Structure of PDB 5w1l Chain A Binding Site BS01
Receptor Information
>5w1l Chain A (length=584) Species:
6210
(Echinococcus granulosus) [
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SAEQVEKLRNKINNAAVLVFAKSFCPYCKKVMERFNNLKIPFGYLDLDLK
KNGSDYQKMLQEITGRTTVPQVFFRGEFIGGCDDVMAIDDDTIVKKANEM
KYDYDMVIIGGGSGGLALAKESAKSGAKVALLDFVVPTPMGTTWGLGGTC
VNVGCIPKKLMHQAALLNHYMEDAKSFGWDVDKGPHDWVKMVEGIQDHIH
ALNFGYRSSMMNANVKYLNALGEIVDPHTIKTTNKQGIVKNITTNTIIVA
TGERPRYPPIPGAKEYGITSDDLFTLDHNPGKTLCVGASYVSLECAGFLS
SIGCDVTVMVRSIFLRGFDQQMAGLISDYIAKYGVKFVRPCVPTSVRCLE
EYDPESGKLAIYEVEGKHEDGTPFKDTFNTVLFAVGRDPCTTNIGLQNVD
VKTTNGRVVVDDEERTNVPNIYAIGDVSNAGYQLTPLAIQAGKNLARRLY
TADDCRTDYTNVPTTVFTPLEYGCIGLSEENAISKFGEDNIEVFHSYFQP
LEWTVPHRPDNTCYAKLIINKQDDNRVVGFHVFGPNAGEVTQGYAVAMHL
GARKEDFDRTIGIHPTCSETFTTLRVTKSSGASA
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
5w1l Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
5w1l
The Enzymatic and Structural Basis for Inhibition of Echinococcus granulosus Thioredoxin Glutathione Reductase by Gold(I).
Resolution
2.88 Å
Binding residue
(original residue number in PDB)
I115 G116 G118 D139 F140 G154 T155 G160 C161 K164 L227 G228 T257 G258 Y296 V297 R393 G431 D432 Q439 L440 T441
Binding residue
(residue number reindexed from 1)
I109 G110 G112 D133 F134 G148 T149 G154 C155 K158 L221 G222 T251 G252 Y290 V291 R387 G425 D426 Q433 L434 T435
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
L152 C156 C161 K164 Y296 E300 G568 H570 E575
Catalytic site (residue number reindexed from 1)
L146 C150 C155 K158 Y290 E294 G562 H564 E569
Enzyme Commision number
1.8.1.9
: thioredoxin-disulfide reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004362
glutathione-disulfide reductase (NADPH) activity
GO:0004791
thioredoxin-disulfide reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016668
oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0006749
glutathione metabolic process
GO:0034599
cellular response to oxidative stress
GO:0045454
cell redox homeostasis
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005739
mitochondrion
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5w1l
,
PDBe:5w1l
,
PDBj:5w1l
PDBsum
5w1l
PubMed
28463568
UniProt
Q869D7
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