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: A4I8X3
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_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.814 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.634 |
CLV_PCSK_FUR_1 | 164 | 168 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.559 |
CLV_PCSK_PC7_1 | 166 | 172 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.592 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.813 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.654 |
DOC_CYCLIN_yCln2_LP_2 | 363 | 369 | PF00134 | 0.611 |
DOC_MAPK_JIP1_4 | 249 | 255 | PF00069 | 0.736 |
DOC_PP1_RVXF_1 | 150 | 157 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.561 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.711 |
DOC_PP4_FxxP_1 | 14 | 17 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 156 | 159 | PF00568 | 0.476 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.476 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.831 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.772 |
DOC_USP7_UBL2_3 | 440 | 444 | PF12436 | 0.613 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 266 | 271 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 386 | 392 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 55 | 63 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 67 | 76 | PF00244 | 0.386 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.700 |
LIG_BIR_III_4 | 42 | 46 | PF00653 | 0.654 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.517 |
LIG_CSL_BTD_1 | 237 | 240 | PF09270 | 0.684 |
LIG_eIF4E_1 | 247 | 253 | PF01652 | 0.742 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.546 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.676 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.488 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.554 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.476 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.719 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.743 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.571 |
LIG_LIR_Apic_2 | 13 | 17 | PF02991 | 0.527 |
LIG_LIR_Apic_2 | 161 | 165 | PF02991 | 0.509 |
LIG_LIR_Apic_2 | 246 | 250 | PF02991 | 0.693 |
LIG_LIR_Apic_2 | 370 | 374 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 145 | 156 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 372 | 383 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.514 |
LIG_MYND_3 | 314 | 318 | PF01753 | 0.594 |
LIG_Pex14_1 | 371 | 375 | PF04695 | 0.407 |
LIG_Pex14_2 | 367 | 371 | PF04695 | 0.571 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.444 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.739 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.424 |
LIG_SH2_SRC | 18 | 21 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 328 | 331 | PF00017 | 0.482 |
LIG_SH2_STAT3 | 382 | 385 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.410 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.783 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.665 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.425 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.715 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.695 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.586 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.613 |
LIG_SUMO_SIM_anti_2 | 280 | 287 | PF11976 | 0.606 |
LIG_SUMO_SIM_anti_2 | 298 | 303 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 388 | 395 | PF11976 | 0.593 |
LIG_SUMO_SIM_par_1 | 251 | 257 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 280 | 287 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 423 | 429 | PF11976 | 0.586 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.547 |
LIG_TYR_ITIM | 146 | 151 | PF00017 | 0.525 |
LIG_WW_1 | 217 | 220 | PF00397 | 0.684 |
MOD_CDC14_SPxK_1 | 34 | 37 | PF00782 | 0.789 |
MOD_CDC14_SPxK_1 | 51 | 54 | PF00782 | 0.693 |
MOD_CDK_SPxK_1 | 31 | 37 | PF00069 | 0.770 |
MOD_CDK_SPxK_1 | 48 | 54 | PF00069 | 0.694 |
MOD_CDK_SPxxK_3 | 48 | 55 | PF00069 | 0.695 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.700 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.465 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.677 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.578 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.657 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.622 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.476 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.543 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.342 |
MOD_DYRK1A_RPxSP_1 | 344 | 348 | PF00069 | 0.702 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.736 |
MOD_GlcNHglycan | 114 | 118 | PF01048 | 0.732 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.741 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.626 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.784 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.588 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.705 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.627 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.812 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.749 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.665 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.768 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.749 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.608 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.776 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.776 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.659 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.480 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.597 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.720 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.512 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.584 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.600 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.700 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.580 |
MOD_PK_1 | 251 | 257 | PF00069 | 0.619 |
MOD_PKA_1 | 266 | 272 | PF00069 | 0.604 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.579 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.604 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.536 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.480 |
MOD_PKB_1 | 54 | 62 | PF00069 | 0.714 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.476 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.524 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.680 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.553 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.652 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.561 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.518 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.561 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.671 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.538 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.780 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.501 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.728 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.689 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.718 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.522 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.715 |
MOD_SUMO_for_1 | 401 | 404 | PF00179 | 0.532 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.678 |
TRG_DiLeu_BaEn_4 | 417 | 423 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.524 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.801 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.622 |
TRG_NES_CRM1_1 | 15 | 28 | PF08389 | 0.571 |
TRG_NES_CRM1_1 | 417 | 430 | PF08389 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.572 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6S1 | Leptomonas seymouri | 47% | 93% |
A0A3R7LCY2 | Trypanosoma rangeli | 27% | 96% |
A0A3S7X6P8 | Leishmania donovani | 99% | 100% |
A4HLG2 | Leishmania braziliensis | 80% | 100% |
D0A4W8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 92% |
E9B3U2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q482 | Leishmania major | 94% | 100% |
V5DG54 | Trypanosoma cruzi | 27% | 82% |