Structure of PDB 5lxd Chain A Binding Site BS01
Receptor Information
>5lxd Chain A (length=386) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
PMTPEQAMKQYMQKLTAFEHHEIFSYPEIYFLGLNAKKRQGMTGGPNNGG
YDDDQGSYVQVPHDHVAYRYEVLKVIGKGSFGQVVKAYDHKVHQHVALKM
VRNEKRFHRQAAEEIRILEHLRKQDKDNTMNVIHMLENFTFRNHICMTFE
LLSMNLYELIKKNKFQGFSLPLVRKFAHSILQCLDALHKNRIIHCDLKPE
NILLKQQGRSGIKVIDFGSSCYEHQRVYTYIQSRFYRAPEVILGARYGMP
IDMWSLGCILAELLTGYPLLPGEDEGDQLACMIELLGMPSQKLLDASKRA
KNFVSSKGYPRYCTVTTLSDGSVVLNGGRSRRGKLRGPPESREWGNALKG
CDDPLFLDFLKQCLEWDPAVRMTPGQALRHPWLRRR
Ligand information
Ligand ID
7A7
InChI
InChI=1S/C18H14FN5O2S/c1-25-9-3-4-11(10(19)7-9)23-17-14-12(21-8-22-17)5-6-13-15(14)27-18(24-13)16(20)26-2/h3-8,20H,1-2H3,(H,21,22,23)/b20-16+
InChIKey
RYBNARZBIXTFJS-CAPFRKAQSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.5
COc1ccc(c(c1)F)Nc2c3c(ccc4c3sc(n4)C(=N)OC)ncn2
CACTVS 3.385
COC(=N)c1sc2c(ccc3ncnc(Nc4ccc(OC)cc4F)c23)n1
OpenEye OEToolkits 2.0.5
[H]/N=C(\c1nc2ccc3c(c2s1)c(ncn3)Nc4ccc(cc4F)OC)/OC
Formula
C18 H14 F N5 O2 S
Name
methyl 9-[(2-fluoranyl-4-methoxy-phenyl)amino]-[1,3]thiazolo[5,4-f]quinazoline-2-carboximidate
ChEMBL
DrugBank
ZINC
PDB chain
5lxd Chain A Residue 501 [
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
5lxd
An Unusual Binding Model of the Methyl 9-Anilinothiazolo[5,4-f] quinazoline-2-carbimidates (EHT 1610 and EHT 5372) Confers High Selectivity for Dual-Specificity Tyrosine Phosphorylation-Regulated Kinases.
Resolution
2.58 Å
Binding residue
(original residue number in PDB)
G156 V163 F228 L231 L282 I294 D295
Binding residue
(residue number reindexed from 1)
G77 V84 F149 L152 L203 I215 D216
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=8.50,IC50=3.16nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D275 K277 N280 D295 S312
Catalytic site (residue number reindexed from 1)
D196 K198 N201 D216 S233
Enzyme Commision number
2.7.12.1
: dual-specificity kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004712
protein serine/threonine/tyrosine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5lxd
,
PDBe:5lxd
,
PDBj:5lxd
PDBsum
5lxd
PubMed
27766861
UniProt
Q92630
|DYRK2_HUMAN Dual specificity tyrosine-phosphorylation-regulated kinase 2 (Gene Name=DYRK2)
[
Back to BioLiP
]