STRINGSTRING
F4RKD9_MELLP F4RKD9_MELLP F4RK62_MELLP F4RK62_MELLP F4RJT8_MELLP F4RJT8_MELLP F4RJP3_MELLP F4RJP3_MELLP F4RJM2_MELLP F4RJM2_MELLP F4RJK5_MELLP F4RJK5_MELLP F4RJG7_MELLP F4RJG7_MELLP F4RJG6_MELLP F4RJG6_MELLP F4RJ38_MELLP F4RJ38_MELLP SUS1 SUS1 F4RIT2_MELLP F4RIT2_MELLP F4RIL9_MELLP F4RIL9_MELLP F4RIL3_MELLP F4RIL3_MELLP F4RHX2_MELLP F4RHX2_MELLP F4RHN7_MELLP F4RHN7_MELLP F4RHJ3_MELLP F4RHJ3_MELLP F4RG78_MELLP F4RG78_MELLP F4RFW4_MELLP F4RFW4_MELLP F4RFS7_MELLP F4RFS7_MELLP F4RFN8_MELLP F4RFN8_MELLP F4RFN0_MELLP F4RFN0_MELLP F4RFA9_MELLP F4RFA9_MELLP F4REB0_MELLP F4REB0_MELLP F4RDR3_MELLP F4RDR3_MELLP F4RDQ3_MELLP F4RDQ3_MELLP F4RDE5_MELLP F4RDE5_MELLP F4RD78_MELLP F4RD78_MELLP F4RD40_MELLP F4RD40_MELLP F4RD26_MELLP F4RD26_MELLP F4RCT5_MELLP F4RCT5_MELLP F4RCB7_MELLP F4RCB7_MELLP F4RBY7_MELLP F4RBY7_MELLP F4RBY4_MELLP F4RBY4_MELLP F4RBH3_MELLP F4RBH3_MELLP F4RB35_MELLP F4RB35_MELLP F4RB28_MELLP F4RB28_MELLP F4RB26_MELLP F4RB26_MELLP F4RAS5_MELLP F4RAS5_MELLP F4RAE0_MELLP F4RAE0_MELLP F4RA27_MELLP F4RA27_MELLP F4RA15_MELLP F4RA15_MELLP F4R9Z0_MELLP F4R9Z0_MELLP F4R9S1_MELLP F4R9S1_MELLP F4R9B6_MELLP F4R9B6_MELLP F4R9B5_MELLP F4R9B5_MELLP F4R997_MELLP F4R997_MELLP F4R926_MELLP F4R926_MELLP F4R924_MELLP F4R924_MELLP F4R8Y9_MELLP F4R8Y9_MELLP F4R8Y0_MELLP F4R8Y0_MELLP F4R8P6_MELLP F4R8P6_MELLP F4R8G7_MELLP F4R8G7_MELLP F4R8B1_MELLP F4R8B1_MELLP F4R885_MELLP F4R885_MELLP F4R7Z5_MELLP F4R7Z5_MELLP F4R7Z4_MELLP F4R7Z4_MELLP F4R7Q0_MELLP F4R7Q0_MELLP F4R7H6_MELLP F4R7H6_MELLP F4R7G7_MELLP F4R7G7_MELLP KAE1 KAE1 F4R722_MELLP F4R722_MELLP F4R708_MELLP F4R708_MELLP F4R6Y0_MELLP F4R6Y0_MELLP F4R6V8_MELLP F4R6V8_MELLP F4R6V5_MELLP F4R6V5_MELLP F4R6R7_MELLP F4R6R7_MELLP F4R6G2_MELLP F4R6G2_MELLP F4R6F7_MELLP F4R6F7_MELLP F4R699_MELLP F4R699_MELLP F4R681_MELLP F4R681_MELLP F4R664_MELLP F4R664_MELLP F4R603_MELLP F4R603_MELLP F4R5Q8_MELLP F4R5Q8_MELLP F4R5J2_MELLP F4R5J2_MELLP F4R5C8_MELLP F4R5C8_MELLP F4R5A3_MELLP F4R5A3_MELLP F4R509_MELLP F4R509_MELLP F4R508_MELLP F4R508_MELLP F4R4Y8_MELLP F4R4Y8_MELLP F4R4P7_MELLP F4R4P7_MELLP F4R4M3_MELLP F4R4M3_MELLP F4R4I3_MELLP F4R4I3_MELLP F4R4F2_MELLP F4R4F2_MELLP F4R4D7_MELLP F4R4D7_MELLP F4R467_MELLP F4R467_MELLP F4R3N8_MELLP F4R3N8_MELLP F4SEM0_MELLP F4SEM0_MELLP F4SEL5_MELLP F4SEL5_MELLP F4SDC2_MELLP F4SDC2_MELLP F4SD89_MELLP F4SD89_MELLP F4SD41_MELLP F4SD41_MELLP F4SC58_MELLP F4SC58_MELLP F4SBM1_MELLP F4SBM1_MELLP F4SBE1_MELLP F4SBE1_MELLP F4SB49_MELLP F4SB49_MELLP F4SAZ5_MELLP F4SAZ5_MELLP F4SAP2_MELLP F4SAP2_MELLP F4SAK6_MELLP F4SAK6_MELLP F4SA54_MELLP F4SA54_MELLP F4S9Z2_MELLP F4S9Z2_MELLP F4S9Y2_MELLP F4S9Y2_MELLP F4S9W5_MELLP F4S9W5_MELLP F4S9S5_MELLP F4S9S5_MELLP F4S986_MELLP F4S986_MELLP F4S968_MELLP F4S968_MELLP F4S8Z4_MELLP F4S8Z4_MELLP F4S8Z1_MELLP F4S8Z1_MELLP F4S8X8_MELLP F4S8X8_MELLP F4S8Q2_MELLP F4S8Q2_MELLP F4S8K2_MELLP F4S8K2_MELLP F4S8G9_MELLP F4S8G9_MELLP F4S824_MELLP F4S824_MELLP F4S7X9_MELLP F4S7X9_MELLP F4S7X8_MELLP F4S7X8_MELLP F4S7W4_MELLP F4S7W4_MELLP F4S7V8_MELLP F4S7V8_MELLP F4S7G9_MELLP F4S7G9_MELLP F4S7G5_MELLP F4S7G5_MELLP F4S7G4_MELLP F4S7G4_MELLP F4S771_MELLP F4S771_MELLP F4S6W4_MELLP F4S6W4_MELLP F4S6J2_MELLP F4S6J2_MELLP F4S694_MELLP F4S694_MELLP F4S673_MELLP F4S673_MELLP F4S650_MELLP F4S650_MELLP F4S631_MELLP F4S631_MELLP F4S620_MELLP F4S620_MELLP MED10 MED10 F4S5Y3_MELLP F4S5Y3_MELLP F4S5X0_MELLP F4S5X0_MELLP F4S5W0_MELLP F4S5W0_MELLP F4S5Q2_MELLP F4S5Q2_MELLP F4S5Q0_MELLP F4S5Q0_MELLP F4S5N3_MELLP F4S5N3_MELLP F4S5L5_MELLP F4S5L5_MELLP F4S5K3_MELLP F4S5K3_MELLP MED6 MED6 F4S4T1_MELLP F4S4T1_MELLP F4S4G8_MELLP F4S4G8_MELLP F4S3X2_MELLP F4S3X2_MELLP F4S3T6_MELLP F4S3T6_MELLP F4S3L2_MELLP F4S3L2_MELLP F4S387_MELLP F4S387_MELLP F4S367_MELLP F4S367_MELLP F4S2S4_MELLP F4S2S4_MELLP F4S2H6_MELLP F4S2H6_MELLP F4S2H0_MELLP F4S2H0_MELLP F4S2G0_MELLP F4S2G0_MELLP F4S2F9_MELLP F4S2F9_MELLP F4S2E8_MELLP F4S2E8_MELLP F4S221_MELLP F4S221_MELLP F4S1Y3_MELLP F4S1Y3_MELLP F4S1X0_MELLP F4S1X0_MELLP F4S1P6_MELLP F4S1P6_MELLP F4S1K7_MELLP F4S1K7_MELLP F4S1F3_MELLP F4S1F3_MELLP F4S1B7_MELLP F4S1B7_MELLP F4S1B5_MELLP F4S1B5_MELLP F4S1B4_MELLP F4S1B4_MELLP F4S1B1_MELLP F4S1B1_MELLP F4S186_MELLP F4S186_MELLP F4S118_MELLP F4S118_MELLP F4S114_MELLP F4S114_MELLP F4S0T4_MELLP F4S0T4_MELLP F4S0K6_MELLP F4S0K6_MELLP F4S093_MELLP F4S093_MELLP F4S085_MELLP F4S085_MELLP F4S023_MELLP F4S023_MELLP F4RZV5_MELLP F4RZV5_MELLP F4RZU5_MELLP F4RZU5_MELLP F4RZU4_MELLP F4RZU4_MELLP F4RZK2_MELLP F4RZK2_MELLP F4RZG4_MELLP F4RZG4_MELLP F4RZF3_MELLP F4RZF3_MELLP F4RZD0_MELLP F4RZD0_MELLP F4RZA7_MELLP F4RZA7_MELLP F4RZ36_MELLP F4RZ36_MELLP F4RZ35_MELLP F4RZ35_MELLP F4RYV6_MELLP F4RYV6_MELLP F4RYV5_MELLP F4RYV5_MELLP F4RYV2_MELLP F4RYV2_MELLP F4RYV1_MELLP F4RYV1_MELLP F4RY07_MELLP F4RY07_MELLP F4RXN2_MELLP F4RXN2_MELLP F4RXF6_MELLP F4RXF6_MELLP F4RXF0_MELLP F4RXF0_MELLP F4RXE3_MELLP F4RXE3_MELLP F4RXE2_MELLP F4RXE2_MELLP F4RX98_MELLP F4RX98_MELLP F4RX17_MELLP F4RX17_MELLP F4RWY5_MELLP F4RWY5_MELLP F4RWX1_MELLP F4RWX1_MELLP F4RWS4_MELLP F4RWS4_MELLP F4RWF1_MELLP F4RWF1_MELLP F4RW68_MELLP F4RW68_MELLP F4RVU9_MELLP F4RVU9_MELLP F4RVI7_MELLP F4RVI7_MELLP F4RVB5_MELLP F4RVB5_MELLP F4RUL9_MELLP F4RUL9_MELLP PAN2 PAN2 F4RUI0_MELLP F4RUI0_MELLP F4RUH5_MELLP F4RUH5_MELLP F4RUF1_MELLP F4RUF1_MELLP F4RUC4_MELLP F4RUC4_MELLP F4RUC3_MELLP F4RUC3_MELLP F4RU01_MELLP F4RU01_MELLP F4RTX5_MELLP F4RTX5_MELLP F4RTU8_MELLP F4RTU8_MELLP F4RTU4_MELLP F4RTU4_MELLP F4RTS5_MELLP F4RTS5_MELLP F4RTQ9_MELLP F4RTQ9_MELLP F4RTQ4_MELLP F4RTQ4_MELLP F4RTM4_MELLP F4RTM4_MELLP F4RTJ9_MELLP F4RTJ9_MELLP F4RTH6_MELLP F4RTH6_MELLP F4RTC1_MELLP F4RTC1_MELLP F4RTB0_MELLP F4RTB0_MELLP F4RT31_MELLP F4RT31_MELLP F4RT05_MELLP F4RT05_MELLP F4RSU9_MELLP F4RSU9_MELLP F4RSU0_MELLP F4RSU0_MELLP F4RSH7_MELLP F4RSH7_MELLP F4RSC3_MELLP F4RSC3_MELLP F4RRW8_MELLP F4RRW8_MELLP F4RRS3_MELLP F4RRS3_MELLP F4RRI9_MELLP F4RRI9_MELLP F4RRF2_MELLP F4RRF2_MELLP F4RQZ4_MELLP F4RQZ4_MELLP F4RQL4_MELLP F4RQL4_MELLP F4RQ77_MELLP F4RQ77_MELLP F4RPW9_MELLP F4RPW9_MELLP F4RPD8_MELLP F4RPD8_MELLP F4RPA4_MELLP F4RPA4_MELLP F4RP79_MELLP F4RP79_MELLP F4RP78_MELLP F4RP78_MELLP F4RP77_MELLP F4RP77_MELLP F4RP53_MELLP F4RP53_MELLP F4RP25_MELLP F4RP25_MELLP F4RNW0_MELLP F4RNW0_MELLP LSM1 LSM1 F4RNS4_MELLP F4RNS4_MELLP F4RNL8_MELLP F4RNL8_MELLP F4RNK6_MELLP F4RNK6_MELLP F4RNF7_MELLP F4RNF7_MELLP F4RNB4_MELLP F4RNB4_MELLP F4RNA3_MELLP F4RNA3_MELLP F4RN16_MELLP F4RN16_MELLP F4RMX8_MELLP F4RMX8_MELLP F4RMD6_MELLP F4RMD6_MELLP F4RMA9_MELLP F4RMA9_MELLP F4RLY3_MELLP F4RLY3_MELLP F4RLN6_MELLP F4RLN6_MELLP F4RLE3_MELLP F4RLE3_MELLP F4RK98_MELLP F4RK98_MELLP
Nodes:
Network nodes represent proteins
splice isoforms or post-translational modifications are collapsed, i.e. each node represents all the proteins produced by a single, protein-coding gene locus.
Node Color
colored nodes:
query proteins and first shell of interactors
white nodes:
second shell of interactors
Node Content
empty nodes:
proteins of unknown 3D structure
filled nodes:
a 3D structure is known or predicted
Edges:
Edges represent protein-protein associations
associations are meant to be specific and meaningful, i.e. proteins jointly contribute to a shared function; this does not necessarily mean they are physically binding to each other.
Known Interactions
from curated databases
experimentally determined
Predicted Interactions
gene neighborhood
gene fusions
gene co-occurrence
Others
textmining
co-expression
protein homology
Your Input:
F4RKD9_MELLPUncharacterized protein. (1336 aa)
F4RK62_MELLPSGF29 C-terminal domain-containing protein. (323 aa)
F4RJT8_MELLPCBFD_NFYB_HMF domain-containing protein. (143 aa)
F4RJP3_MELLPUncharacterized protein. (1199 aa)
F4RJM2_MELLPSCA7 domain-containing protein. (474 aa)
F4RJK5_MELLPBZIP domain-containing protein. (334 aa)
F4RJG7_MELLPUncharacterized protein. (101 aa)
F4RJG6_MELLPUncharacterized protein. (229 aa)
F4RJ38_MELLPWD_REPEATS_REGION domain-containing protein. (315 aa)
SUS1Transcription and mRNA export factor SUS1; Involved in mRNA export coupled transcription activation by association with both the TREX-2 and the SAGA complexes. At the promoters, SAGA is required for recruitment of the basal transcription machinery. It influences RNA polymerase II transcriptional activity through different activities such as TBP interaction and promoter selectivity, interaction with transcription activators, and chromatin modification through histone acetylation and deubiquitination. Within the SAGA complex, participates to a subcomplex required for deubiquitination of [...] (129 aa)
F4RIT2_MELLPCID domain-containing protein. (388 aa)
F4RIL9_MELLPUncharacterized protein. (153 aa)
F4RIL3_MELLPUncharacterized protein. (186 aa)
F4RHX2_MELLPUncharacterized protein. (209 aa)
F4RHN7_MELLPUncharacterized protein. (298 aa)
F4RHJ3_MELLPRNase_PH domain-containing protein. (285 aa)
F4RG78_MELLPHTH cro/C1-type domain-containing protein. (149 aa)
F4RFW4_MELLPFork-head domain-containing protein. (83 aa)
F4RFS7_MELLPBromo domain-containing protein. (667 aa)
F4RFN8_MELLPUncharacterized protein. (1078 aa)
F4RFN0_MELLPUncharacterized protein; Belongs to the cyclin family. (493 aa)
F4RFA9_MELLPUncharacterized protein. (966 aa)
F4REB0_MELLPUncharacterized protein. (220 aa)
F4RDR3_MELLPAcyl_transf_3 domain-containing protein. (488 aa)
F4RDQ3_MELLPUncharacterized protein. (711 aa)
F4RDE5_MELLPSerine/threonine-protein phosphatase. (316 aa)
F4RD78_MELLPRRM domain-containing protein. (304 aa)
F4RD40_MELLPTAF domain-containing protein. (562 aa)
F4RD26_MELLPProtein kinase domain-containing protein; Belongs to the protein kinase superfamily. (387 aa)
F4RCT5_MELLPUncharacterized protein. (676 aa)
F4RCB7_MELLPUncharacterized protein. (656 aa)
F4RBY7_MELLPUncharacterized protein. (984 aa)
F4RBY4_MELLPPeptidase_M50 domain-containing protein. (728 aa)
F4RBH3_MELLPUncharacterized protein. (454 aa)
F4RB35_MELLPUncharacterized protein. (558 aa)
F4RB28_MELLPUncharacterized protein. (290 aa)
F4RB26_MELLPHMG box domain-containing protein. (983 aa)
F4RAS5_MELLPUncharacterized protein. (91 aa)
F4RAE0_MELLPAmino_oxidase domain-containing protein. (586 aa)
F4RA27_MELLPHistone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. (460 aa)
F4RA15_MELLPDBF4-type domain-containing protein. (707 aa)
F4R9Z0_MELLPRING-type domain-containing protein. (483 aa)
F4R9S1_MELLPUncharacterized protein. (310 aa)
F4R9B6_MELLPCleavage and polyadenylation specificity factor subunit 5; Component of the cleavage factor Im (CFIm) complex that functions as an activator of the pre-mRNA 3'-end cleavage and polyadenylation processing required for the maturation of pre-mRNA into functional mRNAs. CFIm contributes to the recruitment of multiprotein complexes on specific sequences on the pre-mRNA 3'-end, so called cleavage and polyadenylation signals (pA signals). Most pre-mRNAs contain multiple pA signals, resulting in alternative cleavage and polyadenylation (APA) producing mRNAs with variable 3'-end formation. The [...] (205 aa)
F4R9B5_MELLPCBFD_NFYB_HMF domain-containing protein. (94 aa)
F4R997_MELLPPHD-type domain-containing protein. (1472 aa)
F4R926_MELLPFe2OG dioxygenase domain-containing protein. (565 aa)
F4R924_MELLPUncharacterized protein. (286 aa)
F4R8Y9_MELLPUncharacterized protein; Belongs to the eukaryotic ribosomal protein P1/P2 family. (108 aa)
F4R8Y0_MELLPWW domain-containing protein. (1017 aa)
F4R8P6_MELLPARID domain-containing protein. (1708 aa)
F4R8G7_MELLPMitochondrial processing peptidase. (531 aa)
F4R8B1_MELLPRNase_PH domain-containing protein. (292 aa)
F4R885_MELLPUncharacterized protein. (67 aa)
F4R7Z5_MELLPUncharacterized protein. (1138 aa)
F4R7Z4_MELLPProteasome subunit beta. (201 aa)
F4R7Q0_MELLPUncharacterized protein. (136 aa)
F4R7H6_MELLPUncharacterized protein. (144 aa)
F4R7G7_MELLPPA28_beta domain-containing protein. (132 aa)
KAE1tRNA N6-adenosine threonylcarbamoyltransferase; Component of the EKC/KEOPS complex that is required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. The complex is probably involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37. KAE1 likely plays a direct catalytic role in this reaction, but requires other protein(s) of the complex to fulfill this activity. The EKC/KEOPS complex also promotes both telomere uncapping and telomere elongation. Th [...] (367 aa)
F4R722_MELLPzf-C2HC5 domain-containing protein. (524 aa)
F4R708_MELLPPITH domain-containing protein. (174 aa)
F4R6Y0_MELLPUncharacterized protein. (511 aa)
F4R6V8_MELLPCyclin-dependent kinases regulatory subunit; Binds to the catalytic subunit of the cyclin dependent kinases and is essential for their biological function. (98 aa)
F4R6V5_MELLPUsp domain-containing protein. (608 aa)
F4R6R7_MELLPUncharacterized protein. (1926 aa)
F4R6G2_MELLPUncharacterized protein. (1027 aa)
F4R6F7_MELLPRBR-type E3 ubiquitin transferase. (521 aa)
F4R699_MELLPEndo/exonuclease/phosphatase domain-containing protein. (556 aa)
F4R681_MELLPUncharacterized protein. (1308 aa)
F4R664_MELLPUncharacterized protein. (1315 aa)
F4R603_MELLPWD_REPEATS_REGION domain-containing protein. (577 aa)
F4R5Q8_MELLPProtein phosphatase PP2A regulatory subunit B; Belongs to the phosphatase 2A regulatory subunit B family. (454 aa)
F4R5J2_MELLPANK_REP_REGION domain-containing protein. (267 aa)
F4R5C8_MELLPProtein kinase domain-containing protein; Belongs to the protein kinase superfamily. (362 aa)
F4R5A3_MELLPUncharacterized protein. (264 aa)
F4R509_MELLPTranscription initiation factor TFIID subunit 9. (216 aa)
F4R508_MELLPPlus3 domain-containing protein. (554 aa)
F4R4Y8_MELLPUncharacterized protein; Belongs to the actin family. (695 aa)
F4R4P7_MELLPUncharacterized protein. (162 aa)
F4R4M3_MELLPExonuclease domain-containing protein. (321 aa)
F4R4I3_MELLPUncharacterized protein. (1261 aa)
F4R4F2_MELLPArf-GAP domain-containing protein. (501 aa)
F4R4D7_MELLPPUM-HD domain-containing protein. (938 aa)
F4R467_MELLPFACT complex subunit POB3; Component of the FACT complex, a general chromatin factor that acts to reorganize nucleosomes. The FACT complex is involved in multiple processes that require DNA as a template such as mRNA elongation, DNA replication and DNA repair. During transcription elongation the FACT complex acts as a histone chaperone that both destabilizes and restores nucleosomal structure. It facilitates the passage of RNA polymerase II and transcription by promoting the dissociation of one histone H2A-H2B dimer from the nucleosome, then subsequently promotes the reestablishment of [...] (529 aa)
F4R3N8_MELLPUncharacterized protein. (253 aa)
F4SEM0_MELLPHistone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. (124 aa)
F4SEL5_MELLPUncharacterized protein. (162 aa)
F4SDC2_MELLPPCNA_C domain-containing protein. (153 aa)
F4SD89_MELLPS4 RNA-binding domain-containing protein. (136 aa)
F4SD41_MELLPRING-type domain-containing protein. (156 aa)
F4SC58_MELLPU-box domain-containing protein. (898 aa)
F4SBM1_MELLPUncharacterized protein. (77 aa)
F4SBE1_MELLPTr-type G domain-containing protein. (453 aa)
F4SB49_MELLPUncharacterized protein. (556 aa)
F4SAZ5_MELLPUncharacterized protein. (219 aa)
F4SAP2_MELLPUncharacterized protein. (247 aa)
F4SAK6_MELLPUncharacterized protein. (337 aa)
F4SA54_MELLPATP-dependent 26S proteasome regulatory subunit; Belongs to the AAA ATPase family. (480 aa)
F4S9Z2_MELLPUncharacterized protein. (88 aa)
F4S9Y2_MELLPHomeobox domain-containing protein. (405 aa)
F4S9W5_MELLPPUM-HD domain-containing protein. (370 aa)
F4S9S5_MELLPPI3K/PI4K domain-containing protein; Belongs to the PI3/PI4-kinase family. (92 aa)
F4S986_MELLPHist_deacetyl domain-containing protein. (659 aa)
F4S968_MELLPSWIB domain-containing protein. (452 aa)
F4S8Z4_MELLPHORMA domain-containing protein. (171 aa)
F4S8Z1_MELLPUncharacterized protein. (287 aa)
F4S8X8_MELLPNudix hydrolase domain-containing protein. (293 aa)
F4S8Q2_MELLPUncharacterized protein. (759 aa)
F4S8K2_MELLPUncharacterized protein. (772 aa)
F4S8G9_MELLPTranscription initiation factor IIA subunit 2; TFIIA is a component of the transcription machinery of RNA polymerase II and plays an important role in transcriptional activation; Belongs to the TFIIA subunit 2 family. (122 aa)
F4S824_MELLPProtein kinase domain-containing protein; Belongs to the protein kinase superfamily. (247 aa)
F4S7X9_MELLPUncharacterized protein. (226 aa)
F4S7X8_MELLPUncharacterized protein. (665 aa)
F4S7W4_MELLPMed12 domain-containing protein. (1895 aa)
F4S7V8_MELLPUncharacterized protein. (306 aa)
F4S7G9_MELLPPan3_PK domain-containing protein. (493 aa)
F4S7G5_MELLPBP28CT domain-containing protein. (1978 aa)
F4S7G4_MELLPUncharacterized protein. (123 aa)
F4S771_MELLPS4 RNA-binding domain-containing protein. (335 aa)
F4S6W4_MELLPTranscription elongation factor Spt6; Plays a role in maintenance of chromatin structure during RNA polymerase II transcription elongation thereby repressing transcription initiation from cryptic promoters. Mediates the reassembly of nucleosomes onto the promoters of at least a selected set of genes during repression; the nucleosome reassembly is essential for transcriptional repression; Belongs to the SPT6 family. (1598 aa)
F4S6J2_MELLPProtein kinase domain-containing protein. (326 aa)
F4S694_MELLPUncharacterized protein. (959 aa)
F4S673_MELLPRNase_PH domain-containing protein. (252 aa)
F4S650_MELLPCBFD_NFYB_HMF domain-containing protein. (87 aa)
F4S631_MELLPCCHC-type domain-containing protein. (406 aa)
F4S620_MELLPRING-type domain-containing protein. (171 aa)
MED10Mediator of RNA polymerase II transcription subunit 10; Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene- specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors. (196 aa)
F4S5Y3_MELLPUncharacterized protein. (621 aa)
F4S5X0_MELLPUncharacterized protein. (133 aa)
F4S5W0_MELLPUncharacterized protein. (1095 aa)
F4S5Q2_MELLPCBFD_NFYB_HMF domain-containing protein. (154 aa)
F4S5Q0_MELLPTr-type G domain-containing protein. (510 aa)
F4S5N3_MELLPUncharacterized protein. (246 aa)
F4S5L5_MELLPUncharacterized protein; Belongs to the cyclin family. (411 aa)
F4S5K3_MELLPAAA ATPase. (745 aa)
MED6Mediator of RNA polymerase II transcription subunit 6; Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene- specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors. (344 aa)
F4S4T1_MELLPPITH domain-containing protein. (216 aa)
F4S4G8_MELLPATP-dependent 26S proteasome regulatory subunit; Belongs to the AAA ATPase family. (413 aa)
F4S3X2_MELLPUncharacterized protein. (301 aa)
F4S3T6_MELLPTranscription elongation factor SPT4; The SPT4-SPT5 complex mediates both activation and inhibition of transcription elongation, and plays a role in pre-mRNA processing. This complex seems to be important for the stability of the RNA polymerase II elongation machinery on the chromatin template but not for the inherent ability of this machinery to translocate down the gene. (107 aa)
F4S3L2_MELLPWD_REPEATS_REGION domain-containing protein. (676 aa)
F4S387_MELLPPITH domain-containing protein. (216 aa)
F4S367_MELLPSAM domain-containing protein. (813 aa)
F4S2S4_MELLPPeptidyl-prolyl cis-trans isomerase. (188 aa)
F4S2H6_MELLPMADS-box domain-containing protein. (58 aa)
F4S2H0_MELLPUncharacterized protein. (304 aa)
F4S2G0_MELLPProliferating cell nuclear antigen; This protein is an auxiliary protein of DNA polymerase delta and is involved in the control of eukaryotic DNA replication by increasing the polymerase's processibility during elongation of the leading strand; Belongs to the PCNA family. (261 aa)
F4S2F9_MELLPS1 motif domain-containing protein. (172 aa)
F4S2E8_MELLPTr-type G domain-containing protein. (678 aa)
F4S221_MELLPAcyl_transf_3 domain-containing protein. (431 aa)
F4S1Y3_MELLPUncharacterized protein. (454 aa)
F4S1X0_MELLPUncharacterized protein. (295 aa)
F4S1P6_MELLPMADS-box domain-containing protein. (201 aa)
F4S1K7_MELLPCDC73_C domain-containing protein. (407 aa)
F4S1F3_MELLPRPN13_C domain-containing protein. (286 aa)
F4S1B7_MELLPOTU domain-containing protein. (313 aa)
F4S1B5_MELLPOTU domain-containing protein. (439 aa)
F4S1B4_MELLPUncharacterized protein. (551 aa)
F4S1B1_MELLPOTU domain-containing protein. (274 aa)
F4S186_MELLPUncharacterized protein. (211 aa)
F4S118_MELLPUncharacterized protein. (748 aa)
F4S114_MELLPeIF-5a domain-containing protein. (188 aa)
F4S0T4_MELLPUncharacterized protein. (247 aa)
F4S0K6_MELLPTPR_REGION domain-containing protein. (399 aa)
F4S093_MELLPPAT1 domain-containing protein. (954 aa)
F4S085_MELLPATP-dependent 26S proteasome regulatory subunit; Belongs to the AAA ATPase family. (439 aa)
F4S023_MELLPATP-dependent 26S proteasome regulatory subunit; Belongs to the AAA ATPase family. (393 aa)
F4RZV5_MELLPCYCLIN domain-containing protein; Belongs to the cyclin family. (203 aa)
F4RZU5_MELLPPHD domain-containing protein. (53 aa)
F4RZU4_MELLPHistone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. (284 aa)
F4RZK2_MELLPPITH domain-containing protein. (205 aa)
F4RZG4_MELLPUncharacterized protein. (728 aa)
F4RZF3_MELLPUncharacterized protein. (282 aa)
F4RZD0_MELLPHORMA domain-containing protein. (230 aa)
F4RZA7_MELLPPUM-HD domain-containing protein. (325 aa)
F4RZ36_MELLPJmjN domain-containing protein. (105 aa)
F4RZ35_MELLPJmjC domain-containing protein. (194 aa)
F4RYV6_MELLPUncharacterized protein. (345 aa)
F4RYV5_MELLPFACT-Spt16_Nlob domain-containing protein. (586 aa)
F4RYV2_MELLPFACT-Spt16_Nlob domain-containing protein. (166 aa)
F4RYV1_MELLPPeptidase_M24 domain-containing protein. (674 aa)
F4RY07_MELLPUncharacterized protein. (63 aa)
F4RXN2_MELLPUncharacterized protein; Belongs to the PI3/PI4-kinase family. (1598 aa)
F4RXF6_MELLPRNase_PH domain-containing protein. (319 aa)
F4RXF0_MELLPUncharacterized protein. (364 aa)
F4RXE3_MELLPC2H2-type domain-containing protein. (401 aa)
F4RXE2_MELLPUncharacterized protein. (67 aa)
F4RX98_MELLPUsp domain-containing protein. (593 aa)
F4RX17_MELLPYTH domain-containing protein. (207 aa)
F4RWY5_MELLPJmjC domain-containing protein. (486 aa)
F4RWX1_MELLPDefective in cullin neddylation protein; Neddylation of cullins play an essential role in the regulation of SCF-type complexes activity. (355 aa)
F4RWS4_MELLPS4 RNA-binding domain-containing protein. (182 aa)
F4RWF1_MELLPANK_REP_REGION domain-containing protein. (1421 aa)
F4RW68_MELLPAcyl_transf_3 domain-containing protein. (473 aa)
F4RVU9_MELLPUncharacterized protein. (2290 aa)
F4RVI7_MELLPUncharacterized protein. (670 aa)
F4RVB5_MELLPUncharacterized protein. (392 aa)
F4RUL9_MELLPBHLH domain-containing protein. (405 aa)
PAN2PAN2-PAN3 deadenylation complex catalytic subunit PAN2; Catalytic subunit of the poly(A)-nuclease (PAN) deadenylation complex, one of two cytoplasmic mRNA deadenylases involved in mRNA turnover. PAN specifically shortens poly(A) tails of RNA and the activity is stimulated by poly(A)-binding protein PAB1. PAN deadenylation is followed by rapid degradation of the shortened mRNA tails by the CCR4-NOT complex. Deadenylated mRNAs are then degraded by two alternative mechanisms, namely exosome-mediated 3'-5' exonucleolytic degradation, or deadenlyation-dependent mRNA decaping and subsequent [...] (1214 aa)
F4RUI0_MELLPKH_dom_type_1 domain-containing protein. (143 aa)
F4RUH5_MELLPUncharacterized protein. (1346 aa)
F4RUF1_MELLPUfd2P_core domain-containing protein. (146 aa)
F4RUC4_MELLPUncharacterized protein. (545 aa)
F4RUC3_MELLPAcyl_transf_3 domain-containing protein. (492 aa)
F4RU01_MELLPTAFII28 domain-containing protein. (227 aa)
F4RTX5_MELLPTr-type G domain-containing protein. (764 aa)
F4RTU8_MELLPFork-head domain-containing protein. (98 aa)
F4RTU4_MELLPPA28_beta domain-containing protein. (287 aa)
F4RTS5_MELLPUncharacterized protein. (249 aa)
F4RTQ9_MELLPSmg4_UPF3 domain-containing protein. (460 aa)
F4RTQ4_MELLPUncharacterized protein. (140 aa)
F4RTM4_MELLPNuclear pore complex protein Nup85; Functions as a component of the nuclear pore complex (NPC). (744 aa)
F4RTJ9_MELLPUncharacterized protein. (178 aa)
F4RTH6_MELLPRPOL4c domain-containing protein. (130 aa)
F4RTC1_MELLPRING-type domain-containing protein. (644 aa)
F4RTB0_MELLPUncharacterized protein. (252 aa)
F4RT31_MELLPUncharacterized protein. (803 aa)
F4RT05_MELLPUncharacterized protein. (357 aa)
F4RSU9_MELLPTranscription initiation factor IIF subunit alpha; TFIIF is a general transcription initiation factor that binds to RNA polymerase II and helps to recruit it to the initiation complex in collaboration with TFIIB. It promotes transcription elongation. Belongs to the TFIIF alpha subunit family. (700 aa)
F4RSU0_MELLPWD_REPEATS_REGION domain-containing protein. (517 aa)
F4RSH7_MELLPFork-head domain-containing protein. (1003 aa)
F4RSC3_MELLPUncharacterized protein. (712 aa)
F4RRW8_MELLPHelicase ATP-binding domain-containing protein. (795 aa)
F4RRS3_MELLPATP-dependent 26S proteasome regulatory subunit; Belongs to the AAA ATPase family. (458 aa)
F4RRI9_MELLPUncharacterized protein. (120 aa)
F4RRF2_MELLPcAMP-dependent protein kinase regulatory subunit. (360 aa)
F4RQZ4_MELLPATP-dependent 26S proteasome regulatory subunit; Belongs to the AAA ATPase family. (408 aa)
F4RQL4_MELLPResponse regulatory domain-containing protein. (477 aa)
F4RQ77_MELLPUncharacterized protein. (286 aa)
F4RPW9_MELLPJmjC domain-containing protein. (397 aa)
F4RPD8_MELLPUncharacterized protein. (75 aa)
F4RPA4_MELLPARID domain-containing protein. (1593 aa)
F4RP79_MELLPUncharacterized protein. (742 aa)
F4RP78_MELLPUncharacterized protein. (235 aa)
F4RP77_MELLPGATA-type domain-containing protein. (150 aa)
F4RP53_MELLPSec39 domain-containing protein. (1051 aa)
F4RP25_MELLPBZIP domain-containing protein. (265 aa)
F4RNW0_MELLPFamily 41 glycosyltransferase. (313 aa)
LSM1U6 snRNA-associated Sm-like protein LSm1; Component of the cytoplasmic LSM1-LSM7 complex which is involved in mRNA degradation. (152 aa)
F4RNS4_MELLPProtein kinase domain-containing protein; Belongs to the protein kinase superfamily. (439 aa)
F4RNL8_MELLPGATA-type domain-containing protein. (71 aa)
F4RNK6_MELLPUncharacterized protein. (941 aa)
F4RNF7_MELLPWD_REPEATS_REGION domain-containing protein. (449 aa)
F4RNB4_MELLPMADS-box domain-containing protein. (819 aa)
F4RNA3_MELLPRRM domain-containing protein. (239 aa)
F4RN16_MELLPUncharacterized protein. (256 aa)
F4RMX8_MELLPPHD-type domain-containing protein. (635 aa)
F4RMD6_MELLPUncharacterized protein. (50 aa)
F4RMA9_MELLPUncharacterized protein. (92 aa)
F4RLY3_MELLPWD_REPEATS_REGION domain-containing protein. (1417 aa)
F4RLN6_MELLPTOG domain-containing protein. (2583 aa)
F4RLE3_MELLPABC transporter domain-containing protein. (563 aa)
F4RK98_MELLPUncharacterized protein; Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family. (883 aa)
Your Current Organism:
Melampsora laricipopulina
NCBI taxonomy Id: 747676
Other names: M. larici-populina 98AG31, Melampsora larici-populina 98AG31, Melampsora laricis-populina 98AG31
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