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: Q4QDC4
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 | 333 | 337 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 523 | 525 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 651 | 653 | PF00082 | 0.304 |
CLV_PCSK_PC7_1 | 190 | 196 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.431 |
DEG_APCC_DBOX_1 | 95 | 103 | PF00400 | 0.426 |
DEG_ODPH_VHL_1 | 622 | 634 | PF01847 | 0.354 |
DEG_SPOP_SBC_1 | 299 | 303 | PF00917 | 0.395 |
DOC_CDC14_PxL_1 | 609 | 617 | PF14671 | 0.329 |
DOC_CKS1_1 | 602 | 607 | PF01111 | 0.195 |
DOC_CYCLIN_yCln2_LP_2 | 626 | 632 | PF00134 | 0.373 |
DOC_CYCLIN_yCln2_LP_2 | 633 | 639 | PF00134 | 0.340 |
DOC_MAPK_gen_1 | 259 | 269 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 287 | 294 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 40 | 48 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 523 | 531 | PF00069 | 0.320 |
DOC_MAPK_HePTP_8 | 494 | 506 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 497 | 506 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 523 | 531 | PF00069 | 0.355 |
DOC_PP2B_LxvP_1 | 444 | 447 | PF13499 | 0.370 |
DOC_PP2B_LxvP_1 | 626 | 629 | PF13499 | 0.360 |
DOC_PP2B_LxvP_1 | 632 | 635 | PF13499 | 0.326 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 651 | 655 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.346 |
LIG_14-3-3_CanoR_1 | 106 | 113 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 501 | 505 | PF00244 | 0.492 |
LIG_APCC_ABBA_1 | 250 | 255 | PF00400 | 0.401 |
LIG_APCC_ABBA_1 | 52 | 57 | PF00400 | 0.636 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.758 |
LIG_BRCT_BRCA1_1 | 467 | 471 | PF00533 | 0.314 |
LIG_CSL_BTD_1 | 552 | 555 | PF09270 | 0.393 |
LIG_eIF4E_1 | 87 | 93 | PF01652 | 0.395 |
LIG_EVH1_2 | 605 | 609 | PF00568 | 0.358 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.574 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.617 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.469 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.390 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.265 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.492 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.484 |
LIG_GBD_Chelix_1 | 505 | 513 | PF00786 | 0.472 |
LIG_HP1_1 | 555 | 559 | PF01393 | 0.395 |
LIG_LIR_Apic_2 | 32 | 37 | PF02991 | 0.595 |
LIG_LIR_Apic_2 | 421 | 426 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 126 | 133 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 489 | 495 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 515 | 522 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 570 | 580 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 608 | 617 | PF02991 | 0.271 |
LIG_LIR_LC3C_4 | 503 | 506 | PF02991 | 0.202 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 421 | 425 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 468 | 472 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 515 | 520 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 552 | 556 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 596 | 602 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 608 | 612 | PF02991 | 0.266 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.370 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.361 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.487 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.308 |
LIG_Pex14_2 | 491 | 495 | PF04695 | 0.367 |
LIG_PTB_Apo_2 | 489 | 496 | PF02174 | 0.436 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.510 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.512 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.343 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.687 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.300 |
LIG_SH2_NCK_1 | 472 | 476 | PF00017 | 0.298 |
LIG_SH2_PTP2 | 34 | 37 | PF00017 | 0.591 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 87 | 90 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.525 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.597 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.286 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.310 |
LIG_SUMO_SIM_anti_2 | 179 | 185 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 502 | 508 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 555 | 561 | PF11976 | 0.324 |
LIG_TRAF2_1 | 456 | 459 | PF00917 | 0.195 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.295 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.329 |
LIG_TYR_ITSM | 468 | 475 | PF00017 | 0.400 |
LIG_UBA3_1 | 151 | 159 | PF00899 | 0.349 |
LIG_Vh1_VBS_1 | 392 | 410 | PF01044 | 0.445 |
LIG_WRC_WIRS_1 | 450 | 455 | PF05994 | 0.331 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.357 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.289 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.510 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.284 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.306 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.354 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.314 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.606 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.641 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.418 |
MOD_CMANNOS | 205 | 208 | PF00535 | 0.248 |
MOD_GlcNHglycan | 160 | 164 | PF01048 | 0.359 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.391 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.426 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.692 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.278 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.403 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.309 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.357 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.361 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.375 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.366 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.377 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.371 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.609 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.374 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.336 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.346 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.418 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.362 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.375 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.370 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.302 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.358 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.363 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.351 |
MOD_NEK2_2 | 449 | 454 | PF00069 | 0.332 |
MOD_PK_1 | 106 | 112 | PF00069 | 0.449 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.327 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.349 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.330 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.272 |
MOD_Plk_2-3 | 344 | 350 | PF00069 | 0.298 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.342 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.333 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.357 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.416 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.393 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.335 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.461 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.341 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.322 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.312 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.394 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.335 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.378 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.314 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.454 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.414 |
MOD_SUMO_for_1 | 650 | 653 | PF00179 | 0.373 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.271 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.588 |
TRG_NES_CRM1_1 | 358 | 372 | PF08389 | 0.225 |
TRG_NES_CRM1_1 | 445 | 459 | PF08389 | 0.297 |
TRG_NES_CRM1_1 | 584 | 596 | PF08389 | 0.367 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 50% | 95% |
A0A0N1HY49 | Leptomonas seymouri | 53% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 43% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 45% | 94% |
A0A0N1PAY4 | Leptomonas seymouri | 50% | 76% |
A0A0N1PB77 | Leptomonas seymouri | 42% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 53% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 49% | 100% |
A0A381MBI0 | Leishmania infantum | 47% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 47% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 52% | 96% |
A0A3Q8IH50 | Leishmania donovani | 60% | 93% |
A0A3Q8IVN0 | Leishmania donovani | 42% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5P4 | Leishmania donovani | 49% | 99% |
A0A3S5H5V2 | Leishmania donovani | 46% | 100% |
A0A3S5H6F6 | Leishmania donovani | 51% | 96% |
A0A3S5H763 | Leishmania donovani | 95% | 100% |
A0A3S7WR10 | Leishmania donovani | 48% | 90% |
A0A3S7WR14 | Leishmania donovani | 55% | 98% |
A0A3S7WR15 | Leishmania donovani | 52% | 79% |
A0A3S7WR24 | Leishmania donovani | 51% | 95% |
A4H4T8 | Leishmania braziliensis | 47% | 100% |
A4H5Y4 | Leishmania braziliensis | 48% | 100% |
A4H617 | Leishmania braziliensis | 52% | 96% |
A4H618 | Leishmania braziliensis | 51% | 98% |
A4H619 | Leishmania braziliensis | 51% | 96% |
A4H620 | Leishmania braziliensis | 60% | 95% |
A4H6C3 | Leishmania braziliensis | 48% | 100% |
A4HNH7 | Leishmania braziliensis | 40% | 100% |
A4HSS2 | Leishmania infantum | 50% | 99% |
A4HUE4 | Leishmania infantum | 48% | 90% |
A4HUE5 | Leishmania infantum | 51% | 97% |
A4HUE6 | Leishmania infantum | 55% | 98% |
A4HUE7 | Leishmania infantum | 52% | 96% |
A4HUE8 | Leishmania infantum | 51% | 95% |
A4HUF4 | Leishmania infantum | 51% | 96% |
A4HUF5 | Leishmania infantum | 60% | 100% |
A4HYA9 | Leishmania infantum | 96% | 100% |
A4IC33 | Leishmania infantum | 42% | 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) | 40% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 96% |
E9AG72 | Leishmania infantum | 46% | 100% |
E9AI40 | Leishmania braziliensis | 53% | 99% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 99% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 90% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 94% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
Q4QH81 | Leishmania major | 45% | 100% |
Q4QHH7 | Leishmania major | 61% | 94% |
Q4QHH8 | Leishmania major | 51% | 92% |
Q4QHH9 | Leishmania major | 51% | 95% |
Q4QHI0 | Leishmania major | 51% | 97% |
Q4QHI1 | Leishmania major | 55% | 100% |
Q4QHI2 | Leishmania major | 52% | 100% |
Q4QIU9 | Leishmania major | 46% | 100% |
Q4QJ48 | Leishmania major | 52% | 99% |
Q7KIP2 | Leishmania major | 40% | 99% |