.
|
 |
|
|
|
|
 |
C.M.Maupin,
R.McKenna,
D.N.Silverman,
and
G.A.Voth
(2009).
Elucidation of the proton transport mechanism in human carbonic anhydrase II.
|
| |
J Am Chem Soc,
131,
7598-7608.
|
 |
|
|
|
|
 |
C.M.Maupin,
M.G.Saunders,
I.F.Thorpe,
R.McKenna,
D.N.Silverman,
and
G.A.Voth
(2008).
Origins of enhanced proton transport in the Y7F mutant of human carbonic anhydrase II.
|
| |
J Am Chem Soc,
130,
11399-11408.
|
 |
|
|
|
|
 |
J.Seravalli,
and
S.W.Ragsdale
(2008).
13C NMR characterization of an exchange reaction between CO and CO2 catalyzed by carbon monoxide dehydrogenase.
|
| |
Biochemistry,
47,
6770-6781.
|
 |
|
|
|
|
 |
V.M.Krishnamurthy,
G.K.Kaufman,
A.R.Urbach,
I.Gitlin,
K.L.Gudiksen,
D.B.Weibel,
and
G.M.Whitesides
(2008).
Carbonic anhydrase as a model for biophysical and physical-organic studies of proteins and protein-ligand binding.
|
| |
Chem Rev,
108,
946.
|
 |
|
|
|
|
 |
C.M.Maupin,
and
G.A.Voth
(2007).
Preferred orientations of His64 in human carbonic anhydrase II.
|
| |
Biochemistry,
46,
2938-2947.
|
 |
|
|
|
|
 |
D.Bhatt,
S.Z.Fisher,
C.Tu,
R.McKenna,
and
D.N.Silverman
(2007).
Location of binding sites in small molecule rescue of human carbonic anhydrase II.
|
| |
Biophys J,
92,
562-570.
|
 |
|
PDB codes:
|
 |
|
|
|
|
|
 |
H.Shimahara,
T.Yoshida,
Y.Shibata,
M.Shimizu,
Y.Kyogoku,
F.Sakiyama,
T.Nakazawa,
S.Tate,
S.Y.Ohki,
T.Kato,
H.Moriyama,
K.Kishida,
Y.Tano,
T.Ohkubo,
and
Y.Kobayashi
(2007).
Tautomerism of histidine 64 associated with proton transfer in catalysis of carbonic anhydrase.
|
| |
J Biol Chem,
282,
9646-9656.
|
 |
|
|
|
|
 |
I.Elder,
Z.Fisher,
P.J.Laipis,
C.Tu,
R.McKenna,
and
D.N.Silverman
(2007).
Structural and kinetic analysis of proton shuttle residues in the active site of human carbonic anhydrase III.
|
| |
Proteins,
68,
337-343.
|
 |
|
PDB codes:
|
 |
|
|
|
|
|
 |
J.M.Swanson,
C.M.Maupin,
H.Chen,
M.K.Petersen,
J.Xu,
Y.Wu,
and
G.A.Voth
(2007).
Proton solvation and transport in aqueous and biomolecular systems: insights from computer simulations.
|
| |
J Phys Chem B,
111,
4300-4314.
|
 |
|
|
|
|
 |
A.Roy,
and
S.Taraphder
(2006).
Proton transfer pathways in the mutant His-64-Ala of human carbonic anhydrase II.
|
| |
Biopolymers,
82,
623-630.
|
 |
|
|
|
|
 |
D.Riccardi,
P.König,
X.Prat-Resina,
H.Yu,
M.Elstner,
T.Frauenheim,
and
Q.Cui
(2006).
"Proton holes" in long-range proton transfer reactions in solution and enzymes: A theoretical analysis.
|
| |
J Am Chem Soc,
128,
16302-16311.
|
 |
|
|
|
|
 |
D.Bhatt,
C.Tu,
S.Z.Fisher,
J.A.Hernandez Prada,
R.McKenna,
and
D.N.Silverman
(2005).
Proton transfer in a Thr200His mutant of human carbonic anhydrase II.
|
| |
Proteins,
61,
239-245.
|
 |
|
PDB codes:
|
 |
|
|
|
|
|
 |
P.Venkataraman,
R.A.Lamb,
and
L.H.Pinto
(2005).
Chemical rescue of histidine selectivity filter mutants of the M2 ion channel of influenza A virus.
|
| |
J Biol Chem,
280,
21463-21472.
|
 |
|
|
|
|
 |
T.K.Kim,
P.Lee,
and
R.F.Colman
(2003).
Critical role of Lys212 and Tyr140 in porcine NADP-dependent isocitrate dehydrogenase.
|
| |
J Biol Chem,
278,
49323-49331.
|
 |
|
|
|
|
 |
C.Tu,
M.Qian,
H.An,
N.R.Wadhwa,
D.Duda,
C.Yoshioka,
Y.Pathak,
R.McKenna,
P.J.Laipis,
and
D.N.Silverman
(2002).
Kinetic analysis of multiple proton shuttles in the active site of human carbonic anhydrase.
|
| |
J Biol Chem,
277,
38870-38876.
|
 |
|
PDB code:
|
 |
|
|
|
|
|
 |
H.An,
C.Tu,
D.Duda,
I.Montanez-Clemente,
K.Math,
P.J.Laipis,
R.McKenna,
and
D.N.Silverman
(2002).
Chemical rescue in catalysis by human carbonic anhydrases II and III.
|
| |
Biochemistry,
41,
3235-3242.
|
 |
|
|
|
|
 |
M.Ferraroni,
S.Tilli,
F.Briganti,
W.R.Chegwidden,
C.T.Supuran,
K.E.Wiebauer,
R.E.Tashian,
and
A.Scozzafava
(2002).
Crystal structure of a zinc-activated variant of human carbonic anhydrase I, CA I Michigan 1: evidence for a second zinc binding site involving arginine coordination.
|
| |
Biochemistry,
41,
6237-6244.
|
 |
|
PDB codes:
|
 |
|
|
|
|
|
 |
D.A.Whittington,
A.Waheed,
B.Ulmasov,
G.N.Shah,
J.H.Grubb,
W.S.Sly,
and
D.W.Christianson
(2001).
Crystal structure of the dimeric extracellular domain of human carbonic anhydrase XII, a bitopic membrane protein overexpressed in certain cancer tumor cells.
|
| |
Proc Natl Acad Sci U S A,
98,
9545-9550.
|
 |
|
PDB codes:
|
 |
|
|
 |
 |
|
The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
codes are
shown on the right.
|
');
}
}
 |