Showing entry for Actin, alpha skeletal muscle


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT011578
Protein NameActin, alpha skeletal muscle
Uniport IdP68133
GeneACTA1
Gene Id58
DomainActin
Pfam PF00022  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0071417 cellular response to organonitrogen compound
Biological Process GO:0090131 mesenchyme migration
Biological Process GO:0006936 muscle contraction
Biological Process GO:0030049 muscle filament sliding
Biological Process GO:0010628 positive regulation of gene expression
Biological Process GO:0009991 response to extracellular stimulus
Biological Process GO:0010226 response to lithium ion
Biological Process GO:0009612 response to mechanical stimulus
Biological Process GO:0048545 response to steroid hormone
Biological Process GO:0043503 skeletal muscle fiber adaptation
Biological Process GO:0048741 skeletal muscle fiber development
Biological Process GO:0030240 skeletal muscle thin filament assembly
molecular function GO:0043531 ADP binding
molecular function GO:0005524 ATP binding
molecular function GO:0017022 myosin binding
molecular function GO:0005200 structural constituent of cytoskeleton
cellular component GO:0015629 actin cytoskeleton
cellular component GO:0005884 actin filament
cellular component GO:0072562 blood microparticle
cellular component GO:0044297 cell body
cellular component GO:0005829 cytosol
cellular component GO:0005869 dynactin complex
cellular component GO:0070062 extracellular exosome
cellular component GO:0005615 extracellular space
cellular component GO:0030175 filopodium
cellular component GO:0030027 lamellipodium
cellular component GO:0030017 sarcomere
cellular component GO:0001725 stress fiber
cellular component GO:0005865 striated muscle thin filament
Reactome
Pathway Id Pathway Name
R-HSA-390522 Striated Muscle Contraction
R-HSA-397014 Muscle contraction
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0002736 BXGD000127 Amyotrophic Lateral Sclerosis Nutritional and Metabolic Diseases; Nervous System Diseases
C0003886 BXGD000238 Arthrogryposis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0004096 BXGD000252 Asthma Respiratory Tract Diseases; Immune System Diseases
C0004364 BXGD000270 Autoimmune Diseases Immune System Diseases
C0005745 BXGD000331 Blepharoptosis Eye Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006157 BXGD000377 Breech Presentation Female Urogenital Diseases and Pregnancy Complications
C0007193 BXGD000451 Cardiomyopathy, Dilated Cardiovascular Diseases
C0007194 BXGD000452 Hypertrophic Cardiomyopathy Cardiovascular Diseases
C0009081 BXGD000581 Congenital clubfoot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0010417 BXGD000670 Cryptorchidism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
C0011168 BXGD000700 Deglutition Disorders Digestive System Diseases; Otorhinolaryngologic Diseases
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0015469 BXGD000996 Facial paralysis Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases
C0015544 BXGD001003 Failure to Thrive Pathological Conditions, Signs and Symptoms
C0015934 BXGD001026 Fetal Growth Retardation Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
C0016842 BXGD001083 Congenital pectus excavatum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0018817 BXGD001235 Atrial Septal Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0019196 BXGD001301 Hepatitis C Digestive System Diseases; Infections
C0019553 BXGD001333 Hip Contracture Musculoskeletal Diseases
C0020224 BXGD001366 Polyhydramnios Female Urogenital Diseases and Pregnancy Complications
C0020534 BXGD001421 Orbital separation excessive Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0022821 BXGD001590 Kyphosis deformity of spine Musculoskeletal Diseases
C0023860 BXGD001708 Listeriosis Infections
C0024003 BXGD001726 Lordosis Musculoskeletal Diseases
C0025990 BXGD001884 Micrognathism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C0026827 BXGD001936 Muscle hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0026848 BXGD001941 Myopathy Musculoskeletal Diseases; Nervous System Diseases
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027868 BXGD002053 Neuromuscular Diseases Nervous System Diseases
C0029089 BXGD002107 Ophthalmoplegia Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0029401 BXGD002135 Osteitis Deformans Musculoskeletal Diseases
C0030552 BXGD002238 Paresis Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0032285 BXGD002344 Pneumonia Infections; Respiratory Tract Diseases
C0032460 BXGD002355 Polycystic Ovary Syndrome Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0033377 BXGD002406 Ptosis Pathological Conditions, Signs and Symptoms
C0035229 BXGD002516 Respiratory Insufficiency Respiratory Tract Diseases
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0036690 BXGD002632 Septicemia Pathological Conditions, Signs and Symptoms; Infections
C0039273 BXGD002806 Talipes cavus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0040485 BXGD002871 Torticollis Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0042510 BXGD002987 Ventricular Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0043116 BXGD003028 HMN (Hereditary Motor Neuropathy) Proximal Type I Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0085215 BXGD003141 Ovarian Failure, Premature Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0085436 BXGD003177 Meningitis, Cryptococcal Infections; Nervous System Diseases
C0086437 BXGD003282 Joint laxity Musculoskeletal Diseases
C0086439 BXGD003284 Hypokinesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0149721 BXGD003349 Left Ventricular Hypertrophy Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0151526 BXGD003432 Premature Birth Female Urogenital Diseases and Pregnancy Complications
C0151786 BXGD003475 Muscle Weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0151888 BXGD003497 Hyporeflexia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0175709 BXGD004013 Centronuclear myopathy Musculoskeletal Diseases; Nervous System Diseases
C0206157 BXGD004165 Myopathies, Nemaline Musculoskeletal Diseases; Nervous System Diseases
C0221170 BXGD004400 Muscular stiffness Nervous System Diseases
C0221629 BXGD004467 Proximal muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0231666 BXGD004505 Wrist-Drop Nervous System Diseases
C0231712 BXGD004519 Waddling gait Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0232466 BXGD004543 Feeding difficulties
C0233565 BXGD004590 Bradykinesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0233844 BXGD004620 Clumsiness Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
C0234146 BXGD004626 Absent reflex Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0234182 BXGD004631 Gowers sign
C0234860 BXGD004698 Weak cry
C0234958 BXGD004702 Muscle degeneration Musculoskeletal Diseases
C0235659 BXGD004763 Reduced fetal movement Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
C0239067 BXGD004961 Difficulty walking up stairs Pathological Conditions, Signs and Symptoms
C0239234 BXGD004974 Low set ears
C0239830 BXGD004998 Hand muscle atrophy
C0239946 BXGD005010 Fibrosis, Liver Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0240421 BXGD005037 Progressive muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0240479 BXGD005039 Neck muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0240635 BXGD005047 Byzanthine arch palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases
C0240953 BXGD005067 Winged scapula
C0241005 BXGD005072 Creatine phosphokinase serum increased
C0241910 BXGD005123 Autoimmune Chronic Hepatitis Digestive System Diseases; Immune System Diseases
C0243026 BXGD005210 Sepsis Pathological Conditions, Signs and Symptoms; Infections
C0265783 BXGD005575 Congenital hypoplasia of lung Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
C0270960 BXGD006141 Congenital myopathy (disorder) Musculoskeletal Diseases; Nervous System Diseases
C0270969 BXGD006144 Zebra body myopathy Musculoskeletal Diseases; Nervous System Diseases
C0270971 BXGD006146 Floppy infant syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0270992 BXGD006151 Secondary myopathy Musculoskeletal Diseases; Nervous System Diseases
C0311394 BXGD006884 Difficulty walking Pathological Conditions, Signs and Symptoms
C0332615 BXGD006898 Myopathic facies
C0341858 BXGD007425 Endometriosis of uterus Female Urogenital Diseases and Pregnancy Complications
C0345392 BXGD007732 Congenital kyphoscoliosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0349588 BXGD007933 Short stature
C0409338 BXGD008381 Flexion contracture - elbow
C0410180 BXGD008412 Eichsfeld type congenital muscular dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0410203 BXGD008417 X-linked centronuclear myopathy Musculoskeletal Diseases; Nervous System Diseases
C0410207 BXGD008419 Tubular Aggregate Myopathy Musculoskeletal Diseases; Nervous System Diseases
C0410264 BXGD008423 Contracture of tendo achilles
C0410266 BXGD008424 Contracture of hamstring(s) Musculoskeletal Diseases
C0424448 BXGD008529 Mask-like facies Nervous System Diseases
C0424551 BXGD008533 Impaired exercise tolerance
C0426790 BXGD008577 Narrow thorax
C0426818 BXGD008586 Thin rib
C0427065 BXGD008604 Distal muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0432072 BXGD008718 Dysmorphic features
C0456132 BXGD008869 Large fontanelle
C0476405 BXGD008993 Lung function testing abnormal
C0476408 BXGD008994 Reduced vital capacity
C0520459 BXGD009084 Necrotizing Enterocolitis Digestive System Diseases
C0520947 BXGD009126 Clumsiness - motor delay Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0521525 BXGD009139 Short neck
C0541794 BXGD009262 Skeletal muscle atrophy
C0544755 BXGD009310 Genu varum Musculoskeletal Diseases
C0544966 BXGD009320 Autophagic vaculoes (finding)
C0546125 BXGD009327 Nemaline Myopathy, Childhood Onset Musculoskeletal Diseases; Nervous System Diseases
C0546264 BXGD009330 Congenital Fiber Type Disproportion Musculoskeletal Diseases; Nervous System Diseases
C0557874 BXGD009444 Global developmental delay
C0575158 BXGD009515 Kyphoscoliosis deformity of spine Musculoskeletal Diseases
C0576093 BXGD009525 Knee joint valgus deformity Musculoskeletal Diseases
C0587246 BXGD009616 Muscle weakness of limb Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0600033 BXGD009682 Acquired Kyphoscoliosis Musculoskeletal Diseases
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0686353 BXGD009833 Muscular Dystrophies, Limb-Girdle Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0699743 BXGD009862 Congenital muscular dystrophy (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0746674 BXGD010147 Generalized muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0751336 BXGD010392 Distal Muscular Dystrophies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0751656 BXGD010540 Nemaline Myopathy, Autosomal Dominant Musculoskeletal Diseases; Nervous System Diseases
C0751657 BXGD010541 Nemaline Myopathy, Autosomal Recessive Musculoskeletal Diseases; Nervous System Diseases
C0752282 BXGD010709 Congenital Structural Myopathy Musculoskeletal Diseases; Nervous System Diseases
C0848558 BXGD010882 Hypospadias Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0850703 BXGD010905 Frequent falls Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0878544 BXGD011368 Cardiomyopathies Cardiovascular Diseases
C1142253 BXGD011742 Arthrofibrosis Musculoskeletal Diseases
C1145670 BXGD011764 Respiratory Failure Respiratory Tract Diseases
C1168401 BXGD011792 Squamous cell carcinoma of the head and neck Neoplasms
C1184923 BXGD011800 Lumbar hyperlordosis Musculoskeletal Diseases
C1269955 BXGD012005 Tumor Cell Invasion
C1276035 BXGD012100 Pena-Shokeir syndrome type I Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1387005 BXGD012953 Penis agenesis Male Urogenital Diseases
C1611743 BXGD013456 Familial (FPAH)
C1833662 BXGD013936 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders
C1834339 BXGD013967 Myopathy, Actin, Congenital, with Excess of Thin Myofilaments Musculoskeletal Diseases; Nervous System Diseases
C1834558 BXGD013978 Myopathy, Centronuclear, Autosomal Dominant Musculoskeletal Diseases; Nervous System Diseases
C1836003 BXGD014069 Facial diplegia Infections; Nervous System Diseases; Stomatognathic Diseases
C1836038 BXGD014073 Poor head control Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1836047 BXGD014074 Long face
C1836057 BXGD014076 Muscle fiber splitting
C1837142 BXGD014201 Poor suck
C1837262 BXGD014215 Increased muscle lipid content
C1837404 BXGD014229 High, narrow palate
C1837463 BXGD014235 Narrow face
C1838114 BXGD014297 Generalized limb muscle atrophy
C1839615 BXGD014390 X-linked myopathy with excessive autophagy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C1839630 BXGD014391 Severe muscular hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1839767 BXGD014404 Tented upper lip vermilion
C1842170 BXGD014503 Centrally nucleated skeletal muscle fibers
C1842820 BXGD014538 Cardiac conduction abnormality
C1843057 BXGD014552 Calf muscle hypertrophy
C1843637 BXGD014597 Neck flexor weakness
C1843643 BXGD014598 Nocturnal hypoventilation Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C1843697 BXGD014603 Axial muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1843700 BXGD014604 Increased variability in muscle fiber diameter
C1848873 BXGD014981 Abnormality of the diaphragm
C1850573 BXGD015154 Slender build Pathological Conditions, Signs and Symptoms
C1850848 BXGD015182 Muscle fiber necrosis
C1853171 BXGD015310 Multiple prenatal fractures
C1853926 BXGD015365 NONAKA MYOPATHY Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C1853932 BXGD015366 Rimmed vacuoles on biopsy
C1854301 BXGD015391 Motor delay Mental Disorders
C1854387 BXGD015396 Type 1 muscle fiber predominance
C1854494 BXGD015409 Slow progression
C1856507 BXGD015614 Bulbar signs
C1857304 BXGD015694 Flexion contracture of finger
C1858025 BXGD015760 Spinal rigidity
C1858120 BXGD015774 Generalized hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1858127 BXGD015775 Limb-girdle muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1861403 BXGD016045 Variable expressivity
C1865014 BXGD016282 Long philtrum
C1866021 BXGD016363 Increased connective tissue
C1866141 BXGD016379 Foot dorsiflexor weakness
C1866934 BXGD016427 Reduced tendon reflexes Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1868623 BXGD016517 Handgrip myotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C2267233 BXGD017017 Neonatal Hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C2674608 BXGD017250 Feeding difficulties in infancy
C2678065 BXGD017398 Myofibrillar Myopathy Musculoskeletal Diseases; Nervous System Diseases
C2732374 BXGD017553 Edema of dorsum of hand Pathological Conditions, Signs and Symptoms
C2750536 BXGD017670 Nemaline Myopathy 3, With Intranuclear Rods Musculoskeletal Diseases; Nervous System Diseases
C2750537 BXGD017671 Myopathy, Actin, Congenital, With Cores Musculoskeletal Diseases; Nervous System Diseases
C2919142 BXGD017867 Short Stature, CTCAE
C2931230 BXGD017985 Vacuolar myopathy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
C2931268 BXGD017993 Scapuloperoneal myopathy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C3494422 BXGD018966 Retrognathia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C3554617 BXGD019228 Adducted thumb Musculoskeletal Diseases
C3645536 BXGD019247 Autosomal Recessive Centronuclear Myopathy Musculoskeletal Diseases; Nervous System Diseases
C3661489 BXGD019263 Autosomal Dominant Myotubular Myopathy Musculoskeletal Diseases; Nervous System Diseases
C3710589 BXGD019375 Cap Myopathy Musculoskeletal Diseases; Nervous System Diseases
C3711377 BXGD019384 Intranuclear Rod Myopathy Musculoskeletal Diseases; Nervous System Diseases
C3711389 BXGD019393 Actin-Accumulation Myopathy Musculoskeletal Diseases; Nervous System Diseases
C3714756 BXGD019429 Intellectual Disability Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C3806467 BXGD019513 Respiratory insufficiency due to muscle weakness Respiratory Tract Diseases
C3806482 BXGD019514 Recurrent respiratory infections Infections; Respiratory Tract Diseases
C3808039 BXGD019537 Nemaline bodies
C3808250 BXGD019542 Reduced forced vital capacity
C4021726 BXGD020735 EMG: myopathic abnormalities Musculoskeletal Diseases; Nervous System Diseases
C4021727 BXGD020736 EMG: neuropathic changes
C4021797 BXGD020787 Abnormality of the thorax
C4022583 BXGD020924 Fatiguable weakness of proximal limb muscles
C4022585 BXGD020926 Fatigable weakness of distal limb muscles
C4022587 BXGD020928 Fatigable weakness of respiratory muscles
C4022591 BXGD020931 Fatigable weakness of bulbar muscles
C4023180 BXGD021139 Type 1 muscle fiber atrophy
C4024911 BXGD021468 Acute infantile spinal muscular atrophy Nervous System Diseases
C4025565 BXGD021665 Late-onset distal muscle weakness
C4025571 BXGD021670 Type 1 fibers relatively smaller than type 2 fibers
C4025729 BXGD021761 Neuromuscular dysphagia Digestive System Diseases; Otorhinolaryngologic Diseases
C4082299 BXGD022088 Bulbar palsy Nervous System Diseases
C4082937 BXGD022095 Necrotizing enterocolitis in fetus OR newborn Digestive System Diseases
C4225181 BXGD022170 MYOPATHY, SCAPULOHUMEROPERONEAL
C4551472 BXGD023303 Hypertrophic obstructive cardiomyopathy Cardiovascular Diseases
C4551649 BXGD023382 Congenital Dysplasia Of The Hip Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C4551952 BXGD023444 Myopathy, Centronuclear, 1 Musculoskeletal Diseases; Nervous System Diseases
C4552811 BXGD023526 Generalized Muscle Weakness, CTCAE
C4721555 BXGD023755 Autoimmune hepatitis Digestive System Diseases
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0002675 Sugars 342.3
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein