RNA Processing, poly(A)-specific ribonuclease PARN Uncharacterized
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: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 3 |
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:0110165 | cellular anatomical entity | 1 | 3 |
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: A0A3Q8ICI3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 26 |
GO:0005488 | binding | 1 | 26 |
GO:0097159 | organic cyclic compound binding | 2 | 26 |
GO:1901363 | heterocyclic compound binding | 2 | 26 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 4 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004518 | nuclease activity | 4 | 4 |
GO:0004527 | exonuclease activity | 5 | 4 |
GO:0004532 | RNA exonuclease activity | 5 | 4 |
GO:0004535 | poly(A)-specific ribonuclease activity | 8 | 1 |
GO:0004540 | RNA nuclease activity | 4 | 4 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 4 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 4 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 4 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 4 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 4 |
GO:0003723 | RNA binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.401 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.344 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.319 |
CLV_PCSK_FUR_1 | 258 | 262 | PF00082 | 0.324 |
CLV_PCSK_FUR_1 | 597 | 601 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.178 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.168 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.338 |
CLV_Separin_Metazoa | 17 | 21 | PF03568 | 0.385 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.524 |
DEG_COP1_1 | 28 | 39 | PF00400 | 0.488 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.322 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.504 |
DOC_MAPK_gen_1 | 130 | 136 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 209 | 218 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 238 | 248 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 241 | 248 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 250 | 257 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 60 | 68 | PF00069 | 0.463 |
DOC_MAPK_NFAT4_5 | 241 | 249 | PF00069 | 0.524 |
DOC_PP1_RVXF_1 | 299 | 305 | PF00149 | 0.449 |
DOC_PP4_FxxP_1 | 568 | 571 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.468 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.421 |
LIG_14-3-3_CanoR_1 | 187 | 194 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 589 | 593 | PF00244 | 0.692 |
LIG_Actin_WH2_2 | 523 | 541 | PF00022 | 0.315 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.384 |
LIG_BRCT_BRCA1_1 | 366 | 370 | PF00533 | 0.446 |
LIG_deltaCOP1_diTrp_1 | 322 | 325 | PF00928 | 0.524 |
LIG_eIF4E_1 | 400 | 406 | PF01652 | 0.524 |
LIG_eIF4E_1 | 96 | 102 | PF01652 | 0.524 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.514 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.468 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.560 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.407 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.439 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.417 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.342 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.463 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.419 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.404 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.467 |
LIG_LIR_Apic_2 | 566 | 571 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 416 | 427 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.431 |
LIG_LYPXL_yS_3 | 252 | 255 | PF13949 | 0.372 |
LIG_NRBOX | 427 | 433 | PF00104 | 0.464 |
LIG_NRP_CendR_1 | 599 | 601 | PF00754 | 0.639 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.524 |
LIG_Pex14_2 | 300 | 304 | PF04695 | 0.432 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.453 |
LIG_Pex14_2 | 8 | 12 | PF04695 | 0.414 |
LIG_RPA_C_Fungi | 182 | 194 | PF08784 | 0.432 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.338 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.263 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.313 |
LIG_SH2_PTP2 | 543 | 546 | PF00017 | 0.331 |
LIG_SH2_SRC | 400 | 403 | PF00017 | 0.230 |
LIG_SH2_SRC | 543 | 546 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 457 | 461 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.479 |
LIG_SH3_1 | 539 | 545 | PF00018 | 0.313 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.314 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.327 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.272 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.456 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 270 | 275 | PF11976 | 0.401 |
LIG_SUMO_SIM_anti_2 | 401 | 407 | PF11976 | 0.230 |
LIG_SUMO_SIM_par_1 | 267 | 272 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 475 | 480 | PF11976 | 0.302 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.351 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.357 |
LIG_TRFH_1 | 100 | 104 | PF08558 | 0.291 |
LIG_WW_1 | 90 | 93 | PF00397 | 0.195 |
LIG_WW_3 | 89 | 93 | PF00397 | 0.195 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.346 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.345 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.432 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.448 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.692 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.386 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.316 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.413 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.257 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.376 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.215 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.509 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.377 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.288 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.230 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.364 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.321 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.439 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.481 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.356 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.333 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.266 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.259 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.442 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.599 |
MOD_N-GLC_1 | 462 | 467 | PF02516 | 0.507 |
MOD_N-GLC_1 | 532 | 537 | PF02516 | 0.467 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.335 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.351 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.278 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.237 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.360 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.272 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.381 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.316 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.656 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.401 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.412 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.265 |
MOD_PK_1 | 369 | 375 | PF00069 | 0.252 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.230 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.330 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.690 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.358 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.415 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.285 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.360 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.489 |
MOD_Plk_1 | 532 | 538 | PF00069 | 0.414 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.201 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.195 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.397 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.237 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.414 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.399 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.359 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.283 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.359 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.313 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.616 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.258 |
TRG_DiLeu_BaEn_1 | 290 | 295 | PF01217 | 0.230 |
TRG_DiLeu_BaEn_1 | 532 | 537 | PF01217 | 0.272 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.298 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 588 | 590 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 596 | 599 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 528 | 532 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P603 | Leptomonas seymouri | 27% | 100% |
A0A0N1ILJ1 | Leptomonas seymouri | 67% | 99% |
A0A0S4IMW3 | Bodo saltans | 26% | 100% |
A0A0S4IR41 | Bodo saltans | 28% | 94% |
A0A0S4J225 | Bodo saltans | 28% | 83% |
A0A1X0NLC6 | Trypanosomatidae | 24% | 100% |
A0A1X0NXI3 | Trypanosomatidae | 42% | 99% |
A0A3R7K5K5 | Trypanosoma rangeli | 26% | 100% |
A0A3S7X9D8 | Leishmania donovani | 27% | 89% |
A0A3S7XC77 | Leishmania donovani | 26% | 100% |
A0A422N5N5 | Trypanosoma rangeli | 48% | 100% |
A4HCS6 | Leishmania braziliensis | 87% | 99% |
A4HQF5 | Leishmania braziliensis | 26% | 100% |
A4I0A0 | Leishmania infantum | 100% | 100% |
A4IBC6 | Leishmania infantum | 27% | 89% |
A4IC91 | Leishmania infantum | 26% | 100% |
B2RXZ1 | Mus musculus | 26% | 100% |
C9ZV58 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
D0A3T2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AF58 | Leishmania major | 26% | 89% |
E9AU71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AW65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
E9B6B4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 89% |
H9JAQ7 | Bombyx mori | 23% | 100% |
O95453 | Homo sapiens | 22% | 94% |
P69341 | Bos taurus | 22% | 94% |
Q4Q0C3 | Leishmania major | 26% | 100% |
Q4QBB3 | Leishmania major | 93% | 100% |
Q5RC51 | Pongo abelii | 22% | 94% |
Q7ZU92 | Danio rerio | 25% | 91% |
Q8NA58 | Homo sapiens | 22% | 100% |
Q8VDG3 | Mus musculus | 24% | 96% |
Q90ZA1 | Xenopus laevis | 23% | 95% |
Q9LG26 | Arabidopsis thaliana | 21% | 87% |
V5ASU9 | Trypanosoma cruzi | 26% | 100% |
V5BCG2 | Trypanosoma cruzi | 46% | 100% |