Appears to be a transporter, related to vertebrate MFSD6 proteins (whose function is likewise unexplored).. Only expanded in Leptomonas.
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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3S7X6L2
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.791 |
CLV_C14_Caspase3-7 | 329 | 333 | PF00656 | 0.421 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.673 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.433 |
CLV_PCSK_FUR_1 | 8 | 12 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.441 |
DEG_SIAH_1 | 32 | 40 | PF03145 | 0.661 |
DOC_CDC14_PxL_1 | 161 | 169 | PF14671 | 0.358 |
DOC_MAPK_gen_1 | 173 | 182 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 293 | 301 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 312 | 318 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 566 | 572 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 377 | 384 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 399 | 406 | PF00069 | 0.333 |
DOC_MAPK_NFAT4_5 | 399 | 407 | PF00069 | 0.265 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.718 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 235 | 242 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 550 | 554 | PF00244 | 0.786 |
LIG_AP2alpha_1 | 330 | 334 | PF02296 | 0.421 |
LIG_BIR_III_4 | 94 | 98 | PF00653 | 0.657 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.274 |
LIG_BRCT_BRCA1_1 | 257 | 261 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.667 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.764 |
LIG_CaM_IQ_9 | 481 | 496 | PF13499 | 0.469 |
LIG_CSL_BTD_1 | 417 | 420 | PF09270 | 0.374 |
LIG_EH1_1 | 146 | 154 | PF00400 | 0.342 |
LIG_eIF4E_1 | 147 | 153 | PF01652 | 0.342 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.697 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.498 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.296 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.290 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.529 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.425 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.439 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.685 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.757 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.461 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.711 |
LIG_GBD_Chelix_1 | 268 | 276 | PF00786 | 0.400 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 264 | 275 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 31 | 39 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 413 | 422 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 459 | 469 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.145 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.737 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.646 |
LIG_MAD2 | 489 | 497 | PF02301 | 0.505 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.315 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.171 |
LIG_Pex14_2 | 330 | 334 | PF04695 | 0.306 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.280 |
LIG_PTB_Apo_2 | 330 | 337 | PF02174 | 0.421 |
LIG_PTB_Apo_2 | 67 | 74 | PF02174 | 0.660 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.252 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.382 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.280 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.307 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 291 | 295 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.342 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 135 | 139 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.145 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.302 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.259 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.386 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.687 |
LIG_SUMO_SIM_anti_2 | 181 | 189 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 351 | 356 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 568 | 576 | PF11976 | 0.684 |
LIG_TYR_ITIM | 281 | 286 | PF00017 | 0.421 |
LIG_TYR_ITSM | 324 | 331 | PF00017 | 0.405 |
LIG_TYR_ITSM | 457 | 464 | PF00017 | 0.421 |
LIG_UBA3_1 | 226 | 232 | PF00899 | 0.456 |
LIG_WRC_WIRS_1 | 252 | 257 | PF05994 | 0.435 |
LIG_WRC_WIRS_1 | 441 | 446 | PF05994 | 0.393 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.321 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.256 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.737 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.530 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.463 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.681 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.755 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.302 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.287 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.814 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.679 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.616 |
MOD_Cter_Amidation | 564 | 567 | PF01082 | 0.436 |
MOD_Cter_Amidation | 8 | 11 | PF01082 | 0.514 |
MOD_Cter_Amidation | 86 | 89 | PF01082 | 0.418 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.541 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.280 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.322 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.284 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.288 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.289 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.598 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.604 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.576 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.466 |
MOD_GlcNHglycan | 94 | 98 | PF01048 | 0.494 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.475 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.736 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.295 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.511 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.421 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.340 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.278 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.484 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.460 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.729 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.677 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.655 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.732 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.491 |
MOD_N-GLC_1 | 51 | 56 | PF02516 | 0.547 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.533 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.333 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.389 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.323 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.280 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.376 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.340 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.340 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.301 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.341 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.473 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.488 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.280 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.255 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.786 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.667 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.639 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.530 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.758 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.790 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.725 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.766 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.726 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.672 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.759 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.348 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.186 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.309 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.362 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.358 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.307 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.333 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.306 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.333 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.739 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.736 |
TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.302 |
TRG_DiLeu_BaEn_1 | 303 | 308 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 154 | 159 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.252 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.716 |
TRG_NES_CRM1_1 | 346 | 360 | PF08389 | 0.396 |
TRG_NES_CRM1_1 | 488 | 501 | PF08389 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4U9 | Leptomonas seymouri | 57% | 100% |
A0A0S4J6V2 | Bodo saltans | 36% | 100% |
A0A0S4JFI6 | Bodo saltans | 34% | 100% |
A0A1X0P0X3 | Trypanosomatidae | 45% | 100% |
A0A1X0P2H7 | Trypanosomatidae | 34% | 100% |
A0A3R7NAF7 | Trypanosoma rangeli | 37% | 100% |
A4HLI5 | Leishmania braziliensis | 70% | 100% |
A4I8Z5 | Leishmania infantum | 99% | 100% |
E9B3W4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q460 | Leishmania major | 91% | 100% |