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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S7XAJ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0030258 | lipid modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0046486 | glycerolipid metabolic process | 4 | 7 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 7 |
GO:0046839 | phospholipid dephosphorylation | 5 | 7 |
GO:0046856 | phosphatidylinositol dephosphorylation | 6 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0043647 | inositol phosphate metabolic process | 4 | 1 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046164 | alcohol catabolic process | 4 | 1 |
GO:0046174 | polyol catabolic process | 5 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046838 | obsolete phosphorylated carbohydrate dephosphorylation | 4 | 1 |
GO:0046855 | obsolete inositol phosphate dephosphorylation | 5 | 1 |
GO:0071545 | inositol phosphate catabolic process | 5 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004518 | nuclease activity | 4 | 7 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0004527 | exonuclease activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0004439 | phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity | 8 | 1 |
GO:0034593 | phosphatidylinositol bisphosphate phosphatase activity | 7 | 1 |
GO:0034595 | phosphatidylinositol phosphate 5-phosphatase activity | 7 | 1 |
GO:0052866 | phosphatidylinositol phosphate phosphatase activity | 6 | 1 |
GO:0106019 | phosphatidylinositol-4,5-bisphosphate phosphatase activity | 8 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.712 |
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 598 | 602 | PF00656 | 0.819 |
CLV_C14_Caspase3-7 | 640 | 644 | PF00656 | 0.718 |
CLV_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 718 | 720 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 781 | 783 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 804 | 806 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 894 | 896 | PF00675 | 0.492 |
CLV_PCSK_FUR_1 | 266 | 270 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 781 | 783 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 887 | 889 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 894 | 896 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 536 | 538 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 777 | 779 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 887 | 889 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 782 | 786 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 819 | 823 | PF00082 | 0.508 |
DEG_Kelch_Keap1_1 | 173 | 178 | PF01344 | 0.588 |
DEG_SCF_FBW7_1 | 16 | 23 | PF00400 | 0.588 |
DOC_CKS1_1 | 118 | 123 | PF01111 | 0.711 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.374 |
DOC_CYCLIN_RxL_1 | 100 | 112 | PF00134 | 0.524 |
DOC_MAPK_gen_1 | 723 | 730 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 894 | 900 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 486 | 495 | PF00069 | 0.458 |
DOC_MAPK_RevD_3 | 764 | 778 | PF00069 | 0.637 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.517 |
DOC_PP2B_LxvP_1 | 766 | 769 | PF13499 | 0.690 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.817 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 769 | 773 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.755 |
DOC_USP7_MATH_2 | 625 | 631 | PF00917 | 0.696 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 677 | 682 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 104 | 109 | PF00244 | 0.813 |
LIG_14-3-3_CanoR_1 | 110 | 114 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 185 | 193 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 468 | 478 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 537 | 542 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 631 | 637 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 888 | 896 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 899 | 907 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 908 | 916 | PF00244 | 0.239 |
LIG_14-3-3_CanoR_1 | 94 | 102 | PF00244 | 0.636 |
LIG_14-3-3_CterR_2 | 924 | 928 | PF00244 | 0.666 |
LIG_APCC_ABBA_1 | 898 | 903 | PF00400 | 0.484 |
LIG_BIR_III_2 | 168 | 172 | PF00653 | 0.699 |
LIG_BIR_III_2 | 501 | 505 | PF00653 | 0.672 |
LIG_BIR_III_4 | 585 | 589 | PF00653 | 0.570 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.706 |
LIG_CSL_BTD_1 | 369 | 372 | PF09270 | 0.480 |
LIG_eIF4E_1 | 401 | 407 | PF01652 | 0.474 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.784 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.638 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.784 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.604 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.603 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.494 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.505 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.633 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.667 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.465 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.702 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.671 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.715 |
LIG_FHA_2 | 631 | 637 | PF00498 | 0.529 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.583 |
LIG_FHA_2 | 861 | 867 | PF00498 | 0.594 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.735 |
LIG_GBD_Chelix_1 | 489 | 497 | PF00786 | 0.468 |
LIG_HP1_1 | 914 | 918 | PF01393 | 0.455 |
LIG_IBAR_NPY_1 | 579 | 581 | PF08397 | 0.684 |
LIG_Integrin_RGD_1 | 364 | 366 | PF01839 | 0.655 |
LIG_Integrin_RGD_1 | 663 | 665 | PF01839 | 0.607 |
LIG_LIR_Apic_2 | 350 | 355 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 248 | 258 | PF02991 | 0.648 |
LIG_LIR_Gen_1 | 680 | 691 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.752 |
LIG_LIR_Nem_3 | 680 | 686 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 706 | 710 | PF02991 | 0.488 |
LIG_MYND_1 | 117 | 121 | PF01753 | 0.702 |
LIG_PTAP_UEV_1 | 120 | 125 | PF05743 | 0.603 |
LIG_Rb_pABgroove_1 | 913 | 921 | PF01858 | 0.456 |
LIG_REV1ctd_RIR_1 | 723 | 731 | PF16727 | 0.489 |
LIG_SH2_CRK | 590 | 594 | PF00017 | 0.696 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.483 |
LIG_SH2_CRK | 707 | 711 | PF00017 | 0.500 |
LIG_SH2_GRB2like | 199 | 202 | PF00017 | 0.689 |
LIG_SH2_NCK_1 | 901 | 905 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 854 | 858 | PF00017 | 0.629 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.689 |
LIG_SH2_STAT3 | 712 | 715 | PF00017 | 0.519 |
LIG_SH2_STAT3 | 810 | 813 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.669 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 810 | 813 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 879 | 882 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 901 | 904 | PF00017 | 0.466 |
LIG_SH3_2 | 372 | 377 | PF14604 | 0.492 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.761 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.712 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.797 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.703 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.514 |
LIG_SH3_3 | 515 | 521 | PF00018 | 0.599 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.612 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.768 |
LIG_SH3_5 | 195 | 199 | PF00018 | 0.639 |
LIG_SUMO_SIM_anti_2 | 235 | 241 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 405 | 411 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 493 | 498 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 914 | 920 | PF11976 | 0.455 |
LIG_UBA3_1 | 478 | 486 | PF00899 | 0.563 |
MOD_CDC14_SPxK_1 | 263 | 266 | PF00782 | 0.667 |
MOD_CDK_SPK_2 | 219 | 224 | PF00069 | 0.607 |
MOD_CDK_SPK_2 | 495 | 500 | PF00069 | 0.535 |
MOD_CDK_SPxK_1 | 260 | 266 | PF00069 | 0.661 |
MOD_CDK_SPxK_1 | 368 | 374 | PF00069 | 0.387 |
MOD_CDK_SPxK_1 | 530 | 536 | PF00069 | 0.779 |
MOD_CDK_SPxxK_3 | 530 | 537 | PF00069 | 0.581 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.812 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.665 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.794 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.700 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.691 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.789 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.635 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.643 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.633 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.777 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.731 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.582 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.537 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.640 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.647 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.720 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.667 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.691 |
MOD_CK2_1 | 769 | 775 | PF00069 | 0.634 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.590 |
MOD_Cter_Amidation | 716 | 719 | PF01082 | 0.472 |
MOD_Cter_Amidation | 730 | 733 | PF01082 | 0.589 |
MOD_DYRK1A_RPxSP_1 | 189 | 193 | PF00069 | 0.582 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.765 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.621 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.641 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.744 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.673 |
MOD_GlcNHglycan | 394 | 398 | PF01048 | 0.494 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.685 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.713 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.667 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.587 |
MOD_GlcNHglycan | 554 | 558 | PF01048 | 0.597 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.759 |
MOD_GlcNHglycan | 71 | 75 | PF01048 | 0.634 |
MOD_GlcNHglycan | 855 | 859 | PF01048 | 0.655 |
MOD_GlcNHglycan | 890 | 893 | PF01048 | 0.494 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.730 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.683 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.841 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.749 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.683 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.639 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.632 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.690 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.708 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.741 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.692 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.542 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.527 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.514 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.484 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.752 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.779 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.714 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.785 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.482 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.569 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.716 |
MOD_GSK3_1 | 920 | 927 | PF00069 | 0.603 |
MOD_LATS_1 | 423 | 429 | PF00433 | 0.422 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.629 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.818 |
MOD_N-GLC_1 | 602 | 607 | PF02516 | 0.820 |
MOD_N-GLC_1 | 631 | 636 | PF02516 | 0.691 |
MOD_N-GLC_1 | 677 | 682 | PF02516 | 0.727 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.506 |
MOD_N-GLC_1 | 801 | 806 | PF02516 | 0.499 |
MOD_N-GLC_1 | 867 | 872 | PF02516 | 0.551 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.714 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.572 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.757 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.534 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.599 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.657 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.749 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.461 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.584 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.443 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.662 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.752 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.581 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.657 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.763 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.578 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.615 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.431 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.480 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.767 |
MOD_PK_1 | 278 | 284 | PF00069 | 0.720 |
MOD_PKA_1 | 425 | 431 | PF00069 | 0.518 |
MOD_PKA_1 | 887 | 893 | PF00069 | 0.604 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.674 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.787 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.743 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.565 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.518 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.742 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.654 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.545 |
MOD_PKA_2 | 887 | 893 | PF00069 | 0.604 |
MOD_PKA_2 | 907 | 913 | PF00069 | 0.244 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.637 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.694 |
MOD_Plk_1 | 788 | 794 | PF00069 | 0.442 |
MOD_Plk_2-3 | 612 | 618 | PF00069 | 0.661 |
MOD_Plk_2-3 | 742 | 748 | PF00069 | 0.777 |
MOD_Plk_2-3 | 826 | 832 | PF00069 | 0.464 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.617 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.723 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.769 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.435 |
MOD_Plk_4 | 788 | 794 | PF00069 | 0.442 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.704 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.721 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.578 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.777 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.724 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.532 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.552 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.728 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.797 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.632 |
MOD_ProDKin_1 | 677 | 683 | PF00069 | 0.734 |
MOD_SUMO_rev_2 | 360 | 369 | PF00179 | 0.612 |
TRG_DiLeu_BaEn_1 | 589 | 594 | PF01217 | 0.726 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.736 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 901 | 904 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.701 |
TRG_ER_diArg_1 | 266 | 269 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 780 | 782 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 894 | 896 | PF00400 | 0.492 |
TRG_NLS_Bipartite_1 | 718 | 736 | PF00514 | 0.511 |
TRG_NLS_Bipartite_1 | 872 | 890 | PF00514 | 0.588 |
TRG_NLS_MonoExtC_3 | 731 | 737 | PF00514 | 0.643 |
TRG_NLS_MonoExtC_3 | 776 | 781 | PF00514 | 0.744 |
TRG_NLS_MonoExtN_4 | 777 | 782 | PF00514 | 0.710 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEB1 | Leptomonas seymouri | 57% | 100% |
A4HNX5 | Leishmania braziliensis | 54% | 99% |
A4ICL9 | Leishmania infantum | 99% | 100% |
E9ASN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q1W1 | Leishmania major | 85% | 100% |