Transporters, folate/biopterin transporter FT5
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) | yes | yes: 9 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 52 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 70 |
NetGPI | no | yes: 0, no: 70 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HUF5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0015877 | biopterin transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0015224 | biopterin transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 656 | 658 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.380 |
DEG_APCC_DBOX_1 | 228 | 236 | PF00400 | 0.451 |
DEG_COP1_1 | 276 | 284 | PF00400 | 0.416 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.525 |
DOC_CDC14_PxL_1 | 574 | 582 | PF14671 | 0.357 |
DOC_CYCLIN_yCln2_LP_2 | 591 | 597 | PF00134 | 0.404 |
DOC_MAPK_gen_1 | 226 | 234 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 244 | 253 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 488 | 496 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 87 | 93 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 17 | 24 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 181 | 188 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 488 | 496 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 464 | 470 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.400 |
DOC_PP2B_LxvP_1 | 591 | 594 | PF13499 | 0.390 |
DOC_PP2B_LxvP_1 | 597 | 600 | PF13499 | 0.356 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 614 | 618 | PF00917 | 0.437 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.375 |
LIG_14-3-3_CanoR_1 | 466 | 470 | PF00244 | 0.517 |
LIG_APCC_ABBA_1 | 4 | 9 | PF00400 | 0.666 |
LIG_APCC_ABBAyCdc20_2 | 266 | 272 | PF00400 | 0.413 |
LIG_CSL_BTD_1 | 517 | 520 | PF09270 | 0.424 |
LIG_EVH1_2 | 570 | 574 | PF00568 | 0.386 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.382 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.285 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.448 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.518 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.442 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.830 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.588 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.596 |
LIG_LIR_Apic_2 | 385 | 391 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 137 | 148 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 156 | 167 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 435 | 444 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 454 | 460 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 480 | 487 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 535 | 544 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.546 |
LIG_LIR_LC3C_4 | 298 | 303 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 433 | 437 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.521 |
LIG_MYND_3 | 281 | 285 | PF01753 | 0.410 |
LIG_Pex14_1 | 157 | 161 | PF04695 | 0.400 |
LIG_Pex14_2 | 200 | 204 | PF04695 | 0.312 |
LIG_Pex14_2 | 432 | 436 | PF04695 | 0.337 |
LIG_Pex14_2 | 456 | 460 | PF04695 | 0.398 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.353 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.541 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.372 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.329 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.538 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 437 | 441 | PF00017 | 0.327 |
LIG_SH2_PTP2 | 493 | 496 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 538 | 542 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.527 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.528 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.326 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.624 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.311 |
LIG_SUMO_SIM_anti_2 | 248 | 255 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 520 | 526 | PF11976 | 0.355 |
LIG_TRAF2_1 | 276 | 279 | PF00917 | 0.416 |
LIG_TRAF2_1 | 291 | 294 | PF00917 | 0.591 |
LIG_TRFH_1 | 105 | 109 | PF08558 | 0.388 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.407 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.222 |
LIG_TYR_ITSM | 433 | 440 | PF00017 | 0.430 |
LIG_UBA3_1 | 328 | 336 | PF00899 | 0.412 |
LIG_Vh1_VBS_1 | 357 | 375 | PF01044 | 0.474 |
LIG_Vh1_VBS_1 | 436 | 454 | PF01044 | 0.413 |
LIG_WRC_WIRS_1 | 415 | 420 | PF05994 | 0.361 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.378 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.324 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.549 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.313 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.793 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.383 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.398 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.362 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.287 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.450 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.401 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.405 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.390 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.400 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.371 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.423 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.230 |
MOD_N-GLC_1 | 636 | 641 | PF02516 | 0.766 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.371 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.398 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.379 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.324 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.496 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.389 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.319 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.393 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.381 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.402 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.309 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.364 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.363 |
MOD_OFUCOSY | 354 | 361 | PF10250 | 0.424 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.376 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.361 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.507 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.371 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.382 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.337 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.420 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.379 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.365 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.490 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.345 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.353 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.408 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.407 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.444 |
MOD_SUMO_rev_2 | 606 | 615 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 650 | 658 | PF00179 | 0.479 |
TRG_DiLeu_BaEn_4 | 306 | 312 | PF01217 | 0.228 |
TRG_DiLeu_BaLyEn_6 | 586 | 591 | PF01217 | 0.347 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.379 |
TRG_NES_CRM1_1 | 410 | 424 | PF08389 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 51% | 93% |
A0A0N1HY49 | Leptomonas seymouri | 54% | 98% |
A0A0N1HZ06 | Leptomonas seymouri | 40% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 43% | 92% |
A0A0N1PAY4 | Leptomonas seymouri | 52% | 75% |
A0A0N1PB77 | Leptomonas seymouri | 39% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 61% | 98% |
A0A0N1PCC1 | Leptomonas seymouri | 46% | 99% |
A0A381MBI0 | Leishmania infantum | 48% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 49% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 59% | 94% |
A0A3Q8IH50 | Leishmania donovani | 99% | 91% |
A0A3Q8IVN0 | Leishmania donovani | 40% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 45% | 100% |
A0A3S5H5P4 | Leishmania donovani | 50% | 97% |
A0A3S5H5V2 | Leishmania donovani | 45% | 100% |
A0A3S5H6F6 | Leishmania donovani | 58% | 94% |
A0A3S5H763 | Leishmania donovani | 62% | 98% |
A0A3S7WR10 | Leishmania donovani | 49% | 88% |
A0A3S7WR14 | Leishmania donovani | 60% | 96% |
A0A3S7WR15 | Leishmania donovani | 58% | 77% |
A0A3S7WR24 | Leishmania donovani | 59% | 93% |
A4H4T8 | Leishmania braziliensis | 44% | 100% |
A4H5Y4 | Leishmania braziliensis | 49% | 100% |
A4H617 | Leishmania braziliensis | 57% | 100% |
A4H618 | Leishmania braziliensis | 57% | 100% |
A4H619 | Leishmania braziliensis | 57% | 100% |
A4H620 | Leishmania braziliensis | 82% | 100% |
A4H6C3 | Leishmania braziliensis | 49% | 100% |
A4HNH7 | Leishmania braziliensis | 37% | 100% |
A4HSS2 | Leishmania infantum | 49% | 100% |
A4HUE4 | Leishmania infantum | 49% | 100% |
A4HUE5 | Leishmania infantum | 58% | 100% |
A4HUE6 | Leishmania infantum | 60% | 100% |
A4HUE7 | Leishmania infantum | 58% | 100% |
A4HUE8 | Leishmania infantum | 58% | 100% |
A4HUF4 | Leishmania infantum | 58% | 100% |
A4HYA9 | Leishmania infantum | 63% | 98% |
A4IC33 | Leishmania infantum | 39% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AG72 | Leishmania infantum | 45% | 100% |
E9AI40 | Leishmania braziliensis | 60% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 98% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 99% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 99% |
Q4QDC4 | Leishmania major | 60% | 100% |
Q4QH81 | Leishmania major | 48% | 100% |
Q4QHH7 | Leishmania major | 93% | 100% |
Q4QHH8 | Leishmania major | 57% | 100% |
Q4QHH9 | Leishmania major | 56% | 100% |
Q4QHI0 | Leishmania major | 59% | 100% |
Q4QHI1 | Leishmania major | 59% | 97% |
Q4QHI2 | Leishmania major | 57% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 48% | 100% |
Q7KIP2 | Leishmania major | 39% | 99% |