| 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: A4HNU0
| 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 | 476 | 480 | PF00656 | 0.632 |
| CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.385 |
| CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.322 |
| CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.349 |
| CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.622 |
| CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.728 |
| CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.562 |
| CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.439 |
| CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.526 |
| CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.271 |
| CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.322 |
| CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.588 |
| CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.729 |
| CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.565 |
| CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.425 |
| CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.526 |
| CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.528 |
| CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.416 |
| CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.350 |
| CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.398 |
| CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.467 |
| CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.366 |
| CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.406 |
| CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.463 |
| CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.323 |
| DEG_APCC_DBOX_1 | 117 | 125 | PF00400 | 0.525 |
| DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.310 |
| DEG_SPOP_SBC_1 | 454 | 458 | PF00917 | 0.700 |
| DOC_CYCLIN_RxL_1 | 115 | 122 | PF00134 | 0.542 |
| DOC_CYCLIN_RxL_1 | 232 | 243 | PF00134 | 0.391 |
| DOC_MAPK_FxFP_2 | 278 | 281 | PF00069 | 0.394 |
| DOC_MAPK_MEF2A_6 | 193 | 200 | PF00069 | 0.321 |
| DOC_MAPK_RevD_3 | 192 | 207 | PF00069 | 0.352 |
| DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.426 |
| DOC_PP1_RVXF_1 | 500 | 507 | PF00149 | 0.448 |
| DOC_PP2B_LxvP_1 | 484 | 487 | PF13499 | 0.489 |
| DOC_PP2B_LxvP_1 | 555 | 558 | PF13499 | 0.470 |
| DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.646 |
| DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.578 |
| DOC_PP2B_PxIxI_1 | 10 | 16 | PF00149 | 0.280 |
| DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.611 |
| DOC_PP4_FxxP_1 | 278 | 281 | PF00568 | 0.394 |
| DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.546 |
| DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.321 |
| DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.483 |
| DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.501 |
| DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.394 |
| DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.310 |
| DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.739 |
| LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.533 |
| LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.561 |
| LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.478 |
| LIG_14-3-3_CanoR_1 | 164 | 171 | PF00244 | 0.403 |
| LIG_14-3-3_CanoR_1 | 241 | 245 | PF00244 | 0.449 |
| LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.327 |
| LIG_14-3-3_CanoR_1 | 422 | 427 | PF00244 | 0.334 |
| LIG_14-3-3_CanoR_1 | 472 | 478 | PF00244 | 0.551 |
| LIG_14-3-3_CanoR_1 | 514 | 524 | PF00244 | 0.513 |
| LIG_Actin_WH2_2 | 149 | 166 | PF00022 | 0.460 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
| LIG_BIR_III_4 | 176 | 180 | PF00653 | 0.348 |
| LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.517 |
| LIG_BRCT_BRCA1_1 | 315 | 319 | PF00533 | 0.334 |
| LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.322 |
| LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.738 |
| LIG_BRCT_BRCA1_1 | 473 | 477 | PF00533 | 0.357 |
| LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.556 |
| LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.441 |
| LIG_CaM_IQ_9 | 41 | 57 | PF13499 | 0.649 |
| LIG_FHA_1 | 166 | 172 | PF00498 | 0.463 |
| LIG_FHA_1 | 255 | 261 | PF00498 | 0.409 |
| LIG_FHA_1 | 357 | 363 | PF00498 | 0.413 |
| LIG_FHA_1 | 416 | 422 | PF00498 | 0.335 |
| LIG_FHA_1 | 473 | 479 | PF00498 | 0.664 |
| LIG_FHA_1 | 480 | 486 | PF00498 | 0.535 |
| LIG_FHA_1 | 523 | 529 | PF00498 | 0.534 |
| LIG_FHA_2 | 474 | 480 | PF00498 | 0.680 |
| LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.567 |
| LIG_LIR_Apic_2 | 456 | 462 | PF02991 | 0.545 |
| LIG_LIR_Gen_1 | 215 | 221 | PF02991 | 0.453 |
| LIG_LIR_Gen_1 | 541 | 552 | PF02991 | 0.416 |
| LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.587 |
| LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.323 |
| LIG_LIR_LC3C_4 | 482 | 486 | PF02991 | 0.523 |
| LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.453 |
| LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.200 |
| LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.295 |
| LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.420 |
| LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.387 |
| LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.534 |
| LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.318 |
| LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.357 |
| LIG_LYPXL_S_1 | 302 | 306 | PF13949 | 0.322 |
| LIG_LYPXL_yS_3 | 303 | 306 | PF13949 | 0.322 |
| LIG_MLH1_MIPbox_1 | 93 | 97 | PF16413 | 0.343 |
| LIG_NRBOX | 260 | 266 | PF00104 | 0.311 |
| LIG_NRBOX | 62 | 68 | PF00104 | 0.602 |
| LIG_PCNA_PIPBox_1 | 521 | 530 | PF02747 | 0.547 |
| LIG_PCNA_yPIPBox_3 | 181 | 189 | PF02747 | 0.486 |
| LIG_PCNA_yPIPBox_3 | 224 | 237 | PF02747 | 0.453 |
| LIG_PCNA_yPIPBox_3 | 514 | 528 | PF02747 | 0.546 |
| LIG_Pex14_2 | 72 | 76 | PF04695 | 0.465 |
| LIG_SH2_CRK | 544 | 548 | PF00017 | 0.439 |
| LIG_SH2_SRC | 37 | 40 | PF00017 | 0.508 |
| LIG_SH2_STAP1 | 37 | 41 | PF00017 | 0.479 |
| LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.394 |
| LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.369 |
| LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.306 |
| LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.549 |
| LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.460 |
| LIG_SH3_1 | 193 | 199 | PF00018 | 0.380 |
| LIG_SH3_3 | 143 | 149 | PF00018 | 0.557 |
| LIG_SH3_3 | 193 | 199 | PF00018 | 0.496 |
| LIG_SH3_3 | 253 | 259 | PF00018 | 0.414 |
| LIG_SH3_3 | 311 | 317 | PF00018 | 0.363 |
| LIG_SUMO_SIM_anti_2 | 234 | 240 | PF11976 | 0.372 |
| LIG_SUMO_SIM_par_1 | 148 | 153 | PF11976 | 0.547 |
| LIG_SUMO_SIM_par_1 | 234 | 240 | PF11976 | 0.363 |
| LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.453 |
| LIG_SUMO_SIM_par_1 | 32 | 38 | PF11976 | 0.530 |
| LIG_TRFH_1 | 145 | 149 | PF08558 | 0.567 |
| LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.363 |
| LIG_TYR_ITIM | 35 | 40 | PF00017 | 0.464 |
| LIG_WRC_WIRS_1 | 69 | 74 | PF05994 | 0.349 |
| LIG_WW_3 | 461 | 465 | PF00397 | 0.502 |
| MOD_CK1_1 | 2 | 8 | PF00069 | 0.641 |
| MOD_CK1_1 | 243 | 249 | PF00069 | 0.423 |
| MOD_CK1_1 | 251 | 257 | PF00069 | 0.400 |
| MOD_CK1_1 | 349 | 355 | PF00069 | 0.427 |
| MOD_CK1_1 | 457 | 463 | PF00069 | 0.702 |
| MOD_CK1_1 | 70 | 76 | PF00069 | 0.370 |
| MOD_CK2_1 | 68 | 74 | PF00069 | 0.473 |
| MOD_Cter_Amidation | 46 | 49 | PF01082 | 0.547 |
| MOD_GlcNHglycan | 172 | 176 | PF01048 | 0.450 |
| MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.368 |
| MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.353 |
| MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.403 |
| MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.641 |
| MOD_GSK3_1 | 240 | 247 | PF00069 | 0.388 |
| MOD_GSK3_1 | 250 | 257 | PF00069 | 0.438 |
| MOD_GSK3_1 | 266 | 273 | PF00069 | 0.149 |
| MOD_GSK3_1 | 442 | 449 | PF00069 | 0.659 |
| MOD_GSK3_1 | 453 | 460 | PF00069 | 0.692 |
| MOD_GSK3_1 | 468 | 475 | PF00069 | 0.577 |
| MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.406 |
| MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.200 |
| MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.440 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.608 |
| MOD_NEK2_1 | 156 | 161 | PF00069 | 0.416 |
| MOD_NEK2_1 | 162 | 167 | PF00069 | 0.397 |
| MOD_NEK2_1 | 237 | 242 | PF00069 | 0.334 |
| MOD_NEK2_1 | 331 | 336 | PF00069 | 0.352 |
| MOD_NEK2_1 | 339 | 344 | PF00069 | 0.323 |
| MOD_NEK2_1 | 346 | 351 | PF00069 | 0.250 |
| MOD_NEK2_1 | 54 | 59 | PF00069 | 0.633 |
| MOD_NEK2_1 | 67 | 72 | PF00069 | 0.465 |
| MOD_PIKK_1 | 107 | 113 | PF00454 | 0.408 |
| MOD_PIKK_1 | 119 | 125 | PF00454 | 0.489 |
| MOD_PIKK_1 | 415 | 421 | PF00454 | 0.335 |
| MOD_PIKK_1 | 80 | 86 | PF00454 | 0.691 |
| MOD_PKA_2 | 101 | 107 | PF00069 | 0.494 |
| MOD_PKA_2 | 240 | 246 | PF00069 | 0.323 |
| MOD_PKA_2 | 254 | 260 | PF00069 | 0.223 |
| MOD_PKA_2 | 349 | 355 | PF00069 | 0.401 |
| MOD_PKA_2 | 400 | 406 | PF00069 | 0.315 |
| MOD_PKA_2 | 471 | 477 | PF00069 | 0.580 |
| MOD_PKA_2 | 54 | 60 | PF00069 | 0.687 |
| MOD_Plk_1 | 346 | 352 | PF00069 | 0.260 |
| MOD_Plk_4 | 266 | 272 | PF00069 | 0.442 |
| MOD_Plk_4 | 3 | 9 | PF00069 | 0.398 |
| MOD_Plk_4 | 358 | 364 | PF00069 | 0.306 |
| MOD_Plk_4 | 428 | 434 | PF00069 | 0.445 |
| MOD_Plk_4 | 473 | 479 | PF00069 | 0.612 |
| MOD_Plk_4 | 480 | 486 | PF00069 | 0.517 |
| MOD_Plk_4 | 92 | 98 | PF00069 | 0.506 |
| MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.394 |
| MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.310 |
| MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.738 |
| MOD_SUMO_for_1 | 205 | 208 | PF00179 | 0.371 |
| MOD_SUMO_rev_2 | 110 | 117 | PF00179 | 0.357 |
| MOD_SUMO_rev_2 | 438 | 448 | PF00179 | 0.569 |
| TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.453 |
| TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.411 |
| TRG_DiLeu_BaEn_1 | 375 | 380 | PF01217 | 0.200 |
| TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.414 |
| TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.392 |
| TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.322 |
| TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.423 |
| TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.387 |
| TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.325 |
| TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.592 |
| TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.717 |
| TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.440 |
| TRG_Pf-PMV_PEXEL_1 | 118 | 123 | PF00026 | 0.527 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P7V5 | Leptomonas seymouri | 65% | 100% |
| A0A0S4JS94 | Bodo saltans | 31% | 100% |
| A0A1X0P966 | Trypanosomatidae | 42% | 100% |
| A0A3S5H816 | Leishmania donovani | 81% | 100% |
| A0A422NK89 | Trypanosoma rangeli | 44% | 100% |
| A4ICQ4 | Leishmania infantum | 81% | 100% |
| D0A2Q5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
| E9ASK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
| Q02939 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
| Q4Q1Z6 | Leishmania major | 83% | 100% |
| V5B9Y1 | Trypanosoma cruzi | 42% | 100% |