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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YLL001W DNM1 / SGDID:S000003924
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
YLL001W DNM1 SGDID:S000003924
Dnm1
Dnm1
Cyanidioschyzon merolae
6fgz_a Q84Y91 100.00 1.90E-47 2.30E-51 409.90 0 0 0 0 0 0 0 0
YLL001W DNM1 SGDID:S000003924
MX2
Interferon-induced GTP-binding protein Mx2 (Interferon-regulated resistance GTP-binding protein MxB) (Myxovirus resistance protein 2) (p78-related protein)
Homo sapiens
Influenza,Pediculus Humanus Corporis Infestation,Hantavirus Hemorrhagic Fever With Renal Syndrome,Danubian Endemic Familial Nephropathy,Aicardi-Goutieres Syndrome,Microphthalmia With Limb Anomalies
4whj_a P20592 ENSG00000183486 MX2 100.00 8.40E-38 1.00E-41 325.10 1 1 0 0 0 0 0 0
YLL001W DNM1 SGDID:S000003924
CTHT_0065850
CTHT_0065850
Chaetomium thermophilum
6ql4_a G0SGC7 99.90 7.60E-31 7.20E-35 297.10 0 0 0 0 0 0 0 0
YLL001W DNM1 SGDID:S000003924
DNM3 KIAA0820
Dynamin-3 (EC 3.6.5.5) (Dynamin, testicular) (T-dynamin)
3.6.5.5 Homo sapiens
Myopathy, Centronuclear, 1,Sezary'S Disease,Centronuclear Myopathy,Neuropathy, Hereditary Sensory, Type Id
5a3f_d Q9UQ16 ENSG00000197959 DNM3 100.00 2.80E-51 3.40E-55 439.40 1 1 0 0 0 0 0 0
YLL001W DNM1 SGDID:S000003924
DNM1 DNM
Dynamin-1 (EC 3.6.5.5)
3.6.5.5 Homo sapiens
Zellweger Syndrome,Seizure Disorder,Optic Nerve Disease,Cohen Syndrome,Myopathy, Centronuclear, 1,Undetermined Early-Onset Epileptic Encephalopathy,Peroxisome Biogenesis Disorder 1b,Optic Atrophy 1,Charcot-Marie-Tooth Disease,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 2,Neuronal Intranuclear Inclusion Disease,Centronuclear Myopathy,Disease Of Mental Health,Neuropathy, Hereditary Sensory, Type Id,Aceruloplasminemia,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Lennox-Gastaut Syndrome,Early Infantile Epileptic Encephalopathy,Charcot-Marie-Tooth Disease, Dominant Intermediate B,Developmental And Epileptic Encephalopathy 31,Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive,Rett Syndrome
6dlu_p Q05193 ENSG00000106976 DNM1 100.00 1.00E-50 1.20E-54 433.90 1 1 0 0 0 0 0 0
YLL001W DNM1 SGDID:S000003924
DNM1L DLP1 DRP1
Dynamin-1-like protein (EC 3.6.5.5) (Dnm1p/Vps1p-like protein) (DVLP) (Dynamin family member proline-rich carboxyl-terminal domain less) (Dymple) (Dynamin-like protein) (Dynamin-like protein 4) (Dynamin-like protein IV) (HdynIV) (Dynamin-related protein 1)
3.6.5.5 Homo sapiens
Myopathy, Lactic Acidosis, And Sideroblastic Anemia,Zellweger Syndrome,Myopathy,Optic Nerve Disease,Scotoma,Cockayne Syndrome A,Alzheimer Disease,Mitochondrial Myopathy,Paroxysmal Dystonia,Hereditary Spastic Paraplegia,Skin Amelanotic Melanoma,Autosomal Recessive Spastic Ataxia,Optic Atrophy 1,Brain Cancer,Obesity Due To Melanocortin 4 Receptor Deficiency,Spastic Paraplegia 8,Charcot-Marie-Tooth Disease,Cranial Nerve Disease,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Microcephaly,Encephalopathy,Tooth Disease,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Lactic Acidosis,Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy,Spinocerebellar Ataxia 12,Optic Atrophy 5,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Spastic Ataxia,Leigh Syndrome,3-Methylglutaconic Aciduria, Type Iii
4bej_b O00429 ENSG00000087470 DNM1L 100.00 1.40E-40 1.80E-44 339.90 1 1 0 0 0 0 0 0
YLL001W DNM1 SGDID:S000003924
Dynamin_M
Dynamin central region
pfam Family
PF01031 99.90 5.50E-30 7.10E-34 236.90 0 0 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab