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:0005840 | ribosome | 5 | 4 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043228 | non-membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
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 |
GO:1990904 | ribonucleoprotein complex | 2 | 4 |
Related structures:
AlphaFold database: A4HL72
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 | 436 | 440 | PF00656 | 0.414 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 711 | 713 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 561 | 563 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.582 |
CLV_PCSK_PC7_1 | 41 | 47 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.447 |
CLV_Separin_Metazoa | 279 | 283 | PF03568 | 0.562 |
DEG_Kelch_Keap1_1 | 403 | 408 | PF01344 | 0.448 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.676 |
DEG_SCF_FBW7_1 | 141 | 146 | PF00400 | 0.504 |
DEG_SCF_FBW7_1 | 165 | 170 | PF00400 | 0.636 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.501 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.539 |
DOC_MAPK_DCC_7 | 454 | 464 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 454 | 464 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 491 | 499 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 637 | 644 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 429 | 437 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 457 | 464 | PF00069 | 0.352 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.390 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.381 |
DOC_USP7_MATH_2 | 301 | 307 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 225 | 234 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 308 | 313 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 535 | 540 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 612 | 620 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 645 | 651 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.681 |
LIG_APCC_ABBAyCdc20_2 | 712 | 718 | PF00400 | 0.492 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.427 |
LIG_EH1_1 | 617 | 625 | PF00400 | 0.417 |
LIG_eIF4E_1 | 618 | 624 | PF01652 | 0.275 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.603 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.635 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.622 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.447 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.392 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.454 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.434 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.588 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.391 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.683 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.424 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.654 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.310 |
LIG_IBAR_NPY_1 | 129 | 131 | PF08397 | 0.603 |
LIG_Integrin_isoDGR_2 | 16 | 18 | PF01839 | 0.555 |
LIG_LIR_Apic_2 | 137 | 143 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 169 | 180 | PF02991 | 0.769 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 449 | 460 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 648 | 658 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.778 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 654 | 659 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.348 |
LIG_MAD2 | 368 | 376 | PF02301 | 0.394 |
LIG_PCNA_yPIPBox_3 | 612 | 624 | PF02747 | 0.430 |
LIG_Pex14_2 | 688 | 692 | PF04695 | 0.358 |
LIG_RPA_C_Fungi | 198 | 210 | PF08784 | 0.499 |
LIG_RPA_C_Fungi | 443 | 455 | PF08784 | 0.394 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.608 |
LIG_SH2_PTP2 | 140 | 143 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.729 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.490 |
LIG_SH3_2 | 373 | 378 | PF14604 | 0.482 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.514 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.437 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.420 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.351 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.647 |
LIG_SH3_4 | 713 | 720 | PF00018 | 0.492 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 411 | 417 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 472 | 479 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 494 | 501 | PF11976 | 0.245 |
LIG_TRAF2_1 | 592 | 595 | PF00917 | 0.611 |
LIG_TRAF2_1 | 672 | 675 | PF00917 | 0.422 |
LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.638 |
LIG_WRC_WIRS_1 | 309 | 314 | PF05994 | 0.500 |
LIG_WRC_WIRS_1 | 653 | 658 | PF05994 | 0.412 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.625 |
MOD_CDK_SPK_2 | 289 | 294 | PF00069 | 0.614 |
MOD_CDK_SPK_2 | 536 | 541 | PF00069 | 0.474 |
MOD_CDK_SPxK_1 | 362 | 368 | PF00069 | 0.450 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.606 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.626 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.579 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.611 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.656 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.674 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.639 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.527 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.531 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.642 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.358 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.416 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.329 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.376 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.638 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.657 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.602 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.574 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.397 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.719 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.544 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.413 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.311 |
MOD_Cter_Amidation | 710 | 713 | PF01082 | 0.502 |
MOD_DYRK1A_RPxSP_1 | 536 | 540 | PF00069 | 0.474 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.548 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.693 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.548 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.694 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.663 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.668 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.725 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.716 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.429 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.292 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.657 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.596 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.668 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.619 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.608 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.680 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.613 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.786 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.457 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.543 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.774 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.599 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.600 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.626 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.579 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.444 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.615 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.385 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.448 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.573 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.449 |
MOD_N-GLC_2 | 388 | 390 | PF02516 | 0.409 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.569 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.528 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.631 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.574 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.394 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.410 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.427 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.457 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.481 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.571 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.534 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.498 |
MOD_NEK2_2 | 257 | 262 | PF00069 | 0.511 |
MOD_NEK2_2 | 506 | 511 | PF00069 | 0.224 |
MOD_NEK2_2 | 543 | 548 | PF00069 | 0.514 |
MOD_NEK2_2 | 682 | 687 | PF00069 | 0.421 |
MOD_OFUCOSY | 661 | 667 | PF10250 | 0.363 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.400 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.494 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.531 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.685 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.577 |
MOD_PKA_1 | 535 | 541 | PF00069 | 0.476 |
MOD_PKA_1 | 645 | 651 | PF00069 | 0.437 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.616 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.613 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.447 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.635 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.480 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.649 |
MOD_PKB_1 | 340 | 348 | PF00069 | 0.591 |
MOD_PKB_1 | 562 | 570 | PF00069 | 0.415 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.541 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.605 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.628 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.422 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.408 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.632 |
MOD_Plk_2-3 | 587 | 593 | PF00069 | 0.487 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.537 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.496 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.527 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.385 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.495 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.586 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.637 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.641 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.623 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.692 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.596 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.456 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.504 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.609 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 562 | 565 | PF00400 | 0.436 |
TRG_NLS_MonoExtN_4 | 559 | 565 | PF00514 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 274 | 279 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6N4 | Leptomonas seymouri | 59% | 98% |
A0A1X0P1T2 | Trypanosomatidae | 40% | 100% |
A0A3Q8ILY5 | Leishmania donovani | 82% | 100% |
A4I8Q1 | Leishmania infantum | 82% | 100% |
E9B3L5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q4H0 | Leishmania major | 82% | 100% |