Ribosomal Protein, NOL1/NOP2/sun family, putative
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 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: E9AHJ5
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.594 |
CLV_PCSK_FUR_1 | 380 | 384 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.446 |
CLV_PCSK_PC7_1 | 107 | 113 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.197 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.460 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.440 |
DEG_SPOP_SBC_1 | 558 | 562 | PF00917 | 0.434 |
DOC_CYCLIN_RxL_1 | 434 | 446 | PF00134 | 0.435 |
DOC_CYCLIN_yCln2_LP_2 | 221 | 224 | PF00134 | 0.482 |
DOC_MAPK_MEF2A_6 | 164 | 173 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 595 | 602 | PF00069 | 0.407 |
DOC_MAPK_NFAT4_5 | 595 | 603 | PF00069 | 0.468 |
DOC_PP1_RVXF_1 | 498 | 504 | PF00149 | 0.320 |
DOC_PP1_RVXF_1 | 97 | 104 | PF00149 | 0.446 |
DOC_PP2B_LxvP_1 | 221 | 224 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 441 | 444 | PF13499 | 0.317 |
DOC_PP2B_LxvP_1 | 598 | 601 | PF13499 | 0.458 |
DOC_PP4_MxPP_1 | 140 | 143 | PF00568 | 0.320 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.454 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.433 |
LIG_14-3-3_CanoR_1 | 271 | 281 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 357 | 361 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 502 | 511 | PF00244 | 0.324 |
LIG_Actin_WH2_2 | 228 | 246 | PF00022 | 0.415 |
LIG_Actin_WH2_2 | 482 | 497 | PF00022 | 0.406 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.651 |
LIG_BRCT_BRCA1_1 | 486 | 490 | PF00533 | 0.329 |
LIG_BRCT_BRCA1_1 | 61 | 65 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.421 |
LIG_deltaCOP1_diTrp_1 | 248 | 253 | PF00928 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 47 | 51 | PF00928 | 0.355 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.413 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.426 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.450 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.425 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.416 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.468 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.399 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.469 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.428 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.494 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.484 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.320 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.415 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.488 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.447 |
LIG_Integrin_RGD_1 | 107 | 109 | PF01839 | 0.473 |
LIG_LIR_Gen_1 | 226 | 236 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 446 | 454 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 46 | 55 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 487 | 496 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 32 | 37 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 487 | 493 | PF02991 | 0.329 |
LIG_MAD2 | 153 | 161 | PF02301 | 0.426 |
LIG_MYND_1 | 220 | 224 | PF01753 | 0.482 |
LIG_NRBOX | 167 | 173 | PF00104 | 0.476 |
LIG_PTB_Apo_2 | 28 | 35 | PF02174 | 0.375 |
LIG_SH2_GRB2like | 496 | 499 | PF00017 | 0.374 |
LIG_SH2_SRC | 344 | 347 | PF00017 | 0.493 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.319 |
LIG_SH3_1 | 90 | 96 | PF00018 | 0.387 |
LIG_SH3_2 | 513 | 518 | PF14604 | 0.238 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.414 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.467 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.337 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.490 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 190 | 196 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 519 | 524 | PF11976 | 0.384 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.342 |
LIG_TRAF2_1 | 605 | 608 | PF00917 | 0.632 |
LIG_TRAF2_1 | 613 | 616 | PF00917 | 0.666 |
LIG_TRFH_1 | 219 | 223 | PF08558 | 0.415 |
LIG_UBA3_1 | 269 | 277 | PF00899 | 0.455 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.685 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.415 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.520 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.415 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.536 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.333 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.457 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.315 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.575 |
MOD_CMANNOS | 250 | 253 | PF00535 | 0.215 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.399 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.215 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.320 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.307 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.550 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.401 |
MOD_GlcNHglycan | 541 | 545 | PF01048 | 0.485 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.551 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.348 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.415 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.448 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.415 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.466 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.432 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.404 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.428 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.441 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.490 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.520 |
MOD_N-GLC_1 | 622 | 627 | PF02516 | 0.648 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.415 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.435 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.426 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.422 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.439 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.429 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.369 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.359 |
MOD_NEK2_2 | 115 | 120 | PF00069 | 0.412 |
MOD_NEK2_2 | 239 | 244 | PF00069 | 0.415 |
MOD_NEK2_2 | 272 | 277 | PF00069 | 0.501 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.415 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.426 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.464 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.419 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.485 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.415 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.471 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.449 |
MOD_PKB_1 | 410 | 418 | PF00069 | 0.589 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.489 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.439 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.332 |
MOD_Plk_1 | 622 | 628 | PF00069 | 0.554 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.302 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.413 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.380 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.363 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.372 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.424 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.466 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.436 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.406 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.431 |
MOD_SUMO_rev_2 | 345 | 350 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 414 | 422 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 457 | 464 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 84 | 92 | PF00179 | 0.464 |
TRG_DiLeu_BaEn_2 | 46 | 52 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 313 | 318 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.461 |
TRG_NLS_MonoCore_2 | 110 | 115 | PF00514 | 0.568 |
TRG_NLS_MonoExtC_3 | 11 | 17 | PF00514 | 0.639 |
TRG_NLS_MonoExtN_4 | 111 | 116 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.215 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Y2 | Leptomonas seymouri | 72% | 99% |
A0A0S4IKI3 | Bodo saltans | 50% | 94% |
A0A1X0P924 | Trypanosomatidae | 54% | 92% |
A0A3Q8IJ07 | Leishmania donovani | 99% | 100% |
A0A3Q8INR5 | Leishmania donovani | 32% | 83% |
A0A3S5IQZ3 | Trypanosoma rangeli | 57% | 100% |
A4HIZ4 | Leishmania braziliensis | 27% | 100% |
A4IDJ1 | Leishmania infantum | 32% | 83% |
A8GDM6 | Serratia proteamaculans (strain 568) | 28% | 100% |
C9ZKZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 97% |
D0A386 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 86% |
E9AEB6 | Leishmania major | 95% | 100% |
E9AIT8 | Leishmania braziliensis | 85% | 100% |
E9ALH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9ASZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 83% |
O13935 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 93% |
P38205 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 93% |
Q08J23 | Homo sapiens | 35% | 83% |
Q1HFZ0 | Mus musculus | 38% | 84% |
Q4Q1K4 | Leishmania major | 32% | 83% |
Q4Q6P5 | Leishmania major | 27% | 100% |
Q4V7N2 | Xenopus laevis | 36% | 91% |
Q9HGQ2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 92% |
Q9W4M9 | Drosophila melanogaster | 35% | 85% |
V5BSK4 | Trypanosoma cruzi | 54% | 100% |