RNA Processing, U3 small nucleolar ribonucleo MPP10
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005732 | sno(s)RNA-containing ribonucleoprotein complex | 3 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
GO:0034457 | Mpp10 complex | 3 | 9 |
GO:0140513 | nuclear protein-containing complex | 2 | 9 |
GO:1990904 | ribonucleoprotein complex | 2 | 9 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I4C8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006364 | rRNA processing | 8 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0016072 | rRNA metabolic process | 7 | 9 |
GO:0034470 | ncRNA processing | 7 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034660 | ncRNA metabolic process | 6 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.367 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.557 |
CLV_PCSK_FUR_1 | 236 | 240 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.179 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.179 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 662 | 664 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 236 | 242 | PF00082 | 0.351 |
CLV_PCSK_PC7_1 | 640 | 646 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.103 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.480 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.340 |
DEG_APCC_DBOX_1 | 440 | 448 | PF00400 | 0.340 |
DEG_APCC_DBOX_1 | 53 | 61 | PF00400 | 0.409 |
DEG_MDM2_SWIB_1 | 424 | 431 | PF02201 | 0.351 |
DEG_SCF_TRCP1_1 | 231 | 237 | PF00400 | 0.190 |
DOC_MAPK_gen_1 | 438 | 447 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 511 | 519 | PF00069 | 0.248 |
DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.545 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.190 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.317 |
DOC_USP7_UBL2_3 | 186 | 190 | PF12436 | 0.288 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.226 |
DOC_USP7_UBL2_3 | 417 | 421 | PF12436 | 0.351 |
DOC_USP7_UBL2_3 | 648 | 652 | PF12436 | 0.308 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.190 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 422 | 431 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 488 | 493 | PF00244 | 0.227 |
LIG_14-3-3_CanoR_1 | 621 | 630 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 85 | 93 | PF00244 | 0.279 |
LIG_Actin_WH2_2 | 542 | 557 | PF00022 | 0.226 |
LIG_Actin_WH2_2 | 60 | 75 | PF00022 | 0.521 |
LIG_BIR_III_4 | 328 | 332 | PF00653 | 0.263 |
LIG_BRCT_BRCA1_1 | 623 | 627 | PF00533 | 0.340 |
LIG_Clathr_ClatBox_1 | 444 | 448 | PF01394 | 0.340 |
LIG_deltaCOP1_diTrp_1 | 205 | 212 | PF00928 | 0.252 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.283 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.253 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.319 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.300 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.190 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.249 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.248 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.283 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.340 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.534 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 624 | 635 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 624 | 630 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.283 |
LIG_Pex14_1 | 208 | 212 | PF04695 | 0.248 |
LIG_Pex14_2 | 424 | 428 | PF04695 | 0.283 |
LIG_PTB_Apo_2 | 446 | 453 | PF02174 | 0.351 |
LIG_PTB_Apo_2 | 569 | 576 | PF02174 | 0.248 |
LIG_PTB_Phospho_1 | 569 | 575 | PF10480 | 0.340 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.476 |
LIG_SH2_SRC | 483 | 486 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.103 |
LIG_SH2_STAT3 | 334 | 337 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.340 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.621 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.319 |
LIG_SH3_4 | 578 | 585 | PF00018 | 0.283 |
LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.340 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.342 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.292 |
LIG_TRAF2_1 | 284 | 287 | PF00917 | 0.245 |
LIG_UBA3_1 | 516 | 522 | PF00899 | 0.248 |
MOD_CDC14_SPxK_1 | 10 | 13 | PF00782 | 0.658 |
MOD_CDK_SPK_2 | 573 | 578 | PF00069 | 0.248 |
MOD_CDK_SPK_2 | 633 | 638 | PF00069 | 0.340 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.656 |
MOD_CDK_SPxxK_3 | 258 | 265 | PF00069 | 0.190 |
MOD_CDK_SPxxK_3 | 633 | 640 | PF00069 | 0.340 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.538 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.301 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.562 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.290 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.419 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.441 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.324 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.301 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.262 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.283 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.295 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.308 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.525 |
MOD_Cter_Amidation | 650 | 653 | PF01082 | 0.340 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.392 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.366 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.328 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.313 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.643 |
MOD_GlcNHglycan | 230 | 234 | PF01048 | 0.392 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.353 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.635 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.397 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.295 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.551 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.249 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.260 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.438 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.331 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.604 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.593 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.500 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.452 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.351 |
MOD_PKA_1 | 487 | 493 | PF00069 | 0.324 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.351 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.539 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.511 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.231 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.490 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.265 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.339 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.340 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.337 |
MOD_Plk_2-3 | 397 | 403 | PF00069 | 0.351 |
MOD_Plk_2-3 | 544 | 550 | PF00069 | 0.248 |
MOD_Plk_2-3 | 629 | 635 | PF00069 | 0.319 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.263 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.248 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.190 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.248 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.340 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.531 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.654 |
MOD_SUMO_for_1 | 468 | 471 | PF00179 | 0.283 |
MOD_SUMO_for_1 | 541 | 544 | PF00179 | 0.292 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.283 |
TRG_DiLeu_BaEn_3 | 419 | 425 | PF01217 | 0.161 |
TRG_DiLeu_BaEn_4 | 286 | 292 | PF01217 | 0.245 |
TRG_DiLeu_BaEn_4 | 317 | 323 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.233 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 660 | 663 | PF00400 | 0.477 |
TRG_NLS_Bipartite_1 | 644 | 666 | PF00514 | 0.317 |
TRG_NLS_MonoCore_2 | 660 | 665 | PF00514 | 0.573 |
TRG_NLS_MonoExtC_3 | 189 | 194 | PF00514 | 0.288 |
TRG_NLS_MonoExtN_4 | 190 | 195 | PF00514 | 0.234 |
TRG_NLS_MonoExtN_4 | 661 | 666 | PF00514 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 191 | 196 | PF00026 | 0.248 |
TRG_Pf-PMV_PEXEL_1 | 292 | 297 | PF00026 | 0.351 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Q4 | Leptomonas seymouri | 71% | 99% |
A0A0S4JKJ8 | Bodo saltans | 45% | 100% |
A0A3S7X283 | Leishmania donovani | 100% | 100% |
A4HH82 | Leishmania braziliensis | 82% | 100% |
C9ZL36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9ADS7 | Leishmania major | 93% | 100% |
E9AM03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |