Histone/chromosome structure, histone deacetylase
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 | 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: A4HTR2
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 | 392 | 396 | PF00656 | 0.619 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.619 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 616 | 618 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.287 |
DEG_APCC_DBOX_1 | 520 | 528 | PF00400 | 0.581 |
DEG_SCF_FBW7_1 | 50 | 57 | PF00400 | 0.729 |
DEG_SCF_FBW7_2 | 326 | 332 | PF00400 | 0.592 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.676 |
DEG_SPOP_SBC_1 | 419 | 423 | PF00917 | 0.721 |
DEG_SPOP_SBC_1 | 427 | 431 | PF00917 | 0.663 |
DOC_ANK_TNKS_1 | 178 | 185 | PF00023 | 0.581 |
DOC_CDC14_PxL_1 | 52 | 60 | PF14671 | 0.734 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.498 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.733 |
DOC_CYCLIN_RxL_1 | 269 | 279 | PF00134 | 0.544 |
DOC_CYCLIN_RxL_1 | 582 | 591 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 48 | 51 | PF00134 | 0.743 |
DOC_MAPK_gen_1 | 518 | 527 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 12 | 21 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 518 | 526 | PF00069 | 0.487 |
DOC_PP2B_LxvP_1 | 48 | 51 | PF13499 | 0.733 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.699 |
DOC_PP2B_PxIxI_1 | 270 | 276 | PF00149 | 0.537 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.739 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.665 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 313 | 323 | PF00244 | 0.581 |
LIG_BIR_III_2 | 481 | 485 | PF00653 | 0.547 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 401 | 405 | PF01394 | 0.709 |
LIG_EH1_1 | 549 | 557 | PF00400 | 0.562 |
LIG_eIF4E_1 | 550 | 556 | PF01652 | 0.562 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.466 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.684 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.633 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.487 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.446 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.526 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.712 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.701 |
LIG_IRF3_LxIS_1 | 294 | 300 | PF10401 | 0.562 |
LIG_LIR_Apic_2 | 118 | 122 | PF02991 | 0.348 |
LIG_LIR_Apic_2 | 288 | 294 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 87 | 91 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 382 | 390 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 502 | 513 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 382 | 386 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.487 |
LIG_MYND_1 | 42 | 46 | PF01753 | 0.759 |
LIG_MYND_1 | 50 | 54 | PF01753 | 0.635 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.642 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.562 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.653 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.328 |
LIG_SH2_NCK_1 | 241 | 245 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 291 | 295 | PF00017 | 0.476 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.476 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.501 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.754 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.605 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.573 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.502 |
LIG_SUMO_SIM_anti_2 | 130 | 136 | PF11976 | 0.454 |
LIG_SUMO_SIM_anti_2 | 295 | 300 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 523 | 528 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 272 | 277 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 523 | 528 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 563 | 568 | PF11976 | 0.488 |
LIG_TRAF2_1 | 462 | 465 | PF00917 | 0.744 |
LIG_TYR_ITIM | 381 | 386 | PF00017 | 0.606 |
LIG_TYR_ITIM | 503 | 508 | PF00017 | 0.487 |
MOD_CDK_SPK_2 | 451 | 456 | PF00069 | 0.568 |
MOD_CDK_SPxK_1 | 325 | 331 | PF00069 | 0.498 |
MOD_CDK_SPxxK_3 | 451 | 458 | PF00069 | 0.706 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.519 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.623 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.525 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.637 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.633 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.509 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.602 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.669 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.672 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.636 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.688 |
MOD_Cter_Amidation | 373 | 376 | PF01082 | 0.765 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.369 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.610 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.367 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.610 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.732 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.674 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.707 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.271 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.234 |
MOD_GlcNHglycan | 589 | 593 | PF01048 | 0.472 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.744 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.644 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.655 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.518 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.571 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.596 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.613 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.621 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.652 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.707 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.501 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.676 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.768 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.747 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.560 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.478 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.427 |
MOD_NEK2_2 | 285 | 290 | PF00069 | 0.482 |
MOD_NEK2_2 | 621 | 626 | PF00069 | 0.566 |
MOD_PKA_1 | 313 | 319 | PF00069 | 0.581 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.569 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.718 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.774 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.535 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.802 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.715 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.494 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.373 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.553 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.475 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.479 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.724 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.451 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.564 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.560 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.785 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.550 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.707 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.501 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.388 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.694 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.668 |
MOD_SUMO_rev_2 | 609 | 618 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 9 | 14 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_1 | 504 | 509 | PF01217 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.737 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.573 |
TRG_NLS_MonoExtC_3 | 4 | 10 | PF00514 | 0.708 |
TRG_NLS_MonoExtN_4 | 4 | 9 | PF00514 | 0.717 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 272 | 277 | PF00026 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 585 | 589 | PF00026 | 0.287 |
TRG_Pf-PMV_PEXEL_1 | 602 | 607 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R2 | Leptomonas seymouri | 61% | 94% |
A0A0S4JEE2 | Bodo saltans | 34% | 100% |
A0A1X0NJV3 | Trypanosomatidae | 47% | 96% |
A0A3S7WWW4 | Leishmania donovani | 99% | 100% |
A0A422N700 | Trypanosoma rangeli | 49% | 99% |
A4HLD0 | Leishmania braziliensis | 82% | 100% |
C9ZIZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 92% |
E9AVI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QBZ5 | Leishmania major | 93% | 100% |
V5BFA4 | Trypanosoma cruzi | 46% | 100% |