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. | no | yes: 0 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q5C8V6
Term | Name | Level | Count |
---|---|---|---|
GO:0000296 | spermine transport | 6 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015695 | organic cation transport | 5 | 2 |
GO:0015846 | polyamine transport | 5 | 2 |
GO:0015847 | putrescine transport | 6 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 2 |
GO:1902047 | polyamine transmembrane transport | 3 | 2 |
GO:1903710 | spermine transmembrane transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 9 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 2 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 2 |
GO:0015101 | organic cation transmembrane transporter activity | 5 | 2 |
GO:0015203 | polyamine transmembrane transporter activity | 3 | 9 |
GO:0015489 | putrescine transmembrane transporter activity | 4 | 2 |
GO:0015606 | spermidine transmembrane transporter activity | 4 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 552 | 556 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 616 | 620 | PF00656 | 0.655 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 793 | 795 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.390 |
CLV_PCSK_FUR_1 | 59 | 63 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.413 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.504 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.739 |
DEG_ODPH_VHL_1 | 209 | 222 | PF01847 | 0.261 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.276 |
DEG_SPOP_SBC_1 | 742 | 746 | PF00917 | 0.659 |
DOC_CKS1_1 | 410 | 415 | PF01111 | 0.268 |
DOC_CYCLIN_RxL_1 | 444 | 454 | PF00134 | 0.268 |
DOC_CYCLIN_yCln2_LP_2 | 410 | 416 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 465 | 471 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 482 | 488 | PF00134 | 0.268 |
DOC_CYCLIN_yCln2_LP_2 | 583 | 589 | PF00134 | 0.615 |
DOC_MAPK_DCC_7 | 409 | 419 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 56 | 66 | PF00069 | 0.693 |
DOC_MAPK_JIP1_4 | 467 | 473 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 264 | 271 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 309 | 316 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 59 | 68 | PF00069 | 0.674 |
DOC_MAPK_NFAT4_5 | 309 | 317 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 270 | 277 | PF00149 | 0.503 |
DOC_PP2B_LxvP_1 | 583 | 586 | PF13499 | 0.653 |
DOC_PP2B_LxvP_1 | 587 | 590 | PF13499 | 0.634 |
DOC_PP2B_LxvP_1 | 759 | 762 | PF13499 | 0.705 |
DOC_PP2B_PxIxI_1 | 414 | 420 | PF00149 | 0.360 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.268 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.246 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 763 | 767 | PF00917 | 0.796 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 661 | 666 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 750 | 755 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 769 | 774 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.705 |
LIG_14-3-3_CanoR_1 | 612 | 621 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 57 | 75 | PF00022 | 0.658 |
LIG_APCC_ABBAyCdc20_2 | 264 | 270 | PF00400 | 0.471 |
LIG_BIR_III_4 | 619 | 623 | PF00653 | 0.683 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.249 |
LIG_deltaCOP1_diTrp_1 | 357 | 364 | PF00928 | 0.283 |
LIG_eIF4E_1 | 444 | 450 | PF01652 | 0.268 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.268 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.461 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.268 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.363 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.474 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.672 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.585 |
LIG_FHA_1 | 783 | 789 | PF00498 | 0.679 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.360 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.667 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.683 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 278 | 288 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 518 | 526 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 461 | 465 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.685 |
LIG_LYPXL_yS_3 | 193 | 196 | PF13949 | 0.438 |
LIG_LYPXL_yS_3 | 462 | 465 | PF13949 | 0.504 |
LIG_MYND_2 | 747 | 751 | PF01753 | 0.651 |
LIG_NRBOX | 445 | 451 | PF00104 | 0.300 |
LIG_PDZ_Class_1 | 798 | 803 | PF00595 | 0.666 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.360 |
LIG_Pex14_1 | 276 | 280 | PF04695 | 0.504 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.273 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.467 |
LIG_PTB_Apo_2 | 187 | 194 | PF02174 | 0.438 |
LIG_PTB_Phospho_1 | 187 | 193 | PF10480 | 0.438 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.268 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.438 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.565 |
LIG_SH2_GRB2like | 287 | 290 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.484 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.487 |
LIG_SH2_PTP2 | 322 | 325 | PF00017 | 0.360 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.482 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 200 | 204 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.268 |
LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.504 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.495 |
LIG_SH3_1 | 794 | 800 | PF00018 | 0.661 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.438 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.427 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.364 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.747 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.631 |
LIG_SH3_3 | 793 | 799 | PF00018 | 0.639 |
LIG_SUMO_SIM_anti_2 | 250 | 256 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 421 | 428 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 477 | 484 | PF11976 | 0.312 |
LIG_SUMO_SIM_anti_2 | 641 | 650 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 312 | 318 | PF11976 | 0.368 |
LIG_SxIP_EBH_1 | 409 | 420 | PF03271 | 0.360 |
LIG_TRAF2_1 | 565 | 568 | PF00917 | 0.718 |
LIG_TRAF2_1 | 625 | 628 | PF00917 | 0.688 |
LIG_TRAF2_1 | 711 | 714 | PF00917 | 0.741 |
LIG_TYR_ITIM | 266 | 271 | PF00017 | 0.487 |
LIG_TYR_ITIM | 450 | 455 | PF00017 | 0.268 |
LIG_TYR_ITIM | 460 | 465 | PF00017 | 0.504 |
LIG_UBA3_1 | 251 | 260 | PF00899 | 0.261 |
LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.449 |
LIG_WRC_WIRS_1 | 184 | 189 | PF05994 | 0.421 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.462 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.300 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.300 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.493 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.238 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.296 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.726 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.717 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.698 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.707 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.676 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.796 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.337 |
MOD_CK2_1 | 708 | 714 | PF00069 | 0.738 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.734 |
MOD_DYRK1A_RPxSP_1 | 771 | 775 | PF00069 | 0.674 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.442 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.238 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.268 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.362 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.503 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.446 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.431 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.446 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.431 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.368 |
MOD_GlcNHglycan | 6 | 10 | PF01048 | 0.518 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.524 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.563 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.513 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.509 |
MOD_GlcNHglycan | 725 | 729 | PF01048 | 0.540 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.540 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.475 |
MOD_GlcNHglycan | 785 | 788 | PF01048 | 0.442 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.456 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.449 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.268 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.399 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.355 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.583 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.277 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.594 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.775 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.651 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.735 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.722 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.671 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.719 |
MOD_LATS_1 | 3 | 9 | PF00433 | 0.659 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.238 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.484 |
MOD_N-GLC_1 | 647 | 652 | PF02516 | 0.538 |
MOD_N-GLC_1 | 788 | 793 | PF02516 | 0.478 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.496 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.268 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.309 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.269 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.266 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.235 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.243 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.393 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.605 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.739 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.683 |
MOD_NEK2_1 | 790 | 795 | PF00069 | 0.682 |
MOD_NEK2_2 | 665 | 670 | PF00069 | 0.612 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.667 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.659 |
MOD_PIKK_1 | 620 | 626 | PF00454 | 0.600 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.438 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.604 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.668 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.616 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.447 |
MOD_PKB_1 | 685 | 693 | PF00069 | 0.740 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.438 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.267 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.599 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.690 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.445 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.429 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.399 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.360 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.260 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.273 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.229 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.320 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.192 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.361 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.300 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.629 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.268 |
MOD_ProDKin_1 | 661 | 667 | PF00069 | 0.719 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.747 |
MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.736 |
MOD_ProDKin_1 | 750 | 756 | PF00069 | 0.689 |
MOD_ProDKin_1 | 769 | 775 | PF00069 | 0.722 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.706 |
MOD_SUMO_rev_2 | 45 | 50 | PF00179 | 0.626 |
TRG_DiLeu_BaLyEn_6 | 124 | 129 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 381 | 386 | PF01217 | 0.289 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 682 | 685 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3U3 | Leptomonas seymouri | 64% | 99% |
A0A3R7M6P3 | Trypanosoma rangeli | 61% | 100% |
A0A3S7WSV4 | Leishmania donovani | 95% | 100% |
A4H7J1 | Leishmania braziliensis | 78% | 100% |
A4HVX4 | Leishmania infantum | 95% | 100% |
E9APM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DDZ5 | Trypanosoma cruzi | 60% | 100% |