An MFS-superfamily protein homologous to human FLVCR2 hem transporter. Only duplicated extensively in Strigomonas
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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4H9A1
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 8 |
GO:0022857 | transmembrane transporter activity | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.193 |
CLV_C14_Caspase3-7 | 51 | 55 | PF00656 | 0.683 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.456 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.301 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.761 |
DOC_CDC14_PxL_1 | 175 | 183 | PF14671 | 0.354 |
DOC_CDC14_PxL_1 | 383 | 391 | PF14671 | 0.478 |
DOC_CYCLIN_RxL_1 | 268 | 281 | PF00134 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 39 | 45 | PF00134 | 0.564 |
DOC_CYCLIN_yCln2_LP_2 | 392 | 398 | PF00134 | 0.437 |
DOC_PP1_RVXF_1 | 271 | 278 | PF00149 | 0.393 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.407 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.354 |
DOC_PP2B_LxvP_1 | 392 | 395 | PF13499 | 0.437 |
DOC_PP2B_PxIxI_1 | 111 | 117 | PF00149 | 0.270 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.356 |
DOC_SPAK_OSR1_1 | 65 | 69 | PF12202 | 0.584 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.193 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.437 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 192 | 202 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.393 |
LIG_Actin_WH2_2 | 134 | 151 | PF00022 | 0.389 |
LIG_BRCT_BRCA1_1 | 231 | 235 | PF00533 | 0.210 |
LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.407 |
LIG_CSL_BTD_1 | 153 | 156 | PF09270 | 0.193 |
LIG_CSL_BTD_1 | 185 | 188 | PF09270 | 0.533 |
LIG_CtBP_PxDLS_1 | 42 | 46 | PF00389 | 0.563 |
LIG_eIF4E_1 | 349 | 355 | PF01652 | 0.278 |
LIG_eIF4E_1 | 383 | 389 | PF01652 | 0.313 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.403 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.257 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.363 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.321 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.498 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.370 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.395 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.505 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.277 |
LIG_GBD_Chelix_1 | 194 | 202 | PF00786 | 0.210 |
LIG_GBD_Chelix_1 | 242 | 250 | PF00786 | 0.478 |
LIG_GBD_Chelix_1 | 301 | 309 | PF00786 | 0.407 |
LIG_GBD_Chelix_1 | 399 | 407 | PF00786 | 0.407 |
LIG_GBD_Chelix_1 | 457 | 465 | PF00786 | 0.210 |
LIG_LIR_Apic_2 | 264 | 270 | PF02991 | 0.533 |
LIG_LIR_Apic_2 | 406 | 412 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 379 | 389 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 446 | 457 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.317 |
LIG_NRBOX | 105 | 111 | PF00104 | 0.478 |
LIG_NRBOX | 240 | 246 | PF00104 | 0.465 |
LIG_PDZ_Class_3 | 477 | 482 | PF00595 | 0.521 |
LIG_Pex14_1 | 154 | 158 | PF04695 | 0.295 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.252 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.299 |
LIG_PTAP_UEV_1 | 22 | 27 | PF05743 | 0.600 |
LIG_REV1ctd_RIR_1 | 465 | 474 | PF16727 | 0.549 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.538 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.375 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.193 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.514 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.581 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 126 | 130 | PF00017 | 0.522 |
LIG_SH2_PTP2 | 383 | 386 | PF00017 | 0.407 |
LIG_SH2_SRC | 383 | 386 | PF00017 | 0.210 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.193 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.254 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.725 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.356 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.752 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 240 | 246 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 350 | 356 | PF11976 | 0.378 |
LIG_SUMO_SIM_anti_2 | 358 | 363 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 285 | 290 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 353 | 358 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 360 | 366 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 416 | 423 | PF11976 | 0.536 |
LIG_TYR_ITIM | 131 | 136 | PF00017 | 0.523 |
LIG_UBA3_1 | 181 | 190 | PF00899 | 0.210 |
LIG_UBA3_1 | 246 | 254 | PF00899 | 0.478 |
LIG_UBA3_1 | 271 | 276 | PF00899 | 0.584 |
LIG_WRC_WIRS_1 | 426 | 431 | PF05994 | 0.407 |
MOD_CDK_SPxK_1 | 59 | 65 | PF00069 | 0.597 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.764 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.501 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.338 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.409 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.616 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.533 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.397 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.498 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.360 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.362 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.409 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.732 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.370 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.495 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.425 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.149 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.325 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.210 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.512 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.446 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.398 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.584 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.385 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.717 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.425 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.357 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.350 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.346 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.299 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.379 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.390 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.590 |
MOD_PK_1 | 33 | 39 | PF00069 | 0.762 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.584 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.393 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.384 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.722 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.533 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.584 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.333 |
MOD_Plk_2-3 | 441 | 447 | PF00069 | 0.440 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.247 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.478 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.475 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.407 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.228 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.415 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.567 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.341 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.407 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.355 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.650 |
MOD_SUMO_rev_2 | 310 | 319 | PF00179 | 0.384 |
TRG_DiLeu_BaLyEn_6 | 177 | 182 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 384 | 389 | PF01217 | 0.252 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.283 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILZ7 | Leptomonas seymouri | 62% | 90% |
A0A0S4J692 | Bodo saltans | 32% | 80% |
A0A0S4JN91 | Bodo saltans | 27% | 100% |
A0A1X0NWR8 | Trypanosomatidae | 28% | 100% |
A0A1X0PA49 | Trypanosomatidae | 27% | 84% |
A0A3R7LY82 | Trypanosoma rangeli | 28% | 88% |
A0A3S7WUW1 | Leishmania donovani | 74% | 94% |
A0A3S7WW86 | Leishmania donovani | 23% | 100% |
A0A422NQJ7 | Trypanosoma rangeli | 26% | 84% |
A4HBK5 | Leishmania braziliensis | 24% | 100% |
A4HXM1 | Leishmania infantum | 74% | 94% |
B2RXV4 | Mus musculus | 26% | 86% |
D0A244 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 88% |
E9AGU5 | Leishmania infantum | 23% | 100% |
E9ARB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
O01735 | Caenorhabditis elegans | 23% | 82% |
P60815 | Rattus norvegicus | 28% | 88% |
Q11073 | Caenorhabditis elegans | 23% | 95% |
Q28FF3 | Xenopus tropicalis | 26% | 100% |
Q4H425 | Epichloe festucae (strain Fl1) | 22% | 100% |
Q4QCK8 | Leishmania major | 23% | 100% |
Q4QE46 | Leishmania major | 74% | 100% |
Q501I9 | Xenopus tropicalis | 25% | 100% |
Q503P5 | Danio rerio | 23% | 100% |
Q66H95 | Rattus norvegicus | 22% | 100% |
Q6GNV7 | Xenopus laevis | 24% | 100% |
Q6UXD7 | Homo sapiens | 26% | 86% |
Q8BFQ6 | Mus musculus | 22% | 100% |
Q8CE47 | Mus musculus | 26% | 93% |
Q91X85 | Mus musculus | 27% | 87% |
Q96SL1 | Homo sapiens | 23% | 100% |
Q9ES43 | Mus terricolor | 26% | 86% |
Q9N1F2 | Felis catus | 27% | 86% |
Q9UPI3 | Homo sapiens | 28% | 92% |
Q9Y5Y0 | Homo sapiens | 29% | 87% |
V5BQV3 | Trypanosoma cruzi | 26% | 88% |
V5DGX2 | Trypanosoma cruzi | 23% | 100% |