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: E9AVI4
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 | 676 | 680 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.606 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.242 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.580 |
DEG_SCF_FBW7_1 | 48 | 55 | PF00400 | 0.684 |
DEG_SPOP_SBC_1 | 406 | 410 | PF00917 | 0.647 |
DEG_SPOP_SBC_1 | 417 | 421 | PF00917 | 0.659 |
DEG_SPOP_SBC_1 | 425 | 429 | PF00917 | 0.602 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.634 |
DOC_ANK_TNKS_1 | 176 | 183 | PF00023 | 0.496 |
DOC_CKS1_1 | 49 | 54 | PF01111 | 0.677 |
DOC_CYCLIN_RxL_1 | 580 | 589 | PF00134 | 0.442 |
DOC_CYCLIN_yCln2_LP_2 | 46 | 49 | PF00134 | 0.624 |
DOC_MAPK_DCC_7 | 264 | 273 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 516 | 525 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 516 | 524 | PF00069 | 0.442 |
DOC_PIKK_1 | 330 | 337 | PF02985 | 0.694 |
DOC_PP2B_LxvP_1 | 46 | 49 | PF13499 | 0.731 |
DOC_PP2B_PxIxI_1 | 268 | 274 | PF00149 | 0.536 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.657 |
DOC_USP7_MATH_2 | 686 | 692 | PF00917 | 0.433 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 311 | 321 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 632 | 638 | PF00244 | 0.506 |
LIG_BRCT_BRCA1_1 | 525 | 529 | PF00533 | 0.442 |
LIG_Clathr_ClatBox_1 | 399 | 403 | PF01394 | 0.608 |
LIG_EH1_1 | 547 | 555 | PF00400 | 0.536 |
LIG_eIF4E_1 | 548 | 554 | PF01652 | 0.536 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.442 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.638 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.574 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.455 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.450 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.393 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.716 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.664 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.439 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.639 |
LIG_IRF3_LxIS_1 | 292 | 298 | PF10401 | 0.536 |
LIG_LIR_Apic_2 | 116 | 120 | PF02991 | 0.282 |
LIG_LIR_Apic_2 | 286 | 292 | PF02991 | 0.439 |
LIG_LIR_Apic_2 | 85 | 89 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 380 | 388 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.442 |
LIG_LIR_LC3C_4 | 559 | 563 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.443 |
LIG_MYND_1 | 40 | 44 | PF01753 | 0.728 |
LIG_MYND_1 | 48 | 52 | PF01753 | 0.647 |
LIG_MYND_1 | 640 | 644 | PF01753 | 0.439 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.593 |
LIG_NRP_CendR_1 | 699 | 701 | PF00754 | 0.456 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.536 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.604 |
LIG_SH2_GRB2like | 381 | 384 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 117 | 121 | PF00017 | 0.264 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.442 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 683 | 686 | PF00017 | 0.433 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.473 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.577 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.602 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.526 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 293 | 298 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 521 | 526 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 270 | 275 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 521 | 526 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 561 | 566 | PF11976 | 0.443 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.676 |
LIG_TYR_ITIM | 379 | 384 | PF00017 | 0.538 |
LIG_TYR_ITIM | 501 | 506 | PF00017 | 0.442 |
LIG_WRC_WIRS_1 | 690 | 695 | PF05994 | 0.445 |
LIG_WW_3 | 261 | 265 | PF00397 | 0.367 |
LIG_WW_3 | 267 | 271 | PF00397 | 0.362 |
MOD_CDK_SPxxK_3 | 449 | 456 | PF00069 | 0.618 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.625 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.501 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.757 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.595 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.584 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.588 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.330 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.649 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.524 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.446 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.687 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.622 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.602 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.573 |
MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.600 |
MOD_Cter_Amidation | 371 | 374 | PF01082 | 0.706 |
MOD_Cter_Amidation | 630 | 633 | PF01082 | 0.433 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.166 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.615 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.349 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.732 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.636 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.636 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.641 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.744 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.166 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.239 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.249 |
MOD_GlcNHglycan | 587 | 591 | PF01048 | 0.440 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.600 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.609 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.446 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.527 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.554 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.576 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.574 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.540 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.638 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.610 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.446 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.266 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.463 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.442 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.809 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.703 |
MOD_N-GLC_1 | 556 | 561 | PF02516 | 0.211 |
MOD_N-GLC_1 | 663 | 668 | PF02516 | 0.489 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.536 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.436 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.507 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.377 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.439 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.475 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.410 |
MOD_PIKK_1 | 622 | 628 | PF00454 | 0.547 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.616 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.427 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.451 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.690 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.610 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.494 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.640 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.367 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.457 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.480 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.441 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.443 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.655 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.537 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.590 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.666 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.654 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.455 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.654 |
MOD_SUMO_rev_2 | 607 | 616 | PF00179 | 0.491 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.744 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.623 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 373 | 376 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 698 | 701 | PF00400 | 0.441 |
TRG_NES_CRM1_1 | 162 | 174 | PF08389 | 0.508 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 270 | 275 | PF00026 | 0.235 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.242 |
TRG_Pf-PMV_PEXEL_1 | 600 | 605 | PF00026 | 0.405 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R2 | Leptomonas seymouri | 60% | 100% |
A0A1X0NJV3 | Trypanosomatidae | 47% | 100% |
A0A3S7WWW4 | Leishmania donovani | 91% | 100% |
A0A422N700 | Trypanosoma rangeli | 48% | 100% |
A4HLD0 | Leishmania braziliensis | 80% | 100% |
A4HTR2 | Leishmania infantum | 91% | 100% |
C9ZIZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
Q4QBZ5 | Leishmania major | 91% | 100% |
V5BFA4 | Trypanosoma cruzi | 47% | 100% |