Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.6.3.1 (
Mg2+-ATPase
)
1,484
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The effects of trypsin digestion and low temperature on Ca2+ binding and on Ca2+ activation of ATP hydrolysis by the high-affinity transport sites of the Ca2+,
Mg2+-ATPase
of sarcoplasmic reticulum were examined. Sarcoplasmic reticulum vesicles contain 0.7-1.1 high-affinity Ca2+ sites per 10(5) g sarcoplasmic reticulum with K = 3-5 X 10(5) M-1, as well as sites of lower affinity. The first cleavage of the ATPase with trypsin (
TD1
) has no effect on the binding properties of the high affinity sites. The second tryptic cleavage (
TD2
) decreases the affinity of the high sites to K = 3 X 10(4) M-1 with conservation of the total number of sites. The purified ATPase contains 1.6-2.0 high affinity Ca2+ sites per 10(5) g protein when measured at 23 degrees C, while at 0-4 degrees C there is approximately equal to 1 high-affinity (K = 5 - 10 X 10(5) M-1) affinity site and approximately equal to 1 intermediate-affinity (K = 3 X 10(4) M-1) site per 10(5) g. Trypsin digestion to the point of
TD1
has no effect on either the number or the binding constants of the high-affinity sites. Upon
TD2
cleavage, one of the sites is converted to the intermediate-affinity state, while the other remains at high affinity. After
TD2
modification of the enzyme both of the sites are in the intermediate affinity state at 4 degrees C. On the basis of the binding data, several models for the roles of the Ca2+ sites in the activation of ATP hydrolysis are derived. The results are summarized by a scheme in which the two high-affinity Ca2+ sites are heterogeneous with respect to sensitivity to temperature and to
TD2
modification. The results of this and a previous study [Scott, T. L. and Shamoo, A. E. (1982) J. Membr. Biol. 64, 137-144] indicate that while occupation of either of the two Ca2+ sites can stimulate ATP hydrolysis, the site which is sensitive to
TD2
is essential for the coupling of hydrolysis to Ca2+ transport.
...
PMID:Distinction of the roles of the two high-affinity calcium sites in the functional activities of the Ca2+-ATPase of sarcoplasmic reticulum. 623 83