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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H336
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 | 131 | 135 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 36 | 40 | PF00656 | 0.573 |
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 | 0.561 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.330 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.603 |
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_APCC_KENBOX_2 | 481 | 485 | PF00400 | 0.193 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.546 |
DEG_ODPH_VHL_1 | 151 | 163 | PF01847 | 0.193 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.459 |
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 | 0.613 |
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 | 507 | 510 | PF13499 | 0.271 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.279 |
DOC_PP4_FxxP_1 | 495 | 498 | PF00568 | 0.289 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.592 |
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_UBL2_3 | 478 | 482 | PF12436 | 0.314 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.360 |
LIG_APCC_ABBA_1 | 531 | 536 | PF00400 | 0.342 |
LIG_BIR_III_4 | 104 | 108 | PF00653 | 0.518 |
LIG_BIR_III_4 | 304 | 308 | PF00653 | 0.335 |
LIG_BRCT_BRCA1_1 | 338 | 342 | PF00533 | 0.193 |
LIG_deltaCOP1_diTrp_1 | 185 | 192 | PF00928 | 0.270 |
LIG_deltaCOP1_diTrp_1 | 536 | 543 | PF00928 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 92 | 99 | PF00928 | 0.356 |
LIG_eIF4E_1 | 155 | 161 | PF01652 | 0.362 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.517 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.273 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.349 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.193 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.289 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.446 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.363 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.367 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.443 |
LIG_LIR_Apic_2 | 492 | 498 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 98 | 105 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.369 |
LIG_MLH1_MIPbox_1 | 338 | 342 | PF16413 | 0.193 |
LIG_MYND_1 | 149 | 153 | PF01753 | 0.279 |
LIG_NRBOX | 159 | 165 | PF00104 | 0.270 |
LIG_PCNA_yPIPBox_3 | 179 | 190 | PF02747 | 0.310 |
LIG_Pex14_1 | 539 | 543 | PF04695 | 0.515 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.271 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.335 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.405 |
LIG_SH2_SRC | 496 | 499 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.407 |
LIG_SH2_STAT3 | 488 | 491 | 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 | 0.375 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.289 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.298 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.426 |
LIG_SUMO_SIM_anti_2 | 472 | 478 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 298 | 304 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 505 | 514 | 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 | 0.371 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.314 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.284 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.363 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.440 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.429 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.367 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.685 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.485 |
MOD_CMANNOS | 353 | 356 | PF00535 | 0.271 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.622 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.658 |
MOD_GlcNHglycan | 459 | 462 | 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 | 0.704 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.271 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.477 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.268 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.206 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.322 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.399 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.475 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.226 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.311 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.257 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.303 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.725 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.307 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.193 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.451 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.289 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.543 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.488 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.271 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.589 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.682 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.591 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.548 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.446 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.377 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.294 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.226 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.311 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.284 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.319 |
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 | 0.613 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.683 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.402 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.521 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.507 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.368 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.396 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.384 |
MOD_SUMO_rev_2 | 45 | 52 | PF00179 | 0.574 |
TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 423 | 428 | PF01217 | 0.193 |
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 | 155 | 157 | PF00400 | 0.197 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.566 |
TRG_NLS_MonoExtC_3 | 477 | 482 | PF00514 | 0.193 |
TRG_NLS_MonoExtN_4 | 70 | 77 | PF00514 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 549 | 553 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6Q6 | Leptomonas seymouri | 64% | 100% |
A0A0S4JIK0 | Bodo saltans | 41% | 87% |
A0A1X0P355 | Trypanosomatidae | 48% | 99% |
A0A3S5H4S7 | Leishmania donovani | 84% | 100% |
A4HRC4 | Leishmania infantum | 83% | 100% |
C9ZXH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9ABZ1 | Leishmania major | 87% | 99% |
E9AJ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5B795 | Trypanosoma cruzi | 50% | 99% |