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: A4HLS3
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 | 37 | 41 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.411 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.709 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 11 | 17 | PF00082 | 0.692 |
CLV_PCSK_PC7_1 | 433 | 439 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.819 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.588 |
DEG_APCC_DBOX_1 | 253 | 261 | PF00400 | 0.352 |
DEG_MDM2_SWIB_1 | 435 | 442 | PF02201 | 0.398 |
DEG_SCF_FBW7_1 | 102 | 109 | PF00400 | 0.824 |
DEG_SPOP_SBC_1 | 127 | 131 | PF00917 | 0.661 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.730 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.559 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.745 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.578 |
DOC_CKS1_1 | 210 | 215 | PF01111 | 0.411 |
DOC_CKS1_1 | 328 | 333 | PF01111 | 0.545 |
DOC_CYCLIN_RxL_1 | 493 | 504 | PF00134 | 0.593 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 477 | 486 | PF00134 | 0.575 |
DOC_MAPK_gen_1 | 437 | 444 | PF00069 | 0.354 |
DOC_PP1_RVXF_1 | 412 | 418 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.517 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.634 |
DOC_USP7_UBL2_3 | 493 | 497 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 196 | 206 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 35 | 39 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 402 | 407 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 6 | 13 | PF00244 | 0.699 |
LIG_Actin_WH2_2 | 346 | 362 | PF00022 | 0.411 |
LIG_AP2alpha_1 | 406 | 410 | PF02296 | 0.411 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.787 |
LIG_BIR_III_2 | 44 | 48 | PF00653 | 0.597 |
LIG_BIR_III_4 | 139 | 143 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.567 |
LIG_eIF4E_1 | 494 | 500 | PF01652 | 0.576 |
LIG_FAT_LD_1 | 370 | 378 | PF03623 | 0.304 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.516 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.411 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.411 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.822 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.595 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.792 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.509 |
LIG_Integrin_isoDGR_2 | 197 | 199 | PF01839 | 0.411 |
LIG_LIR_Apic_2 | 183 | 188 | PF02991 | 0.635 |
LIG_LIR_Apic_2 | 212 | 218 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.631 |
LIG_MYND_1 | 121 | 125 | PF01753 | 0.624 |
LIG_PCNA_yPIPBox_3 | 196 | 210 | 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_REV1ctd_RIR_1 | 384 | 390 | PF16727 | 0.411 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 367 | 371 | PF00017 | 0.509 |
LIG_SH2_STAT3 | 259 | 262 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.509 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.746 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.411 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.568 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.583 |
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 | 0.592 |
LIG_WRC_WIRS_1 | 403 | 408 | PF05994 | 0.352 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.411 |
MOD_CDK_SPK_2 | 133 | 138 | PF00069 | 0.724 |
MOD_CDK_SPxxK_3 | 209 | 216 | PF00069 | 0.352 |
MOD_CDK_SPxxK_3 | 245 | 252 | PF00069 | 0.352 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.792 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.565 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.769 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.602 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.613 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.699 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.411 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.635 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.614 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.789 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.703 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.431 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.678 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.411 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.618 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.735 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.575 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.509 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.553 |
MOD_Cter_Amidation | 222 | 225 | PF01082 | 0.447 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.814 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.642 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.783 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.692 |
MOD_GlcNHglycan | 280 | 285 | PF01048 | 0.642 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.504 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.527 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.691 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.352 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.597 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.612 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.756 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.720 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.641 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.737 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.711 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.717 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.761 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.304 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.698 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.691 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.528 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.411 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.633 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.747 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.590 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.707 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.591 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.642 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.711 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.561 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.523 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.625 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.650 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.808 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.603 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.836 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.536 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.579 |
MOD_PK_1 | 366 | 372 | PF00069 | 0.276 |
MOD_PKA_1 | 15 | 21 | PF00069 | 0.737 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.768 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.532 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.352 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.518 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.492 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.509 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.352 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.698 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.570 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.276 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.562 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.635 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.752 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.304 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.658 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.352 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.586 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.823 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.747 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.352 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.352 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.637 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.546 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.730 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.411 |
TRG_DiLeu_BaEn_3 | 281 | 287 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.509 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZZ8 | Leptomonas seymouri | 55% | 85% |
A0A3S7X6Z7 | Leishmania donovani | 78% | 100% |
A4I982 | Leishmania infantum | 78% | 100% |
E9B449 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q3X6 | Leishmania major | 78% | 100% |