Structure of PDB 5hzn Chain H Binding Site BS01
Receptor Information
>5hzn Chain H (length=303) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
AADVYVPDEWEVAREKITMSRELGQGSFGMVYEGVAKGVVKDEPETRVAI
KTVNEAASMRERIEFLNEASVMKEFNCHHVVRLLGVVSQGQPTLVIMELM
TRGDLKSYLRSLRPAMANNPVLAPPSLSKMIQMAGEIADGMAYLNANKFV
HRDLAARNCMVAEDFTVKIGDFGMTRDIYETDYYRKGGKGLLPVRWMSPE
SLKDGVFTTYSDVWSFGVVLWEIATLAEQPYQGLSNEQVLRFVMEGGLLD
KPDNCPDMLFELMRMCWQYNPKMRPSFLEIISSIKEEMEPGFREVSFYYS
EEN
Ligand information
Ligand ID
66A
InChI
InChI=1S/C27H29N5O/c28-26-25-24(21-8-4-9-23(14-21)33-17-19-6-2-1-3-7-19)16-32(27(25)30-18-29-26)22-12-20(13-22)15-31-10-5-11-31/h1-4,6-9,14,16,18,20,22H,5,10-13,15,17H2,(H2,28,29,30)/t20-,22+
InChIKey
AECDBHGVIIRMOI-GRGXKFILSA-N
SMILES
Software
SMILES
CACTVS 3.385
Nc1ncnc2n(cc(c3cccc(OCc4ccccc4)c3)c12)[CH]5C[CH](C5)CN6CCC6
CACTVS 3.385
Nc1ncnc2n(cc(c3cccc(OCc4ccccc4)c3)c12)[C@@H]5C[C@@H](C5)CN6CCC6
ACDLabs 12.01
c2(cc(OCc1ccccc1)ccc2)c6c3c(N)ncnc3n(C5CC(CN4CCC4)C5)c6
OpenEye OEToolkits 2.0.4
c1ccc(cc1)COc2cccc(c2)c3cn(c4c3c(ncn4)N)C5CC(C5)CN6CCC6
Formula
C27 H29 N5 O
Name
7-[cis-3-(azetidin-1-ylmethyl)cyclobutyl]-5-[3-(benzyloxy)phenyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
ChEMBL
CHEMBL1614712
DrugBank
ZINC
ZINC000100073728
PDB chain
5hzn Chain H Residue 1301 [
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
5hzn
Identification of a 5-[3-phenyl-(2-cyclic-ether)-methylether]-4-aminopyrrolo[2,3-d]pyrimidine series of IGF-1R inhibitors.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
L1002 G1003 Q1004 V1010 A1028 K1030 F1044 E1047 A1048 V1060 M1076 M1079 D1083 M1139 G1149 D1150
Binding residue
(residue number reindexed from 1)
L23 G24 Q25 V31 A49 K51 F65 E68 A69 V81 M97 M100 D104 M160 G170 D171
Annotation score
1
Binding affinity
MOAD
: ic50=0.061uM
BindingDB: IC50=61nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D1132 R1136 N1137 D1150 E1159
Catalytic site (residue number reindexed from 1)
D153 R157 N158 D171 E180
Enzyme Commision number
2.7.10.1
: receptor protein-tyrosine kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004713
protein tyrosine kinase activity
GO:0004714
transmembrane receptor protein tyrosine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
GO:0007169
cell surface receptor protein tyrosine kinase signaling pathway
Cellular Component
GO:0016020
membrane
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5hzn
,
PDBe:5hzn
,
PDBj:5hzn
PDBsum
5hzn
PubMed
26951750
UniProt
P08069
|IGF1R_HUMAN Insulin-like growth factor 1 receptor (Gene Name=IGF1R)
[
Back to BioLiP
]