Structure of PDB 6sar Chain A Binding Site BS01
Receptor Information
>6sar Chain A (length=392) Species:
83333
(Escherichia coli K-12) [
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LSIGQEMQMGDYYVRQLRGSAPLINDPLLTQYINSLGMRLVSHANSVKTP
FHFFLINNDEINAFAFFGGNVVLHSALFRYSDNESQLASVMAHEISHVTQ
RHSFTQQNEQEADRIGIQVLQRSGFDPQAMPTFLEKLLDQARYSSRPPEI
LLTHPLPESRLADARNRANQMRPMVVQSSEDFYLAKARTLGMYNSGRNQL
TSDLLDEWAKGNVRQQRAAQYGRALQAMEANKYDEARKTLQPLLAAEPGN
AWYLDLATDIDLGQNKANEAINRLKNARDLRTNPVLQLNLANAYLQGGQP
QEAANILNRYTFNNKDDSNGWDLLAQAEAALNNRDQELAARAEGYALAGR
LDQAISLLSSASSQVKLGSLQQARYDARIDQLRQLQERFKPY
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
6sar Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6sar
Structure-Function Characterization of the Conserved Regulatory Mechanism of the Escherichia coli M48 Metalloprotease BepA.
Resolution
2.18 Å
Binding residue
(original residue number in PDB)
H136 H140 E201 H246
Binding residue
(residue number reindexed from 1)
H93 H97 E109 H154
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.4.-.-
Gene Ontology
Molecular Function
GO:0004222
metalloendopeptidase activity
GO:0008237
metallopeptidase activity
Biological Process
GO:0006508
proteolysis
GO:0061077
chaperone-mediated protein folding
Cellular Component
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6sar
,
PDBe:6sar
,
PDBj:6sar
PDBsum
6sar
PubMed
33106348
UniProt
P66948
|BEPA_ECOLI Beta-barrel assembly-enhancing protease (Gene Name=bepA)
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