| 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: A0A3S5H686
| 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_MEL_PAP_1 | 43 | 49 | PF00089 | 0.523 |
| CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.568 |
| CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.650 |
| CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.426 |
| CLV_PCSK_FUR_1 | 585 | 589 | PF00082 | 0.458 |
| CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.661 |
| CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.221 |
| CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.432 |
| CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.462 |
| CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.221 |
| CLV_PCSK_PC1ET2_1 | 587 | 589 | PF00082 | 0.547 |
| CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.412 |
| CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.232 |
| DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.504 |
| DOC_CKS1_1 | 142 | 147 | PF01111 | 0.434 |
| DOC_CYCLIN_yCln2_LP_2 | 169 | 175 | PF00134 | 0.473 |
| DOC_CYCLIN_yCln2_LP_2 | 36 | 42 | PF00134 | 0.601 |
| DOC_MAPK_DCC_7 | 160 | 169 | PF00069 | 0.473 |
| DOC_MAPK_MEF2A_6 | 160 | 169 | PF00069 | 0.473 |
| DOC_MAPK_MEF2A_6 | 280 | 287 | PF00069 | 0.395 |
| DOC_MAPK_MEF2A_6 | 332 | 340 | PF00069 | 0.418 |
| DOC_MAPK_MEF2A_6 | 479 | 487 | PF00069 | 0.478 |
| DOC_PP1_RVXF_1 | 467 | 473 | PF00149 | 0.378 |
| DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.473 |
| DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.421 |
| DOC_PP2B_PxIxI_1 | 118 | 124 | PF00149 | 0.413 |
| DOC_PP2B_PxIxI_1 | 330 | 336 | PF00149 | 0.418 |
| DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.544 |
| DOC_PP4_FxxP_1 | 214 | 217 | PF00568 | 0.512 |
| DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.684 |
| DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.546 |
| DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.606 |
| DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.513 |
| DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.473 |
| DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.363 |
| DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.472 |
| DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.479 |
| DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.615 |
| DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.481 |
| DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.543 |
| DOC_USP7_UBL2_3 | 33 | 37 | PF12436 | 0.559 |
| DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.492 |
| DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.477 |
| DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.396 |
| DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.757 |
| LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.432 |
| LIG_14-3-3_CanoR_1 | 249 | 256 | PF00244 | 0.475 |
| LIG_14-3-3_CanoR_1 | 321 | 330 | PF00244 | 0.473 |
| LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.526 |
| LIG_APCC_ABBA_1 | 173 | 178 | PF00400 | 0.473 |
| LIG_BIR_III_4 | 91 | 95 | PF00653 | 0.516 |
| LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.418 |
| LIG_CaM_IQ_9 | 594 | 609 | PF13499 | 0.389 |
| LIG_EVH1_2 | 2 | 6 | PF00568 | 0.588 |
| LIG_FHA_1 | 101 | 107 | PF00498 | 0.715 |
| LIG_FHA_1 | 241 | 247 | PF00498 | 0.460 |
| LIG_FHA_1 | 379 | 385 | PF00498 | 0.450 |
| LIG_FHA_1 | 478 | 484 | PF00498 | 0.438 |
| LIG_FHA_1 | 510 | 516 | PF00498 | 0.466 |
| LIG_FHA_1 | 83 | 89 | PF00498 | 0.500 |
| LIG_FHA_2 | 205 | 211 | PF00498 | 0.432 |
| LIG_Integrin_RGD_1 | 378 | 380 | PF01839 | 0.250 |
| LIG_LIR_Apic_2 | 213 | 217 | PF02991 | 0.478 |
| LIG_LIR_Apic_2 | 447 | 453 | PF02991 | 0.432 |
| LIG_LIR_Gen_1 | 207 | 214 | PF02991 | 0.550 |
| LIG_LIR_Gen_1 | 286 | 293 | PF02991 | 0.481 |
| LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.524 |
| LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.512 |
| LIG_LIR_Gen_1 | 460 | 470 | PF02991 | 0.475 |
| LIG_LIR_Gen_1 | 541 | 550 | PF02991 | 0.576 |
| LIG_LIR_LC3C_4 | 480 | 485 | PF02991 | 0.473 |
| LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.482 |
| LIG_LIR_Nem_3 | 286 | 290 | PF02991 | 0.481 |
| LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.524 |
| LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.493 |
| LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.475 |
| LIG_LIR_Nem_3 | 541 | 545 | PF02991 | 0.490 |
| LIG_SH2_SRC | 208 | 211 | PF00017 | 0.473 |
| LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.523 |
| LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.432 |
| LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.418 |
| LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.432 |
| LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.617 |
| LIG_SH3_2 | 142 | 147 | PF14604 | 0.432 |
| LIG_SH3_2 | 327 | 332 | PF14604 | 0.429 |
| LIG_SH3_3 | 113 | 119 | PF00018 | 0.510 |
| LIG_SH3_3 | 139 | 145 | PF00018 | 0.274 |
| LIG_SH3_3 | 287 | 293 | PF00018 | 0.432 |
| LIG_SH3_3 | 324 | 330 | PF00018 | 0.429 |
| LIG_SUMO_SIM_anti_2 | 69 | 74 | PF11976 | 0.484 |
| LIG_SUMO_SIM_par_1 | 334 | 339 | PF11976 | 0.418 |
| LIG_SUMO_SIM_par_1 | 438 | 443 | PF11976 | 0.418 |
| LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.431 |
| LIG_TYR_ITIM | 359 | 364 | PF00017 | 0.432 |
| LIG_UBA3_1 | 72 | 79 | PF00899 | 0.610 |
| LIG_WRC_WIRS_1 | 211 | 216 | PF05994 | 0.512 |
| LIG_WRC_WIRS_1 | 284 | 289 | PF05994 | 0.473 |
| LIG_WW_3 | 2 | 6 | PF00397 | 0.539 |
| LIG_WW_3 | 329 | 333 | PF00397 | 0.475 |
| MOD_CDK_SPK_2 | 521 | 526 | PF00069 | 0.396 |
| MOD_CDK_SPxK_1 | 141 | 147 | PF00069 | 0.299 |
| MOD_CK1_1 | 141 | 147 | PF00069 | 0.446 |
| MOD_CK1_1 | 180 | 186 | PF00069 | 0.423 |
| MOD_CK1_1 | 300 | 306 | PF00069 | 0.487 |
| MOD_CK1_1 | 392 | 398 | PF00069 | 0.460 |
| MOD_CK1_1 | 465 | 471 | PF00069 | 0.540 |
| MOD_CK1_1 | 56 | 62 | PF00069 | 0.635 |
| MOD_CK1_1 | 95 | 101 | PF00069 | 0.673 |
| MOD_CK2_1 | 204 | 210 | PF00069 | 0.429 |
| MOD_CK2_1 | 345 | 351 | PF00069 | 0.432 |
| MOD_CK2_1 | 419 | 425 | PF00069 | 0.464 |
| MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.354 |
| MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.255 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.372 |
| MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.317 |
| MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.340 |
| MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.276 |
| MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.264 |
| MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.255 |
| MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.611 |
| MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.655 |
| MOD_GSK3_1 | 176 | 183 | PF00069 | 0.508 |
| MOD_GSK3_1 | 266 | 273 | PF00069 | 0.443 |
| MOD_GSK3_1 | 321 | 328 | PF00069 | 0.521 |
| MOD_GSK3_1 | 505 | 512 | PF00069 | 0.438 |
| MOD_GSK3_1 | 52 | 59 | PF00069 | 0.520 |
| MOD_GSK3_1 | 556 | 563 | PF00069 | 0.588 |
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.669 |
| MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.547 |
| MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.307 |
| MOD_NEK2_1 | 106 | 111 | PF00069 | 0.717 |
| MOD_NEK2_1 | 223 | 228 | PF00069 | 0.473 |
| MOD_NEK2_1 | 360 | 365 | PF00069 | 0.418 |
| MOD_NEK2_1 | 419 | 424 | PF00069 | 0.512 |
| MOD_NEK2_1 | 505 | 510 | PF00069 | 0.421 |
| MOD_NEK2_2 | 13 | 18 | PF00069 | 0.500 |
| MOD_PIKK_1 | 195 | 201 | PF00454 | 0.438 |
| MOD_PIKK_1 | 297 | 303 | PF00454 | 0.512 |
| MOD_PIKK_1 | 96 | 102 | PF00454 | 0.589 |
| MOD_PKA_2 | 176 | 182 | PF00069 | 0.360 |
| MOD_PKA_2 | 248 | 254 | PF00069 | 0.475 |
| MOD_PKA_2 | 51 | 57 | PF00069 | 0.680 |
| MOD_PKA_2 | 560 | 566 | PF00069 | 0.547 |
| MOD_PKB_1 | 319 | 327 | PF00069 | 0.473 |
| MOD_PKB_1 | 50 | 58 | PF00069 | 0.531 |
| MOD_Plk_1 | 119 | 125 | PF00069 | 0.399 |
| MOD_Plk_1 | 195 | 201 | PF00069 | 0.491 |
| MOD_Plk_1 | 241 | 247 | PF00069 | 0.509 |
| MOD_Plk_1 | 256 | 262 | PF00069 | 0.557 |
| MOD_Plk_2-3 | 210 | 216 | PF00069 | 0.473 |
| MOD_Plk_4 | 345 | 351 | PF00069 | 0.432 |
| MOD_Plk_4 | 355 | 361 | PF00069 | 0.432 |
| MOD_Plk_4 | 419 | 425 | PF00069 | 0.512 |
| MOD_Plk_4 | 462 | 468 | PF00069 | 0.512 |
| MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.470 |
| MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.395 |
| MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.757 |
| MOD_SUMO_rev_2 | 559 | 568 | PF00179 | 0.685 |
| TRG_DiLeu_BaEn_1 | 578 | 583 | PF01217 | 0.408 |
| TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.414 |
| TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.509 |
| TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.408 |
| TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.432 |
| TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.588 |
| TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.473 |
| TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.671 |
| TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.381 |
| TRG_ER_diArg_1 | 537 | 540 | PF00400 | 0.394 |
| TRG_Pf-PMV_PEXEL_1 | 518 | 522 | PF00026 | 0.581 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PD56 | Leptomonas seymouri | 64% | 100% |
| A0A0S4J6F0 | Bodo saltans | 36% | 90% |
| A0A1X0NP71 | Trypanosomatidae | 43% | 98% |
| A0A422NJU7 | Trypanosoma rangeli | 45% | 100% |
| A4HTP2 | Leishmania infantum | 99% | 100% |
| E9AI33 | Leishmania braziliensis | 81% | 100% |
| E9AMH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
| O13298 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
| P53973 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 86% |
| Q4QI60 | Leishmania major | 96% | 100% |
| Q5A960 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 73% |
| V5BR24 | Trypanosoma cruzi | 46% | 100% |