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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000123 | histone acetyltransferase complex | 4 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0031248 | protein acetyltransferase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0035267 | NuA4 histone acetyltransferase complex | 7 | 1 |
GO:0043189 | H4/H2A histone acetyltransferase complex | 6 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902493 | acetyltransferase complex | 4 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902562 | H4 histone acetyltransferase complex | 5 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HLG2
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 10 |
GO:0009889 | regulation of biosynthetic process | 4 | 10 |
GO:0010468 | regulation of gene expression | 5 | 10 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 10 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 10 |
GO:0019222 | regulation of metabolic process | 3 | 10 |
GO:0031323 | regulation of cellular metabolic process | 4 | 10 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 10 |
GO:0050789 | regulation of biological process | 2 | 10 |
GO:0050794 | regulation of cellular process | 3 | 10 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 10 |
GO:0051252 | regulation of RNA metabolic process | 5 | 10 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 10 |
GO:0065007 | biological regulation | 1 | 10 |
GO:0080090 | regulation of primary metabolic process | 4 | 10 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 10 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 10 |
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006475 | internal protein amino acid acetylation | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016573 | histone acetylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0018393 | internal peptidyl-lysine acetylation | 8 | 1 |
GO:0018394 | peptidyl-lysine acetylation | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 505 | 507 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.588 |
DEG_SPOP_SBC_1 | 209 | 213 | PF00917 | 0.522 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.539 |
DOC_CDC14_PxL_1 | 414 | 422 | PF14671 | 0.343 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.811 |
DOC_CKS1_1 | 431 | 436 | PF01111 | 0.570 |
DOC_CKS1_1 | 466 | 471 | PF01111 | 0.657 |
DOC_CYCLIN_RxL_1 | 308 | 322 | PF00134 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 466 | 472 | PF00134 | 0.617 |
DOC_MAPK_gen_1 | 29 | 38 | PF00069 | 0.455 |
DOC_MAPK_JIP1_4 | 352 | 358 | PF00069 | 0.707 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.455 |
DOC_PP1_RVXF_1 | 253 | 260 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 299 | 302 | PF13499 | 0.561 |
DOC_PP2B_LxvP_1 | 57 | 60 | PF13499 | 0.442 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.419 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.499 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.476 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.476 |
DOC_PP4_FxxP_1 | 53 | 56 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.544 |
DOC_USP7_UBL2_3 | 543 | 547 | PF12436 | 0.625 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 159 | 167 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 17 | 21 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 171 | 180 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 489 | 495 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 410 | 426 | PF00022 | 0.338 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.439 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.604 |
LIG_BRCT_BRCA1_1 | 474 | 478 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.457 |
LIG_CSL_BTD_1 | 340 | 343 | PF09270 | 0.694 |
LIG_eIF4E_1 | 350 | 356 | PF01652 | 0.723 |
LIG_EVH1_1 | 71 | 75 | PF00568 | 0.435 |
LIG_EVH1_1 | 99 | 103 | PF00568 | 0.470 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.528 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.550 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.496 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.495 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.730 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.553 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.476 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.532 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.715 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.356 |
LIG_GBD_Chelix_1 | 404 | 412 | PF00786 | 0.317 |
LIG_LIR_Apic_2 | 117 | 121 | PF02991 | 0.511 |
LIG_LIR_Apic_2 | 264 | 268 | PF02991 | 0.509 |
LIG_LIR_Apic_2 | 348 | 353 | PF02991 | 0.685 |
LIG_LIR_Apic_2 | 428 | 434 | PF02991 | 0.519 |
LIG_LIR_Apic_2 | 473 | 477 | PF02991 | 0.601 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 7 | 11 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.451 |
LIG_MYND_1 | 56 | 60 | PF01753 | 0.439 |
LIG_MYND_3 | 417 | 421 | PF01753 | 0.597 |
LIG_OCRL_FandH_1 | 13 | 25 | PF00620 | 0.460 |
LIG_Pex14_1 | 474 | 478 | PF04695 | 0.447 |
LIG_Pex14_2 | 470 | 474 | PF04695 | 0.599 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.452 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.428 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.444 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.728 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.559 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.559 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 485 | 488 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.453 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.410 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.800 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.664 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.702 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.614 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.611 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.437 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.461 |
LIG_SUMO_SIM_anti_2 | 401 | 406 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 491 | 498 | PF11976 | 0.600 |
LIG_SUMO_SIM_par_1 | 354 | 360 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 383 | 390 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 520 | 527 | PF11976 | 0.546 |
LIG_TYR_ITIM | 249 | 254 | PF00017 | 0.525 |
LIG_WW_3 | 138 | 142 | PF00397 | 0.517 |
MOD_CDC14_SPxK_1 | 138 | 141 | PF00782 | 0.768 |
MOD_CDK_SPxK_1 | 135 | 141 | PF00069 | 0.748 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.661 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.684 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.461 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.692 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.574 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.711 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.611 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.622 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.715 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.476 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.600 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.612 |
MOD_DYRK1A_RPxSP_1 | 222 | 226 | PF00069 | 0.562 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.723 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.686 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.622 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.780 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.716 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.460 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.792 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.425 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.739 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.458 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.754 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.673 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.614 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.651 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.748 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.543 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.715 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.601 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.720 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.735 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.604 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.722 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.636 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.543 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.407 |
MOD_N-GLC_1 | 439 | 444 | PF02516 | 0.680 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.699 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.625 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.670 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.481 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.592 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.518 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.631 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.468 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.629 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.445 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.516 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.684 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.436 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.461 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.516 |
MOD_PIKK_1 | 529 | 535 | PF00454 | 0.580 |
MOD_PK_1 | 354 | 360 | PF00069 | 0.592 |
MOD_PKA_1 | 171 | 177 | PF00069 | 0.580 |
MOD_PKA_1 | 314 | 320 | PF00069 | 0.498 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.456 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.481 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.498 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.553 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.634 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.476 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.412 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.655 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.541 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.561 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.557 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.518 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.561 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.607 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.667 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.679 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.746 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.780 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.502 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.559 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.744 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.523 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.438 |
MOD_SUMO_for_1 | 504 | 507 | PF00179 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.738 |
TRG_NES_CRM1_1 | 119 | 132 | PF08389 | 0.557 |
TRG_NES_CRM1_1 | 520 | 533 | PF08389 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6S1 | Leptomonas seymouri | 45% | 100% |
A0A3R7LCY2 | Trypanosoma rangeli | 28% | 100% |
A0A3S7X6P8 | Leishmania donovani | 80% | 100% |
A4I8X3 | Leishmania infantum | 80% | 100% |
D0A4W8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B3U2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q482 | Leishmania major | 80% | 100% |
V5DG54 | Trypanosoma cruzi | 30% | 100% |