Structure of PDB 2a3b Chain B Binding Site BS01
Receptor Information
>2a3b Chain B (length=394) [
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ASSGYRSVVYFVNWAIYGRNHNPQDLPVERLTHVLYAFANVRPETGEVYM
TDSWADIEKHYPGDSWSDTGNNVYGCIKQLYLLKKQNRNLKVLLSIGGWT
YSPNFAPAASTDAGRKNFAKTAVKLLQDLGFDGLDIDWEYPENDQQANDF
VLLLKEVRTALDSYSAANAGGQHFLLTVASPAGPDKIKVLHLKDMDQQLD
FWNLMAYDYAGSFSSLSGHQANVYNDTSNPLSTPFNTQTALDLYRAGGVP
ANKIVLGMPLYGRSFANTDGPGKPYNGVGQGSWENGVWDYKALPQAGATE
HVLPDIMASYSYDATNKFLISYDNPQVANLKSGYIKSLGLGGAMWWDSSS
DKTGSDSLITTVVNALGGTGVFEQSQNELDYPVSQYDNLRNGMQ
Ligand information
Ligand ID
CFF
InChI
InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3
InChIKey
RYYVLZVUVIJVGH-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cn1cnc2N(C)C(=O)N(C)C(=O)c12
ACDLabs 10.04
O=C2N(c1ncn(c1C(=O)N2C)C)C
OpenEye OEToolkits 1.5.0
Cn1cnc2c1C(=O)N(C(=O)N2C)C
Formula
C8 H10 N4 O2
Name
CAFFEINE;
3,7-DIHYDRO-1,3,7-TRIMETHYL-1H-PURINE-2,6-DIONE
ChEMBL
CHEMBL113
DrugBank
DB00201
ZINC
ZINC000000001084
PDB chain
2a3b Chain B Residue 2434 [
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Receptor-Ligand Complex Structure
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PDB
2a3b
Methylxanthine drugs are chitinase inhibitors: investigation of inhibition and binding modes.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
W137 Y178 D246 F251
Binding residue
(residue number reindexed from 1)
W99 Y140 D208 F213
Annotation score
3
Binding affinity
MOAD
: ic50=469uM
BindingDB: IC50=469000nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D173 D175 E177 Y245
Catalytic site (residue number reindexed from 1)
D135 D137 E139 Y207
Enzyme Commision number
3.2.1.14
: chitinase.
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0008061
chitin binding
Biological Process
GO:0005975
carbohydrate metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2a3b
,
PDBe:2a3b
,
PDBj:2a3b
PDBsum
2a3b
PubMed
16183021
UniProt
Q873X9
|CHIB1_ASPFM Endochitinase B1 (Gene Name=chiB1)
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