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

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YPL208W RKM1 / SGDID:S000006129
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
YPL208W RKM1 SGDID:S000006129
SETD6
N-lysine methyltransferase SETD6 (EC 2.1.1.-) (SET domain-containing protein 6)
2.1.1.- Homo sapiens
Familial Colorectal Cancer Type X,Meningioma, Familial
3qxy_a Q8TBK2 ENSG00000103037 SETD6 100.00 1.60E-34 1.60E-38 305.20 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
EZH2 KMT6
Histone-lysine N-methyltransferase EZH2 (EC 2.1.1.356) (ENX-1) (Enhancer of zeste homolog 2) (Lysine N-methyltransferase 6)
2.1.1.356 Homo sapiens
Skin Melanoma,Retinitis Pigmentosa,Cll/Sll,Chronic Myelomonocytic Leukemia,Melanoma,Breast Myoepithelial Carcinoma,Clear Cell Renal Cell Carcinoma,Diffuse Midline Glioma, H3 K27m-Mutant,B-Cell Lymphoma,Atypical Teratoid Rhabdoid Tumor,Essential Thrombocythemia,Posterior Fossa Ependymoma,Cholangiolocellular Carcinoma,Neuroblastoma,Primary Cutaneous Follicle Center Lymphoma,Leukemia, Acute Myeloid,Secondary Hemophagocytic Lymphohistiocytosis,Bone Marrow Cancer,Transitional Cell Carcinoma,Ezh2-Related Overgrowth,Bladder Cancer,Bile Duct Adenoma,Primary Hyperoxaluria,Ovarian Cancer,T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Malignant Peripheral Nerve Sheath Tumor,Rhabdomyosarcoma,Weaver Syndrome,Tongue Disease,Sotos Syndrome 1,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Rhabdoid Cancer,Fragile X Syndrome,Lymphoma, Non-Hodgkin, Familial,Beckwith-Wiedemann Syndrome,Esophageal Cancer,Myelodysplastic Syndrome,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Splenic Marginal Zone Lymphoma,Tongue Squamous Cell Carcinoma,Acute Promyelocytic Leukemia,Follicular Lymphoma,Ovarian Clear Cell Carcinoma,Nasopharyngeal Carcinoma,Lymphoma,Brain Glioma,Kabuki Syndrome 1,Juvenile Myelomonocytic Leukemia,Autosomal Dominant Non-Syndromic Intellectual Disability,Rett Syndrome,Myelofibrosis,Myeloma, Multiple,Medulloblastoma,Melanoma, Uveal,Childhood Acute Myeloid Leukemia,Lung Cancer,Hyperoxaluria, Primary, Type I,Pancreatic Cancer,Polycythemia Vera
4mi5_a Q15910 ENSG00000106462 EZH2 96.70 3.70E-06 3.50E-10 78.80 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
SETD3 C14orf154
Actin-histidine N-methyltransferase (EC 2.1.1.85) (SET domain-containing protein 3) (hSETD3)
2.1.1.85 Homo sapiens
Meier-Gorlin Syndrome 1
6icv_b Q86TU7 ENSG00000183576 SETD3 100.00 6.50E-35 6.30E-39 313.00 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
Smyd1 Bop
Histone-lysine N-methyltransferase Smyd1 (EC 2.1.1.354) (CD8b-opposite) (SET and MYND domain-containing protein 1) (Zinc finger protein BOP) (m-BOP)
2.1.1.354 Mus musculus
3n71_a P97443 99.00 4.00E-14 4.30E-18 144.00 0 0 1 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
set7 SPCC297.04c
SET domain-containing protein 7 (EC 2.1.1.-)
2.1.1.- Schizosaccharomyces pombe
5h6z_a Q9Y7Q6 98.30 2.60E-10 2.60E-14 101.70 0 0 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
SET1 KLLA0F24134g
Histone-lysine N-methyltransferase, H3 lysine-4 specific (EC 2.1.1.354) (COMPASS component SET1) (SET domain-containing protein 1)
2.1.1.354 Kluyveromyces lactis
6chg_c Q6CIT4 96.60 6.40E-06 6.60E-10 69.90 0 0 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
KMT2D ALR MLL2 MLL4
Histone-lysine N-methyltransferase 2D (Lysine N-methyltransferase 2D) (EC 2.1.1.354) (ALL1-related protein) (Myeloid/lymphoid or mixed-lineage leukemia protein 2)
2.1.1.354 Homo sapiens
Charge Syndrome,Plasma Cell Neoplasm,Cold Agglutinin Disease,Kleefstra Syndrome,Cavernous Sinus Meningioma,Rasopathy,Holoprosencephaly,Hypoplastic Left Heart Syndrome,Leukemia, Acute Myeloid,Dandy-Walker Syndrome,Rubinstein Taybi Like Syndrome,Breast Malignant Phyllodes Tumor,Microphthalmia,Microcephaly,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Complement Component C1s Deficiency,Chromosome 16p13.3 Deletion Syndrome, Proximal,Mental Retardation, Autosomal Dominant 26,Childhood Medulloblastoma,Lung Squamous Cell Carcinoma,Smith-Magenis Syndrome,Spinocerebellar Ataxia 2,Tetralogy Of Fallot,Peripheral T-Cell Lymphoma,Congenital Disorder Of Glycosylation, Type Ig,Autism Spectrum Disorder,Lymphoma,Kabuki Syndrome 1,Kbg Syndrome,Methylmalonic Acidemia And Homocysteinemia, Cblx Type,Scoliosis,Autosomal Dominant Non-Syndromic Intellectual Disability,Myeloma, Multiple,Medulloblastoma,Isolated Growth Hormone Deficiency Type Iii,Postaxial Acrofacial Dysostosis
4z4p_a O14686 ENSG00000167548 KMT2D 96.40 1.40E-05 1.40E-09 69.30 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
KMT5A PRSET7 SET07 SET8 SETD8
N-lysine methyltransferase KMT5A (EC 2.1.1.-) (H4-K20-HMTase KMT5A) (Histone-lysine N-methyltransferase KMT5A) (EC 2.1.1.361) (Lysine N-methyltransferase 5A) (Lysine-specific methylase 5A) (PR/SET domain-containing protein 07) (PR-Set7) (PR/SET07) (SET domain-containing protein 8)
2.1.1.361 Homo sapiens
Meier-Gorlin Syndrome 1
3f9x_c Q9NQR1 ENSG00000183955 KMT5A 96.30 1.40E-05 1.50E-09 69.00 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
KMT5B SUV420H1 CGI-85
Histone-lysine N-methyltransferase KMT5B (Lysine N-methyltransferase 5B) (Lysine-specific methyltransferase 5B) (Suppressor of variegation 4-20 homolog 1) (Su(var)4-20 homolog 1) (Suv4-20h1) ([histone H4]-N-methyl-L-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.362) ([histone H4]-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.361)
2.1.1.361,2.1.1.362, Homo sapiens
Primary Hyperoxaluria,Meier-Gorlin Syndrome 1,Mental Retardation, Autosomal Dominant 51,Autism Spectrum Disorder,Autism,Hyperoxaluria, Primary, Type I
3s8p_a Q4FZB7 ENSG00000110066 KMT5B 96.40 1.40E-05 1.30E-09 77.60 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
SETD7 KIAA1717 KMT7 SET7 SET9
Histone-lysine N-methyltransferase SETD7 (EC 2.1.1.364) (Histone H3-K4 methyltransferase SETD7) (H3-K4-HMTase SETD7) (Lysine N-methyltransferase 7) (SET domain-containing protein 7) (SET7/9)
2.1.1.364 Homo sapiens
1muf_a Q8WTS6 ENSG00000145391 SETD7 96.60 6.30E-06 6.50E-10 76.20 0 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
Kmt5b Suv420h1
Histone-lysine N-methyltransferase KMT5B (Lysine-specific methyltransferase 5B) (Suppressor of variegation 4-20 homolog 1) (Su(var)4-20 homolog 1) (Suv4-20h1) ([histone H4]-N-methyl-L-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.362) ([histone H4]-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.361)
2.1.1.361,2.1.1.362, Mus musculus
4bup_b Q3U8K7 96.30 1.70E-05 1.50E-09 76.90 0 0 1 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
KMT5C SUV420H2 PP7130
Histone-lysine N-methyltransferase KMT5C (Lysine N-methyltransferase 5C) (Lysine-specific methyltransferase 5C) (Suppressor of variegation 4-20 homolog 2) (Su(var)4-20 homolog 2) (Suv4-20h2) ([histone H4]-N-methyl-L-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.362) ([histone H4]-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.361)
2.1.1.361,2.1.1.362, Homo sapiens
Primary Hyperoxaluria,Hyperoxaluria, Primary, Type I
3rq4_a Q86Y97 ENSG00000133247 KMT5C 96.30 1.70E-05 1.60E-09 75.20 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
KMT2A ALL1 CXXC7 HRX HTRX MLL MLL1 TRX1
Histone-lysine N-methyltransferase 2A (Lysine N-methyltransferase 2A) (EC 2.1.1.354) (ALL-1) (CXXC-type zinc finger protein 7) (Myeloid/lymphoid or mixed-lineage leukemia) (Myeloid/lymphoid or mixed-lineage leukemia protein 1) (Trithorax-like protein) (Zinc finger protein HRX) [Cleaved into: MLL cleavage product N320 (N-terminal cleavage product of 320 kDa) (p320); MLL cleavage product C180 (C-terminal cleavage product of 180 kDa) (p180)]
2.1.1.354 Homo sapiens
Childhood Acute Lymphocytic Leukemia,Lymphoblastic Lymphoma,Hypertrichosis,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Cornelia De Lange Syndrome,Leukemia, Chronic Myeloid,Acute Myeloid Leukemia With T(9;11)(P22;Q23),B-Lymphoblastic Leukemia/Lymphoma,B-Lymphoblastic Leukemia/Lymphoma With Bcr-Abl1,B-Lymphoblastic Leukemia/Lymphoma With Iamp21,Rare Genetic Intellectual Disability,Myeloproliferative Neoplasm,Leukemia,Pancytopenia,Mixed Phenotype Acute Leukemia,Childhood Leukemia,Acute Leukemia,Leukemia, Acute Myeloid,Acute Myeloid Leukemia With 11q23 Abnormalities,Intravascular Large B-Cell Lymphoma,Familial Isolated Trichomegaly,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Ring Chromosome 21,Acute Megakaryoblastic Leukemia Without Down Syndrome,Rubinstein Taybi Like Syndrome,Central Nervous System Leukemia,Monocytic Leukemia,Ring Chromosome,Myeloid Sarcoma,Myeloid Leukemia,Acute Megakaryocytic Leukemia,Acute Monoblastic Leukemia,Colon Leiomyoma,Cytogenetically Normal Acute Myeloid Leukemia,Microcephaly,Hypoxia,Chronic Granulomatous Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Leukemia, Acute Lymphoblastic 3,Disease Of Mental Health,Cornelia De Lange Syndrome 1,Lymphoma, Non-Hodgkin, Familial,Wiedemann-Steiner Syndrome,Myelodysplastic Syndrome,Hairy Elbows,Acute Promyelocytic Leukemia,Wilms Tumor 1,Kabuki Syndrome 1,Kbg Syndrome,Leukemia, Acute Monocytic,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Autosomal Dominant Non-Syndromic Intellectual Disability,Autism
5f5e_a Q03164 ENSG00000118058 KMT2A 96.70 4.50E-06 4.60E-10 71.60 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
PFAG_03779
PFAG_03779
Plasmodium falciparum
4rz0_a W7FLI1 96.70 3.20E-06 3.30E-10 71.40 0 0 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
Kmt5c Suv420h2
Histone-lysine N-methyltransferase KMT5C (Lysine-specific methyltransferase 5C) (Suppressor of variegation 4-20 homolog 2) (Su(var)4-20 homolog 2) (Suv4-20h2) ([histone H4]-N-methyl-L-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.362) ([histone H4]-lysine20 N-methyltransferase KMT5B) (EC 2.1.1.361)
2.1.1.361,2.1.1.362, Mus musculus
4au7_a Q6Q783 96.50 8.50E-06 8.00E-10 77.60 0 0 1 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
A612L
A612L
Paramecium bursaria
2g46_b O41094 96.70 3.10E-06 3.20E-10 69.00 0 0 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
SMYD2 KMT3C
N-lysine methyltransferase SMYD2 (EC 2.1.1.-) (HSKM-B) (Histone methyltransferase SMYD2) (EC 2.1.1.354) (Lysine N-methyltransferase 3C) (SET and MYND domain-containing protein 2)
2.1.1.354 Homo sapiens
4wuy_a Q9NRG4 ENSG00000143499 SMYD2 99.20 3.40E-15 3.60E-19 152.00 0 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
legAS4 lpg1718
legAS4 lpg1718
Legionella pneumophila
5czy_a Q5ZUS4 96.20 2.70E-05 2.70E-09 79.20 0 0 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
BN1205_038210 TGVEG_216080
BN1205_038210 TGVEG_216080
Toxoplasma gondii
6fnd_b B9Q0K5 99.20 6.50E-16 7.00E-20 154.30 0 0 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
SMYD3 ZMYND1 ZNFN3A1
Histone-lysine N-methyltransferase SMYD3 (EC 2.1.1.354) (SET and MYND domain-containing protein 3) (Zinc finger MYND domain-containing protein 1)
2.1.1.354 Homo sapiens
Cerebellar Ataxia, Nonprogressive, With Mental Retardation,Renal Wilms' Tumor,Hepatocellular Carcinoma
5v37_a Q9H7B4 ENSG00000185420 SMYD3 99.10 4.00E-15 4.40E-19 147.80 1 1 0 0 0 0 0 0
YPL208W RKM1 SGDID:S000006129
RBCMT
Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplastic (EC 2.1.1.127) ([Fructose-bisphosphate aldolase]-lysine N-methyltransferase) (EC 2.1.1.259) ([Ribulose-bisphosphate carboxylase]-lysine N-methyltransferase) (PsLSMT) (RuBisCO LSMT) (RuBisCO methyltransferase) (rbcMT)
2.1.1.127,2.1.1.259, Pisum sativum
2h21_b Q43088 99.90 1.40E-33 1.30E-37 298.30 0 0 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab