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. | yes | yes: 52 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | 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:0005737 | cytoplasm | 2 | 7 |
GO:0016020 | membrane | 2 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: Q4QHI0
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 | 658 | 662 | PF00656 | 0.833 |
CLV_MEL_PAP_1 | 431 | 437 | PF00089 | 0.318 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.486 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 512 | 514 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.416 |
DEG_SPOP_SBC_1 | 656 | 660 | PF00917 | 0.669 |
DOC_CDC14_PxL_1 | 602 | 610 | PF14671 | 0.399 |
DOC_CKS1_1 | 614 | 619 | PF01111 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 619 | 625 | PF00134 | 0.445 |
DOC_MAPK_gen_1 | 126 | 132 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 250 | 260 | PF00069 | 0.616 |
DOC_MAPK_gen_1 | 512 | 520 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 630 | 639 | PF00069 | 0.655 |
DOC_MAPK_MEF2A_6 | 220 | 227 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 512 | 520 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 488 | 494 | PF00149 | 0.587 |
DOC_PP2B_LxvP_1 | 619 | 622 | PF13499 | 0.432 |
DOC_PP2B_PxIxI_1 | 220 | 226 | PF00149 | 0.355 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.840 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 250 | 260 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 490 | 494 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.494 |
LIG_APCC_ABBA_1 | 43 | 48 | PF00400 | 0.706 |
LIG_APCC_ABBAyCdc20_2 | 42 | 48 | PF00400 | 0.577 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.860 |
LIG_BIR_III_4 | 17 | 21 | PF00653 | 0.659 |
LIG_Clathr_ClatBox_1 | 258 | 262 | PF01394 | 0.515 |
LIG_EH1_1 | 492 | 500 | PF00400 | 0.409 |
LIG_eIF4E_1 | 602 | 608 | PF01652 | 0.298 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.637 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.405 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.658 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.424 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.326 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.462 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.559 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.485 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.638 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.295 |
LIG_GBD_Chelix_1 | 471 | 479 | PF00786 | 0.300 |
LIG_GBD_Chelix_1 | 494 | 502 | PF00786 | 0.542 |
LIG_GBD_Chelix_1 | 532 | 540 | PF00786 | 0.572 |
LIG_LIR_Apic_2 | 22 | 28 | PF02991 | 0.701 |
LIG_LIR_Apic_2 | 341 | 347 | PF02991 | 0.597 |
LIG_LIR_Apic_2 | 409 | 415 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 585 | 589 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 117 | 124 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 195 | 202 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 478 | 485 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 559 | 568 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 80 | 88 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 457 | 461 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.410 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.433 |
LIG_Pex14_2 | 456 | 460 | PF04695 | 0.378 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.440 |
LIG_PTB_Apo_2 | 452 | 459 | PF02174 | 0.440 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.507 |
LIG_PTB_Phospho_1 | 452 | 458 | PF10480 | 0.473 |
LIG_SH2_CRK | 129 | 133 | PF00017 | 0.443 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.395 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.582 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.686 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.413 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.396 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.370 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.393 |
LIG_SH2_CRK | 602 | 606 | PF00017 | 0.425 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.580 |
LIG_SH2_GRB2like | 602 | 605 | PF00017 | 0.419 |
LIG_SH2_NCK_1 | 327 | 331 | PF00017 | 0.504 |
LIG_SH2_PTP2 | 25 | 28 | PF00017 | 0.693 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.699 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.507 |
LIG_SH2_SRC | 331 | 334 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.595 |
LIG_SH3_1 | 344 | 350 | PF00018 | 0.653 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.664 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.427 |
LIG_SUMO_SIM_anti_2 | 507 | 512 | PF11976 | 0.388 |
LIG_SUMO_SIM_anti_2 | 616 | 622 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 473 | 478 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 544 | 550 | PF11976 | 0.397 |
LIG_TRFH_1 | 144 | 148 | PF08558 | 0.429 |
LIG_TYR_ITIM | 142 | 147 | PF00017 | 0.449 |
LIG_TYR_ITSM | 457 | 464 | PF00017 | 0.472 |
LIG_UBA3_1 | 142 | 150 | PF00899 | 0.427 |
LIG_UBA3_1 | 258 | 266 | PF00899 | 0.589 |
LIG_UBA3_1 | 479 | 486 | PF00899 | 0.484 |
LIG_UBA3_1 | 625 | 630 | PF00899 | 0.303 |
LIG_Vh1_VBS_1 | 370 | 388 | PF01044 | 0.476 |
LIG_Vh1_VBS_1 | 460 | 478 | PF01044 | 0.454 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.415 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.314 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.686 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.430 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.500 |
MOD_Cter_Amidation | 290 | 293 | PF01082 | 0.538 |
MOD_DYRK1A_RPxSP_1 | 434 | 438 | PF00069 | 0.484 |
MOD_GlcNHglycan | 151 | 155 | PF01048 | 0.427 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.440 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.595 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.387 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.510 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.489 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.548 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.442 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.317 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.447 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.432 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.442 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.702 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.475 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.424 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.444 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.351 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.406 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.394 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.478 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.440 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.366 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.521 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.431 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.435 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.423 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.517 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.537 |
MOD_OFUCOSY | 158 | 165 | PF10250 | 0.280 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.395 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.575 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.527 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.417 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.402 |
MOD_PKB_1 | 268 | 276 | PF00069 | 0.282 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.441 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.414 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.405 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.585 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.423 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.462 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.531 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.394 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.274 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.413 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.449 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.449 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.542 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.399 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.482 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.295 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 16 | 26 | PF00179 | 0.651 |
MOD_SUMO_rev_2 | 635 | 644 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_2 | 254 | 260 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 603 | 608 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 614 | 619 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 250 | 255 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 98% |
A0A0N1HY49 | Leptomonas seymouri | 46% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 34% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 37% | 97% |
A0A0N1PAY4 | Leptomonas seymouri | 45% | 79% |
A0A0N1PB77 | Leptomonas seymouri | 34% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 67% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 42% | 100% |
A0A381MBI0 | Leishmania infantum | 44% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 44% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 95% | 99% |
A0A3Q8IH50 | Leishmania donovani | 59% | 96% |
A0A3Q8IVN0 | Leishmania donovani | 37% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 42% | 100% |
A0A3S5H5P4 | Leishmania donovani | 43% | 100% |
A0A3S5H5V2 | Leishmania donovani | 44% | 100% |
A0A3S5H6F6 | Leishmania donovani | 91% | 99% |
A0A3S5H763 | Leishmania donovani | 52% | 100% |
A0A3S7WR10 | Leishmania donovani | 43% | 93% |
A0A3S7WR14 | Leishmania donovani | 82% | 100% |
A0A3S7WR15 | Leishmania donovani | 71% | 81% |
A0A3S7WR24 | Leishmania donovani | 88% | 98% |
A4H4T8 | Leishmania braziliensis | 42% | 100% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 79% | 99% |
A4H618 | Leishmania braziliensis | 80% | 100% |
A4H619 | Leishmania braziliensis | 80% | 99% |
A4H620 | Leishmania braziliensis | 57% | 98% |
A4H6C3 | Leishmania braziliensis | 42% | 100% |
A4HNH7 | Leishmania braziliensis | 35% | 100% |
A4HSS2 | Leishmania infantum | 43% | 100% |
A4HUE4 | Leishmania infantum | 43% | 93% |
A4HUE5 | Leishmania infantum | 71% | 100% |
A4HUE6 | Leishmania infantum | 83% | 100% |
A4HUE7 | Leishmania infantum | 95% | 99% |
A4HUE8 | Leishmania infantum | 88% | 98% |
A4HUF4 | Leishmania infantum | 89% | 99% |
A4HUF5 | Leishmania infantum | 59% | 100% |
A4HYA9 | Leishmania infantum | 52% | 100% |
A4IC33 | Leishmania infantum | 35% | 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) | 39% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
E9AG72 | Leishmania infantum | 44% | 100% |
E9AI40 | Leishmania braziliensis | 74% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 93% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 97% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4QDC4 | Leishmania major | 51% | 99% |
Q4QH81 | Leishmania major | 44% | 100% |
Q4QHH7 | Leishmania major | 59% | 100% |
Q4QHH8 | Leishmania major | 91% | 100% |
Q4QHH9 | Leishmania major | 90% | 100% |
Q4QHI1 | Leishmania major | 88% | 100% |
Q4QHI2 | Leishmania major | 79% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 42% | 100% |
Q7KIP2 | Leishmania major | 36% | 98% |