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Phenotype ontology term - FYPO:0003591 - abnormal protein complex binding

Term summary

ID
FYPO:0003591
Name
abnormal protein complex binding
Ontology or CV name
Phenotype
Definition
A molecular function phenotype in which the binding of one protein to a protein complex is abnormal. The protein whose binding to the protein complex is affected may be encoded by the mutated gene, or may be encoded by a different gene.

Parents

Annotation

Multi-locus phenotype

FYPO:0007597 - abolished CLRC complex binding

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Single locus phenotype

FYPO:0003591 - abnormal protein complex binding

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FYPO:0006025 - abolished actin filament binding

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FYPO:0005861 - abolished CCR4-NOT complex binding

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FYPO:0007597 - abolished CLRC complex binding

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FYPO:0007884 - abolished Lsm2-8 complex binding

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FYPO:0005234 - abolished MCM complex binding

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FYPO:0005862 - abolished MTREC complex binding

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FYPO:0006799 - abolished nuclear MIS12/MIND complex binding

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FYPO:0004226 - abolished nucleosome binding

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FYPO:0003297 - abolished ribosome binding

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FYPO:0003633 - abolished U1 snRNP binding

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FYPO:0003635 - abolished U2 snRNP binding

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FYPO:0002656 - decreased actin filament binding

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FYPO:0010031 - decreased CCR4-NOT complex binding

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FYPO:0007885 - decreased Lsm2-8 complex binding

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FYPO:0007173 - decreased mitotic checkpoint complex binding

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FYPO:0004227 - decreased nucleosome binding

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FYPO:0005142 - decreased proteasome core complex binding

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FYPO:0003634 - decreased U1 snRNP binding

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FYPO:0003636 - decreased U2 snRNP binding

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FYPO:0003592 - increased anaphase-promoting complex binding

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