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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9B491
Term | Name | Level | Count |
---|---|---|---|
GO:0006040 | amino sugar metabolic process | 4 | 1 |
GO:0006047 | UDP-N-acetylglucosamine metabolic process | 4 | 1 |
GO:0006048 | UDP-N-acetylglucosamine biosynthetic process | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009225 | nucleotide-sugar metabolic process | 4 | 1 |
GO:0009226 | nucleotide-sugar biosynthetic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046349 | amino sugar biosynthetic process | 5 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
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 | 290 | 296 | PF00089 | 0.251 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.247 |
CLV_PCSK_FUR_1 | 426 | 430 | PF00082 | 0.134 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.144 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.134 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.187 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 53 | 61 | PF00400 | 0.463 |
DEG_SPOP_SBC_1 | 489 | 493 | PF00917 | 0.453 |
DOC_CDC14_PxL_1 | 89 | 97 | PF14671 | 0.509 |
DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 183 | 190 | PF00069 | 0.473 |
DOC_MAPK_NFAT4_5 | 183 | 191 | PF00069 | 0.451 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.474 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.405 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.385 |
LIG_14-3-3_CanoR_1 | 221 | 226 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 32 | 41 | PF00244 | 0.279 |
LIG_14-3-3_CanoR_1 | 345 | 352 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 503 | 510 | PF00244 | 0.465 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.341 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.451 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.421 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.472 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.406 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.429 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.436 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.412 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.420 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.508 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.383 |
LIG_LIR_Gen_1 | 21 | 28 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 331 | 342 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 370 | 381 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.433 |
LIG_REV1ctd_RIR_1 | 216 | 225 | PF16727 | 0.528 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.416 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.390 |
LIG_SH2_GRB2like | 59 | 62 | PF00017 | 0.238 |
LIG_SH2_NCK_1 | 228 | 232 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.405 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.496 |
LIG_SH2_SRC | 228 | 231 | PF00017 | 0.509 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.241 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 155 | 158 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 498 | 501 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 533 | 536 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.280 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.451 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.447 |
LIG_SUMO_SIM_par_1 | 185 | 194 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 283 | 288 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 467 | 473 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 545 | 552 | PF11976 | 0.346 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.442 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.532 |
LIG_TRFH_1 | 210 | 214 | PF08558 | 0.496 |
LIG_TYR_ITIM | 337 | 342 | PF00017 | 0.405 |
LIG_UBA3_1 | 467 | 474 | PF00899 | 0.412 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.509 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.490 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.649 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.418 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.334 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.383 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.429 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.451 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.424 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.335 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.239 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.406 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.278 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.296 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.235 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.288 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.310 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.474 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.490 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.482 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.490 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.473 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.459 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.308 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.488 |
MOD_N-GLC_1 | 266 | 271 | PF02516 | 0.134 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.401 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.480 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.419 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.500 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.540 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.286 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.377 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.455 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.555 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.516 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.559 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.505 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.451 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.474 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.377 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.358 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.557 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.451 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.460 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.517 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.472 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.556 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.390 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.492 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.309 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.385 |
MOD_SUMO_for_1 | 404 | 407 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 549 | 555 | PF00179 | 0.312 |
TRG_DiLeu_BaEn_1 | 118 | 123 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 516 | 519 | PF00928 | 0.191 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.205 |
TRG_Pf-PMV_PEXEL_1 | 32 | 37 | PF00026 | 0.322 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG62 | Leptomonas seymouri | 64% | 99% |
A0A0S4IVW9 | Bodo saltans | 39% | 100% |
A0A1X0P444 | Trypanosomatidae | 44% | 100% |
A0A3S7X721 | Leishmania donovani | 86% | 98% |
A0A422P028 | Trypanosoma rangeli | 40% | 100% |
D0A658 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AHS0 | Leishmania infantum | 85% | 98% |
E9AIV6 | Leishmania braziliensis | 81% | 100% |
O64765 | Arabidopsis thaliana | 34% | 100% |
O74933 | Candida albicans | 35% | 100% |
O94617 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
P43123 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
Q16222 | Homo sapiens | 31% | 100% |
Q18493 | Caenorhabditis elegans | 29% | 100% |
Q28CH3 | Xenopus tropicalis | 32% | 100% |
Q2FEW1 | Staphylococcus aureus (strain USA300) | 28% | 100% |
Q2FW81 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 28% | 100% |
Q2YYH4 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 28% | 100% |
Q3KQV9 | Homo sapiens | 33% | 100% |
Q3TW96 | Mus musculus | 33% | 100% |
Q49ZB5 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 27% | 100% |
Q4Q3T5 | Leishmania major | 87% | 100% |
Q54GN5 | Dictyostelium discoideum | 31% | 100% |
Q5HE34 | Staphylococcus aureus (strain COL) | 28% | 100% |
Q5HM59 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 30% | 100% |
Q6G7E3 | Staphylococcus aureus (strain MSSA476) | 28% | 100% |
Q6GEQ8 | Staphylococcus aureus (strain MRSA252) | 28% | 100% |
Q7A0A0 | Staphylococcus aureus (strain MW2) | 28% | 100% |
Q7A4A4 | Staphylococcus aureus (strain N315) | 28% | 100% |
Q7ZWD4 | Danio rerio | 32% | 100% |
Q8CNG6 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 30% | 100% |
Q91YN5 | Mus musculus | 32% | 100% |
Q940S3 | Arabidopsis thaliana | 34% | 100% |
Q99S95 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 28% | 100% |
V5BYI4 | Trypanosoma cruzi | 43% | 93% |