Mitochondrial protein, mitochondrial edited mRNA stability factor 1 subunit Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.507 |
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.332 |
CLV_PCSK_FUR_1 | 599 | 603 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.368 |
CLV_PCSK_PC7_1 | 637 | 643 | PF00082 | 0.449 |
CLV_PCSK_PC7_1 | 74 | 80 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.169 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.371 |
CLV_Separin_Metazoa | 265 | 269 | PF03568 | 0.516 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.393 |
DEG_ODPH_VHL_1 | 416 | 427 | PF01847 | 0.476 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.383 |
DOC_CYCLIN_RxL_1 | 329 | 338 | PF00134 | 0.301 |
DOC_MAPK_gen_1 | 119 | 128 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 544 | 551 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 601 | 610 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 641 | 649 | PF00069 | 0.308 |
DOC_MAPK_HePTP_8 | 105 | 117 | PF00069 | 0.315 |
DOC_MAPK_MEF2A_6 | 108 | 117 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 544 | 551 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 586 | 595 | PF00069 | 0.332 |
DOC_PP1_RVXF_1 | 330 | 337 | PF00149 | 0.260 |
DOC_PP1_RVXF_1 | 506 | 512 | PF00149 | 0.456 |
DOC_PP2B_LxvP_1 | 212 | 215 | PF13499 | 0.364 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.496 |
DOC_PP2B_PxIxI_1 | 112 | 118 | PF00149 | 0.294 |
DOC_PP4_FxxP_1 | 255 | 258 | PF00568 | 0.358 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.486 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 490 | 494 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 617 | 625 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 641 | 649 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.398 |
LIG_Actin_RPEL_3 | 115 | 134 | PF02755 | 0.293 |
LIG_Actin_WH2_2 | 13 | 31 | PF00022 | 0.498 |
LIG_APCC_ABBA_1 | 126 | 131 | PF00400 | 0.334 |
LIG_APCC_ABBA_1 | 333 | 338 | PF00400 | 0.244 |
LIG_APCC_ABBAyCdc20_2 | 332 | 338 | PF00400 | 0.264 |
LIG_CtBP_PxDLS_1 | 174 | 180 | PF00389 | 0.448 |
LIG_deltaCOP1_diTrp_1 | 135 | 144 | PF00928 | 0.446 |
LIG_deltaCOP1_diTrp_1 | 471 | 475 | PF00928 | 0.324 |
LIG_EH_1 | 345 | 349 | PF12763 | 0.317 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.402 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.332 |
LIG_GBD_Chelix_1 | 580 | 588 | PF00786 | 0.402 |
LIG_LIR_Apic_2 | 252 | 258 | PF02991 | 0.361 |
LIG_LIR_Apic_2 | 379 | 384 | PF02991 | 0.559 |
LIG_LIR_Apic_2 | 471 | 477 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 345 | 356 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 446 | 457 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 470 | 480 | PF02991 | 0.315 |
LIG_LIR_LC3C_4 | 578 | 582 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 644 | 649 | PF02991 | 0.370 |
LIG_LYPXL_yS_3 | 315 | 318 | PF13949 | 0.315 |
LIG_MAD2 | 652 | 660 | PF02301 | 0.444 |
LIG_PCNA_PIPBox_1 | 264 | 273 | PF02747 | 0.386 |
LIG_PCNA_PIPBox_1 | 99 | 108 | PF02747 | 0.364 |
LIG_PCNA_yPIPBox_3 | 261 | 271 | PF02747 | 0.471 |
LIG_PCNA_yPIPBox_3 | 323 | 334 | PF02747 | 0.366 |
LIG_PCNA_yPIPBox_3 | 92 | 106 | PF02747 | 0.373 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.241 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.280 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.557 |
LIG_SH2_GRB2like | 474 | 477 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 499 | 503 | PF00017 | 0.309 |
LIG_SH2_NCK_1 | 561 | 565 | PF00017 | 0.499 |
LIG_SH2_SRC | 499 | 502 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 668 | 672 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.234 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 646 | 649 | PF00017 | 0.379 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.290 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.483 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.320 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.343 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.345 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.435 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.465 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.308 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.429 |
LIG_TYR_ITIM | 148 | 153 | PF00017 | 0.241 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.605 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.594 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.642 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.486 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.419 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.396 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.503 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.343 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.720 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.609 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.402 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.663 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.710 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.604 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.548 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.416 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.537 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.418 |
MOD_GlcNHglycan | 655 | 659 | PF01048 | 0.394 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.307 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.644 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.631 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.519 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.644 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.411 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.433 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.373 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.534 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.472 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.400 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.349 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.393 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.539 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.411 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.347 |
MOD_NEK2_2 | 67 | 72 | PF00069 | 0.500 |
MOD_NEK2_2 | 73 | 78 | PF00069 | 0.453 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.575 |
MOD_PK_1 | 282 | 288 | PF00069 | 0.629 |
MOD_PKA_1 | 641 | 647 | PF00069 | 0.414 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.591 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.542 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.541 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.535 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.435 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.399 |
MOD_PKA_2 | 641 | 647 | PF00069 | 0.346 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.459 |
MOD_PKB_1 | 308 | 316 | PF00069 | 0.417 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.629 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.320 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.505 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.430 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.412 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.357 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.301 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.309 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.558 |
MOD_SUMO_for_1 | 260 | 263 | PF00179 | 0.425 |
MOD_SUMO_rev_2 | 32 | 37 | PF00179 | 0.380 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.356 |
TRG_DiLeu_BaEn_1 | 338 | 343 | PF01217 | 0.364 |
TRG_DiLeu_BaEn_4 | 460 | 466 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_4 | 483 | 489 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 599 | 602 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 641 | 643 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.330 |
TRG_NES_CRM1_1 | 583 | 594 | PF08389 | 0.207 |
TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 435 | 439 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 652 | 656 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7Z6 | Leptomonas seymouri | 70% | 92% |
A0A0S4IW89 | Bodo saltans | 35% | 100% |
A0A1X0P3U7 | Trypanosomatidae | 50% | 93% |
A0A3S7X701 | Leishmania donovani | 100% | 100% |
A0A422P030 | Trypanosoma rangeli | 52% | 96% |
A4HLW2 | Leishmania braziliensis | 87% | 100% |
D0A659 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 91% |
E9B490 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q3T6 | Leishmania major | 95% | 100% |
V5BP67 | Trypanosoma cruzi | 50% | 98% |