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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B449
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006090 | pyruvate metabolic process | 7 | 1 |
GO:0006091 | generation of precursor metabolites and energy | 3 | 1 |
GO:0006096 | glycolytic process | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
GO:0006165 | obsolete nucleoside diphosphate phosphorylation | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006757 | obsolete ATP generation from ADP | 4 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009117 | nucleotide metabolic process | 5 | 1 |
GO:0009132 | nucleoside diphosphate metabolic process | 5 | 1 |
GO:0009135 | purine nucleoside diphosphate metabolic process | 6 | 1 |
GO:0009141 | nucleoside triphosphate metabolic process | 5 | 1 |
GO:0009144 | purine nucleoside triphosphate metabolic process | 6 | 1 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 1 |
GO:0009179 | purine ribonucleoside diphosphate metabolic process | 7 | 1 |
GO:0009185 | ribonucleoside diphosphate metabolic process | 6 | 1 |
GO:0009199 | ribonucleoside triphosphate metabolic process | 6 | 1 |
GO:0009205 | purine ribonucleoside triphosphate metabolic process | 7 | 1 |
GO:0009259 | ribonucleotide metabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016052 | carbohydrate catabolic process | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046031 | ADP metabolic process | 7 | 1 |
GO:0046034 | ATP metabolic process | 7 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046939 | obsolete nucleotide phosphorylation | 6 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004619 | phosphoglycerate mutase activity | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0016853 | isomerase activity | 2 | 1 |
GO:0016866 | intramolecular transferase activity | 3 | 1 |
GO:0016868 | intramolecular transferase activity, phosphotransferases | 4 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
GO:0050897 | cobalt ion binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 131 | 135 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.411 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.732 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.820 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 11 | 17 | PF00082 | 0.723 |
CLV_PCSK_PC7_1 | 433 | 439 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.809 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.630 |
DEG_APCC_DBOX_1 | 252 | 260 | PF00400 | 0.352 |
DEG_MDM2_SWIB_1 | 435 | 442 | PF02201 | 0.398 |
DEG_SPOP_SBC_1 | 111 | 115 | PF00917 | 0.699 |
DEG_SPOP_SBC_1 | 128 | 132 | PF00917 | 0.650 |
DEG_SPOP_SBC_1 | 49 | 53 | PF00917 | 0.689 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.763 |
DOC_CKS1_1 | 209 | 214 | PF01111 | 0.411 |
DOC_CYCLIN_RxL_1 | 493 | 504 | PF00134 | 0.602 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 477 | 486 | PF00134 | 0.576 |
DOC_MAPK_gen_1 | 437 | 444 | PF00069 | 0.354 |
DOC_PP1_RVXF_1 | 412 | 418 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 313 | 316 | PF13499 | 0.714 |
DOC_PP4_FxxP_1 | 184 | 187 | PF00568 | 0.529 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.699 |
DOC_USP7_UBL2_3 | 493 | 497 | PF12436 | 0.552 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 170 | 179 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 183 | 187 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 195 | 205 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 251 | 257 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 366 | 374 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 38 | 47 | PF00244 | 0.825 |
LIG_14-3-3_CanoR_1 | 402 | 407 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 6 | 13 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 71 | 80 | PF00244 | 0.824 |
LIG_14-3-3_CanoR_1 | 99 | 104 | PF00244 | 0.554 |
LIG_Actin_WH2_2 | 346 | 362 | PF00022 | 0.411 |
LIG_AP2alpha_1 | 406 | 410 | PF02296 | 0.411 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.805 |
LIG_BIR_III_2 | 141 | 145 | PF00653 | 0.735 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.545 |
LIG_eIF4E_1 | 494 | 500 | PF01652 | 0.588 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.528 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.649 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.560 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.411 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.411 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.588 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.835 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.780 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.509 |
LIG_Integrin_isoDGR_2 | 196 | 198 | PF01839 | 0.411 |
LIG_LIR_Apic_2 | 182 | 187 | PF02991 | 0.651 |
LIG_LIR_Apic_2 | 211 | 217 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.632 |
LIG_MYND_1 | 312 | 316 | PF01753 | 0.710 |
LIG_PCNA_yPIPBox_3 | 195 | 209 | PF02747 | 0.411 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.411 |
LIG_Pex14_2 | 406 | 410 | PF04695 | 0.183 |
LIG_Pex14_2 | 435 | 439 | PF04695 | 0.398 |
LIG_PTAP_UEV_1 | 125 | 130 | PF05743 | 0.728 |
LIG_PTAP_UEV_1 | 156 | 161 | PF05743 | 0.532 |
LIG_REV1ctd_RIR_1 | 384 | 390 | PF16727 | 0.411 |
LIG_RPA_C_Fungi | 339 | 351 | PF08784 | 0.548 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 367 | 371 | PF00017 | 0.509 |
LIG_SH2_STAT3 | 258 | 261 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.509 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.761 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.696 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.630 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.411 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.551 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.567 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.411 |
LIG_SUMO_SIM_anti_2 | 420 | 427 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 420 | 427 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.593 |
LIG_WRC_WIRS_1 | 403 | 408 | PF05994 | 0.352 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.411 |
MOD_CDK_SPxxK_3 | 208 | 215 | PF00069 | 0.352 |
MOD_CDK_SPxxK_3 | 244 | 251 | PF00069 | 0.352 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.802 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.604 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.774 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.595 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.628 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.411 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.642 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.796 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.704 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.411 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.618 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.638 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.733 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.790 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.509 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.801 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.554 |
MOD_Cter_Amidation | 221 | 224 | PF01082 | 0.447 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.817 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.566 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.717 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.641 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.704 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.807 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.687 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.497 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.680 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.672 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.416 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.352 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.600 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.608 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.723 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.777 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.757 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.656 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.755 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.728 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.768 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.692 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.521 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.411 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.576 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.757 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.662 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.511 |
MOD_N-GLC_2 | 94 | 96 | PF02516 | 0.735 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.726 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.655 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.523 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.416 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.638 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.800 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.613 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.838 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.547 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.352 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.515 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.560 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.509 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.352 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.727 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.822 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.416 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.758 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.644 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.352 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.416 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.690 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.756 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.352 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.352 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.509 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.651 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.733 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.411 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.688 |
MOD_SUMO_rev_2 | 87 | 97 | PF00179 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 309 | 314 | PF01217 | 0.701 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.509 |
TRG_ER_diArg_1 | 250 | 253 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZZ8 | Leptomonas seymouri | 58% | 85% |
A0A3S7X6Z7 | Leishmania donovani | 93% | 100% |
A4HLS3 | Leishmania braziliensis | 75% | 100% |
A4I982 | Leishmania infantum | 93% | 100% |
Q4Q3X6 | Leishmania major | 91% | 100% |