Histone/chromosome structure, histone acetyltransferase
| 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. | yes | yes: 25 | 
| 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:0006355 | regulation of DNA-templated transcription | 6 | 11 | 
| GO:0009889 | regulation of biosynthetic process | 4 | 11 | 
| GO:0010468 | regulation of gene expression | 5 | 11 | 
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 11 | 
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 11 | 
| GO:0019222 | regulation of metabolic process | 3 | 11 | 
| GO:0031323 | regulation of cellular metabolic process | 4 | 11 | 
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 11 | 
| GO:0050789 | regulation of biological process | 2 | 11 | 
| GO:0050794 | regulation of cellular process | 3 | 11 | 
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 | 
| GO:0051252 | regulation of RNA metabolic process | 5 | 11 | 
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 | 
| GO:0065007 | biological regulation | 1 | 11 | 
| GO:0080090 | regulation of primary metabolic process | 4 | 11 | 
| GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 11 | 
| GO:2001141 | regulation of RNA biosynthetic process | 6 | 11 | 
| GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 | 
| GO:0009890 | negative regulation of biosynthetic process | 5 | 1 | 
| GO:0009891 | positive regulation of biosynthetic process | 5 | 1 | 
| GO:0009892 | negative regulation of metabolic process | 4 | 1 | 
| GO:0009893 | positive regulation of metabolic process | 4 | 1 | 
| GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 | 
| GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 | 
| GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 | 
| GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 | 
| GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 | 
| GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 | 
| GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 | 
| GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 | 
| GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 | 
| GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 | 
| GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 | 
| GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 | 
| GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 | 
| GO:0048518 | positive regulation of biological process | 3 | 1 | 
| GO:0048519 | negative regulation of biological process | 3 | 1 | 
| GO:0048522 | positive regulation of cellular process | 4 | 1 | 
| GO:0048523 | negative regulation of cellular process | 4 | 1 | 
| GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 | 
| GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 | 
| GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 | 
| GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 | 
| GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 | 
| GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 | 
| GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 | 
| GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 | 
| GO:0004402 | histone acetyltransferase activity | 4 | 11 | 
| GO:0008080 | N-acetyltransferase activity | 6 | 11 | 
| GO:0016407 | acetyltransferase activity | 5 | 11 | 
| GO:0016410 | N-acyltransferase activity | 5 | 11 | 
| GO:0016740 | transferase activity | 2 | 11 | 
| GO:0016746 | acyltransferase activity | 3 | 11 | 
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 11 | 
| GO:0034212 | peptide N-acetyltransferase activity | 7 | 11 | 
| GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 11 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 11 | 
| GO:0003712 | transcription coregulator activity | 2 | 1 | 
| GO:0005488 | binding | 1 | 1 | 
| GO:0005515 | protein binding | 2 | 1 | 
| GO:0042393 | histone binding | 3 | 1 | 
| GO:0140110 | transcription regulator activity | 1 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.503 | 
| CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.402 | 
| CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.307 | 
| CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.728 | 
| CLV_PCSK_FUR_1 | 136 | 140 | PF00082 | 0.631 | 
| CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.587 | 
| CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.426 | 
| CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.307 | 
| CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.460 | 
| CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.728 | 
| CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.473 | 
| CLV_PCSK_PC7_1 | 286 | 292 | PF00082 | 0.402 | 
| CLV_PCSK_PC7_1 | 469 | 475 | PF00082 | 0.437 | 
| CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.469 | 
| CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.307 | 
| CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.556 | 
| CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.525 | 
| DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.615 | 
| DOC_CKS1_1 | 392 | 397 | PF01111 | 0.602 | 
| DOC_CKS1_1 | 80 | 85 | PF01111 | 0.617 | 
| DOC_MAPK_gen_1 | 290 | 297 | PF00069 | 0.602 | 
| DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.520 | 
| DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.507 | 
| DOC_SPAK_OSR1_1 | 376 | 380 | PF12202 | 0.507 | 
| DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.631 | 
| DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.379 | 
| DOC_USP7_UBL2_3 | 473 | 477 | PF12436 | 0.537 | 
| DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.481 | 
| DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.543 | 
| DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.507 | 
| DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.507 | 
| DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.507 | 
| DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.781 | 
| LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.459 | 
| LIG_APCC_ABBA_1 | 258 | 263 | PF00400 | 0.469 | 
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.565 | 
| LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.487 | 
| LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.507 | 
| LIG_BRCT_BRCA1_1 | 482 | 486 | PF00533 | 0.518 | 
| LIG_Clathr_ClatBox_1 | 292 | 296 | PF01394 | 0.520 | 
| LIG_deltaCOP1_diTrp_1 | 161 | 165 | PF00928 | 0.474 | 
| LIG_FHA_1 | 100 | 106 | PF00498 | 0.570 | 
| LIG_FHA_1 | 145 | 151 | PF00498 | 0.596 | 
| LIG_FHA_1 | 202 | 208 | PF00498 | 0.600 | 
| LIG_FHA_1 | 325 | 331 | PF00498 | 0.507 | 
| LIG_FHA_1 | 337 | 343 | PF00498 | 0.507 | 
| LIG_FHA_1 | 414 | 420 | PF00498 | 0.624 | 
| LIG_FHA_1 | 436 | 442 | PF00498 | 0.553 | 
| LIG_FHA_1 | 470 | 476 | PF00498 | 0.483 | 
| LIG_FHA_1 | 486 | 492 | PF00498 | 0.538 | 
| LIG_FHA_2 | 302 | 308 | PF00498 | 0.563 | 
| LIG_FHA_2 | 459 | 465 | PF00498 | 0.507 | 
| LIG_GBD_Chelix_1 | 293 | 301 | PF00786 | 0.402 | 
| LIG_LIR_Apic_2 | 161 | 167 | PF02991 | 0.566 | 
| LIG_LIR_Apic_2 | 283 | 288 | PF02991 | 0.507 | 
| LIG_LIR_Gen_1 | 485 | 495 | PF02991 | 0.497 | 
| LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.471 | 
| LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.528 | 
| LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.521 | 
| LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.529 | 
| LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.516 | 
| LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.523 | 
| LIG_MLH1_MIPbox_1 | 140 | 144 | PF16413 | 0.487 | 
| LIG_Pex14_1 | 493 | 497 | PF04695 | 0.479 | 
| LIG_Pex14_2 | 497 | 501 | PF04695 | 0.538 | 
| LIG_PTB_Apo_2 | 17 | 24 | PF02174 | 0.602 | 
| LIG_REV1ctd_RIR_1 | 141 | 150 | PF16727 | 0.472 | 
| LIG_SH2_CRK | 16 | 20 | PF00017 | 0.507 | 
| LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.516 | 
| LIG_SH2_STAP1 | 471 | 475 | PF00017 | 0.454 | 
| LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.381 | 
| LIG_SH2_STAT3 | 433 | 436 | PF00017 | 0.507 | 
| LIG_SH2_STAT3 | 46 | 49 | PF00017 | 0.507 | 
| LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.485 | 
| LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.486 | 
| LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.507 | 
| LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.507 | 
| LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.507 | 
| LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.512 | 
| LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.541 | 
| LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.556 | 
| LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.331 | 
| LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.617 | 
| LIG_SH3_1 | 502 | 508 | PF00018 | 0.545 | 
| LIG_SH3_3 | 389 | 395 | PF00018 | 0.514 | 
| LIG_SH3_3 | 502 | 508 | PF00018 | 0.435 | 
| LIG_SH3_3 | 513 | 519 | PF00018 | 0.541 | 
| LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.538 | 
| LIG_SUMO_SIM_anti_2 | 361 | 367 | PF11976 | 0.507 | 
| LIG_SUMO_SIM_par_1 | 27 | 34 | PF11976 | 0.602 | 
| LIG_SUMO_SIM_par_1 | 291 | 296 | PF11976 | 0.508 | 
| LIG_SUMO_SIM_par_1 | 377 | 382 | PF11976 | 0.515 | 
| LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.507 | 
| LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.557 | 
| LIG_TRFH_1 | 256 | 260 | PF08558 | 0.354 | 
| LIG_UBA3_1 | 311 | 320 | PF00899 | 0.507 | 
| MOD_CDK_SPxK_1 | 391 | 397 | PF00069 | 0.507 | 
| MOD_CK1_1 | 201 | 207 | PF00069 | 0.676 | 
| MOD_CK1_1 | 336 | 342 | PF00069 | 0.553 | 
| MOD_CK1_1 | 74 | 80 | PF00069 | 0.734 | 
| MOD_CK1_1 | 92 | 98 | PF00069 | 0.641 | 
| MOD_CK2_1 | 301 | 307 | PF00069 | 0.582 | 
| MOD_CK2_1 | 383 | 389 | PF00069 | 0.507 | 
| MOD_CK2_1 | 458 | 464 | PF00069 | 0.560 | 
| MOD_GlcNHglycan | 115 | 119 | PF01048 | 0.553 | 
| MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.695 | 
| MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.596 | 
| MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.627 | 
| MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.607 | 
| MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.417 | 
| MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.526 | 
| MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.657 | 
| MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.627 | 
| MOD_GSK3_1 | 110 | 117 | PF00069 | 0.475 | 
| MOD_GSK3_1 | 138 | 145 | PF00069 | 0.515 | 
| MOD_GSK3_1 | 159 | 166 | PF00069 | 0.448 | 
| MOD_GSK3_1 | 180 | 187 | PF00069 | 0.667 | 
| MOD_GSK3_1 | 194 | 201 | PF00069 | 0.506 | 
| MOD_GSK3_1 | 202 | 209 | PF00069 | 0.569 | 
| MOD_GSK3_1 | 218 | 225 | PF00069 | 0.666 | 
| MOD_GSK3_1 | 243 | 250 | PF00069 | 0.445 | 
| MOD_GSK3_1 | 297 | 304 | PF00069 | 0.602 | 
| MOD_GSK3_1 | 379 | 386 | PF00069 | 0.513 | 
| MOD_GSK3_1 | 469 | 476 | PF00069 | 0.645 | 
| MOD_GSK3_1 | 485 | 492 | PF00069 | 0.428 | 
| MOD_GSK3_1 | 81 | 88 | PF00069 | 0.613 | 
| MOD_GSK3_1 | 99 | 106 | PF00069 | 0.482 | 
| MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.402 | 
| MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.307 | 
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.696 | 
| MOD_NEK2_1 | 144 | 149 | PF00069 | 0.598 | 
| MOD_NEK2_1 | 19 | 24 | PF00069 | 0.433 | 
| MOD_NEK2_1 | 194 | 199 | PF00069 | 0.741 | 
| MOD_NEK2_1 | 406 | 411 | PF00069 | 0.598 | 
| MOD_PIKK_1 | 180 | 186 | PF00454 | 0.629 | 
| MOD_PKA_1 | 138 | 144 | PF00069 | 0.491 | 
| MOD_PKA_1 | 473 | 479 | PF00069 | 0.415 | 
| MOD_PKA_1 | 89 | 95 | PF00069 | 0.719 | 
| MOD_PKA_2 | 138 | 144 | PF00069 | 0.624 | 
| MOD_PKA_2 | 473 | 479 | PF00069 | 0.415 | 
| MOD_PKA_2 | 89 | 95 | PF00069 | 0.719 | 
| MOD_PKB_1 | 136 | 144 | PF00069 | 0.492 | 
| MOD_Plk_1 | 358 | 364 | PF00069 | 0.507 | 
| MOD_Plk_1 | 379 | 385 | PF00069 | 0.507 | 
| MOD_Plk_1 | 479 | 485 | PF00069 | 0.487 | 
| MOD_Plk_4 | 159 | 165 | PF00069 | 0.558 | 
| MOD_Plk_4 | 406 | 412 | PF00069 | 0.564 | 
| MOD_Plk_4 | 482 | 488 | PF00069 | 0.514 | 
| MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.481 | 
| MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.541 | 
| MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.507 | 
| MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.507 | 
| MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.507 | 
| MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.780 | 
| MOD_SUMO_rev_2 | 313 | 322 | PF00179 | 0.507 | 
| MOD_SUMO_rev_2 | 384 | 392 | PF00179 | 0.520 | 
| TRG_DiLeu_BaEn_1 | 307 | 312 | PF01217 | 0.507 | 
| TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.507 | 
| TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.365 | 
| TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.386 | 
| TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.630 | 
| TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.602 | 
| TRG_NES_CRM1_1 | 307 | 318 | PF08389 | 0.507 | 
| TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.576 | 
| TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.307 | 
| TRG_Pf-PMV_PEXEL_1 | 447 | 452 | PF00026 | 0.402 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P5B0 | Leptomonas seymouri | 80% | 100% | 
| A0A1X0NNT9 | Trypanosomatidae | 58% | 100% | 
| A0A3R7M6T2 | Trypanosoma rangeli | 57% | 100% | 
| A4H7H5 | Leishmania braziliensis | 87% | 100% | 
| A4HVV6 | Leishmania infantum | 100% | 100% | 
| C9ZT70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% | 
| E9APK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% | 
| E9B048 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 68% | 
| O94446 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% | 
| Q4QFX1 | Leishmania major | 97% | 100% | 
| V5BHR3 | Trypanosoma cruzi | 58% | 100% |