Structure of PDB 3c9e Chain A Binding Site BS07
Receptor Information
>3c9e Chain A (length=215) Species:
9606
(Homo sapiens) [
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APDSVDYRKKGYVTPVKNQGQCGSCWAFSSVGALEGQLKKKTGKLLNLSP
QNLVDCVSENDGCGGGYMTNAFQYVQKNRGIDSEDAYPYVGQEESCMYNP
TGKAAKCRGYREIPEGNEKALKRAVARVGPVSVAIDASLTSFQFYSKGVY
YDESCNSDNLNHAVLAVGYGIQKGNKHWIIKNSWGENWGNKGYILMARNK
NNACGIANLASFPKM
Ligand information
Ligand ID
E64
InChI
InChI=1S/C15H29N5O5/c1-9(2)7-10(20-14(25)11(21)8-12(22)23)13(24)18-5-3-4-6-19-15(16)17/h9-11,21H,3-8H2,1-2H3,(H,18,24)(H,20,25)(H,22,23)(H4,16,17,19)/p+1/t10-,11-/m0/s1
InChIKey
QPQNJAXBPHVASB-QWRGUYRKSA-O
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)C[C@@H](C(=O)NCCCCNC(=[NH2+])N)NC(=O)[C@H](CC(=O)O)O
OpenEye OEToolkits 1.5.0
CC(C)CC(C(=O)NCCCCNC(=[NH2+])N)NC(=O)C(CC(=O)O)O
CACTVS 3.341
CC(C)C[C@H](NC(=O)[C@@H](O)CC(O)=O)C(=O)NCCCCNC(N)=[NH2+]
CACTVS 3.341
CC(C)C[CH](NC(=O)[CH](O)CC(O)=O)C(=O)NCCCCNC(N)=[NH2+]
ACDLabs 10.04
O=C(O)CC(O)C(=O)NC(C(=O)NCCCCNC(=[NH2+])\N)CC(C)C
Formula
C15 H30 N5 O5
Name
N-[N-[1-HYDROXYCARBOXYETHYL-CARBONYL]LEUCYLAMINO-BUTYL]-GUANIDINE
ChEMBL
DrugBank
DB04276
ZINC
PDB chain
3c9e Chain A Residue 308 [
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Receptor-Ligand Complex Structure
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PDB
3c9e
The crystal and molecular structures of a cathepsin K:chondroitin sulfate complex.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
Q19 G23 C25 E59 N60 G65 G66 Y67 L160 H162
Binding residue
(residue number reindexed from 1)
Q19 G23 C25 E59 N60 G65 G66 Y67 L160 H162
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=8.00,Kd=10nM
Enzymatic activity
Catalytic site (original residue number in PDB)
Q19 C25 H162 N182
Catalytic site (residue number reindexed from 1)
Q19 C25 H162 N182
Enzyme Commision number
3.4.22.38
: cathepsin K.
Gene Ontology
Molecular Function
GO:0008234
cysteine-type peptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:3c9e
,
PDBe:3c9e
,
PDBj:3c9e
PDBsum
3c9e
PubMed
18692071
UniProt
P43235
|CATK_HUMAN Cathepsin K (Gene Name=CTSK)
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