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: E9B1G7
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
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:0022613 | ribonucleoprotein complex biogenesis | 4 | 11 |
GO:0032259 | methylation | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0042254 | ribosome biogenesis | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044085 | cellular component biogenesis | 3 | 11 |
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:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031167 | rRNA methylation | 5 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0070475 | rRNA base methylation | 6 | 1 |
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:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 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 |
GO:0008169 | C-methyltransferase activity | 5 | 1 |
GO:0008173 | RNA methyltransferase activity | 4 | 1 |
GO:0008649 | rRNA methyltransferase activity | 5 | 1 |
GO:0009383 | rRNA (cytosine-C5-)-methyltransferase activity | 6 | 1 |
GO:0016434 | rRNA (cytosine) methyltransferase activity | 6 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.696 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.704 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 269 | 271 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 617 | 619 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.811 |
CLV_Separin_Metazoa | 217 | 221 | PF03568 | 0.471 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.441 |
DEG_APCC_DBOX_1 | 478 | 486 | PF00400 | 0.348 |
DEG_ODPH_VHL_1 | 329 | 340 | PF01847 | 0.451 |
DEG_SPOP_SBC_1 | 554 | 558 | PF00917 | 0.687 |
DOC_CYCLIN_RxL_1 | 435 | 449 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 189 | 198 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 210 | 218 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 255 | 263 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 289 | 297 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 398 | 408 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 478 | 484 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 500 | 510 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 579 | 588 | PF00069 | 0.760 |
DOC_MAPK_MEF2A_6 | 289 | 297 | PF00069 | 0.451 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 599 | 602 | PF13499 | 0.758 |
DOC_PP4_FxxP_1 | 491 | 494 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.547 |
DOC_USP7_MATH_2 | 286 | 292 | PF00917 | 0.451 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.691 |
DOC_USP7_UBL2_3 | 38 | 42 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.660 |
DOC_USP7_UBL2_3 | 591 | 595 | PF12436 | 0.727 |
DOC_USP7_UBL2_3 | 613 | 617 | PF12436 | 0.733 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 370 | 375 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 435 | 443 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 503 | 509 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 561 | 571 | PF00244 | 0.639 |
LIG_AP_GAE_1 | 107 | 113 | PF02883 | 0.561 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.627 |
LIG_CaM_IQ_9 | 568 | 584 | PF13499 | 0.677 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.451 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.464 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.680 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.534 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.451 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.444 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.480 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.513 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.464 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.463 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.747 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 288 | 298 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 394 | 403 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 427 | 436 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 95 | 100 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 95 | 99 | PF02991 | 0.620 |
LIG_MAD2 | 12 | 20 | PF02301 | 0.650 |
LIG_MAD2 | 336 | 344 | PF02301 | 0.451 |
LIG_PCNA_PIPBox_1 | 234 | 243 | PF02747 | 0.503 |
LIG_REV1ctd_RIR_1 | 522 | 532 | PF16727 | 0.463 |
LIG_SH2_GRB2like | 504 | 507 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 430 | 434 | PF00017 | 0.412 |
LIG_SH2_SRC | 227 | 230 | PF00017 | 0.427 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.588 |
LIG_SH2_STAT3 | 315 | 318 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 350 | 353 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.486 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.476 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.518 |
LIG_SUMO_SIM_anti_2 | 214 | 222 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 221 | 228 | PF11976 | 0.442 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.692 |
LIG_TRAF2_1 | 184 | 187 | PF00917 | 0.357 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.463 |
LIG_TYR_ITSM | 392 | 399 | PF00017 | 0.502 |
LIG_UBA3_1 | 444 | 452 | PF00899 | 0.499 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.435 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.451 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.574 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.671 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.567 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.467 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.537 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.710 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.726 |
MOD_Cter_Amidation | 40 | 43 | PF01082 | 0.575 |
MOD_GlcNHglycan | 339 | 343 | PF01048 | 0.312 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.282 |
MOD_GlcNHglycan | 84 | 90 | PF01048 | 0.670 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.626 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.537 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.453 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.448 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.496 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.510 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.614 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.573 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.686 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.542 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.695 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.609 |
MOD_N-GLC_1 | 566 | 571 | PF02516 | 0.484 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.724 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.635 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.522 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.500 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.367 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.463 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.481 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.589 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.661 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.463 |
MOD_PK_1 | 420 | 426 | PF00069 | 0.451 |
MOD_PKA_1 | 530 | 536 | PF00069 | 0.432 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.451 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.463 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.446 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.700 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.451 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.447 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.425 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.451 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.623 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.662 |
MOD_SUMO_for_1 | 122 | 125 | PF00179 | 0.488 |
MOD_SUMO_for_1 | 202 | 205 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 116 | 124 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 605 | 614 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_1 | 214 | 219 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_2 | 227 | 233 | PF01217 | 0.351 |
TRG_DiLeu_BaEn_2 | 244 | 250 | PF01217 | 0.376 |
TRG_DiLeu_BaEn_3 | 467 | 473 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 477 | 480 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 577 | 580 | PF00400 | 0.710 |
TRG_NLS_Bipartite_1 | 559 | 580 | PF00514 | 0.715 |
TRG_NLS_MonoExtC_3 | 575 | 581 | PF00514 | 0.750 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 405 | 409 | PF00026 | 0.251 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P967 | Leptomonas seymouri | 72% | 100% |
A0A0S4KG56 | Bodo saltans | 64% | 100% |
A0A1X0NJV9 | Trypanosomatidae | 68% | 100% |
A0A3Q8IJS8 | Leishmania donovani | 90% | 100% |
A0A422N5J0 | Trypanosoma rangeli | 70% | 100% |
A4HIZ4 | Leishmania braziliensis | 81% | 100% |
A4I6B1 | Leishmania infantum | 90% | 100% |
C9ZN38 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
Q08J23 | Homo sapiens | 25% | 81% |
Q1HFZ0 | Mus musculus | 25% | 83% |
Q28E61 | Xenopus tropicalis | 25% | 78% |
Q4Q6P5 | Leishmania major | 90% | 100% |
Q4V7N2 | Xenopus laevis | 25% | 90% |
Q922K7 | Mus musculus | 48% | 79% |
V5BIK5 | Trypanosoma cruzi | 66% | 100% |