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Ligands
Code Name Style Show Link
JNB ~{N}-[(2~{R},3~{R},4~{S},5~{S},6~{R})-6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]-4-phenyl-benzamide
PLP Pyridoxal-5'-phosphate
Non-standard Residues
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Glycosylation
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Modification
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Code : 6R0I   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : Glycogen Phosphorylase B in complex with 4
Release Data : 2019-04-17
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 : Koulas, M.S., Tsagkarakou, S.A., Kyriakis, E., Stravodimos, G.A., Skamnaki, V.T., Leonidas, D.D.
Keywords : TRANSFERASE
Exp. method : X-RAY DIFFRACTION ( 2.40 Å )
Citation :

High Consistency of Structure-Based Design and X-Ray Crystallography: Design, Synthesis, Kinetic Evaluation and Crystallographic Binding Mode Determination of Biphenyl-N-acyl-beta-d-Glucopyranosylamines as Glycogen Phosphorylase Inhibitors.

Fischer, T.,Koulas, S.M.,Tsagkarakou, A.S.  et al.
(2019)  Molecules  24

PubMed: 30987252
DOI: 10.3390/molecules24071322

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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