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Receptor Information

>6txx Chain A (length=128) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]

GAPATVTEQGEDITSKKDRGVLKIVKRVGNGEETPMIGDKVYVHYKGKLS
NGKKFDSSHDRNEPFVFSLGKGQVIKAWDIGVATMKKGEICHLLCKPEYA
YGSAGSLPKIPSNATLFFEIELLDFKGE

Ligand ID

37K

InChI

InChI=1S/C46H60N2O10/c1-51-39-20-18-32(28-40(39)52-2)17-19-38(34-14-11-15-36(29-34)57-27-24-47-22-25-56-26-23-47)58-46(50)37-16-9-10-21-48(37)45(49)43(33-12-7-6-8-13-33)35-30-41(53-3)44(55-5)42(31-35)54-4/h7,11-12,14-15,18,20,28-31,33,37-38,43H,6,8-10,13,16-17,19,21-27H2,1-5H3/t33-,37+,38-,43+/m1/s1

InChIKey

LMMQNDBBWIKJQS-CNKHDIINSA-N

SMILES

Software	SMILES
CACTVS 3.385	COc1ccc(CC[CH](OC(=O)[CH]2CCCCN2C(=O)[CH]([CH]3CCCC=C3)c4cc(OC)c(OC)c(OC)c4)c5cccc(OCCN6CCOCC6)c5)cc1OC
ACDLabs 12.01	O=C(N1CCCCC1C(=O)OC(c3cc(OCCN2CCOCC2)ccc3)CCc4ccc(OC)c(OC)c4)C(c5cc(OC)c(OC)c(OC)c5)C6C=CCCC6
OpenEye OEToolkits 1.9.2	COc1ccc(cc1OC)CC[C@H](c2cccc(c2)OCCN3CCOCC3)OC(=O)[C@@H]4CCCCN4C(=O)[C@H](c5cc(c(c(c5)OC)OC)OC)[C@H]6CCCC=C6
CACTVS 3.385	COc1ccc(CC[C@@H](OC(=O)[C@@H]2CCCCN2C(=O)[C@@H]([C@H]3CCCC=C3)c4cc(OC)c(OC)c(OC)c4)c5cccc(OCCN6CCOCC6)c5)cc1OC
OpenEye OEToolkits 1.9.2	COc1ccc(cc1OC)CCC(c2cccc(c2)OCCN3CCOCC3)OC(=O)C4CCCCN4C(=O)C(c5cc(c(c(c5)OC)OC)OC)C6CCCC=C6

Formula

C46 H60 N2 O10

Name

(1R)-3-(3,4-dimethoxyphenyl)-1-{3-[2-(morpholin-4-yl)ethoxy]phenyl}propyl (2S)-1-[(2S)-2-[(1S)-cyclohex-2-en-1-yl]-2-(3,4,5-trimethoxyphenyl)acetyl]piperidine-2-carboxylate

PDB chain

6txx Chain A Residue 201 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]

Receptor-Ligand Complex Structure

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Structure summary

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PDB	6txx Hybrid Screening Approach for Very Small Fragments: X-ray and Computational Screening on FKBP51.
Resolution	2.1 Å
Binding residue (original residue number in PDB)	Y57 D68 F77 G84 Q85 V86 W90 Y113 S118 K121
Binding residue (residue number reindexed from 1)	Y45 D56 F65 G72 Q73 V74 W78 Y101 S106 K109
Annotation score	1

Catalytic site (original residue number in PDB)	Y57 F67 D68 I87 Y113 F130
Catalytic site (residue number reindexed from 1)	Y45 F55 D56 I75 Y101 F118
Enzyme Commision number	5.2.1.8: peptidylprolyl isomerase.

	Molecular Function
GO:0003755	peptidyl-prolyl cis-trans isomerase activity

PDB	RCSB:6txx, PDBe:6txx, PDBj:6txx
PDBsum	6txx
PubMed	32420743
UniProt	Q13451\|FKBP5_HUMAN Peptidyl-prolyl cis-trans isomerase FKBP5 (Gene Name=FKBP5)

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Structure of PDB 6txx Chain A Binding Site BS01