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 |
Related structures:
AlphaFold database: A0A3S7X9K6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006370 | 7-methylguanosine mRNA capping | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009452 | 7-methylguanosine RNA capping | 8 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0036260 | RNA capping | 7 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003746 | translation elongation factor activity | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004483 | mRNA (nucleoside-2'-O-)-methyltransferase activity | 6 | 12 |
GO:0005488 | binding | 1 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008171 | O-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008174 | mRNA methyltransferase activity | 5 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.344 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.344 |
CLV_Separin_Metazoa | 412 | 416 | PF03568 | 0.518 |
DEG_SPOP_SBC_1 | 22 | 26 | PF00917 | 0.629 |
DOC_CYCLIN_RxL_1 | 221 | 230 | PF00134 | 0.484 |
DOC_CYCLIN_RxL_1 | 235 | 245 | PF00134 | 0.372 |
DOC_CYCLIN_RxL_1 | 77 | 87 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 50 | 56 | PF00134 | 0.422 |
DOC_MAPK_DCC_7 | 165 | 175 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 236 | 243 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 360 | 367 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 410 | 416 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 433 | 440 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 236 | 243 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 316 | 323 | PF00069 | 0.412 |
DOC_MAPK_NFAT4_5 | 316 | 324 | PF00069 | 0.433 |
DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.377 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.470 |
DOC_PP2B_LxvP_1 | 319 | 322 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 334 | 337 | PF13499 | 0.352 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.389 |
DOC_PP4_FxxP_1 | 396 | 399 | PF00568 | 0.426 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.486 |
DOC_USP7_UBL2_3 | 445 | 449 | PF12436 | 0.629 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 164 | 173 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 284 | 294 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 326 | 336 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.516 |
LIG_Actin_WH2_2 | 387 | 404 | PF00022 | 0.470 |
LIG_BIR_III_4 | 457 | 461 | PF00653 | 0.643 |
LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.654 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.607 |
LIG_BRCT_BRCA1_1 | 48 | 52 | PF00533 | 0.522 |
LIG_CaM_IQ_9 | 182 | 197 | PF13499 | 0.636 |
LIG_eIF4E_1 | 314 | 320 | PF01652 | 0.470 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.333 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.510 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.496 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.486 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.473 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.597 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.561 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.532 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.287 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.634 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.459 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.552 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.496 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.399 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.470 |
LIG_GBD_Chelix_1 | 416 | 424 | PF00786 | 0.546 |
LIG_HCF-1_HBM_1 | 378 | 381 | PF13415 | 0.413 |
LIG_Integrin_RGD_1 | 316 | 318 | PF01839 | 0.459 |
LIG_IRF3_LxIS_1 | 239 | 244 | PF10401 | 0.479 |
LIG_LIR_Apic_2 | 42 | 47 | PF02991 | 0.433 |
LIG_LIR_Apic_2 | 92 | 97 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 268 | 274 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 33 | 43 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 392 | 401 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 98 | 109 | PF02991 | 0.364 |
LIG_LIR_LC3C_4 | 331 | 336 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 392 | 396 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.344 |
LIG_PCNA_PIPBox_1 | 13 | 22 | PF02747 | 0.632 |
LIG_PCNA_yPIPBox_3 | 7 | 20 | PF02747 | 0.647 |
LIG_PTB_Apo_2 | 14 | 21 | PF02174 | 0.632 |
LIG_PTB_Apo_2 | 147 | 154 | PF02174 | 0.328 |
LIG_PTB_Phospho_1 | 14 | 20 | PF10480 | 0.631 |
LIG_REV1ctd_RIR_1 | 354 | 364 | PF16727 | 0.362 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.379 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.670 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.460 |
LIG_SH2_GRB2like | 177 | 180 | PF00017 | 0.424 |
LIG_SH2_NCK_1 | 381 | 385 | PF00017 | 0.396 |
LIG_SH2_SRC | 177 | 180 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.387 |
LIG_SH3_2 | 61 | 66 | PF14604 | 0.537 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.386 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.480 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.535 |
LIG_SUMO_SIM_par_1 | 52 | 59 | PF11976 | 0.471 |
LIG_TYR_ITIM | 99 | 104 | PF00017 | 0.385 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.473 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.561 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.572 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.716 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.755 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.602 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.613 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.385 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.541 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.715 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.411 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.412 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.738 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.591 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.528 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.437 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.425 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.552 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.373 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.515 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.390 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.502 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.374 |
MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.728 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.523 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.651 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.479 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.593 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.339 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.603 |
MOD_PK_1 | 247 | 253 | PF00069 | 0.445 |
MOD_PK_1 | 518 | 524 | PF00069 | 0.444 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.467 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.363 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.439 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.522 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.643 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.385 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.540 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.374 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.450 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.515 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.364 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.450 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.420 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.389 |
MOD_SUMO_rev_2 | 183 | 192 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 462 | 472 | PF00179 | 0.677 |
MOD_SUMO_rev_2 | 67 | 75 | PF00179 | 0.363 |
TRG_DiLeu_BaEn_1 | 386 | 391 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.596 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.402 |
TRG_ER_diArg_1 | 146 | 149 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 432 | 435 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.363 |
TRG_ER_FFAT_2 | 14 | 25 | PF00635 | 0.661 |
TRG_NLS_MonoCore_2 | 6 | 11 | PF00514 | 0.634 |
TRG_NLS_MonoExtC_3 | 7 | 12 | PF00514 | 0.579 |
TRG_NLS_MonoExtN_4 | 7 | 13 | PF00514 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB31 | Leptomonas seymouri | 74% | 100% |
A0A0S4IHM6 | Bodo saltans | 53% | 100% |
A0A0S4JS06 | Bodo saltans | 45% | 100% |
A0A1X0P597 | Trypanosomatidae | 63% | 100% |
A0A422NR92 | Trypanosoma rangeli | 58% | 100% |
A4HN05 | Leishmania braziliensis | 87% | 99% |
A4IBM8 | Leishmania infantum | 99% | 100% |
C9ZZ04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AFG2 | Leishmania major | 97% | 100% |
E9B6L7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |