Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Ca(2+)-dependent and Ca(2+)-independent calmodulin binding sites in erythrocyte protein 4.1. Implications for regulation of protein 4.1 interactions with transmembrane proteins.
Calmodulin regulation of basal and agonist-stimulated G protein coupling by the mu-opioid receptor (OP(3)) in morphine-pretreated cell.
Structural basis for the activation of anthrax adenylyl cyclase exotoxin by calmodulin.
The Chediak-Higashi protein interacts with SNARE complex and signal transduction proteins.
Ca2+-binding protein-1 facilitates and forms a postsynaptic complex with Cav1.2 (L-type) Ca2+ channels.
Myristoyl moiety of HIV Nef is involved in regulation of the interaction with calmodulin in vivo.
CP110 cooperates with two calcium-binding proteins to regulate cytokinesis and genome stability.
Characterization of exosome-like vesicles released from human tracheobronchial ciliated epithelium: a possible role in innate defense.
Structural analysis of the complex between calmodulin and full-length myelin basic protein, an intrinsically disordered molecule.
Defective calmodulin binding to the cardiac ryanodine receptor plays a key role in CPVT-associated channel dysfunction.
Structure of the CaMKIIdelta/calmodulin complex reveals the molecular mechanism of CaMKII kinase activation.
Solution NMR structure of Apo-calmodulin in complex with the IQ motif of human cardiac sodium channel NaV1.5.
IQ-motif selectivity in human IQGAP2 and IQGAP3: binding of calmodulin and myosin essential light chain.
Proteomic characterization of the human sperm nucleus.
Quantitative proteomic analysis of human substantia nigra in Alzheimer's disease, Huntington's disease and Multiple sclerosis.
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
Distinctive malfunctions of calmodulin mutations associated with heart RyR2-mediated arrhythmic disease.
Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G.
Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current.
Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks.
Comparison of S100b protein with calmodulin: interactions with melittin and microtubule-associated tau proteins and inhibition of phosphorylation of tau proteins by protein kinase C.
A family of conserved bacterial virulence factors dampens interferon responses by blocking calcium signaling.
A calmodulin-binding sequence in the C-terminus of human cardiac titin kinase.
Blocking the Ca2+-induced conformational transitions in calmodulin with disulfide bonds.
CALM binds bacterial OspC3
OspC3 ADP-riboxanates CASP4
Calmodulin is an auxiliary subunit of KCNQ2/3 potassium channels.
Protein Kinase C and Calmodulin Serve As Calcium Sensors for Calcium-Stimulated Endocytosis at Synapses.
The expression characteristics of FAM71D and its association with sperm motility.
Calmodulin binds and modulates K(+)-dependent Na(+)/Ca(2+)-exchanger isoform 4, NCKX4.
Translocation of CaN:CaM:NFAT to nucleus
Translocation of NFATC1:CaN:CaM to nucleus
UniProtKB reviewed entry P0DP24 (CALM2_HUMAN)