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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q6P5
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 2 |
GO:0000470 | maturation of LSU-rRNA | 9 | 2 |
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 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:0016072 | rRNA metabolic process | 7 | 2 |
GO:0031167 | rRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 12 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
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:0070475 | rRNA base methylation | 6 | 2 |
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 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 10 |
GO:0042254 | ribosome biogenesis | 5 | 10 |
GO:0044085 | cellular component biogenesis | 3 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
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:0008169 | C-methyltransferase activity | 5 | 2 |
GO:0008173 | RNA methyltransferase activity | 4 | 2 |
GO:0008649 | rRNA methyltransferase activity | 5 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0009383 | rRNA (cytosine-C5-)-methyltransferase activity | 6 | 2 |
GO:0016434 | rRNA (cytosine) methyltransferase activity | 6 | 2 |
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:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.430 |
CLV_C14_Caspase3-7 | 71 | 75 | PF00656 | 0.792 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 627 | 629 | PF00675 | 0.685 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.224 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.213 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.213 |
CLV_PCSK_PC1ET2_1 | 564 | 566 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 621 | 623 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.799 |
CLV_Separin_Metazoa | 221 | 225 | PF03568 | 0.429 |
DEG_APCC_DBOX_1 | 223 | 231 | PF00400 | 0.399 |
DEG_ODPH_VHL_1 | 333 | 344 | PF01847 | 0.413 |
DOC_CYCLIN_RxL_1 | 439 | 453 | PF00134 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 244 | 250 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 193 | 202 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 214 | 222 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 259 | 267 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 293 | 301 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 402 | 412 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 482 | 488 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 504 | 514 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 583 | 592 | PF00069 | 0.731 |
DOC_MAPK_MEF2A_6 | 293 | 301 | PF00069 | 0.421 |
DOC_PP2B_LxvP_1 | 244 | 247 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 412 | 415 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 603 | 606 | PF13499 | 0.715 |
DOC_PP4_FxxP_1 | 495 | 498 | PF00568 | 0.413 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.571 |
DOC_USP7_MATH_2 | 290 | 296 | PF00917 | 0.413 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.660 |
DOC_USP7_UBL2_3 | 39 | 43 | PF12436 | 0.513 |
DOC_USP7_UBL2_3 | 619 | 623 | PF12436 | 0.671 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 266 | 271 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 284 | 289 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 439 | 447 | PF00244 | 0.434 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.585 |
LIG_BIR_III_4 | 74 | 78 | PF00653 | 0.505 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.749 |
LIG_CaM_IQ_9 | 572 | 588 | PF13499 | 0.560 |
LIG_EH1_1 | 235 | 243 | PF00400 | 0.417 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.400 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.437 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.484 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.575 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.430 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.464 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.476 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.516 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.423 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.426 |
LIG_FHA_2 | 610 | 616 | PF00498 | 0.694 |
LIG_LIR_Gen_1 | 218 | 227 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 232 | 241 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 292 | 302 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 97 | 104 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 326 | 330 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.572 |
LIG_MAD2 | 13 | 21 | PF02301 | 0.565 |
LIG_MAD2 | 340 | 348 | PF02301 | 0.413 |
LIG_PCNA_PIPBox_1 | 238 | 247 | PF02747 | 0.321 |
LIG_REV1ctd_RIR_1 | 526 | 536 | PF16727 | 0.424 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 319 | 322 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 354 | 357 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.480 |
LIG_SH3_1 | 621 | 627 | PF00018 | 0.568 |
LIG_SH3_2 | 624 | 629 | PF14604 | 0.560 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.439 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.568 |
LIG_SUMO_SIM_anti_2 | 218 | 226 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 225 | 232 | PF11976 | 0.393 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.669 |
LIG_TRAF2_1 | 188 | 191 | PF00917 | 0.330 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.424 |
LIG_TYR_ITSM | 396 | 403 | PF00017 | 0.467 |
LIG_UBA3_1 | 448 | 456 | PF00899 | 0.464 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.425 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.413 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.523 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.776 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.600 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.452 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.516 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.595 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.708 |
MOD_Cter_Amidation | 619 | 622 | PF01082 | 0.710 |
MOD_GlcNHglycan | 343 | 347 | PF01048 | 0.280 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.272 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.224 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.685 |
MOD_GlcNHglycan | 88 | 94 | PF01048 | 0.731 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.577 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.642 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.526 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.430 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.413 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.497 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.468 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.547 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.620 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.666 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.747 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.619 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.426 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.394 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.476 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.414 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.424 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.419 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.475 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.541 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.572 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.424 |
MOD_PK_1 | 284 | 290 | PF00069 | 0.364 |
MOD_PK_1 | 424 | 430 | PF00069 | 0.413 |
MOD_PKA_1 | 534 | 540 | PF00069 | 0.374 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.428 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.429 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.413 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.633 |
MOD_Plk_2-3 | 566 | 572 | PF00069 | 0.501 |
MOD_Plk_2-3 | 94 | 100 | PF00069 | 0.533 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.429 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.413 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.413 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.413 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.574 |
MOD_SUMO_for_1 | 126 | 129 | PF00179 | 0.437 |
MOD_SUMO_for_1 | 206 | 209 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 120 | 128 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 545 | 552 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 218 | 223 | PF01217 | 0.382 |
TRG_DiLeu_BaEn_2 | 231 | 237 | PF01217 | 0.306 |
TRG_DiLeu_BaEn_2 | 248 | 254 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_3 | 471 | 477 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 581 | 584 | PF00400 | 0.649 |
TRG_NLS_Bipartite_1 | 563 | 584 | PF00514 | 0.661 |
TRG_NLS_MonoExtC_3 | 579 | 585 | PF00514 | 0.719 |
TRG_NLS_MonoExtC_3 | 620 | 625 | PF00514 | 0.672 |
TRG_NLS_MonoExtN_4 | 619 | 625 | PF00514 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.213 |
TRG_Pf-PMV_PEXEL_1 | 409 | 413 | PF00026 | 0.213 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P967 | Leptomonas seymouri | 72% | 100% |
A0A0S4KG56 | Bodo saltans | 65% | 100% |
A0A1X0NJV9 | Trypanosomatidae | 62% | 100% |
A0A3Q8IJ07 | Leishmania donovani | 28% | 99% |
A0A3Q8IJS8 | Leishmania donovani | 93% | 100% |
A0A422N5J0 | Trypanosoma rangeli | 71% | 100% |
A4HIZ4 | Leishmania braziliensis | 82% | 100% |
A4I6B1 | Leishmania infantum | 93% | 100% |
C9ZN38 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9AEB6 | Leishmania major | 27% | 99% |
E9AHJ5 | Leishmania infantum | 27% | 99% |
E9B1G7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q5ZLV4 | Gallus gallus | 22% | 79% |
Q8VYM6 | Arabidopsis thaliana | 46% | 94% |
Q9FG73 | Arabidopsis thaliana | 44% | 92% |
V5BIK5 | Trypanosoma cruzi | 67% | 100% |