Structure of PDB 5wve Chain M Binding Site BS02
Receptor Information
>5wve Chain M (length=1144) Species:
9606
(Homo sapiens) [
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GITSYVRTVLCEGGVPQRPVVFVTRKKLVNAIQQKLSKLKGEPGWVTIHG
MAGCGKSVLAAEAVRDHSLLEGCFPGGVHWVSVGKQDKSGLLMKLQNLCT
RLDQDESFSQRLPLNIEEAKDRLRILMLRKHPRSLLILDDVWDSWVLKAF
DSQCQILLTTRDKSVTDSVMGPKYVVPVESSLGKEKGLEILSLFVNMKKA
DLPEQAHSIIKECKGSPLVVSLIGALLRDFPNRWEYYLKQLQNKQFKRIR
KSSSYDYEALDEAMSISVEMLREDIKDYYTDLSILQKDVKVPTKVLCILW
DMETEEVEDILQEFVNKSLLFCDRNGKSFRYYLHDLQVDFLTEKNCSQLQ
DLHKKIITQFQRYHQPHTLSPDQEDCMYWYNFLAYHMASAKMHKELCALM
FSLDWIKAKTELVGPAHLIHEFVEYRHILDEKDCAVSENFQEFLSLNGHL
LGRQPFPNIVQLGLCEPETSEVYQQAKLQAKQEVDNGMLYLEWINKKNIT
NLSRLVVRPHTDAVYHACFSEDGQRIASCGADKTLQVFKAETGEKLLEIK
AHEDEVLCCAFSTDDRFIATCSVDKKVKIWNSMTGELVHTYDEHSEQVNC
CHFTNSSHHLLLATGSSDCFLKLWDLNQKECRNTMFGHTNSVNHCRFSPD
DKLLASCSADGTLKLWDATSANERKSINVKQFFLNLEDPQEDMEVIVKCC
SWSADGARIMVAAKNKIFLFDIHTSGLLGEIHTGHHSTIQYCDFSPQNHL
AVVALSQYCVELWNTDSRSKVADCRGHLSWVHGVMFSPDGSSFLTSSDDQ
TIRLWETKKVCKNSAVMLKQEVDVVFQENEVMVLAVDHIRRLQLINGRTG
QIDYLTEAQVSCCCLSPHLQYIAFGDENGAIEILELVNNRIFQSRFQHKK
TVWHIQFTADEKTLISSSDDAEIQVWNWQLDKCIFLRGHQETVKDFRLLK
NSRLLSWSFDGTVKVWNIITGNKEKDFVCHQGTVLSCDISHDATKFSSTS
ADKTAKIWSFDLLLPLHELRGHNGCVRCSAFSVDSTLLATGDDNGEIRIW
NVSNGELLHLCAPLSEEGAATHGGWVTDLCFSPDGKMLISAGGYIKWWNV
VTGESSQTFYTNGTNLKKIHVSPDFKTYVTVDNLGILYILQTLE
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
5wve Chain M Residue 1302 [
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Receptor-Ligand Complex Structure
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PDB
5wve
Mechanistic insights into caspase-9 activation by the structure of the apoptosome holoenzyme
Resolution
4.4 Å
Binding residue
(original residue number in PDB)
S161 D243
Binding residue
(residue number reindexed from 1)
S57 D139
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0008656
cysteine-type endopeptidase activator activity involved in apoptotic process
GO:0031072
heat shock protein binding
GO:0042802
identical protein binding
GO:0043531
ADP binding
Biological Process
GO:0001666
response to hypoxia
GO:0001822
kidney development
GO:0001843
neural tube closure
GO:0006915
apoptotic process
GO:0006919
activation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0007399
nervous system development
GO:0007420
brain development
GO:0007584
response to nutrient
GO:0008635
activation of cysteine-type endopeptidase activity involved in apoptotic process by cytochrome c
GO:0010659
cardiac muscle cell apoptotic process
GO:0030154
cell differentiation
GO:0030900
forebrain development
GO:0042981
regulation of apoptotic process
GO:0043065
positive regulation of apoptotic process
GO:0051402
neuron apoptotic process
GO:0070059
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress
GO:0071560
cellular response to transforming growth factor beta stimulus
GO:0072432
response to G1 DNA damage checkpoint signaling
GO:0097190
apoptotic signaling pathway
GO:0097193
intrinsic apoptotic signaling pathway
GO:1902510
regulation of apoptotic DNA fragmentation
GO:2001235
positive regulation of apoptotic signaling pathway
Cellular Component
GO:0005576
extracellular region
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0032991
protein-containing complex
GO:0034774
secretory granule lumen
GO:0043293
apoptosome
GO:0070062
extracellular exosome
GO:1904813
ficolin-1-rich granule lumen
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5wve
,
PDBe:5wve
,
PDBj:5wve
PDBsum
5wve
PubMed
28143931
UniProt
O14727
|APAF_HUMAN Apoptotic protease-activating factor 1 (Gene Name=APAF1)
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