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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YBL024W | NCL1 | SGDID:S000000120 | NSUN6 NOPD1 |
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6 (EC 2.1.1.-) (NOL1/NOP2/Sun and PUA domain-containing protein 1) (NOL1/NOP2/Sun domain family member 6) |
2.1.1.- | Homo sapiens | Dubowitz Syndrome,Cardiomyopathy, Familial Restrictive, 1,Brugada Syndrome,Brugada Syndrome 4,Williams-Beuren Syndrome,Autosomal Recessive Non-Syndromic Intellectual Disability |
5wwq_b | Q8TEA1 | ENSG00000241058 | NSUN6 | 99.50 | 2.80E-19 | 2.40E-23 | 197.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBL024W | NCL1 | SGDID:S000000120 | PH1374 |
315aa long hypothetical proliferating-cell nucleolar protein p120 |
Pyrococcus horikoshii | 1ixk_a | O50082 | 100.00 | 6.50E-38 | 5.40E-42 | 330.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBL024W | NCL1 | SGDID:S000000120 | rsmF TTHA1387 |
Ribosomal RNA small subunit methyltransferase F (EC 2.1.1.-) (EC 2.1.1.178) (rRNA (cytosine-C(5)-)-methyltransferase RsmF) |
2.1.1.178 | Thermus thermophilus | 3m6w_a | Q5SII2 | 99.90 | 8.60E-29 | 7.20E-33 | 273.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YBL024W | NCL1 | SGDID:S000000120 | rsmF yebU b1835 JW5301 |
Ribosomal RNA small subunit methyltransferase F (EC 2.1.1.178) (16S rRNA m5C1407 methyltransferase) (rRNA (cytosine-C(5)-)-methyltransferase RsmF) |
2.1.1.178 | Escherichia coli | 2frx_a | P76273 | 99.90 | 3.10E-28 | 2.70E-32 | 269.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YBL024W | NCL1 | SGDID:S000000120 | rsmB fmu/fmv rrmB sun yhdB b3289 JW3250 |
Ribosomal RNA small subunit methyltransferase B (EC 2.1.1.176) (16S rRNA m5C967 methyltransferase) (rRNA (cytosine-C(5)-)-methyltransferase RsmB) |
2.1.1.176 | Escherichia coli | 1sqf_a | P36929 | 99.80 | 1.40E-25 | 1.30E-29 | 242.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YBL024W | NCL1 | SGDID:S000000120 | NSUN4 |
5-methylcytosine rRNA methyltransferase NSUN4 (EC 2.1.1.-) (NOL1/NOP2/Sun domain family member 4) |
2.1.1.- | Homo sapiens | Cardiomyopathy, Familial Restrictive, 1,Restrictive Cardiomyopathy |
4fzv_a | Q96CB9 | ENSG00000117481 | NSUN4 | 99.70 | 1.60E-21 | 1.40E-25 | 206.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBL024W | NCL1 | SGDID:S000000120 | PH1991 |
tRNA (cytosine(72)-C(5))-methyltransferase (tRNA:m(5)C72 MTase) (EC 2.1.1.-) (PhNSun6) |
2.1.1.- | Pyrococcus horikoshii | 5zve_a | O57712 | 99.80 | 5.70E-24 | 5.00E-28 | 228.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YBL024W | NCL1 | SGDID:S000000120 | trm4 MJ0026 |
tRNA (cytosine(48)-C(5))-methyltransferase (EC 2.1.1.-) (aTrm4) (tRNA (cytosine-5-)-methyltransferase Trm4) |
2.1.1.- | Methanocaldococcus jannaschii | 3a4t_a | Q60343 | 99.70 | 5.30E-23 | 4.80E-27 | 208.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YBL024W | NCL1 | SGDID:S000000120 | HMPREF0351_12218 |
HMPREF0351_12218 |
2.1.1.- | Enterococcus faecium | 3m4x_a | Q3Y1J9 | 99.80 | 2.40E-26 | 2.20E-30 | 252.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YBL024W | NCL1 | SGDID:S000000120 | NOP2 YNA1 YNL061W N2428 YNL2428W |
25S rRNA (cytosine(2870)-C(5))-methyltransferase (EC 2.1.1.310) (Nucleolar protein 2) |
2.1.1.310 | Saccharomyces cerevisiae | 6elz_q | P40991 | 99.90 | 5.10E-31 | 4.00E-35 | 296.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YBL024W | NCL1 | SGDID:S000000120 | NSUN5 NSUN5A WBSCR20 WBSCR20A |
28S rRNA (cytosine-C(5))-methyltransferase (EC 2.1.1.-) (NOL1-related protein) (NOL1R) (NOL1/NOP2/Sun domain family member 5) (Williams-Beuren syndrome chromosomal region 20A protein) |
2.1.1.- | Homo sapiens | Ehrlichiosis,Dubowitz Syndrome,Cardiomyopathy, Familial Restrictive, 1,Osteogenesis Imperfecta, Type Xviii,Restrictive Cardiomyopathy,Osteogenesis Imperfecta, Type Xx,Williams-Beuren Syndrome,Autosomal Recessive Non-Syndromic Intellectual Disability,Bowen-Conradi Syndrome |
2b9e_a | Q96P11 | ENSG00000130305 | NSUN5 | 99.80 | 4.90E-25 | 4.40E-29 | 228.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBL024W | NCL1 | SGDID:S000000120 | PH0851 |
PH0851 |
Pyrococcus horikoshii | 2yxl_a | O58581 | 99.90 | 4.60E-27 | 4.10E-31 | 257.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |