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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 8 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9B1H4
Term | Name | Level | Count |
---|---|---|---|
GO:0006482 | protein demethylation | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008214 | protein dealkylation | 5 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016577 | histone demethylation | 4 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034720 | histone H3-K4 demethylation | 6 | 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:0070076 | histone lysine demethylation | 5 | 1 |
GO:0070544 | histone H3-K36 demethylation | 6 | 1 |
GO:0070988 | demethylation | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005506 | iron ion binding | 6 | 9 |
GO:0016491 | oxidoreductase activity | 2 | 9 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 9 |
GO:0016706 | 2-oxoglutarate-dependent dioxygenase activity | 4 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0046914 | transition metal ion binding | 5 | 9 |
GO:0051213 | dioxygenase activity | 3 | 9 |
GO:0032451 | demethylase activity | 2 | 1 |
GO:0032452 | histone demethylase activity | 4 | 1 |
GO:0032453 | histone H3K4 demethylase activity | 5 | 1 |
GO:0051864 | histone H3K36 demethylase activity | 5 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0140457 | protein demethylase activity | 3 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.403 |
CLV_MEL_PAP_1 | 240 | 246 | PF00089 | 0.440 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.195 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.387 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.387 |
DEG_MDM2_SWIB_1 | 67 | 74 | PF02201 | 0.424 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.445 |
DEG_SPOP_SBC_1 | 509 | 513 | PF00917 | 0.355 |
DEG_SPOP_SBC_1 | 77 | 81 | PF00917 | 0.422 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.259 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.324 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 88 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 379 | 389 | PF00069 | 0.166 |
DOC_MAPK_HePTP_8 | 522 | 534 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 382 | 391 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 525 | 534 | PF00069 | 0.402 |
DOC_MAPK_NFAT4_5 | 525 | 533 | PF00069 | 0.387 |
DOC_PP1_RVXF_1 | 416 | 422 | PF00149 | 0.391 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 368 | 371 | PF13499 | 0.283 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.434 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.451 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.295 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.330 |
DOC_PP4_FxxP_1 | 589 | 592 | PF00568 | 0.328 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.259 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.280 |
DOC_USP7_UBL2_3 | 235 | 239 | PF12436 | 0.414 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.324 |
DOC_USP7_UBL2_3 | 460 | 464 | PF12436 | 0.278 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 382 | 388 | PF00244 | 0.247 |
LIG_14-3-3_CanoR_1 | 545 | 550 | PF00244 | 0.348 |
LIG_APCC_ABBA_1 | 308 | 313 | PF00400 | 0.259 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.292 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.259 |
LIG_Clathr_ClatBox_1 | 319 | 323 | PF01394 | 0.233 |
LIG_Clathr_ClatBox_1 | 600 | 604 | PF01394 | 0.419 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.355 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.509 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.455 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.542 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.475 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.361 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.403 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.425 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.228 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.354 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.294 |
LIG_LIR_Apic_2 | 298 | 302 | PF02991 | 0.259 |
LIG_LIR_Apic_2 | 351 | 356 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.383 |
LIG_MYND_1 | 350 | 354 | PF01753 | 0.225 |
LIG_NRBOX | 471 | 477 | PF00104 | 0.352 |
LIG_PCNA_yPIPBox_3 | 458 | 469 | PF02747 | 0.390 |
LIG_Pex14_1 | 265 | 269 | PF04695 | 0.292 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.322 |
LIG_Pex14_2 | 560 | 564 | PF04695 | 0.319 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.421 |
LIG_PTB_Apo_2 | 435 | 442 | PF02174 | 0.403 |
LIG_Rb_pABgroove_1 | 325 | 333 | PF01858 | 0.324 |
LIG_REV1ctd_RIR_1 | 176 | 185 | PF16727 | 0.344 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.323 |
LIG_SH2_GRB2like | 36 | 39 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 312 | 316 | PF00017 | 0.259 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.259 |
LIG_SH2_SRC | 312 | 315 | PF00017 | 0.294 |
LIG_SH2_SRC | 331 | 334 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.438 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.448 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.417 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.443 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 229 | 235 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 335 | 341 | PF11976 | 0.293 |
LIG_SUMO_SIM_anti_2 | 471 | 479 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 471 | 479 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 599 | 605 | PF11976 | 0.417 |
LIG_TYR_ITIM | 56 | 61 | PF00017 | 0.413 |
LIG_UBA3_1 | 319 | 326 | PF00899 | 0.233 |
MOD_CDC14_SPxK_1 | 110 | 113 | PF00782 | 0.483 |
MOD_CDK_SPK_2 | 352 | 357 | PF00069 | 0.280 |
MOD_CDK_SPxK_1 | 107 | 113 | PF00069 | 0.488 |
MOD_CDK_SPxxK_3 | 107 | 114 | PF00069 | 0.509 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.621 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.423 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.427 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.259 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.709 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.329 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.584 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.442 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.414 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.260 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.259 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.413 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.499 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.450 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.664 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.586 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.455 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.259 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.243 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.377 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.470 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.377 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.413 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.453 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.362 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.460 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.409 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.310 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.326 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.519 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.259 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.483 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.401 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.433 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.372 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.432 |
MOD_NEK2_2 | 263 | 268 | PF00069 | 0.272 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.334 |
MOD_NEK2_2 | 490 | 495 | PF00069 | 0.477 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.512 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.621 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.259 |
MOD_PK_1 | 577 | 583 | PF00069 | 0.240 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.540 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.598 |
MOD_PKA_1 | 242 | 248 | PF00069 | 0.445 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.490 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.445 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.297 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.293 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.484 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.349 |
MOD_PKB_1 | 131 | 139 | PF00069 | 0.583 |
MOD_PKB_1 | 519 | 527 | PF00069 | 0.390 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.583 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.374 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.411 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.259 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.480 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.399 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.314 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.412 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.423 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.545 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.259 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.324 |
MOD_SUMO_for_1 | 145 | 148 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 232 | 240 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_1 | 184 | 189 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.372 |
TRG_DiLeu_BaEn_1 | 597 | 602 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 518 | 523 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 526 | 531 | PF01217 | 0.352 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.444 |
TRG_NES_CRM1_1 | 471 | 483 | PF08389 | 0.299 |
TRG_NLS_MonoCore_2 | 103 | 108 | PF00514 | 0.489 |
TRG_NLS_MonoExtN_4 | 103 | 108 | PF00514 | 0.489 |
TRG_NLS_MonoExtN_4 | 238 | 245 | PF00514 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 423 | 428 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDT4 | Leptomonas seymouri | 70% | 100% |
A0A1X0NJI1 | Trypanosomatidae | 53% | 100% |
A0A3S7X447 | Leishmania donovani | 92% | 100% |
A3KP59 | Danio rerio | 27% | 100% |
A4HIZ9 | Leishmania braziliensis | 78% | 100% |
A4I6B6 | Leishmania infantum | 92% | 100% |
A5PK74 | Bos taurus | 30% | 94% |
A8QFQ3 | Brugia malayi | 26% | 88% |
A8XEA2 | Caenorhabditis briggsae | 24% | 80% |
B0WMG3 | Culex quinquefasciatus | 30% | 96% |
B3MSI4 | Drosophila ananassae | 30% | 74% |
B3NU20 | Drosophila erecta | 27% | 95% |
B4GUZ2 | Drosophila persimilis | 28% | 91% |
B4I100 | Drosophila sechellia | 30% | 95% |
B4JMQ2 | Drosophila grimshawi | 29% | 86% |
B4L6Q5 | Drosophila mojavensis | 30% | 70% |
B4M7P8 | Drosophila virilis | 27% | 69% |
B4NP88 | Drosophila willistoni | 30% | 81% |
B4Q068 | Drosophila yakuba | 27% | 91% |
B4R4H1 | Drosophila simulans | 30% | 74% |
C3XRY1 | Branchiostoma floridae | 28% | 100% |
D3ZU57 | Rattus norvegicus | 31% | 100% |
Q16W06 | Aedes aegypti | 27% | 98% |
Q4Q6P0 | Leishmania major | 87% | 100% |
Q54K96 | Dictyostelium discoideum | 28% | 100% |
Q5ZMM1 | Gallus gallus | 30% | 100% |
Q7K4H4 | Drosophila melanogaster | 29% | 96% |
Q9H6W3 | Homo sapiens | 30% | 97% |
Q9JJF3 | Mus musculus | 31% | 100% |
V5AYK7 | Trypanosoma cruzi | 53% | 100% |