Structure of PDB 2fhn Chain X Binding Site BS01
Receptor Information
>2fhn Chain X (length=118) Species:
9031
(Gallus gallus) [
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CSLTGKWTNNLGSIMTIRAVNSRGEFTGTYLTAVADNPGNITLSPLLGIQ
HKRASQPTFGFTVHWNFSESTTVFTGQCFIDRNGKEVLKTMWLLRSSVND
ISYDWIATRVGYNNFTRL
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
2fhn Chain X Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
2fhn
Factors dictating the pseudocatalytic efficiency of avidins
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
L14 S16 Y33 T35 V37 A38 D39 W68 S73 T75 W95 S99 R112
Binding residue
(residue number reindexed from 1)
L11 S13 Y30 T32 V34 A35 D36 W65 S70 T72 W92 S96 R109
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:2fhn
,
PDBe:2fhn
,
PDBj:2fhn
PDBsum
2fhn
PubMed
16546211
UniProt
P56734
|AVR4_CHICK Avidin-related protein 4/5 (Gene Name=AVR4)
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