Structure of PDB 5xtq Chain B Binding Site BS01
Receptor Information
>5xtq Chain B (length=254) Species:
46015
(Autographa californica nucleopolyhedrovirus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
RGSMIPLTPLFSRYKDSYLLYSFRLIDLLRASKSTHLTKLLSSQATYLYH
FACLKDIQKYEVQQLIEWAINASPDMDLQQFRIEFMDKTTELNLRSCQPK
SFTYTFTTIWDTMHFLSLIIDDMVYTRDKSSLDFVMQQLKTMKVLFYNVF
FILQCAMCRDHYMNVKGFIIYHIELIEIALDKEKYGTDITFVDSYQQETA
GADVSNNMLMKNLMAYVSMTFHNDINDYKWIQRNKKPPAYERMTWGEYKK
LLNL
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
5xtq Chain B Residue 301 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
5xtq
Three Conserved Regions in Baculovirus Sulfhydryl Oxidase P33 Are Critical for Enzymatic Activity and Function
Resolution
2.04 Å
Binding residue
(original residue number in PDB)
R10 F106 I109 W110 H114 F150 M157 C158 M222 H225 N226 I228 N229 K232 Q235 M247
Binding residue
(residue number reindexed from 1)
R13 F106 I109 W110 H114 F150 M157 C158 M219 H222 N223 I225 N226 K229 Q232 M243
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.8.3.2
: thiol oxidase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0016972
thiol oxidase activity
Cellular Component
GO:0030430
host cell cytoplasm
GO:0042025
host cell nucleus
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:5xtq
,
PDBe:5xtq
,
PDBj:5xtq
PDBsum
5xtq
PubMed
28904203
UniProt
P41480
|FLSO_NPVAC FAD-linked sulfhydryl oxidase (Gene Name=P33)
[
Back to BioLiP
]