Structure of PDB 3c9e Chain A Binding Site BS04
Receptor Information
>3c9e Chain A (length=215) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
APDSVDYRKKGYVTPVKNQGQCGSCWAFSSVGALEGQLKKKTGKLLNLSP
QNLVDCVSENDGCGGGYMTNAFQYVQKNRGIDSEDAYPYVGQEESCMYNP
TGKAAKCRGYREIPEGNEKALKRAVARVGPVSVAIDASLTSFQFYSKGVY
YDESCNSDNLNHAVLAVGYGIQKGNKHWIIKNSWGENWGNKGYILMARNK
NNACGIANLASFPKM
Ligand information
Ligand ID
ASG
InChI
InChI=1S/C8H15NO9S/c1-3(11)9-5-6(12)7(18-19(14,15)16)4(2-10)17-8(5)13/h4-8,10,12-13H,2H2,1H3,(H,9,11)(H,14,15,16)/t4-,5-,6-,7+,8-/m1/s1
InChIKey
WHCJUIFHMJFEFZ-UIAUGNHASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)N[C@@H]1[C@H]([C@H]([C@H](O[C@H]1O)CO)OS(=O)(=O)O)O
ACDLabs 10.04
O=S(=O)(O)OC1C(OC(O)C(NC(=O)C)C1O)CO
CACTVS 3.341
CC(=O)N[CH]1[CH](O)O[CH](CO)[CH](O[S](O)(=O)=O)[CH]1O
CACTVS 3.341
CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@H](O[S](O)(=O)=O)[C@@H]1O
OpenEye OEToolkits 1.5.0
CC(=O)NC1C(C(C(OC1O)CO)OS(=O)(=O)O)O
Formula
C8 H15 N O9 S
Name
2-acetamido-2-deoxy-4-O-sulfo-beta-D-galactopyranose;
2-DEOXY-2-ACETAMIDO-BETA-D-GALACTOSE-4-SULFATE;
N-acetyl-4-O-sulfo-beta-D-galactosamine;
2-acetamido-2-deoxy-4-O-sulfo-beta-D-galactose;
2-acetamido-2-deoxy-4-O-sulfo-D-galactose;
2-acetamido-2-deoxy-4-O-sulfo-galactose
ChEMBL
DrugBank
DB01872
ZINC
ZINC000013513371
PDB chain
3c9e Chain B Residue 4 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
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)
G170 I171
Binding residue
(residue number reindexed from 1)
G170 I171
Annotation score
1
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3c9e
,
PDBe:3c9e
,
PDBj:3c9e
PDBsum
3c9e
PubMed
18692071
UniProt
P43235
|CATK_HUMAN Cathepsin K (Gene Name=CTSK)
[
Back to BioLiP
]