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Ligands
Code Name Style Show Link
CKQ 4-[4-[5-[(2~{S},3~{R},4~{R},5~{S},6~{R})-6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]-4~{H}-1,2,4-triazol-3-yl]phenyl]benzoic acid
IMP Inosinic acid
PLP Pyridoxal-5'-phosphate
Non-standard Residues
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Glycosylation
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Modification
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Code : 6F3J   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : The crystal structure of Glycogen Phosphorylase in complex with 10a
Release Data : 2018-02-28
Compound :
mol_id molecule chains synonym
1 Glycogen phosphorylase, muscle form A Myophosphorylase
ec: 2.4.1.1
Source :
mol_id organism_scientific organism_common
1 Oryctolagus cuniculus  (taxid:9986) Rabbit
tissue: muscle
Authors : Kyriakis, E., Stamati, E.C.V., Stravodimos, G.A., Skamnaki, V.T., Leonidas, D.D.
Keywords : Transferase
Exp. method : X-RAY DIFFRACTION ( 2.20 Å )
Citation :

A multidisciplinary study of 3-( beta-d-glucopyranosyl)-5-substituted-1,2,4-triazole derivatives as glycogen phosphorylase inhibitors: Computation, synthesis, crystallography and kinetics reveal new potent inhibitors.

Kun, S.,Begum, J.,Kyriakis, E.  et al.
(2018)  Eur J Med Chem  147 : 266 - 278

PubMed: 29453094
DOI: 10.1016/j.ejmech.2018.01.095

Chain : A
UniProt : P00489 (PYGM_RABIT)
Reaction: EC: Evidence:
Physiological Direction:
[(1->4)-alpha-D-glucosyl](n) + phosphate = [(1->4)-alpha-D- glucosyl](n-1) + alpha-D-glucose 1-phosphate 2.4.1.1 UniProtKB:P11217
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