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: E9AI33
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 | 52 | 58 | PF00089 | 0.424 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.157 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.343 |
CLV_PCSK_FUR_1 | 593 | 597 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.329 |
DEG_APCC_DBOX_1 | 443 | 451 | PF00400 | 0.491 |
DEG_APCC_DBOX_1 | 45 | 53 | PF00400 | 0.286 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.441 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.395 |
DOC_CYCLIN_yCln2_LP_2 | 177 | 183 | PF00134 | 0.448 |
DOC_CYCLIN_yCln2_LP_2 | 45 | 51 | PF00134 | 0.499 |
DOC_MAPK_DCC_7 | 168 | 177 | PF00069 | 0.372 |
DOC_MAPK_FxFP_2 | 29 | 32 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 168 | 177 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 340 | 348 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 444 | 452 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 487 | 495 | PF00069 | 0.474 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.410 |
DOC_PP2B_LxvP_1 | 515 | 518 | PF13499 | 0.412 |
DOC_PP2B_PxIxI_1 | 126 | 132 | PF00149 | 0.384 |
DOC_PP2B_PxIxI_1 | 338 | 344 | PF00149 | 0.415 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.440 |
DOC_PP4_MxPP_1 | 573 | 576 | PF00568 | 0.470 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.553 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 212 | 217 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 257 | 264 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 329 | 334 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 396 | 404 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 59 | 68 | PF00244 | 0.533 |
LIG_APCC_ABBA_1 | 181 | 186 | PF00400 | 0.528 |
LIG_BRCT_BRCA1_1 | 450 | 454 | PF00533 | 0.415 |
LIG_EVH1_2 | 11 | 15 | PF00568 | 0.566 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.506 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.416 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.452 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.549 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.459 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.449 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.325 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.357 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.481 |
LIG_Integrin_RGD_1 | 386 | 388 | PF01839 | 0.246 |
LIG_LIR_Apic_2 | 221 | 225 | PF02991 | 0.381 |
LIG_LIR_Apic_2 | 455 | 461 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 215 | 222 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 294 | 301 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 311 | 321 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 366 | 375 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 549 | 558 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 67 | 74 | PF02991 | 0.330 |
LIG_LIR_LC3C_4 | 488 | 493 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 468 | 474 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.621 |
LIG_NRBOX | 523 | 529 | PF00104 | 0.261 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.552 |
LIG_SH3_1 | 6 | 12 | PF00018 | 0.434 |
LIG_SH3_2 | 150 | 155 | PF14604 | 0.391 |
LIG_SH3_2 | 335 | 340 | PF14604 | 0.426 |
LIG_SH3_2 | 9 | 14 | PF14604 | 0.438 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.469 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.422 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.428 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.426 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.318 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.524 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 78 | 83 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 237 | 244 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 342 | 347 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 446 | 451 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 491 | 496 | PF11976 | 0.429 |
LIG_TRAF2_1 | 577 | 580 | PF00917 | 0.644 |
LIG_TYR_ITIM | 367 | 372 | PF00017 | 0.428 |
LIG_UBA3_1 | 79 | 84 | PF00899 | 0.554 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.469 |
LIG_WW_3 | 337 | 341 | PF00397 | 0.471 |
MOD_CDK_SPK_2 | 103 | 108 | PF00069 | 0.495 |
MOD_CDK_SPxK_1 | 149 | 155 | PF00069 | 0.418 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.607 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.557 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.419 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.357 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.374 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.498 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.430 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.536 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.324 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.451 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.492 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.461 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.692 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.602 |
MOD_GlcNHglycan | 19 | 23 | PF01048 | 0.523 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.493 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.269 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.343 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.329 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.340 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.273 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.274 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.642 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.367 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.448 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.439 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.357 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.428 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.528 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.474 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.479 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.428 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.509 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.412 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.509 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.417 |
MOD_PK_1 | 329 | 335 | PF00069 | 0.357 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.598 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.471 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.512 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.661 |
MOD_PKB_1 | 327 | 335 | PF00069 | 0.469 |
MOD_PKB_1 | 59 | 67 | PF00069 | 0.531 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.352 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.496 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.534 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.430 |
MOD_Plk_2-3 | 218 | 224 | PF00069 | 0.362 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.533 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.280 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.481 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.357 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.428 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.428 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.351 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.364 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.509 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.516 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.628 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.451 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.537 |
MOD_SUMO_rev_2 | 371 | 380 | PF00179 | 0.357 |
MOD_SUMO_rev_2 | 570 | 576 | PF00179 | 0.596 |
TRG_DiLeu_BaEn_1 | 586 | 591 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 519 | 524 | PF01217 | 0.397 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 539 | 542 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 553 | 555 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 593 | 596 | PF00400 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.328 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD56 | Leptomonas seymouri | 63% | 100% |
A0A0S4J6F0 | Bodo saltans | 37% | 91% |
A0A1X0NP71 | Trypanosomatidae | 42% | 99% |
A0A3S5H686 | Leishmania donovani | 81% | 100% |
A0A422NJU7 | Trypanosoma rangeli | 43% | 100% |
A4HTP2 | Leishmania infantum | 81% | 94% |
E9AMH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
P53973 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 87% |
Q4QI60 | Leishmania major | 81% | 100% |
Q5A960 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 74% |
V5BR24 | Trypanosoma cruzi | 43% | 100% |