Structure of PDB 5fpv Chain D Binding Site BS02
Receptor Information
>5fpv Chain D (length=342) Species:
9606
(Homo sapiens) [
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LNPSARIMTFYPTMEEFRNFSRYIAYIESQGAHRAGLAKVVPPKEWKPRA
SYDDIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFRKIANSDKYC
TPRYSEFEELERKYWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTIL
DLVEKEGVNTPYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPP
EHGKRLERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKYGIPFDKVTQE
AGEFMITFPYGYHAGFNHGFNCAESTNFATRRWIEYGKQAVLCSCRKDMV
KISMDVFVRKFQPERYKLWKAGKDNTVIDHTLPTPEAAEFLK
Ligand information
Ligand ID
MMK
InChI
InChI=1S/C15H22N4O3/c1-4-19(8-7-18(2)3)14(20)11-16-10-13-9-12(15(21)22)5-6-17-13/h5-9,16H,4,10-11H2,1-3H3,(H,21,22)/b8-7+
InChIKey
RTKGUAPXWDCFNW-BQYQJAHWSA-N
SMILES
Software
SMILES
CACTVS 3.385
CCN(C=CN(C)C)C(=O)CNCc1cc(ccn1)C(O)=O
CACTVS 3.385
CCN(\C=C\N(C)C)C(=O)CNCc1cc(ccn1)C(O)=O
OpenEye OEToolkits 1.7.6
CCN(/C=C/N(C)C)C(=O)CNCc1cc(ccn1)C(=O)O
OpenEye OEToolkits 1.7.6
CCN(C=CN(C)C)C(=O)CNCc1cc(ccn1)C(=O)O
ACDLabs 12.01
O=C(O)c1ccnc(c1)CNCC(=O)N(\C=C\N(C)C)CC
Formula
C15 H22 N4 O3
Name
2-{[(2-{[(E)-2-(dimethylamino)ethenyl](ethyl)amino}-2-oxoethyl)amino]methyl}pyridine-4-carboxylic acid
ChEMBL
DrugBank
ZINC
ZINC000263620993
PDB chain
5fpv Chain D Residue 1358 [
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Receptor-Ligand Complex Structure
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PDB
5fpv
Structural Analysis of Human Kdm5B Guides Histone Demethylase Inhibitor Development.
Resolution
2.44 Å
Binding residue
(original residue number in PDB)
Y133 Y176 Y178 F186 H189 E191 K207 W209 K242 H277 S289
Binding residue
(residue number reindexed from 1)
Y125 Y162 Y164 F172 H175 E177 K193 W195 K228 H263 S275
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G171 Y178 H189 E191 H277 S289
Catalytic site (residue number reindexed from 1)
G157 Y164 H175 E177 H263 S275
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:5fpv
,
PDBe:5fpv
,
PDBj:5fpv
PDBsum
5fpv
PubMed
27214403
UniProt
O75164
|KDM4A_HUMAN Lysine-specific demethylase 4A (Gene Name=KDM4A)
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