| 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:0000439 | transcription factor TFIIH core complex | 4 | 12 |
| GO:0005667 | transcription regulator complex | 2 | 12 |
| GO:0032991 | protein-containing complex | 1 | 12 |
| GO:0090575 | RNA polymerase II transcription regulator complex | 3 | 12 |
| GO:0140513 | nuclear protein-containing complex | 2 | 12 |
| GO:0005654 | nucleoplasm | 2 | 1 |
| GO:0005675 | transcription factor TFIIH holo complex | 4 | 1 |
| GO:0032806 | carboxy-terminal domain protein kinase complex | 3 | 1 |
| GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| GO:1902494 | catalytic complex | 2 | 1 |
| GO:1902554 | serine/threonine protein kinase complex | 6 | 1 |
| GO:1902911 | protein kinase complex | 5 | 1 |
| GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9ASK0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
| GO:0006259 | DNA metabolic process | 4 | 12 |
| GO:0006281 | DNA repair | 5 | 12 |
| GO:0006289 | nucleotide-excision repair | 6 | 12 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
| GO:0006950 | response to stress | 2 | 12 |
| GO:0006974 | DNA damage response | 4 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0033554 | cellular response to stress | 3 | 12 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
| GO:0043170 | macromolecule metabolic process | 3 | 12 |
| GO:0044237 | cellular metabolic process | 2 | 12 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
| GO:0046483 | heterocycle metabolic process | 3 | 12 |
| GO:0050896 | response to stimulus | 1 | 12 |
| GO:0051716 | cellular response to stimulus | 2 | 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 |
| GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
| GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
| GO:0006468 | protein phosphorylation | 5 | 1 |
| GO:0006793 | phosphorus metabolic process | 3 | 1 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
| GO:0009889 | regulation of biosynthetic process | 4 | 1 |
| GO:0010468 | regulation of gene expression | 5 | 1 |
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
| GO:0016310 | phosphorylation | 5 | 1 |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
| GO:0019222 | regulation of metabolic process | 3 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
| GO:0036211 | protein modification process | 4 | 1 |
| GO:0043412 | macromolecule modification | 4 | 1 |
| GO:0050789 | regulation of biological process | 2 | 1 |
| GO:0050794 | regulation of cellular process | 3 | 1 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
| GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
| GO:0065007 | biological regulation | 1 | 1 |
| GO:0070816 | obsolete phosphorylation of RNA polymerase II C-terminal domain | 6 | 1 |
| GO:0080090 | regulation of primary metabolic process | 4 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
| GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0001671 | ATPase activator activity | 3 | 12 |
| GO:0098772 | molecular function regulator activity | 1 | 12 |
| GO:0140677 | molecular function activator activity | 2 | 12 |
| GO:0003676 | nucleic acid binding | 3 | 1 |
| GO:0003677 | DNA binding | 4 | 1 |
| GO:0003690 | double-stranded DNA binding | 5 | 1 |
| GO:0005488 | binding | 1 | 1 |
| GO:0097159 | organic cyclic compound binding | 2 | 1 |
| GO:1901363 | heterocyclic compound binding | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.636 |
| CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.354 |
| CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.268 |
| CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.347 |
| CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.632 |
| CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.612 |
| CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.409 |
| CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.493 |
| CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.268 |
| CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.587 |
| CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.615 |
| CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.406 |
| CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.493 |
| CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.489 |
| CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.360 |
| CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.378 |
| CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.312 |
| CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.384 |
| CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.464 |
| CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.320 |
| CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.374 |
| CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.433 |
| CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.289 |
| DEG_APCC_DBOX_1 | 117 | 125 | PF00400 | 0.488 |
| DOC_ANK_TNKS_1 | 462 | 469 | PF00023 | 0.433 |
| DOC_CKS1_1 | 196 | 201 | PF01111 | 0.280 |
| DOC_CYCLIN_RxL_1 | 113 | 122 | PF00134 | 0.426 |
| DOC_CYCLIN_RxL_1 | 232 | 240 | PF00134 | 0.346 |
| DOC_MAPK_FxFP_2 | 278 | 281 | PF00069 | 0.350 |
| DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.396 |
| DOC_PP1_RVXF_1 | 499 | 505 | PF00149 | 0.419 |
| DOC_PP2B_LxvP_1 | 553 | 556 | PF13499 | 0.424 |
| DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.460 |
| DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.588 |
| DOC_PP4_FxxP_1 | 278 | 281 | PF00568 | 0.350 |
| DOC_PP4_FxxP_1 | 457 | 460 | PF00568 | 0.476 |
| DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.268 |
| DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.571 |
| DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.411 |
| DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.466 |
| DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.300 |
| DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.351 |
| DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.261 |
| LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.475 |
| LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.519 |
| LIG_14-3-3_CanoR_1 | 161 | 171 | PF00244 | 0.391 |
| LIG_14-3-3_CanoR_1 | 246 | 256 | PF00244 | 0.388 |
| LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.264 |
| LIG_14-3-3_CanoR_1 | 409 | 418 | PF00244 | 0.280 |
| LIG_14-3-3_CanoR_1 | 419 | 424 | PF00244 | 0.345 |
| LIG_14-3-3_CanoR_1 | 512 | 517 | PF00244 | 0.470 |
| LIG_Actin_WH2_2 | 149 | 166 | PF00022 | 0.407 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.644 |
| LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.482 |
| LIG_BRCT_BRCA1_1 | 315 | 319 | PF00533 | 0.276 |
| LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.396 |
| LIG_BRCT_BRCA1_1 | 453 | 457 | PF00533 | 0.688 |
| LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.483 |
| LIG_CaM_IQ_9 | 41 | 57 | PF13499 | 0.445 |
| LIG_CtBP_PxDLS_1 | 330 | 334 | PF00389 | 0.378 |
| LIG_FHA_1 | 166 | 172 | PF00498 | 0.439 |
| LIG_FHA_1 | 173 | 179 | PF00498 | 0.440 |
| LIG_FHA_1 | 19 | 25 | PF00498 | 0.233 |
| LIG_FHA_1 | 238 | 244 | PF00498 | 0.431 |
| LIG_FHA_1 | 255 | 261 | PF00498 | 0.416 |
| LIG_FHA_1 | 354 | 360 | PF00498 | 0.418 |
| LIG_FHA_1 | 471 | 477 | PF00498 | 0.679 |
| LIG_FHA_1 | 479 | 485 | PF00498 | 0.502 |
| LIG_FHA_1 | 521 | 527 | PF00498 | 0.505 |
| LIG_FHA_2 | 138 | 144 | PF00498 | 0.627 |
| LIG_FHA_2 | 472 | 478 | PF00498 | 0.693 |
| LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.519 |
| LIG_LIR_Apic_2 | 454 | 460 | PF02991 | 0.480 |
| LIG_LIR_Gen_1 | 215 | 221 | PF02991 | 0.419 |
| LIG_LIR_Gen_1 | 539 | 550 | PF02991 | 0.358 |
| LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.496 |
| LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.419 |
| LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.290 |
| LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.384 |
| LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.391 |
| LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.437 |
| LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.455 |
| LIG_LYPXL_S_1 | 302 | 306 | PF13949 | 0.268 |
| LIG_LYPXL_yS_3 | 303 | 306 | PF13949 | 0.268 |
| LIG_NRBOX | 260 | 266 | PF00104 | 0.268 |
| LIG_NRBOX | 62 | 68 | PF00104 | 0.469 |
| LIG_PCNA_PIPBox_1 | 519 | 528 | PF02747 | 0.509 |
| LIG_PCNA_yPIPBox_3 | 181 | 189 | PF02747 | 0.452 |
| LIG_PCNA_yPIPBox_3 | 224 | 237 | PF02747 | 0.328 |
| LIG_PCNA_yPIPBox_3 | 512 | 526 | PF02747 | 0.511 |
| LIG_SH2_CRK | 542 | 546 | PF00017 | 0.384 |
| LIG_SH2_SRC | 37 | 40 | PF00017 | 0.444 |
| LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.378 |
| LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.350 |
| LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.252 |
| LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.510 |
| LIG_SH3_3 | 143 | 149 | PF00018 | 0.474 |
| LIG_SH3_3 | 193 | 199 | PF00018 | 0.346 |
| LIG_SH3_3 | 253 | 259 | PF00018 | 0.378 |
| LIG_SH3_3 | 311 | 317 | PF00018 | 0.303 |
| LIG_SUMO_SIM_anti_2 | 234 | 240 | PF11976 | 0.323 |
| LIG_SUMO_SIM_par_1 | 148 | 153 | PF11976 | 0.519 |
| LIG_SUMO_SIM_par_1 | 234 | 240 | PF11976 | 0.312 |
| LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.328 |
| LIG_SUMO_SIM_par_1 | 328 | 334 | PF11976 | 0.378 |
| LIG_SUMO_SIM_par_1 | 64 | 71 | PF11976 | 0.483 |
| LIG_TRFH_1 | 145 | 149 | PF08558 | 0.541 |
| LIG_TRFH_1 | 313 | 317 | PF08558 | 0.264 |
| LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.312 |
| LIG_TYR_ITIM | 35 | 40 | PF00017 | 0.387 |
| MOD_CK1_1 | 18 | 24 | PF00069 | 0.350 |
| MOD_CK1_1 | 2 | 8 | PF00069 | 0.642 |
| MOD_CK1_1 | 251 | 257 | PF00069 | 0.390 |
| MOD_CK1_1 | 439 | 445 | PF00069 | 0.635 |
| MOD_CK1_1 | 453 | 459 | PF00069 | 0.647 |
| MOD_CK2_1 | 137 | 143 | PF00069 | 0.464 |
| MOD_CK2_1 | 84 | 90 | PF00069 | 0.608 |
| MOD_Cter_Amidation | 46 | 49 | PF01082 | 0.420 |
| MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.318 |
| MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.341 |
| MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.403 |
| MOD_GlcNHglycan | 437 | 441 | PF01048 | 0.601 |
| MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.603 |
| MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.597 |
| MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.537 |
| MOD_GSK3_1 | 246 | 253 | PF00069 | 0.431 |
| MOD_GSK3_1 | 266 | 273 | PF00069 | 0.170 |
| MOD_GSK3_1 | 325 | 332 | PF00069 | 0.298 |
| MOD_GSK3_1 | 439 | 446 | PF00069 | 0.607 |
| MOD_GSK3_1 | 449 | 456 | PF00069 | 0.618 |
| MOD_GSK3_1 | 466 | 473 | PF00069 | 0.471 |
| MOD_GSK3_1 | 80 | 87 | PF00069 | 0.487 |
| MOD_GSK3_1 | 88 | 95 | PF00069 | 0.625 |
| MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.310 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.619 |
| MOD_NEK2_1 | 156 | 161 | PF00069 | 0.407 |
| MOD_NEK2_1 | 162 | 167 | PF00069 | 0.380 |
| MOD_NEK2_1 | 237 | 242 | PF00069 | 0.297 |
| MOD_NEK2_1 | 331 | 336 | PF00069 | 0.370 |
| MOD_NEK2_1 | 339 | 344 | PF00069 | 0.309 |
| MOD_NEK2_1 | 455 | 460 | PF00069 | 0.734 |
| MOD_NEK2_1 | 54 | 59 | PF00069 | 0.522 |
| MOD_NEK2_1 | 82 | 87 | PF00069 | 0.629 |
| MOD_NEK2_1 | 88 | 93 | PF00069 | 0.637 |
| MOD_PIKK_1 | 119 | 125 | PF00454 | 0.376 |
| MOD_PIKK_1 | 80 | 86 | PF00454 | 0.620 |
| MOD_PIKK_1 | 92 | 98 | PF00454 | 0.402 |
| MOD_PKA_2 | 101 | 107 | PF00069 | 0.469 |
| MOD_PKA_2 | 294 | 300 | PF00069 | 0.264 |
| MOD_PKA_2 | 397 | 403 | PF00069 | 0.276 |
| MOD_PKA_2 | 54 | 60 | PF00069 | 0.594 |
| MOD_Plk_4 | 266 | 272 | PF00069 | 0.420 |
| MOD_Plk_4 | 355 | 361 | PF00069 | 0.252 |
| MOD_Plk_4 | 425 | 431 | PF00069 | 0.415 |
| MOD_Plk_4 | 478 | 484 | PF00069 | 0.493 |
| MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.464 |
| MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.300 |
| MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.351 |
| MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.261 |
| MOD_SUMO_rev_2 | 307 | 313 | PF00179 | 0.280 |
| TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.370 |
| TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.367 |
| TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.378 |
| TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.274 |
| TRG_DiLeu_BaLyEn_6 | 553 | 558 | PF01217 | 0.369 |
| TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.275 |
| TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.335 |
| TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.326 |
| TRG_ER_diArg_1 | 351 | 353 | PF00400 | 0.271 |
| TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.628 |
| TRG_Pf-PMV_PEXEL_1 | 118 | 123 | PF00026 | 0.490 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P7V5 | Leptomonas seymouri | 65% | 100% |
| A0A0S4JS94 | Bodo saltans | 31% | 100% |
| A0A1X0P966 | Trypanosomatidae | 41% | 100% |
| A0A3S5H816 | Leishmania donovani | 92% | 100% |
| A0A422NK89 | Trypanosoma rangeli | 43% | 100% |
| A4HNU0 | Leishmania braziliensis | 82% | 100% |
| A4ICQ4 | Leishmania infantum | 91% | 100% |
| D0A2Q5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
| Q02939 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
| Q4Q1Z6 | Leishmania major | 91% | 100% |
| V5B9Y1 | Trypanosoma cruzi | 42% | 100% |