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 | 2 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 2 |
GO:0005680 | anaphase-promoting complex | 4 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q1L9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 7 |
GO:0009894 | regulation of catabolic process | 4 | 2 |
GO:0009896 | positive regulation of catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 7 |
GO:0019222 | regulation of metabolic process | 3 | 7 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030162 | regulation of proteolysis | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031329 | regulation of cellular catabolic process | 5 | 2 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 2 |
GO:0032434 | regulation of proteasomal ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0032436 | positive regulation of proteasomal ubiquitin-dependent protein catabolic process | 8 | 2 |
GO:0042176 | regulation of protein catabolic process | 5 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0045732 | positive regulation of protein catabolic process | 6 | 2 |
GO:0045862 | positive regulation of proteolysis | 7 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 7 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 2 |
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:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 7 |
GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 2 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901800 | positive regulation of proteasomal protein catabolic process | 7 | 2 |
GO:1903050 | regulation of proteolysis involved in protein catabolic process | 7 | 2 |
GO:1903052 | positive regulation of proteolysis involved in protein catabolic process | 8 | 2 |
GO:1905784 | regulation of anaphase-promoting complex-dependent catabolic process | 8 | 2 |
GO:1905786 | positive regulation of anaphase-promoting complex-dependent catabolic process | 9 | 2 |
GO:2000058 | regulation of ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:2000060 | positive regulation of ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0031396 | regulation of protein ubiquitination | 8 | 5 |
GO:0031398 | positive regulation of protein ubiquitination | 9 | 5 |
GO:0031399 | regulation of protein modification process | 6 | 5 |
GO:0031401 | positive regulation of protein modification process | 7 | 5 |
GO:0043085 | positive regulation of catalytic activity | 4 | 5 |
GO:0044093 | positive regulation of molecular function | 3 | 5 |
GO:0050790 | regulation of catalytic activity | 3 | 5 |
GO:0051338 | regulation of transferase activity | 4 | 5 |
GO:0051347 | positive regulation of transferase activity | 5 | 5 |
GO:0051438 | regulation of ubiquitin-protein transferase activity | 5 | 5 |
GO:0051443 | positive regulation of ubiquitin-protein transferase activity | 6 | 5 |
GO:0065009 | regulation of molecular function | 2 | 5 |
GO:1903320 | regulation of protein modification by small protein conjugation or removal | 7 | 5 |
GO:1903322 | positive regulation of protein modification by small protein conjugation or removal | 8 | 5 |
GO:1904666 | regulation of ubiquitin protein ligase activity | 6 | 5 |
GO:1904668 | positive regulation of ubiquitin protein ligase activity | 7 | 5 |
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 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 649 | 653 | PF00656 | 0.497 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.574 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.575 |
CLV_PCSK_PC7_1 | 539 | 545 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.470 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.639 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.553 |
DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.600 |
DEG_SPOP_SBC_1 | 375 | 379 | PF00917 | 0.402 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.671 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.644 |
DOC_CKS1_1 | 104 | 109 | PF01111 | 0.625 |
DOC_CKS1_1 | 676 | 681 | PF01111 | 0.571 |
DOC_CYCLIN_RxL_1 | 199 | 210 | PF00134 | 0.624 |
DOC_MAPK_MEF2A_6 | 242 | 250 | PF00069 | 0.493 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.531 |
DOC_PP1_RVXF_1 | 339 | 346 | PF00149 | 0.503 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.604 |
DOC_PP2B_LxvP_1 | 322 | 325 | PF13499 | 0.479 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.609 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.519 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.475 |
DOC_PP4_MxPP_1 | 172 | 175 | PF00568 | 0.607 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 129 | 136 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 208 | 217 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 234 | 240 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 264 | 269 | PF00244 | 0.750 |
LIG_14-3-3_CanoR_1 | 285 | 290 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 327 | 333 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 40 | 48 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 447 | 453 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 50 | 56 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.510 |
LIG_Actin_WH2_2 | 564 | 582 | PF00022 | 0.551 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.574 |
LIG_Clathr_ClatBox_1 | 236 | 240 | PF01394 | 0.422 |
LIG_eIF4E_1 | 531 | 537 | PF01652 | 0.688 |
LIG_EVH1_1 | 413 | 417 | PF00568 | 0.536 |
LIG_EVH1_2 | 414 | 418 | PF00568 | 0.536 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.711 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.525 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.502 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.544 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.426 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.436 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.604 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.422 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.579 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.404 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.499 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.627 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.725 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.512 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.557 |
LIG_GBD_Chelix_1 | 79 | 87 | PF00786 | 0.308 |
LIG_HP1_1 | 350 | 354 | PF01393 | 0.481 |
LIG_Integrin_RGD_1 | 159 | 161 | PF01839 | 0.509 |
LIG_LIR_Apic_2 | 122 | 128 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 52 | 63 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 640 | 646 | PF02991 | 0.591 |
LIG_OCRL_FandH_1 | 288 | 300 | PF00620 | 0.389 |
LIG_PCNA_PIPBox_1 | 326 | 335 | PF02747 | 0.420 |
LIG_Pex14_1 | 601 | 605 | PF04695 | 0.717 |
LIG_Pex14_2 | 643 | 647 | PF04695 | 0.504 |
LIG_SH2_CRK | 55 | 59 | PF00017 | 0.465 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.724 |
LIG_SH2_CRK | 630 | 634 | PF00017 | 0.459 |
LIG_SH2_NCK_1 | 605 | 609 | PF00017 | 0.724 |
LIG_SH2_NCK_1 | 630 | 634 | PF00017 | 0.577 |
LIG_SH2_PTP2 | 351 | 354 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 630 | 634 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.753 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.423 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.642 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.490 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.480 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.399 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.630 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.585 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.696 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.502 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.457 |
LIG_SUMO_SIM_par_1 | 235 | 240 | PF11976 | 0.427 |
LIG_TRAF2_1 | 668 | 671 | PF00917 | 0.557 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.552 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.425 |
MOD_CDK_SPxxK_3 | 192 | 199 | PF00069 | 0.575 |
MOD_CDK_SPxxK_3 | 675 | 682 | PF00069 | 0.572 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.626 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.327 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.353 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.730 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.629 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.629 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.530 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.625 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.653 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.654 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.704 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.585 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.515 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.559 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.404 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.631 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.547 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.451 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.761 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.528 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.719 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.594 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.535 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.590 |
MOD_GlcNHglycan | 272 | 276 | PF01048 | 0.698 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.298 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.470 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.467 |
MOD_GlcNHglycan | 368 | 372 | PF01048 | 0.452 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.737 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.533 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.656 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.593 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.768 |
MOD_GlcNHglycan | 502 | 506 | PF01048 | 0.558 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.657 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.445 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.569 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.650 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.626 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.579 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.439 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.730 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.457 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.680 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.644 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.613 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.492 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.492 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.609 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.417 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.476 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.632 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.562 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.659 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.524 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.656 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.639 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.626 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.733 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.630 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.274 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.503 |
MOD_LATS_1 | 293 | 299 | PF00433 | 0.576 |
MOD_LATS_1 | 94 | 100 | PF00433 | 0.512 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.292 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.602 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.465 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.379 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.538 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.488 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.728 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.497 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.530 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.731 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.591 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.619 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.471 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.756 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.505 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.425 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.699 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.442 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.559 |
MOD_PK_1 | 264 | 270 | PF00069 | 0.695 |
MOD_PK_1 | 295 | 301 | PF00069 | 0.492 |
MOD_PKA_1 | 129 | 135 | PF00069 | 0.416 |
MOD_PKA_1 | 543 | 549 | PF00069 | 0.728 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.581 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.416 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.630 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.485 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.695 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.616 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.655 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.465 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.728 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.682 |
MOD_PKB_1 | 542 | 550 | PF00069 | 0.586 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.415 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.663 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.420 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.803 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.655 |
MOD_Plk_2-3 | 558 | 564 | PF00069 | 0.713 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.544 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.695 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.740 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.492 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.429 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.532 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.790 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.692 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.621 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.664 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.621 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.525 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.603 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.757 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.511 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.568 |
TRG_DiLeu_BaEn_1 | 671 | 676 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_2 | 140 | 146 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 611 | 616 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 542 | 544 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 611 | 614 | PF00400 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZD9 | Leptomonas seymouri | 57% | 89% |
A0A3S7XAS2 | Leishmania donovani | 94% | 100% |
A4HP71 | Leishmania braziliensis | 80% | 90% |
A4IDH6 | Leishmania infantum | 94% | 100% |
E9ASX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |