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MYO5A and MLPH
Number of citations of the paper that reports this interaction (PubMedID
12006666
)
44
Data Source:
HPRD
(in vitro, in vivo)
MYO5A
MLPH
Description
myosin VA
melanophilin
Image
No pdb structure
GO Annotations
Cellular Component
Ruffle
Cytoplasm
Lysosome
Early Endosome
Late Endosome
Peroxisome
Endoplasmic Reticulum
Cytosol
Actin Filament
Actin Cytoskeleton
Membrane
Myosin Complex
Growth Cone
Cytoplasmic Vesicle
Vesicle
Filopodium Tip
Insulin-responsive Compartment
Melanosome
Neuron Projection
Recycling Endosome
Extracellular Exosome
Cytoplasm
Cytosol
Dendrite
Cortical Actin Cytoskeleton
Perinuclear Region Of Cytoplasm
Extracellular Exosome
Molecular Function
Microfilament Motor Activity
Nucleotide Binding
RNA Binding
Cytoskeletal Motor Activity
Actin Binding
Catalytic Activity
Protein Binding
Calmodulin Binding
ATP Binding
ATP Hydrolysis Activity
Small GTPase Binding
Actin Filament Binding
Actin Binding
Protein Binding
Zinc Ion Binding
Myosin Binding
Protein-macromolecule Adaptor Activity
Small GTPase Binding
Metal Ion Binding
Biological Process
Post-Golgi Vesicle-mediated Transport
Endocytosis
Actin Filament Organization
Protein Transport
Vesicle-mediated Transport
Actin Filament-based Movement
Vesicle Transport Along Actin Filament
Melanosome Transport
Cellular Response To Insulin Stimulus
Protein Localization To Plasma Membrane
Regulation Of Golgi Organization
Intracellular Protein Transport
Melanosome Transport
Pathways
Translocation of SLC2A4 (GLUT4) to the plasma membrane
Regulation of actin dynamics for phagocytic cup formation
Insulin processing
FCGR3A-mediated phagocytosis
Regulation of MITF-M-dependent genes involved in pigmentation
Regulation of MITF-M-dependent genes involved in pigmentation
Regulation of MITF-M-dependent genes involved in pigmentation
Drugs
Diseases
Other phagocyte defects, including the following eight diseases: Chediak-Higashi syndrome; Griscelli syndrome, type 1 (GS1); Griscelli syndrome, type 2 (GS2); Griscelli syndrome, type 3 (GS3); beta-actin deficiency; Neutrophil-specific granule deficiency; Myeloperoxidase deficiency; Glucose 6-phosphate dehydrogenase deficiency; Shwachman syndrome
Other phagocyte defects, including the following eight diseases: Chediak-Higashi syndrome; Griscelli syndrome, type 1 (GS1); Griscelli syndrome, type 2 (GS2); Griscelli syndrome, type 3 (GS3); beta-actin deficiency; Neutrophil-specific granule deficiency; Myeloperoxidase deficiency; Glucose 6-phosphate dehydrogenase deficiency; Shwachman syndrome
GWAS
Mean platelet volume (
32888494
)
Metabolite levels (Pyroglutamine) (
23934736
)
Central corneal thickness (
32528159
)
Heel bone mineral density (
28869591
30598549
)
Height (
33713608
)
Intraocular pressure (
29617998
)
Prostate cancer (
21743057
)
Interacting Genes
20 interacting genes:
AKAP9
BMF
CALM1
DLGAP1
DYNLL1
DYNLL2
ERG
KIF5B
MLPH
NDEL1
NEFL
PDE4B
PRPH
RAB11A
RAB27A
RAB3A
RPH3A
TRIM2
TRIM3
USP7
7 interacting genes:
BLOC1S6
C1orf216
MTDH
MYO5A
RAB27A
RAB27B
RECK
Entrez ID
4644
79083
HPRD ID
01179
09409
Ensembl ID
ENSG00000197535
ENSG00000115648
Uniprot IDs
A0A8I5KTF1
A0A8J8YWI7
A8CDT9
Q9UES4
Q9Y4I1
Q9BV36
PDB IDs
4D07
4J5L
4LLI
4LX1
4LX2
5JCY
5JCZ
Enriched GO Terms of Interacting Partners
?
Establishment Of Vesicle Localization
Vesicle Localization
Establishment Of Organelle Localization
Organelle Localization
Axon Cytoplasm
Myosin V Binding
Establishment Of Localization In Cell
Retrograde Axonal Transport
Protein-containing Complex Binding
Establishment Of Melanosome Localization
Melanosome Localization
Melanosome Transport
Pigment Granule Transport
Pigment Granule Localization
Regulation Of Transport
Centrosome
Centrosome Localization
Exosomal Secretion
Synaptic Vesicle Transport
Microtubule Associated Complex
Synaptic Vesicle Membrane
Modulation Of Chemical Synaptic Transmission
Synaptic Vesicle
Microtubule-based Process
Positive Regulation Of Regulated Secretory Pathway
Lysosome Localization
Transport Along Microtubule
Vesicle
Axonal Transport
Neurofilament Cytoskeleton Organization
Microtubule-based Movement
Cytoskeleton-dependent Intracellular Transport
Cytosol
Microtubule-based Transport
Axo-dendritic Transport
Positive Regulation Of Exocytosis
Cytoskeleton
Organelle Transport Along Microtubule
Protein Transport
Vesicle-mediated Transport In Synapse
Intermediate Filament Cytoskeleton Organization
Intermediate Filament-based Process
Regulation Of Cellular Component Organization
Positive Regulation Of Cellular Component Organization
Organelle Organization
Secretory Granule
Regulation Of Intracellular Transport
Intracellular Transport
Regulation Of Cellular Localization
Regulation Of Synaptic Vesicle Fusion To Presynaptic Active Zone Membrane
Pigment Granule Localization
Establishment Of Melanosome Localization
Melanosome Localization
Melanosome Transport
Pigment Granule Transport
Melanosome
Establishment Of Vesicle Localization
Vesicle Localization
Myosin V Binding
Late Endosome
Melanocyte Differentiation
Pigment Cell Differentiation
Exocytic Vesicle
Cytoskeleton-dependent Intracellular Transport
Multivesicular Body Membrane
Synaptic Vesicle Transport
Establishment Of Organelle Localization
Anterograde Axonal Transport
Pigmentation
Multivesicular Body Sorting Pathway
Vesicle Cytoskeletal Trafficking
Axon Cytoplasm
Axonal Transport
Apical Plasma Membrane
Secretion By Cell
GDP Binding
Cytotoxic T Cell Degranulation
Positive Regulation Of Constitutive Secretory Pathway
G Protein Activity
Bradykinin Biosynthetic Process
Circadian Sleep/wake Cycle
Protein Transport
Axo-dendritic Transport
Positive Regulation Of Exocytosis
Organelle Localization
Blood Coagulation
Secretory Granule
Ruffle
Coagulation
Secretion
Hemostasis
Establishment Of Protein Localization
Protein Localization To Extracellular Region
Establishment Of Protein Localization To Extracellular Region
Protein Secretion
Complement-dependent Cytotoxicity
Regulation Of Establishment Of Blood-brain Barrier
Intracellular Nitric Oxide Homeostasis
Exosomal Secretion
Establishment Of Localization In Cell
Tagcloud
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Tagcloud (Difference)
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Tagcloud (Intersection)
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