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 |
Related structures:
AlphaFold database: A4H971
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 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016779 | nucleotidyltransferase activity | 4 | 10 |
GO:0051748 | UTP-monosaccharide-1-phosphate uridylyltransferase activity | 6 | 5 |
GO:0070569 | uridylyltransferase activity | 5 | 10 |
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0002134 | UTP binding | 4 | 1 |
GO:0003977 | UDP-N-acetylglucosamine diphosphorylase activity | 6 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0017103 | UTP:galactose-1-phosphate uridylyltransferase activity | 7 | 1 |
GO:0019103 | pyrimidine nucleotide binding | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032557 | pyrimidine ribonucleotide binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0043763 | UTP:glucose-1-phosphate uridylyltransferase regulator activity | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 583 | 587 | PF00656 | 0.401 |
CLV_C14_Caspase3-7 | 616 | 620 | PF00656 | 0.449 |
CLV_MEL_PAP_1 | 424 | 430 | PF00089 | 0.413 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.408 |
DEG_APCC_DBOX_1 | 464 | 472 | PF00400 | 0.409 |
DEG_COP1_1 | 375 | 383 | PF00400 | 0.412 |
DOC_AGCK_PIF_1 | 425 | 430 | PF00069 | 0.323 |
DOC_ANK_TNKS_1 | 466 | 473 | PF00023 | 0.369 |
DOC_CDC14_PxL_1 | 88 | 96 | PF14671 | 0.449 |
DOC_MAPK_gen_1 | 113 | 120 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 465 | 475 | PF00069 | 0.347 |
DOC_MAPK_HePTP_8 | 463 | 475 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 113 | 120 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 466 | 475 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 493 | 500 | PF00069 | 0.243 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.287 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.452 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.399 |
DOC_PP4_FxxP_1 | 383 | 386 | PF00568 | 0.382 |
DOC_PP4_FxxP_1 | 396 | 399 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 517 | 520 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 89 | 92 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.431 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 113 | 117 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 127 | 137 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 393 | 397 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 528 | 532 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.328 |
LIG_Actin_WH2_2 | 181 | 197 | PF00022 | 0.469 |
LIG_Actin_WH2_2 | 352 | 367 | PF00022 | 0.440 |
LIG_Actin_WH2_2 | 456 | 471 | PF00022 | 0.406 |
LIG_AP2alpha_2 | 319 | 321 | PF02296 | 0.383 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.441 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.354 |
LIG_CtBP_PxDLS_1 | 281 | 285 | PF00389 | 0.282 |
LIG_EVH1_2 | 85 | 89 | PF00568 | 0.433 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.520 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.498 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.442 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.287 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.433 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.266 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.416 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.288 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.513 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.432 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.480 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.297 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.406 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.220 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.411 |
LIG_GBD_Chelix_1 | 120 | 128 | PF00786 | 0.215 |
LIG_LIR_Apic_2 | 382 | 386 | PF02991 | 0.381 |
LIG_LIR_Apic_2 | 395 | 399 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 515 | 520 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 115 | 124 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 293 | 303 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 327 | 334 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 423 | 433 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.393 |
LIG_LIR_LC3C_4 | 529 | 533 | PF02991 | 0.202 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 429 | 433 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.414 |
LIG_PTB_Apo_2 | 322 | 329 | PF02174 | 0.393 |
LIG_PTB_Apo_2 | 382 | 389 | PF02174 | 0.367 |
LIG_PTB_Phospho_1 | 322 | 328 | PF10480 | 0.386 |
LIG_PTB_Phospho_1 | 382 | 388 | PF10480 | 0.424 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.458 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.286 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.216 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.374 |
LIG_SH2_STAT3 | 461 | 464 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.305 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.458 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.269 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.335 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.466 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.431 |
LIG_SUMO_SIM_anti_2 | 408 | 417 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 495 | 501 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 529 | 534 | PF11976 | 0.312 |
LIG_TYR_ITIM | 128 | 133 | PF00017 | 0.432 |
LIG_UBA3_1 | 309 | 315 | PF00899 | 0.235 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.362 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.420 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.405 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.421 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.317 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.368 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.496 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.362 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.237 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.372 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.543 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.393 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.312 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.400 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.225 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.452 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.391 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.269 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.338 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.331 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.405 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.497 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.640 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.711 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.548 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.463 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.434 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.614 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.298 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.338 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.360 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.436 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.623 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.497 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.252 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.336 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.287 |
MOD_N-GLC_1 | 587 | 592 | PF02516 | 0.304 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.458 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.364 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.462 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.377 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.384 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.349 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.416 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.494 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.452 |
MOD_NEK2_2 | 232 | 237 | PF00069 | 0.502 |
MOD_NEK2_2 | 571 | 576 | PF00069 | 0.384 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.212 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.427 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.471 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.407 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.609 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.338 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.356 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.501 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.444 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.452 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.525 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.525 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.340 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.438 |
MOD_Plk_1 | 600 | 606 | PF00069 | 0.349 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.379 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.432 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.462 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.432 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.364 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.491 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.304 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.300 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.400 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.333 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.424 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.428 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.448 |
MOD_SUMO_rev_2 | 212 | 218 | PF00179 | 0.357 |
TRG_AP2beta_CARGO_1 | 457 | 467 | PF09066 | 0.366 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.308 |
TRG_DiLeu_BaEn_1 | 438 | 443 | PF01217 | 0.313 |
TRG_DiLeu_BaEn_2 | 263 | 269 | PF01217 | 0.337 |
TRG_DiLeu_LyEn_5 | 83 | 88 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.280 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 336 | 341 | PF00026 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 536 | 540 | PF00026 | 0.367 |
TRG_PTS1 | 627 | 630 | PF00515 | 0.620 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6W2 | Leptomonas seymouri | 66% | 98% |
A0A0S4IQX2 | Bodo saltans | 34% | 83% |
A0A1X0NSQ3 | Trypanosomatidae | 50% | 100% |
A0A3R7KRK2 | Trypanosoma rangeli | 48% | 100% |
A0A3S7WUL7 | Leishmania donovani | 83% | 100% |
A2YGP6 | Oryza sativa subsp. indica | 32% | 100% |
A4HXJ3 | Leishmania infantum | 83% | 100% |
E9AR88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q09WE7 | Glycine max | 34% | 100% |
Q0GZS3 | Cucumis melo | 35% | 100% |
Q4QE75 | Leishmania major | 84% | 100% |
Q5W915 | Pisum sativum | 34% | 100% |
Q5Z8Y4 | Oryza sativa subsp. japonica | 32% | 100% |
Q9C5I1 | Arabidopsis thaliana | 35% | 100% |
V5DFP2 | Trypanosoma cruzi | 49% | 100% |