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 | 2 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 2 |
GO:0005680 | anaphase-promoting complex | 4 | 2 |
GO:0005840 | ribosome | 5 | 5 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043228 | non-membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
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 |
GO:1990904 | ribonucleoprotein complex | 2 | 5 |
Related structures:
AlphaFold database: Q4Q4H0
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 | 8 |
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 | 8 |
GO:0019222 | regulation of metabolic process | 3 | 8 |
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 | 8 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050794 | regulation of cellular process | 3 | 2 |
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:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 8 |
GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 2 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 8 |
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 | 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:0050790 | regulation of catalytic activity | 3 | 6 |
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:0065009 | regulation of molecular function | 2 | 6 |
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 |
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 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.557 |
CLV_MEL_PAP_1 | 85 | 91 | PF00089 | 0.716 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.808 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.760 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.808 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.760 |
CLV_PCSK_PC1ET2_1 | 561 | 563 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.800 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.733 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.813 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.482 |
CLV_Separin_Metazoa | 279 | 283 | PF03568 | 0.798 |
DEG_Kelch_Keap1_1 | 403 | 408 | PF01344 | 0.607 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.742 |
DEG_SCF_FBW7_1 | 165 | 170 | PF00400 | 0.708 |
DEG_SCF_FBW7_1 | 227 | 233 | PF00400 | 0.556 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.670 |
DOC_ANK_TNKS_1 | 261 | 268 | PF00023 | 0.671 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.697 |
DOC_CKS1_1 | 57 | 62 | PF01111 | 0.738 |
DOC_MAPK_gen_1 | 454 | 464 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 637 | 644 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 420 | 427 | PF00149 | 0.385 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.624 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 656 | 659 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.452 |
DOC_USP7_MATH_2 | 301 | 307 | PF00917 | 0.722 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 308 | 313 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 37 | 42 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 535 | 540 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 645 | 651 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.834 |
LIG_Actin_WH2_2 | 292 | 310 | PF00022 | 0.751 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.509 |
LIG_EH1_1 | 617 | 625 | PF00400 | 0.501 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.566 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.726 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.718 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.507 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.478 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.476 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.685 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.531 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.523 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.491 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.814 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.486 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.700 |
LIG_IBAR_NPY_1 | 129 | 131 | PF08397 | 0.776 |
LIG_LIR_Apic_2 | 655 | 659 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 449 | 459 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 648 | 658 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.444 |
LIG_MAD2 | 368 | 376 | PF02301 | 0.548 |
LIG_PCNA_yPIPBox_3 | 612 | 624 | PF02747 | 0.582 |
LIG_Pex14_2 | 688 | 692 | PF04695 | 0.402 |
LIG_PTB_Apo_2 | 506 | 513 | PF02174 | 0.547 |
LIG_PTB_Phospho_1 | 506 | 512 | PF10480 | 0.547 |
LIG_RPA_C_Fungi | 443 | 455 | PF08784 | 0.516 |
LIG_SH2_NCK_1 | 131 | 135 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.795 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.815 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.549 |
LIG_SH3_2 | 373 | 378 | PF14604 | 0.635 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.712 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.492 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.508 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.492 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.805 |
LIG_SUMO_SIM_par_1 | 410 | 416 | PF11976 | 0.531 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.605 |
LIG_TRAF2_1 | 592 | 595 | PF00917 | 0.686 |
LIG_TRAF2_1 | 672 | 675 | PF00917 | 0.559 |
LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.728 |
LIG_WRC_WIRS_1 | 653 | 658 | PF05994 | 0.502 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.713 |
MOD_CDC14_SPxK_1 | 114 | 117 | PF00782 | 0.711 |
MOD_CDK_SPK_2 | 289 | 294 | PF00069 | 0.709 |
MOD_CDK_SPK_2 | 536 | 541 | PF00069 | 0.549 |
MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.709 |
MOD_CDK_SPxK_1 | 362 | 368 | PF00069 | 0.491 |
MOD_CDK_SPxK_1 | 56 | 62 | PF00069 | 0.729 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.794 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.658 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.691 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.686 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.643 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.643 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.722 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.801 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.681 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.499 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.486 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.535 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.472 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.496 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.727 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.809 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.612 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.674 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.498 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.814 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.506 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.487 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.616 |
MOD_Cter_Amidation | 72 | 75 | PF01082 | 0.758 |
MOD_DYRK1A_RPxSP_1 | 536 | 540 | PF00069 | 0.550 |
MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.805 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.687 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.812 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.819 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.774 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.710 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.748 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.714 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.677 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.694 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.775 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.771 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.516 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.512 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.226 |
MOD_GlcNHglycan | 693 | 697 | PF01048 | 0.588 |
MOD_GlcNHglycan | 701 | 705 | PF01048 | 0.709 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.763 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.686 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.665 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.684 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.661 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.567 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.747 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.597 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.534 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.721 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.784 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.777 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.721 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.711 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.704 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.514 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.593 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.478 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.658 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.542 |
MOD_N-GLC_2 | 388 | 390 | PF02516 | 0.558 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.663 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.754 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.666 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.769 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.691 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.477 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.286 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.485 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.225 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.514 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.560 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.591 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.663 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.644 |
MOD_NEK2_2 | 682 | 687 | PF00069 | 0.502 |
MOD_OFUCOSY | 661 | 667 | PF10250 | 0.511 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.466 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.577 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.814 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.669 |
MOD_PKA_1 | 535 | 541 | PF00069 | 0.623 |
MOD_PKA_1 | 645 | 651 | PF00069 | 0.521 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.765 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.781 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.735 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.516 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.730 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.623 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.719 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.737 |
MOD_PKB_1 | 340 | 348 | PF00069 | 0.778 |
MOD_PKB_1 | 562 | 570 | PF00069 | 0.498 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.641 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.765 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.583 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.498 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.717 |
MOD_Plk_2-3 | 718 | 724 | PF00069 | 0.562 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.686 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.633 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.585 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.588 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.475 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.543 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.623 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.727 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.802 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.713 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.700 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.700 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.634 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.491 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.544 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.736 |
MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.804 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.682 |
MOD_SUMO_for_1 | 29 | 32 | PF00179 | 0.708 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.645 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 562 | 565 | PF00400 | 0.518 |
TRG_NLS_MonoExtN_4 | 559 | 565 | PF00514 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 274 | 279 | PF00026 | 0.727 |
TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.685 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6N4 | Leptomonas seymouri | 60% | 98% |
A0A3Q8ILY5 | Leishmania donovani | 93% | 100% |
A4HL72 | Leishmania braziliensis | 82% | 100% |
A4I8Q1 | Leishmania infantum | 93% | 100% |
D0A4N8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9B3L5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |