Structure of PDB 1ssx Chain A Binding Site BS03
Receptor Information
>1ssx Chain A (length=198) Species:
69
(Lysobacter enzymogenes) [
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ANIVGGIEYSINNASLCSVGFSVTRGATKGFVTAGHCGTVNATARIGGAV
VGTFAARVFPGNDRAWVSLTSAQTLLPRVANGSSFVTVRGSTEAAVGAAV
CRSGRTTGYQCGTITAKNVTANYAEGAVRGLTQGNACMGRGDSGGSWITS
AGQAQGVMSGGNVQSNGNNCGIPASQRSSLFERLQPILSQYGLSLVTG
Ligand information
Ligand ID
SO4
InChI
InChI=1S/H2O4S/c1-5(2,3)4/h(H2,1,2,3,4)/p-2
InChIKey
QAOWNCQODCNURD-UHFFFAOYSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
[O-]S(=O)(=O)[O-]
CACTVS 3.341
[O-][S]([O-])(=O)=O
ACDLabs 10.04
[O-]S([O-])(=O)=O
Formula
O4 S
Name
SULFATE ION
ChEMBL
DrugBank
DB14546
ZINC
PDB chain
1ssx Chain A Residue 203 [
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Receptor-Ligand Complex Structure
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PDB
1ssx
The 0.83A Resolution Crystal Structure of alpha-Lytic Protease Reveals the Detailed Structure of the Active Site and Identifies a Source of Conformational Strain.
Resolution
0.83 Å
Binding residue
(original residue number in PDB)
A176 R178
Binding residue
(residue number reindexed from 1)
A127 R129
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D102 G193 S195 S214
Catalytic site (residue number reindexed from 1)
H36 D63 G141 S143 S159
Enzyme Commision number
3.4.21.12
: alpha-lytic endopeptidase.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:1ssx
,
PDBe:1ssx
,
PDBj:1ssx
PDBsum
1ssx
PubMed
15111063
UniProt
P00778
|PRLA_LYSEN Alpha-lytic protease (Gene Name=alpha-LP)
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