







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 |
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YDR363W | ESC2 | SGDID:S000002771 | UBL5 |
Ubiquitin-like protein 5 |
Homo sapiens | 4pyu_g | Q9BZL1 | ENSG00000198258 | UBL5 | 97.00 | 6.90E-07 | 1.00E-10 | 56.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDR363W | ESC2 | SGDID:S000002771 | DSK2 SHE4 YMR276W YM8021.02 |
Ubiquitin domain-containing protein DSK2 |
Saccharomyces cerevisiae | 2bwf_a | P48510 | 97.00 | 8.00E-07 | 1.20E-10 | 57.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | tas3 SPBC83.03c |
RNA-induced transcriptional silencing complex protein tas3 (RITS protein tas3) |
Schizosaccharomyces pombe | 3tix_a | O94687 | 97.50 | 4.30E-08 | 5.00E-12 | 82.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | thyA BMEI0608 |
Thymidylate synthase (TS) (TSase) (EC 2.1.1.45) |
2.1.1.45 | Brucella melitensis | 3ix6_b | P67042 | 98.10 | 9.60E-10 | 1.00E-13 | 102.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR363W | ESC2 | SGDID:S000002771 | NFATC2IP NIP45 |
NFATC2-interacting protein (45 kDa NF-AT-interacting protein) (45 kDa NFAT-interacting protein) (Nuclear factor of activated T-cells, cytoplasmic 2-interacting protein) |
Homo sapiens | Tracheitis,Friedreich Ataxia 2,Cone-Rod Dystrophy 2 |
2l76_a | Q8NCF5 | ENSG00000176953 | NFATC2IP | 98.70 | 1.60E-12 | 1.90E-16 | 97.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | POL30 YBR088C YBR0811 |
Proliferating cell nuclear antigen (PCNA) |
Saccharomyces cerevisiae | 3pge_a | P15873 | 98.30 | 1.20E-10 | 1.30E-14 | 99.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | bqt4 SPBC19C7.10 |
Bouquet formation protein 4 |
Schizosaccharomyces pombe | 5yca_a | O60158 | 97.40 | 9.50E-08 | 1.10E-11 | 81.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | UBA52 UBCEP2 |
Ubiquitin-60S ribosomal protein L40 (CEP52) (Ubiquitin A-52 residue ribosomal protein fusion product 1) [Cleaved into: Ubiquitin; 60S ribosomal protein L40 (Large ribosomal subunit protein eL40)] |
Homo sapiens | Stomatitis,Myoclonic Epilepsy Of Lafora |
5hps_b | P62987 | ENSG00000221983 | UBA52 | 97.10 | 5.10E-07 | 7.60E-11 | 58.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | Isg15 G1p2 Ucrp |
Ubiquitin-like protein ISG15 (Interferon-induced 15 kDa protein) (Interferon-induced 17 kDa protein) (IP17) (Ubiquitin cross-reactive protein) |
Mus musculus | 5jze_d | Q64339 | 96.90 | 1.10E-06 | 1.60E-10 | 55.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | Ubc |
Polyubiquitin-C [Cleaved into: Ubiquitin; Ubiquitin-related 1; Ubiquitin-related 2] |
Mus musculus | 3a9j_b | P0CG50 | 97.00 | 7.60E-07 | 1.10E-10 | 56.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | rad60 SPBC1921.02 |
DNA repair protein rad60 |
Schizosaccharomyces pombe | 3goe_a | Q9USX3 | 97.60 | 2.60E-08 | 3.20E-12 | 70.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | CSUB_C1474 HGMM_F04B03C03 HGMM_F21D07C21 HGMM_F30C12C33 |
CSUB_C1474 HGMM_F04B03C03 HGMM_F21D07C21 HGMM_F30C12C33 |
Caldiarchaeum subterraneum | 5zew_a | E6N8B8 | 96.90 | 9.90E-07 | 1.50E-10 | 54.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | SUMO3 SMT3A SMT3H1 |
Small ubiquitin-related modifier 3 (SUMO-3) (SMT3 homolog 1) (SUMO-2) (Ubiquitin-like protein SMT3A) (Smt3A) |
Homo sapiens | Brachydactyly, Type A1 |
2io1_d | P55854 | ENSG00000184900 | SUMO3 | 97.40 | 1.00E-07 | 1.40E-11 | 65.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | UBB |
Polyubiquitin-B [Cleaved into: Ubiquitin] |
Homo sapiens | Alzheimer Disease,Submucosal Cleft Palate,Cleft Hard Palate,Parkinson Disease, Late-Onset,Patella, Chondromalacia Of,Pick Disease Of Brain,Xeroderma Pigmentosum, Complementation Group C,Cleft Soft Palate,Encephalopathy, Familial, With Neuroserpin Inclusion Bodies,Smith-Magenis Syndrome,Down Syndrome,Uvula, Bifid,Leukodystrophy, Hypomyelinating, 7, With Or Without Oligodontia And/Or Hypogonadotropic Hypogonadism,Mulibrey Nanism,Myoclonic Epilepsy Of Lafora |
2y5b_f | P0CG47 | ENSG00000170315 | UBB | 97.00 | 7.70E-07 | 1.10E-10 | 64.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | BURPS1710b_A0907 |
BURPS1710b_A0907 |
5.2.1.8 | Burkholderia pseudomallei | 3uf8_a | Q3JK38 | 98.40 | 3.80E-11 | 4.70E-15 | 99.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR363W | ESC2 | SGDID:S000002771 | FPV170 |
Protein A6 homolog |
Fowlpox virus | 6br9_a | Q9J563 | 98.00 | 2.40E-09 | 2.00E-13 | 103.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | RUB1 NEDD8 UBQ15 At1g31340 T19E23.13 |
Ubiquitin-NEDD8-like protein RUB1 [Cleaved into: Ubiquitin; NEDD8-like protein RUB1 (Ubiquitin-related protein 1) (AtRUB1)] |
Arabidopsis thaliana | 1bt0_a | Q9SHE7 | 98.00 | 1.70E-09 | 1.80E-13 | 80.10 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | RAD23A |
UV excision repair protein RAD23 homolog A (HR23A) (hHR23A) |
Homo sapiens | Brain Sarcoma,Angelman Syndrome,Paget'S Disease Of Bone,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group G |
2wyq_a | P54725 | ENSG00000179262 | RAD23A | 97.00 | 6.90E-07 | 9.70E-11 | 59.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | smt3 anon-EST:Posey240 Dm0342 Dmel\CG4494 DmSmt3 Dmsmt3 DmSUMO-1 dSmt3 dsmt3 l(2)04493 l(2)SH0182 l(2)SH2 0182 SMT3 Smt3 SUMO Sumo sumo CG4494 Dmel_CG4494 |
smt3 anon-EST:Posey240 Dm0342 Dmel\CG4494 DmSmt3 Dmsmt3 DmSUMO-1 dSmt3 dsmt3 l(2)04493 l(2)SH0182 l(2)SH2 0182 SMT3 Smt3 SUMO Sumo sumo CG4494 Dmel_CG4494 |
Drosophila melanogaster | 2k1f_a | O97102 | 97.30 | 1.20E-07 | 1.80E-11 | 63.40 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | SMT3 YDR510W D9719.15 |
Ubiquitin-like protein SMT3 |
Saccharomyces cerevisiae | 2eke_c | Q12306 | 97.60 | 3.70E-08 | 4.40E-12 | 73.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | Aspscr1 Tug |
Tether containing UBX domain for GLUT4 (Alveolar soft part sarcoma chromosomal region candidate gene 1 protein homolog) |
Mus musculus | 2al3_a | Q8VBT9 | 98.40 | 6.90E-11 | 7.80E-15 | 89.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | RAD23 YEL037C SYGP-ORF29 |
UV excision repair protein RAD23 |
Saccharomyces cerevisiae | 2nbw_b | P32628 | 97.00 | 6.50E-07 | 9.60E-11 | 57.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | PRKN PARK2 |
E3 ubiquitin-protein ligase parkin (Parkin) (EC 2.3.2.31) (Parkin RBR E3 ubiquitin-protein ligase) (Parkinson juvenile disease protein 2) (Parkinson disease protein 2) |
2.3.2.31 | Homo sapiens | Progressive Myoclonus Epilepsy,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Rem Sleep Behavior Disorder,Lung Cancer Susceptibility 3,Tremor,Optic Nerve Disease,Prion Disease,Gaucher'S Disease,Sphingolipidosis,Alzheimer Disease,Ulnar Nerve Lesion,Radial Nerve Lesion,Amyotrophic Lateral Sclerosis 1,Angelman Syndrome,Motor Neuron Disease,Movement Disease,Neurodegeneration With Brain Iron Accumulation,Testicular Disease,Leber Plus Disease,Essential Tremor,Choreatic Disease,Machado-Joseph Disease,Dementia,Optic Atrophy 1,Cerebellar Disease,Leukoencephalopathy, Hereditary Diffuse, With Spheroids,Parkin Type Of Early-Onset Parkinson Disease,Dystonia,Nervous System Disease,Ovarian Cancer,Charcot-Marie-Tooth Disease,Paratyphoid Fever,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Parkinson Disease 3, Autosomal Dominant,Parkinson Disease 1, Autosomal Dominant,Tooth Disease,Pick Disease Of Brain,Postencephalitic Parkinson Disease,Autosomal Dominant Cerebellar Ataxia,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Gaucher Disease, Type I,Toxic Encephalopathy,Body Mass Index Quantitative Trait Locus 11,Dentatorubral-Pallidoluysian Atrophy,Meier-Gorlin Syndrome 2,Dementia, Lewy Body,Dystonia 12,Schizophrenia,Ophthalmomyiasis,Restless Legs Syndrome,Parkinson Disease 21,Kufor-Rakeb Syndrome,Leprosy 3,Focal Dystonia,Parkinson Disease 10,Attention Deficit-Hyperactivity Disorder,Autism Spectrum Disorder,Multiple System Atrophy 1,Color Agnosia,Leber Hereditary Optic Neuropathy, Modifier Of,Leprosy 2,Mitochondrial Complex I Deficiency, Nuclear Type 1,Epilepsy, Idiopathic Generalized 9,Ptosis,Rett Syndrome,Myoclonic Epilepsy Of Lafora,Autism,Juvenile-Onset Parkinson'S Disease,Early-Onset Parkinson'S Disease,Parkinson Disease 2, Autosomal Recessive Juvenile,Lung Cancer,Parkinson Disease 15, Autosomal Recessive Early-Onset |
5tr5_a | O60260 | ENSG00000185345 | PRKN | 96.90 | 1.00E-06 | 1.60E-10 | 54.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR363W | ESC2 | SGDID:S000002771 | SUMO1 SMT3C SMT3H3 UBL1 OK/SW-cl.43 |
Small ubiquitin-related modifier 1 (SUMO-1) (GAP-modifying protein 1) (GMP1) (SMT3 homolog 3) (Sentrin) (Ubiquitin-homology domain protein PIC1) (Ubiquitin-like protein SMT3C) (Smt3C) (Ubiquitin-like protein UBL1) |
Homo sapiens | Progressive Multifocal Leukoencephalopathy,Cleft Lip,Orofacial Cleft 4,Acute Necrotizing Encephalitis,Lip Cancer,Cleft Palate, Isolated,Neuronal Intranuclear Inclusion Disease,Orofacial Cleft 10,Dentatorubral-Pallidoluysian Atrophy,Familial Partial Lipodystrophy,Orofacial Cleft,Tooth Agenesis,Acute Promyelocytic Leukemia,Early-Onset Parkinson'S Disease,Frontotemporal Dementia |
1wyw_b | P63165 | ENSG00000116030 | SUMO1 | 97.30 | 1.70E-07 | 2.40E-11 | 64.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | VP30 |
Transcriptional activator VP30 (EbolaVP30) (eVP30) (Minor nucleoprotein VP30) |
Reston ebolavirus | 3v7o_a | Q8JPX6 | 97.40 | 1.30E-07 | 1.30E-11 | 84.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | UBL4A DXS254E GDX UBL4 |
Ubiquitin-like protein 4A (Ubiquitin-like protein GDX) |
Homo sapiens | Rett Syndrome,Primary Hypomagnesemia |
2dzi_a | P11441 | ENSG00000102178 | UBL4A | 97.20 | 2.60E-07 | 3.90E-11 | 59.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | Nfatc2ip Nip45 |
NFATC2-interacting protein (45 kDa NF-AT-interacting protein) (45 kDa NFAT-interacting protein) (Nuclear factor of activated T-cells, cytoplasmic 2-interacting protein) |
Mus musculus | 3a4r_a | O09130 | 98.00 | 1.60E-09 | 2.30E-13 | 71.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | SUMO2 SMT3B SMT3H2 |
Small ubiquitin-related modifier 2 (SUMO-2) (HSMT3) (SMT3 homolog 2) (SUMO-3) (Sentrin-2) (Ubiquitin-like protein SMT3B) (Smt3B) |
Homo sapiens | Gordon Holmes Syndrome |
1wm2_a | P61956 | ENSG00000188612 | SUMO2 | 97.80 | 9.00E-09 | 1.30E-12 | 67.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | Tb927.5.3210 |
Tb927.5.3210 |
Trypanosoma brucei | 2k8h_a | Q57Z72 | 97.60 | 2.20E-08 | 2.80E-12 | 74.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | UBC |
Polyubiquitin-C [Cleaved into: Ubiquitin] |
Homo sapiens | Retinitis Pigmentosa,Epilepsy,Middle East Respiratory Syndrome,Alzheimer Disease,Ectodermal Dysplasia,Angelman Syndrome,Luteoma,Cystic Fibrosis,Machado-Joseph Disease,Ethmoid Sinus Adenocarcinoma,Xeroderma Pigmentosum, Complementation Group C,Neuronal Ceroid Lipofuscinosis,Ring Dermoid Of Cornea,Ectodermal Dysplasia 10a, Hypohidrotic/Hair/Nail Type, Autosomal Dominant,Myoclonic Epilepsy Of Lafora,Gordon Holmes Syndrome |
2ld9_a | P0CG48 | ENSG00000150991 | UBC | 97.00 | 7.80E-07 | 1.20E-10 | 55.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | sumo 543735 |
sumo 543735 |
Solanum lycopersicum | 5jp1_b | Q9SMD1 | 97.50 | 3.90E-08 | 5.30E-12 | 68.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | PFDG_04583 |
PFDG_04583 |
Plasmodium falciparum | 5gjl_a | A0A0L7M5F7 | 97.50 | 6.00E-08 | 8.30E-12 | 67.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | smo-1 smt3 sumo K12C11.2 |
Small ubiquitin-related modifier (SUMO) (Ubiquitin-like protein SMT3) |
Caenorhabditis elegans | 5xqm_a | P55853 | 97.10 | 3.90E-07 | 5.10E-11 | 64.50 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YDR363W | ESC2 | SGDID:S000002771 | ISG15 G1P2 UCRP |
Ubiquitin-like protein ISG15 (Interferon-induced 15 kDa protein) (Interferon-induced 17 kDa protein) (IP17) (Ubiquitin cross-reactive protein) (hUCRP) |
Homo sapiens | Viral Infectious Disease,Coronavirus Infectious Disease,Hepatitis E,Middle East Respiratory Syndrome,Avian Influenza,Amyotrophic Lateral Sclerosis 1,Crimean-Congo Hemorrhagic Fever,Noonan Syndrome 1,Influenza,Bacterial Infectious Disease,Japanese Encephalitis,Adult Dermatomyositis,Childhood Type Dermatomyositis,Vaccinia,Immunodeficiency 27b,Immunodeficiency 38 With Basal Ganglia Calcification,Aicardi-Goutieres Syndrome,Vasculopathy, Retinal, With Cerebral Leukoencephalopathy And Systemic Manifestations,Acute Promyelocytic Leukemia,Adams-Oliver Syndrome,Basal Ganglia Calcification,Systemic Lupus Erythematosus,Microphthalmia With Limb Anomalies,Oliver Syndrome |
6ffa_b | P05161 | ENSG00000187608 | ISG15 | 97.20 | 2.10E-07 | 3.20E-11 | 59.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR363W | ESC2 | SGDID:S000002771 | NEDD8 |
NEDD8 (Neddylin) (Neural precursor cell expressed developmentally down-regulated protein 8) (NEDD-8) (Ubiquitin-like protein Nedd8) |
Homo sapiens | Parkinson Disease, Late-Onset |
3dbh_i | Q15843 | ENSG00000129559 | NEDD8 | 97.10 | 4.00E-07 | 5.90E-11 | 60.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |