Structure of PDB 6wqp Chain B Binding Site BS01
Receptor Information
>6wqp Chain B (length=354) Species:
1161942
(Ruminococcus champanellensis) [
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SLELLEPPTQMRDLTASQLLDEITIGWNLGNTLDATTTSWLPNPTPAQSE
TAWGCPMTTKAMIDKVKEGGFNTVRVPVSWIDHTGSAPEYQIDEAWMNRV
QEVVNYVIDNDMYCILNIHHENDWLIPTNAQKDSVNARLDAIWTQIATRF
GSYDEHLIFEGMNQPRLVGDPNEWNGGNQEARQVINSYNQTFVNTVRATG
GNNAIRCLMVPTYAASCSSTTVNDFVLPTDTVANKLIVDIHSYSPYNFAL
NTSGTSSFTQSDISQLQWTLQEIYNSFGAKGIPVIIGQFGALNKNNINGR
VLWGENYLRIAKSYNIRCIWWDNNAFDTSGENFGLLNRGTLTWQYPELLE
AMMK
Ligand information
Ligand ID
BCT
InChI
InChI=1S/CH2O3/c2-1(3)4/h(H2,2,3,4)/p-1
InChIKey
BVKZGUZCCUSVTD-UHFFFAOYSA-M
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)(O)[O-]
CACTVS 3.341
OC([O-])=O
ACDLabs 10.04
[O-]C(=O)O
Formula
C H O3
Name
BICARBONATE ION
ChEMBL
DrugBank
ZINC
PDB chain
6wqp Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6wqp
A structural and kinetic survey of GH5_4 endoglucanases reveals determinants of broad substrate specificity and opportunities for biomass hydrolysis.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
N296 N298
Binding residue
(residue number reindexed from 1)
N296 N298
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
Biological Process
GO:0000272
polysaccharide catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6wqp
,
PDBe:6wqp
,
PDBj:6wqp
PDBsum
6wqp
PubMed
33454012
UniProt
D4LAX7
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