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Ligands
Code Name Style Show Link
BME Beta-mercaptoethanol
CL Chloride ion
Non-standard Residues
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Glycosylation
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Modification
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Code : 107L   PDBj   RCSB PDB   PDBe
Header : HYDROLASE(O-GLYCOSYL)
Title : STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME
Release Data : 1993-10-31
Compound :
mol_id molecule chains
1 T4 LYSOZYME A
ec: 3.2.1.17
Source :
mol_id organism_scientific
1 Enterobacteria phage T4  (taxid:10665)
expression_system_vector_type: PLASMID
expression_system_plasmid: M13
Authors : Blaber, M., Matthews, B.W.
Keywords : HYDROLASE(O-GLYCOSYL)
Exp. method : X-RAY DIFFRACTION ( 1.80 Å )
Citation :

Structural basis of amino acid alpha helix propensity.

Blaber, M.,Zhang, X.J.,Matthews, B.W.
(1993)  Science  260 : 1637 - 1640

PubMed: 8503008

Control of Enzyme Activity by an Engineered Disulfide Bond

Matsumura, M.,Matthews, B.W.
(1989)  Science  243 : 792

Structure of Bacteriophage T4 Lysozyme Refined at 1.7 Angstroms Resolution

Weaver, L.H.,Matthews, B.W.
(1987)  J.Mol.Biol.  193 : 189

Chain : A
UniProt : P00720 (ENLYS_BPT4)
Reaction: EC: Evidence:
Physiological Direction:
Hydrolysis of (1->4)-beta-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in a peptidoglycan and between N-acetyl-D-glucosamine residues in chitodextrins. 3.2.1.17 HAMAP-Rule:MF_04110, PubMed:4865643
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