N-acetylglucosamine-1-phosphotransferase homologous protein. Assumed to be a type II TM protein like its distant relatives.. Signal-anchored glycan biogenesis protein essential for mannose 6-P generation (lysosomal signal for the Metazoan hosts). Family only expended in Leishmaniids.. Localization: Golgi (by homology)
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: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 125 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 32 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 38 |
NetGPI | no | yes: 0, no: 38 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0016020 | membrane | 2 | 19 |
Related structures:
AlphaFold database: Q4QER7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 37 |
GO:0016740 | transferase activity | 2 | 37 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 847 | 851 | PF00656 | 0.399 |
CLV_MEL_PAP_1 | 136 | 142 | PF00089 | 0.502 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.615 |
CLV_PCSK_FUR_1 | 456 | 460 | PF00082 | 0.535 |
CLV_PCSK_FUR_1 | 529 | 533 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 737 | 739 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 783 | 787 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.604 |
DEG_APCC_DBOX_1 | 238 | 246 | PF00400 | 0.437 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.558 |
DEG_SPOP_SBC_1 | 41 | 45 | PF00917 | 0.525 |
DEG_SPOP_SBC_1 | 65 | 69 | PF00917 | 0.598 |
DOC_CDC14_PxL_1 | 165 | 173 | PF14671 | 0.381 |
DOC_CKS1_1 | 616 | 621 | PF01111 | 0.629 |
DOC_CYCLIN_yCln2_LP_2 | 499 | 505 | PF00134 | 0.342 |
DOC_CYCLIN_yCln2_LP_2 | 837 | 843 | PF00134 | 0.426 |
DOC_MAPK_DCC_7 | 584 | 593 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 250 | 259 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 324 | 333 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 492 | 501 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 584 | 593 | PF00069 | 0.547 |
DOC_MAPK_HePTP_8 | 612 | 624 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 494 | 503 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 615 | 624 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 680 | 687 | PF00069 | 0.619 |
DOC_PP2B_LxvP_1 | 499 | 502 | PF13499 | 0.419 |
DOC_PP2B_LxvP_1 | 75 | 78 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 786 | 789 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 616 | 619 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 775 | 779 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 830 | 834 | PF00917 | 0.615 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 239 | 243 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 310 | 314 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 326 | 332 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 414 | 424 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 458 | 468 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 532 | 541 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 60 | 64 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 684 | 688 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 705 | 713 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 854 | 858 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 280 | 297 | PF00022 | 0.459 |
LIG_Actin_WH2_2 | 398 | 415 | PF00022 | 0.416 |
LIG_BRCT_BRCA1_1 | 516 | 520 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 642 | 646 | PF00533 | 0.626 |
LIG_eIF4E_1 | 400 | 406 | PF01652 | 0.489 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.592 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.464 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.316 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.618 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.453 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.610 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.691 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.472 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.495 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.474 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.434 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.448 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.573 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.599 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.537 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.306 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.548 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.473 |
LIG_Integrin_RGD_1 | 13 | 15 | PF01839 | 0.574 |
LIG_LIR_Apic_2 | 164 | 169 | PF02991 | 0.646 |
LIG_LIR_Apic_2 | 838 | 842 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 852 | 858 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 407 | 415 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 565 | 575 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 844 | 853 | PF02991 | 0.574 |
LIG_LIR_LC3C_4 | 809 | 814 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 618 | 624 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 796 | 801 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.607 |
LIG_MAD2 | 705 | 713 | PF02301 | 0.541 |
LIG_MYND_1 | 118 | 122 | PF01753 | 0.573 |
LIG_PTB_Apo_2 | 173 | 180 | PF02174 | 0.562 |
LIG_PTB_Apo_2 | 333 | 340 | PF02174 | 0.360 |
LIG_PTB_Apo_2 | 586 | 593 | PF02174 | 0.480 |
LIG_PTB_Phospho_1 | 173 | 179 | PF10480 | 0.414 |
LIG_PTB_Phospho_1 | 333 | 339 | PF10480 | 0.360 |
LIG_PTB_Phospho_1 | 586 | 592 | PF10480 | 0.511 |
LIG_REV1ctd_RIR_1 | 473 | 483 | PF16727 | 0.316 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.497 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.438 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.588 |
LIG_SH2_GRB2like | 209 | 212 | PF00017 | 0.414 |
LIG_SH2_GRB2like | 334 | 337 | PF00017 | 0.453 |
LIG_SH2_GRB2like | 592 | 595 | PF00017 | 0.515 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.589 |
LIG_SH2_SRC | 621 | 624 | PF00017 | 0.546 |
LIG_SH2_SRC | 660 | 663 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 480 | 484 | PF00017 | 0.222 |
LIG_SH2_STAT3 | 717 | 720 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.560 |
LIG_SH3_2 | 454 | 459 | PF14604 | 0.449 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.600 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.465 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.704 |
LIG_SH3_3 | 744 | 750 | PF00018 | 0.512 |
LIG_SUMO_SIM_anti_2 | 37 | 46 | PF11976 | 0.651 |
LIG_SUMO_SIM_anti_2 | 392 | 399 | PF11976 | 0.519 |
LIG_SUMO_SIM_anti_2 | 809 | 815 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 48 | 53 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 791 | 797 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 809 | 815 | PF11976 | 0.361 |
LIG_TRAF2_1 | 636 | 639 | PF00917 | 0.558 |
LIG_TRAF2_1 | 659 | 662 | PF00917 | 0.544 |
LIG_TYR_ITIM | 145 | 150 | PF00017 | 0.566 |
LIG_TYR_ITSM | 79 | 86 | PF00017 | 0.588 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.486 |
MOD_CDC14_SPxK_1 | 57 | 60 | PF00782 | 0.558 |
MOD_CDK_SPK_2 | 514 | 519 | PF00069 | 0.453 |
MOD_CDK_SPxK_1 | 54 | 60 | PF00069 | 0.558 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.398 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.428 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.552 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.440 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.634 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.506 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.445 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.559 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.552 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.306 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.571 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.496 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.568 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.463 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.574 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.609 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.605 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.560 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.642 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.431 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.517 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.686 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.498 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.625 |
MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.596 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.488 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.641 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.383 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.371 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.636 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.608 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.622 |
MOD_LATS_1 | 293 | 299 | PF00433 | 0.360 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.531 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.564 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.571 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.560 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.637 |
MOD_N-GLC_1 | 573 | 578 | PF02516 | 0.456 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.712 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.529 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.345 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.413 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.391 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.462 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.412 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.634 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.554 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.420 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.497 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.396 |
MOD_PIKK_1 | 539 | 545 | PF00454 | 0.488 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.602 |
MOD_PK_1 | 728 | 734 | PF00069 | 0.683 |
MOD_PKA_1 | 127 | 133 | PF00069 | 0.425 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.644 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.435 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.760 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.384 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.337 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.349 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.590 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.616 |
MOD_PKA_2 | 683 | 689 | PF00069 | 0.549 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.562 |
MOD_PKB_1 | 324 | 332 | PF00069 | 0.378 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.487 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.569 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.378 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.465 |
MOD_Plk_2-3 | 175 | 181 | PF00069 | 0.438 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.542 |
MOD_Plk_2-3 | 719 | 725 | PF00069 | 0.630 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.482 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.496 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.493 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.418 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.378 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.388 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.466 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.431 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.586 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.459 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.360 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.502 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.680 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.600 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.608 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.628 |
MOD_TYR_CSK | 104 | 112 | PF07714 | 0.576 |
TRG_DiLeu_BaEn_1 | 116 | 121 | PF01217 | 0.574 |
TRG_DiLeu_BaEn_1 | 832 | 837 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 116 | 122 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 846 | 849 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 489 | 492 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 529 | 532 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 608 | 610 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 760 | 763 | PF00400 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q7 | Leptomonas seymouri | 47% | 100% |
A0A1X0NYY7 | Trypanosomatidae | 44% | 100% |
A0A3Q8IAD3 | Leishmania donovani | 55% | 88% |
A0A3Q8IAF8 | Leishmania donovani | 75% | 89% |
A0A3Q8IAK8 | Leishmania donovani | 82% | 88% |
A0A3Q8IJ32 | Leishmania donovani | 83% | 100% |
A0A3S5H6Y1 | Leishmania donovani | 81% | 91% |
A0A3S7WTZ8 | Leishmania donovani | 62% | 83% |
A0A3S7WU13 | Leishmania donovani | 82% | 91% |
A0A422NAR5 | Trypanosoma rangeli | 43% | 100% |
A4H8M5 | Leishmania braziliensis | 69% | 95% |
A4H8M7 | Leishmania braziliensis | 73% | 93% |
A4H8N0 | Leishmania braziliensis | 48% | 100% |
A4H8N1 | Leishmania braziliensis | 50% | 88% |
A4HWZ5 | Leishmania infantum | 83% | 91% |
A4HWZ6 | Leishmania infantum | 79% | 94% |
A4HWZ8 | Leishmania infantum | 81% | 94% |
A4HX00 | Leishmania infantum | 62% | 83% |
A4HX01 | Leishmania infantum | 55% | 100% |
A4HX05 | Leishmania infantum | 77% | 89% |
E8NHI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 92% |
E9AGP0 | Leishmania infantum | 92% | 100% |
E9AQQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
E9AQR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 87% |
E9AQR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 92% |
E9AQR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 90% |
E9AQR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9AQR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 88% |
Q4QER2 | Leishmania major | 55% | 100% |
Q4QER3 | Leishmania major | 65% | 100% |
Q4QER4 | Leishmania major | 95% | 100% |
Q4QER5 | Leishmania major | 91% | 99% |
Q4QER6 | Leishmania major | 91% | 99% |
Q4QER8 | Leishmania major | 90% | 90% |
Q4QER9 | Leishmania major | 90% | 93% |
Q4QES0 | Leishmania major | 89% | 100% |
V5ANJ8 | Trypanosoma cruzi | 45% | 100% |