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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q9K0
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0034248 | regulation of amide metabolic process | 5 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003729 | mRNA binding | 5 | 2 |
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 | 217 | 219 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.737 |
CLV_PCSK_FUR_1 | 386 | 390 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 503 | 505 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 541 | 543 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 55 | 59 | PF03568 | 0.369 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.393 |
DEG_APCC_DBOX_1 | 467 | 475 | PF00400 | 0.427 |
DEG_SCF_FBW7_1 | 105 | 112 | PF00400 | 0.347 |
DEG_SCF_FBW7_2 | 379 | 385 | PF00400 | 0.335 |
DOC_CDC14_PxL_1 | 171 | 179 | PF14671 | 0.327 |
DOC_CDC14_PxL_1 | 435 | 443 | PF14671 | 0.375 |
DOC_CKS1_1 | 106 | 111 | PF01111 | 0.357 |
DOC_CKS1_1 | 379 | 384 | PF01111 | 0.310 |
DOC_CKS1_1 | 413 | 418 | PF01111 | 0.373 |
DOC_CYCLIN_RxL_1 | 231 | 241 | PF00134 | 0.411 |
DOC_MAPK_MEF2A_6 | 201 | 208 | PF00069 | 0.307 |
DOC_MAPK_NFAT4_5 | 201 | 209 | PF00069 | 0.307 |
DOC_PP1_RVXF_1 | 127 | 134 | PF00149 | 0.333 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.393 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.637 |
DOC_USP7_MATH_2 | 159 | 165 | PF00917 | 0.409 |
DOC_USP7_UBL2_3 | 132 | 136 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 44 | 48 | PF12436 | 0.428 |
DOC_USP7_UBL2_3 | 563 | 567 | PF12436 | 0.693 |
DOC_USP7_UBL2_3 | 568 | 572 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 560 | 570 | PF00244 | 0.651 |
LIG_14-3-3_CterR_2 | 569 | 573 | PF00244 | 0.496 |
LIG_APCC_ABBA_1 | 206 | 211 | PF00400 | 0.367 |
LIG_APCC_ABBA_1 | 380 | 385 | PF00400 | 0.382 |
LIG_BIR_III_4 | 508 | 512 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.350 |
LIG_Clathr_ClatBox_1 | 400 | 404 | PF01394 | 0.396 |
LIG_deltaCOP1_diTrp_1 | 407 | 413 | PF00928 | 0.403 |
LIG_EH1_1 | 148 | 156 | PF00400 | 0.292 |
LIG_eIF4E_1 | 371 | 377 | PF01652 | 0.393 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.386 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.468 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.375 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.339 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.355 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.354 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.655 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.478 |
LIG_LIR_Apic_2 | 192 | 198 | PF02991 | 0.481 |
LIG_LIR_Apic_2 | 330 | 336 | PF02991 | 0.322 |
LIG_LIR_Apic_2 | 412 | 416 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.445 |
LIG_LYPXL_yS_3 | 222 | 225 | PF13949 | 0.345 |
LIG_LYPXL_yS_3 | 259 | 262 | PF13949 | 0.389 |
LIG_LYPXL_yS_3 | 88 | 91 | PF13949 | 0.355 |
LIG_NRBOX | 340 | 346 | PF00104 | 0.425 |
LIG_NRBOX | 375 | 381 | PF00104 | 0.332 |
LIG_PCNA_yPIPBox_3 | 263 | 275 | PF02747 | 0.334 |
LIG_PTB_Apo_2 | 365 | 372 | PF02174 | 0.313 |
LIG_PTB_Phospho_1 | 365 | 371 | PF10480 | 0.411 |
LIG_Rb_pABgroove_1 | 238 | 246 | PF01858 | 0.419 |
LIG_Rb_pABgroove_1 | 336 | 344 | PF01858 | 0.277 |
LIG_RPA_C_Fungi | 455 | 467 | PF08784 | 0.512 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.421 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.284 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.397 |
LIG_SH2_NCK_1 | 516 | 520 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.349 |
LIG_SH2_STAP1 | 84 | 88 | PF00017 | 0.427 |
LIG_SH2_STAT3 | 346 | 349 | PF00017 | 0.357 |
LIG_SH2_STAT3 | 371 | 374 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.509 |
LIG_SH3_1 | 217 | 223 | PF00018 | 0.417 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.414 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.353 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.417 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.381 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.476 |
LIG_SUMO_SIM_anti_2 | 202 | 207 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 211 | 217 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 26 | 32 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 421 | 427 | PF11976 | 0.402 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.549 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.431 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.375 |
LIG_UBA3_1 | 203 | 210 | PF00899 | 0.297 |
LIG_UBA3_1 | 243 | 249 | PF00899 | 0.331 |
LIG_UBA3_1 | 400 | 406 | PF00899 | 0.442 |
LIG_UBA3_1 | 56 | 62 | PF00899 | 0.430 |
LIG_UBA3_1 | 94 | 101 | PF00899 | 0.359 |
LIG_WRC_WIRS_1 | 318 | 323 | PF05994 | 0.502 |
MOD_CDK_SPxxK_3 | 194 | 201 | PF00069 | 0.480 |
MOD_CDK_SPxxK_3 | 534 | 541 | PF00069 | 0.719 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.392 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.568 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.446 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.395 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.321 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.367 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.475 |
MOD_Cter_Amidation | 501 | 504 | PF01082 | 0.663 |
MOD_Cter_Amidation | 558 | 561 | PF01082 | 0.719 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.495 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.260 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.476 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.660 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.340 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.468 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.380 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.327 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.432 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.348 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.689 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.739 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.699 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.533 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.421 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.248 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.355 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.443 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.397 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.789 |
MOD_PK_1 | 107 | 113 | PF00069 | 0.403 |
MOD_PKA_1 | 542 | 548 | PF00069 | 0.772 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.567 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.436 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.457 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.451 |
MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.650 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.351 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.402 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.515 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.352 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.502 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.340 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.484 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.306 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.308 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.376 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.646 |
MOD_SUMO_for_1 | 524 | 527 | PF00179 | 0.815 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 235 | 240 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 560 | 562 | PF00400 | 0.640 |
TRG_NLS_Bipartite_1 | 525 | 547 | PF00514 | 0.721 |
TRG_NLS_MonoExtC_3 | 541 | 546 | PF00514 | 0.714 |
TRG_NLS_MonoExtC_3 | 566 | 571 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 386 | 391 | PF00514 | 0.335 |
TRG_NLS_MonoExtN_4 | 541 | 547 | PF00514 | 0.697 |
TRG_NLS_MonoExtN_4 | 567 | 572 | PF00514 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWV1 | Leptomonas seymouri | 83% | 100% |
A0A0S4IXV1 | Bodo saltans | 48% | 82% |
A0A1X0NZF1 | Trypanosomatidae | 60% | 93% |
A0A3Q8IDL8 | Leishmania donovani | 96% | 100% |
A0A3R7MC19 | Trypanosoma rangeli | 58% | 98% |
A4HED9 | Leishmania braziliensis | 84% | 99% |
A4I1T6 | Leishmania infantum | 96% | 100% |
C9ZKE5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 94% |
E9AXX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5D8H4 | Trypanosoma cruzi | 55% | 98% |