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: 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: A0A3Q8IH50
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 | 271 | 273 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 718 | 720 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 552 | 554 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 720 | 722 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.252 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.426 |
DEG_COP1_1 | 340 | 348 | PF00400 | 0.393 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.621 |
DOC_CDC14_PxL_1 | 638 | 646 | PF14671 | 0.336 |
DOC_CYCLIN_yCln2_LP_2 | 655 | 661 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 151 | 157 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 290 | 298 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 308 | 317 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 552 | 560 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 245 | 252 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 290 | 298 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 552 | 560 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 81 | 88 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 528 | 534 | PF00149 | 0.524 |
DOC_PP2B_LxvP_1 | 473 | 476 | PF13499 | 0.381 |
DOC_PP2B_LxvP_1 | 655 | 658 | PF13499 | 0.371 |
DOC_PP2B_LxvP_1 | 661 | 664 | PF13499 | 0.337 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.580 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 530 | 534 | PF00244 | 0.496 |
LIG_APCC_ABBA_1 | 68 | 73 | PF00400 | 0.648 |
LIG_APCC_ABBAyCdc20_2 | 330 | 336 | PF00400 | 0.388 |
LIG_CSL_BTD_1 | 581 | 584 | PF09270 | 0.404 |
LIG_EVH1_2 | 634 | 638 | PF00568 | 0.364 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.574 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.699 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.363 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.262 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.429 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.497 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.421 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.582 |
LIG_LIR_Apic_2 | 449 | 455 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 142 | 149 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 201 | 212 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 518 | 524 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 544 | 551 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 599 | 608 | PF02991 | 0.521 |
LIG_LIR_LC3C_4 | 362 | 367 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.343 |
LIG_MYND_3 | 345 | 349 | PF01753 | 0.385 |
LIG_Pex14_1 | 221 | 225 | PF04695 | 0.381 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.293 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.316 |
LIG_Pex14_2 | 520 | 524 | PF04695 | 0.378 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.517 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.382 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.333 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.520 |
LIG_SH2_CRK | 412 | 416 | PF00017 | 0.350 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.308 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.306 |
LIG_SH2_PTP2 | 557 | 560 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 602 | 606 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.532 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.694 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.306 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.577 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.290 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 312 | 319 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 584 | 590 | PF11976 | 0.336 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.391 |
LIG_TRAF2_1 | 355 | 358 | PF00917 | 0.569 |
LIG_TRFH_1 | 169 | 173 | PF08558 | 0.368 |
LIG_TYR_ITIM | 167 | 172 | PF00017 | 0.388 |
LIG_TYR_ITIM | 284 | 289 | PF00017 | 0.197 |
LIG_TYR_ITSM | 497 | 504 | PF00017 | 0.410 |
LIG_UBA3_1 | 392 | 400 | PF00899 | 0.392 |
LIG_Vh1_VBS_1 | 421 | 439 | PF01044 | 0.452 |
LIG_Vh1_VBS_1 | 500 | 518 | PF01044 | 0.393 |
LIG_WRC_WIRS_1 | 479 | 484 | PF05994 | 0.342 |
MOD_CDK_SPK_2 | 14 | 19 | PF00069 | 0.519 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.358 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.304 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.528 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.324 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.729 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.364 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.359 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.301 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.261 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.447 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.390 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.369 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.386 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.370 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.377 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.333 |
MOD_N-GLC_1 | 636 | 641 | PF02516 | 0.205 |
MOD_N-GLC_1 | 700 | 705 | PF02516 | 0.467 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.298 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.383 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.289 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.345 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.347 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.372 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.356 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.304 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.413 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.370 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.374 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.364 |
MOD_NEK2_2 | 478 | 483 | PF00069 | 0.342 |
MOD_OFUCOSY | 418 | 425 | PF10250 | 0.404 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.353 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.335 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.354 |
MOD_Plk_1 | 700 | 706 | PF00069 | 0.659 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.353 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.362 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.317 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.389 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.379 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.345 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.468 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.326 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.533 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.333 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.388 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.388 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.688 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.763 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.423 |
MOD_SUMO_rev_2 | 42 | 48 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 670 | 679 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 714 | 722 | PF00179 | 0.460 |
TRG_DiLeu_BaEn_4 | 370 | 376 | PF01217 | 0.203 |
TRG_DiLeu_BaLyEn_6 | 650 | 655 | PF01217 | 0.327 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.347 |
TRG_NES_CRM1_1 | 474 | 488 | PF08389 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 51% | 100% |
A0A0N1HY49 | Leptomonas seymouri | 53% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 40% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 44% | 100% |
A0A0N1PAY4 | Leptomonas seymouri | 49% | 82% |
A0A0N1PB77 | Leptomonas seymouri | 38% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 59% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 46% | 100% |
A0A381MBI0 | Leishmania infantum | 48% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 48% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 58% | 100% |
A0A3Q8IVN0 | Leishmania donovani | 40% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H5P4 | Leishmania donovani | 49% | 100% |
A0A3S5H5V2 | Leishmania donovani | 45% | 100% |
A0A3S5H6F6 | Leishmania donovani | 59% | 100% |
A0A3S5H763 | Leishmania donovani | 62% | 100% |
A0A3S7WR10 | Leishmania donovani | 49% | 97% |
A0A3S7WR14 | Leishmania donovani | 59% | 100% |
A0A3S7WR15 | Leishmania donovani | 56% | 85% |
A0A3S7WR24 | Leishmania donovani | 59% | 100% |
A4H4T8 | Leishmania braziliensis | 44% | 100% |
A4H5Y4 | Leishmania braziliensis | 49% | 100% |
A4H617 | Leishmania braziliensis | 58% | 100% |
A4H618 | Leishmania braziliensis | 58% | 100% |
A4H619 | Leishmania braziliensis | 58% | 100% |
A4H620 | Leishmania braziliensis | 82% | 100% |
A4H6C3 | Leishmania braziliensis | 47% | 98% |
A4HNH7 | Leishmania braziliensis | 37% | 96% |
A4HSS2 | Leishmania infantum | 49% | 100% |
A4HUE4 | Leishmania infantum | 50% | 100% |
A4HUE5 | Leishmania infantum | 58% | 100% |
A4HUE6 | Leishmania infantum | 60% | 100% |
A4HUE7 | Leishmania infantum | 58% | 100% |
A4HUE8 | Leishmania infantum | 59% | 100% |
A4HUF4 | Leishmania infantum | 59% | 100% |
A4HUF5 | Leishmania infantum | 99% | 100% |
A4HYA9 | Leishmania infantum | 60% | 100% |
A4IC33 | Leishmania infantum | 39% | 96% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 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) | 43% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 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) | 49% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 98% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 95% |
Q4QDC4 | Leishmania major | 60% | 100% |
Q4QH81 | Leishmania major | 46% | 98% |
Q4QHH7 | Leishmania major | 91% | 100% |
Q4QHH8 | Leishmania major | 58% | 100% |
Q4QHH9 | Leishmania major | 58% | 100% |
Q4QHI0 | Leishmania major | 59% | 100% |
Q4QHI1 | Leishmania major | 60% | 97% |
Q4QHI2 | Leishmania major | 58% | 97% |
Q4QIU9 | Leishmania major | 45% | 100% |
Q4QJ48 | Leishmania major | 49% | 100% |
Q7KIP2 | Leishmania major | 39% | 95% |