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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 6 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005730 | nucleolus | 5 | 2 |
GO:0031010 | ISWI-type complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0070603 | SWI/SNF superfamily-type complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1904949 | ATPase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q1X0
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 2 |
GO:0006338 | chromatin remodeling | 5 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 2 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 2 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 2 |
GO:0031554 | regulation of termination of DNA-templated transcription | 6 | 2 |
GO:0031555 | transcriptional attenuation | 7 | 2 |
GO:0043244 | regulation of protein-containing complex disassembly | 5 | 2 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 2 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 2 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051128 | regulation of cellular component organization | 4 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 2 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 2 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 2 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 189 | 193 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.676 |
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 837 | 841 | PF00656 | 0.504 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 757 | 759 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 825 | 827 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 857 | 859 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 894 | 896 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 916 | 918 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 959 | 961 | PF00675 | 0.283 |
CLV_PCSK_FUR_1 | 413 | 417 | PF00082 | 0.465 |
CLV_PCSK_FUR_1 | 855 | 859 | PF00082 | 0.317 |
CLV_PCSK_FUR_1 | 960 | 964 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 827 | 829 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 894 | 896 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 915 | 917 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 959 | 961 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 962 | 964 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 827 | 829 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 962 | 964 | PF00082 | 0.274 |
CLV_PCSK_PC7_1 | 202 | 208 | PF00082 | 0.671 |
CLV_PCSK_PC7_1 | 416 | 422 | PF00082 | 0.533 |
CLV_PCSK_PC7_1 | 441 | 447 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 581 | 587 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 899 | 903 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 920 | 924 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 968 | 972 | PF00082 | 0.377 |
DEG_APCC_DBOX_1 | 967 | 975 | PF00400 | 0.283 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.493 |
DEG_SCF_TRCP1_1 | 189 | 195 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 606 | 610 | PF00917 | 0.634 |
DEG_SPOP_SBC_1 | 614 | 618 | PF00917 | 0.561 |
DOC_ANK_TNKS_1 | 445 | 452 | PF00023 | 0.617 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.414 |
DOC_CKS1_1 | 550 | 555 | PF01111 | 0.568 |
DOC_CYCLIN_RxL_1 | 500 | 508 | PF00134 | 0.534 |
DOC_CYCLIN_RxL_1 | 532 | 541 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 371 | 377 | PF00134 | 0.354 |
DOC_MAPK_DCC_7 | 162 | 171 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 89 | 95 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 535 | 542 | PF00069 | 0.476 |
DOC_MAPK_RevD_3 | 744 | 759 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 1002 | 1008 | PF00149 | 0.563 |
DOC_PP1_RVXF_1 | 855 | 862 | PF00149 | 0.319 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.509 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 615 | 619 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 794 | 798 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 897 | 901 | PF00917 | 0.217 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.558 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.786 |
LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 679 | 685 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 69 | 79 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 834 | 839 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.402 |
LIG_Actin_WH2_2 | 300 | 315 | PF00022 | 0.379 |
LIG_AP2alpha_2 | 662 | 664 | PF02296 | 0.611 |
LIG_BIR_III_4 | 525 | 529 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 897 | 901 | PF00533 | 0.282 |
LIG_Clathr_ClatBox_1 | 1002 | 1006 | PF01394 | 0.511 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.343 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.801 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.640 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.516 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.505 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.590 |
LIG_FHA_1 | 879 | 885 | PF00498 | 0.425 |
LIG_FHA_1 | 907 | 913 | PF00498 | 0.427 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.413 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.406 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.572 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.698 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.689 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.699 |
LIG_FHA_2 | 799 | 805 | PF00498 | 0.547 |
LIG_FHA_2 | 977 | 983 | PF00498 | 0.496 |
LIG_LIR_Apic_2 | 391 | 397 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 494 | 502 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 829 | 838 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 494 | 498 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 568 | 572 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 683 | 687 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 829 | 835 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 854 | 859 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 881 | 885 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 940 | 945 | PF02991 | 0.326 |
LIG_MAD2 | 867 | 875 | PF02301 | 0.354 |
LIG_NRBOX | 741 | 747 | PF00104 | 0.532 |
LIG_PALB2_WD40_1 | 558 | 566 | PF16756 | 0.551 |
LIG_PCNA_yPIPBox_3 | 231 | 245 | PF02747 | 0.595 |
LIG_PCNA_yPIPBox_3 | 89 | 99 | PF02747 | 0.386 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.458 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.350 |
LIG_SH2_CRK | 832 | 836 | PF00017 | 0.536 |
LIG_SH2_CRK | 856 | 860 | PF00017 | 0.317 |
LIG_SH2_GRB2like | 999 | 1002 | PF00017 | 0.495 |
LIG_SH2_PTP2 | 78 | 81 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 999 | 1002 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 493 | 497 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 832 | 836 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 949 | 952 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 977 | 980 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 999 | 1002 | PF00017 | 0.551 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.680 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.622 |
LIG_SH3_3 | 877 | 883 | PF00018 | 0.312 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 167 | 174 | PF11976 | 0.652 |
LIG_SUMO_SIM_par_1 | 536 | 541 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 834 | 840 | PF11976 | 0.432 |
LIG_SxIP_EBH_1 | 72 | 84 | PF03271 | 0.387 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.502 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.427 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.516 |
LIG_TRAF2_1 | 627 | 630 | PF00917 | 0.709 |
LIG_TRAF2_1 | 654 | 657 | PF00917 | 0.696 |
LIG_TRAF2_1 | 980 | 983 | PF00917 | 0.523 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.351 |
LIG_TYR_ITIM | 76 | 81 | PF00017 | 0.445 |
LIG_WRC_WIRS_1 | 950 | 955 | PF05994 | 0.366 |
MOD_CDC14_SPxK_1 | 174 | 177 | PF00782 | 0.622 |
MOD_CDK_SPK_2 | 549 | 554 | PF00069 | 0.579 |
MOD_CDK_SPK_2 | 630 | 635 | PF00069 | 0.548 |
MOD_CDK_SPxK_1 | 171 | 177 | PF00069 | 0.622 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.517 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.687 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.717 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.701 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.521 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.716 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.486 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.457 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.494 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.584 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.525 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.686 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.640 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.637 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.575 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.461 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.523 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.555 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.428 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.438 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.577 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.451 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.705 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.642 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.659 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.687 |
MOD_CK2_1 | 976 | 982 | PF00069 | 0.436 |
MOD_Cter_Amidation | 913 | 916 | PF01082 | 0.345 |
MOD_Cter_Amidation | 960 | 963 | PF01082 | 0.274 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.541 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.662 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.507 |
MOD_GlcNHglycan | 920 | 923 | PF01048 | 0.333 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.631 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.632 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.535 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.479 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.731 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.570 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.780 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.686 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.618 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.324 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.561 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.417 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.389 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.663 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.487 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.664 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.550 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.654 |
MOD_N-GLC_1 | 763 | 768 | PF02516 | 0.561 |
MOD_N-GLC_1 | 875 | 880 | PF02516 | 0.354 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.520 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.455 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.498 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.495 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.472 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.510 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.545 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.281 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.656 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.484 |
MOD_PIKK_1 | 763 | 769 | PF00454 | 0.554 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.529 |
MOD_PK_1 | 834 | 840 | PF00069 | 0.388 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.738 |
MOD_PKA_1 | 585 | 591 | PF00069 | 0.662 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.681 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.662 |
MOD_PKA_2 | 987 | 993 | PF00069 | 0.564 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.701 |
MOD_PKB_1 | 268 | 276 | PF00069 | 0.438 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.341 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.595 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.555 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.546 |
MOD_Plk_1 | 809 | 815 | PF00069 | 0.452 |
MOD_Plk_1 | 875 | 881 | PF00069 | 0.304 |
MOD_Plk_1 | 906 | 912 | PF00069 | 0.344 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.544 |
MOD_Plk_2-3 | 593 | 599 | PF00069 | 0.698 |
MOD_Plk_2-3 | 662 | 668 | PF00069 | 0.559 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.341 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.640 |
MOD_Plk_4 | 907 | 913 | PF00069 | 0.238 |
MOD_Plk_4 | 949 | 955 | PF00069 | 0.351 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.633 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.470 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.620 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.416 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.605 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.699 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.787 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.606 |
MOD_SUMO_for_1 | 414 | 417 | PF00179 | 0.426 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 275 | 280 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 425 | 431 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 630 | 640 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 662 | 671 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 722 | 731 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 736 | 745 | PF00179 | 0.390 |
MOD_SUMO_rev_2 | 781 | 790 | PF00179 | 0.566 |
TRG_DiLeu_BaEn_1 | 439 | 444 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.644 |
TRG_DiLeu_BaEn_1 | 741 | 746 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_3 | 906 | 912 | PF01217 | 0.282 |
TRG_DiLeu_BaEn_4 | 907 | 913 | PF01217 | 0.343 |
TRG_DiLeu_BaLyEn_6 | 831 | 836 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 832 | 835 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 856 | 859 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 860 | 863 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 999 | 1002 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 856 | 858 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 915 | 917 | PF00400 | 0.345 |
TRG_NLS_Bipartite_1 | 404 | 424 | PF00514 | 0.543 |
TRG_NLS_MonoCore_2 | 576 | 581 | PF00514 | 0.653 |
TRG_NLS_MonoCore_2 | 757 | 762 | PF00514 | 0.544 |
TRG_NLS_MonoExtC_3 | 419 | 425 | PF00514 | 0.541 |
TRG_NLS_MonoExtC_3 | 576 | 581 | PF00514 | 0.582 |
TRG_NLS_MonoExtN_4 | 577 | 583 | PF00514 | 0.669 |
TRG_NLS_MonoExtN_4 | 758 | 763 | PF00514 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.695 |
TRG_Pf-PMV_PEXEL_1 | 729 | 733 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 834 | 839 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD66 | Leptomonas seymouri | 57% | 94% |
A0A3S7XAG3 | Leishmania donovani | 91% | 100% |
A0A422NTX5 | Trypanosoma rangeli | 38% | 100% |
A4HNW6 | Leishmania braziliensis | 75% | 100% |
A4ICM8 | Leishmania infantum | 91% | 100% |
D0A2T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ASM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |