| ORF |
Std. Name |
|
ACV120_A1B |
|
YHR026w
|
PPA1 |
|
0.354
|
| proteolipid|vacuolar ATPase V0 domain subunit c'' |
|
YBL068w
|
PRS4 |
|
0.355
|
| ribose-phosphate pyrophosphokinase |
|
YPL227c
|
ALG5 |
|
0.355
|
| UDP-glucose:dolichyl-phosphate glucosyltransferase |
|
YLR039c
|
RIC1 |
|
0.355
|
| Ric1p binds to Rgp1p, on the Golgi, and the complex catalyzes nucleotide exchange on Ypt6p. |
|
YOR381w
|
FRE3 |
|
0.355
|
| ferric reductase transmembrane component |
|
YJL078c
|
PRY3 |
|
0.356
|
| Protein of unknown function, has similarity to Pry1p and Pry2p and to the plant PR-1 class of pathogen related proteins |
|
YHR039c-B
|
|
|
0.356
|
| This ORF is a part of YHR039C-A |
|
YGL241w
|
KAP114 |
|
0.356
|
| Karyopherin, responsible for nuclear import of Spt15p, histones H2A and H2B, and Nap1p; amino terminus shows similarity to those of other importins, particularly Cse1p; localization is primarily nuclear |
|
YMR180c
|
CTL1 |
|
0.356
|
| RNA triphosphatase |
|
YOL057w
|
|
|
0.356
|
| Hypothetical ORF |
|
YER059w
|
PCL6 |
|
0.356
|
| PHO85 cyclin |
|
YGR092w
|
DBF2 |
|
0.356
|
| Kinase required for late nuclear division. Cdc15 promotes the exit from mitosis by directly switching on the kinase activity of Dbf2. |
|
YNR049c
|
MSO1 |
|
0.356
|
| Probable component of the secretory vesicle docking complex, acts at a late step in secretion; shows genetic and physical interactions with Sec1p and is enriched in microsomal membrane fractions; required for sporulation |
|
YFL042c
|
|
|
0.356
|
| Due to a sequence change (deletion of G at 46151), YFL043C is now part of YFL042C. |
|
YDR516c
|
EMI2 |
|
0.357
|
| Non-essential protein of unknown function required for transcriptional induction of the early meiotic-specific transcription factor IME1, also required for sporulation |
|
YLR068w
|
FYV7 |
|
0.357
|
| Protein of unknown function, required for survival upon exposure to K1 killer toxin; involved in processing the 35S rRNA primary transcript to generate the 20S and 27SA2 pre-rRNA transcripts |
|
YDR111c
|
|
|
0.357
|
| putative alanine transaminase (glutamyc pyruvic transaminase) |
|
YKR058w
|
GLG1 |
|
0.357
|
| glycogen synthesis initiator |
|
YOR068c
|
VAM10 |
|
0.358
|
| [Abnormal]Vacuole Morphology |
|
YOL058w
|
ARG1 |
|
0.358
|
| Arginosuccinate synthetase, catalyzes the formation of L-argininosuccinate from citrulline and L-aspartate in the arginine biosynthesis pathway: potential Cdc28p substrate |
|
YBR258c
|
SHG1 |
|
0.358
|
| Subunit of the COMPASS complex, which methylates histone H3 on lysine 4 and is required in transcriptional silencing near telomeres |
|
YDR043c
|
NRG1 |
|
0.359
|
| binds to UAS-1 in the STA1 promoter and can interact with Ssn6p|transcriptional repressor |
|
YHR003c
|
|
|
0.359
|
| Hypothetical ORF |
|
YGL232w
|
TAN1 |
|
0.359
|
| Putative tRNA acetyltransferase, RNA-binding protein required for the formation of the modified nucleoside N(4)-acetylcytidine in serine and leucine tRNAs but not required for the same modification in 18S rRNA |
|
YER167w
|
BCK2 |
|
0.359
|
| Protein rich in serine and threonine residues involved in protein kinase C signaling pathway, which controls cell integrity: overproduction suppresses pkc1 mutations |
|
YOR044w
|
|
|
0.359
|
| Hypothetical ORF |
|
YBR003w
|
COQ1 |
|
0.359
|
| hexaprenyl pyrophosphate synthetase |
|
YKL162c-A
|
|
|
0.359
|
| Similar to PIR1, PIR2 and PIR3 proteins |
|
YOL055c
|
THI20 |
|
0.359
|
| Hydroxymethylpyrimidine phosphate kinase, involved in the last steps in thiamine biosynthesis; member of a gene family with THI21 and THI22; functionally redundant with Thi21p |
|
YLR311c
|
|
|
0.360
|
| Hypothetical ORF |
|
YGR212w
|
|
|
0.360
|
| Hypothetical ORF |
|
YDR462w
|
MRPL28 |
|
0.360
|
| Mitochondrial ribosomal protein of the large subunit |
|
YBR223c
|
TDP1 |
|
0.360
|
| Tyrosine-DNA Phosphodiesterase |
|
YLR094c
|
GIS3 |
|
0.361
|
| Protein of unknown function |
|
YOL061w
|
PRS5 |
|
0.361
|
| phosphoribosylpyrophosphate synthetase (ribose-phosphate pyrophosphokinase) |
|
YPR141c
|
KAR3 |
|
0.361
|
| Minus-end-directed microtubule motor that functions in mitosis and meiosis, localizes to the spindle pole body and localization is dependent on functional Cik1p, required for nuclear fusion during mating: potential Cdc28p substrate |
|
YFL019c
|
|
|
0.361
|
| Hypothetical ORF |
|
YDR096w
|
GIS1 |
|
0.361
|
| zinc finger protein (putative) |
|
YOR186w
|
|
|
0.361
|
| Hypothetical ORF |
|
YEL029c
|
BUD16 |
|
0.361
|
| Protein involved in bud-site selection; diploid mutants display a random budding pattern instead of the wild-type bipolar pattern; has similarity to pyridoxal kinases |
|
YEL004w
|
YEA4 |
|
0.362
|
| Shows sequence similarity to GOG5, a gene involved in vanadate resistance |
|
YFL034w
|
|
|
0.362
|
| Hypothetical ORF |
|
YDR116c
|
MRPL1 |
|
0.362
|
| Mitochondrial ribosomal protein of the large subunit |
|
YJL051w
|
|
|
0.363
|
| Protein of unknown function, localized to the bud tip; mRNA is targeted to the bud via the mRNA transport system involving She2p |
|
YKL087c
|
CYT2 |
|
0.363
|
| cytochrome c1 heme lyase (CC1HL) |
|
YNR014w
|
|
|
0.363
|
| Hypothetical ORF |
|
YBR203w
|
COS111 |
|
0.363
|
| Protein required for wild-type resistance to the antifungal drug ciclopirox olamine; not related to the COS family of subtelomerically-encoded proteins |
|
YJL162c
|
JJJ2 |
|
0.363
|
| Protein that may function as a cochaperone, as suggested by the presence of a DnaJ-like domain |
|
YOR018w
|
ROD1 |
|
0.364
|
| Membrane protein; overexpression confers resistance to the GST substrate o-dinitrobenzene as well as to zinc and calcium; contains a PY-motif, which is required for Rod1p interaction with Rsp5p, a hect-type ubiquitin ligase |
|
YGL094c
|
PAN2 |
|
0.364
|
| poly(A) ribonuclease 135 kDa subunit |
