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: E9ASN5
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 | 230 | 234 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 598 | 602 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 615 | 619 | PF00656 | 0.487 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 776 | 778 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 780 | 782 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 893 | 895 | PF00675 | 0.384 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 776 | 778 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 780 | 782 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 886 | 888 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 893 | 895 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 536 | 538 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 596 | 598 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 776 | 778 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 886 | 888 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 781 | 785 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 818 | 822 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 886 | 890 | PF00082 | 0.353 |
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.529 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.503 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.518 |
DEG_SPOP_SBC_1 | 89 | 93 | PF00917 | 0.517 |
DOC_ANK_TNKS_1 | 596 | 603 | PF00023 | 0.549 |
DOC_MAPK_gen_1 | 425 | 436 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 723 | 730 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 893 | 899 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 486 | 495 | PF00069 | 0.348 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.514 |
DOC_PP2B_LxvP_1 | 225 | 228 | PF13499 | 0.524 |
DOC_PP2B_LxvP_1 | 765 | 768 | PF13499 | 0.593 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.649 |
DOC_USP7_MATH_2 | 625 | 631 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 677 | 682 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 108 | 114 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 184 | 193 | PF00244 | 0.759 |
LIG_14-3-3_CanoR_1 | 207 | 216 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 468 | 478 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 537 | 542 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 631 | 637 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 887 | 895 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 898 | 906 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 907 | 915 | PF00244 | 0.237 |
LIG_14-3-3_CterR_2 | 923 | 927 | PF00244 | 0.515 |
LIG_APCC_ABBA_1 | 897 | 902 | PF00400 | 0.376 |
LIG_BIR_III_2 | 501 | 505 | PF00653 | 0.563 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.608 |
LIG_eIF4E_1 | 401 | 407 | PF01652 | 0.376 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.654 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.704 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.552 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.549 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.427 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.498 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.512 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.544 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.352 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.608 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.761 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.521 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.592 |
LIG_FHA_2 | 631 | 637 | PF00498 | 0.516 |
LIG_FHA_2 | 777 | 783 | PF00498 | 0.382 |
LIG_FHA_2 | 860 | 866 | PF00498 | 0.441 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.632 |
LIG_GBD_Chelix_1 | 489 | 497 | PF00786 | 0.358 |
LIG_HP1_1 | 913 | 917 | PF01393 | 0.345 |
LIG_Integrin_RGD_1 | 364 | 366 | PF01839 | 0.496 |
LIG_LIR_Apic_2 | 350 | 355 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 248 | 258 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 527 | 535 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 680 | 691 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 680 | 686 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 706 | 710 | PF02991 | 0.378 |
LIG_Rb_pABgroove_1 | 912 | 920 | PF01858 | 0.345 |
LIG_REV1ctd_RIR_1 | 723 | 731 | PF16727 | 0.400 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.366 |
LIG_SH2_CRK | 707 | 711 | PF00017 | 0.390 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 900 | 904 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 853 | 857 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 712 | 715 | PF00017 | 0.412 |
LIG_SH2_STAT3 | 809 | 812 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 809 | 812 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 878 | 881 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 900 | 903 | PF00017 | 0.360 |
LIG_SH3_2 | 372 | 377 | PF14604 | 0.381 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.652 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.683 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.581 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.551 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.395 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.612 |
LIG_SH3_5 | 195 | 199 | PF00018 | 0.523 |
LIG_SUMO_SIM_par_1 | 405 | 411 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 493 | 498 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 913 | 919 | PF11976 | 0.346 |
LIG_TRAF2_1 | 757 | 760 | PF00917 | 0.490 |
MOD_CDK_SPK_2 | 495 | 500 | PF00069 | 0.426 |
MOD_CDK_SPxK_1 | 760 | 766 | PF00069 | 0.542 |
MOD_CDK_SPxxK_3 | 260 | 267 | PF00069 | 0.497 |
MOD_CDK_SPxxK_3 | 90 | 97 | PF00069 | 0.536 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.554 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.530 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.672 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.721 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.656 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.550 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.627 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.569 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.654 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.614 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.560 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.637 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.558 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.638 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.502 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.484 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.557 |
MOD_CK2_1 | 754 | 760 | PF00069 | 0.534 |
MOD_CK2_1 | 768 | 774 | PF00069 | 0.555 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.446 |
MOD_Cter_Amidation | 730 | 733 | PF01082 | 0.508 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.663 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.610 |
MOD_GlcNHglycan | 394 | 398 | PF01048 | 0.404 |
MOD_GlcNHglycan | 554 | 558 | PF01048 | 0.537 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.691 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.621 |
MOD_GlcNHglycan | 71 | 75 | PF01048 | 0.556 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.526 |
MOD_GlcNHglycan | 854 | 858 | PF01048 | 0.501 |
MOD_GlcNHglycan | 889 | 892 | PF01048 | 0.387 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.592 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.686 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.602 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.556 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.597 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.570 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.579 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.539 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.465 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.521 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.393 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.558 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.652 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.575 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.600 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.667 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.366 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.578 |
MOD_GSK3_1 | 812 | 819 | PF00069 | 0.444 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.600 |
MOD_GSK3_1 | 919 | 926 | PF00069 | 0.451 |
MOD_LATS_1 | 423 | 429 | PF00433 | 0.354 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.507 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.513 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.489 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.572 |
MOD_N-GLC_1 | 566 | 571 | PF02516 | 0.518 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.656 |
MOD_N-GLC_1 | 602 | 607 | PF02516 | 0.643 |
MOD_N-GLC_1 | 631 | 636 | PF02516 | 0.584 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.522 |
MOD_N-GLC_1 | 800 | 805 | PF02516 | 0.398 |
MOD_N-GLC_1 | 866 | 871 | PF02516 | 0.461 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.585 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.601 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.609 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.608 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.718 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.442 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.575 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.760 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.348 |
MOD_NEK2_1 | 787 | 792 | PF00069 | 0.336 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.648 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.494 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.664 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.357 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.385 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.669 |
MOD_PK_1 | 278 | 284 | PF00069 | 0.596 |
MOD_PKA_1 | 184 | 190 | PF00069 | 0.529 |
MOD_PKA_1 | 425 | 431 | PF00069 | 0.402 |
MOD_PKA_1 | 776 | 782 | PF00069 | 0.414 |
MOD_PKA_1 | 886 | 892 | PF00069 | 0.451 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.660 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.578 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.618 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.521 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.402 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.590 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.626 |
MOD_PKA_2 | 776 | 782 | PF00069 | 0.414 |
MOD_PKA_2 | 847 | 853 | PF00069 | 0.469 |
MOD_PKA_2 | 886 | 892 | PF00069 | 0.451 |
MOD_PKA_2 | 906 | 912 | PF00069 | 0.241 |
MOD_PKB_1 | 217 | 225 | PF00069 | 0.537 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.515 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.491 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.618 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.339 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.585 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.537 |
MOD_Plk_1 | 787 | 793 | PF00069 | 0.334 |
MOD_Plk_2-3 | 741 | 747 | PF00069 | 0.716 |
MOD_Plk_2-3 | 825 | 831 | PF00069 | 0.354 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.612 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.621 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.374 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.334 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.665 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.624 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.620 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.649 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.588 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.448 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.601 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.632 |
MOD_ProDKin_1 | 677 | 683 | PF00069 | 0.702 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.536 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.534 |
MOD_SUMO_rev_2 | 360 | 369 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 667 | 676 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_1 | 589 | 594 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 900 | 903 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 893 | 895 | PF00400 | 0.384 |
TRG_NLS_Bipartite_1 | 871 | 889 | PF00514 | 0.442 |
TRG_NLS_MonoExtC_3 | 731 | 737 | PF00514 | 0.545 |
TRG_NLS_MonoExtC_3 | 775 | 780 | PF00514 | 0.609 |
TRG_NLS_MonoExtN_4 | 776 | 781 | PF00514 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEB1 | Leptomonas seymouri | 54% | 100% |
A0A3S7XAJ4 | Leishmania donovani | 79% | 100% |
A4HNX5 | Leishmania braziliensis | 54% | 98% |
A4ICL9 | Leishmania infantum | 79% | 73% |
Q4Q1W1 | Leishmania major | 77% | 100% |