| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 3 |
| GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q3T5
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006040 | amino sugar metabolic process | 4 | 2 |
| GO:0006047 | UDP-N-acetylglucosamine metabolic process | 4 | 2 |
| GO:0006048 | UDP-N-acetylglucosamine biosynthetic process | 5 | 2 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
| GO:0006793 | phosphorus metabolic process | 3 | 2 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
| GO:0008152 | metabolic process | 1 | 2 |
| GO:0009058 | biosynthetic process | 2 | 2 |
| GO:0009225 | nucleotide-sugar metabolic process | 4 | 2 |
| GO:0009226 | nucleotide-sugar biosynthetic process | 5 | 2 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
| GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
| GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
| GO:0044237 | cellular metabolic process | 2 | 2 |
| GO:0044238 | primary metabolic process | 2 | 2 |
| GO:0044249 | cellular biosynthetic process | 3 | 2 |
| GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
| GO:0044281 | small molecule metabolic process | 2 | 2 |
| GO:0046349 | amino sugar biosynthetic process | 5 | 2 |
| GO:0046483 | heterocycle metabolic process | 3 | 2 |
| GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
| GO:0071704 | organic substance metabolic process | 2 | 2 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
| GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 2 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
| GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
| GO:1901576 | organic substance biosynthetic process | 3 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0003977 | UDP-N-acetylglucosamine diphosphorylase activity | 6 | 8 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
| GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
| GO:0070569 | uridylyltransferase activity | 5 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 301 | 307 | PF00089 | 0.354 |
| CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.355 |
| CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.359 |
| CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.290 |
| CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.322 |
| CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.516 |
| CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.516 |
| CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.363 |
| CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.258 |
| CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.506 |
| CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.290 |
| CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.248 |
| CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.506 |
| DEG_APCC_DBOX_1 | 53 | 61 | PF00400 | 0.493 |
| DEG_SPOP_SBC_1 | 500 | 504 | PF00917 | 0.492 |
| DOC_CDC14_PxL_1 | 89 | 97 | PF14671 | 0.512 |
| DOC_MAPK_gen_1 | 288 | 298 | PF00069 | 0.535 |
| DOC_MAPK_MEF2A_6 | 194 | 201 | PF00069 | 0.389 |
| DOC_MAPK_NFAT4_5 | 194 | 202 | PF00069 | 0.449 |
| DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.405 |
| DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.471 |
| DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.527 |
| DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.474 |
| DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.477 |
| DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.651 |
| DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.360 |
| DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.518 |
| DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.449 |
| DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.573 |
| DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.508 |
| DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.372 |
| DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.539 |
| LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.527 |
| LIG_14-3-3_CanoR_1 | 356 | 363 | PF00244 | 0.529 |
| LIG_14-3-3_CanoR_1 | 514 | 521 | PF00244 | 0.493 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.402 |
| LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.467 |
| LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.469 |
| LIG_FHA_1 | 194 | 200 | PF00498 | 0.449 |
| LIG_FHA_1 | 241 | 247 | PF00498 | 0.467 |
| LIG_FHA_1 | 34 | 40 | PF00498 | 0.463 |
| LIG_FHA_1 | 363 | 369 | PF00498 | 0.474 |
| LIG_FHA_1 | 482 | 488 | PF00498 | 0.474 |
| LIG_FHA_1 | 495 | 501 | PF00498 | 0.450 |
| LIG_FHA_2 | 200 | 206 | PF00498 | 0.499 |
| LIG_FHA_2 | 388 | 394 | PF00498 | 0.544 |
| LIG_FHA_2 | 508 | 514 | PF00498 | 0.533 |
| LIG_LIR_Gen_1 | 21 | 28 | PF02991 | 0.510 |
| LIG_LIR_Gen_1 | 342 | 353 | PF02991 | 0.475 |
| LIG_LIR_Gen_1 | 381 | 392 | PF02991 | 0.474 |
| LIG_LIR_Gen_1 | 506 | 517 | PF02991 | 0.339 |
| LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.512 |
| LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.459 |
| LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.463 |
| LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.455 |
| LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.442 |
| LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.464 |
| LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.446 |
| LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.512 |
| LIG_PTB_Apo_2 | 223 | 230 | PF02174 | 0.388 |
| LIG_REV1ctd_RIR_1 | 227 | 236 | PF16727 | 0.547 |
| LIG_SH2_CRK | 23 | 27 | PF00017 | 0.560 |
| LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.534 |
| LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.554 |
| LIG_SH2_NCK_1 | 350 | 354 | PF00017 | 0.449 |
| LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.524 |
| LIG_SH2_NCK_1 | 498 | 502 | PF00017 | 0.453 |
| LIG_SH2_PTP2 | 292 | 295 | PF00017 | 0.453 |
| LIG_SH2_SRC | 239 | 242 | PF00017 | 0.535 |
| LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.510 |
| LIG_SH2_STAP1 | 427 | 431 | PF00017 | 0.554 |
| LIG_SH2_STAT3 | 155 | 158 | PF00017 | 0.480 |
| LIG_SH2_STAT3 | 544 | 547 | PF00017 | 0.447 |
| LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.453 |
| LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.346 |
| LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.449 |
| LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.534 |
| LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.552 |
| LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.454 |
| LIG_SH3_3 | 184 | 190 | PF00018 | 0.464 |
| LIG_SH3_3 | 302 | 308 | PF00018 | 0.490 |
| LIG_SUMO_SIM_par_1 | 196 | 205 | PF11976 | 0.495 |
| LIG_SUMO_SIM_par_1 | 294 | 299 | PF11976 | 0.535 |
| LIG_SUMO_SIM_par_1 | 478 | 484 | PF11976 | 0.510 |
| LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.464 |
| LIG_TRFH_1 | 221 | 225 | PF08558 | 0.527 |
| LIG_TYR_ITIM | 290 | 295 | PF00017 | 0.453 |
| LIG_TYR_ITIM | 348 | 353 | PF00017 | 0.449 |
| MOD_CK1_1 | 148 | 154 | PF00069 | 0.466 |
| MOD_CK1_1 | 175 | 181 | PF00069 | 0.573 |
| MOD_CK1_1 | 231 | 237 | PF00069 | 0.523 |
| MOD_CK1_1 | 272 | 278 | PF00069 | 0.558 |
| MOD_CK1_1 | 29 | 35 | PF00069 | 0.420 |
| MOD_CK1_1 | 358 | 364 | PF00069 | 0.443 |
| MOD_CK1_1 | 374 | 380 | PF00069 | 0.343 |
| MOD_CK1_1 | 502 | 508 | PF00069 | 0.661 |
| MOD_CK2_1 | 11 | 17 | PF00069 | 0.464 |
| MOD_CK2_1 | 24 | 30 | PF00069 | 0.435 |
| MOD_CK2_1 | 327 | 333 | PF00069 | 0.468 |
| MOD_CK2_1 | 387 | 393 | PF00069 | 0.471 |
| MOD_CK2_1 | 430 | 436 | PF00069 | 0.554 |
| MOD_CK2_1 | 507 | 513 | PF00069 | 0.531 |
| MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.407 |
| MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.417 |
| MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.457 |
| MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.198 |
| MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.636 |
| MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.317 |
| MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.319 |
| MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.302 |
| MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.306 |
| MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.600 |
| MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.500 |
| MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.536 |
| MOD_GSK3_1 | 228 | 235 | PF00069 | 0.499 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.506 |
| MOD_GSK3_1 | 269 | 276 | PF00069 | 0.523 |
| MOD_GSK3_1 | 358 | 365 | PF00069 | 0.517 |
| MOD_GSK3_1 | 374 | 381 | PF00069 | 0.444 |
| MOD_GSK3_1 | 387 | 394 | PF00069 | 0.483 |
| MOD_GSK3_1 | 481 | 488 | PF00069 | 0.425 |
| MOD_GSK3_1 | 499 | 506 | PF00069 | 0.620 |
| MOD_GSK3_1 | 528 | 535 | PF00069 | 0.370 |
| MOD_GSK3_1 | 549 | 556 | PF00069 | 0.516 |
| MOD_LATS_1 | 483 | 489 | PF00433 | 0.441 |
| MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.271 |
| MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.462 |
| MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.350 |
| MOD_NEK2_1 | 11 | 16 | PF00069 | 0.482 |
| MOD_NEK2_1 | 132 | 137 | PF00069 | 0.500 |
| MOD_NEK2_1 | 199 | 204 | PF00069 | 0.464 |
| MOD_NEK2_1 | 387 | 392 | PF00069 | 0.534 |
| MOD_NEK2_1 | 39 | 44 | PF00069 | 0.549 |
| MOD_NEK2_1 | 53 | 58 | PF00069 | 0.320 |
| MOD_NEK2_1 | 60 | 65 | PF00069 | 0.467 |
| MOD_PIKK_1 | 172 | 178 | PF00454 | 0.613 |
| MOD_PIKK_1 | 275 | 281 | PF00454 | 0.471 |
| MOD_PIKK_1 | 33 | 39 | PF00454 | 0.482 |
| MOD_PKA_1 | 98 | 104 | PF00069 | 0.424 |
| MOD_PKA_2 | 193 | 199 | PF00069 | 0.416 |
| MOD_PKA_2 | 231 | 237 | PF00069 | 0.503 |
| MOD_PKA_2 | 250 | 256 | PF00069 | 0.563 |
| MOD_PKA_2 | 355 | 361 | PF00069 | 0.520 |
| MOD_PKA_2 | 401 | 407 | PF00069 | 0.549 |
| MOD_PKA_2 | 513 | 519 | PF00069 | 0.499 |
| MOD_PKA_2 | 53 | 59 | PF00069 | 0.424 |
| MOD_PKA_2 | 98 | 104 | PF00069 | 0.476 |
| MOD_Plk_1 | 29 | 35 | PF00069 | 0.419 |
| MOD_Plk_1 | 392 | 398 | PF00069 | 0.547 |
| MOD_Plk_1 | 452 | 458 | PF00069 | 0.554 |
| MOD_Plk_4 | 277 | 283 | PF00069 | 0.474 |
| MOD_Plk_4 | 387 | 393 | PF00069 | 0.515 |
| MOD_Plk_4 | 85 | 91 | PF00069 | 0.478 |
| MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.569 |
| MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.508 |
| MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.372 |
| MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.538 |
| MOD_SUMO_for_1 | 415 | 418 | PF00179 | 0.444 |
| TRG_DiLeu_BaEn_1 | 118 | 123 | PF01217 | 0.462 |
| TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.498 |
| TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.410 |
| TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.282 |
| TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.535 |
| TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.449 |
| TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.453 |
| TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.456 |
| TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.489 |
| TRG_Pf-PMV_PEXEL_1 | 245 | 249 | PF00026 | 0.248 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PG62 | Leptomonas seymouri | 64% | 100% |
| A0A0S4IVW9 | Bodo saltans | 39% | 100% |
| A0A1X0P444 | Trypanosomatidae | 44% | 100% |
| A0A3S7X721 | Leishmania donovani | 93% | 100% |
| A0A422P028 | Trypanosoma rangeli | 39% | 100% |
| D0A658 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
| E9AHS0 | Leishmania infantum | 93% | 100% |
| E9AIV6 | Leishmania braziliensis | 79% | 100% |
| E9B491 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
| O64765 | Arabidopsis thaliana | 34% | 100% |
| O74933 | Candida albicans | 29% | 100% |
| O94617 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
| P43123 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
| Q16222 | Homo sapiens | 30% | 100% |
| Q18493 | Caenorhabditis elegans | 28% | 100% |
| Q28CH3 | Xenopus tropicalis | 31% | 100% |
| Q2FEW1 | Staphylococcus aureus (strain USA300) | 29% | 100% |
| Q2FW81 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 29% | 100% |
| Q2YYH4 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 29% | 100% |
| Q3KQV9 | Homo sapiens | 32% | 100% |
| Q3TW96 | Mus musculus | 33% | 100% |
| Q49ZB5 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 26% | 100% |
| Q4L846 | Staphylococcus haemolyticus (strain JCSC1435) | 28% | 100% |
| Q54GN5 | Dictyostelium discoideum | 28% | 100% |
| Q5HE34 | Staphylococcus aureus (strain COL) | 29% | 100% |
| Q5HM59 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 30% | 100% |
| Q6G7E3 | Staphylococcus aureus (strain MSSA476) | 29% | 100% |
| Q6GEQ8 | Staphylococcus aureus (strain MRSA252) | 29% | 100% |
| Q7A0A0 | Staphylococcus aureus (strain MW2) | 29% | 100% |
| Q7A4A4 | Staphylococcus aureus (strain N315) | 29% | 100% |
| Q7ZWD4 | Danio rerio | 32% | 100% |
| Q8CNG6 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 29% | 100% |
| Q91YN5 | Mus musculus | 31% | 100% |
| Q940S3 | Arabidopsis thaliana | 33% | 100% |
| Q99S95 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 29% | 100% |
| V5BYI4 | Trypanosoma cruzi | 41% | 95% |