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:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005634 | nucleus | 5 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
Related structures:
AlphaFold database: Q4Q6P0
Term | Name | Level | Count |
---|---|---|---|
GO:0006482 | protein demethylation | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0008214 | protein dealkylation | 5 | 2 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016577 | histone demethylation | 4 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0034720 | histone H3-K4 demethylation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070076 | histone lysine demethylation | 5 | 2 |
GO:0070544 | histone H3-K36 demethylation | 6 | 2 |
GO:0070988 | demethylation | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
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:0032451 | demethylase activity | 2 | 2 |
GO:0032452 | histone demethylase activity | 4 | 2 |
GO:0032453 | histone H3K4 demethylase activity | 5 | 2 |
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:0051864 | histone H3K36 demethylase activity | 5 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:0140457 | protein demethylase activity | 3 | 2 |
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 | 0.415 |
CLV_MEL_PAP_1 | 240 | 246 | PF00089 | 0.448 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.360 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.342 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.453 |
DEG_SCF_FBW7_1 | 354 | 359 | PF00400 | 0.309 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.445 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.267 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.343 |
DOC_MAPK_gen_1 | 29 | 37 | PF00069 | 0.453 |
DOC_MAPK_HePTP_8 | 522 | 534 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 383 | 391 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 525 | 534 | PF00069 | 0.421 |
DOC_MAPK_NFAT4_5 | 525 | 533 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 416 | 422 | PF00149 | 0.405 |
DOC_PP2B_LxvP_1 | 368 | 371 | PF13499 | 0.299 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.422 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.464 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.303 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.338 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.294 |
DOC_USP7_UBL2_3 | 235 | 239 | PF12436 | 0.428 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.343 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.475 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 32 | 36 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 512 | 520 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 96 | 103 | PF00244 | 0.470 |
LIG_APCC_ABBA_1 | 308 | 313 | PF00400 | 0.267 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.298 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.267 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.455 |
LIG_Clathr_ClatBox_1 | 600 | 604 | PF01394 | 0.426 |
LIG_deltaCOP1_diTrp_1 | 263 | 269 | PF00928 | 0.299 |
LIG_DLG_GKlike_1 | 133 | 141 | PF00625 | 0.504 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.365 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.437 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.381 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.367 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.483 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.440 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.375 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.443 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.438 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.373 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.468 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.300 |
LIG_LIR_Apic_2 | 298 | 302 | PF02991 | 0.267 |
LIG_LIR_Apic_2 | 351 | 356 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 316 | 327 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 56 | 63 | PF02991 | 0.425 |
LIG_LIR_LC3C_4 | 56 | 61 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.425 |
LIG_MLH1_MIPbox_1 | 33 | 37 | PF16413 | 0.455 |
LIG_NRBOX | 471 | 477 | PF00104 | 0.358 |
LIG_PCNA_yPIPBox_3 | 458 | 469 | PF02747 | 0.403 |
LIG_Pex14_1 | 265 | 269 | PF04695 | 0.298 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.350 |
LIG_Pex14_2 | 560 | 564 | PF04695 | 0.326 |
LIG_PTB_Apo_2 | 435 | 442 | PF02174 | 0.417 |
LIG_Rb_LxCxE_1 | 278 | 298 | PF01857 | 0.351 |
LIG_Rb_pABgroove_1 | 325 | 333 | PF01858 | 0.343 |
LIG_REV1ctd_RIR_1 | 176 | 185 | PF16727 | 0.357 |
LIG_SH2_NCK_1 | 312 | 316 | PF00017 | 0.267 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.267 |
LIG_SH2_SRC | 312 | 315 | PF00017 | 0.267 |
LIG_SH2_SRC | 331 | 334 | PF00017 | 0.301 |
LIG_SH2_STAT3 | 67 | 70 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.451 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.452 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.397 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.518 |
LIG_SUMO_SIM_anti_2 | 230 | 235 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 335 | 341 | PF11976 | 0.301 |
LIG_SUMO_SIM_anti_2 | 471 | 479 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 471 | 479 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 59 | 64 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 599 | 605 | PF11976 | 0.424 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.503 |
LIG_WW_3 | 14 | 18 | PF00397 | 0.439 |
MOD_CDK_SPK_2 | 27 | 32 | PF00069 | 0.451 |
MOD_CDK_SPK_2 | 352 | 357 | PF00069 | 0.294 |
MOD_CDK_SPxxK_3 | 107 | 114 | PF00069 | 0.500 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.631 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.485 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.571 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.267 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.507 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.495 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.774 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.357 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.496 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.609 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.500 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.466 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.291 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.267 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.332 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.494 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.458 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.597 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.606 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.583 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.592 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.267 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.355 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.343 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.410 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.461 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.454 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.358 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.365 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.500 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.447 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.284 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.375 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.449 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.324 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.459 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.524 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.299 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.474 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.389 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.346 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.452 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.454 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.357 |
MOD_NEK2_2 | 378 | 383 | PF00069 | 0.301 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.500 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.631 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.267 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.636 |
MOD_PKA_1 | 242 | 248 | PF00069 | 0.571 |
MOD_PKA_1 | 512 | 518 | PF00069 | 0.304 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.450 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.571 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.486 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.290 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.341 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.491 |
MOD_PKB_1 | 131 | 139 | PF00069 | 0.604 |
MOD_PKB_1 | 519 | 527 | PF00069 | 0.394 |
MOD_PKB_1 | 94 | 102 | PF00069 | 0.443 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.604 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.384 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.419 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.269 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.521 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.406 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.323 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.466 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.546 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.517 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.267 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.343 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.475 |
MOD_SUMO_for_1 | 145 | 148 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 232 | 240 | PF00179 | 0.366 |
TRG_DiLeu_BaEn_1 | 184 | 189 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_1 | 597 | 602 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 518 | 523 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 526 | 531 | PF01217 | 0.361 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.450 |
TRG_NES_CRM1_1 | 471 | 483 | PF08389 | 0.304 |
TRG_NLS_Bipartite_1 | 130 | 147 | PF00514 | 0.609 |
TRG_NLS_MonoExtC_3 | 142 | 148 | PF00514 | 0.546 |
TRG_NLS_MonoExtN_4 | 238 | 245 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 423 | 428 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDT4 | Leptomonas seymouri | 70% | 100% |
A0A1X0NJI1 | Trypanosomatidae | 50% | 100% |
A0A3S7X447 | Leishmania donovani | 93% | 100% |
A3KP59 | Danio rerio | 28% | 100% |
A4HIZ9 | Leishmania braziliensis | 79% | 100% |
A4I6B6 | Leishmania infantum | 93% | 100% |
A5PK74 | Bos taurus | 30% | 94% |
A8QFQ3 | Brugia malayi | 25% | 88% |
A8XEA2 | Caenorhabditis briggsae | 24% | 80% |
B0WMG3 | Culex quinquefasciatus | 30% | 96% |
B3MSI4 | Drosophila ananassae | 30% | 74% |
B3NU20 | Drosophila erecta | 28% | 95% |
B4I100 | Drosophila sechellia | 30% | 95% |
B4L6Q5 | Drosophila mojavensis | 30% | 70% |
B4M7P8 | Drosophila virilis | 28% | 69% |
B4NP88 | Drosophila willistoni | 30% | 81% |
B4Q068 | Drosophila yakuba | 28% | 91% |
B4R4H1 | Drosophila simulans | 30% | 74% |
C3XRY1 | Branchiostoma floridae | 27% | 100% |
D3ZU57 | Rattus norvegicus | 31% | 100% |
E9B1H4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q16W06 | Aedes aegypti | 28% | 98% |
Q54K96 | Dictyostelium discoideum | 30% | 100% |
Q5ZMM1 | Gallus gallus | 29% | 100% |
Q7K4H4 | Drosophila melanogaster | 29% | 96% |
Q9H6W3 | Homo sapiens | 30% | 97% |
Q9JJF3 | Mus musculus | 31% | 100% |
V5AYK7 | Trypanosoma cruzi | 53% | 100% |