Structure of PDB 5a1f Chain A Binding Site BS01
Receptor Information
>5a1f Chain A (length=450) Species:
9606
(Homo sapiens) [
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SMFLPPPECPVFEPSWEEFADPFAFIHKIRPIAEQTGICKVRPPPDWQPP
FACDVDKLHFTPRIQRLNELEAQTRVRDYTLRTFGEMADAFKSDYFNMPV
HMVPTELVEKEFWRLVSTIEEDVTVEYGADIASKEFGSGFPVRDSPEEEE
YLDSGWNLNNMPVMEQSVLAHITADICGMKLPWLYVGMCFSSFCWHIEDH
WSYSINYLHWGEPKTWYGVPGYAAEQLENVMKKLAPELFVSQPDLLHQLV
TIMNPNTLMTHEVPVYRTNQCAGEFVITFPRAYHSGFNQGFNFAEAVNFC
TVDWLPLGRQCVEHYRLLHRYCVFSHDEMICKMASKADVLDVVVASTVQK
DMAIMIEDEKALRETVRKLGVIDSERMDFELLPDDERQCVKCKTTCFMSA
ISCSCKPGLLVCLHHVKELCSCPPYKYKLRYRYTLDDLYPMMNALKLRAE
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
5a1f Chain A Residue 1754 [
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Receptor-Ligand Complex Structure
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PDB
5a1f
Structural Analysis of Human Kdm5B Guides Histone Demethylase Inhibitor Development.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
C692 C695 C715 H718
Binding residue
(residue number reindexed from 1)
C389 C392 C412 H415
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G481 Y488 H499 E501 H587 A599
Catalytic site (residue number reindexed from 1)
G178 Y185 H196 E198 H284 A296
Enzyme Commision number
1.14.11.67
: [histone H3]-trimethyl-L-lysine(4) demethylase.
External links
PDB
RCSB:5a1f
,
PDBe:5a1f
,
PDBj:5a1f
PDBsum
5a1f
PubMed
27214403
UniProt
Q9UGL1
|KDM5B_HUMAN Lysine-specific demethylase 5B (Gene Name=KDM5B)
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