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: Q4QAQ2
Term | Name | Level | Count |
---|---|---|---|
GO:0000459 | exonucleolytic trimming involved in rRNA processing | 8 | 2 |
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 | 2 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0031123 | RNA 3'-end processing | 7 | 2 |
GO:0031125 | rRNA 3'-end processing | 9 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043628 | regulatory ncRNA 3'-end processing | 8 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 2 |
GO:0090503 | RNA phosphodiester bond hydrolysis, exonucleolytic | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 2 |
GO:0000215 | tRNA 2'-phosphotransferase activity | 5 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004518 | nuclease activity | 4 | 2 |
GO:0004527 | exonuclease activity | 5 | 2 |
GO:0004532 | RNA exonuclease activity | 5 | 2 |
GO:0004540 | RNA nuclease activity | 4 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 2 |
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:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 572 | 576 | PF00656 | 0.322 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.319 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.319 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.202 |
CLV_PCSK_PC7_1 | 331 | 337 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.299 |
DEG_ODPH_VHL_1 | 50 | 63 | PF01847 | 0.418 |
DOC_CKS1_1 | 179 | 184 | PF01111 | 0.552 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.677 |
DOC_CKS1_1 | 551 | 556 | PF01111 | 0.318 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 242 | 248 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 192 | 200 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 253 | 260 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 335 | 342 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 418 | 424 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 253 | 262 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 522 | 531 | PF00069 | 0.297 |
DOC_PP1_RVXF_1 | 390 | 397 | PF00149 | 0.415 |
DOC_PP2B_LxvP_1 | 226 | 229 | PF13499 | 0.546 |
DOC_PP4_FxxP_1 | 342 | 345 | PF00568 | 0.482 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.316 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.430 |
DOC_USP7_UBL2_3 | 565 | 569 | PF12436 | 0.467 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 111 | 119 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 397 | 407 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 468 | 474 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.447 |
LIG_AP2alpha_2 | 128 | 130 | PF02296 | 0.538 |
LIG_APCC_ABBA_1 | 527 | 532 | PF00400 | 0.313 |
LIG_BIR_III_2 | 148 | 152 | PF00653 | 0.550 |
LIG_BIR_III_2 | 282 | 286 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 338 | 342 | PF00533 | 0.564 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.673 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.539 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.301 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.454 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.599 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.705 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.477 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.383 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.403 |
LIG_GBD_Chelix_1 | 244 | 252 | PF00786 | 0.273 |
LIG_LIR_Apic_2 | 16 | 21 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 339 | 345 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 46 | 52 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 154 | 162 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.454 |
LIG_LYPXL_SIV_4 | 442 | 450 | PF13949 | 0.415 |
LIG_MYND_1 | 212 | 216 | PF01753 | 0.470 |
LIG_NRBOX | 247 | 253 | PF00104 | 0.387 |
LIG_PDZ_Class_2 | 577 | 582 | PF00595 | 0.565 |
LIG_RPA_C_Fungi | 348 | 360 | PF08784 | 0.565 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.433 |
LIG_SH2_PTP2 | 100 | 103 | PF00017 | 0.297 |
LIG_SH2_PTP2 | 405 | 408 | PF00017 | 0.357 |
LIG_SH2_PTP2 | 49 | 52 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 58 | 61 | PF00017 | 0.301 |
LIG_SH2_SRC | 530 | 533 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.301 |
LIG_SH3_1 | 297 | 303 | PF00018 | 0.774 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.332 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.401 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.753 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.788 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 345 | 351 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 82 | 87 | PF11976 | 0.299 |
LIG_TRAF2_1 | 355 | 358 | PF00917 | 0.562 |
LIG_TRAF2_1 | 472 | 475 | PF00917 | 0.426 |
LIG_WW_3 | 301 | 305 | PF00397 | 0.760 |
MOD_CDK_SPxK_1 | 17 | 23 | PF00069 | 0.678 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.607 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.678 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.353 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.305 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.288 |
MOD_CMANNOS | 485 | 488 | PF00535 | 0.433 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.433 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.450 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.255 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.312 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.742 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.750 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.705 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.302 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.297 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.721 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.790 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.361 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.727 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.445 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.351 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.684 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.393 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.642 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.421 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.314 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.325 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.485 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.649 |
MOD_PK_1 | 336 | 342 | PF00069 | 0.650 |
MOD_PKA_1 | 193 | 199 | PF00069 | 0.246 |
MOD_PKA_1 | 335 | 341 | PF00069 | 0.677 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.288 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.433 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.224 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.609 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.288 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.481 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.313 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.325 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.517 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.370 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.301 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.741 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.405 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.564 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.318 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.364 |
MOD_SUMO_rev_2 | 162 | 168 | PF00179 | 0.313 |
MOD_SUMO_rev_2 | 374 | 381 | PF00179 | 0.591 |
TRG_DiLeu_BaEn_2 | 135 | 141 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.224 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.397 |
TRG_NES_CRM1_1 | 221 | 234 | PF08389 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 254 | 259 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.389 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWH5 | Leptomonas seymouri | 56% | 94% |
A0A0S4J7G0 | Bodo saltans | 40% | 90% |
A0A1X0NVN6 | Trypanosomatidae | 43% | 100% |
A0A3Q8IBU9 | Leishmania donovani | 90% | 100% |
A0A422MZ86 | Trypanosoma rangeli | 46% | 100% |
A4HDD9 | Leishmania braziliensis | 77% | 100% |
A4I0S0 | Leishmania infantum | 90% | 100% |
D0A750 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AWS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5C0L6 | Trypanosoma cruzi | 46% | 91% |