Structure of PDB 4lgu Chain B Binding Site BS02
Receptor Information
>4lgu Chain B (length=94) Species:
9606
(Homo sapiens) [
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SSISNLSMQTHAARMRTFMYWPSSVPVQPEQLASAGFYYVGRNDDVKCFC
CDGGLRCWESGDDPWVEHAKWFPRCEFLIRMKGQEFVDEIQGRY
Ligand information
Ligand ID
1YH
InChI
InChI=1S/C29H43N5O4/c1-19(30-2)27(35)32-26(20-9-4-3-5-10-20)29(37)34-17-21-11-8-15-33(21)18-24(34)28(36)31-23-14-16-38-25-13-7-6-12-22(23)25/h6-7,12-13,19-21,23-24,26,30H,3-5,8-11,14-18H2,1-2H3,(H,31,36)(H,32,35)/t19-,21+,23+,24-,26-/m0/s1
InChIKey
GIAUJOMDUOPYLU-XFCBJTKFSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(NC(C(=O)N2CC1N(CCC1)CC2C(=O)NC3c4c(OCC3)cccc4)C5CCCCC5)C(NC)C
CACTVS 3.385
CN[CH](C)C(=O)N[CH](C1CCCCC1)C(=O)N2C[CH]3CCCN3C[CH]2C(=O)N[CH]4CCOc5ccccc45
OpenEye OEToolkits 1.7.6
CC(C(=O)NC(C1CCCCC1)C(=O)N2CC3CCCN3CC2C(=O)NC4CCOc5c4cccc5)NC
OpenEye OEToolkits 1.7.6
C[C@@H](C(=O)N[C@@H](C1CCCCC1)C(=O)N2C[C@H]3CCCN3C[C@H]2C(=O)N[C@@H]4CCOc5c4cccc5)NC
CACTVS 3.385
CN[C@@H](C)C(=O)N[C@@H](C1CCCCC1)C(=O)N2C[C@H]3CCCN3C[C@H]2C(=O)N[C@@H]4CCOc5ccccc45
Formula
C29 H43 N5 O4
Name
(3S,8aR)-N-((R)-chroman-4-yl)-2-((S)-2-cyclohexyl-2-((S)-2-(methylamino)propanamido)acetyl)octahydropyrrolo[1,2-a]pyrazine-3-carboxamide
ChEMBL
CHEMBL2365533
DrugBank
ZINC
ZINC000095594116
PDB chain
4lgu Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4lgu
Design, stereoselective synthesis, and biological evaluation of novel tri-cyclic compounds as inhibitor of apoptosis proteins (IAP) antagonists.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D297 G306 L307 R308 C309 W310 E311 D314 W323
Binding residue
(residue number reindexed from 1)
D45 G54 L55 R56 C57 W58 E59 D62 W71
Annotation score
1
Binding affinity
MOAD
: ic50=2.1nM
Enzymatic activity
Enzyme Commision number
2.3.2.27
: RING-type E3 ubiquitin transferase.
External links
PDB
RCSB:4lgu
,
PDBe:4lgu
,
PDBj:4lgu
PDBsum
4lgu
PubMed
23928071
UniProt
Q13490
|BIRC2_HUMAN Baculoviral IAP repeat-containing protein 2 (Gene Name=BIRC2)
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