Structure of PDB 5wi6 Chain B Binding Site BS01
Receptor Information
>5wi6 Chain B (length=244) Species:
9606
(Homo sapiens) [
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IVGGQEAPRSKWPWQVSLRVHGPYWMHFCGGSLIHPQWVLTAAHCVGPDV
KDLAALRVQLREQHLYYQDQLLPVSRIIVHPQFYTAQCGADIALLELEEP
VNVSSHVHTVTLPPASETFPPGMPCWVTGWGDVDNDERLPPPFPLKQVKV
PIMENHICDAKYHLGAYTGDDVRIVRDDMLCAGNTRRDSCQGDSGGPLVC
KVNGTWLQAGVVSWGEGCAQPNRPGIYTRVTYYLDWIHHYVPKK
Ligand information
Ligand ID
0GJ
InChI
InChI=1S/C14H27ClN6O5/c15-6-10(22)9(2-1-5-19-14(17)18)21-11(23)7-20-13(26)8(16)3-4-12(24)25/h8-10,22H,1-7,16H2,(H,20,26)(H,21,23)(H,24,25)(H4,17,18,19)/p+1/t8-,9-,10+/m0/s1
InChIKey
XELWNHKFCNMWQO-LPEHRKFASA-O
SMILES
Software
SMILES
CACTVS 3.370
N[CH](CCC(O)=O)C(=O)NCC(=O)N[CH](CCCNC(N)=[NH2+])[CH](O)CCl
CACTVS 3.370
N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H](CCCNC(N)=[NH2+])[C@H](O)CCl
ACDLabs 12.01
O=C(NC(CCCNC(=[NH2+])\N)C(O)CCl)CNC(=O)C(N)CCC(=O)O
OpenEye OEToolkits 1.7.0
C(CC(C(CCl)O)NC(=O)CNC(=O)C(CCC(=O)O)N)CNC(=[NH2+])N
OpenEye OEToolkits 1.7.0
C(C[C@@H]([C@@H](CCl)O)NC(=O)CNC(=O)[C@H](CCC(=O)O)N)CNC(=[NH2+])N
Formula
C14 H28 Cl N6 O5
Name
L-alpha-glutamyl-N-{(1S)-4-{[amino(iminio)methyl]amino}-1-[(1S)-2-chloro-1-hydroxyethyl]butyl}glycinamide
ChEMBL
DrugBank
ZINC
PDB chain
5wi6 Chain B Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5wi6
Dual functionality of beta-tryptase protomers as both proteases and cofactors in the active tetramer.
Resolution
2.72 Å
Binding residue
(original residue number in PDB)
H57 D189 S190 Q192 S195 S214 W215 G216
Binding residue
(residue number reindexed from 1)
H44 D188 S189 Q191 S194 S213 W214 G215
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D102 Q192 G193 D194 S195
Catalytic site (residue number reindexed from 1)
H44 D91 Q191 G192 D193 S194
Enzyme Commision number
3.4.21.59
: tryptase.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0005515
protein binding
GO:0008236
serine-type peptidase activity
GO:0042802
identical protein binding
Biological Process
GO:0006508
proteolysis
GO:0006952
defense response
GO:0022617
extracellular matrix disassembly
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0062023
collagen-containing extracellular matrix
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5wi6
,
PDBe:5wi6
,
PDBj:5wi6
PDBsum
5wi6
PubMed
29661938
UniProt
Q15661
|TRYB1_HUMAN Tryptase alpha/beta-1 (Gene Name=TPSAB1)
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