Structure of PDB 8ihw Chain A Binding Site BS01
Receptor Information
>8ihw Chain A (length=433) Species:
6396
(Eisenia fetida) [
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QYNYDEVLEKSILFYEAERSGRLPANNRIPYRGDSALGDQGNQGQDLTGG
WYDAGDHVKFGFPMAFATTTLAWGILEFRDGYEAAGQYNLALDSIRWTLN
YFLKAHVSDNEFYGQVGDANTDHAYWGRPEDMTMERPAWSISPSAPGSDL
AAETAAALAAGYLVFRDSDAAFANNLLAHSRTLYDFALNNRGIYSQSISN
AAGFYASSAYEDELAWGAAWLYRATEEQEYLDRAYEFGTTTNTAWAYDWN
EKIVGYQLLLTTSAGQTDFLPRVENFLRNWFPGGSVQYTPLGLAWLAQWG
PNRYAANAAFIALVSAKYNILASESEQFARSQIHYMLGDAGRSYVVGFGN
NPPQQPHHRSSSCPDQPAECDWDEFNQPGPNYQILYGALVGGPDQNDQFE
DLRSDYIRNEVANDYNAGFQGAVAALRAIQLRD
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
8ihw Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
8ihw
A single mutation Asp43Arg was increased 2.5-fold the catalytic activity and maintained the stability of cold-adapted endo-1,4-beta glucanase (Ef-EG2) from Eisenia fetida.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
D386 Q404
Binding residue
(residue number reindexed from 1)
D365 Q383
Annotation score
4
Enzymatic activity
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:8ihw
,
PDBe:8ihw
,
PDBj:8ihw
PDBsum
8ihw
PubMed
UniProt
I2FI81
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