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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042555 | MCM complex | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B719
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0032392 | DNA geometric change | 7 | 11 |
GO:0032508 | DNA duplex unwinding | 8 | 11 |
GO:0051276 | chromosome organization | 5 | 11 |
GO:0071103 | DNA conformation change | 6 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 724 | 728 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 684 | 686 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 892 | 894 | PF00675 | 0.602 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 684 | 686 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 835 | 837 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 894 | 896 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.229 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 835 | 837 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 894 | 896 | PF00082 | 0.600 |
CLV_PCSK_PC7_1 | 139 | 145 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.477 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.415 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.612 |
DEG_SCF_FBW7_2 | 495 | 502 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 274 | 278 | PF00917 | 0.628 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.704 |
DEG_SPOP_SBC_1 | 380 | 384 | PF00917 | 0.415 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.388 |
DOC_CKS1_1 | 496 | 501 | PF01111 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 624 | 630 | PF00134 | 0.487 |
DOC_MAPK_gen_1 | 307 | 316 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 472 | 481 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 684 | 692 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 868 | 877 | PF00069 | 0.573 |
DOC_PP1_RVXF_1 | 532 | 539 | PF00149 | 0.319 |
DOC_PP1_RVXF_1 | 900 | 907 | PF00149 | 0.574 |
DOC_PP2B_LxvP_1 | 327 | 330 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 845 | 848 | PF13499 | 0.668 |
DOC_PP2B_LxvP_1 | 875 | 878 | PF13499 | 0.672 |
DOC_SPAK_OSR1_1 | 331 | 335 | PF12202 | 0.435 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 780 | 784 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 799 | 803 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 871 | 875 | PF00917 | 0.750 |
DOC_USP7_UBL2_3 | 307 | 311 | PF12436 | 0.521 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 711 | 716 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 811 | 816 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 869 | 874 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 109 | 117 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 272 | 282 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 287 | 296 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 473 | 481 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 591 | 599 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 619 | 625 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 798 | 804 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 893 | 901 | PF00244 | 0.620 |
LIG_AP2alpha_2 | 677 | 679 | PF02296 | 0.495 |
LIG_BIR_III_2 | 577 | 581 | PF00653 | 0.472 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 902 | 906 | PF00533 | 0.577 |
LIG_Clathr_ClatBox_1 | 218 | 222 | PF01394 | 0.415 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.466 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.352 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.422 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.340 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.509 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.426 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.380 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.588 |
LIG_FHA_1 | 878 | 884 | PF00498 | 0.556 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.429 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.535 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.611 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.503 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.415 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.694 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.410 |
LIG_Integrin_RGD_1 | 685 | 687 | PF01839 | 0.577 |
LIG_LIR_Gen_1 | 487 | 495 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 827 | 833 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 882 | 892 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 827 | 831 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 882 | 888 | PF02991 | 0.581 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.426 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.470 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.441 |
LIG_Pex14_2 | 328 | 332 | PF04695 | 0.435 |
LIG_Pex14_2 | 489 | 493 | PF04695 | 0.415 |
LIG_SH2_CRK | 671 | 675 | PF00017 | 0.591 |
LIG_SH2_CRK | 828 | 832 | PF00017 | 0.532 |
LIG_SH2_CRK | 885 | 889 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 636 | 640 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 828 | 832 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 563 | 566 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 828 | 831 | PF00017 | 0.579 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.467 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.549 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.429 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.415 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.417 |
LIG_SH3_3 | 807 | 813 | PF00018 | 0.709 |
LIG_SUMO_SIM_par_1 | 216 | 224 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 72 | 80 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 745 | 751 | PF11976 | 0.608 |
LIG_TRFH_1 | 885 | 889 | PF08558 | 0.629 |
LIG_TYR_ITIM | 11 | 16 | PF00017 | 0.485 |
LIG_TYR_ITIM | 883 | 888 | PF00017 | 0.579 |
LIG_UBA3_1 | 137 | 143 | PF00899 | 0.384 |
LIG_UBA3_1 | 492 | 500 | PF00899 | 0.365 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.447 |
LIG_WW_2 | 21 | 24 | PF00397 | 0.383 |
MOD_CDK_SPK_2 | 33 | 38 | PF00069 | 0.467 |
MOD_CDK_SPK_2 | 495 | 500 | PF00069 | 0.280 |
MOD_CDK_SPK_2 | 781 | 786 | PF00069 | 0.591 |
MOD_CDK_SPxxK_3 | 427 | 434 | PF00069 | 0.384 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.426 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.296 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.566 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.626 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.258 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.667 |
MOD_CK1_1 | 811 | 817 | PF00069 | 0.672 |
MOD_CK1_1 | 854 | 860 | PF00069 | 0.718 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.407 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.252 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.604 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.524 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.561 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.744 |
MOD_CK2_1 | 873 | 879 | PF00069 | 0.583 |
MOD_Cter_Amidation | 833 | 836 | PF01082 | 0.601 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.271 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.583 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.613 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.284 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.296 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.261 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.602 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.252 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.441 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.533 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.609 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.574 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.631 |
MOD_GlcNHglycan | 854 | 857 | PF01048 | 0.639 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.717 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.398 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.391 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.285 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.261 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.238 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.564 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.508 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.275 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.583 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.275 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.252 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.277 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.312 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.315 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.252 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.515 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.434 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.653 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.708 |
MOD_GSK3_1 | 855 | 862 | PF00069 | 0.714 |
MOD_GSK3_1 | 869 | 876 | PF00069 | 0.753 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.620 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.384 |
MOD_N-GLC_1 | 679 | 684 | PF02516 | 0.503 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.513 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.321 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.331 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.428 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.236 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.331 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.252 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.328 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.488 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.408 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.376 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.655 |
MOD_NEK2_2 | 346 | 351 | PF00069 | 0.328 |
MOD_NEK2_2 | 49 | 54 | PF00069 | 0.411 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.356 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.252 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.373 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.273 |
MOD_PIKK_1 | 704 | 710 | PF00454 | 0.624 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.660 |
MOD_PIKK_1 | 808 | 814 | PF00454 | 0.690 |
MOD_PIKK_1 | 826 | 832 | PF00454 | 0.701 |
MOD_PIKK_1 | 859 | 865 | PF00454 | 0.707 |
MOD_PKA_1 | 893 | 899 | PF00069 | 0.609 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.335 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.366 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.269 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.454 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.252 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.510 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.283 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.252 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.273 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.671 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.678 |
MOD_PKA_2 | 797 | 803 | PF00069 | 0.685 |
MOD_PKB_1 | 310 | 318 | PF00069 | 0.333 |
MOD_PKB_1 | 796 | 804 | PF00069 | 0.448 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.331 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.483 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.380 |
MOD_Plk_1 | 742 | 748 | PF00069 | 0.525 |
MOD_Plk_1 | 826 | 832 | PF00069 | 0.525 |
MOD_Plk_2-3 | 433 | 439 | PF00069 | 0.252 |
MOD_Plk_2-3 | 525 | 531 | PF00069 | 0.516 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.252 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.147 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.494 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.252 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.385 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.597 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.577 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.380 |
MOD_Plk_4 | 883 | 889 | PF00069 | 0.763 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.709 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.384 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.296 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.296 |
MOD_ProDKin_1 | 711 | 717 | PF00069 | 0.523 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.620 |
MOD_ProDKin_1 | 811 | 817 | PF00069 | 0.765 |
MOD_ProDKin_1 | 869 | 875 | PF00069 | 0.719 |
MOD_SUMO_for_1 | 499 | 502 | PF00179 | 0.280 |
MOD_SUMO_rev_2 | 169 | 176 | PF00179 | 0.384 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.252 |
TRG_DiLeu_BaEn_1 | 842 | 847 | PF01217 | 0.692 |
TRG_DiLeu_BaLyEn_6 | 481 | 486 | PF01217 | 0.252 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 828 | 831 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 885 | 888 | PF00928 | 0.584 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 734 | 736 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 796 | 799 | PF00400 | 0.492 |
TRG_NES_CRM1_1 | 186 | 200 | PF08389 | 0.272 |
TRG_NES_CRM1_1 | 5 | 20 | PF08389 | 0.332 |
TRG_NLS_MonoCore_2 | 308 | 313 | PF00514 | 0.435 |
TRG_NLS_MonoExtC_3 | 892 | 898 | PF00514 | 0.662 |
TRG_NLS_MonoExtN_4 | 307 | 314 | PF00514 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P9H0 | Leptomonas seymouri | 74% | 98% |
A0A0S4J4D4 | Bodo saltans | 44% | 97% |
A0A1X0P4W1 | Trypanosomatidae | 59% | 100% |
A0A3Q8IQ79 | Leishmania donovani | 93% | 100% |
A0A3R7MUG3 | Trypanosoma rangeli | 56% | 100% |
A0A3S5H7S8 | Leishmania donovani | 30% | 100% |
A4HKT9 | Leishmania braziliensis | 30% | 100% |
A4HNF5 | Leishmania braziliensis | 85% | 100% |
A4I8B8 | Leishmania infantum | 30% | 100% |
A4IC27 | Leishmania infantum | 93% | 100% |
B8B406 | Oryza sativa subsp. indica | 33% | 100% |
C9ZYH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AFW6 | Leishmania major | 93% | 100% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q561P5 | Xenopus tropicalis | 27% | 100% |
Q69QA6 | Oryza sativa subsp. japonica | 33% | 100% |
Q9U1E0 | Leishmania major | 28% | 100% |