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: 9 |
NetGPI | no | yes: 0, no: 9 |
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 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
Related structures:
AlphaFold database: A4HL13
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 3 |
GO:0006082 | organic acid metabolic process | 3 | 3 |
GO:0006090 | pyruvate metabolic process | 7 | 3 |
GO:0006091 | generation of precursor metabolites and energy | 3 | 3 |
GO:0006096 | glycolytic process | 5 | 3 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006163 | purine nucleotide metabolic process | 5 | 3 |
GO:0006165 | obsolete nucleoside diphosphate phosphorylation | 6 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 3 |
GO:0006757 | obsolete ATP generation from ADP | 4 | 3 |
GO:0006793 | phosphorus metabolic process | 3 | 3 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009056 | catabolic process | 2 | 3 |
GO:0009117 | nucleotide metabolic process | 5 | 3 |
GO:0009132 | nucleoside diphosphate metabolic process | 5 | 3 |
GO:0009135 | purine nucleoside diphosphate metabolic process | 6 | 3 |
GO:0009141 | nucleoside triphosphate metabolic process | 5 | 3 |
GO:0009144 | purine nucleoside triphosphate metabolic process | 6 | 3 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 3 |
GO:0009179 | purine ribonucleoside diphosphate metabolic process | 7 | 3 |
GO:0009185 | ribonucleoside diphosphate metabolic process | 6 | 3 |
GO:0009199 | ribonucleoside triphosphate metabolic process | 6 | 3 |
GO:0009205 | purine ribonucleoside triphosphate metabolic process | 7 | 3 |
GO:0009259 | ribonucleotide metabolic process | 5 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016052 | carbohydrate catabolic process | 4 | 3 |
GO:0016310 | phosphorylation | 5 | 3 |
GO:0019637 | organophosphate metabolic process | 3 | 3 |
GO:0019693 | ribose phosphate metabolic process | 4 | 3 |
GO:0019752 | carboxylic acid metabolic process | 5 | 3 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043436 | oxoacid metabolic process | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044281 | small molecule metabolic process | 2 | 3 |
GO:0046031 | ADP metabolic process | 7 | 3 |
GO:0046034 | ATP metabolic process | 7 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0046939 | obsolete nucleotide phosphorylation | 6 | 3 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0072521 | purine-containing compound metabolic process | 4 | 3 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
GO:1901575 | organic substance catabolic process | 3 | 3 |
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 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 248 | 252 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.610 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 595 | 597 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 606 | 608 | PF00082 | 0.714 |
CLV_PCSK_PC7_1 | 290 | 296 | PF00082 | 0.370 |
CLV_PCSK_PC7_1 | 591 | 597 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.489 |
DEG_APCC_DBOX_1 | 210 | 218 | PF00400 | 0.413 |
DEG_COP1_1 | 356 | 365 | PF00400 | 0.363 |
DEG_SPOP_SBC_1 | 308 | 312 | PF00917 | 0.476 |
DOC_CYCLIN_RxL_1 | 128 | 139 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 465 | 468 | PF00134 | 0.437 |
DOC_MAPK_DCC_7 | 229 | 238 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 178 | 188 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 294 | 304 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 427 | 437 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 501 | 508 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 178 | 186 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 229 | 238 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 257 | 265 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 344 | 353 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 501 | 508 | PF00069 | 0.441 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.481 |
DOC_PP2B_PxIxI_1 | 473 | 479 | PF00149 | 0.261 |
DOC_PP2B_PxIxI_1 | 78 | 84 | PF00149 | 0.283 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.458 |
DOC_USP7_UBL2_3 | 598 | 602 | PF12436 | 0.580 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 211 | 221 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 25 | 35 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 257 | 265 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 454 | 460 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 501 | 507 | PF00244 | 0.432 |
LIG_Actin_WH2_2 | 331 | 346 | PF00022 | 0.341 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
LIG_CaM_NSCaTE_8 | 144 | 151 | PF13499 | 0.428 |
LIG_EH1_1 | 13 | 21 | PF00400 | 0.350 |
LIG_eIF4E_1 | 231 | 237 | PF01652 | 0.431 |
LIG_EVH1_1 | 578 | 582 | PF00568 | 0.522 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.401 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.475 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.356 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.408 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.502 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.430 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.525 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.582 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.363 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.370 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.710 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 228 | 234 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 115 | 126 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 381 | 392 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 482 | 486 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 577 | 581 | PF02991 | 0.539 |
LIG_Pex14_2 | 39 | 43 | PF04695 | 0.550 |
LIG_REV1ctd_RIR_1 | 36 | 45 | PF16727 | 0.508 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.503 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.363 |
LIG_SH2_GRB2like | 10 | 13 | PF00017 | 0.327 |
LIG_SH2_GRB2like | 56 | 59 | PF00017 | 0.312 |
LIG_SH2_NCK_1 | 118 | 122 | PF00017 | 0.503 |
LIG_SH2_PTP2 | 137 | 140 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 262 | 265 | PF00017 | 0.415 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.419 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.363 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.410 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.472 |
LIG_SUMO_SIM_anti_2 | 80 | 85 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 29 | 37 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 504 | 510 | PF11976 | 0.442 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.609 |
LIG_UBA3_1 | 170 | 178 | PF00899 | 0.433 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.394 |
LIG_WW_2 | 579 | 582 | PF00397 | 0.587 |
MOD_CDK_SPxK_1 | 205 | 211 | PF00069 | 0.522 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.574 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.462 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.548 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.410 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.597 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.725 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.501 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.631 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.456 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.443 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.549 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.555 |
MOD_GlcNHglycan | 223 | 227 | PF01048 | 0.507 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.333 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.456 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.392 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.460 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.534 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.399 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.369 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.561 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.538 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.406 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.340 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.482 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.326 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.464 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.421 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.284 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.548 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.471 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.617 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.418 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.500 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.351 |
MOD_N-GLC_2 | 574 | 576 | PF02516 | 0.409 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.574 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.347 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.569 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.312 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.503 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.554 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.477 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.260 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.565 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.306 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.501 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.323 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.333 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.456 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.413 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.472 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.518 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.357 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.393 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.321 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.519 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.485 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.415 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.440 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.571 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.522 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.544 |
MOD_SUMO_rev_2 | 29 | 38 | PF00179 | 0.509 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4A1 | Leptomonas seymouri | 38% | 94% |
A0A1X0NS02 | Trypanosomatidae | 26% | 100% |
A0A3Q8IJR5 | Leishmania donovani | 73% | 100% |
A0A3R7RSQ9 | Trypanosoma rangeli | 26% | 100% |
A4I8J4 | Leishmania infantum | 72% | 100% |
E9B3F4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q4P6 | Leishmania major | 71% | 100% |
V5DME2 | Trypanosoma cruzi | 26% | 100% |