Nucleic acid binding, RNA helicase
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HZ60
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.735 |
CLV_C14_Caspase3-7 | 331 | 335 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.620 |
CLV_MEL_PAP_1 | 307 | 313 | PF00089 | 0.391 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.169 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.514 |
CLV_PCSK_FUR_1 | 14 | 18 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.405 |
DEG_APCC_DBOX_1 | 164 | 172 | PF00400 | 0.400 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.708 |
DOC_CYCLIN_RxL_1 | 127 | 135 | PF00134 | 0.519 |
DOC_CYCLIN_RxL_1 | 515 | 526 | PF00134 | 0.453 |
DOC_CYCLIN_RxL_1 | 653 | 661 | PF00134 | 0.531 |
DOC_CYCLIN_yClb1_LxF_4 | 319 | 325 | PF00134 | 0.394 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 646 | 655 | PF00134 | 0.439 |
DOC_CYCLIN_yCln2_LP_2 | 651 | 657 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 16 | 27 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 316 | 324 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 552 | 562 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 632 | 640 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 174 | 182 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 632 | 640 | PF00069 | 0.590 |
DOC_PP1_RVXF_1 | 410 | 417 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.535 |
DOC_PP1_RVXF_1 | 516 | 523 | PF00149 | 0.453 |
DOC_PP2B_LxvP_1 | 531 | 534 | PF13499 | 0.453 |
DOC_PP4_FxxP_1 | 675 | 678 | PF00568 | 0.370 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 319 | 323 | PF12436 | 0.436 |
DOC_USP7_UBL2_3 | 452 | 456 | PF12436 | 0.734 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.647 |
DOC_USP7_UBL2_3 | 635 | 639 | PF12436 | 0.605 |
DOC_USP7_UBL2_3 | 656 | 660 | PF12436 | 0.430 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.390 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.706 |
LIG_14-3-3_CanoR_1 | 239 | 246 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 310 | 318 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 395 | 403 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 484 | 493 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 546 | 556 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 676 | 685 | PF00244 | 0.506 |
LIG_Actin_WH2_2 | 164 | 181 | PF00022 | 0.521 |
LIG_Actin_WH2_2 | 192 | 207 | PF00022 | 0.416 |
LIG_Actin_WH2_2 | 307 | 325 | PF00022 | 0.441 |
LIG_Actin_WH2_2 | 644 | 662 | PF00022 | 0.418 |
LIG_APCC_ABBA_1 | 379 | 384 | PF00400 | 0.452 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.698 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.550 |
LIG_EH_1 | 628 | 632 | PF12763 | 0.441 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.453 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.453 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.564 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.455 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.519 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.550 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.457 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.569 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.532 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.512 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.550 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.437 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.540 |
LIG_GBD_Chelix_1 | 196 | 204 | PF00786 | 0.240 |
LIG_Integrin_isoDGR_2 | 105 | 107 | PF01839 | 0.350 |
LIG_Integrin_isoDGR_2 | 410 | 412 | PF01839 | 0.488 |
LIG_LIR_Apic_2 | 120 | 126 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 521 | 530 | PF02991 | 0.478 |
LIG_LIR_LC3C_4 | 622 | 627 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 521 | 525 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.502 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.453 |
LIG_RPA_C_Fungi | 48 | 60 | PF08784 | 0.500 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.296 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.296 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.374 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.549 |
LIG_SH2_NCK_1 | 633 | 637 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 172 | 175 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 367 | 370 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 692 | 695 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 692 | 695 | PF00017 | 0.517 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.388 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.414 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.507 |
LIG_SH3_4 | 635 | 642 | PF00018 | 0.567 |
LIG_SUMO_SIM_par_1 | 370 | 376 | PF11976 | 0.437 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.645 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.720 |
LIG_TRAF2_1 | 693 | 696 | PF00917 | 0.487 |
LIG_UBA3_1 | 321 | 327 | PF00899 | 0.390 |
MOD_CDC14_SPxK_1 | 291 | 294 | PF00782 | 0.463 |
MOD_CDK_SPxK_1 | 288 | 294 | PF00069 | 0.468 |
MOD_CDK_SPxxK_3 | 445 | 452 | PF00069 | 0.627 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.296 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.707 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.607 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.608 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.502 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.556 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.513 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.514 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.518 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.552 |
MOD_Cter_Amidation | 235 | 238 | PF01082 | 0.751 |
MOD_Cter_Amidation | 314 | 317 | PF01082 | 0.379 |
MOD_Cter_Amidation | 454 | 457 | PF01082 | 0.732 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.614 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.314 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.750 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.602 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.640 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.759 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.715 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.669 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.663 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.400 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.296 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.524 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.649 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.613 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.433 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.533 |
MOD_LATS_1 | 112 | 118 | PF00433 | 0.296 |
MOD_LATS_1 | 64 | 70 | PF00433 | 0.494 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.432 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.332 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.545 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.539 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.581 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.545 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.512 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.385 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.500 |
MOD_OFUCOSY | 385 | 390 | PF10250 | 0.410 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.312 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.463 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.391 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.571 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.394 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.538 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.555 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.504 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.552 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.363 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.231 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.502 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.707 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.178 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.366 |
TRG_NLS_MonoCore_2 | 237 | 242 | PF00514 | 0.715 |
TRG_NLS_MonoExtC_3 | 16 | 21 | PF00514 | 0.668 |
TRG_NLS_MonoExtC_3 | 236 | 241 | PF00514 | 0.719 |
TRG_NLS_MonoExtN_4 | 14 | 21 | PF00514 | 0.724 |
TRG_NLS_MonoExtN_4 | 235 | 242 | PF00514 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 130 | 135 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 401 | 405 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 484 | 489 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P856 | Leptomonas seymouri | 65% | 100% |
A0A0S4J214 | Bodo saltans | 45% | 100% |
A0A1X0NXJ9 | Trypanosomatidae | 48% | 100% |
A0A3R7MLR3 | Trypanosoma rangeli | 49% | 100% |
A0A3S7WWF8 | Leishmania donovani | 99% | 100% |
A4HBQ8 | Leishmania braziliensis | 82% | 100% |
D0A1I1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AV28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4QCF4 | Leishmania major | 94% | 100% |
V5BDT6 | Trypanosoma cruzi | 48% | 100% |