Structure of PDB 1vbl Chain A Binding Site BS01
Receptor Information
>1vbl Chain A (length=416) Species:
132676
(Bacillus sp. TS-47) [
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KELGHEVLKPYDGWAAYGEGTTGGAMASPQNVFVVTNRTELIQALGGNNH
TNQYNSVPKIIYVKGTIDLNVDDNNQPVGPDFYKDPHFDFEAYLREYDPA
TWGKKEVEGPLEEARVRSQKKQKDRIMVYVGSNTSIIGVGKDAKIKGGGF
LIKNVDNVIIRNIEFEAPLDYFPEWDPTDGTLGEWNSEYDSISIEGSSHI
WIDHNTFTDGDHPDRSLGTYFGRPFQQHDGALDIKNSSDFITISYNVFTN
HDKVTLIGASDSRMADSGHLRVTLHHNYYKNVTQRLPRVRFGQVHIYNNY
YEFSNLADYDFQYAWGVGVFSQIYAQNNYFSFDWDIDPSLIIKVWSKNEE
SMYETGTIVDLPNGRRYIDLVASYNESNTLQLKKEVTWKPMFYHVIHPTP
SVPALVKAKAGAGNLH
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1vbl Chain A Residue 417 [
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Receptor-Ligand Complex Structure
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PDB
1vbl
Structural Basis for Thermostability of Pectate Lyase from Bacillus sp. TS 47
Resolution
1.91 Å
Binding residue
(original residue number in PDB)
D190 D229 D233
Binding residue
(residue number reindexed from 1)
D190 D229 D233
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
E188 D190 D229 D233 R285
Catalytic site (residue number reindexed from 1)
E188 D190 D229 D233 R285
Enzyme Commision number
4.2.2.2
: pectate lyase.
Gene Ontology
Molecular Function
GO:0016829
lyase activity
GO:0030570
pectate lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0000272
polysaccharide catabolic process
Cellular Component
GO:0005576
extracellular region
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1vbl
,
PDBe:1vbl
,
PDBj:1vbl
PDBsum
1vbl
PubMed
UniProt
Q9AJM4
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