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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AWS2
Term | Name | Level | Count |
---|---|---|---|
GO:0000459 | exonucleolytic trimming involved in rRNA processing | 8 | 1 |
GO:0000467 | exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 1 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031125 | rRNA 3'-end processing | 9 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043628 | regulatory ncRNA 3'-end processing | 8 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 1 |
GO:0090503 | RNA phosphodiester bond hydrolysis, exonucleolytic | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000215 | tRNA 2'-phosphotransferase activity | 5 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004532 | RNA exonuclease activity | 5 | 1 |
GO:0004540 | RNA nuclease activity | 4 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.337 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.320 |
DOC_CKS1_1 | 179 | 184 | PF01111 | 0.563 |
DOC_CKS1_1 | 553 | 558 | PF01111 | 0.348 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 241 | 247 | PF00134 | 0.525 |
DOC_MAPK_gen_1 | 192 | 200 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 252 | 259 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 30 | 38 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 335 | 344 | PF00069 | 0.622 |
DOC_MAPK_gen_1 | 381 | 391 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 420 | 426 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 524 | 531 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 252 | 261 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 382 | 391 | PF00069 | 0.184 |
DOC_MAPK_MEF2A_6 | 524 | 533 | PF00069 | 0.328 |
DOC_PP1_RVXF_1 | 392 | 399 | PF00149 | 0.475 |
DOC_PP4_FxxP_1 | 344 | 347 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.347 |
DOC_USP7_UBL2_3 | 381 | 385 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 567 | 571 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 111 | 119 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 337 | 343 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 399 | 409 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 470 | 476 | PF00244 | 0.415 |
LIG_Actin_WH2_2 | 161 | 176 | PF00022 | 0.454 |
LIG_Actin_WH2_2 | 239 | 254 | PF00022 | 0.480 |
LIG_AP2alpha_2 | 128 | 130 | PF02296 | 0.581 |
LIG_APCC_ABBA_1 | 529 | 534 | PF00400 | 0.344 |
LIG_BIR_III_2 | 148 | 152 | PF00653 | 0.562 |
LIG_BIR_III_2 | 281 | 285 | PF00653 | 0.646 |
LIG_BIR_III_2 | 369 | 373 | PF00653 | 0.432 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.321 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.579 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.693 |
LIG_EVH1_2 | 371 | 375 | PF00568 | 0.409 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.330 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.328 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.407 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.475 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.636 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.749 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.512 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.606 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.425 |
LIG_GBD_Chelix_1 | 243 | 251 | PF00786 | 0.274 |
LIG_Integrin_isoDGR_2 | 577 | 579 | PF01839 | 0.417 |
LIG_LIR_Apic_2 | 341 | 347 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 154 | 162 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 384 | 391 | PF02991 | 0.184 |
LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.184 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.440 |
LIG_LYPXL_SIV_4 | 444 | 452 | PF13949 | 0.475 |
LIG_NRBOX | 246 | 252 | PF00104 | 0.536 |
LIG_PDZ_Class_2 | 579 | 584 | PF00595 | 0.588 |
LIG_RPA_C_Fungi | 350 | 362 | PF08784 | 0.587 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 100 | 103 | PF00017 | 0.328 |
LIG_SH2_PTP2 | 407 | 410 | PF00017 | 0.385 |
LIG_SH2_PTP2 | 58 | 61 | PF00017 | 0.332 |
LIG_SH2_SRC | 532 | 535 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.332 |
LIG_SH3_1 | 23 | 29 | PF00018 | 0.491 |
LIG_SH3_2 | 325 | 330 | PF14604 | 0.517 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.362 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.419 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.258 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.693 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.760 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.799 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 82 | 87 | PF11976 | 0.330 |
LIG_TRAF2_1 | 357 | 360 | PF00917 | 0.591 |
LIG_WW_3 | 300 | 304 | PF00397 | 0.774 |
LIG_WW_3 | 370 | 374 | PF00397 | 0.429 |
MOD_CDK_SPxxK_3 | 261 | 268 | PF00069 | 0.321 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.701 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.333 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.378 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.336 |
MOD_CMANNOS | 487 | 490 | PF00535 | 0.449 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.449 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.398 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.243 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.726 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.725 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.334 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.328 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.709 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.349 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.801 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.740 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.361 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.493 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.398 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.696 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.417 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.329 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.338 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.355 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.398 |
MOD_PK_1 | 385 | 391 | PF00069 | 0.184 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.255 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.449 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.440 |
MOD_PKB_1 | 335 | 343 | PF00069 | 0.572 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.506 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.338 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.267 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.394 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.332 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.427 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.441 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.617 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.338 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.398 |
MOD_SUMO_rev_2 | 162 | 168 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 376 | 383 | PF00179 | 0.607 |
TRG_DiLeu_BaEn_2 | 135 | 141 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.184 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.745 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.420 |
TRG_NES_CRM1_1 | 220 | 230 | PF08389 | 0.454 |
TRG_NLS_MonoExtN_4 | 328 | 334 | PF00514 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 253 | 258 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWH5 | Leptomonas seymouri | 56% | 94% |
A0A0S4J7G0 | Bodo saltans | 40% | 90% |
A0A1X0NVN6 | Trypanosomatidae | 42% | 100% |
A0A3Q8IBU9 | Leishmania donovani | 89% | 100% |
A0A422MZ86 | Trypanosoma rangeli | 46% | 100% |
A4HDD9 | Leishmania braziliensis | 77% | 99% |
A4I0S0 | Leishmania infantum | 89% | 100% |
D0A750 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
Q4QAQ2 | Leishmania major | 87% | 99% |
V5C0L6 | Trypanosoma cruzi | 46% | 92% |