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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HNX5
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 6 |
GO:0006644 | phospholipid metabolic process | 4 | 6 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016311 | dephosphorylation | 5 | 6 |
GO:0019637 | organophosphate metabolic process | 3 | 6 |
GO:0030258 | lipid modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044255 | cellular lipid metabolic process | 3 | 6 |
GO:0046486 | glycerolipid metabolic process | 4 | 6 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 6 |
GO:0046839 | phospholipid dephosphorylation | 5 | 6 |
GO:0046856 | phosphatidylinositol dephosphorylation | 6 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
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 | 6 |
GO:0004518 | nuclease activity | 4 | 6 |
GO:0004519 | endonuclease activity | 5 | 6 |
GO:0004527 | exonuclease activity | 5 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 6 |
GO:0016791 | phosphatase activity | 5 | 6 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 6 |
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 | 324 | 328 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 591 | 595 | PF00656 | 0.692 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 711 | 713 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 772 | 774 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 776 | 778 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 799 | 801 | PF00675 | 0.603 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 711 | 713 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 776 | 778 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 882 | 884 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 882 | 884 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 716 | 720 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 777 | 781 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 814 | 818 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.558 |
DEG_APCC_DBOX_1 | 348 | 356 | PF00400 | 0.417 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.581 |
DEG_SCF_FBW7_2 | 511 | 517 | PF00400 | 0.535 |
DEG_SCF_SKP2-CKS1_1 | 664 | 671 | PF00560 | 0.547 |
DEG_SPOP_SBC_1 | 221 | 225 | PF00917 | 0.549 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.540 |
DOC_ANK_TNKS_1 | 589 | 596 | PF00023 | 0.588 |
DOC_CKS1_1 | 511 | 516 | PF01111 | 0.536 |
DOC_CKS1_1 | 583 | 588 | PF01111 | 0.558 |
DOC_CYCLIN_RxL_1 | 126 | 137 | PF00134 | 0.556 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.534 |
DOC_MAPK_gen_1 | 418 | 429 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 479 | 488 | PF00069 | 0.412 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.553 |
DOC_PP2B_LxvP_1 | 247 | 250 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 761 | 764 | PF13499 | 0.644 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.553 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.590 |
DOC_USP7_UBL2_3 | 211 | 215 | PF12436 | 0.556 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 665 | 670 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 756 | 761 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 210 | 218 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 239 | 243 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 244 | 248 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 505 | 515 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 623 | 628 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 84 | 91 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 883 | 891 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 894 | 902 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 903 | 911 | PF00244 | 0.252 |
LIG_14-3-3_CterR_2 | 919 | 923 | PF00244 | 0.538 |
LIG_APCC_ABBA_1 | 893 | 898 | PF00400 | 0.446 |
LIG_eIF4E_1 | 350 | 356 | PF01652 | 0.414 |
LIG_EVH1_1 | 23 | 27 | PF00568 | 0.529 |
LIG_EVH1_2 | 114 | 118 | PF00568 | 0.553 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.558 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.612 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.556 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.474 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.540 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.537 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.603 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.519 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.422 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.572 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.557 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.643 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.497 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.606 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.558 |
LIG_FHA_2 | 856 | 862 | PF00498 | 0.505 |
LIG_GBD_Chelix_1 | 482 | 490 | PF00786 | 0.417 |
LIG_HP1_1 | 909 | 913 | PF01393 | 0.419 |
LIG_Integrin_isoDGR_2 | 82 | 84 | PF01839 | 0.557 |
LIG_LIR_Apic_2 | 343 | 348 | PF02991 | 0.555 |
LIG_LIR_Apic_2 | 580 | 586 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 673 | 684 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 699 | 707 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 612 | 618 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 673 | 679 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 699 | 703 | PF02991 | 0.446 |
LIG_LYPXL_yS_3 | 163 | 166 | PF13949 | 0.568 |
LIG_NRBOX | 351 | 357 | PF00104 | 0.411 |
LIG_Pex14_2 | 783 | 787 | PF04695 | 0.337 |
LIG_Rb_pABgroove_1 | 908 | 916 | PF01858 | 0.419 |
LIG_SH2_CRK | 566 | 570 | PF00017 | 0.544 |
LIG_SH2_CRK | 583 | 587 | PF00017 | 0.621 |
LIG_SH2_CRK | 676 | 680 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 433 | 437 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 896 | 900 | PF00017 | 0.432 |
LIG_SH2_SRC | 106 | 109 | PF00017 | 0.561 |
LIG_SH2_SRC | 410 | 413 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 700 | 704 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 849 | 853 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 805 | 808 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 874 | 877 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 896 | 899 | PF00017 | 0.429 |
LIG_SH3_2 | 365 | 370 | PF14604 | 0.451 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.664 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.551 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.579 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.552 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.558 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.468 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.642 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.660 |
LIG_SH3_3 | 611 | 617 | PF00018 | 0.765 |
LIG_SUMO_SIM_anti_2 | 116 | 124 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 486 | 491 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 533 | 540 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 909 | 915 | PF11976 | 0.420 |
LIG_TRAF2_1 | 732 | 735 | PF00917 | 0.525 |
LIG_TYR_ITIM | 161 | 166 | PF00017 | 0.569 |
LIG_UBA3_1 | 471 | 479 | PF00899 | 0.545 |
LIG_UBA3_1 | 511 | 518 | PF00899 | 0.536 |
LIG_WRC_WIRS_1 | 627 | 632 | PF05994 | 0.497 |
LIG_WW_2 | 24 | 27 | PF00397 | 0.516 |
MOD_CDK_SPK_2 | 488 | 493 | PF00069 | 0.465 |
MOD_CDK_SPxK_1 | 523 | 529 | PF00069 | 0.627 |
MOD_CDK_SPxK_1 | 665 | 671 | PF00069 | 0.544 |
MOD_CDK_SPxK_1 | 756 | 762 | PF00069 | 0.534 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.594 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.546 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.563 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.681 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.565 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.646 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.586 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.666 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.348 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.554 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.606 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.553 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.573 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.575 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.540 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.550 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.611 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.540 |
MOD_CK2_1 | 855 | 861 | PF00069 | 0.513 |
MOD_Cter_Amidation | 709 | 712 | PF01082 | 0.427 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.604 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.568 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.556 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.713 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.542 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.532 |
MOD_GlcNHglycan | 387 | 391 | PF01048 | 0.474 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.555 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.578 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.589 |
MOD_GlcNHglycan | 850 | 854 | PF01048 | 0.505 |
MOD_GlcNHglycan | 885 | 888 | PF01048 | 0.456 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.624 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.686 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.551 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.540 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.558 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.533 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.601 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.548 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.516 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.524 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.616 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.569 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.682 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.491 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.471 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.523 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.527 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.566 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.554 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.541 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.625 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.642 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.576 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.554 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.508 |
MOD_GSK3_1 | 915 | 922 | PF00069 | 0.474 |
MOD_N-GLC_1 | 595 | 600 | PF02516 | 0.684 |
MOD_N-GLC_1 | 619 | 624 | PF02516 | 0.592 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.659 |
MOD_N-GLC_1 | 796 | 801 | PF02516 | 0.471 |
MOD_N-GLC_1 | 862 | 867 | PF02516 | 0.524 |
MOD_N-GLC_2 | 279 | 281 | PF02516 | 0.522 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.568 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.553 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.684 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.433 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.422 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.406 |
MOD_NEK2_1 | 914 | 919 | PF00069 | 0.310 |
MOD_OFUCOSY | 62 | 69 | PF10250 | 0.587 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.558 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.643 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.692 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.423 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.393 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.457 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.631 |
MOD_PKA_1 | 882 | 888 | PF00069 | 0.464 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.580 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.593 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.609 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.578 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.538 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.566 |
MOD_PKA_2 | 843 | 849 | PF00069 | 0.424 |
MOD_PKA_2 | 882 | 888 | PF00069 | 0.464 |
MOD_PKA_2 | 902 | 908 | PF00069 | 0.257 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.563 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.599 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.489 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.366 |
MOD_Plk_1 | 610 | 616 | PF00069 | 0.530 |
MOD_Plk_1 | 783 | 789 | PF00069 | 0.405 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.559 |
MOD_Plk_2-3 | 588 | 594 | PF00069 | 0.581 |
MOD_Plk_2-3 | 655 | 661 | PF00069 | 0.578 |
MOD_Plk_2-3 | 821 | 827 | PF00069 | 0.428 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.567 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.596 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.545 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.630 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.598 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.461 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.405 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.661 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.631 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.693 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.588 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.493 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.542 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.550 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.611 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.628 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.524 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.515 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.532 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.763 |
MOD_ProDKin_1 | 665 | 671 | PF00069 | 0.640 |
MOD_ProDKin_1 | 756 | 762 | PF00069 | 0.527 |
MOD_SUMO_rev_2 | 208 | 216 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 353 | 362 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 565 | 570 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 676 | 679 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 700 | 703 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 896 | 899 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 382 | 385 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 641 | 643 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 693 | 696 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 775 | 777 | PF00400 | 0.501 |
TRG_NLS_Bipartite_1 | 867 | 885 | PF00514 | 0.454 |
TRG_NLS_MonoExtC_3 | 772 | 777 | PF00514 | 0.568 |
TRG_NLS_MonoExtN_4 | 771 | 777 | PF00514 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 590 | 594 | PF00026 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 94 | 98 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAJ4 | Leishmania donovani | 54% | 99% |
A4ICL9 | Leishmania infantum | 54% | 73% |
E9ASN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
Q4Q1W1 | Leishmania major | 54% | 100% |