







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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YMR229C | RRP5 | SGDID:S000004842 | RPS1 SOVF_099990 |
30S ribosomal protein S1, chloroplastic (CS1) (Chloroplastic small ribosomal subunit protein bS1c) |
Spinacia oleracea | 5x8p_8 | P29344 | 99.20 | 5.80E-16 | 6.80E-20 | 167.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YMR229C | RRP5 | SGDID:S000004842 | PARMER_03812 |
PARMER_03812 |
Parabacteroides merdae | 4r7s_a | A7AK45 | 99.20 | 6.70E-16 | 1.00E-19 | 141.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YMR229C | RRP5 | SGDID:S000004842 | RRP5 FMI1 YMR229C YM9959.11C |
rRNA biogenesis protein RRP5 (Ribosomal RNA-processing protein 5) (U3 small nucleolar RNA-associated protein RRP5) (U3 snoRNA-associated protein RRP5) |
Saccharomyces cerevisiae | 5nlg_a | Q05022 | 99.80 | 9.50E-27 | 1.40E-30 | 229.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YMR229C | RRP5 | SGDID:S000004842 | rpsA ssyF b0911 JW0894 |
30S ribosomal protein S1 (Bacteriophage Q beta RNA-directed RNA polymerase subunit I) (Small ribosomal subunit protein bS1) |
Escherichia coli | 4q7j_h | P0AG67 | 99.30 | 4.30E-16 | 5.20E-20 | 160.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YMR229C | RRP5 | SGDID:S000004842 | PEX5 PXR1 |
Peroxisomal targeting signal 1 receptor (PTS1 receptor) (PTS1R) (PTS1-BP) (Peroxin-5) (Peroxisomal C-terminal targeting signal import receptor) (Peroxisome receptor 1) |
Homo sapiens | Refsum Disease, Classic,Peroxisome Biogenesis Disorder 1a,Peroxisome Biogenesis Disorder 2a,Zellweger Syndrome,Peroxisomal Disease,Rhizomelic Chondrodysplasia Punctata, Type 1,Chondrodysplasia Punctata Syndrome,Peroxisomal Biogenesis Disorder,Neonatal Adrenoleukodystrophy,Peroxisome Biogenesis Disorder 1b,Cataract,Rhizomelic Chondrodysplasia Punctata,Sensorineural Hearing Loss,Zellweger Spectrum Disorder,Rhizomelic Chondrodysplasia Punctata, Type 2,Primary Hyperoxaluria,Leukodystrophy,Juvenile Glaucoma,Microcephaly,Adrenoleukodystrophy,Rhizomelic Chondrodysplasia Punctata, Type 5,Peroxisome Biogenesis Disorder 2b,Mulibrey Nanism,Rhizomelic Chondrodysplasia Punctata, Type 3 |
1fch_a | P50542 | 99.30 | 7.00E-17 | 9.30E-21 | 164.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |