Skip to main content Skip to navigation Skip to search
Open toolbar

Accessibility

Disclaimer
Home

Main menu

  • Home
  • Download
  • Information
  • Contact

Mobile Main Menu

  • Home
  • Download
  • Information
  • Contact
AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

Breadcrumb

  1. Home
YML042W CAT2 / SGDID:S000004506
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
Yeast Systematic Name Yeast Symbol SGDID Analog Name Analog Description EC Organism Disease Structure Uniprot Human ID Human Symbol HHsearch Probability HHsearch E_value HHsearch P_value HHsearch Score Flag Disease related Flag Homo sapiens Flag Mus musculus Flag Danio rerio Flag Drosophila melanogaster Flag Caenorhabditis elegans Flag Arabidopsis thaliana Flag Escherichia coli
YML042W CAT2 SGDID:S000004506
Carn_acyltransf
Choline/Carnitine o-acyltransferase
pfam Family
PF00755 100.00 1.00E-119 1.00E-123 1020.70 0 0 0 0 0 0 0 0
YML042W CAT2 SGDID:S000004506
Crat
Carnitine O-acetyltransferase (Carnitine acetylase) (EC 2.3.1.137) (EC 2.3.1.7) (Carnitine acetyltransferase) (CAT) (CrAT)
2.3.1.137,2.3.1.7, Mus musculus
2h3u_b P47934 100.00 7.00E-127 5.00E-131 1089.20 0 0 1 0 0 0 0 0
YML042W CAT2 SGDID:S000004506
Chat
Choline O-acetyltransferase (CHOACTase) (ChAT) (Choline acetylase) (EC 2.3.1.6)
2.3.1.6 Rattus norvegicus
1t1u_a P32738 100.00 5.00E-126 4.00E-130 1088.90 0 0 0 0 0 0 0 0
YML042W CAT2 SGDID:S000004506
Cpt2 Cpt-2
Carnitine O-palmitoyltransferase 2, mitochondrial (EC 2.3.1.21) (Carnitine palmitoyltransferase II) (CPT II)
2.3.1.21 Rattus norvegicus
2deb_b P18886 100.00 2.00E-129 2.00E-133 1116.50 0 0 0 0 0 0 0 0
YML042W CAT2 SGDID:S000004506
Crot Cot
Peroxisomal carnitine O-octanoyltransferase (COT) (EC 2.3.1.137)
2.3.1.137 Mus musculus
1xl7_a Q9DC50 100.00 8.00E-127 6.00E-131 1091.70 0 0 1 0 0 0 0 0
YML042W CAT2 SGDID:S000004506
CRAT CAT1
Carnitine O-acetyltransferase (Carnitine acetylase) (EC 2.3.1.137) (EC 2.3.1.7) (Carnitine acetyltransferase) (CAT) (CrAT)
2.3.1.137,2.3.1.7, Homo sapiens
Mitochondrial Encephalomyopathy,Myopathy,Overnutrition,Basal Ganglia Disease,Neurodegeneration With Brain Iron Accumulation,Peripheral Vascular Disease,Leukoregulin,Neurodegeneration With Brain Iron Accumulation 8,Immune Deficiency Disease,Carnitine Acetyltransferase Deficiency,Carnitine Palmitoyltransferase I Deficiency,Leigh Syndrome,Carnitine Palmitoyltransferase Ii Deficiency, Infantile
1nm8_a P43155 ENSG00000095321 CRAT 100.00 2.00E-126 1.00E-130 1087.90 1 1 0 0 0 0 0 0
YML042W CAT2 SGDID:S000004506
CHAT
Choline O-acetyltransferase (CHOACTase) (ChAT) (Choline acetylase) (EC 2.3.1.6)
2.3.1.6 Homo sapiens
Megacolon,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Central Sleep Apnea,Neuromuscular Junction Disease,Neuromuscular Disease,Congenital Myasthenic Syndrome Associated With Acetylcholine Receptor Deficiency,Congenital Myasthenic Syndrome With Episodic Apnea,Alzheimer Disease,Constipation,Amyotrophic Lateral Sclerosis 1,Mild Cognitive Impairment,Motor Neuron Disease,Neuroblastoma,Myasthenic Syndrome, Congenital, 21, Presynaptic,Apnea, Central Sleep,Riboflavin Deficiency,Chronic Progressive External Ophthalmoplegia,Neurotic Disorder,Presynaptic Congenital Myasthenic Syndromes,Ocular Dominance,Gastroesophageal Reflux,Sudden Infant Death Syndrome,Myasthenic Syndrome, Congenital, 4c, Associated With Acetylcholine Receptor Deficiency,Dementia,Scrapie,Vascular Dementia,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Parkinson Disease 1, Autosomal Dominant,Febrile Seizures,Head Injury,Amnestic Disorder,Pick Disease Of Brain,Wernicke-Korsakoff Syndrome,Central Nervous System Disease,Respiratory Failure,Tendinosis,Olivopontocerebellar Atrophy,Cone-Rod Dystrophy 2,Disease Of Mental Health,Toxic Encephalopathy,Congenital Myasthenic Syndrome,Lactic Acidosis,Retinitis Pigmentosa 23,Generalized Epilepsy With Febrile Seizures Plus, Type 7,Dementia, Lewy Body,Schizophrenia,Aspiration Pneumonia,Down Syndrome,Vertical Talus, Congenital,Huntington Disease,Cataract 38,Multiple System Atrophy 1,Myasthenic Syndrome, Congenital, 19,Ptosis,Rett Syndrome,Myasthenic Syndrome, Congenital, 6, Presynaptic,Thiamine Deficiency Disease
2fy3_a P28329 ENSG00000070748 CHAT 100.00 1.00E-126 8.00E-131 1091.00 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab