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ACTA1 and TNNI3
Data Source:
HPRD
(in vitro)
ACTA1
TNNI3
Description
actin alpha 1, skeletal muscle
troponin I3, cardiac type
Image
No pdb structure
GO Annotations
Cellular Component
Stress Fiber
Extracellular Space
Cytosol
Striated Muscle Thin Filament
Dynactin Complex
Actin Filament
Actin Cytoskeleton
Sarcomere
Lamellipodium
Filopodium
Cell Body
Extracellular Exosome
Blood Microparticle
Cytosol
Troponin Complex
Sarcomere
Cardiac Myofibril
Cardiac Troponin Complex
Molecular Function
Structural Constituent Of Cytoskeleton
Protein Binding
ATP Binding
Myosin Binding
ADP Binding
Actin Binding
Protein Binding
Calcium Channel Inhibitor Activity
Protein Kinase Binding
Protein Domain Specific Binding
Troponin C Binding
Troponin T Binding
Metal Ion Binding
Calcium-dependent Protein Binding
Actin Filament Binding
Biological Process
Muscle Contraction
Response To Mechanical Stimulus
Response To Extracellular Stimulus
Response To Lithium Ion
Positive Regulation Of Gene Expression
Muscle Filament Sliding
Skeletal Muscle Thin Filament Assembly
Skeletal Muscle Fiber Adaptation
Response To Steroid Hormone
Skeletal Muscle Fiber Development
Cellular Response To Organonitrogen Compound
Mesenchyme Migration
Vasculogenesis
Regulation Of Systemic Arterial Blood Pressure By Ischemic Conditions
Skeletal Muscle Contraction
Cellular Calcium Ion Homeostasis
Muscle Contraction
Heart Development
Regulation Of Cardiac Muscle Contraction By Calcium Ion Signaling
Muscle Filament Sliding
Negative Regulation Of ATPase Activity
Ventricular Cardiac Muscle Tissue Morphogenesis
Heart Contraction
Cardiac Muscle Contraction
Pathways
Striated Muscle Contraction
Striated Muscle Contraction
Ion homeostasis
Drugs
Latrunculin A
Sucrose
Ulapualide A
Kabiramide C
Jaspisamide A
Tmr
1-Methylhistidine
Phosphoaminophosphonic Acid-Adenylate Ester
Aplyronine A
Reidispongiolide A
Reidispongiolide C
Sphinxolide B
Latrunculin B
N-(6-Aminohexyl)-5-Chloro-1-Naphthalenesulfonamide
Diseases
Congenital fiber type disproportion (CFTD)
Cap myopathy
Nemaline myopathy
Hypertrophic cardiomyopathy (HCM)
GWAS
Platelet count (
32888494
)
Interacting Genes
114 interacting genes:
ABL1
ABRA
ACTR10
ACTR1B
ADSS2
AFAP1
AIF1
AJUBA
AMOT
ANXA2
BIN1
CCIN
CCT2
CCT4
CCT5
CFL1
CLIC5
CNN1
CORO2B
COTL1
CTNND1
CTTN
CYFIP1
CYTH1
DHX9
DLG1
DMD
DNASE1
DNMBP
DTNA
DUX4L9
EGFR
EPB41
EPB41L2
EPS8
FGD4
FHOD1
FSCN1
GAS2
GAS7
GC
GSN
HCLS1
HDAC4
HIP1R
HSPB2
HTRA2
IQGAP1
ITGA2
ITPKA
KIF23
KLHL20
LASP1
MACF1
MAP1A
MAPT
MIB2
MINPP1
MYL1
MYLK
MYO10
MYO6
MYO7A
MYO9B
NEXN
NR3C2
NRAP
PAK1
PARVA
PCYT1B
PFDN1
PFN1
PHACTR1
PLD1
PPP1R9B
PRKCA
PRKCD
PRKCE
RAC1
RNF167
RPS6KB1
S100A1
S100A4
SCIN
SMTN
SNCA
SORBS1
SPRR1A
SPTA1
SPTAN1
SPTBN2
TAGLN
TJP1
TLN1
TMSB4X
TMSB4Y
TNNI1
TNNI3
TNNI3K
TP53
TPM2
TPM3
TRIM55
TRIM63
TTN
UBC
USP25
USP6NL
UTRN
VASP
VAV1
VCL
VIL1
XIRP1
19 interacting genes:
ACTA1
HSPB2
LYST
MST1
PAPPA
PKD2
PKD2L1
PRKCA
PSMC5
RASSF10
RCAN3
SOX4
TNNC1
TNNC2
TNNI3K
TNNT1
TNNT2
TRIM55
TRIM63
Entrez ID
58
7137
HPRD ID
00030
11769
Ensembl ID
ENSG00000143632
ENSG00000129991
Uniprot IDs
P68133
P19429
Q6FGX2
PDB IDs
1J1D
1J1E
1LXF
1MXL
1OZS
2KGB
2KRD
2L1R
2MZP
2N7L
4Y99
5VLN
5W88
5WCL
6KN7
6KN8
6MV3
7JGI
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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