Nucleic acid binding, RNA-binding
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. | yes | yes: 25 |
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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S7X388
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.698 |
CLV_PCSK_FUR_1 | 614 | 618 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.751 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.857 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.447 |
DEG_APCC_DBOX_1 | 591 | 599 | PF00400 | 0.507 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.660 |
DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 213 | 222 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 601 | 610 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 215 | 224 | PF00069 | 0.754 |
DOC_MAPK_MEF2A_6 | 334 | 342 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 337 | 343 | PF00149 | 0.623 |
DOC_PP1_RVXF_1 | 561 | 567 | PF00149 | 0.567 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.726 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.630 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.745 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.419 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 440 | 445 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 563 | 567 | PF00244 | 0.568 |
LIG_Actin_WH2_2 | 480 | 496 | PF00022 | 0.652 |
LIG_BIR_III_4 | 235 | 239 | PF00653 | 0.720 |
LIG_BRCT_BRCA1_1 | 42 | 46 | PF00533 | 0.528 |
LIG_DLG_GKlike_1 | 440 | 448 | PF00625 | 0.541 |
LIG_EH1_1 | 544 | 552 | PF00400 | 0.556 |
LIG_eIF4E_1 | 545 | 551 | PF01652 | 0.472 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.551 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.498 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.499 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.752 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.478 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.562 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.539 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.573 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.689 |
LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.764 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.573 |
LIG_NRBOX | 440 | 446 | PF00104 | 0.542 |
LIG_NRBOX | 545 | 551 | PF00104 | 0.565 |
LIG_Pex14_1 | 9 | 13 | PF04695 | 0.633 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.771 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.497 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.689 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.642 |
LIG_SH2_NCK_1 | 349 | 353 | PF00017 | 0.709 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.682 |
LIG_SH2_STAP1 | 587 | 591 | PF00017 | 0.603 |
LIG_SH2_STAT3 | 587 | 590 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.687 |
LIG_SH3_1 | 136 | 142 | PF00018 | 0.778 |
LIG_SH3_1 | 507 | 513 | PF00018 | 0.560 |
LIG_SH3_2 | 139 | 144 | PF14604 | 0.838 |
LIG_SH3_2 | 510 | 515 | PF14604 | 0.564 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.821 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.642 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.560 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.713 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.730 |
LIG_SH3_CIN85_PxpxPR_1 | 139 | 144 | PF14604 | 0.821 |
LIG_SUMO_SIM_par_1 | 547 | 554 | PF11976 | 0.510 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.695 |
LIG_TYR_ITIM | 197 | 202 | PF00017 | 0.642 |
LIG_WRC_WIRS_1 | 568 | 573 | PF05994 | 0.568 |
LIG_WW_3 | 141 | 145 | PF00397 | 0.828 |
MOD_CDC14_SPxK_1 | 491 | 494 | PF00782 | 0.639 |
MOD_CDK_SPxK_1 | 333 | 339 | PF00069 | 0.642 |
MOD_CDK_SPxK_1 | 488 | 494 | PF00069 | 0.638 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.642 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.601 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.605 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.770 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.626 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.633 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.677 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.599 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.620 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.455 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.470 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.559 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.579 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.657 |
MOD_N-GLC_2 | 450 | 452 | PF02516 | 0.547 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.615 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.554 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.671 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.726 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.539 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.648 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.657 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.642 |
MOD_NEK2_2 | 479 | 484 | PF00069 | 0.656 |
MOD_NEK2_2 | 492 | 497 | PF00069 | 0.542 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.629 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.638 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.601 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.598 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.644 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.569 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.581 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.482 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.622 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.559 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.566 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.642 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.519 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.511 |
MOD_SUMO_for_1 | 602 | 605 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 149 | 155 | PF00179 | 0.797 |
MOD_SUMO_rev_2 | 283 | 289 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 35 | 43 | PF00179 | 0.733 |
MOD_SUMO_rev_2 | 53 | 58 | PF00179 | 0.469 |
TRG_DiLeu_BaEn_4 | 83 | 89 | PF01217 | 0.704 |
TRG_DiLeu_BaLyEn_6 | 606 | 611 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.773 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.563 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 614 | 617 | PF00400 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.790 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMQ3 | Leptomonas seymouri | 72% | 72% |
A0A0S4IX72 | Bodo saltans | 35% | 84% |
A0A1X0P281 | Trypanosomatidae | 47% | 79% |
A0A3R7N4R9 | Trypanosoma rangeli | 46% | 80% |
A4HI65 | Leishmania braziliensis | 91% | 100% |
A4I5E2 | Leishmania infantum | 100% | 100% |
C9ZQS2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 82% |
E9B0P0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4Q7J2 | Leishmania major | 99% | 100% |
V5B929 | Trypanosoma cruzi | 48% | 83% |