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: A0A3S7WX62
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 | 63 | 67 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 774 | 778 | PF00656 | 0.710 |
CLV_C14_Caspase3-7 | 837 | 841 | PF00656 | 0.621 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.793 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 869 | 871 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 869 | 871 | PF00082 | 0.706 |
CLV_PCSK_PC7_1 | 640 | 646 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 792 | 796 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 827 | 831 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 854 | 858 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 453 | 457 | PF03568 | 0.558 |
CLV_Separin_Metazoa | 722 | 726 | PF03568 | 0.529 |
DEG_APCC_DBOX_1 | 536 | 544 | PF00400 | 0.603 |
DEG_APCC_DBOX_1 | 610 | 618 | PF00400 | 0.449 |
DEG_APCC_DBOX_1 | 688 | 696 | PF00400 | 0.529 |
DEG_SCF_FBW7_1 | 319 | 325 | PF00400 | 0.539 |
DEG_SCF_FBW7_1 | 543 | 549 | PF00400 | 0.712 |
DEG_SCF_TRCP1_1 | 239 | 244 | PF00400 | 0.615 |
DEG_SCF_TRCP1_1 | 337 | 342 | PF00400 | 0.390 |
DOC_CDC14_PxL_1 | 597 | 605 | PF14671 | 0.469 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.595 |
DOC_CKS1_1 | 407 | 412 | PF01111 | 0.672 |
DOC_CKS1_1 | 543 | 548 | PF01111 | 0.710 |
DOC_CYCLIN_RxL_1 | 531 | 541 | PF00134 | 0.628 |
DOC_CYCLIN_RxL_1 | 827 | 837 | PF00134 | 0.599 |
DOC_CYCLIN_yClb1_LxF_4 | 35 | 40 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 454 | 460 | PF00134 | 0.584 |
DOC_MAPK_gen_1 | 439 | 448 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 683 | 692 | PF00069 | 0.577 |
DOC_MAPK_RevD_3 | 216 | 231 | PF00069 | 0.556 |
DOC_PP1_RVXF_1 | 454 | 461 | PF00149 | 0.414 |
DOC_PP1_RVXF_1 | 613 | 620 | PF00149 | 0.446 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 865 | 868 | PF00568 | 0.621 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 825 | 829 | PF00917 | 0.565 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 840 | 845 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 328 | 333 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 439 | 446 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 515 | 523 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 581 | 587 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 644 | 648 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 70 | 75 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 725 | 729 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 849 | 854 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 312 | 329 | PF00022 | 0.459 |
LIG_Actin_WH2_2 | 600 | 617 | PF00022 | 0.447 |
LIG_Actin_WH2_2 | 688 | 706 | PF00022 | 0.629 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.588 |
LIG_BIR_III_2 | 693 | 697 | PF00653 | 0.616 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.691 |
LIG_BRCT_BRCA1_1 | 382 | 386 | PF00533 | 0.624 |
LIG_CSL_BTD_1 | 543 | 546 | PF09270 | 0.609 |
LIG_deltaCOP1_diTrp_1 | 343 | 346 | PF00928 | 0.561 |
LIG_EH_1 | 260 | 264 | PF12763 | 0.478 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.667 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.537 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.539 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.595 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.571 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.760 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.729 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.590 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.542 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.706 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.686 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.389 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.702 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.663 |
LIG_FHA_2 | 772 | 778 | PF00498 | 0.711 |
LIG_FHA_2 | 850 | 856 | PF00498 | 0.476 |
LIG_Integrin_RGD_1 | 640 | 642 | PF01839 | 0.562 |
LIG_LIR_Gen_1 | 20 | 31 | PF02991 | 0.732 |
LIG_LIR_Gen_1 | 311 | 319 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 343 | 354 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 805 | 814 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 846 | 853 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 534 | 539 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 599 | 603 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 667 | 671 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 805 | 809 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 828 | 833 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 846 | 850 | PF02991 | 0.360 |
LIG_LYPXL_yS_3 | 600 | 603 | PF13949 | 0.473 |
LIG_MYND_1 | 400 | 404 | PF01753 | 0.688 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.437 |
LIG_Pex14_2 | 312 | 316 | PF04695 | 0.247 |
LIG_SH2_NCK_1 | 363 | 367 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 731 | 735 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.491 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.653 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.632 |
LIG_SH3_3 | 540 | 546 | PF00018 | 0.697 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.445 |
LIG_SH3_3 | 693 | 699 | PF00018 | 0.513 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.726 |
LIG_Sin3_3 | 495 | 502 | PF02671 | 0.569 |
LIG_SUMO_SIM_anti_2 | 810 | 816 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 204 | 210 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 351 | 356 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 560 | 566 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 627 | 634 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 812 | 818 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 90 | 96 | PF11976 | 0.462 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.584 |
LIG_TRAF2_1 | 588 | 591 | PF00917 | 0.460 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.594 |
LIG_TRAF2_1 | 653 | 656 | PF00917 | 0.541 |
LIG_TYR_ITIM | 598 | 603 | PF00017 | 0.467 |
LIG_WRC_WIRS_1 | 315 | 320 | PF05994 | 0.454 |
MOD_CDK_SPK_2 | 510 | 515 | PF00069 | 0.623 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.713 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.618 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.641 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.693 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.689 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.714 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.696 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.709 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.517 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.715 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.719 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.711 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.441 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.699 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.696 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.546 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.696 |
MOD_CK2_1 | 780 | 786 | PF00069 | 0.652 |
MOD_CK2_1 | 820 | 826 | PF00069 | 0.509 |
MOD_CK2_1 | 840 | 846 | PF00069 | 0.270 |
MOD_CK2_1 | 849 | 855 | PF00069 | 0.515 |
MOD_CMANNOS | 529 | 532 | PF00535 | 0.712 |
MOD_Cter_Amidation | 371 | 374 | PF01082 | 0.550 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.661 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.632 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.635 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.607 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.768 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.693 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.589 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.685 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.411 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.723 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.556 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.676 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.824 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.782 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.569 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.668 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.712 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.650 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.654 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.700 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.637 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.720 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.544 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.438 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.402 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.795 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.683 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.754 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.614 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.727 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.573 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.736 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.761 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.550 |
MOD_GSK3_1 | 836 | 843 | PF00069 | 0.513 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.714 |
MOD_N-GLC_1 | 503 | 508 | PF02516 | 0.671 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.597 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.506 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.651 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.547 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.328 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.580 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.521 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.484 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.590 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.438 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.587 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.544 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.749 |
MOD_NEK2_1 | 815 | 820 | PF00069 | 0.412 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.601 |
MOD_NEK2_2 | 322 | 327 | PF00069 | 0.433 |
MOD_NEK2_2 | 699 | 704 | PF00069 | 0.545 |
MOD_NEK2_2 | 80 | 85 | PF00069 | 0.501 |
MOD_NEK2_2 | 825 | 830 | PF00069 | 0.511 |
MOD_OFUCOSY | 550 | 555 | PF10250 | 0.759 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.537 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.705 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.539 |
MOD_PIKK_1 | 609 | 615 | PF00454 | 0.433 |
MOD_PIKK_1 | 714 | 720 | PF00454 | 0.647 |
MOD_PIKK_1 | 752 | 758 | PF00454 | 0.808 |
MOD_PIKK_1 | 817 | 823 | PF00454 | 0.441 |
MOD_PK_1 | 328 | 334 | PF00069 | 0.521 |
MOD_PK_1 | 70 | 76 | PF00069 | 0.652 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.559 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.552 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.714 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.740 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.626 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.578 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.581 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.480 |
MOD_PKA_2 | 724 | 730 | PF00069 | 0.646 |
MOD_PKA_2 | 799 | 805 | PF00069 | 0.486 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.585 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.548 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.521 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.532 |
MOD_Plk_1 | 590 | 596 | PF00069 | 0.591 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.570 |
MOD_Plk_1 | 699 | 705 | PF00069 | 0.546 |
MOD_Plk_1 | 825 | 831 | PF00069 | 0.565 |
MOD_Plk_2-3 | 157 | 163 | PF00069 | 0.695 |
MOD_Plk_2-3 | 780 | 786 | PF00069 | 0.654 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.636 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.548 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.464 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.605 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.556 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.445 |
MOD_Plk_4 | 724 | 730 | PF00069 | 0.518 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.539 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.664 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.735 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.675 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.732 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.588 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.793 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.652 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.743 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.703 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.747 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.675 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.792 |
MOD_ProDKin_1 | 840 | 846 | PF00069 | 0.499 |
MOD_SUMO_for_1 | 647 | 650 | PF00179 | 0.654 |
MOD_SUMO_rev_2 | 473 | 481 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 777 | 784 | PF00179 | 0.743 |
TRG_DiLeu_BaEn_1 | 345 | 350 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 454 | 459 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 634 | 639 | PF01217 | 0.586 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.783 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.460 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 636 | 638 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.548 |
TRG_NES_CRM1_1 | 324 | 337 | PF08389 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 637 | 642 | PF00026 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 831 | 835 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.691 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6M5 | Leptomonas seymouri | 38% | 100% |
A4HCE3 | Leishmania braziliensis | 63% | 97% |
A4HZW6 | Leishmania infantum | 99% | 100% |
E9AVS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 97% |
Q4QBQ5 | Leishmania major | 88% | 100% |