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 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQ80
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
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: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:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
GO:0000365 | mRNA trans splicing, via spliceosome | 9 | 1 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045291 | mRNA trans splicing, SL addition | 10 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
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_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.421 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.749 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.523 |
CLV_PCSK_FUR_1 | 483 | 487 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.813 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 484 | 486 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.650 |
CLV_PCSK_PC7_1 | 176 | 182 | PF00082 | 0.419 |
CLV_PCSK_PC7_1 | 480 | 486 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.391 |
DEG_APCC_DBOX_1 | 119 | 127 | PF00400 | 0.610 |
DEG_APCC_DBOX_1 | 72 | 80 | PF00400 | 0.655 |
DEG_SPOP_SBC_1 | 343 | 347 | PF00917 | 0.322 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.677 |
DOC_CYCLIN_yCln2_LP_2 | 129 | 135 | PF00134 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 297 | 303 | PF00134 | 0.523 |
DOC_MAPK_DCC_7 | 120 | 129 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.645 |
DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 72 | 78 | PF00069 | 0.655 |
DOC_MAPK_HePTP_8 | 117 | 129 | PF00069 | 0.640 |
DOC_MAPK_MEF2A_6 | 120 | 129 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 168 | 175 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.383 |
DOC_MAPK_RevD_3 | 165 | 181 | PF00069 | 0.325 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.539 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.251 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.648 |
DOC_PP2B_PxIxI_1 | 162 | 168 | PF00149 | 0.301 |
DOC_PP4_FxxP_1 | 423 | 426 | PF00568 | 0.751 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.561 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.571 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 362 | 370 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 452 | 462 | PF00244 | 0.659 |
LIG_Actin_WH2_2 | 11 | 28 | PF00022 | 0.439 |
LIG_Actin_WH2_2 | 164 | 182 | PF00022 | 0.542 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.524 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 321 | 327 | PF00928 | 0.444 |
LIG_eIF4E_1 | 33 | 39 | PF01652 | 0.371 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.600 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.428 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.611 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.443 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.458 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.402 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.447 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.552 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.542 |
LIG_LIR_Apic_2 | 108 | 112 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 422 | 426 | PF02991 | 0.748 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.407 |
LIG_LYPXL_SIV_4 | 224 | 232 | PF13949 | 0.487 |
LIG_NRBOX | 231 | 237 | PF00104 | 0.294 |
LIG_Pex14_1 | 323 | 327 | PF04695 | 0.403 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.394 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.579 |
LIG_SH2_GRB2like | 231 | 234 | PF00017 | 0.504 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 307 | 310 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.652 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.374 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.612 |
LIG_SxIP_EBH_1 | 362 | 373 | PF03271 | 0.357 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.421 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.688 |
LIG_TRAF2_2 | 453 | 458 | PF00917 | 0.542 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.511 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.409 |
MOD_CDC14_SPxK_1 | 223 | 226 | PF00782 | 0.444 |
MOD_CDK_SPxK_1 | 220 | 226 | PF00069 | 0.454 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.607 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.635 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.371 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.589 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.574 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.704 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.541 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.666 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.372 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.413 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.555 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.668 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.656 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.754 |
MOD_DYRK1A_RPxSP_1 | 181 | 185 | PF00069 | 0.521 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.597 |
MOD_GlcNHglycan | 246 | 250 | PF01048 | 0.650 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.445 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.583 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.630 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.679 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.546 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.476 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.454 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.553 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.602 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.559 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.572 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.558 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.599 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.651 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.548 |
MOD_N-GLC_2 | 172 | 174 | PF02516 | 0.482 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.429 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.369 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.543 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.405 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.577 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.649 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.529 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.628 |
MOD_PKA_1 | 352 | 358 | PF00069 | 0.630 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.524 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.403 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.504 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.756 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.627 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.699 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.526 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.515 |
MOD_Plk_2-3 | 237 | 243 | PF00069 | 0.526 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.350 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.413 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.445 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.574 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.454 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.405 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.635 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.565 |
MOD_SUMO_rev_2 | 193 | 202 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 68 | 74 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_1 | 431 | 436 | PF01217 | 0.699 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 329 | 334 | PF01217 | 0.535 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.527 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.701 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.731 |
TRG_NLS_Bipartite_1 | 450 | 468 | PF00514 | 0.652 |
TRG_NLS_Bipartite_1 | 470 | 488 | PF00514 | 0.545 |
TRG_NLS_MonoCore_2 | 482 | 487 | PF00514 | 0.784 |
TRG_NLS_MonoExtC_3 | 463 | 469 | PF00514 | 0.736 |
TRG_NLS_MonoExtN_4 | 480 | 487 | PF00514 | 0.673 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDY9 | Leptomonas seymouri | 59% | 100% |
A0A0S4IZS7 | Bodo saltans | 26% | 86% |
A0A1X0P050 | Trypanosomatidae | 40% | 71% |
A0A3S7XBU2 | Leishmania donovani | 83% | 99% |
A0A422NSB3 | Trypanosoma rangeli | 35% | 100% |
A4IDX8 | Leishmania infantum | 84% | 99% |
D0A432 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 77% |
E9ATZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
Q4Q0J7 | Leishmania major | 82% | 100% |
V5BNQ3 | Trypanosoma cruzi | 42% | 81% |