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: A4HDD9
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 | 274 | 278 | PF00656 | 0.722 |
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.337 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.243 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.525 |
DEG_ODPH_VHL_1 | 44 | 57 | PF01847 | 0.486 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.729 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.472 |
DOC_CDC14_PxL_1 | 140 | 148 | PF14671 | 0.430 |
DOC_CKS1_1 | 173 | 178 | PF01111 | 0.563 |
DOC_CKS1_1 | 544 | 549 | PF01111 | 0.348 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.769 |
DOC_CYCLIN_yCln2_LP_2 | 286 | 292 | PF00134 | 0.547 |
DOC_MAPK_gen_1 | 186 | 194 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 410 | 417 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 410 | 417 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 515 | 524 | PF00069 | 0.328 |
DOC_PP1_RVXF_1 | 382 | 389 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.558 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.367 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.223 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.812 |
DOC_USP7_UBL2_3 | 367 | 371 | PF12436 | 0.616 |
DOC_USP7_UBL2_3 | 558 | 562 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.338 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 22 | 26 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 272 | 276 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 318 | 328 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 389 | 399 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 461 | 467 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 65 | 73 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 83 | 91 | PF00244 | 0.387 |
LIG_Actin_WH2_2 | 182 | 197 | PF00022 | 0.400 |
LIG_Actin_WH2_2 | 227 | 242 | PF00022 | 0.480 |
LIG_AP2alpha_2 | 122 | 124 | PF02296 | 0.581 |
LIG_APCC_ABBA_1 | 520 | 525 | PF00400 | 0.344 |
LIG_BIR_III_2 | 142 | 146 | PF00653 | 0.562 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.646 |
LIG_BRCT_BRCA1_2 | 361 | 367 | PF00533 | 0.429 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.328 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.399 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.475 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.704 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.520 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.409 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.425 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.502 |
LIG_GBD_Chelix_1 | 231 | 239 | PF00786 | 0.274 |
LIG_LIR_Apic_2 | 255 | 260 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 148 | 156 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 394 | 404 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.440 |
LIG_LYPXL_SIV_4 | 435 | 443 | PF13949 | 0.475 |
LIG_NRBOX | 234 | 240 | PF00104 | 0.540 |
LIG_PDZ_Class_2 | 570 | 575 | PF00595 | 0.550 |
LIG_RPA_C_Fungi | 338 | 350 | PF08784 | 0.587 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 397 | 400 | PF00017 | 0.385 |
LIG_SH2_PTP2 | 52 | 55 | PF00017 | 0.332 |
LIG_SH2_PTP2 | 94 | 97 | PF00017 | 0.328 |
LIG_SH2_SRC | 523 | 526 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.323 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.580 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.362 |
LIG_SUMO_SIM_par_1 | 53 | 58 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 76 | 81 | PF11976 | 0.330 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.404 |
LIG_TRAF2_1 | 345 | 348 | PF00917 | 0.575 |
LIG_TRAF2_1 | 465 | 468 | PF00917 | 0.444 |
MOD_CDK_SPxK_1 | 5 | 11 | PF00069 | 0.767 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.333 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.381 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.336 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.413 |
MOD_CMANNOS | 478 | 481 | PF00535 | 0.449 |
MOD_Cter_Amidation | 63 | 66 | PF01082 | 0.358 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.449 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.367 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.243 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.784 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.774 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.682 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.423 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.298 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.334 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.451 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.734 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.328 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.279 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.372 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.794 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.794 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.535 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.361 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.358 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.721 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.567 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.629 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.145 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.223 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.338 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.355 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.298 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.570 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.674 |
MOD_PIKK_1 | 445 | 451 | PF00454 | 0.320 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.223 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.548 |
MOD_PKA_1 | 65 | 71 | PF00069 | 0.320 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.619 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.449 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.808 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.696 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.440 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.312 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.320 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.532 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.338 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.332 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.427 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.591 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.783 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.338 |
MOD_SUMO_rev_2 | 156 | 162 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 366 | 373 | PF00179 | 0.615 |
MOD_SUMO_rev_2 | 452 | 460 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_2 | 129 | 135 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.342 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 409 | 411 | PF00400 | 0.223 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.420 |
TRG_NES_CRM1_1 | 205 | 218 | PF08389 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 241 | 246 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWH5 | Leptomonas seymouri | 60% | 93% |
A0A0S4J7G0 | Bodo saltans | 41% | 88% |
A0A1X0NVN6 | Trypanosomatidae | 44% | 98% |
A0A3Q8IBU9 | Leishmania donovani | 77% | 100% |
A0A422MZ86 | Trypanosoma rangeli | 47% | 100% |
A4I0S0 | Leishmania infantum | 77% | 100% |
D0A750 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AWS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 98% |
Q4QAQ2 | Leishmania major | 77% | 100% |
V5C0L6 | Trypanosoma cruzi | 46% | 90% |