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: A4HIZ9
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 | 576 | 580 | PF00656 | 0.396 |
CLV_MEL_PAP_1 | 211 | 217 | PF00089 | 0.439 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.376 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.341 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.299 |
DEG_SCF_FBW7_1 | 324 | 330 | PF00400 | 0.297 |
DEG_SPOP_SBC_1 | 478 | 482 | PF00917 | 0.339 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.260 |
DOC_CKS1_1 | 324 | 329 | PF01111 | 0.325 |
DOC_MAPK_gen_1 | 230 | 240 | PF00069 | 0.272 |
DOC_MAPK_HePTP_8 | 493 | 505 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 496 | 505 | PF00069 | 0.397 |
DOC_MAPK_NFAT4_5 | 496 | 504 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 131 | 138 | PF00149 | 0.320 |
DOC_PP1_RVXF_1 | 144 | 150 | PF00149 | 0.206 |
DOC_PP1_RVXF_1 | 387 | 393 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.509 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.284 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.440 |
DOC_PP4_FxxP_1 | 240 | 243 | PF00568 | 0.293 |
DOC_PP4_FxxP_1 | 560 | 563 | PF00568 | 0.318 |
DOC_PP4_MxPP_1 | 468 | 471 | PF00568 | 0.309 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.260 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.403 |
DOC_USP7_UBL2_3 | 110 | 114 | PF12436 | 0.569 |
DOC_USP7_UBL2_3 | 152 | 156 | PF12436 | 0.249 |
DOC_USP7_UBL2_3 | 206 | 210 | PF12436 | 0.412 |
DOC_USP7_UBL2_3 | 350 | 354 | PF12436 | 0.325 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.260 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 313 | 321 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 413 | 421 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 516 | 522 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 72 | 82 | PF00244 | 0.475 |
LIG_APCC_ABBA_1 | 279 | 284 | PF00400 | 0.260 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.288 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.260 |
LIG_Clathr_ClatBox_1 | 290 | 294 | PF01394 | 0.234 |
LIG_Clathr_ClatBox_1 | 571 | 575 | PF01394 | 0.413 |
LIG_CtBP_PxDLS_1 | 470 | 474 | PF00389 | 0.300 |
LIG_eIF4E_1 | 217 | 223 | PF01652 | 0.353 |
LIG_eIF4E_1 | 546 | 552 | PF01652 | 0.252 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.435 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.312 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.445 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.387 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.343 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.530 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.455 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.398 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.356 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.303 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.348 |
LIG_LIR_Apic_2 | 237 | 243 | PF02991 | 0.291 |
LIG_LIR_Apic_2 | 269 | 273 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 369 | 378 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 369 | 373 | PF02991 | 0.377 |
LIG_Pex14_1 | 236 | 240 | PF04695 | 0.288 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.321 |
LIG_Pex14_2 | 531 | 535 | PF04695 | 0.308 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.354 |
LIG_Rb_LxCxE_1 | 249 | 269 | PF01857 | 0.302 |
LIG_Rb_pABgroove_1 | 296 | 304 | PF01858 | 0.325 |
LIG_REV1ctd_RIR_1 | 147 | 156 | PF16727 | 0.341 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.324 |
LIG_SH2_NCK_1 | 283 | 287 | PF00017 | 0.260 |
LIG_SH2_NCK_1 | 302 | 306 | PF00017 | 0.260 |
LIG_SH2_SRC | 283 | 286 | PF00017 | 0.299 |
LIG_SH2_SRC | 302 | 305 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.494 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.443 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 306 | 312 | PF11976 | 0.294 |
LIG_SUMO_SIM_anti_2 | 442 | 451 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 442 | 451 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 570 | 576 | PF11976 | 0.410 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.182 |
LIG_UBA3_1 | 187 | 192 | PF00899 | 0.259 |
LIG_UBA3_1 | 290 | 297 | PF00899 | 0.234 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.618 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.425 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.260 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.478 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.328 |
MOD_Cter_Amidation | 99 | 102 | PF01082 | 0.511 |
MOD_DYRK1A_RPxSP_1 | 78 | 82 | PF00069 | 0.467 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.443 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.261 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.495 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.433 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.260 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.328 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.489 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.427 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.636 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.615 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.509 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.446 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.518 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.260 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.260 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.372 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.275 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.249 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.383 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.459 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.340 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.544 |
MOD_LATS_1 | 490 | 496 | PF00433 | 0.243 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.519 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.182 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.435 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.437 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.525 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.308 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.323 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.520 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.260 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.335 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.473 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.448 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.389 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.370 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.559 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.335 |
MOD_NEK2_2 | 461 | 466 | PF00069 | 0.477 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.479 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.618 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.260 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.757 |
MOD_PKA_1 | 125 | 131 | PF00069 | 0.517 |
MOD_PKA_1 | 213 | 219 | PF00069 | 0.444 |
MOD_PKA_1 | 428 | 434 | PF00069 | 0.463 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.499 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.449 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.444 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.298 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.294 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.473 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.468 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.342 |
MOD_PKB_1 | 8 | 16 | PF00069 | 0.421 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.182 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.380 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.260 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.405 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.308 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.252 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.260 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.325 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 116 | 119 | PF00179 | 0.569 |
TRG_DiLeu_BaEn_1 | 442 | 447 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_1 | 568 | 573 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_4 | 306 | 312 | PF01217 | 0.182 |
TRG_DiLeu_BaLyEn_6 | 44 | 49 | PF01217 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.420 |
TRG_NLS_Bipartite_1 | 101 | 118 | PF00514 | 0.584 |
TRG_NLS_MonoExtC_3 | 113 | 119 | PF00514 | 0.496 |
TRG_NLS_MonoExtC_3 | 5 | 10 | PF00514 | 0.412 |
TRG_NLS_MonoExtN_4 | 210 | 216 | PF00514 | 0.448 |
TRG_NLS_MonoExtN_4 | 6 | 11 | PF00514 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDT4 | Leptomonas seymouri | 73% | 100% |
A0A1X0NJI1 | Trypanosomatidae | 54% | 100% |
A0A3S7X447 | Leishmania donovani | 81% | 100% |
A3KP59 | Danio rerio | 29% | 100% |
A4I6B6 | Leishmania infantum | 81% | 100% |
A5PK74 | Bos taurus | 28% | 89% |
A8QFQ3 | Brugia malayi | 27% | 84% |
A8XEA2 | Caenorhabditis briggsae | 23% | 77% |
B0WMG3 | Culex quinquefasciatus | 28% | 92% |
B3MSI4 | Drosophila ananassae | 29% | 71% |
B3NU20 | Drosophila erecta | 29% | 91% |
B4GUZ2 | Drosophila persimilis | 28% | 87% |
B4I100 | Drosophila sechellia | 30% | 91% |
B4L6Q5 | Drosophila mojavensis | 29% | 67% |
B4NP88 | Drosophila willistoni | 29% | 78% |
B4Q068 | Drosophila yakuba | 29% | 87% |
B4R4H1 | Drosophila simulans | 30% | 70% |
C3XRY1 | Branchiostoma floridae | 27% | 98% |
D3ZU57 | Rattus norvegicus | 29% | 100% |
E9B1H4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 95% |
O01658 | Caenorhabditis elegans | 25% | 80% |
Q16W06 | Aedes aegypti | 27% | 94% |
Q4Q6P0 | Leishmania major | 79% | 100% |
Q54K96 | Dictyostelium discoideum | 31% | 100% |
Q5ZMM1 | Gallus gallus | 29% | 99% |
Q7K4H4 | Drosophila melanogaster | 28% | 91% |
Q9H6W3 | Homo sapiens | 28% | 93% |
Q9JJF3 | Mus musculus | 29% | 99% |
V5AYK7 | Trypanosoma cruzi | 52% | 100% |