Structure of PDB 1ksd Chain A Binding Site BS01
Receptor Information
>1ksd Chain A (length=433) Species:
62960
(Nasutitermes takasagoensis) [
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MAYDYKQVLRDSLLFYEAQRSGRLPADQKVTWRKDSALNDQGDQGQDLTG
GYFDAGDFVKFGFPMAYTATVLAWGLIDFEAGYSSAGALDDGRKAVKWAT
DYFIKAHTSQNEFYGQVGQGDADHAFWGRPEDMTMARPAYKIDTSRPGSD
LAGETAAALAAASIVFRNVDGTYSNNLLTHARQLFDFANNYRGKYSDSIT
DARNFYASADYRDELVWAAAWLYRATNDNTYLNTAESLYDEFGLQNWGGG
LNWDSKVSGVQVLLAKLTNKQAYKDTVQSYVNYLINNQQKTPKGLLYIDM
WGTLRHAANAAFIMLEAAELGLSASSYRQFAQTQIDYALGDGGRSFVCGF
GSNPPTRPHHRSSSCPPAPATCDWNTFNSPDPNYHVLSGALVGGPDQNDN
YVDDRSDYVHNEVATDYNAGFQSALAALVALGY
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
1ksd Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1ksd
Structure of an endoglucanase from termite, Nasutitermes takasagoensis.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
D210 D213 E214 D254
Binding residue
(residue number reindexed from 1)
D210 D213 E214 D254
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D54 D57 Y206 E412
Catalytic site (residue number reindexed from 1)
D54 D57 Y206 E412
Enzyme Commision number
3.2.1.4
: cellulase.
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0008810
cellulase activity
GO:0016798
hydrolase activity, acting on glycosyl bonds
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0030245
cellulose catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1ksd
,
PDBe:1ksd
,
PDBj:1ksd
PDBsum
1ksd
PubMed
11914490
UniProt
O77044
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