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1 of phosphorylase that lacked the N-terminus (phosphorylase b').
2 ) have been determined for the rabbit muscle phosphorylase b.
3 inimal binding requirements of rabbit muscle phosphorylase b.
4 N-oxide on the self-association behaviour of phosphorylase b.
5 e mutants are more like phosphorylase a than phosphorylase b.
6 sphorylase a, and unlike the dephospho-form, phosphorylase b.
7 accommodates the phosphorylatable serine in phosphorylase b.
8 lation by gamma(1-300) compared to wild-type phosphorylase b.
9 iency for gamma(1-300), compared to that for phosphorylase b.
10 time the full thermodynamic effect of AMP on phosphorylase b.
11 ing the allosteric effect of AMP on glycogen phosphorylase b.
12 of glycerol, sucrose and ethylene glycol on phosphorylase b activity, phenomena that have been attri
14 are) on an extensive time-course analysis of phosphorylase B and an epitope analysis of single-domain
15 digests, using a standard dilution series of phosphorylase B and carbonic anhydrase, separated by SDS
16 lamide gel electrophoresis with cross-linked phosphorylase B as standard is a suitable gel system for
17 determinants employed in the recognition of phosphorylase b as substrate are utilized in the recogni
19 ing studies to 2.4 A resolution with T state phosphorylase b crystals showed that nojirimycin tetrazo
21 o enzyme-catalyzed reaction using the enzyme phosphorylase b from rabbit muscle and Deinococcus geoth
22 x that phosphorylates and activates glycogen phosphorylase b (GP b) in a Ca (2+)-dependent reaction t
26 strates and allosteric effectors to glycogen phosphorylase b has provided evidence that the device is
27 inants for protein phosphatase-1, mutants of phosphorylase b have been converted to phosphorylase a a
28 sedimentation equilibrium distributions for phosphorylase b in 40 mM Hepes buffer (pH 6.8) supplemen
31 16 subunits of the (alphabetagammadelta)(4) phosphorylase b kinase (PhK) complex can only be achieve
32 the glycogen branching enzyme (GBE) and the phosphorylase b kinase alpha subunit (PhKalpha) protein,
33 to be discovered for some glycogenoses (e.g. phosphorylase-b-kinase deficiency or branching enzyme de
34 hrombospondin 1) and 3 new markers (glycogen phosphorylase B, lipoprotein a and profilin 1) were elev
36 t interact with the amino terminus in either phosphorylase b or a, showed little difference in phosph
37 ion opposite the regulatory face of glycogen phosphorylase b (P-b), providing a probe for detecting a
38 nd the physical interaction between glycogen phosphorylase-b (P-b) and its only known kinase, phospho
39 atured rTromp1 eluted at the position of the phosphorylase b protein standard (97 kDa), suggesting a
40 hose terms the marginally enhanced extent of phosphorylase b self-association observed in the presenc
42 to 'open-loop' Ca2+-dependent conversion of phosphorylase b to a, and partly to the 'closed loop' in
43 25 fmol, and the lowest gel loading in which phosphorylase B was identified using electroextraction w
45 the presence of the inhibitor glucose, while phosphorylase b was phosphorylated normally with this in
46 hK is the only kinase that can phosphorylate phosphorylase b, which in turn is the only physiological