Structure of PDB 2ybs Chain B Binding Site BS03
Receptor Information
>2ybs Chain B (length=349) Species:
9606
(Homo sapiens) [
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TLNPSARIMTFYPTMEEFRNFSRYIAYIESQGAHRAGLAKVVPPKEWKPR
ASYDDIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFRKIANSDKY
CTPRYSEFEELERKYWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTI
LDLVEKESGITIEGVNTPYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPK
SWYSVPPEHGKRLERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKYGIP
FDKVTQEAGEFMITFPYGYHAGFNHGFNCAESTNFATRRWIEYGKQAVLC
SCRKDMVKISMDVFVRKFQPERYKLWKAGKDNTVIDHTLPTPEAAEFLK
Ligand information
Ligand ID
S2G
InChI
InChI=1S/C5H8O5/c6-3(5(9)10)1-2-4(7)8/h3,6H,1-2H2,(H,7,8)(H,9,10)/t3-/m0/s1
InChIKey
HWXBTNAVRSUOJR-VKHMYHEASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(CC(=O)O)[C@@H](C(=O)O)O
CACTVS 3.370
O[CH](CCC(O)=O)C(O)=O
CACTVS 3.370
O[C@@H](CCC(O)=O)C(O)=O
ACDLabs 12.01
O=C(O)C(O)CCC(=O)O
OpenEye OEToolkits 1.7.0
C(CC(=O)O)C(C(=O)O)O
Formula
C5 H8 O5
Name
(2S)-2-HYDROXYPENTANEDIOIC ACID
ChEMBL
CHEMBL1615211
DrugBank
ZINC
ZINC000000402967
PDB chain
2ybs Chain B Residue 1358 [
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Receptor-Ligand Complex Structure
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PDB
2ybs
The oncometabolite 2-hydroxyglutarate inhibits histone lysine demethylases.
Resolution
2.32 Å
Binding residue
(original residue number in PDB)
Y132 Y177 F185 H188 S196 N198 K206 W208
Binding residue
(residue number reindexed from 1)
Y126 Y171 F179 H182 S190 N192 K200 W202
Annotation score
2
Binding affinity
BindingDB: IC50=26000nM
Enzymatic activity
Catalytic site (original residue number in PDB)
G170 Y177 H188 E190 H276 S288
Catalytic site (residue number reindexed from 1)
G164 Y171 H182 E184 H270 S282
Enzyme Commision number
1.14.11.66
: [histone H3]-trimethyl-L-lysine(9) demethylase.
1.14.11.69
: [histone H3]-trimethyl-L-lysine(36) demethylase.
External links
PDB
RCSB:2ybs
,
PDBe:2ybs
,
PDBj:2ybs
PDBsum
2ybs
PubMed
21460794
UniProt
O75164
|KDM4A_HUMAN Lysine-specific demethylase 4A (Gene Name=KDM4A)
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