| 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: 5 |
| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3S0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005975 | carbohydrate metabolic process | 3 | 12 |
| GO:0006040 | amino sugar metabolic process | 4 | 11 |
| GO:0006047 | UDP-N-acetylglucosamine metabolic process | 4 | 11 |
| GO:0006048 | UDP-N-acetylglucosamine biosynthetic process | 5 | 11 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
| GO:0006793 | phosphorus metabolic process | 3 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009058 | biosynthetic process | 2 | 11 |
| GO:0009225 | nucleotide-sugar metabolic process | 4 | 11 |
| GO:0009226 | nucleotide-sugar biosynthetic process | 5 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
| GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
| GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
| GO:0044237 | cellular metabolic process | 2 | 11 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0044249 | cellular biosynthetic process | 3 | 11 |
| GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
| GO:0044281 | small molecule metabolic process | 2 | 11 |
| GO:0046349 | amino sugar biosynthetic process | 5 | 11 |
| GO:0046483 | heterocycle metabolic process | 3 | 11 |
| GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 12 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 11 |
| GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 11 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
| GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
| GO:1901576 | organic substance biosynthetic process | 3 | 11 |
| GO:0006041 | glucosamine metabolic process | 6 | 1 |
| GO:1901071 | glucosamine-containing compound metabolic process | 5 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000287 | magnesium ion binding | 5 | 7 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004610 | phosphoacetylglucosamine mutase activity | 5 | 11 |
| GO:0005488 | binding | 1 | 12 |
| GO:0016853 | isomerase activity | 2 | 12 |
| GO:0016866 | intramolecular transferase activity | 3 | 12 |
| GO:0016868 | intramolecular transferase activity, phosphotransferases | 4 | 12 |
| GO:0043167 | ion binding | 2 | 12 |
| GO:0043169 | cation binding | 3 | 12 |
| GO:0046872 | metal ion binding | 4 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 540 | 544 | PF00656 | 0.383 |
| CLV_MEL_PAP_1 | 59 | 65 | PF00089 | 0.415 |
| CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.468 |
| CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.431 |
| CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.543 |
| CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.468 |
| CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.420 |
| CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.487 |
| CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.543 |
| CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.487 |
| CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.505 |
| CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.493 |
| CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.389 |
| CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.372 |
| CLV_Separin_Metazoa | 22 | 26 | PF03568 | 0.370 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.646 |
| DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.400 |
| DOC_CKS1_1 | 195 | 200 | PF01111 | 0.352 |
| DOC_CYCLIN_yCln2_LP_2 | 55 | 58 | PF00134 | 0.364 |
| DOC_MAPK_gen_1 | 355 | 363 | PF00069 | 0.461 |
| DOC_MAPK_gen_1 | 429 | 437 | PF00069 | 0.424 |
| DOC_MAPK_MEF2A_6 | 429 | 437 | PF00069 | 0.424 |
| DOC_PP1_RVXF_1 | 344 | 351 | PF00149 | 0.300 |
| DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.364 |
| DOC_PP4_FxxP_1 | 559 | 562 | PF00568 | 0.298 |
| DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.454 |
| DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.517 |
| DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.528 |
| DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.398 |
| DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.570 |
| DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.392 |
| DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.500 |
| DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.418 |
| DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.315 |
| DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.467 |
| DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.503 |
| DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.407 |
| LIG_14-3-3_CanoR_1 | 522 | 528 | PF00244 | 0.319 |
| LIG_14-3-3_CanoR_1 | 62 | 66 | PF00244 | 0.380 |
| LIG_APCC_ABBA_1 | 433 | 438 | PF00400 | 0.320 |
| LIG_APCC_ABBA_1 | 569 | 574 | PF00400 | 0.298 |
| LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.477 |
| LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.423 |
| LIG_FHA_1 | 178 | 184 | PF00498 | 0.489 |
| LIG_FHA_1 | 401 | 407 | PF00498 | 0.339 |
| LIG_FHA_1 | 442 | 448 | PF00498 | 0.377 |
| LIG_FHA_1 | 522 | 528 | PF00498 | 0.303 |
| LIG_FHA_1 | 563 | 569 | PF00498 | 0.298 |
| LIG_FHA_1 | 86 | 92 | PF00498 | 0.418 |
| LIG_FHA_2 | 281 | 287 | PF00498 | 0.471 |
| LIG_FHA_2 | 456 | 462 | PF00498 | 0.505 |
| LIG_FHA_2 | 495 | 501 | PF00498 | 0.487 |
| LIG_FHA_2 | 523 | 529 | PF00498 | 0.409 |
| LIG_IBAR_NPY_1 | 98 | 100 | PF08397 | 0.419 |
| LIG_KLC1_Yacidic_2 | 503 | 507 | PF13176 | 0.358 |
| LIG_LIR_Gen_1 | 17 | 27 | PF02991 | 0.454 |
| LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.230 |
| LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.399 |
| LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.389 |
| LIG_LIR_Gen_1 | 369 | 380 | PF02991 | 0.362 |
| LIG_LIR_Gen_1 | 500 | 509 | PF02991 | 0.410 |
| LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.377 |
| LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.465 |
| LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.430 |
| LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.382 |
| LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.384 |
| LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.406 |
| LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.324 |
| LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.331 |
| LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.388 |
| LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.325 |
| LIG_LIR_Nem_3 | 500 | 504 | PF02991 | 0.401 |
| LIG_LYPXL_yS_3 | 192 | 195 | PF13949 | 0.496 |
| LIG_MAD2 | 346 | 354 | PF02301 | 0.444 |
| LIG_MLH1_MIPbox_1 | 16 | 20 | PF16413 | 0.477 |
| LIG_Pex14_1 | 501 | 505 | PF04695 | 0.346 |
| LIG_Pex14_2 | 15 | 19 | PF04695 | 0.485 |
| LIG_Rb_pABgroove_1 | 346 | 354 | PF01858 | 0.449 |
| LIG_SH2_CRK | 372 | 376 | PF00017 | 0.358 |
| LIG_SH2_GRB2like | 397 | 400 | PF00017 | 0.322 |
| LIG_SH2_NCK_1 | 415 | 419 | PF00017 | 0.363 |
| LIG_SH2_NCK_1 | 572 | 576 | PF00017 | 0.373 |
| LIG_SH2_SRC | 397 | 400 | PF00017 | 0.322 |
| LIG_SH2_SRC | 505 | 508 | PF00017 | 0.265 |
| LIG_SH2_SRC | 572 | 575 | PF00017 | 0.342 |
| LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.314 |
| LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.487 |
| LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.246 |
| LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.335 |
| LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.317 |
| LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.334 |
| LIG_SH3_3 | 503 | 509 | PF00018 | 0.379 |
| LIG_SH3_5 | 354 | 358 | PF00018 | 0.305 |
| LIG_SUMO_SIM_anti_2 | 366 | 372 | PF11976 | 0.267 |
| LIG_SUMO_SIM_anti_2 | 389 | 395 | PF11976 | 0.461 |
| LIG_SUMO_SIM_par_1 | 443 | 449 | PF11976 | 0.462 |
| LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.279 |
| LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.430 |
| LIG_TYR_ITIM | 370 | 375 | PF00017 | 0.355 |
| LIG_UBA3_1 | 264 | 273 | PF00899 | 0.253 |
| LIG_UBA3_1 | 370 | 378 | PF00899 | 0.440 |
| LIG_WRC_WIRS_1 | 281 | 286 | PF05994 | 0.439 |
| MOD_CDK_SPK_2 | 185 | 190 | PF00069 | 0.312 |
| MOD_CK1_1 | 163 | 169 | PF00069 | 0.437 |
| MOD_CK1_1 | 237 | 243 | PF00069 | 0.578 |
| MOD_CK1_1 | 276 | 282 | PF00069 | 0.408 |
| MOD_CK1_1 | 457 | 463 | PF00069 | 0.360 |
| MOD_CK1_1 | 8 | 14 | PF00069 | 0.375 |
| MOD_CK2_1 | 115 | 121 | PF00069 | 0.381 |
| MOD_CK2_1 | 166 | 172 | PF00069 | 0.467 |
| MOD_CK2_1 | 280 | 286 | PF00069 | 0.475 |
| MOD_CK2_1 | 455 | 461 | PF00069 | 0.566 |
| MOD_CK2_1 | 523 | 529 | PF00069 | 0.408 |
| MOD_CK2_1 | 548 | 554 | PF00069 | 0.503 |
| MOD_CK2_1 | 560 | 566 | PF00069 | 0.298 |
| MOD_CK2_1 | 576 | 582 | PF00069 | 0.298 |
| MOD_CMANNOS | 119 | 122 | PF00535 | 0.415 |
| MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.400 |
| MOD_DYRK1A_RPxSP_1 | 531 | 535 | PF00069 | 0.376 |
| MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.522 |
| MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.403 |
| MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.488 |
| MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.518 |
| MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.493 |
| MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.464 |
| MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.298 |
| MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.419 |
| MOD_GSK3_1 | 213 | 220 | PF00069 | 0.569 |
| MOD_GSK3_1 | 269 | 276 | PF00069 | 0.443 |
| MOD_GSK3_1 | 295 | 302 | PF00069 | 0.523 |
| MOD_GSK3_1 | 313 | 320 | PF00069 | 0.388 |
| MOD_GSK3_1 | 332 | 339 | PF00069 | 0.431 |
| MOD_GSK3_1 | 388 | 395 | PF00069 | 0.269 |
| MOD_GSK3_1 | 441 | 448 | PF00069 | 0.422 |
| MOD_GSK3_1 | 450 | 457 | PF00069 | 0.399 |
| MOD_GSK3_1 | 544 | 551 | PF00069 | 0.405 |
| MOD_GSK3_1 | 576 | 583 | PF00069 | 0.345 |
| MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.540 |
| MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.466 |
| MOD_NEK2_1 | 234 | 239 | PF00069 | 0.390 |
| MOD_NEK2_1 | 299 | 304 | PF00069 | 0.491 |
| MOD_NEK2_1 | 388 | 393 | PF00069 | 0.240 |
| MOD_NEK2_1 | 494 | 499 | PF00069 | 0.461 |
| MOD_NEK2_1 | 548 | 553 | PF00069 | 0.488 |
| MOD_NEK2_2 | 177 | 182 | PF00069 | 0.485 |
| MOD_NEK2_2 | 280 | 285 | PF00069 | 0.467 |
| MOD_PIKK_1 | 237 | 243 | PF00454 | 0.513 |
| MOD_PIKK_1 | 471 | 477 | PF00454 | 0.327 |
| MOD_PKA_2 | 163 | 169 | PF00069 | 0.358 |
| MOD_PKA_2 | 366 | 372 | PF00069 | 0.304 |
| MOD_PKA_2 | 521 | 527 | PF00069 | 0.485 |
| MOD_PKA_2 | 560 | 566 | PF00069 | 0.298 |
| MOD_PKA_2 | 61 | 67 | PF00069 | 0.388 |
| MOD_PKB_1 | 520 | 528 | PF00069 | 0.310 |
| MOD_Plk_1 | 276 | 282 | PF00069 | 0.372 |
| MOD_Plk_1 | 295 | 301 | PF00069 | 0.444 |
| MOD_Plk_1 | 388 | 394 | PF00069 | 0.237 |
| MOD_Plk_1 | 494 | 500 | PF00069 | 0.466 |
| MOD_Plk_4 | 14 | 20 | PF00069 | 0.454 |
| MOD_Plk_4 | 217 | 223 | PF00069 | 0.504 |
| MOD_Plk_4 | 259 | 265 | PF00069 | 0.352 |
| MOD_Plk_4 | 280 | 286 | PF00069 | 0.451 |
| MOD_Plk_4 | 295 | 301 | PF00069 | 0.402 |
| MOD_Plk_4 | 388 | 394 | PF00069 | 0.237 |
| MOD_Plk_4 | 441 | 447 | PF00069 | 0.302 |
| MOD_Plk_4 | 61 | 67 | PF00069 | 0.363 |
| MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.417 |
| MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.313 |
| MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.473 |
| MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.508 |
| MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.402 |
| MOD_SUMO_rev_2 | 131 | 138 | PF00179 | 0.280 |
| MOD_SUMO_rev_2 | 353 | 361 | PF00179 | 0.470 |
| TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.278 |
| TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.264 |
| TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.450 |
| TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.411 |
| TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.451 |
| TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.449 |
| TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.343 |
| TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.471 |
| TRG_NES_CRM1_1 | 21 | 36 | PF08389 | 0.463 |
| TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.521 |
| TRG_Pf-PMV_PEXEL_1 | 470 | 475 | PF00026 | 0.392 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I5G0 | Leptomonas seymouri | 53% | 100% |
| A0A0S4KHH8 | Bodo saltans | 39% | 100% |
| A0A1X0NPH2 | Trypanosomatidae | 45% | 99% |
| A0A3R7KD29 | Trypanosoma rangeli | 46% | 98% |
| A0A3S5H601 | Leishmania donovani | 85% | 100% |
| A4HTA8 | Leishmania infantum | 84% | 100% |
| C9ZUL6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
| E9AL97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
| F1RQM2 | Sus scrofa | 39% | 100% |
| O95394 | Homo sapiens | 39% | 100% |
| P38628 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
| P57750 | Arabidopsis thaliana | 35% | 100% |
| Q042H3 | Lactobacillus gasseri (strain ATCC 33323 / DSM 20243 / BCRC 14619 / CIP 102991 / JCM 1131 / KCTC 3163 / NCIMB 11718 / NCTC 13722 / AM63) | 23% | 100% |
| Q09687 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
| Q09770 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
| Q4QIK7 | Leishmania major | 84% | 100% |
| Q5Z1H8 | Nocardia farcinica (strain IFM 10152) | 24% | 100% |
| Q6ZDQ1 | Oryza sativa subsp. japonica | 36% | 100% |
| Q74K59 | Lactobacillus johnsonii (strain CNCM I-12250 / La1 / NCC 533) | 23% | 100% |
| Q8SSL7 | Encephalitozoon cuniculi (strain GB-M1) | 32% | 100% |
| Q9CYR6 | Mus musculus | 37% | 100% |
| Q9P4V2 | Candida albicans | 35% | 100% |
| V5B892 | Trypanosoma cruzi | 44% | 98% |