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: 7 |
NetGPI | no | yes: 0, no: 7 |
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: A4IDH6
Term | Name | Level | Count |
---|---|---|---|
GO:0009893 | positive regulation of metabolic process | 4 | 8 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 8 |
GO:0019222 | regulation of metabolic process | 3 | 8 |
GO:0031396 | regulation of protein ubiquitination | 8 | 7 |
GO:0031398 | positive regulation of protein ubiquitination | 9 | 7 |
GO:0031399 | regulation of protein modification process | 6 | 7 |
GO:0031401 | positive regulation of protein modification process | 7 | 7 |
GO:0043085 | positive regulation of catalytic activity | 4 | 7 |
GO:0044093 | positive regulation of molecular function | 3 | 7 |
GO:0048518 | positive regulation of biological process | 3 | 8 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050790 | regulation of catalytic activity | 3 | 7 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 8 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 8 |
GO:0051246 | regulation of protein metabolic process | 5 | 8 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 8 |
GO:0051338 | regulation of transferase activity | 4 | 7 |
GO:0051347 | positive regulation of transferase activity | 5 | 7 |
GO:0051438 | regulation of ubiquitin-protein transferase activity | 5 | 7 |
GO:0051443 | positive regulation of ubiquitin-protein transferase activity | 6 | 7 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0065009 | regulation of molecular function | 2 | 7 |
GO:0080090 | regulation of primary metabolic process | 4 | 8 |
GO:1903320 | regulation of protein modification by small protein conjugation or removal | 7 | 7 |
GO:1903322 | positive regulation of protein modification by small protein conjugation or removal | 8 | 7 |
GO:1904666 | regulation of ubiquitin protein ligase activity | 6 | 7 |
GO:1904668 | positive regulation of ubiquitin protein ligase activity | 7 | 7 |
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:0009987 | cellular process | 1 | 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 | 8 |
GO:0008047 | enzyme activator activity | 3 | 8 |
GO:0010997 | anaphase-promoting complex binding | 3 | 8 |
GO:0030234 | enzyme regulator activity | 2 | 8 |
GO:0044877 | protein-containing complex binding | 2 | 8 |
GO:0055106 | ubiquitin-protein transferase regulator activity | 3 | 8 |
GO:0097027 | ubiquitin-protein transferase activator activity | 4 | 8 |
GO:0098772 | molecular function regulator activity | 1 | 8 |
GO:0140677 | molecular function activator activity | 2 | 8 |
GO:1990757 | ubiquitin ligase activator activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 652 | 656 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.643 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.643 |
CLV_PCSK_PC7_1 | 525 | 531 | PF00082 | 0.584 |
CLV_PCSK_PC7_1 | 542 | 548 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.507 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.664 |
DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.570 |
DEG_SPOP_SBC_1 | 411 | 415 | PF00917 | 0.696 |
DOC_CKS1_1 | 104 | 109 | PF01111 | 0.644 |
DOC_CKS1_1 | 679 | 684 | PF01111 | 0.663 |
DOC_CYCLIN_RxL_1 | 202 | 213 | PF00134 | 0.640 |
DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.546 |
DOC_PP1_RVXF_1 | 342 | 349 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.627 |
DOC_PP2B_LxvP_1 | 325 | 328 | PF13499 | 0.520 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.606 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.498 |
DOC_PP4_MxPP_1 | 172 | 175 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.595 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 129 | 136 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.792 |
LIG_14-3-3_CanoR_1 | 211 | 220 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 40 | 48 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 450 | 456 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 50 | 56 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.585 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.657 |
LIG_Clathr_ClatBox_1 | 239 | 243 | PF01394 | 0.429 |
LIG_eIF4E_1 | 534 | 540 | PF01652 | 0.716 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.731 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.513 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.692 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.536 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.581 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.495 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.452 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.508 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.670 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.578 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.701 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.639 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.471 |
LIG_FHA_2 | 650 | 656 | PF00498 | 0.530 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.460 |
LIG_HP1_1 | 353 | 357 | PF01393 | 0.508 |
LIG_Integrin_RGD_1 | 159 | 161 | PF01839 | 0.582 |
LIG_LIR_Apic_2 | 122 | 128 | PF02991 | 0.638 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 352 | 362 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 476 | 485 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 52 | 63 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.554 |
LIG_LYPXL_yS_3 | 421 | 424 | PF13949 | 0.693 |
LIG_OCRL_FandH_1 | 291 | 303 | PF00620 | 0.424 |
LIG_PCNA_PIPBox_1 | 329 | 338 | PF02747 | 0.497 |
LIG_Pex14_1 | 604 | 608 | PF04695 | 0.615 |
LIG_Pex14_2 | 646 | 650 | PF04695 | 0.439 |
LIG_SH2_CRK | 55 | 59 | PF00017 | 0.475 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.605 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.489 |
LIG_SH2_NCK_1 | 608 | 612 | PF00017 | 0.605 |
LIG_SH2_NCK_1 | 633 | 637 | PF00017 | 0.560 |
LIG_SH2_PTP2 | 354 | 357 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 633 | 637 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.710 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.441 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.742 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.562 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.556 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.501 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.413 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.666 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.694 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.732 |
LIG_SH3_3 | 622 | 628 | PF00018 | 0.474 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.533 |
LIG_SUMO_SIM_par_1 | 238 | 243 | PF11976 | 0.491 |
LIG_TRAF2_1 | 671 | 674 | PF00917 | 0.637 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.596 |
LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.508 |
MOD_CDK_SPxxK_3 | 195 | 202 | PF00069 | 0.605 |
MOD_CDK_SPxxK_3 | 678 | 685 | PF00069 | 0.663 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.703 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.307 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.399 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.780 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.688 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.692 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.498 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.632 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.744 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.739 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.740 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.589 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.576 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.515 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.429 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.682 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.511 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.532 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.811 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.768 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.671 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.557 |
MOD_GlcNHglycan | 275 | 279 | PF01048 | 0.767 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.351 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.262 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.487 |
MOD_GlcNHglycan | 371 | 375 | PF01048 | 0.436 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.730 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.585 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.741 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.689 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.758 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.700 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.614 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.699 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.524 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.635 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.739 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.474 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.495 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.423 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.782 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.451 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.716 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.662 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.714 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.546 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.517 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.680 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.493 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.474 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.642 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.748 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.428 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.743 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.692 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.796 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.619 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.252 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.543 |
MOD_LATS_1 | 296 | 302 | PF00433 | 0.607 |
MOD_LATS_1 | 94 | 100 | PF00433 | 0.585 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.317 |
MOD_N-GLC_1 | 506 | 511 | PF02516 | 0.663 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.466 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.409 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.350 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.514 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.690 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.781 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.532 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.509 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.765 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.514 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.792 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.513 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.365 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.728 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.454 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.574 |
MOD_PIKK_1 | 669 | 675 | PF00454 | 0.636 |
MOD_PK_1 | 267 | 273 | PF00069 | 0.675 |
MOD_PK_1 | 298 | 304 | PF00069 | 0.556 |
MOD_PKA_1 | 129 | 135 | PF00069 | 0.508 |
MOD_PKA_1 | 546 | 552 | PF00069 | 0.767 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.643 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.508 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.472 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.656 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.623 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.748 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.454 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.767 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.719 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.493 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.493 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.795 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.630 |
MOD_Plk_2-3 | 561 | 567 | PF00069 | 0.786 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.564 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.737 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.623 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.402 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.506 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.456 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.812 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.678 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.721 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.751 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.699 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.566 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.655 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.806 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.524 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.659 |
TRG_DiLeu_BaEn_1 | 27 | 32 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_1 | 674 | 679 | PF01217 | 0.637 |
TRG_DiLeu_BaEn_2 | 140 | 146 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 614 | 619 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 529 | 531 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 545 | 547 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 614 | 617 | PF00400 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZD9 | Leptomonas seymouri | 57% | 89% |
A0A3S7XAS2 | Leishmania donovani | 100% | 100% |
A4HP71 | Leishmania braziliensis | 78% | 100% |
D0A364 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9ASX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q1L9 | Leishmania major | 94% | 100% |