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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: Q4QBB3
Term | Name | Level | Count |
---|---|---|---|
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 5 |
GO:0003676 | nucleic acid binding | 3 | 25 |
GO:0003723 | RNA binding | 4 | 4 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004518 | nuclease activity | 4 | 5 |
GO:0004527 | exonuclease activity | 5 | 5 |
GO:0004532 | RNA exonuclease activity | 5 | 5 |
GO:0004540 | RNA nuclease activity | 4 | 5 |
GO:0005488 | binding | 1 | 25 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 5 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 5 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 25 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 25 |
GO:0004535 | poly(A)-specific ribonuclease activity | 8 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.406 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.346 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.151 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.315 |
CLV_PCSK_FUR_1 | 258 | 262 | PF00082 | 0.320 |
CLV_PCSK_FUR_1 | 594 | 598 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.189 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.194 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.173 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.328 |
CLV_Separin_Metazoa | 17 | 21 | PF03568 | 0.389 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.520 |
DEG_COP1_1 | 28 | 39 | PF00400 | 0.482 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.302 |
DEG_ODPH_VHL_1 | 88 | 100 | PF01847 | 0.356 |
DOC_ANK_TNKS_1 | 577 | 584 | PF00023 | 0.450 |
DOC_MAPK_gen_1 | 130 | 136 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 209 | 218 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 238 | 248 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 241 | 250 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 60 | 68 | PF00069 | 0.465 |
DOC_MAPK_NFAT4_5 | 241 | 249 | PF00069 | 0.520 |
DOC_MAPK_RevD_3 | 246 | 261 | PF00069 | 0.356 |
DOC_PP1_RVXF_1 | 213 | 219 | PF00149 | 0.365 |
DOC_PP1_RVXF_1 | 299 | 305 | PF00149 | 0.451 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.391 |
DOC_PP4_FxxP_1 | 568 | 571 | PF00568 | 0.670 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.488 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 187 | 194 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 215 | 219 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 586 | 590 | PF00244 | 0.692 |
LIG_Actin_WH2_2 | 523 | 541 | PF00022 | 0.322 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.381 |
LIG_BRCT_BRCA1_1 | 366 | 370 | PF00533 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 322 | 325 | PF00928 | 0.520 |
LIG_eIF4E_1 | 400 | 406 | PF01652 | 0.520 |
LIG_eIF4E_1 | 96 | 102 | PF01652 | 0.520 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.522 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.463 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.563 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.438 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.417 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.423 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.434 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.425 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.502 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.360 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.457 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.409 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 566 | 571 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 416 | 427 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.437 |
LIG_NRBOX | 427 | 433 | PF00104 | 0.460 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.520 |
LIG_Pex14_2 | 300 | 304 | PF04695 | 0.432 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.460 |
LIG_Pex14_2 | 8 | 12 | PF04695 | 0.419 |
LIG_RPA_C_Fungi | 182 | 194 | PF08784 | 0.428 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.321 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.262 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.329 |
LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.333 |
LIG_SH2_PTP2 | 543 | 546 | PF00017 | 0.321 |
LIG_SH2_SRC | 400 | 403 | PF00017 | 0.234 |
LIG_SH2_SRC | 543 | 546 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 457 | 461 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.456 |
LIG_SH3_1 | 539 | 545 | PF00018 | 0.311 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.287 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.341 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.297 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.440 |
LIG_SUMO_SIM_anti_2 | 270 | 275 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 401 | 407 | PF11976 | 0.234 |
LIG_SUMO_SIM_par_1 | 267 | 272 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 475 | 480 | PF11976 | 0.307 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.341 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.394 |
LIG_TRFH_1 | 100 | 104 | PF08558 | 0.280 |
LIG_WW_1 | 90 | 93 | PF00397 | 0.199 |
LIG_WW_3 | 89 | 93 | PF00397 | 0.199 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.373 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.400 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.362 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.471 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.671 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.407 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.305 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.376 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.279 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.393 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.515 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.407 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.350 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.254 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.412 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.485 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.510 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.393 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.379 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.474 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.250 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.425 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.411 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.439 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.617 |
MOD_N-GLC_1 | 532 | 537 | PF02516 | 0.500 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.321 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.350 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.298 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.330 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.451 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.262 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.397 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.321 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.638 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.383 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.400 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.266 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.267 |
MOD_PK_1 | 369 | 375 | PF00069 | 0.272 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.234 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.176 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.371 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.686 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.400 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.199 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.465 |
MOD_Plk_1 | 532 | 538 | PF00069 | 0.413 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.350 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.303 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.375 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.239 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.439 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.398 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.300 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.367 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.644 |
TRG_DiLeu_BaEn_1 | 290 | 295 | PF01217 | 0.252 |
TRG_DiLeu_BaLyEn_6 | 533 | 538 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.211 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 593 | 596 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.372 |
TRG_NLS_Bipartite_1 | 195 | 214 | PF00514 | 0.164 |
TRG_NLS_MonoExtN_4 | 209 | 214 | PF00514 | 0.164 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 528 | 532 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P603 | Leptomonas seymouri | 26% | 100% |
A0A0N1ILJ1 | Leptomonas seymouri | 67% | 98% |
A0A0S4IMW3 | Bodo saltans | 26% | 100% |
A0A1X0NLC6 | Trypanosomatidae | 25% | 100% |
A0A1X0NXI3 | Trypanosomatidae | 43% | 99% |
A0A3Q8ICI3 | Leishmania donovani | 93% | 100% |
A0A3R7K5K5 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X9D8 | Leishmania donovani | 27% | 88% |
A0A3S7XC77 | Leishmania donovani | 26% | 100% |
A0A422N5N5 | Trypanosoma rangeli | 49% | 100% |
A4HCS6 | Leishmania braziliensis | 89% | 100% |
A4HQF5 | Leishmania braziliensis | 27% | 100% |
A4I0A0 | Leishmania infantum | 93% | 100% |
A4IBC6 | Leishmania infantum | 27% | 88% |
A4IC91 | Leishmania infantum | 26% | 100% |
B2RXZ1 | Mus musculus | 25% | 100% |
C9ZV58 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A3T2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AF58 | Leishmania major | 27% | 88% |
E9AU71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AW65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B6B4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 88% |
H9JAQ7 | Bombyx mori | 24% | 100% |
O95453 | Homo sapiens | 22% | 94% |
P69341 | Bos taurus | 23% | 94% |
Q4Q0C3 | Leishmania major | 26% | 100% |
Q5RC51 | Pongo abelii | 23% | 94% |
Q7ZU92 | Danio rerio | 23% | 91% |
Q8NA58 | Homo sapiens | 23% | 100% |
Q8VDG3 | Mus musculus | 23% | 96% |
Q90ZA1 | Xenopus laevis | 23% | 95% |
Q9LG26 | Arabidopsis thaliana | 22% | 87% |
V5ASU9 | Trypanosoma cruzi | 27% | 100% |
V5BCG2 | Trypanosoma cruzi | 46% | 100% |