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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000118 | histone deacetylase complex | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A4HLD0
Term | Name | Level | Count |
---|---|---|---|
GO:0000122 | negative regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0006476 | protein deacetylation | 6 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016575 | histone deacetylation | 6 | 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:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0035601 | protein deacylation | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 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:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0098732 | macromolecule deacylation | 5 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004407 | histone deacetylase activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 1 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 1 |
GO:0019213 | deacetylase activity | 3 | 1 |
GO:0033558 | protein lysine deacetylase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 612 | 614 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.253 |
CLV_Separin_Metazoa | 355 | 359 | PF03568 | 0.543 |
DEG_APCC_DBOX_1 | 516 | 524 | PF00400 | 0.583 |
DEG_SCF_FBW7_1 | 48 | 55 | PF00400 | 0.680 |
DEG_SCF_FBW7_1 | 64 | 71 | PF00400 | 0.703 |
DEG_SPOP_SBC_1 | 406 | 410 | PF00917 | 0.685 |
DEG_SPOP_SBC_1 | 68 | 72 | PF00917 | 0.649 |
DOC_ANK_TNKS_1 | 176 | 183 | PF00023 | 0.527 |
DOC_CDC14_PxL_1 | 50 | 58 | PF14671 | 0.671 |
DOC_CKS1_1 | 49 | 54 | PF01111 | 0.672 |
DOC_CYCLIN_RxL_1 | 267 | 277 | PF00134 | 0.518 |
DOC_CYCLIN_RxL_1 | 578 | 587 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 46 | 49 | PF00134 | 0.664 |
DOC_MAPK_gen_1 | 514 | 523 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 514 | 522 | PF00069 | 0.453 |
DOC_PIKK_1 | 330 | 337 | PF02985 | 0.734 |
DOC_PP2B_LxvP_1 | 46 | 49 | PF13499 | 0.735 |
DOC_PP2B_PxIxI_1 | 268 | 274 | PF00149 | 0.544 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.673 |
LIG_14-3-3_CanoR_1 | 122 | 130 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 311 | 317 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 374 | 381 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 435 | 439 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 556 | 572 | PF00022 | 0.411 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.623 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 585 | 589 | PF00533 | 0.317 |
LIG_Clathr_ClatBox_1 | 399 | 403 | PF01394 | 0.662 |
LIG_EH1_1 | 545 | 553 | PF00400 | 0.544 |
LIG_eIF4E_1 | 546 | 552 | PF01652 | 0.544 |
LIG_EVH1_1 | 353 | 357 | PF00568 | 0.543 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.415 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.391 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.453 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.546 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.468 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.379 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.490 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.629 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.543 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.477 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.664 |
LIG_Integrin_isoDGR_2 | 433 | 435 | PF01839 | 0.549 |
LIG_IRF3_LxIS_1 | 292 | 298 | PF10401 | 0.544 |
LIG_LIR_Apic_2 | 116 | 120 | PF02991 | 0.298 |
LIG_LIR_Apic_2 | 286 | 292 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 498 | 509 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 498 | 504 | PF02991 | 0.453 |
LIG_MYND_1 | 44 | 48 | PF01753 | 0.696 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.656 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.544 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.642 |
LIG_SH2_NCK_1 | 117 | 121 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.453 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.468 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.496 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.584 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.579 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.628 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.667 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 293 | 298 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 519 | 525 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 270 | 275 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 519 | 525 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 559 | 564 | PF11976 | 0.454 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.665 |
LIG_TYR_ITIM | 379 | 384 | PF00017 | 0.580 |
LIG_TYR_ITIM | 499 | 504 | PF00017 | 0.453 |
LIG_WW_3 | 355 | 359 | PF00397 | 0.543 |
MOD_CDK_SPxxK_3 | 36 | 43 | PF00069 | 0.469 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.616 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.512 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.671 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.615 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.609 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.538 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.653 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.306 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.674 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.580 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.581 |
MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.581 |
MOD_Cter_Amidation | 433 | 436 | PF01082 | 0.546 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.602 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.366 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.793 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.715 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.806 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.271 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.262 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.251 |
MOD_GlcNHglycan | 585 | 589 | PF01048 | 0.435 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.658 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.602 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.622 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.544 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.563 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.622 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.598 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.623 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.571 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.618 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.500 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.463 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.500 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.515 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.544 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.478 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.446 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.392 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.450 |
MOD_NEK2_2 | 434 | 439 | PF00069 | 0.520 |
MOD_NEK2_2 | 617 | 622 | PF00069 | 0.491 |
MOD_PIKK_1 | 620 | 626 | PF00454 | 0.533 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.682 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.701 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.649 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.629 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.706 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.478 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.452 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.454 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.665 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.566 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.537 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.697 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.599 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.739 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.654 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.483 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.568 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.673 |
MOD_SUMO_rev_2 | 605 | 614 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 7 | 12 | PF00179 | 0.653 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.735 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.575 |
TRG_NES_CRM1_1 | 162 | 175 | PF08389 | 0.518 |
TRG_NLS_MonoExtC_3 | 2 | 8 | PF00514 | 0.688 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 270 | 275 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 581 | 585 | PF00026 | 0.253 |
TRG_Pf-PMV_PEXEL_1 | 598 | 603 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R2 | Leptomonas seymouri | 60% | 93% |
A0A1X0NJV3 | Trypanosomatidae | 46% | 95% |
A0A3S7WWW4 | Leishmania donovani | 81% | 100% |
A0A422N700 | Trypanosoma rangeli | 50% | 99% |
A4HTR2 | Leishmania infantum | 82% | 99% |
C9ZIZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 91% |
E9AVI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 89% |
Q4QBZ5 | Leishmania major | 81% | 100% |
V5BFA4 | Trypanosoma cruzi | 48% | 100% |