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: E9AMH8
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 | 43 | 49 | PF00089 | 0.450 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 147 | 151 | PF00082 | 0.138 |
CLV_PCSK_FUR_1 | 537 | 541 | PF00082 | 0.291 |
CLV_PCSK_FUR_1 | 585 | 589 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.138 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.138 |
CLV_PCSK_PC1ET2_1 | 587 | 589 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 534 | 540 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.226 |
DEG_APCC_DBOX_1 | 435 | 443 | PF00400 | 0.489 |
DEG_SCF_TRCP1_1 | 178 | 183 | PF00400 | 0.338 |
DEG_SPOP_SBC_1 | 106 | 110 | PF00917 | 0.373 |
DOC_CKS1_1 | 142 | 147 | PF01111 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 169 | 175 | PF00134 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 36 | 42 | PF00134 | 0.533 |
DOC_MAPK_DCC_7 | 160 | 169 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 160 | 169 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 280 | 287 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 332 | 340 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 436 | 444 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 479 | 487 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 511 | 519 | PF00069 | 0.221 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.467 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.406 |
DOC_PP2B_PxIxI_1 | 118 | 124 | PF00149 | 0.387 |
DOC_PP2B_PxIxI_1 | 330 | 336 | PF00149 | 0.413 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.491 |
DOC_PP4_FxxP_1 | 214 | 217 | PF00568 | 0.507 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.680 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.559 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 33 | 37 | PF12436 | 0.468 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.467 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 249 | 256 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.534 |
LIG_Actin_WH2_2 | 502 | 520 | PF00022 | 0.375 |
LIG_APCC_ABBA_1 | 173 | 178 | PF00400 | 0.467 |
LIG_BIR_III_4 | 91 | 95 | PF00653 | 0.469 |
LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.413 |
LIG_EVH1_2 | 2 | 6 | PF00568 | 0.598 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.483 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.455 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.444 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.433 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.442 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.453 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.426 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.475 |
LIG_Integrin_RGD_1 | 378 | 380 | PF01839 | 0.244 |
LIG_LIR_Apic_2 | 213 | 217 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 447 | 453 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 207 | 214 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 286 | 293 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 422 | 432 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 460 | 470 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 541 | 550 | PF02991 | 0.571 |
LIG_LIR_LC3C_4 | 480 | 485 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 286 | 290 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 541 | 545 | PF02991 | 0.486 |
LIG_Pex14_2 | 424 | 428 | PF04695 | 0.338 |
LIG_PTB_Apo_2 | 418 | 425 | PF02174 | 0.338 |
LIG_SH2_SRC | 208 | 211 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.574 |
LIG_SH3_2 | 142 | 147 | PF14604 | 0.426 |
LIG_SH3_2 | 327 | 332 | PF14604 | 0.424 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.467 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.268 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.377 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.426 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.424 |
LIG_SUMO_SIM_anti_2 | 69 | 74 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 334 | 339 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 438 | 443 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.426 |
LIG_TRAF2_1 | 569 | 572 | PF00917 | 0.565 |
LIG_TYR_ITIM | 359 | 364 | PF00017 | 0.426 |
LIG_UBA3_1 | 515 | 523 | PF00899 | 0.230 |
LIG_UBA3_1 | 72 | 79 | PF00899 | 0.598 |
LIG_WRC_WIRS_1 | 211 | 216 | PF05994 | 0.507 |
LIG_WRC_WIRS_1 | 284 | 289 | PF05994 | 0.467 |
LIG_WW_3 | 2 | 6 | PF00397 | 0.550 |
LIG_WW_3 | 329 | 333 | PF00397 | 0.469 |
MOD_CDK_SPK_2 | 521 | 526 | PF00069 | 0.373 |
MOD_CDK_SPK_2 | 98 | 103 | PF00069 | 0.456 |
MOD_CDK_SPxK_1 | 141 | 147 | PF00069 | 0.294 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.612 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.482 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.455 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.534 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.667 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.545 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.599 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.424 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.426 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.459 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.650 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.354 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.250 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.367 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.312 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.121 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.335 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.271 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.250 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.597 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.502 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.438 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.516 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.425 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.537 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.584 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.615 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.325 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.301 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.557 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.467 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.413 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.507 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.407 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.400 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.433 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.507 |
MOD_PIKK_1 | 567 | 573 | PF00454 | 0.413 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.539 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.469 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.690 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.548 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.558 |
MOD_PKB_1 | 319 | 327 | PF00069 | 0.467 |
MOD_PKB_1 | 50 | 58 | PF00069 | 0.538 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.375 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.486 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.503 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.552 |
MOD_Plk_2-3 | 210 | 216 | PF00069 | 0.467 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.426 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.426 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.507 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.507 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.417 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.370 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.519 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.716 |
MOD_SUMO_rev_2 | 559 | 568 | PF00179 | 0.688 |
TRG_DiLeu_BaEn_1 | 578 | 583 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.390 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 537 | 540 | PF00400 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD56 | Leptomonas seymouri | 65% | 100% |
A0A0S4J6F0 | Bodo saltans | 37% | 90% |
A0A1X0NP71 | Trypanosomatidae | 44% | 97% |
A0A3S5H686 | Leishmania donovani | 92% | 100% |
A0A422NJU7 | Trypanosoma rangeli | 46% | 100% |
A4HTP2 | Leishmania infantum | 91% | 93% |
E9AI33 | Leishmania braziliensis | 80% | 100% |
P53973 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 86% |
Q4QI60 | Leishmania major | 90% | 100% |
Q5A960 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 29% | 73% |
V5BR24 | Trypanosoma cruzi | 45% | 100% |