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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9B3W4
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 | 0.742 |
CLV_C14_Caspase3-7 | 329 | 333 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.701 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.446 |
CLV_PCSK_FUR_1 | 8 | 12 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.407 |
DEG_APCC_DBOX_1 | 295 | 303 | PF00400 | 0.549 |
DEG_SPOP_SBC_1 | 107 | 111 | PF00917 | 0.538 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.370 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.638 |
DOC_CDC14_PxL_1 | 161 | 169 | PF14671 | 0.407 |
DOC_MAPK_gen_1 | 173 | 182 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 200 | 208 | PF00069 | 0.169 |
DOC_MAPK_gen_1 | 293 | 301 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 312 | 318 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 566 | 572 | PF00069 | 0.695 |
DOC_MAPK_MEF2A_6 | 293 | 301 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 377 | 384 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 399 | 406 | PF00069 | 0.337 |
DOC_MAPK_NFAT4_5 | 399 | 407 | PF00069 | 0.280 |
DOC_MAPK_RevD_3 | 185 | 201 | PF00069 | 0.233 |
DOC_PP1_RVXF_1 | 304 | 310 | PF00149 | 0.416 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.723 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.207 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.754 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 494 | 499 | PF00244 | 0.461 |
LIG_AP2alpha_1 | 330 | 334 | PF02296 | 0.420 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.320 |
LIG_BRCT_BRCA1_1 | 257 | 261 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.717 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.694 |
LIG_CaM_IQ_9 | 481 | 496 | PF13499 | 0.465 |
LIG_CSL_BTD_1 | 417 | 420 | PF09270 | 0.370 |
LIG_CtBP_PxDLS_1 | 179 | 183 | PF00389 | 0.178 |
LIG_CtBP_PxDLS_1 | 53 | 57 | PF00389 | 0.553 |
LIG_EH1_1 | 146 | 154 | PF00400 | 0.342 |
LIG_eIF4E_1 | 147 | 153 | PF01652 | 0.342 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.700 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.169 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.440 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.438 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.705 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.706 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.712 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 264 | 275 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 31 | 39 | PF02991 | 0.740 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 413 | 424 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 459 | 469 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.783 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.648 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.310 |
LIG_Pex14_2 | 330 | 334 | PF04695 | 0.327 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.291 |
LIG_PTB_Apo_2 | 330 | 337 | PF02174 | 0.420 |
LIG_PTB_Apo_2 | 67 | 74 | PF02174 | 0.663 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.264 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.178 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.378 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.291 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.305 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.178 |
LIG_SH2_NCK_1 | 291 | 295 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.342 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 135 | 139 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.150 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.320 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.269 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.383 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.656 |
LIG_SUMO_SIM_anti_2 | 181 | 187 | PF11976 | 0.262 |
LIG_SUMO_SIM_anti_2 | 529 | 535 | PF11976 | 0.601 |
LIG_SUMO_SIM_anti_2 | 569 | 576 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 353 | 360 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 568 | 576 | PF11976 | 0.687 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.592 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.178 |
LIG_TYR_ITIM | 281 | 286 | PF00017 | 0.420 |
LIG_TYR_ITSM | 324 | 331 | PF00017 | 0.402 |
LIG_TYR_ITSM | 457 | 464 | PF00017 | 0.420 |
LIG_UBA3_1 | 226 | 232 | PF00899 | 0.470 |
LIG_WRC_WIRS_1 | 122 | 127 | PF05994 | 0.181 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.574 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.343 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.763 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.549 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.722 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.736 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.320 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.655 |
MOD_Cter_Amidation | 198 | 201 | PF01082 | 0.370 |
MOD_Cter_Amidation | 564 | 567 | PF01082 | 0.437 |
MOD_Cter_Amidation | 8 | 11 | PF01082 | 0.523 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.333 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.398 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.461 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.298 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.318 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.594 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.610 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.497 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.538 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.733 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.717 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.526 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.402 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.770 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.363 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.738 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.740 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.743 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.738 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.686 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.768 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.582 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.566 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.503 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.511 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.327 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.385 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.368 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.318 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.414 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.370 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.484 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.350 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.500 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.498 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.300 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.264 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.774 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.573 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.676 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.267 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.727 |
MOD_PK_1 | 494 | 500 | PF00069 | 0.464 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.639 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.595 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.530 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.687 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.794 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.771 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.745 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.716 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.659 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.709 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.741 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.348 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.192 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.340 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.394 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.378 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.321 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.360 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.728 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.150 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.452 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.684 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.207 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.483 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.753 |
TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_1 | 303 | 308 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_2 | 53 | 59 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 154 | 159 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.185 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.178 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.264 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.210 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 346 | 360 | PF08389 | 0.370 |
TRG_NES_CRM1_1 | 488 | 501 | PF08389 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4U9 | Leptomonas seymouri | 57% | 100% |
A0A0S4J6V2 | Bodo saltans | 35% | 100% |
A0A0S4JFI6 | Bodo saltans | 31% | 100% |
A0A1X0P0X3 | Trypanosomatidae | 41% | 100% |
A0A3R7NAF7 | Trypanosoma rangeli | 35% | 100% |
A0A3S7X6L2 | Leishmania donovani | 85% | 100% |
A4HLI5 | Leishmania braziliensis | 68% | 100% |
A4I8Z5 | Leishmania infantum | 85% | 100% |
Q4Q460 | Leishmania major | 82% | 100% |