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:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7WSV4
Term | Name | Level | Count |
---|---|---|---|
GO:0000296 | spermine transport | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015695 | organic cation transport | 5 | 1 |
GO:0015846 | polyamine transport | 5 | 1 |
GO:0015847 | putrescine transport | 6 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:1902047 | polyamine transmembrane transport | 3 | 1 |
GO:1903710 | spermine transmembrane transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 9 |
GO:0015203 | polyamine transmembrane transporter activity | 3 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015101 | organic cation transmembrane transporter activity | 5 | 1 |
GO:0015489 | putrescine transmembrane transporter activity | 4 | 1 |
GO:0015606 | spermidine transmembrane transporter activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 551 | 555 | PF00656 | 0.776 |
CLV_C14_Caspase3-7 | 616 | 620 | PF00656 | 0.721 |
CLV_C14_Caspase3-7 | 635 | 639 | PF00656 | 0.667 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 793 | 795 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.458 |
CLV_PCSK_FUR_1 | 59 | 63 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.357 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.560 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.795 |
DEG_ODPH_VHL_1 | 209 | 222 | PF01847 | 0.376 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.339 |
DEG_SPOP_SBC_1 | 593 | 597 | PF00917 | 0.720 |
DEG_SPOP_SBC_1 | 742 | 746 | PF00917 | 0.742 |
DOC_CKS1_1 | 410 | 415 | PF01111 | 0.357 |
DOC_CYCLIN_RxL_1 | 444 | 454 | PF00134 | 0.357 |
DOC_CYCLIN_yCln2_LP_2 | 410 | 416 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 465 | 471 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 482 | 488 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 583 | 589 | PF00134 | 0.704 |
DOC_MAPK_DCC_7 | 409 | 419 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 56 | 66 | PF00069 | 0.749 |
DOC_MAPK_JIP1_4 | 467 | 473 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 264 | 271 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 309 | 316 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 59 | 68 | PF00069 | 0.736 |
DOC_MAPK_NFAT4_5 | 309 | 317 | PF00069 | 0.510 |
DOC_PP1_RVXF_1 | 270 | 277 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 583 | 586 | PF13499 | 0.787 |
DOC_PP2B_LxvP_1 | 587 | 590 | PF13499 | 0.742 |
DOC_PP2B_LxvP_1 | 759 | 762 | PF13499 | 0.767 |
DOC_PP2B_PxIxI_1 | 414 | 420 | PF00149 | 0.438 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.310 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.820 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 763 | 767 | PF00917 | 0.821 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 661 | 666 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 750 | 755 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 769 | 774 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.763 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.598 |
LIG_Actin_WH2_2 | 60 | 75 | PF00022 | 0.727 |
LIG_APCC_ABBAyCdc20_2 | 264 | 270 | PF00400 | 0.598 |
LIG_BIR_III_4 | 619 | 623 | PF00653 | 0.784 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.602 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.333 |
LIG_deltaCOP1_diTrp_1 | 357 | 364 | PF00928 | 0.344 |
LIG_eIF4E_1 | 444 | 450 | PF01652 | 0.357 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.357 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.487 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.345 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.388 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.459 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.811 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.667 |
LIG_FHA_1 | 783 | 789 | PF00498 | 0.772 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.438 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.638 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.795 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.746 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.777 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 278 | 288 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 518 | 526 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 461 | 465 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.759 |
LIG_LYPXL_yS_3 | 193 | 196 | PF13949 | 0.501 |
LIG_LYPXL_yS_3 | 462 | 465 | PF13949 | 0.560 |
LIG_MYND_2 | 747 | 751 | PF01753 | 0.734 |
LIG_NRBOX | 445 | 451 | PF00104 | 0.391 |
LIG_PDZ_Class_1 | 798 | 803 | PF00595 | 0.765 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.438 |
LIG_Pex14_1 | 276 | 280 | PF04695 | 0.560 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.363 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.531 |
LIG_PTB_Apo_2 | 187 | 194 | PF02174 | 0.501 |
LIG_PTB_Phospho_1 | 187 | 193 | PF10480 | 0.501 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.357 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.501 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.620 |
LIG_SH2_GRB2like | 287 | 290 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.598 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.548 |
LIG_SH2_PTP2 | 322 | 325 | PF00017 | 0.438 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.548 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 200 | 204 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.560 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.823 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.747 |
LIG_SH3_1 | 794 | 800 | PF00018 | 0.767 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.677 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.483 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.484 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.503 |
LIG_SH3_3 | 793 | 799 | PF00018 | 0.711 |
LIG_SUMO_SIM_anti_2 | 250 | 256 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 421 | 428 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 477 | 484 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 312 | 318 | PF11976 | 0.492 |
LIG_SxIP_EBH_1 | 409 | 420 | PF03271 | 0.438 |
LIG_TRAF2_1 | 565 | 568 | PF00917 | 0.766 |
LIG_TRAF2_1 | 625 | 628 | PF00917 | 0.819 |
LIG_TRAF2_1 | 711 | 714 | PF00917 | 0.803 |
LIG_TYR_ITIM | 266 | 271 | PF00017 | 0.548 |
LIG_TYR_ITIM | 450 | 455 | PF00017 | 0.357 |
LIG_TYR_ITIM | 460 | 465 | PF00017 | 0.501 |
LIG_UBA3_1 | 251 | 260 | PF00899 | 0.376 |
LIG_ULM_U2AF65_1 | 272 | 277 | PF00076 | 0.445 |
LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.514 |
LIG_WRC_WIRS_1 | 184 | 189 | PF05994 | 0.480 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.534 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.376 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.391 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.505 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.318 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.387 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.733 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.779 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.775 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.801 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.422 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.744 |
MOD_CK2_1 | 708 | 714 | PF00069 | 0.797 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.791 |
MOD_CMANNOS | 609 | 612 | PF00535 | 0.455 |
MOD_DYRK1A_RPxSP_1 | 771 | 775 | PF00069 | 0.771 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.492 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.301 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.357 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.425 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.569 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.391 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.477 |
MOD_GlcNHglycan | 554 | 558 | PF01048 | 0.457 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.379 |
MOD_GlcNHglycan | 6 | 10 | PF01048 | 0.578 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.608 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.579 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.574 |
MOD_GlcNHglycan | 725 | 729 | PF01048 | 0.596 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.599 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.576 |
MOD_GlcNHglycan | 785 | 788 | PF01048 | 0.491 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.501 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.501 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.357 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.436 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.360 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.542 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.296 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.806 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.770 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.795 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.785 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.769 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.778 |
MOD_LATS_1 | 3 | 9 | PF00433 | 0.744 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.301 |
MOD_N-GLC_1 | 604 | 609 | PF02516 | 0.550 |
MOD_N-GLC_1 | 649 | 654 | PF02516 | 0.590 |
MOD_N-GLC_1 | 788 | 793 | PF02516 | 0.573 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.554 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.340 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.401 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.353 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.355 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.298 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.325 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.679 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.438 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.586 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.793 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.797 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.799 |
MOD_NEK2_1 | 790 | 795 | PF00069 | 0.779 |
MOD_NEK2_2 | 678 | 683 | PF00069 | 0.780 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.749 |
MOD_PIKK_1 | 620 | 626 | PF00454 | 0.615 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.636 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.501 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.737 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.655 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.511 |
MOD_PKB_1 | 685 | 693 | PF00069 | 0.801 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.501 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.331 |
MOD_Plk_1 | 604 | 610 | PF00069 | 0.652 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.827 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.500 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.474 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.438 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.438 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.333 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.347 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.290 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.383 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.251 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.383 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.390 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.357 |
MOD_ProDKin_1 | 661 | 667 | PF00069 | 0.782 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.799 |
MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.790 |
MOD_ProDKin_1 | 750 | 756 | PF00069 | 0.757 |
MOD_ProDKin_1 | 769 | 775 | PF00069 | 0.781 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.765 |
TRG_DiLeu_BaLyEn_6 | 124 | 129 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 381 | 386 | PF01217 | 0.357 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.602 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 682 | 685 | PF00400 | 0.793 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.655 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3U3 | Leptomonas seymouri | 64% | 99% |
A0A3R7M6P3 | Trypanosoma rangeli | 62% | 100% |
A4H7J1 | Leishmania braziliensis | 79% | 99% |
A4HVX4 | Leishmania infantum | 100% | 100% |
E9APM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q5C8V6 | Leishmania major | 95% | 100% |
V5DDZ5 | Trypanosoma cruzi | 60% | 100% |