Structure of PDB 7ccr Chain L Binding Site BS02
Receptor Information
>7ccr Chain L (length=95) Species:
9606
(Homo sapiens) [
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RYRPGTVALREIRRYQKSTELLIRKLPFQRLVREIAQDFKTDLRFQSSAV
MALQEACEAYLVGLFEDTNLCAIHAKRVTIMPKDIQLARRIRGER
Ligand information
>7ccr Chain U (length=147) [
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ctggagaatcccggtgccgaggccgctcaattggtcgtagacagctctag
caccgcttaaacgcacgtacgcgctgtcccccgcgttttaaccgccaagg
ggattactccctagtctccaggcacgtgtcagatatatacatcctgt
Receptor-Ligand Complex Structure
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PDB
7ccr
Structural basis for nucleosome-mediated inhibition of cGAS activity.
Resolution
4.9 Å
Binding residue
(original residue number in PDB)
R40 Y41 P43 G44 V46 R49 R63 K64 L65 P66 R83
Binding residue
(residue number reindexed from 1)
R1 Y2 P4 G5 V7 R10 R24 K25 L26 P27 R44
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003677
DNA binding
GO:0030527
structural constituent of chromatin
GO:0046982
protein heterodimerization activity
Cellular Component
GO:0000786
nucleosome
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Molecular Function
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Cellular Component
External links
PDB
RCSB:7ccr
,
PDBe:7ccr
,
PDBj:7ccr
PDBsum
7ccr
PubMed
33051594
UniProt
P68431
|H31_HUMAN Histone H3.1 (Gene Name=H3C1)
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