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:0000118 | histone deacetylase complex | 3 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QBZ5
Term | Name | Level | Count |
---|---|---|---|
GO:0000122 | negative regulation of transcription by RNA polymerase II | 8 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0006476 | protein deacetylation | 6 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016575 | histone deacetylation | 6 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 2 |
GO:0035601 | protein deacylation | 5 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 2 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0098732 | macromolecule deacylation | 5 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004407 | histone deacetylase activity | 4 | 2 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 2 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 2 |
GO:0019213 | deacetylase activity | 3 | 2 |
GO:0033558 | protein lysine deacetylase activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.577 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 614 | 616 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.240 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.576 |
DEG_SCF_FBW7_1 | 48 | 55 | PF00400 | 0.697 |
DEG_SCF_FBW7_2 | 324 | 330 | PF00400 | 0.589 |
DEG_SPOP_SBC_1 | 407 | 411 | PF00917 | 0.659 |
DEG_SPOP_SBC_1 | 425 | 429 | PF00917 | 0.597 |
DOC_ANK_TNKS_1 | 176 | 183 | PF00023 | 0.474 |
DOC_CDC14_PxL_1 | 50 | 58 | PF14671 | 0.691 |
DOC_CKS1_1 | 324 | 329 | PF01111 | 0.428 |
DOC_CKS1_1 | 49 | 54 | PF01111 | 0.697 |
DOC_CYCLIN_RxL_1 | 580 | 589 | PF00134 | 0.440 |
DOC_CYCLIN_yCln2_LP_2 | 46 | 49 | PF00134 | 0.612 |
DOC_MAPK_gen_1 | 516 | 525 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 516 | 524 | PF00069 | 0.440 |
DOC_PIKK_1 | 330 | 337 | PF02985 | 0.582 |
DOC_PP2B_LxvP_1 | 46 | 49 | PF13499 | 0.725 |
DOC_PP2B_PxIxI_1 | 268 | 274 | PF00149 | 0.497 |
DOC_PP4_FxxP_1 | 117 | 120 | PF00568 | 0.198 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.665 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.639 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 311 | 321 | PF00244 | 0.474 |
LIG_BIR_III_2 | 479 | 483 | PF00653 | 0.511 |
LIG_BRCT_BRCA1_1 | 525 | 529 | PF00533 | 0.440 |
LIG_Clathr_ClatBox_1 | 399 | 403 | PF01394 | 0.585 |
LIG_EH1_1 | 547 | 555 | PF00400 | 0.534 |
LIG_eIF4E_1 | 548 | 554 | PF01652 | 0.534 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.430 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.624 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.552 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.440 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.385 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.504 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.640 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.675 |
LIG_IRF3_LxIS_1 | 292 | 298 | PF10401 | 0.534 |
LIG_LIR_Apic_2 | 116 | 120 | PF02991 | 0.282 |
LIG_LIR_Apic_2 | 286 | 292 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 85 | 89 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 380 | 388 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.440 |
LIG_MYND_1 | 40 | 44 | PF01753 | 0.760 |
LIG_MYND_1 | 48 | 52 | PF01753 | 0.582 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.534 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.534 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.534 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.430 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.440 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.454 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.545 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.628 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.528 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.455 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 293 | 298 | PF11976 | 0.440 |
LIG_SUMO_SIM_anti_2 | 521 | 526 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 270 | 275 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 521 | 526 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 561 | 566 | PF11976 | 0.441 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.647 |
LIG_TYR_ITIM | 379 | 384 | PF00017 | 0.534 |
LIG_TYR_ITIM | 501 | 506 | PF00017 | 0.440 |
MOD_CDK_SPxK_1 | 323 | 329 | PF00069 | 0.438 |
MOD_CDK_SPxxK_3 | 449 | 456 | PF00069 | 0.593 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.623 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.474 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.571 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.525 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.585 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.566 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.487 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.437 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.638 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.570 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.556 |
MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.598 |
MOD_Cter_Amidation | 371 | 374 | PF01082 | 0.731 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.615 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.274 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.388 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.659 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.684 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.635 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.637 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.237 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.230 |
MOD_GlcNHglycan | 587 | 591 | PF01048 | 0.452 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.550 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.491 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.557 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.571 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.558 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.557 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.619 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.663 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.444 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.592 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.725 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.683 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.687 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.552 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.434 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.384 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.443 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.377 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.398 |
MOD_PIKK_1 | 622 | 628 | PF00454 | 0.489 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.474 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.698 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.714 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.494 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.631 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.646 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.794 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.733 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.434 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.451 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.462 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.708 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.340 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.523 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.535 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.635 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.421 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.663 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.454 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.639 |
MOD_SUMO_rev_2 | 7 | 12 | PF00179 | 0.635 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 373 | 376 | PF00400 | 0.618 |
TRG_NES_CRM1_1 | 162 | 175 | PF08389 | 0.506 |
TRG_NLS_MonoExtC_3 | 2 | 8 | PF00514 | 0.676 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.240 |
TRG_Pf-PMV_PEXEL_1 | 600 | 605 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R2 | Leptomonas seymouri | 61% | 93% |
A0A0S4JEE2 | Bodo saltans | 38% | 100% |
A0A1X0NJV3 | Trypanosomatidae | 47% | 96% |
A0A3S7WWW4 | Leishmania donovani | 93% | 100% |
A0A422N700 | Trypanosoma rangeli | 49% | 99% |
A4HLD0 | Leishmania braziliensis | 81% | 100% |
A4HTR2 | Leishmania infantum | 93% | 100% |
C9ZIZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 92% |
E9AVI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 90% |
V5BFA4 | Trypanosoma cruzi | 47% | 100% |