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: A0A3S7X447
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 | 488 | 492 | PF00656 | 0.471 |
CLV_MEL_PAP_1 | 123 | 129 | PF00089 | 0.497 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.569 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.727 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.410 |
DEG_SCF_FBW7_1 | 235 | 242 | PF00400 | 0.415 |
DOC_CKS1_1 | 182 | 187 | PF01111 | 0.332 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.467 |
DOC_MAPK_gen_1 | 122 | 129 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 14 | 23 | PF00069 | 0.574 |
DOC_MAPK_HePTP_8 | 405 | 417 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 266 | 274 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 408 | 417 | PF00069 | 0.471 |
DOC_MAPK_NFAT4_5 | 408 | 416 | PF00069 | 0.535 |
DOC_PP1_RVXF_1 | 123 | 130 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 299 | 305 | PF00149 | 0.497 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.356 |
DOC_PP2B_LxvP_1 | 380 | 383 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.519 |
DOC_PP4_FxxP_1 | 152 | 155 | PF00568 | 0.368 |
DOC_PP4_FxxP_1 | 236 | 239 | PF00568 | 0.362 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.688 |
DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.554 |
DOC_USP7_UBL2_3 | 262 | 266 | PF12436 | 0.467 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 225 | 233 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 396 | 403 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.536 |
LIG_APCC_ABBA_1 | 191 | 196 | PF00400 | 0.332 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.332 |
LIG_Clathr_ClatBox_1 | 202 | 206 | PF01394 | 0.301 |
LIG_Clathr_ClatBox_1 | 483 | 487 | PF01394 | 0.481 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.559 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.406 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.364 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.546 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.602 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.501 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.485 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.553 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.433 |
LIG_LIR_Apic_2 | 149 | 155 | PF02991 | 0.367 |
LIG_LIR_Apic_2 | 181 | 185 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 234 | 239 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.392 |
LIG_MYND_1 | 233 | 237 | PF01753 | 0.292 |
LIG_NRBOX | 354 | 360 | PF00104 | 0.431 |
LIG_PCNA_yPIPBox_3 | 341 | 352 | PF02747 | 0.502 |
LIG_Pex14_1 | 148 | 152 | PF04695 | 0.365 |
LIG_Pex14_2 | 443 | 447 | PF04695 | 0.394 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.400 |
LIG_PTB_Apo_2 | 318 | 325 | PF02174 | 0.504 |
LIG_Rb_LxCxE_1 | 161 | 181 | PF01857 | 0.428 |
LIG_Rb_pABgroove_1 | 208 | 216 | PF01858 | 0.467 |
LIG_REV1ctd_RIR_1 | 59 | 68 | PF16727 | 0.434 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.332 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.332 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.332 |
LIG_SH2_SRC | 214 | 217 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.505 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.472 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.502 |
LIG_SUMO_SIM_anti_2 | 113 | 118 | PF11976 | 0.437 |
LIG_SUMO_SIM_anti_2 | 218 | 224 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 354 | 362 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 354 | 362 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.479 |
LIG_UBA3_1 | 202 | 209 | PF00899 | 0.301 |
MOD_CDK_SPK_2 | 235 | 240 | PF00069 | 0.390 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.565 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.332 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.502 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.622 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.493 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.391 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.739 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.325 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.309 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.540 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.532 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.716 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.518 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.482 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.700 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.307 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.399 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.318 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.437 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.508 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.460 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.370 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.425 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.438 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.491 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.473 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.487 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.649 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.332 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.593 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.446 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.414 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.368 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.388 |
MOD_NEK2_2 | 146 | 151 | PF00069 | 0.338 |
MOD_NEK2_2 | 254 | 259 | PF00069 | 0.400 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.365 |
MOD_NEK2_2 | 373 | 378 | PF00069 | 0.473 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.332 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.651 |
MOD_PKA_1 | 125 | 131 | PF00069 | 0.502 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.728 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.454 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.307 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.365 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.529 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.451 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.537 |
MOD_PKB_1 | 15 | 23 | PF00069 | 0.711 |
MOD_PKB_1 | 402 | 410 | PF00069 | 0.455 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.713 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.453 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.494 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.310 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.462 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.366 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.332 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.467 |
MOD_SUMO_for_1 | 28 | 31 | PF00179 | 0.697 |
MOD_SUMO_rev_2 | 115 | 123 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_1 | 354 | 359 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_1 | 480 | 485 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_1 | 67 | 72 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 409 | 414 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.269 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.428 |
TRG_NLS_MonoExtN_4 | 121 | 128 | PF00514 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDT4 | Leptomonas seymouri | 70% | 99% |
A0A1X0NJI1 | Trypanosomatidae | 53% | 100% |
A3KP59 | Danio rerio | 28% | 93% |
A4HIZ9 | Leishmania braziliensis | 81% | 100% |
A4I6B6 | Leishmania infantum | 99% | 100% |
A5PK74 | Bos taurus | 31% | 76% |
A8QFQ3 | Brugia malayi | 25% | 71% |
B0WMG3 | Culex quinquefasciatus | 30% | 78% |
B3NU20 | Drosophila erecta | 28% | 77% |
B4GUZ2 | Drosophila persimilis | 30% | 74% |
B4I100 | Drosophila sechellia | 30% | 77% |
B4JMQ2 | Drosophila grimshawi | 33% | 70% |
B4NP88 | Drosophila willistoni | 30% | 66% |
B4Q068 | Drosophila yakuba | 28% | 74% |
C3XRY1 | Branchiostoma floridae | 28% | 84% |
D3ZU57 | Rattus norvegicus | 31% | 85% |
E9B1H4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O01658 | Caenorhabditis elegans | 25% | 68% |
Q16W06 | Aedes aegypti | 28% | 80% |
Q4Q6P0 | Leishmania major | 93% | 100% |
Q54K96 | Dictyostelium discoideum | 30% | 99% |
Q5ZMM1 | Gallus gallus | 29% | 84% |
Q7K4H4 | Drosophila melanogaster | 29% | 78% |
Q9H6W3 | Homo sapiens | 31% | 79% |
Q9JJF3 | Mus musculus | 31% | 84% |
V5AYK7 | Trypanosoma cruzi | 54% | 100% |