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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A4HTP2
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 | 12 | 16 | PF00656 | 0.442 |
CLV_MEL_PAP_1 | 87 | 93 | PF00089 | 0.400 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.474 |
CLV_PCSK_FUR_1 | 629 | 633 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.222 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.222 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.220 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.394 |
DOC_CKS1_1 | 186 | 191 | PF01111 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.484 |
DOC_MAPK_DCC_7 | 204 | 213 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 204 | 213 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 324 | 331 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 376 | 384 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 523 | 531 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 511 | 517 | PF00149 | 0.379 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.474 |
DOC_PP2B_LxvP_1 | 551 | 554 | PF13499 | 0.361 |
DOC_PP2B_PxIxI_1 | 162 | 168 | PF00149 | 0.400 |
DOC_PP2B_PxIxI_1 | 374 | 380 | PF00149 | 0.420 |
DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.474 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.628 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.442 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.496 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.358 |
DOC_USP7_UBL2_3 | 77 | 81 | PF12436 | 0.420 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.390 |
LIG_14-3-3_CanoR_1 | 21 | 29 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 293 | 300 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 365 | 374 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 94 | 102 | PF00244 | 0.532 |
LIG_APCC_ABBA_1 | 217 | 222 | PF00400 | 0.474 |
LIG_BIR_III_4 | 135 | 139 | PF00653 | 0.487 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 486 | 490 | PF00533 | 0.420 |
LIG_CaM_IQ_9 | 638 | 653 | PF13499 | 0.388 |
LIG_EVH1_2 | 28 | 32 | PF00568 | 0.405 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.412 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.661 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.448 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.437 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.439 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.393 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.420 |
LIG_Integrin_RGD_1 | 422 | 424 | PF01839 | 0.262 |
LIG_LIR_Apic_2 | 257 | 261 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 47 | 53 | PF02991 | 0.404 |
LIG_LIR_Apic_2 | 491 | 497 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 251 | 258 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 330 | 337 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 347 | 357 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 402 | 411 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 504 | 514 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 585 | 594 | PF02991 | 0.559 |
LIG_LIR_LC3C_4 | 524 | 529 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 585 | 589 | PF02991 | 0.468 |
LIG_NRP_CendR_1 | 651 | 653 | PF00754 | 0.465 |
LIG_SH2_SRC | 252 | 255 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.437 |
LIG_SH3_2 | 186 | 191 | PF14604 | 0.420 |
LIG_SH3_2 | 371 | 376 | PF14604 | 0.431 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.478 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.256 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.437 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.431 |
LIG_SH3_CIN85_PxpxPR_1 | 44 | 49 | PF14604 | 0.422 |
LIG_SUMO_SIM_anti_2 | 113 | 118 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 482 | 487 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 526 | 532 | PF11976 | 0.436 |
LIG_TYR_ITIM | 403 | 408 | PF00017 | 0.437 |
LIG_UBA3_1 | 116 | 123 | PF00899 | 0.495 |
LIG_WRC_WIRS_1 | 255 | 260 | PF05994 | 0.474 |
LIG_WRC_WIRS_1 | 328 | 333 | PF05994 | 0.474 |
LIG_WW_3 | 373 | 377 | PF00397 | 0.462 |
MOD_CDK_SPK_2 | 44 | 49 | PF00069 | 0.422 |
MOD_CDK_SPK_2 | 565 | 570 | PF00069 | 0.390 |
MOD_CDK_SPxK_1 | 185 | 191 | PF00069 | 0.281 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.597 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.703 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.440 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.475 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.424 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.500 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.465 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.533 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.434 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.437 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.494 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.435 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.350 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.259 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.274 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.308 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.127 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.334 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.457 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.304 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.291 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.235 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.665 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.551 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.647 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.432 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.497 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.447 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.512 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.395 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.376 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.598 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.539 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.539 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.296 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.662 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.474 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.515 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.420 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.474 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.361 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.564 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.320 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.574 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.439 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.474 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.434 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.435 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.442 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.503 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.564 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.652 |
MOD_PKB_1 | 363 | 371 | PF00069 | 0.474 |
MOD_PKB_1 | 94 | 102 | PF00069 | 0.533 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.372 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.480 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.463 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.482 |
MOD_Plk_2-3 | 254 | 260 | PF00069 | 0.474 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.437 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.437 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.474 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.474 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.702 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.442 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.553 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.587 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.385 |
MOD_SUMO_rev_2 | 603 | 612 | PF00179 | 0.626 |
TRG_DiLeu_BaEn_1 | 622 | 627 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 555 | 560 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 575 | 578 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 581 | 584 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 61 | 63 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 562 | 566 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J6F0 | Bodo saltans | 36% | 97% |
A0A1X0NP71 | Trypanosomatidae | 43% | 100% |
A0A3S5H686 | Leishmania donovani | 99% | 100% |
A0A422NJU7 | Trypanosoma rangeli | 44% | 100% |
E9AI33 | Leishmania braziliensis | 81% | 100% |
E9AMH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
P53973 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 92% |
Q4QI60 | Leishmania major | 96% | 100% |
Q5A960 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 78% |
V5BR24 | Trypanosoma cruzi | 45% | 100% |