Nucleases, ribonuclease
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4IBC6
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0000175 | 3'-5'-RNA exonuclease activity | 7 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004518 | nuclease activity | 4 | 2 |
GO:0004527 | exonuclease activity | 5 | 2 |
GO:0004532 | RNA exonuclease activity | 5 | 2 |
GO:0004540 | RNA nuclease activity | 4 | 2 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 388 | 392 | PF00656 | 0.431 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.251 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.548 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.401 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.421 |
DEG_SPOP_SBC_1 | 409 | 413 | PF00917 | 0.431 |
DOC_CDC14_PxL_1 | 187 | 195 | PF14671 | 0.406 |
DOC_CYCLIN_yClb3_PxF_3 | 469 | 475 | PF00134 | 0.396 |
DOC_MAPK_gen_1 | 268 | 276 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 316 | 324 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 665 | 672 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.505 |
DOC_PP1_RVXF_1 | 442 | 449 | PF00149 | 0.593 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.396 |
DOC_SPAK_OSR1_1 | 333 | 337 | PF12202 | 0.431 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.359 |
DOC_USP7_UBL2_3 | 400 | 404 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 178 | 186 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 417 | 423 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 665 | 673 | PF00244 | 0.491 |
LIG_APCC_ABBA_1 | 78 | 83 | PF00400 | 0.451 |
LIG_APCC_ABBAyCdc20_2 | 382 | 388 | PF00400 | 0.431 |
LIG_BIR_III_4 | 88 | 92 | PF00653 | 0.543 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 525 | 529 | PF00533 | 0.523 |
LIG_eIF4E_1 | 380 | 386 | PF01652 | 0.431 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.451 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.529 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.575 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.465 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.425 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.512 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.460 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.383 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.377 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.414 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.557 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.315 |
LIG_LIR_Gen_1 | 233 | 242 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 454 | 465 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 582 | 591 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 79 | 89 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 454 | 460 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 474 | 478 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 582 | 586 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.578 |
LIG_NRBOX | 431 | 437 | PF00104 | 0.451 |
LIG_PCNA_PIPBox_1 | 456 | 465 | PF02747 | 0.431 |
LIG_PDZ_Class_2 | 672 | 677 | PF00595 | 0.441 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.451 |
LIG_Pex14_2 | 483 | 487 | PF04695 | 0.568 |
LIG_SH2_CRK | 583 | 587 | PF00017 | 0.384 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.553 |
LIG_SH2_GRB2like | 576 | 579 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 71 | 75 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 576 | 580 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 463 | 466 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 640 | 643 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.363 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.423 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.451 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 167 | 172 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 334 | 340 | PF11976 | 0.584 |
LIG_WRC_WIRS_1 | 231 | 236 | PF05994 | 0.523 |
LIG_WRC_WIRS_1 | 362 | 367 | PF05994 | 0.523 |
LIG_WRC_WIRS_1 | 472 | 477 | PF05994 | 0.451 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.586 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.582 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.513 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.451 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.451 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.525 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.405 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.501 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.487 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.514 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.471 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.330 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.339 |
MOD_Cter_Amidation | 314 | 317 | PF01082 | 0.226 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.251 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.284 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.228 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.325 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.313 |
MOD_GlcNHglycan | 30 | 34 | PF01048 | 0.355 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.340 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.404 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.323 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.348 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.476 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.305 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.310 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.542 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.482 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.472 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.477 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.585 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.409 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.521 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.396 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.510 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.241 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.283 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.361 |
MOD_N-GLC_1 | 610 | 615 | PF02516 | 0.581 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.386 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.431 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.596 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.446 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.539 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.482 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.413 |
MOD_NEK2_2 | 569 | 574 | PF00069 | 0.551 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.451 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.444 |
MOD_PK_1 | 507 | 513 | PF00069 | 0.576 |
MOD_PK_1 | 517 | 523 | PF00069 | 0.507 |
MOD_PKA_1 | 55 | 61 | PF00069 | 0.451 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.580 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.512 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.476 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.457 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.481 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.501 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.506 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.364 |
MOD_Plk_2-3 | 131 | 137 | PF00069 | 0.421 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.546 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.480 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.548 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.448 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.467 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.508 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.587 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.606 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.532 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.474 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.380 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.444 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.567 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.431 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.496 |
MOD_SUMO_for_1 | 386 | 389 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 289 | 294 | PF00179 | 0.521 |
TRG_DiLeu_BaEn_2 | 113 | 119 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.431 |
TRG_NES_CRM1_1 | 312 | 328 | PF08389 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 316 | 320 | PF00026 | 0.206 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGE9 | Leptomonas seymouri | 42% | 96% |
A0A0S4J225 | Bodo saltans | 22% | 93% |
A0A1X0P5M9 | Trypanosomatidae | 26% | 100% |
A0A3Q8ICI3 | Leishmania donovani | 27% | 100% |
A0A3R7LZW8 | Trypanosoma rangeli | 25% | 100% |
A0A3S7X9D8 | Leishmania donovani | 100% | 100% |
A4HCS6 | Leishmania braziliensis | 26% | 100% |
A4HMQ8 | Leishmania braziliensis | 67% | 100% |
A4I0A0 | Leishmania infantum | 27% | 100% |
C9ZZC3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AF58 | Leishmania major | 92% | 100% |
E9AW65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B6B4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QBB3 | Leishmania major | 27% | 100% |