Structure of PDB 7neu Chain A Binding Site BS02
Receptor Information
>7neu Chain A (length=398) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
QSGQVLAALPRTSRQVQVLQNLTTTYEIVLWQPVTADLIVKKKQVHFFVN
ASDVDNVKAHLNVSGIPCSVLLADVEDLIQQQISNDTVSPRASASYYEQY
HSLNEIYSWIEFITERHPDMLTKIHIGSSFEKYPLYVLKVSGQTAKNAIW
IDCGIHAREWISPAFCLWFIGHITQFYGIIGQYTNLLRLVDFYVMPVVNV
DGYDYSWKKNRMWRKNRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCS
ETYCGLYPESEPEVKAVASFLRRNINQIKAYISMHSYSQHIVFPYSYTRS
KCKDHEELSLVASEAVRAIEKISKNIRYTYGQGSETLYLAPGGGDDWIYD
LGIKYSFTIELRDTGTYGFLLPERYIKPTCREAFAAVSKIAWHVIRNV
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
7neu Chain A Residue 502 [
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
7neu
Phosphinanes and Azaphosphinanes as Potent and Selective Inhibitors of Activated Thrombin-Activatable Fibrinolysis Inhibitor (TAFIa).
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
H159 E162 H288
Binding residue
(residue number reindexed from 1)
H156 E159 H285
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H159 E162 R217 H288 E363
Catalytic site (residue number reindexed from 1)
H156 E159 R214 H285 E360
Enzyme Commision number
3.4.17.20
: carboxypeptidase U.
Gene Ontology
Molecular Function
GO:0004180
carboxypeptidase activity
GO:0004181
metallocarboxypeptidase activity
GO:0008237
metallopeptidase activity
GO:0008270
zinc ion binding
GO:0046872
metal ion binding
Biological Process
GO:0003331
positive regulation of extracellular matrix constituent secretion
GO:0006508
proteolysis
GO:0007596
blood coagulation
GO:0009410
response to xenobiotic stimulus
GO:0010757
negative regulation of plasminogen activation
GO:0030163
protein catabolic process
GO:0042730
fibrinolysis
GO:0051918
negative regulation of fibrinolysis
GO:0071333
cellular response to glucose stimulus
GO:0097421
liver regeneration
GO:2000346
negative regulation of hepatocyte proliferation
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0070062
extracellular exosome
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:7neu
,
PDBe:7neu
,
PDBj:7neu
PDBsum
7neu
PubMed
33764059
UniProt
Q96IY4
|CBPB2_HUMAN Carboxypeptidase B2 (Gene Name=CPB2)
[
Back to BioLiP
]