Structure of PDB 1ks4 Chain A Binding Site BS03
Receptor Information
>1ks4 Chain A (length=223) Species:
5061
(Aspergillus niger) [
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QTMCSQYDSASSPPYSVNQNLWGEYQGTGSQCVYVDKLSSSGASWHTEWT
WSGGEGTVKSYSNSGVTFNKKLVSDVSSIPTSVEWKQDNTNVNADVAYDL
FTAANVDHATSSGDYELMIWLARYGNIQPIGKQIATATVGGKSWEVWYGS
TTQAGAEQRTYSFVSESPINSYSGDINAFFSYLTQNQGFPASSQYLINLQ
FGTEAFTGGPATFTVDNWTASVN
Ligand information
Ligand ID
PD
InChI
InChI=1S/Pd/q+2
InChIKey
MUJIDPITZJWBSW-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Pd++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Pd+2]
Formula
Pd
Name
PALLADIUM ION
ChEMBL
DrugBank
ZINC
PDB chain
1ks4 Chain A Residue 226 [
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Receptor-Ligand Complex Structure
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PDB
1ks4
Determination of the structure of an endoglucanase from Aspergillus niger and its mode of inhibition by palladium chloride.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
T2 M3 C32 V33 Y34
Binding residue
(residue number reindexed from 1)
T2 M3 C32 V33 Y34
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E116 E204
Catalytic site (residue number reindexed from 1)
E116 E204
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:0016740
transferase activity
GO:0016798
hydrolase activity, acting on glycosyl bonds
Biological Process
GO:0000272
polysaccharide catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1ks4
,
PDBe:1ks4
,
PDBj:1ks4
PDBsum
1ks4
PubMed
11914491
UniProt
O74705
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