Nucleic acid binding, RNA-binding 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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I171
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003723 | RNA binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.551 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.539 |
DOC_CKS1_1 | 470 | 475 | PF01111 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 184 | 190 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 482 | 488 | PF00134 | 0.705 |
DOC_CYCLIN_yCln2_LP_2 | 528 | 534 | PF00134 | 0.607 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 517 | 526 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 519 | 528 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 535 | 543 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 154 | 161 | PF00149 | 0.474 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.371 |
DOC_PP2B_LxvP_1 | 188 | 191 | PF13499 | 0.606 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.697 |
DOC_PP2B_LxvP_1 | 482 | 485 | PF13499 | 0.714 |
DOC_PP2B_LxvP_1 | 528 | 531 | PF13499 | 0.663 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.511 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.537 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.758 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 519 | 525 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 577 | 583 | PF00244 | 0.615 |
LIG_APCC_ABBAyCdc20_2 | 163 | 169 | PF00400 | 0.498 |
LIG_deltaCOP1_diTrp_1 | 315 | 324 | PF00928 | 0.474 |
LIG_EVH1_1 | 189 | 193 | PF00568 | 0.602 |
LIG_EVH1_2 | 347 | 351 | PF00568 | 0.424 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.491 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.438 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.304 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.428 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.388 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.399 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.579 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.558 |
LIG_Integrin_isoDGR_2 | 138 | 140 | PF01839 | 0.500 |
LIG_LIR_Apic_2 | 247 | 251 | PF02991 | 0.699 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 315 | 320 | PF02991 | 0.506 |
LIG_LIR_Apic_2 | 423 | 428 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 119 | 129 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 178 | 189 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.470 |
LIG_MYND_1 | 187 | 191 | PF01753 | 0.615 |
LIG_MYND_1 | 211 | 215 | PF01753 | 0.579 |
LIG_MYND_1 | 70 | 74 | PF01753 | 0.490 |
LIG_PROFILIN_1 | 208 | 214 | PF00235 | 0.609 |
LIG_PROFILIN_1 | 454 | 460 | PF00235 | 0.582 |
LIG_PTB_Apo_2 | 318 | 325 | PF02174 | 0.412 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.448 |
LIG_PTB_Phospho_1 | 72 | 78 | PF10480 | 0.448 |
LIG_REV1ctd_RIR_1 | 79 | 84 | PF16727 | 0.482 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.657 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.661 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.438 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.367 |
LIG_SH2_GRB2like | 19 | 22 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 97 | 100 | PF00017 | 0.448 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 353 | 357 | PF00017 | 0.367 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.755 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.459 |
LIG_SH3_1 | 248 | 254 | PF00018 | 0.698 |
LIG_SH3_1 | 453 | 459 | PF00018 | 0.635 |
LIG_SH3_2 | 191 | 196 | PF14604 | 0.597 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.652 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.723 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.672 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.698 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.659 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.632 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.657 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.760 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.476 |
LIG_SH3_CIN85_PxpxPR_1 | 191 | 196 | PF14604 | 0.623 |
LIG_SUMO_SIM_anti_2 | 149 | 155 | PF11976 | 0.447 |
LIG_SUMO_SIM_anti_2 | 23 | 30 | PF11976 | 0.421 |
LIG_TYR_ITSM | 93 | 100 | PF00017 | 0.386 |
LIG_WRC_WIRS_1 | 118 | 123 | PF05994 | 0.470 |
LIG_WW_2 | 211 | 214 | PF00397 | 0.574 |
LIG_WW_3 | 193 | 197 | PF00397 | 0.551 |
LIG_WW_3 | 51 | 55 | PF00397 | 0.460 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.580 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.642 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.427 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.724 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.664 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.753 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.713 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.726 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.388 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.466 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.423 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.504 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.533 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.598 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.418 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.704 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.630 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.675 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.699 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.520 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.681 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.665 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.763 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.497 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.732 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.764 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.731 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.673 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.558 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.519 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.369 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.810 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.744 |
MOD_N-GLC_1 | 559 | 564 | PF02516 | 0.670 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.668 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.431 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.597 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.514 |
MOD_NEK2_2 | 282 | 287 | PF00069 | 0.604 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.707 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.693 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.423 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.442 |
MOD_PKB_1 | 402 | 410 | PF00069 | 0.423 |
MOD_PKB_1 | 517 | 525 | PF00069 | 0.551 |
MOD_Plk_2-3 | 23 | 29 | PF00069 | 0.423 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.683 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.526 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.428 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.427 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.509 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.614 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.448 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.700 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.727 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.478 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.753 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.605 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.701 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.751 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.757 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 438 | 441 | PF00400 | 0.672 |
TRG_NES_CRM1_1 | 112 | 126 | PF08389 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM94 | Leptomonas seymouri | 54% | 93% |
A0A3R7MBU5 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WYR7 | Leishmania donovani | 100% | 100% |
A4HDX6 | Leishmania braziliensis | 80% | 100% |
D0A5F7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AXA5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QA67 | Leishmania major | 95% | 100% |
V5B7N8 | Trypanosoma cruzi | 36% | 100% |