Related to plant TauE sulfite exporters. Due to a re-entrant loop, the number of full TM segments is only 10
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 | yes | yes: 12, no: 0 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0031464 | Cul4A-RING E3 ubiquitin ligase complex | 6 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0080008 | Cul4-RING E3 ubiquitin ligase complex | 5 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IGK2
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.715 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.521 |
DEG_APCC_DBOX_1 | 197 | 205 | PF00400 | 0.299 |
DEG_APCC_DBOX_1 | 343 | 351 | PF00400 | 0.504 |
DEG_APCC_DBOX_1 | 459 | 467 | PF00400 | 0.524 |
DEG_APCC_DBOX_1 | 91 | 99 | PF00400 | 0.294 |
DEG_SCF_FBW7_1 | 274 | 281 | PF00400 | 0.727 |
DOC_CKS1_1 | 275 | 280 | PF01111 | 0.726 |
DOC_CYCLIN_yCln2_LP_2 | 175 | 178 | PF00134 | 0.330 |
DOC_MAPK_gen_1 | 459 | 468 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 11 | 20 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 198 | 206 | PF00069 | 0.299 |
DOC_MAPK_NFAT4_5 | 198 | 206 | PF00069 | 0.364 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.327 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.449 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 315 | 320 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 348 | 355 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 460 | 466 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.406 |
LIG_Actin_WH2_2 | 182 | 200 | PF00022 | 0.306 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.375 |
LIG_BRCT_BRCA1_1 | 435 | 439 | PF00533 | 0.220 |
LIG_BRCT_BRCA1_1 | 469 | 473 | PF00533 | 0.400 |
LIG_eIF4E_1 | 169 | 175 | PF01652 | 0.467 |
LIG_eIF4E_1 | 325 | 331 | PF01652 | 0.372 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.492 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.341 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.275 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.339 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.495 |
LIG_GBD_Chelix_1 | 302 | 310 | PF00786 | 0.368 |
LIG_LIR_Apic_2 | 159 | 165 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 213 | 221 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 414 | 423 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 434 | 442 | PF02991 | 0.117 |
LIG_LIR_Gen_1 | 464 | 473 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 84 | 91 | PF02991 | 0.365 |
LIG_LIR_LC3C_4 | 428 | 433 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.363 |
LIG_LRP6_Inhibitor_1 | 453 | 459 | PF00058 | 0.313 |
LIG_LYPXL_yS_3 | 370 | 373 | PF13949 | 0.521 |
LIG_MYND_2 | 177 | 181 | PF01753 | 0.261 |
LIG_NRBOX | 198 | 204 | PF00104 | 0.320 |
LIG_NRBOX | 305 | 311 | PF00104 | 0.447 |
LIG_PCNA_yPIPBox_3 | 451 | 461 | PF02747 | 0.518 |
LIG_Pex14_2 | 415 | 419 | PF04695 | 0.322 |
LIG_Pex14_2 | 435 | 439 | PF04695 | 0.200 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.382 |
LIG_PTB_Apo_2 | 165 | 172 | PF02174 | 0.447 |
LIG_PTB_Phospho_1 | 165 | 171 | PF10480 | 0.447 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.287 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.456 |
LIG_SH2_CRK | 488 | 492 | PF00017 | 0.336 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.287 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.518 |
LIG_SH2_SRC | 465 | 468 | PF00017 | 0.394 |
LIG_SH2_STAT3 | 293 | 296 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.313 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.426 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 105 | 110 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 270 | 277 | PF11976 | 0.761 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.419 |
LIG_TYR_ITIM | 167 | 172 | PF00017 | 0.447 |
LIG_TYR_ITIM | 368 | 373 | PF00017 | 0.529 |
LIG_TYR_ITIM | 463 | 468 | PF00017 | 0.515 |
LIG_UBA3_1 | 184 | 191 | PF00899 | 0.400 |
LIG_UBA3_1 | 454 | 459 | PF00899 | 0.570 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.316 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.364 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.440 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.553 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.630 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.309 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.646 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.520 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.279 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.602 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.428 |
MOD_GlcNHglycan | 405 | 409 | PF01048 | 0.508 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.444 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.362 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.527 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.674 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.590 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.615 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.688 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.596 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.532 |
MOD_N-GLC_2 | 64 | 66 | PF02516 | 0.606 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.476 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.347 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.525 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.677 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.584 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.361 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.155 |
MOD_NEK2_2 | 411 | 416 | PF00069 | 0.282 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.447 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.734 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.652 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.568 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.344 |
MOD_PIKK_1 | 491 | 497 | PF00454 | 0.355 |
MOD_PKA_1 | 348 | 354 | PF00069 | 0.475 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.743 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.547 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.553 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.504 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.220 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.301 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.293 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.332 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.396 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.271 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.274 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.464 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.272 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.361 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.356 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.679 |
MOD_SUMO_rev_2 | 47 | 56 | PF00179 | 0.416 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P810 | Leptomonas seymouri | 64% | 100% |
A0A0S4IUN5 | Bodo saltans | 36% | 96% |
A0A0S4IWE0 | Bodo saltans | 38% | 97% |
A0A1X0NUS8 | Trypanosomatidae | 48% | 100% |
A0A3R7KFU6 | Trypanosoma rangeli | 45% | 100% |
A0A3R7KMV5 | Trypanosoma rangeli | 46% | 100% |
A4HK28 | Leishmania braziliensis | 70% | 100% |
A4I7M8 | Leishmania infantum | 100% | 100% |
E9B2H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
F4I8X6 | Arabidopsis thaliana | 24% | 100% |
Q4Q5M9 | Leishmania major | 90% | 100% |
Q8L7A0 | Arabidopsis thaliana | 26% | 100% |
Q8S9J0 | Arabidopsis thaliana | 25% | 100% |
V5BFC3 | Trypanosoma cruzi | 46% | 100% |