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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 1 |
GO:0005680 | anaphase-promoting complex | 4 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9AX17
Term | Name | Level | Count |
---|---|---|---|
GO:0009893 | positive regulation of metabolic process | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 7 |
GO:0019222 | regulation of metabolic process | 3 | 7 |
GO:0031396 | regulation of protein ubiquitination | 8 | 6 |
GO:0031398 | positive regulation of protein ubiquitination | 9 | 6 |
GO:0031399 | regulation of protein modification process | 6 | 6 |
GO:0031401 | positive regulation of protein modification process | 7 | 6 |
GO:0043085 | positive regulation of catalytic activity | 4 | 6 |
GO:0044093 | positive regulation of molecular function | 3 | 6 |
GO:0048518 | positive regulation of biological process | 3 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050790 | regulation of catalytic activity | 3 | 6 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 7 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 7 |
GO:0051246 | regulation of protein metabolic process | 5 | 7 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 7 |
GO:0051301 | cell division | 2 | 7 |
GO:0051338 | regulation of transferase activity | 4 | 6 |
GO:0051347 | positive regulation of transferase activity | 5 | 6 |
GO:0051438 | regulation of ubiquitin-protein transferase activity | 5 | 6 |
GO:0051443 | positive regulation of ubiquitin-protein transferase activity | 6 | 6 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 6 |
GO:0080090 | regulation of primary metabolic process | 4 | 7 |
GO:1903320 | regulation of protein modification by small protein conjugation or removal | 7 | 6 |
GO:1903322 | positive regulation of protein modification by small protein conjugation or removal | 8 | 6 |
GO:1904666 | regulation of ubiquitin protein ligase activity | 6 | 6 |
GO:1904668 | positive regulation of ubiquitin protein ligase activity | 7 | 6 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009896 | positive regulation of catabolic process | 5 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030162 | regulation of proteolysis | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 1 |
GO:0032434 | regulation of proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0032436 | positive regulation of proteasomal ubiquitin-dependent protein catabolic process | 8 | 1 |
GO:0042176 | regulation of protein catabolic process | 5 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0045732 | positive regulation of protein catabolic process | 6 | 1 |
GO:0045862 | positive regulation of proteolysis | 7 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901800 | positive regulation of proteasomal protein catabolic process | 7 | 1 |
GO:1903050 | regulation of proteolysis involved in protein catabolic process | 7 | 1 |
GO:1903052 | positive regulation of proteolysis involved in protein catabolic process | 8 | 1 |
GO:1905784 | regulation of anaphase-promoting complex-dependent catabolic process | 8 | 1 |
GO:1905786 | positive regulation of anaphase-promoting complex-dependent catabolic process | 9 | 1 |
GO:2000058 | regulation of ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:2000060 | positive regulation of ubiquitin-dependent protein catabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0008047 | enzyme activator activity | 3 | 7 |
GO:0010997 | anaphase-promoting complex binding | 3 | 7 |
GO:0030234 | enzyme regulator activity | 2 | 7 |
GO:0044877 | protein-containing complex binding | 2 | 7 |
GO:0055106 | ubiquitin-protein transferase regulator activity | 3 | 7 |
GO:0097027 | ubiquitin-protein transferase activator activity | 4 | 7 |
GO:0098772 | molecular function regulator activity | 1 | 7 |
GO:0140677 | molecular function activator activity | 2 | 7 |
GO:1990757 | ubiquitin ligase activator activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.640 |
CLV_Separin_Metazoa | 445 | 449 | PF03568 | 0.416 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.635 |
DEG_SCF_FBW7_1 | 13 | 20 | PF00400 | 0.580 |
DEG_SPOP_SBC_1 | 789 | 793 | PF00917 | 0.621 |
DOC_CDC14_PxL_1 | 700 | 708 | PF14671 | 0.373 |
DOC_CKS1_1 | 172 | 177 | PF01111 | 0.535 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.606 |
DOC_CKS1_1 | 386 | 391 | PF01111 | 0.586 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.381 |
DOC_CYCLIN_RxL_1 | 241 | 251 | PF00134 | 0.593 |
DOC_CYCLIN_RxL_1 | 715 | 725 | PF00134 | 0.469 |
DOC_MAPK_gen_1 | 98 | 106 | PF00069 | 0.665 |
DOC_MAPK_MEF2A_6 | 369 | 378 | PF00069 | 0.586 |
DOC_PP1_RVXF_1 | 630 | 637 | PF00149 | 0.473 |
DOC_PP1_RVXF_1 | 651 | 658 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.572 |
DOC_PP4_FxxP_1 | 18 | 21 | PF00568 | 0.623 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.664 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.542 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 789 | 793 | PF00917 | 0.639 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 752 | 757 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 384 | 389 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 448 | 456 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 509 | 514 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 656 | 662 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 760 | 769 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 78 | 83 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.602 |
LIG_BIR_III_2 | 31 | 35 | PF00653 | 0.558 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.589 |
LIG_BRCT_BRCA1_1 | 815 | 819 | PF00533 | 0.495 |
LIG_BRCT_BRCA1_2 | 180 | 186 | PF00533 | 0.586 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.606 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.612 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.681 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.674 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.490 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.548 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.273 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.317 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.345 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.414 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.304 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.658 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.474 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.360 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.469 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.638 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.620 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.621 |
LIG_LIR_Apic_2 | 383 | 389 | PF02991 | 0.541 |
LIG_LIR_Apic_2 | 699 | 704 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 409 | 420 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 553 | 562 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 761 | 771 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 512 | 518 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 553 | 557 | PF02991 | 0.441 |
LIG_LYPXL_yS_3 | 703 | 706 | PF13949 | 0.373 |
LIG_PCNA_yPIPBox_3 | 73 | 85 | PF02747 | 0.610 |
LIG_Pex14_2 | 742 | 746 | PF04695 | 0.505 |
LIG_PTB_Apo_2 | 428 | 435 | PF02174 | 0.404 |
LIG_PTB_Phospho_1 | 428 | 434 | PF10480 | 0.407 |
LIG_REV1ctd_RIR_1 | 620 | 630 | PF16727 | 0.516 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.644 |
LIG_SH2_CRK | 412 | 416 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 412 | 415 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 693 | 696 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.618 |
LIG_SH3_1 | 392 | 398 | PF00018 | 0.425 |
LIG_SH3_2 | 395 | 400 | PF14604 | 0.423 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.642 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.552 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.572 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.751 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.425 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.469 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.591 |
LIG_SUMO_SIM_par_1 | 508 | 514 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 529 | 536 | PF11976 | 0.391 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.556 |
LIG_WRC_WIRS_1 | 551 | 556 | PF05994 | 0.425 |
MOD_CDC14_SPxK_1 | 121 | 124 | PF00782 | 0.580 |
MOD_CDC14_SPxK_1 | 287 | 290 | PF00782 | 0.634 |
MOD_CDK_SPK_2 | 155 | 160 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 118 | 124 | PF00069 | 0.589 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.605 |
MOD_CDK_SPxK_1 | 284 | 290 | PF00069 | 0.639 |
MOD_CDK_SPxK_1 | 394 | 400 | PF00069 | 0.416 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.609 |
MOD_CDK_SPxxK_3 | 385 | 392 | PF00069 | 0.523 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.769 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.644 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.566 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.607 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.674 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.637 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.773 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.620 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.349 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.501 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.627 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.368 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.572 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.464 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.493 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.593 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.599 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.569 |
MOD_CK1_1 | 770 | 776 | PF00069 | 0.575 |
MOD_CK1_1 | 788 | 794 | PF00069 | 0.501 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.600 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.685 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.654 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.534 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.504 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.600 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.597 |
MOD_GlcNHglycan | 190 | 194 | PF01048 | 0.538 |
MOD_GlcNHglycan | 200 | 204 | PF01048 | 0.654 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.698 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.600 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.601 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.581 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.342 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.338 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.334 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.619 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.360 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.284 |
MOD_GlcNHglycan | 608 | 612 | PF01048 | 0.745 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.270 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.325 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.262 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.670 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.553 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.663 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.600 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.647 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.584 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.537 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.591 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.591 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.630 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.657 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.496 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.613 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.630 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.395 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.304 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.387 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.419 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.484 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.560 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.516 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.600 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.361 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.600 |
MOD_GSK3_1 | 767 | 774 | PF00069 | 0.546 |
MOD_GSK3_1 | 780 | 787 | PF00069 | 0.671 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.584 |
MOD_LATS_1 | 41 | 47 | PF00433 | 0.642 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.620 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.548 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.631 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.549 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.728 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.629 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.720 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.366 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.469 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.485 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.581 |
MOD_NEK2_1 | 751 | 756 | PF00069 | 0.587 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.555 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.515 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.605 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.668 |
MOD_NEK2_2 | 736 | 741 | PF00069 | 0.469 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.284 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.567 |
MOD_PIKK_1 | 670 | 676 | PF00454 | 0.358 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.605 |
MOD_PIKK_1 | 808 | 814 | PF00454 | 0.656 |
MOD_PK_1 | 179 | 185 | PF00069 | 0.567 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.614 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.575 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.603 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.501 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.278 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.368 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.514 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.431 |
MOD_PKA_2 | 751 | 757 | PF00069 | 0.712 |
MOD_PKA_2 | 759 | 765 | PF00069 | 0.707 |
MOD_PKA_2 | 813 | 819 | PF00069 | 0.638 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.616 |
MOD_PKB_1 | 382 | 390 | PF00069 | 0.606 |
MOD_PKB_1 | 538 | 546 | PF00069 | 0.577 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.629 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.675 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.586 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.554 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.252 |
MOD_Plk_1 | 507 | 513 | PF00069 | 0.304 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.374 |
MOD_Plk_1 | 736 | 742 | PF00069 | 0.469 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.599 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.636 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.571 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.599 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.433 |
MOD_Plk_4 | 696 | 702 | PF00069 | 0.345 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.469 |
MOD_Plk_4 | 815 | 821 | PF00069 | 0.495 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.609 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.618 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.647 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.593 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.605 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.526 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.635 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.691 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.614 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.607 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.536 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.416 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.504 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.632 |
MOD_ProDKin_1 | 752 | 758 | PF00069 | 0.574 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.788 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.663 |
MOD_SUMO_rev_2 | 97 | 103 | PF00179 | 0.591 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 703 | 706 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 763 | 766 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 706 | 708 | PF00400 | 0.381 |
TRG_NES_CRM1_1 | 423 | 437 | PF08389 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 244 | 249 | PF00026 | 0.593 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM82 | Leptomonas seymouri | 59% | 98% |
A0A3Q8IG81 | Leishmania donovani | 90% | 99% |
A4HDN2 | Leishmania braziliensis | 82% | 100% |
E9AH79 | Leishmania infantum | 91% | 99% |
Q4QAF9 | Leishmania major | 91% | 100% |