Structure of PDB 1ks4 Chain A Binding Site BS03

Receptor Information
>1ks4 Chain A (length=223) Species: 5061 (Aspergillus niger) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
QTMCSQYDSASSPPYSVNQNLWGEYQGTGSQCVYVDKLSSSGASWHTEWT
WSGGEGTVKSYSNSGVTFNKKLVSDVSSIPTSVEWKQDNTNVNADVAYDL
FTAANVDHATSSGDYELMIWLARYGNIQPIGKQIATATVGGKSWEVWYGS
TTQAGAEQRTYSFVSESPINSYSGDINAFFSYLTQNQGFPASSQYLINLQ
FGTEAFTGGPATFTVDNWTASVN
Ligand information
Ligand IDPD
InChIInChI=1S/Pd/q+2
InChIKeyMUJIDPITZJWBSW-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Pd++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Pd+2]
FormulaPd
NamePALLADIUM ION
ChEMBL
DrugBank
ZINC
PDB chain1ks4 Chain A Residue 226 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB1ks4 Determination of the structure of an endoglucanase from Aspergillus niger and its mode of inhibition by palladium chloride.
Resolution2.5 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 score1
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

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:1ks4, PDBe:1ks4, PDBj:1ks4
PDBsum1ks4
PubMed11914491
UniProtO74705

[Back to BioLiP]