| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0005829 | cytosol | 2 | 1 |
| GO:0005930 | axoneme | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| GO:0000015 | phosphopyruvate hydratase complex | 3 | 4 |
| GO:0032991 | protein-containing complex | 1 | 4 |
| GO:1902494 | catalytic complex | 2 | 4 |
Related structures:
AlphaFold database: E9B3F4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005975 | carbohydrate metabolic process | 3 | 4 |
| GO:0006082 | organic acid metabolic process | 3 | 4 |
| GO:0006090 | pyruvate metabolic process | 7 | 4 |
| GO:0006091 | generation of precursor metabolites and energy | 3 | 4 |
| GO:0006096 | glycolytic process | 5 | 4 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 4 |
| GO:0006163 | purine nucleotide metabolic process | 5 | 4 |
| GO:0006165 | obsolete nucleoside diphosphate phosphorylation | 6 | 4 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 4 |
| GO:0006753 | nucleoside phosphate metabolic process | 4 | 4 |
| GO:0006757 | obsolete ATP generation from ADP | 4 | 4 |
| GO:0006793 | phosphorus metabolic process | 3 | 4 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
| GO:0008152 | metabolic process | 1 | 4 |
| GO:0009056 | catabolic process | 2 | 4 |
| GO:0009117 | nucleotide metabolic process | 5 | 4 |
| GO:0009132 | nucleoside diphosphate metabolic process | 5 | 4 |
| GO:0009135 | purine nucleoside diphosphate metabolic process | 6 | 4 |
| GO:0009141 | nucleoside triphosphate metabolic process | 5 | 4 |
| GO:0009144 | purine nucleoside triphosphate metabolic process | 6 | 4 |
| GO:0009150 | purine ribonucleotide metabolic process | 6 | 4 |
| GO:0009179 | purine ribonucleoside diphosphate metabolic process | 7 | 4 |
| GO:0009185 | ribonucleoside diphosphate metabolic process | 6 | 4 |
| GO:0009199 | ribonucleoside triphosphate metabolic process | 6 | 4 |
| GO:0009205 | purine ribonucleoside triphosphate metabolic process | 7 | 4 |
| GO:0009259 | ribonucleotide metabolic process | 5 | 4 |
| GO:0009987 | cellular process | 1 | 4 |
| GO:0016052 | carbohydrate catabolic process | 4 | 4 |
| GO:0016310 | phosphorylation | 5 | 4 |
| GO:0019637 | organophosphate metabolic process | 3 | 4 |
| GO:0019693 | ribose phosphate metabolic process | 4 | 4 |
| GO:0019752 | carboxylic acid metabolic process | 5 | 4 |
| GO:0032787 | monocarboxylic acid metabolic process | 6 | 4 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 4 |
| GO:0043436 | oxoacid metabolic process | 4 | 4 |
| GO:0044237 | cellular metabolic process | 2 | 4 |
| GO:0044238 | primary metabolic process | 2 | 4 |
| GO:0044281 | small molecule metabolic process | 2 | 4 |
| GO:0046031 | ADP metabolic process | 7 | 4 |
| GO:0046034 | ATP metabolic process | 7 | 4 |
| GO:0046483 | heterocycle metabolic process | 3 | 4 |
| GO:0046939 | obsolete nucleotide phosphorylation | 6 | 4 |
| GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 4 |
| GO:0071704 | organic substance metabolic process | 2 | 4 |
| GO:0072521 | purine-containing compound metabolic process | 4 | 4 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 4 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 4 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
| GO:1901575 | organic substance catabolic process | 3 | 4 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 8 |
| GO:0004634 | phosphopyruvate hydratase activity | 5 | 8 |
| GO:0016829 | lyase activity | 2 | 8 |
| GO:0016835 | carbon-oxygen lyase activity | 3 | 8 |
| GO:0016836 | hydro-lyase activity | 4 | 8 |
| GO:0000287 | magnesium ion binding | 5 | 4 |
| GO:0005488 | binding | 1 | 4 |
| GO:0043167 | ion binding | 2 | 4 |
| GO:0043169 | cation binding | 3 | 4 |
| GO:0046872 | metal ion binding | 4 | 4 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 248 | 252 | PF00656 | 0.476 |
| CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.537 |
| CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.547 |
| CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.564 |
| CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.634 |
| CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.547 |
| CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.561 |
| CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.413 |
| CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.559 |
| CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.622 |
| CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.552 |
| DEG_SIAH_1 | 581 | 589 | PF03145 | 0.584 |
| DEG_SPOP_SBC_1 | 267 | 271 | PF00917 | 0.451 |
| DEG_SPOP_SBC_1 | 308 | 312 | PF00917 | 0.627 |
| DOC_ANK_TNKS_1 | 43 | 50 | PF00023 | 0.335 |
| DOC_CYCLIN_RxL_1 | 128 | 139 | PF00134 | 0.526 |
| DOC_CYCLIN_yCln2_LP_2 | 460 | 466 | PF00134 | 0.556 |
| DOC_MAPK_DCC_7 | 229 | 238 | PF00069 | 0.519 |
| DOC_MAPK_gen_1 | 430 | 437 | PF00069 | 0.491 |
| DOC_MAPK_gen_1 | 501 | 508 | PF00069 | 0.573 |
| DOC_MAPK_MEF2A_6 | 229 | 238 | PF00069 | 0.519 |
| DOC_MAPK_MEF2A_6 | 257 | 265 | PF00069 | 0.497 |
| DOC_MAPK_MEF2A_6 | 501 | 508 | PF00069 | 0.573 |
| DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.572 |
| DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.263 |
| DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.549 |
| DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.498 |
| DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.472 |
| DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.525 |
| DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.518 |
| DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.543 |
| DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.524 |
| DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.321 |
| DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.501 |
| DOC_USP7_UBL2_3 | 404 | 408 | PF12436 | 0.508 |
| DOC_USP7_UBL2_3 | 592 | 596 | PF12436 | 0.575 |
| DOC_USP7_UBL2_3 | 598 | 602 | PF12436 | 0.601 |
| DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.559 |
| DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.589 |
| LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.743 |
| LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.483 |
| LIG_14-3-3_CanoR_1 | 243 | 253 | PF00244 | 0.427 |
| LIG_14-3-3_CanoR_1 | 25 | 35 | PF00244 | 0.634 |
| LIG_14-3-3_CanoR_1 | 257 | 265 | PF00244 | 0.407 |
| LIG_14-3-3_CanoR_1 | 302 | 308 | PF00244 | 0.518 |
| LIG_14-3-3_CanoR_1 | 501 | 507 | PF00244 | 0.494 |
| LIG_Actin_WH2_2 | 486 | 503 | PF00022 | 0.284 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.651 |
| LIG_BIR_III_4 | 112 | 116 | PF00653 | 0.595 |
| LIG_BIR_III_4 | 274 | 278 | PF00653 | 0.674 |
| LIG_BIR_III_4 | 375 | 379 | PF00653 | 0.515 |
| LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.367 |
| LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.553 |
| LIG_EH1_1 | 13 | 21 | PF00400 | 0.387 |
| LIG_EVH1_1 | 578 | 582 | PF00568 | 0.553 |
| LIG_FHA_1 | 237 | 243 | PF00498 | 0.467 |
| LIG_FHA_1 | 267 | 273 | PF00498 | 0.662 |
| LIG_FHA_1 | 326 | 332 | PF00498 | 0.470 |
| LIG_FHA_1 | 333 | 339 | PF00498 | 0.462 |
| LIG_FHA_1 | 357 | 363 | PF00498 | 0.632 |
| LIG_FHA_1 | 455 | 461 | PF00498 | 0.553 |
| LIG_FHA_1 | 503 | 509 | PF00498 | 0.446 |
| LIG_FHA_1 | 553 | 559 | PF00498 | 0.557 |
| LIG_FHA_1 | 581 | 587 | PF00498 | 0.575 |
| LIG_FHA_1 | 68 | 74 | PF00498 | 0.443 |
| LIG_FHA_1 | 83 | 89 | PF00498 | 0.413 |
| LIG_FHA_2 | 109 | 115 | PF00498 | 0.707 |
| LIG_FHA_2 | 483 | 489 | PF00498 | 0.430 |
| LIG_FHA_2 | 82 | 88 | PF00498 | 0.530 |
| LIG_LIR_Gen_1 | 117 | 126 | PF02991 | 0.463 |
| LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.488 |
| LIG_LIR_Gen_1 | 531 | 540 | PF02991 | 0.430 |
| LIG_LIR_Nem_3 | 117 | 121 | PF02991 | 0.626 |
| LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.510 |
| LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.594 |
| LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.483 |
| LIG_LIR_Nem_3 | 531 | 535 | PF02991 | 0.460 |
| LIG_LIR_Nem_3 | 577 | 581 | PF02991 | 0.659 |
| LIG_MLH1_MIPbox_1 | 39 | 43 | PF16413 | 0.553 |
| LIG_MYND_1 | 463 | 467 | PF01753 | 0.386 |
| LIG_Pex14_2 | 39 | 43 | PF04695 | 0.598 |
| LIG_REV1ctd_RIR_1 | 36 | 45 | PF16727 | 0.632 |
| LIG_SH2_CRK | 118 | 122 | PF00017 | 0.604 |
| LIG_SH2_NCK_1 | 118 | 122 | PF00017 | 0.604 |
| LIG_SH2_NCK_1 | 137 | 141 | PF00017 | 0.356 |
| LIG_SH2_PTP2 | 262 | 265 | PF00017 | 0.473 |
| LIG_SH2_PTP2 | 532 | 535 | PF00017 | 0.430 |
| LIG_SH2_SRC | 137 | 140 | PF00017 | 0.440 |
| LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.567 |
| LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.414 |
| LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.473 |
| LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.452 |
| LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.490 |
| LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.360 |
| LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.472 |
| LIG_SH3_1 | 576 | 582 | PF00018 | 0.621 |
| LIG_SH3_3 | 474 | 480 | PF00018 | 0.495 |
| LIG_SH3_3 | 576 | 582 | PF00018 | 0.528 |
| LIG_SUMO_SIM_par_1 | 504 | 510 | PF11976 | 0.569 |
| LIG_UBA3_1 | 170 | 178 | PF00899 | 0.476 |
| LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.509 |
| LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.394 |
| LIG_WW_2 | 579 | 582 | PF00397 | 0.628 |
| MOD_CK1_1 | 159 | 165 | PF00069 | 0.386 |
| MOD_CK1_1 | 215 | 221 | PF00069 | 0.765 |
| MOD_CK1_1 | 224 | 230 | PF00069 | 0.539 |
| MOD_CK1_1 | 3 | 9 | PF00069 | 0.570 |
| MOD_CK1_1 | 306 | 312 | PF00069 | 0.578 |
| MOD_CK1_1 | 455 | 461 | PF00069 | 0.706 |
| MOD_CK1_1 | 541 | 547 | PF00069 | 0.477 |
| MOD_CK1_1 | 82 | 88 | PF00069 | 0.486 |
| MOD_CK2_1 | 108 | 114 | PF00069 | 0.720 |
| MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.550 |
| MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.523 |
| MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.475 |
| MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.660 |
| MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.765 |
| MOD_GlcNHglycan | 225 | 229 | PF01048 | 0.620 |
| MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.536 |
| MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.598 |
| MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.495 |
| MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.597 |
| MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.637 |
| MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.708 |
| MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.534 |
| MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.463 |
| MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.635 |
| MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.577 |
| MOD_GSK3_1 | 100 | 107 | PF00069 | 0.747 |
| MOD_GSK3_1 | 116 | 123 | PF00069 | 0.602 |
| MOD_GSK3_1 | 14 | 21 | PF00069 | 0.440 |
| MOD_GSK3_1 | 143 | 150 | PF00069 | 0.468 |
| MOD_GSK3_1 | 152 | 159 | PF00069 | 0.477 |
| MOD_GSK3_1 | 166 | 173 | PF00069 | 0.404 |
| MOD_GSK3_1 | 252 | 259 | PF00069 | 0.551 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.480 |
| MOD_GSK3_1 | 278 | 285 | PF00069 | 0.588 |
| MOD_GSK3_1 | 303 | 310 | PF00069 | 0.535 |
| MOD_GSK3_1 | 332 | 339 | PF00069 | 0.563 |
| MOD_GSK3_1 | 351 | 358 | PF00069 | 0.526 |
| MOD_GSK3_1 | 370 | 377 | PF00069 | 0.421 |
| MOD_GSK3_1 | 437 | 444 | PF00069 | 0.464 |
| MOD_GSK3_1 | 450 | 457 | PF00069 | 0.620 |
| MOD_GSK3_1 | 546 | 553 | PF00069 | 0.520 |
| MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.466 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.635 |
| MOD_NEK2_1 | 14 | 19 | PF00069 | 0.537 |
| MOD_NEK2_1 | 236 | 241 | PF00069 | 0.408 |
| MOD_NEK2_1 | 268 | 273 | PF00069 | 0.635 |
| MOD_NEK2_1 | 303 | 308 | PF00069 | 0.563 |
| MOD_NEK2_1 | 355 | 360 | PF00069 | 0.584 |
| MOD_NEK2_1 | 418 | 423 | PF00069 | 0.517 |
| MOD_NEK2_1 | 437 | 442 | PF00069 | 0.271 |
| MOD_NEK2_1 | 507 | 512 | PF00069 | 0.584 |
| MOD_NEK2_2 | 252 | 257 | PF00069 | 0.615 |
| MOD_PK_1 | 229 | 235 | PF00069 | 0.471 |
| MOD_PKA_2 | 100 | 106 | PF00069 | 0.575 |
| MOD_PKA_2 | 256 | 262 | PF00069 | 0.529 |
| MOD_PKA_2 | 450 | 456 | PF00069 | 0.662 |
| MOD_PKA_2 | 566 | 572 | PF00069 | 0.624 |
| MOD_Plk_1 | 278 | 284 | PF00069 | 0.474 |
| MOD_Plk_1 | 79 | 85 | PF00069 | 0.482 |
| MOD_Plk_2-3 | 108 | 114 | PF00069 | 0.642 |
| MOD_Plk_2-3 | 482 | 488 | PF00069 | 0.506 |
| MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.651 |
| MOD_Plk_4 | 116 | 122 | PF00069 | 0.536 |
| MOD_Plk_4 | 166 | 172 | PF00069 | 0.398 |
| MOD_Plk_4 | 236 | 242 | PF00069 | 0.484 |
| MOD_Plk_4 | 284 | 290 | PF00069 | 0.374 |
| MOD_Plk_4 | 382 | 388 | PF00069 | 0.483 |
| MOD_Plk_4 | 437 | 443 | PF00069 | 0.495 |
| MOD_Plk_4 | 473 | 479 | PF00069 | 0.490 |
| MOD_Plk_4 | 502 | 508 | PF00069 | 0.530 |
| MOD_Plk_4 | 528 | 534 | PF00069 | 0.490 |
| MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.568 |
| MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.587 |
| MOD_SUMO_rev_2 | 29 | 38 | PF00179 | 0.646 |
| MOD_SUMO_rev_2 | 373 | 383 | PF00179 | 0.615 |
| TRG_DiLeu_BaLyEn_6 | 460 | 465 | PF01217 | 0.416 |
| TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.622 |
| TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.473 |
| TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.411 |
| TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.523 |
| TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.498 |
| TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.439 |
| TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.413 |
| TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.538 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P4A1 | Leptomonas seymouri | 39% | 94% |
| A0A0S4IQJ6 | Bodo saltans | 25% | 100% |
| A0A1X0NS02 | Trypanosomatidae | 26% | 100% |
| A0A3Q8IJR5 | Leishmania donovani | 86% | 100% |
| A4HL13 | Leishmania braziliensis | 75% | 100% |
| A4I8J4 | Leishmania infantum | 86% | 100% |
| D0AAM4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
| Q4Q4P6 | Leishmania major | 88% | 100% |
| V5DME2 | Trypanosoma cruzi | 27% | 100% |