Structure of PDB 3b7e Chain B Binding Site BS03
Receptor Information
>3b7e Chain B (length=385) Species:
11320
(Influenza A virus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
VILTGNSSLCPISGWAIYSKDNGIRIGSKGDVFVIREPFISCSHLECRTF
FLTQGALLNDKHSNGTVKDRSPYRTLMSCPVGEAPSPYNSRFESVAWSAS
ACHDGMGWLTIGISGPDNGAVAVLKYNGIITDTIKSWRNNILRTQESECA
CVNGSCFTIMTDGPSNGQASYKILKIEKGKVTKSIELNAPNYHYEECSCY
PDTGKVMCVCRDNWHGSNRPWVSFDQNLDYQIGYICSGVFGDNPRPNDGT
GSCGPVSSNGANGIKGFSFRYDNGVWIGRTKSTSSRSGFEMIWDPNGWTE
TDSSFSVRQDIVAITDWSGYSGSFVQHPELTGLDCMRPCFWVELIRGQPK
ENTIWTSGSSISFCGVNSDTVGWSWPDGAELPFSI
Ligand information
Ligand ID
ZMR
InChI
InChI=1S/C12H20N4O7/c1-4(18)15-8-5(16-12(13)14)2-7(11(21)22)23-10(8)9(20)6(19)3-17/h2,5-6,8-10,17,19-20H,3H2,1H3,(H,15,18)(H,21,22)(H4,13,14,16)/t5-,6+,8+,9+,10+/m0/s1
InChIKey
ARAIBEBZBOPLMB-UFGQHTETSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(=O)N[CH]1[CH](NC(N)=N)C=C(O[CH]1[CH](O)[CH](O)CO)C(O)=O
ACDLabs 12.01
C(=O)(O)C1=CC(C(NC(=O)C)C(O1)C(O)C(O)CO)N\C(=N)N
CACTVS 3.385
CC(=O)N[C@@H]1[C@@H](NC(N)=N)C=C(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O
OpenEye OEToolkits 2.0.7
CC(=O)NC1C(C=C(OC1C(C(CO)O)O)C(=O)O)NC(=N)N
OpenEye OEToolkits 2.0.7
[H]/N=C(\N)/N[C@H]1C=C(O[C@H]([C@@H]1NC(=O)C)[C@@H]([C@@H](CO)O)O)C(=O)O
Formula
C12 H20 N4 O7
Name
ZANAMIVIR;
4-GUANIDINO-2-DEOXY-2,3-DEHYDRO-N-ACETYL-NEURAMINIC ACID;
4-guanidino-Neu5Ac2en;
MODIFIED SIALIC ACID
ChEMBL
CHEMBL222813
DrugBank
DB00558
ZINC
ZINC000003918138
PDB chain
3b7e Chain B Residue 1002 [
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
3b7e
Structural characterization of the 1918 influenza virus H1N1 neuraminidase
Resolution
1.45 Å
Binding residue
(original residue number in PDB)
R118 E119 D151 R152 W178 E227 S246 E276 R292 R371 Y406
Binding residue
(residue number reindexed from 1)
R36 E37 D69 R70 W97 E146 S165 E195 R211 R286 Y320
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D151 E277 R292 R371 Y406
Catalytic site (residue number reindexed from 1)
D69 E196 R211 R286 Y320
Enzyme Commision number
3.2.1.18
: exo-alpha-sialidase.
Gene Ontology
Molecular Function
GO:0004308
exo-alpha-sialidase activity
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0046761
viral budding from plasma membrane
Cellular Component
GO:0016020
membrane
GO:0033644
host cell membrane
GO:0055036
virion membrane
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3b7e
,
PDBe:3b7e
,
PDBj:3b7e
PDBsum
3b7e
PubMed
18715929
UniProt
Q9IGQ6
|NRAM_I18A0 Neuraminidase (Gene Name=NA)
[
Back to BioLiP
]