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:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q0J7
Term | Name | Level | Count |
---|---|---|---|
GO:0000365 | mRNA trans splicing, via spliceosome | 9 | 2 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 12 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045291 | mRNA trans splicing, SL addition | 10 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051252 | regulation of RNA metabolic process | 5 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016538 | cyclin-dependent protein serine/threonine kinase regulator activity | 5 | 12 |
GO:0019207 | kinase regulator activity | 3 | 12 |
GO:0019887 | protein kinase regulator activity | 4 | 12 |
GO:0030234 | enzyme regulator activity | 2 | 12 |
GO:0098772 | molecular function regulator activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.718 |
CLV_PCSK_FUR_1 | 295 | 299 | PF00082 | 0.531 |
CLV_PCSK_FUR_1 | 487 | 491 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.764 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 474 | 476 | PF00082 | 0.719 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 176 | 182 | PF00082 | 0.414 |
CLV_PCSK_PC7_1 | 475 | 481 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.291 |
DEG_APCC_DBOX_1 | 119 | 127 | PF00400 | 0.612 |
DEG_APCC_DBOX_1 | 72 | 80 | PF00400 | 0.660 |
DEG_SCF_FBW7_1 | 84 | 91 | PF00400 | 0.513 |
DEG_SPOP_SBC_1 | 413 | 417 | PF00917 | 0.755 |
DOC_CYCLIN_yCln2_LP_2 | 129 | 135 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 300 | 306 | PF00134 | 0.525 |
DOC_MAPK_DCC_7 | 120 | 129 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 180 | 186 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 295 | 302 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 72 | 78 | PF00069 | 0.654 |
DOC_MAPK_HePTP_8 | 117 | 129 | PF00069 | 0.640 |
DOC_MAPK_MEF2A_6 | 120 | 129 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 166 | 175 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.385 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 300 | 303 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 320 | 323 | PF13499 | 0.264 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.656 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.746 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.672 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.630 |
LIG_Actin_WH2_2 | 11 | 28 | PF00022 | 0.446 |
LIG_Actin_WH2_2 | 164 | 182 | PF00022 | 0.550 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.439 |
LIG_CtBP_PxDLS_1 | 317 | 321 | PF00389 | 0.517 |
LIG_deltaCOP1_diTrp_1 | 324 | 330 | PF00928 | 0.455 |
LIG_eIF4E_1 | 33 | 39 | PF01652 | 0.374 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.602 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.437 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.606 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.441 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.467 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.402 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.569 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.552 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.580 |
LIG_Integrin_RGD_1 | 251 | 253 | PF01839 | 0.655 |
LIG_LIR_Apic_2 | 108 | 112 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 426 | 430 | PF02991 | 0.744 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.409 |
LIG_LYPXL_SIV_4 | 224 | 232 | PF13949 | 0.488 |
LIG_Pex14_1 | 326 | 330 | PF04695 | 0.412 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.407 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.584 |
LIG_SH2_GRB2like | 231 | 234 | PF00017 | 0.506 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.499 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 310 | 313 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.638 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.556 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.362 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.587 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.703 |
LIG_SUMO_SIM_par_1 | 77 | 83 | PF11976 | 0.450 |
LIG_TRAF2_1 | 432 | 435 | PF00917 | 0.672 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.513 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.408 |
MOD_CDC14_SPxK_1 | 223 | 226 | PF00782 | 0.444 |
MOD_CDK_SPxK_1 | 220 | 226 | PF00069 | 0.453 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.536 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.605 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.591 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.609 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.704 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.686 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.598 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.379 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.413 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.545 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.573 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.655 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.757 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.756 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.597 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.654 |
MOD_GlcNHglycan | 253 | 257 | PF01048 | 0.637 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.552 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.577 |
MOD_GlcNHglycan | 398 | 402 | PF01048 | 0.618 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.676 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.626 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.543 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.461 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.533 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.461 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.661 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.583 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.731 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.547 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.635 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.716 |
MOD_N-GLC_2 | 172 | 174 | PF02516 | 0.493 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.456 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.377 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.209 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.413 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.581 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.668 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.532 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.600 |
MOD_PKA_1 | 454 | 460 | PF00069 | 0.725 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.520 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.456 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.630 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.405 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.595 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.767 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.631 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.539 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.512 |
MOD_Plk_2-3 | 86 | 92 | PF00069 | 0.506 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.405 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.449 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.453 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.412 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.634 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.628 |
MOD_SUMO_rev_2 | 193 | 202 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 69 | 74 | PF00179 | 0.642 |
TRG_DiLeu_BaEn_1 | 435 | 440 | PF01217 | 0.717 |
TRG_DiLeu_BaLyEn_6 | 295 | 300 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 478 | 480 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 487 | 490 | PF00400 | 0.726 |
TRG_ER_FFAT_2 | 52 | 59 | PF00635 | 0.564 |
TRG_NLS_Bipartite_1 | 454 | 472 | PF00514 | 0.654 |
TRG_NLS_MonoExtC_3 | 467 | 473 | PF00514 | 0.740 |
TRG_NLS_MonoExtN_4 | 466 | 472 | PF00514 | 0.604 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDY9 | Leptomonas seymouri | 58% | 100% |
A0A0S4IZS7 | Bodo saltans | 25% | 86% |
A0A1X0P050 | Trypanosomatidae | 40% | 72% |
A0A3S7XBU2 | Leishmania donovani | 93% | 100% |
A0A422NSB3 | Trypanosoma rangeli | 42% | 100% |
A4HQ80 | Leishmania braziliensis | 82% | 100% |
A4IDX8 | Leishmania infantum | 93% | 100% |
D0A432 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 77% |
E9ATZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BNQ3 | Trypanosoma cruzi | 42% | 82% |