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: A0A3S5H763
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_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.725 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.371 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.268 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.274 |
CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 652 | 654 | PF00082 | 0.283 |
CLV_PCSK_PC7_1 | 191 | 197 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.412 |
DEG_ODPH_VHL_1 | 623 | 635 | PF01847 | 0.325 |
DEG_SPOP_SBC_1 | 300 | 304 | PF00917 | 0.393 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.188 |
DOC_CDC14_PxL_1 | 610 | 618 | PF14671 | 0.309 |
DOC_CKS1_1 | 603 | 608 | PF01111 | 0.190 |
DOC_CYCLIN_yCln2_LP_2 | 627 | 633 | PF00134 | 0.345 |
DOC_CYCLIN_yCln2_LP_2 | 634 | 640 | PF00134 | 0.312 |
DOC_MAPK_gen_1 | 260 | 270 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 288 | 295 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 41 | 49 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 524 | 532 | PF00069 | 0.300 |
DOC_MAPK_HePTP_8 | 495 | 507 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 41 | 49 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 498 | 507 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 524 | 532 | PF00069 | 0.337 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.341 |
DOC_PP2B_LxvP_1 | 627 | 630 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 633 | 636 | PF13499 | 0.299 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 652 | 656 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 107 | 114 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.468 |
LIG_Actin_WH2_2 | 310 | 328 | PF00022 | 0.380 |
LIG_APCC_ABBA_1 | 251 | 256 | PF00400 | 0.374 |
LIG_APCC_ABBA_1 | 53 | 58 | PF00400 | 0.625 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.294 |
LIG_CSL_BTD_1 | 553 | 556 | PF09270 | 0.365 |
LIG_eIF4E_1 | 88 | 94 | PF01652 | 0.390 |
LIG_EVH1_2 | 606 | 610 | PF00568 | 0.340 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.552 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.616 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.451 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.323 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.240 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.469 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.553 |
LIG_HP1_1 | 556 | 560 | PF01393 | 0.367 |
LIG_LIR_Apic_2 | 32 | 38 | PF02991 | 0.596 |
LIG_LIR_Apic_2 | 422 | 427 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 127 | 134 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 186 | 197 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 490 | 496 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 516 | 523 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 571 | 581 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 609 | 618 | PF02991 | 0.249 |
LIG_LIR_LC3C_4 | 504 | 507 | PF02991 | 0.195 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 469 | 473 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 490 | 495 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 553 | 557 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 609 | 613 | PF02991 | 0.245 |
LIG_Pex14_1 | 206 | 210 | PF04695 | 0.342 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.332 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.468 |
LIG_Pex14_2 | 468 | 472 | PF04695 | 0.287 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.339 |
LIG_PTB_Apo_2 | 490 | 497 | PF02174 | 0.413 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.489 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.491 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.313 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.280 |
LIG_SH2_NCK_1 | 473 | 477 | PF00017 | 0.278 |
LIG_SH2_PTP2 | 35 | 38 | PF00017 | 0.591 |
LIG_SH2_PTP2 | 44 | 47 | PF00017 | 0.584 |
LIG_SH2_SRC | 35 | 38 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 574 | 578 | PF00017 | 0.307 |
LIG_SH2_STAT3 | 88 | 91 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.504 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.587 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.529 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.263 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.290 |
LIG_SUMO_SIM_par_1 | 503 | 510 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 556 | 562 | PF11976 | 0.297 |
LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.190 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.272 |
LIG_TYR_ITIM | 442 | 447 | PF00017 | 0.302 |
LIG_TYR_ITSM | 469 | 476 | PF00017 | 0.372 |
LIG_UBA3_1 | 152 | 160 | PF00899 | 0.301 |
LIG_Vh1_VBS_1 | 382 | 400 | PF01044 | 0.377 |
LIG_Vh1_VBS_1 | 472 | 490 | PF01044 | 0.354 |
LIG_WRC_WIRS_1 | 451 | 456 | PF05994 | 0.303 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.329 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.243 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.263 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.271 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.319 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.288 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.576 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.612 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.393 |
MOD_CMANNOS | 206 | 209 | PF00535 | 0.232 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.260 |
MOD_GlcNHglycan | 161 | 165 | PF01048 | 0.326 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.394 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.401 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.661 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.376 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.268 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.386 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.342 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.346 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.331 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.357 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.341 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.578 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.343 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.258 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.306 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.335 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.425 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.339 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.270 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.330 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.334 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.322 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.305 |
MOD_NEK2_2 | 487 | 492 | PF00069 | 0.188 |
MOD_OFUCOSY | 390 | 397 | PF10250 | 0.365 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.619 |
MOD_PK_1 | 107 | 113 | PF00069 | 0.428 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.344 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.317 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.303 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.251 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.273 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.313 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.305 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.323 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.387 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.362 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.307 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.442 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.313 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.296 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.288 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.349 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.307 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.349 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.288 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.471 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.387 |
MOD_SUMO_for_1 | 651 | 654 | PF00179 | 0.345 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.240 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.581 |
TRG_NES_CRM1_1 | 359 | 373 | PF08389 | 0.212 |
TRG_NES_CRM1_1 | 446 | 460 | PF08389 | 0.273 |
TRG_NES_CRM1_1 | 585 | 597 | PF08389 | 0.339 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 50% | 96% |
A0A0N1HY49 | Leptomonas seymouri | 55% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 43% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 46% | 94% |
A0A0N1PAY4 | Leptomonas seymouri | 49% | 76% |
A0A0N1PB77 | Leptomonas seymouri | 42% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 54% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 48% | 100% |
A0A381MBI0 | Leishmania infantum | 48% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 48% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 52% | 100% |
A0A3Q8IH50 | Leishmania donovani | 62% | 100% |
A0A3Q8IVN0 | Leishmania donovani | 42% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 41% | 100% |
A0A3S5H5P4 | Leishmania donovani | 49% | 100% |
A0A3S5H5V2 | Leishmania donovani | 45% | 100% |
A0A3S5H6F6 | Leishmania donovani | 51% | 100% |
A0A3S7WR10 | Leishmania donovani | 47% | 90% |
A0A3S7WR14 | Leishmania donovani | 56% | 98% |
A0A3S7WR15 | Leishmania donovani | 52% | 79% |
A0A3S7WR24 | Leishmania donovani | 52% | 96% |
A4H4T8 | Leishmania braziliensis | 45% | 99% |
A4H5Y4 | Leishmania braziliensis | 48% | 100% |
A4H617 | Leishmania braziliensis | 53% | 100% |
A4H618 | Leishmania braziliensis | 52% | 100% |
A4H619 | Leishmania braziliensis | 53% | 100% |
A4H620 | Leishmania braziliensis | 62% | 100% |
A4H6C3 | Leishmania braziliensis | 48% | 100% |
A4HNH7 | Leishmania braziliensis | 40% | 96% |
A4HSS2 | Leishmania infantum | 49% | 100% |
A4HUE4 | Leishmania infantum | 48% | 100% |
A4HUE5 | Leishmania infantum | 53% | 100% |
A4HUE6 | Leishmania infantum | 55% | 100% |
A4HUE7 | Leishmania infantum | 52% | 100% |
A4HUE8 | Leishmania infantum | 51% | 100% |
A4HUF4 | Leishmania infantum | 51% | 100% |
A4HUF5 | Leishmania infantum | 62% | 100% |
A4HYA9 | Leishmania infantum | 99% | 100% |
A4IC33 | Leishmania infantum | 43% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 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) | 42% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AG72 | Leishmania infantum | 45% | 100% |
E9AI40 | Leishmania braziliensis | 52% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 99% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
Q4QDC4 | Leishmania major | 95% | 100% |
Q4QH81 | Leishmania major | 47% | 100% |
Q4QHH7 | Leishmania major | 62% | 100% |
Q4QHH8 | Leishmania major | 51% | 100% |
Q4QHH9 | Leishmania major | 51% | 100% |
Q4QHI0 | Leishmania major | 52% | 100% |
Q4QHI1 | Leishmania major | 56% | 100% |
Q4QHI2 | Leishmania major | 53% | 100% |
Q4QIU9 | Leishmania major | 44% | 99% |
Q4QJ48 | Leishmania major | 49% | 100% |
Q7KIP2 | Leishmania major | 41% | 100% |