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: A4HK28
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_NRD_NRD_1 | 347 | 349 | PF00675 | 0.372 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.501 |
DEG_APCC_DBOX_1 | 197 | 205 | PF00400 | 0.259 |
DOC_CYCLIN_yCln2_LP_2 | 174 | 180 | PF00134 | 0.286 |
DOC_MAPK_gen_1 | 52 | 58 | PF00069 | 0.160 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 11 | 20 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 198 | 206 | PF00069 | 0.259 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.287 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.559 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.262 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.424 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 92 | 98 | PF00244 | 0.312 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.392 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.160 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 469 | 473 | PF00533 | 0.371 |
LIG_eIF4E_1 | 169 | 175 | PF01652 | 0.439 |
LIG_eIF4E_1 | 325 | 331 | PF01652 | 0.338 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.628 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.377 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.269 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.263 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.371 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.237 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.248 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.177 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.175 |
LIG_GBD_Chelix_1 | 306 | 314 | PF00786 | 0.308 |
LIG_GBD_Chelix_1 | 471 | 479 | PF00786 | 0.244 |
LIG_LIR_Apic_2 | 159 | 165 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 148 | 158 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 414 | 423 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.321 |
LIG_LIR_LC3C_4 | 428 | 433 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.202 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.137 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.321 |
LIG_LYPXL_S_1 | 369 | 373 | PF13949 | 0.239 |
LIG_LYPXL_yS_3 | 370 | 373 | PF13949 | 0.498 |
LIG_NRBOX | 196 | 202 | PF00104 | 0.286 |
LIG_NRBOX | 305 | 311 | PF00104 | 0.449 |
LIG_Pex14_2 | 435 | 439 | PF04695 | 0.352 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.294 |
LIG_PTB_Apo_2 | 165 | 172 | PF02174 | 0.419 |
LIG_PTB_Phospho_1 | 165 | 171 | PF10480 | 0.419 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.428 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.282 |
LIG_SH2_CRK | 488 | 492 | PF00017 | 0.320 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.568 |
LIG_SH2_NCK_1 | 255 | 259 | PF00017 | 0.528 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.502 |
LIG_SH2_SRC | 465 | 468 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 488 | 492 | PF00017 | 0.269 |
LIG_SH2_STAT3 | 293 | 296 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.226 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.407 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 105 | 110 | PF11976 | 0.342 |
LIG_SUMO_SIM_anti_2 | 420 | 428 | PF11976 | 0.221 |
LIG_SUMO_SIM_par_1 | 22 | 27 | PF11976 | 0.402 |
LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.571 |
LIG_TYR_ITIM | 167 | 172 | PF00017 | 0.419 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.407 |
LIG_TYR_ITIM | 368 | 373 | PF00017 | 0.509 |
LIG_TYR_ITIM | 463 | 468 | PF00017 | 0.494 |
LIG_UBA3_1 | 121 | 127 | PF00899 | 0.453 |
LIG_UBA3_1 | 184 | 191 | PF00899 | 0.372 |
LIG_WRC_WIRS_1 | 98 | 103 | PF05994 | 0.407 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.424 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.446 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.442 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.565 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.635 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.386 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.192 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.210 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.451 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.352 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.416 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.485 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.318 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.443 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.656 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.609 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.637 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.552 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.599 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.384 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.261 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.301 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.503 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.307 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.330 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.286 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.506 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.740 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.664 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.250 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.271 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.577 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.355 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.228 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.240 |
MOD_NEK2_2 | 411 | 416 | PF00069 | 0.257 |
MOD_NEK2_2 | 84 | 89 | PF00069 | 0.181 |
MOD_NEK2_2 | 90 | 95 | PF00069 | 0.184 |
MOD_OFUCOSY | 66 | 73 | PF10250 | 0.381 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.419 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.561 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.583 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.529 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.253 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.500 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.362 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.397 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.291 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.288 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.660 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.364 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.487 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.245 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.253 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.268 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.316 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.282 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.296 |
MOD_SUMO_for_1 | 264 | 267 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 47 | 54 | PF00179 | 0.285 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.364 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P810 | Leptomonas seymouri | 62% | 100% |
A0A0S4IUN5 | Bodo saltans | 38% | 96% |
A0A0S4IWE0 | Bodo saltans | 38% | 97% |
A0A1X0NUS8 | Trypanosomatidae | 44% | 100% |
A0A3Q8IGK2 | Leishmania donovani | 70% | 100% |
A0A3R7KFU6 | Trypanosoma rangeli | 42% | 100% |
A0A3R7KMV5 | Trypanosoma rangeli | 44% | 100% |
A4I7M8 | Leishmania infantum | 70% | 100% |
E9B2H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
F4I8X6 | Arabidopsis thaliana | 22% | 100% |
Q4Q5M9 | Leishmania major | 69% | 100% |
Q8L7A0 | Arabidopsis thaliana | 26% | 100% |
Q8S9J0 | Arabidopsis thaliana | 24% | 100% |
V5BFC3 | Trypanosoma cruzi | 43% | 100% |