Structure of PDB 5i53 Chain A Binding Site BS03
Receptor Information
>5i53 Chain A (length=129) Species:
9031
(Gallus gallus) [
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KVFGRCELAAAMKRHGLDNYRGYSLGNWVCAAKFESNFNTQATNRNTDGS
TDYGILQINSRWWCNDGRTPGSRNLCNIPCSALLSSDITASVNCAKKIVS
DGNGMNAWVAWRNRCKGTDVQAWIRGCRL
Ligand information
Ligand ID
URE
InChI
InChI=1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)
InChIKey
XSQUKJJJFZCRTK-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)(N)N
CACTVS 3.341
NC(N)=O
ACDLabs 10.04
O=C(N)N
Formula
C H4 N2 O
Name
UREA
ChEMBL
CHEMBL985
DrugBank
DB03904
ZINC
ZINC000008214514
PDB chain
5i53 Chain A Residue 204 [
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Receptor-Ligand Complex Structure
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PDB
5i53
Time-dependent X-ray diffraction studies on urea/hen egg white lysozyme complexes reveal structural changes that indicate onset of denaturation
Resolution
1.608 Å
Binding residue
(original residue number in PDB)
C127 L129
Binding residue
(residue number reindexed from 1)
C127 L129
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
E35 N46 D48 S50 D52 N59
Catalytic site (residue number reindexed from 1)
E35 N46 D48 S50 D52 N59
Enzyme Commision number
3.2.1.17
: lysozyme.
Gene Ontology
Molecular Function
GO:0003796
lysozyme activity
GO:0005515
protein binding
GO:0016231
beta-N-acetylglucosaminidase activity
GO:0016798
hydrolase activity, acting on glycosyl bonds
GO:0042802
identical protein binding
Biological Process
GO:0016998
cell wall macromolecule catabolic process
GO:0031640
killing of cells of another organism
GO:0042742
defense response to bacterium
GO:0050829
defense response to Gram-negative bacterium
GO:0050830
defense response to Gram-positive bacterium
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0005737
cytoplasm
GO:0005783
endoplasmic reticulum
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Molecular Function
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Cellular Component
External links
PDB
RCSB:5i53
,
PDBe:5i53
,
PDBj:5i53
PDBsum
5i53
PubMed
27573790
UniProt
P00698
|LYSC_CHICK Lysozyme C (Gene Name=LYZ)
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