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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ABZ1
Term | Name | Level | Count |
---|---|---|---|
GO:0007623 | circadian rhythm | 2 | 11 |
GO:0010468 | regulation of gene expression | 5 | 11 |
GO:0019222 | regulation of metabolic process | 3 | 11 |
GO:0032501 | multicellular organismal process | 1 | 11 |
GO:0032922 | circadian regulation of gene expression | 2 | 11 |
GO:0048511 | rhythmic process | 1 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0004527 | exonuclease activity | 5 | 11 |
GO:0004532 | RNA exonuclease activity | 5 | 11 |
GO:0004535 | poly(A)-specific ribonuclease activity | 8 | 11 |
GO:0004540 | RNA nuclease activity | 4 | 11 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 11 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0004519 | endonuclease activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 36 | 40 | PF00656 | 0.595 |
CLV_C14_Caspase3-7 | 534 | 538 | PF00656 | 0.359 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.314 |
CLV_PCSK_FUR_1 | 393 | 397 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 178 | 180 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.423 |
CLV_Separin_Metazoa | 162 | 166 | PF03568 | 0.335 |
CLV_Separin_Metazoa | 335 | 339 | PF03568 | 0.404 |
DEG_APCC_DBOX_1 | 156 | 164 | PF00400 | 0.270 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.349 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.554 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.270 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.459 |
DOC_CKS1_1 | 437 | 442 | PF01111 | 0.376 |
DOC_MAPK_gen_1 | 156 | 163 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 265 | 273 | PF00069 | 0.271 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.630 |
DOC_MAPK_MEF2A_6 | 267 | 275 | PF00069 | 0.271 |
DOC_PP1_RVXF_1 | 186 | 193 | PF00149 | 0.414 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.404 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.271 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.279 |
DOC_PP4_FxxP_1 | 491 | 494 | PF00568 | 0.289 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.270 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.457 |
DOC_USP7_UBL2_3 | 474 | 478 | PF12436 | 0.314 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 340 | 348 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.365 |
LIG_APCC_ABBA_1 | 527 | 532 | PF00400 | 0.347 |
LIG_BIR_III_4 | 104 | 108 | PF00653 | 0.569 |
LIG_BIR_III_4 | 304 | 308 | PF00653 | 0.335 |
LIG_BIR_III_4 | 398 | 402 | PF00653 | 0.292 |
LIG_deltaCOP1_diTrp_1 | 185 | 192 | PF00928 | 0.270 |
LIG_deltaCOP1_diTrp_1 | 532 | 539 | PF00928 | 0.476 |
LIG_deltaCOP1_diTrp_1 | 92 | 99 | PF00928 | 0.357 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.519 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.273 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.349 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.254 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.289 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.450 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.363 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.204 |
LIG_LIR_Apic_2 | 488 | 494 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 98 | 105 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 537 | 542 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.368 |
LIG_MYND_1 | 149 | 153 | PF01753 | 0.279 |
LIG_NRBOX | 159 | 165 | PF00104 | 0.270 |
LIG_PCNA_yPIPBox_3 | 178 | 190 | PF02747 | 0.317 |
LIG_Pex14_1 | 535 | 539 | PF04695 | 0.501 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.271 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.335 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.406 |
LIG_SH2_SRC | 492 | 495 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.407 |
LIG_SH2_STAT3 | 484 | 487 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.351 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.391 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.289 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.300 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.432 |
LIG_SUMO_SIM_anti_2 | 468 | 476 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 298 | 304 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 501 | 510 | PF11976 | 0.271 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.404 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.334 |
LIG_TYR_ITIM | 193 | 198 | PF00017 | 0.349 |
LIG_WRC_WIRS_1 | 96 | 101 | PF05994 | 0.379 |
MOD_CDK_SPK_2 | 427 | 432 | PF00069 | 0.270 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.371 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.314 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.363 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.438 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.432 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.700 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.307 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.474 |
MOD_CMANNOS | 353 | 356 | PF00535 | 0.271 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.635 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.677 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.414 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.412 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.234 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.725 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.271 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.347 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.392 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.472 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.311 |
MOD_N-GLC_2 | 134 | 136 | PF02516 | 0.318 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.303 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.748 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.373 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.448 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.289 |
MOD_NEK2_2 | 543 | 548 | PF00069 | 0.531 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.271 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.584 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.700 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.609 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.673 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.566 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.468 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.294 |
MOD_PKB_1 | 338 | 346 | PF00069 | 0.243 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.311 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.317 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.281 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.408 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.390 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.630 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.706 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.397 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.550 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.510 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.371 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.368 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.386 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.384 |
MOD_SUMO_rev_2 | 170 | 180 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 45 | 52 | PF00179 | 0.599 |
TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.314 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.318 |
TRG_NLS_MonoExtN_4 | 474 | 481 | PF00514 | 0.292 |
TRG_NLS_MonoExtN_4 | 70 | 77 | PF00514 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.292 |
TRG_Pf-PMV_PEXEL_1 | 545 | 549 | PF00026 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6Q6 | Leptomonas seymouri | 64% | 99% |
A0A0S4JIK0 | Bodo saltans | 39% | 86% |
A0A1X0P355 | Trypanosomatidae | 47% | 99% |
A0A3S5H4S7 | Leishmania donovani | 94% | 99% |
A4H336 | Leishmania braziliensis | 87% | 99% |
A4HRC4 | Leishmania infantum | 94% | 100% |
C9ZXH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AJ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5B795 | Trypanosoma cruzi | 51% | 98% |