Structure of PDB 2fhl Chain B Binding Site BS01
Receptor Information
>2fhl Chain B (length=120) Species:
9031
(Gallus gallus) [
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KCSLTGKWTNNLGSIMTIRAVNSRGEFTGTYLTAVADNPGNITLSPLLGI
QHKRASQPTFGFTVHWNFSESTTVFTGQCFIDRNGKEVLKTMWLLRSSVN
DISYDWKATRVGYNNFTRLS
Ligand information
Ligand ID
BNI
InChI
InChI=1S/C16H20N4O4S/c21-14(17-10-5-7-11(8-6-10)20(23)24)4-2-1-3-13-15-12(9-25-13)18-16(22)19-15/h5-8,12-13,15H,1-4,9H2,(H,17,21)(H2,18,19,22)/t12-,13-,15-/m0/s1
InChIKey
PORZMUYPQKOFQY-YDHLFZDLSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(ccc1NC(=O)CCCCC2C3C(CS2)NC(=O)N3)[N+](=O)[O-]
ACDLabs 10.04
O=C1NC2C(SCC2N1)CCCCC(=O)Nc3ccc([N+]([O-])=O)cc3
CACTVS 3.341
[O-][N+](=O)c1ccc(NC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)cc1
OpenEye OEToolkits 1.5.0
c1cc(ccc1NC(=O)CCCC[C@H]2[C@@H]3[C@H](CS2)NC(=O)N3)[N+](=O)[O-]
CACTVS 3.341
[O-][N+](=O)c1ccc(NC(=O)CCCC[CH]2SC[CH]3NC(=O)N[CH]23)cc1
Formula
C16 H20 N4 O4 S
Name
5-(2-OXO-HEXAHYDRO-THIENO[3,4-D]IMIDAZOL-6-YL)-PENTANOIC ACID (4-NITRO-PHENYL)-AMIDE;
BIOTINYL P-NITROANILINE
ChEMBL
DrugBank
DB03549
ZINC
ZINC000006535889
PDB chain
2fhl Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
2fhl
Factors dictating the pseudocatalytic efficiency of avidins
Resolution
1.05 Å
Binding residue
(original residue number in PDB)
S216 Y233 T235 V237 A238 D239 W268 S273 T275 W295 R312
Binding residue
(residue number reindexed from 1)
S14 Y31 T33 V35 A36 D37 W66 S71 T73 W93 R110
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0009374
biotin binding
Cellular Component
GO:0005576
extracellular region
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:2fhl
,
PDBe:2fhl
,
PDBj:2fhl
PDBsum
2fhl
PubMed
16546211
UniProt
P56734
|AVR4_CHICK Avidin-related protein 4/5 (Gene Name=AVR4)
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