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) | yes | yes: 2 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016604 | nuclear body | 2 | 1 |
GO:0016607 | nuclear speck | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I2Y0
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 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:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 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:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.617 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.452 |
CLV_PCSK_FUR_1 | 344 | 348 | PF00082 | 0.536 |
CLV_PCSK_FUR_1 | 357 | 361 | PF00082 | 0.391 |
CLV_PCSK_FUR_1 | 370 | 374 | PF00082 | 0.530 |
CLV_PCSK_FUR_1 | 380 | 384 | PF00082 | 0.532 |
CLV_PCSK_FUR_1 | 390 | 394 | PF00082 | 0.384 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.406 |
CLV_PCSK_FUR_1 | 425 | 429 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.244 |
CLV_PCSK_PC7_1 | 220 | 226 | PF00082 | 0.573 |
CLV_PCSK_PC7_1 | 340 | 346 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 357 | 363 | PF00082 | 0.363 |
CLV_PCSK_PC7_1 | 400 | 406 | PF00082 | 0.447 |
CLV_PCSK_PC7_1 | 411 | 417 | PF00082 | 0.572 |
CLV_PCSK_PC7_1 | 421 | 427 | PF00082 | 0.602 |
CLV_PCSK_PC7_1 | 443 | 449 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.197 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.411 |
DOC_CYCLIN_RxL_1 | 185 | 193 | PF00134 | 0.483 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 237 | 244 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 237 | 246 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 275 | 282 | PF00069 | 0.483 |
DOC_PP2B_PxIxI_1 | 275 | 281 | PF00149 | 0.444 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.445 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.523 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.501 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.229 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.402 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.466 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.498 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 51 | 57 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.413 |
LIG_MAD2 | 139 | 147 | PF02301 | 0.350 |
LIG_NRP_CendR_1 | 447 | 449 | PF00754 | 0.631 |
LIG_REV1ctd_RIR_1 | 21 | 30 | PF16727 | 0.400 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.422 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.411 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.550 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.483 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.411 |
LIG_TRFH_1 | 167 | 171 | PF08558 | 0.400 |
LIG_WW_3 | 207 | 211 | PF00397 | 0.542 |
LIG_WW_3 | 412 | 416 | PF00397 | 0.608 |
LIG_WW_3 | 422 | 426 | PF00397 | 0.698 |
LIG_WW_3 | 432 | 436 | PF00397 | 0.488 |
LIG_WW_3 | 438 | 442 | PF00397 | 0.560 |
LIG_WW_3 | 444 | 448 | PF00397 | 0.517 |
MOD_CDC14_SPxK_1 | 412 | 415 | PF00782 | 0.537 |
MOD_CDC14_SPxK_1 | 422 | 425 | PF00782 | 0.535 |
MOD_CDC14_SPxK_1 | 432 | 435 | PF00782 | 0.535 |
MOD_CDC14_SPxK_1 | 438 | 441 | PF00782 | 0.528 |
MOD_CDC14_SPxK_1 | 444 | 447 | PF00782 | 0.502 |
MOD_CDK_SPxK_1 | 409 | 415 | PF00069 | 0.534 |
MOD_CDK_SPxK_1 | 419 | 425 | PF00069 | 0.537 |
MOD_CDK_SPxK_1 | 429 | 435 | PF00069 | 0.538 |
MOD_CDK_SPxK_1 | 441 | 447 | PF00069 | 0.525 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.674 |
MOD_CDK_SPxxK_3 | 419 | 426 | PF00069 | 0.607 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.600 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.461 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.501 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.523 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.552 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.371 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.480 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.486 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.418 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.473 |
MOD_DYRK1A_RPxSP_1 | 409 | 413 | PF00069 | 0.537 |
MOD_DYRK1A_RPxSP_1 | 419 | 423 | PF00069 | 0.536 |
MOD_DYRK1A_RPxSP_1 | 435 | 439 | PF00069 | 0.536 |
MOD_DYRK1A_RPxSP_1 | 441 | 445 | PF00069 | 0.545 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.521 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.650 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.696 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.288 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.614 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.233 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.192 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.226 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.345 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.157 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.480 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.482 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.463 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.654 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.563 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.586 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.526 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.612 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.602 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.483 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.374 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.552 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.495 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.453 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.511 |
MOD_PKA_1 | 347 | 353 | PF00069 | 0.481 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.351 |
MOD_PKA_1 | 372 | 378 | PF00069 | 0.518 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.520 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.398 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.436 |
MOD_PKA_1 | 415 | 421 | PF00069 | 0.606 |
MOD_PKA_1 | 427 | 433 | PF00069 | 0.479 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.581 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.488 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.601 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.610 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.351 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.518 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.520 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.398 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.436 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.606 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.479 |
MOD_PKB_1 | 345 | 353 | PF00069 | 0.530 |
MOD_PKB_1 | 360 | 368 | PF00069 | 0.358 |
MOD_PKB_1 | 370 | 378 | PF00069 | 0.518 |
MOD_PKB_1 | 380 | 388 | PF00069 | 0.525 |
MOD_PKB_1 | 390 | 398 | PF00069 | 0.324 |
MOD_PKB_1 | 403 | 411 | PF00069 | 0.418 |
MOD_PKB_1 | 425 | 433 | PF00069 | 0.588 |
MOD_Plk_2-3 | 265 | 271 | PF00069 | 0.331 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.444 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.461 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.411 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.444 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.544 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.537 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.538 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.525 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 311 | 316 | PF01217 | 0.461 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 440 | 443 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMB5 | Leptomonas seymouri | 51% | 100% |
A0A1X0NSK5 | Trypanosomatidae | 30% | 97% |
A0A3R7LQ31 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X0Y2 | Leishmania donovani | 99% | 99% |
A4HFY7 | Leishmania braziliensis | 81% | 100% |
C9ZJH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ADJ0 | Leishmania major | 98% | 100% |
E9AZB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |