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: 1, no: 5 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034702 | monoatomic ion channel complex | 4 | 1 |
GO:0034703 | cation channel complex | 5 | 1 |
GO:0034704 | calcium channel complex | 6 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
GO:1902495 | transmembrane transporter complex | 3 | 1 |
GO:1990246 | uniplex complex | 4 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
Related structures:
AlphaFold database: E9AVS4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0006811 | monoatomic ion transport | 4 | 7 |
GO:0006812 | monoatomic cation transport | 5 | 7 |
GO:0006816 | calcium ion transport | 7 | 7 |
GO:0006851 | mitochondrial calcium ion transmembrane transport | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0030001 | metal ion transport | 6 | 7 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0055085 | transmembrane transport | 2 | 7 |
GO:0070588 | calcium ion transmembrane transport | 6 | 7 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 7 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 7 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 7 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 7 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0036444 | calcium import into the mitochondrion | 5 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051560 | mitochondrial calcium ion homeostasis | 8 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055074 | calcium ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 752 | 756 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 815 | 819 | PF00656 | 0.489 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.391 |
CLV_PCSK_FUR_1 | 3 | 7 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 847 | 849 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 847 | 849 | PF00082 | 0.571 |
CLV_PCSK_PC7_1 | 617 | 623 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 805 | 809 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 832 | 836 | PF00082 | 0.474 |
CLV_Separin_Metazoa | 678 | 682 | PF03568 | 0.393 |
DEG_APCC_DBOX_1 | 587 | 595 | PF00400 | 0.370 |
DEG_APCC_DBOX_1 | 665 | 673 | PF00400 | 0.548 |
DEG_SCF_FBW7_1 | 319 | 325 | PF00400 | 0.436 |
DEG_SCF_TRCP1_1 | 239 | 244 | PF00400 | 0.549 |
DOC_CDC14_PxL_1 | 574 | 582 | PF14671 | 0.374 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.474 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.588 |
DOC_CYCLIN_RxL_1 | 3 | 11 | PF00134 | 0.461 |
DOC_CYCLIN_RxL_1 | 508 | 518 | PF00134 | 0.539 |
DOC_CYCLIN_RxL_1 | 805 | 815 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 455 | 461 | PF00134 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 464 | 470 | PF00134 | 0.436 |
DOC_MAPK_gen_1 | 3 | 10 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 441 | 449 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 805 | 812 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 660 | 669 | PF00069 | 0.457 |
DOC_PP1_RVXF_1 | 590 | 597 | PF00149 | 0.378 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.424 |
DOC_PP4_FxxP_1 | 598 | 601 | PF00568 | 0.314 |
DOC_PP4_FxxP_1 | 843 | 846 | PF00568 | 0.495 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 846 | 850 | PF00917 | 0.386 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 741 | 746 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.401 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 328 | 333 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 492 | 500 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 621 | 625 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 73 | 78 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 770 | 779 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 827 | 832 | PF00244 | 0.381 |
LIG_Actin_WH2_2 | 577 | 594 | PF00022 | 0.359 |
LIG_Actin_WH2_2 | 665 | 683 | PF00022 | 0.492 |
LIG_Actin_WH2_2 | 694 | 709 | PF00022 | 0.445 |
LIG_BIR_III_2 | 469 | 473 | PF00653 | 0.469 |
LIG_BIR_III_2 | 670 | 674 | PF00653 | 0.481 |
LIG_BIR_III_4 | 755 | 759 | PF00653 | 0.485 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.643 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.584 |
LIG_deltaCOP1_diTrp_1 | 343 | 346 | PF00928 | 0.439 |
LIG_eIF4E_1 | 771 | 777 | PF01652 | 0.346 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.545 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.563 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.654 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.497 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.442 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.591 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.539 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.590 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.589 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.626 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.554 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.523 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.674 |
LIG_FHA_2 | 750 | 756 | PF00498 | 0.628 |
LIG_Integrin_RGD_1 | 617 | 619 | PF01839 | 0.489 |
LIG_LIR_Apic_2 | 595 | 601 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 311 | 319 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 343 | 354 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 783 | 792 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 824 | 831 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 644 | 648 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 783 | 787 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 824 | 828 | PF02991 | 0.299 |
LIG_LYPXL_yS_3 | 577 | 580 | PF13949 | 0.377 |
LIG_Pex14_2 | 312 | 316 | PF04695 | 0.233 |
LIG_SH2_CRK | 648 | 652 | PF00017 | 0.312 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 708 | 712 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 771 | 774 | PF00017 | 0.369 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.371 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.576 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.388 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.399 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.681 |
LIG_SUMO_SIM_par_1 | 163 | 170 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 204 | 210 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 215 | 222 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 351 | 356 | PF11976 | 0.445 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.495 |
LIG_TYR_ITIM | 575 | 580 | PF00017 | 0.370 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.463 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.393 |
LIG_WRC_WIRS_1 | 315 | 320 | PF05994 | 0.363 |
MOD_CDK_SPK_2 | 487 | 492 | PF00069 | 0.559 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.605 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.535 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.511 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.597 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.262 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.587 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.602 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.579 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.480 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.590 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.624 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.501 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.447 |
MOD_CK1_1 | 744 | 750 | PF00069 | 0.647 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.531 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.637 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.347 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.572 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.579 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.611 |
MOD_CK2_1 | 798 | 804 | PF00069 | 0.409 |
MOD_CK2_1 | 818 | 824 | PF00069 | 0.269 |
MOD_CK2_1 | 827 | 833 | PF00069 | 0.411 |
MOD_CMANNOS | 506 | 509 | PF00535 | 0.597 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.552 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.633 |
MOD_GlcNHglycan | 17 | 21 | PF01048 | 0.577 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.630 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.594 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.482 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.559 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.676 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.633 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.534 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.601 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.685 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.781 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.511 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.481 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.555 |
MOD_GlcNHglycan | 772 | 775 | PF01048 | 0.424 |
MOD_GlcNHglycan | 848 | 851 | PF01048 | 0.378 |
MOD_GlcNHglycan | 93 | 97 | PF01048 | 0.397 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.692 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.488 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.472 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.361 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.685 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.520 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.557 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.682 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.710 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.670 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.503 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.525 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.408 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.600 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.461 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.574 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.479 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.480 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.642 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.490 |
MOD_NEK2_1 | 772 | 777 | PF00069 | 0.420 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.682 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.503 |
MOD_NEK2_2 | 80 | 85 | PF00069 | 0.430 |
MOD_OFUCOSY | 527 | 532 | PF10250 | 0.634 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.566 |
MOD_PIKK_1 | 492 | 498 | PF00454 | 0.608 |
MOD_PIKK_1 | 557 | 563 | PF00454 | 0.462 |
MOD_PIKK_1 | 691 | 697 | PF00454 | 0.514 |
MOD_PIKK_1 | 730 | 736 | PF00454 | 0.667 |
MOD_PIKK_1 | 795 | 801 | PF00454 | 0.478 |
MOD_PK_1 | 328 | 334 | PF00069 | 0.425 |
MOD_PK_1 | 73 | 79 | PF00069 | 0.591 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.501 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.597 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.437 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.541 |
MOD_PKA_2 | 655 | 661 | PF00069 | 0.395 |
MOD_PKA_2 | 706 | 712 | PF00069 | 0.453 |
MOD_PKA_2 | 777 | 783 | PF00069 | 0.375 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.466 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.437 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.517 |
MOD_Plk_1 | 567 | 573 | PF00069 | 0.473 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.493 |
MOD_Plk_2-3 | 157 | 163 | PF00069 | 0.617 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.466 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.551 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.443 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.400 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.448 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.487 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.348 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.421 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.532 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.467 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.678 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.563 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.635 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.600 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.760 |
MOD_ProDKin_1 | 741 | 747 | PF00069 | 0.664 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.398 |
MOD_SUMO_for_1 | 624 | 627 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 331 | 339 | PF00179 | 0.305 |
MOD_SUMO_rev_2 | 844 | 849 | PF00179 | 0.393 |
TRG_DiLeu_BaEn_1 | 345 | 350 | PF01217 | 0.352 |
TRG_DiLeu_BaLyEn_6 | 455 | 460 | PF01217 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 611 | 616 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 648 | 651 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 620 | 622 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 805 | 807 | PF00400 | 0.306 |
TRG_NES_CRM1_1 | 324 | 336 | PF08389 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 614 | 619 | PF00026 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 809 | 813 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6M5 | Leptomonas seymouri | 38% | 100% |
A0A3S7WX62 | Leishmania donovani | 78% | 98% |
A4HCE3 | Leishmania braziliensis | 62% | 99% |
A4HZW6 | Leishmania infantum | 78% | 98% |
Q4QBQ5 | Leishmania major | 80% | 100% |