Structure of PDB 5tfa Chain A Binding Site BS01
Receptor Information
>5tfa Chain A (length=216) Species:
9606
(Homo sapiens) [
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TEVVMENVTAFWEEGGTPVLKDINFKIERGQLLAVAGSTGAGKTSLLMMI
MGELEPSEGKIKHSGRISFCSQFSWIMPGTIKENIIFGVSYDEYRYRSVI
KACQLEEDISKFAEKDNIVLGEGGITLSGGQRARISLARAVYKDADLYLL
DSPFGYLDVLTEKEIFESCVCKLMANKTRILVTSKMEHLKKADKILILHE
GSSYFYGTFSELQNLQ
Ligand information
Ligand ID
DUT
InChI
InChI=1S/C9H15N2O14P3/c12-5-3-8(11-2-1-7(13)10-9(11)14)23-6(5)4-22-27(18,19)25-28(20,21)24-26(15,16)17/h1-2,5-6,8,12H,3-4H2,(H,18,19)(H,20,21)(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1
InChIKey
AHCYMLUZIRLXAA-SHYZEUOFSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1[C@@H]([C@H](O[C@H]1N2C=CC(=O)NC2=O)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O
OpenEye OEToolkits 1.5.0
C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O
CACTVS 3.341
O[CH]1C[CH](O[CH]1CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)N2C=CC(=O)NC2=O
CACTVS 3.341
O[C@H]1C[C@@H](O[C@@H]1CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)N2C=CC(=O)NC2=O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)NC(=O)C=C1)CC2O
Formula
C9 H15 N2 O14 P3
Name
DEOXYURIDINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL374361
DrugBank
DB02333
ZINC
ZINC000008215971
PDB chain
5tfa Chain A Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
5tfa
Thermodynamic correction of F508del-CFTR by ligand binding to a remote site in the mutated domain
Resolution
1.87 Å
Binding residue
(original residue number in PDB)
W401 V440 T460 G461 G463 K464 T465 S466 Q493
Binding residue
(residue number reindexed from 1)
W12 V19 T39 G40 G42 K43 T44 S45 Q72
Annotation score
1
Enzymatic activity
Enzyme Commision number
5.6.1.6
: channel-conductance-controlling ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
View graph for
Molecular Function
External links
PDB
RCSB:5tfa
,
PDBe:5tfa
,
PDBj:5tfa
PDBsum
5tfa
PubMed
UniProt
P13569
|CFTR_HUMAN Cystic fibrosis transmembrane conductance regulator (Gene Name=CFTR)
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