Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
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:0005829 | cytosol | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006011 | UDP-glucose metabolic process | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009225 | nucleotide-sugar metabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0005976 | polysaccharide metabolic process | 4 | 1 |
GO:0005977 | glycogen metabolic process | 6 | 1 |
GO:0006073 | obsolete cellular glucan metabolic process | 5 | 1 |
GO:0006091 | generation of precursor metabolites and energy | 3 | 1 |
GO:0006112 | energy reserve metabolic process | 5 | 1 |
GO:0015980 | energy derivation by oxidation of organic compounds | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044042 | glucan metabolic process | 5 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0044264 | obsolete cellular polysaccharide metabolic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003983 | UTP:glucose-1-phosphate uridylyltransferase activity | 7 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0051748 | UTP-monosaccharide-1-phosphate uridylyltransferase activity | 6 | 12 |
GO:0070569 | uridylyltransferase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.436 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.298 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.179 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.254 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.183 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.256 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.615 |
DEG_SPOP_SBC_1 | 489 | 493 | PF00917 | 0.471 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 305 | 314 | PF00134 | 0.467 |
DOC_MAPK_DCC_7 | 406 | 416 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 237 | 246 | PF00069 | 0.481 |
DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.497 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.456 |
DOC_PP4_FxxP_1 | 473 | 476 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.529 |
DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 261 | 265 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 443 | 447 | PF00244 | 0.547 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.555 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.488 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.460 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.443 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.383 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.630 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.501 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.474 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.476 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.428 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.456 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.531 |
LIG_GBD_Chelix_1 | 77 | 85 | PF00786 | 0.296 |
LIG_LIR_Apic_2 | 185 | 189 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 471 | 476 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 105 | 114 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 193 | 199 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 425 | 435 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 105 | 109 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.610 |
LIG_LYPXL_yS_3 | 147 | 150 | PF13949 | 0.480 |
LIG_MAD2 | 167 | 175 | PF02301 | 0.523 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.456 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.465 |
LIG_SH2_STAT3 | 116 | 119 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.480 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.457 |
LIG_SUMO_SIM_anti_2 | 157 | 162 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 278 | 285 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 278 | 285 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 314 | 320 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 384 | 391 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 412 | 418 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.523 |
LIG_UBA3_1 | 317 | 322 | PF00899 | 0.505 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.456 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.350 |
LIG_WRC_WIRS_1 | 293 | 298 | PF05994 | 0.549 |
MOD_CDK_SPK_2 | 343 | 348 | PF00069 | 0.559 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.456 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.428 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.422 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.556 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.539 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.313 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.256 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.244 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.411 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.272 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.281 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.165 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.578 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.346 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.413 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.457 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.493 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.398 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.596 |
MOD_LATS_1 | 420 | 426 | PF00433 | 0.480 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.395 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.558 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.473 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.469 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.497 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.459 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.459 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.444 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.468 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.477 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.489 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.557 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.568 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.510 |
MOD_NEK2_2 | 260 | 265 | PF00069 | 0.549 |
MOD_PKA_1 | 442 | 448 | PF00069 | 0.428 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.511 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.524 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.444 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.428 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.467 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.412 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.534 |
MOD_Plk_2-3 | 102 | 108 | PF00069 | 0.471 |
MOD_Plk_2-3 | 292 | 298 | PF00069 | 0.511 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.481 |
MOD_Plk_2-3 | 93 | 99 | PF00069 | 0.520 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.461 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.560 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.468 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.521 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.485 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.466 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.559 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.337 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.590 |
MOD_SUMO_for_1 | 462 | 465 | PF00179 | 0.398 |
MOD_SUMO_rev_2 | 2 | 8 | PF00179 | 0.635 |
MOD_SUMO_rev_2 | 437 | 444 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 99 | 106 | PF00179 | 0.485 |
TRG_DiLeu_BaEn_1 | 276 | 281 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_2 | 122 | 128 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.523 |
TRG_NES_CRM1_1 | 56 | 67 | PF08389 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 447 | 451 | PF00026 | 0.240 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H7 | Leptomonas seymouri | 79% | 100% |
A0A0S4JER9 | Bodo saltans | 57% | 100% |
A0A1X0P7U0 | Trypanosomatidae | 66% | 100% |
A0A3S7WUZ9 | Leishmania donovani | 95% | 100% |
A0A422P1Z6 | Trypanosoma rangeli | 62% | 100% |
A4HXX2 | Leishmania infantum | 95% | 100% |
C9ZZT0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AI58 | Leishmania braziliensis | 85% | 100% |
O35156 | Cricetulus griseus | 36% | 97% |
O59819 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 99% |
O64459 | Pyrus pyrifolia | 36% | 100% |
P08800 | Dictyostelium discoideum | 32% | 97% |
P19595 | Solanum tuberosum | 34% | 100% |
P32861 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 99% |
P38709 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P57751 | Arabidopsis thaliana | 35% | 100% |
P78811 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 98% |
P79303 | Sus scrofa | 35% | 97% |
Q07130 | Bos taurus | 36% | 97% |
Q16851 | Homo sapiens | 36% | 97% |
Q43772 | Hordeum vulgare | 36% | 100% |
Q4QDU3 | Leishmania major | 94% | 100% |
Q54YZ0 | Dictyostelium discoideum | 36% | 98% |
Q59KI0 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 39% | 99% |
Q8SSC5 | Encephalitozoon cuniculi (strain GB-M1) | 37% | 100% |
Q91ZJ5 | Mus musculus | 36% | 97% |
Q9LKG7 | Astragalus penduliflorus | 35% | 100% |
Q9M9P3 | Arabidopsis thaliana | 34% | 100% |
Q9SDX3 | Musa acuminata | 34% | 100% |
V5B6M0 | Trypanosoma cruzi | 60% | 100% |