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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: A4HQB0
Term | Name | Level | Count |
---|---|---|---|
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010629 | negative regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031047 | RNA-mediated gene silencing | 7 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060147 | regulation of post-transcriptional gene silencing | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0060964 | regulation of miRNA-mediated gene silencing | 8 | 1 |
GO:0060966 | regulation of gene silencing by RNA | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1900368 | regulation of post-transcriptional gene silencing by RNA | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.638 |
CLV_C14_Caspase3-7 | 51 | 55 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.648 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.580 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.600 |
DEG_SPOP_SBC_1 | 321 | 325 | PF00917 | 0.682 |
DOC_CKS1_1 | 466 | 471 | PF01111 | 0.768 |
DOC_MAPK_MEF2A_6 | 154 | 162 | PF00069 | 0.478 |
DOC_PIKK_1 | 97 | 104 | PF02985 | 0.767 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.669 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.379 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.567 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.619 |
DOC_USP7_UBL2_3 | 238 | 242 | PF12436 | 0.625 |
DOC_USP7_UBL2_3 | 251 | 255 | PF12436 | 0.656 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 258 | 262 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 82 | 92 | PF00244 | 0.604 |
LIG_BIR_III_2 | 109 | 113 | PF00653 | 0.754 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.729 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.491 |
LIG_Clathr_ClatBox_1 | 159 | 163 | PF01394 | 0.423 |
LIG_deltaCOP1_diTrp_1 | 284 | 290 | PF00928 | 0.545 |
LIG_eIF4E_1 | 371 | 377 | PF01652 | 0.543 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.636 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.530 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.728 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.536 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.442 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.562 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.692 |
LIG_GBD_Chelix_1 | 513 | 521 | PF00786 | 0.547 |
LIG_LIR_Apic_2 | 63 | 68 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 295 | 306 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 310 | 316 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 422 | 431 | PF02991 | 0.694 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.551 |
LIG_PDZ_Class_2 | 518 | 523 | PF00595 | 0.597 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.490 |
LIG_REV1ctd_RIR_1 | 54 | 62 | PF16727 | 0.557 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.517 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.558 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.543 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 410 | 414 | PF00017 | 0.516 |
LIG_SH2_NCK_1 | 46 | 50 | PF00017 | 0.543 |
LIG_SH2_NCK_1 | 511 | 515 | PF00017 | 0.519 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 410 | 414 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.497 |
LIG_SH3_1 | 392 | 398 | PF00018 | 0.616 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.428 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.626 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.498 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.604 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.576 |
LIG_SUMO_SIM_anti_2 | 386 | 391 | PF11976 | 0.455 |
LIG_SUMO_SIM_anti_2 | 448 | 453 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 266 | 271 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 386 | 391 | PF11976 | 0.522 |
LIG_TRAF2_1 | 174 | 177 | PF00917 | 0.607 |
LIG_TRAF2_1 | 425 | 428 | PF00917 | 0.666 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.750 |
LIG_TYR_ITIM | 348 | 353 | PF00017 | 0.543 |
LIG_UBA3_1 | 267 | 272 | PF00899 | 0.545 |
MOD_CDK_SPxxK_3 | 141 | 148 | PF00069 | 0.530 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.670 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.449 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.637 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.639 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.530 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.605 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.583 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.718 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.566 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.644 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.464 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.589 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.624 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.536 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.497 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.544 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.548 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.648 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.547 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.499 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.595 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.624 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.290 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.655 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.448 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.525 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.654 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.535 |
MOD_N-GLC_2 | 494 | 496 | PF02516 | 0.590 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.749 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.527 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.590 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.587 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.497 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.467 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.624 |
MOD_OFUCOSY | 151 | 157 | PF10250 | 0.582 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.644 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.740 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.557 |
MOD_PK_1 | 383 | 389 | PF00069 | 0.543 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.557 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.652 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.604 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.702 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.530 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.532 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.503 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.597 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.412 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.455 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.498 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.460 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.540 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.723 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.528 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.521 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.582 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.608 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.764 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.589 |
MOD_SUMO_rev_2 | 135 | 144 | PF00179 | 0.682 |
TRG_DiLeu_BaEn_1 | 155 | 160 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.699 |
TRG_DiLeu_BaEn_1 | 26 | 31 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_4 | 427 | 433 | PF01217 | 0.694 |
TRG_DiLeu_BaLyEn_6 | 271 | 276 | PF01217 | 0.532 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.543 |
TRG_NES_CRM1_1 | 448 | 458 | PF08389 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NNC5 | Trypanosomatidae | 28% | 100% |
A0A3R7RJN8 | Trypanosoma rangeli | 27% | 100% |
D0A3Z5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |