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. | yes | 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: A0A3Q8IJS8
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 | 101 | 105 | PF00656 | 0.746 |
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 449 | 453 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.727 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.753 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 620 | 622 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.806 |
CLV_Separin_Metazoa | 220 | 224 | PF03568 | 0.468 |
DEG_APCC_DBOX_1 | 222 | 230 | PF00400 | 0.444 |
DEG_ODPH_VHL_1 | 332 | 343 | PF01847 | 0.452 |
DOC_CYCLIN_RxL_1 | 438 | 452 | PF00134 | 0.477 |
DOC_CYCLIN_yCln2_LP_2 | 243 | 249 | PF00134 | 0.477 |
DOC_MAPK_gen_1 | 192 | 201 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 258 | 266 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 292 | 300 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 401 | 411 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 481 | 487 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 503 | 513 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 582 | 591 | PF00069 | 0.718 |
DOC_MAPK_MEF2A_6 | 292 | 300 | PF00069 | 0.452 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.452 |
DOC_PP2B_LxvP_1 | 602 | 605 | PF13499 | 0.751 |
DOC_PP4_FxxP_1 | 494 | 497 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.657 |
DOC_USP7_MATH_2 | 289 | 295 | PF00917 | 0.452 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.701 |
DOC_USP7_UBL2_3 | 39 | 43 | PF12436 | 0.544 |
DOC_USP7_UBL2_3 | 594 | 598 | PF12436 | 0.721 |
DOC_USP7_UBL2_3 | 618 | 622 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 265 | 270 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 438 | 446 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 564 | 574 | PF00244 | 0.621 |
LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.470 |
LIG_CaM_IQ_9 | 571 | 587 | PF13499 | 0.641 |
LIG_EH1_1 | 234 | 242 | PF00400 | 0.459 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.444 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.463 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.684 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.452 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.452 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.486 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.529 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.475 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.464 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.738 |
LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 291 | 301 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 397 | 406 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 217 | 221 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 397 | 402 | PF02991 | 0.489 |
LIG_MAD2 | 13 | 21 | PF02301 | 0.667 |
LIG_MAD2 | 339 | 347 | PF02301 | 0.452 |
LIG_PCNA_PIPBox_1 | 237 | 246 | PF02747 | 0.452 |
LIG_REV1ctd_RIR_1 | 525 | 535 | PF16727 | 0.464 |
LIG_SH2_NCK_1 | 71 | 75 | PF00017 | 0.559 |
LIG_SH2_SRC | 230 | 233 | PF00017 | 0.427 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.598 |
LIG_SH2_STAT3 | 318 | 321 | PF00017 | 0.452 |
LIG_SH2_STAT3 | 353 | 356 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.513 |
LIG_SH3_1 | 620 | 626 | PF00018 | 0.658 |
LIG_SH3_2 | 623 | 628 | PF14604 | 0.651 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.477 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.658 |
LIG_SUMO_SIM_anti_2 | 217 | 225 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 224 | 231 | PF11976 | 0.439 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.657 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.365 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.464 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.754 |
LIG_TYR_ITSM | 395 | 402 | PF00017 | 0.503 |
LIG_UBA3_1 | 447 | 455 | PF00899 | 0.494 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.436 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.452 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.553 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.778 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.665 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.503 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.538 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.703 |
MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.516 |
MOD_Cter_Amidation | 618 | 621 | PF01082 | 0.752 |
MOD_GlcNHglycan | 342 | 346 | PF01048 | 0.313 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.283 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.672 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.256 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.718 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.606 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.538 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.686 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.454 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.449 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.513 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.500 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.617 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.677 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.699 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.756 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.649 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.459 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.431 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.505 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.355 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.464 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.450 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.493 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.500 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.676 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.464 |
MOD_PK_1 | 423 | 429 | PF00069 | 0.452 |
MOD_PKA_1 | 533 | 539 | PF00069 | 0.423 |
MOD_PKA_1 | 548 | 554 | PF00069 | 0.623 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.452 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.464 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.452 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.731 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.665 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.465 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.444 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.443 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.452 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.556 |
MOD_SUMO_for_1 | 125 | 128 | PF00179 | 0.529 |
MOD_SUMO_for_1 | 205 | 208 | PF00179 | 0.472 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.694 |
MOD_SUMO_rev_2 | 119 | 127 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 544 | 551 | PF00179 | 0.627 |
TRG_DiLeu_BaEn_1 | 217 | 222 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_2 | 230 | 236 | PF01217 | 0.358 |
TRG_DiLeu_BaEn_2 | 247 | 253 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_3 | 470 | 476 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 580 | 583 | PF00400 | 0.654 |
TRG_NLS_Bipartite_1 | 548 | 566 | PF00514 | 0.697 |
TRG_NLS_MonoExtC_3 | 578 | 584 | PF00514 | 0.706 |
TRG_NLS_MonoExtN_4 | 618 | 624 | PF00514 | 0.748 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.252 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.252 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P967 | Leptomonas seymouri | 72% | 100% |
A0A0S4KG56 | Bodo saltans | 65% | 100% |
A0A1X0NJV9 | Trypanosomatidae | 69% | 100% |
A0A422N5J0 | Trypanosoma rangeli | 70% | 100% |
A4HIZ4 | Leishmania braziliensis | 80% | 99% |
A4I6B1 | Leishmania infantum | 99% | 100% |
C9ZN38 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
E9B1G7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q08J23 | Homo sapiens | 26% | 82% |
Q1HFZ0 | Mus musculus | 25% | 83% |
Q28E61 | Xenopus tropicalis | 24% | 79% |
Q4Q6P5 | Leishmania major | 93% | 100% |
Q5ZLV4 | Gallus gallus | 24% | 79% |
V5BIK5 | Trypanosoma cruzi | 68% | 100% |