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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005778 | peroxisomal membrane | 6 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0031903 | microbody membrane | 5 | 12 |
GO:0042579 | microbody | 5 | 12 |
GO:0043226 | organelle | 2 | 13 |
GO:0043227 | membrane-bounded organelle | 3 | 13 |
GO:0043229 | intracellular organelle | 3 | 13 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 13 |
GO:0098588 | bounding membrane of organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
Related structures:
AlphaFold database: A4HB70
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 12 |
GO:0006625 | protein targeting to peroxisome | 5 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007031 | peroxisome organization | 5 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 13 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0033365 | protein localization to organelle | 5 | 12 |
GO:0043574 | peroxisomal transport | 4 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
GO:0072662 | protein localization to peroxisome | 6 | 12 |
GO:0072663 | establishment of protein localization to peroxisome | 5 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0042254 | ribosome biogenesis | 5 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051054 | positive regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0051972 | regulation of telomerase activity | 5 | 1 |
GO:0051973 | positive regulation of telomerase activity | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000278 | regulation of DNA biosynthetic process | 6 | 1 |
GO:2000573 | positive regulation of DNA biosynthetic process | 7 | 1 |
GO:0015919 | peroxisomal membrane transport | 5 | 1 |
GO:0016558 | protein import into peroxisome matrix | 5 | 1 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 1 |
GO:0071806 | protein transmembrane transport | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:1990275 | preribosome binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 495 | 499 | PF00656 | 0.391 |
CLV_C14_Caspase3-7 | 751 | 755 | PF00656 | 0.279 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.590 |
CLV_PCSK_FUR_1 | 184 | 188 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.508 |
CLV_PCSK_PC7_1 | 798 | 804 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 739 | 743 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 782 | 786 | PF00082 | 0.440 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.556 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.391 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.550 |
DOC_ANK_TNKS_1 | 186 | 193 | PF00023 | 0.468 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.552 |
DOC_CYCLIN_RxL_1 | 777 | 789 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 334 | 340 | PF00134 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 435 | 441 | PF00134 | 0.391 |
DOC_CYCLIN_yCln2_LP_2 | 620 | 626 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 71 | 77 | PF00134 | 0.407 |
DOC_MAPK_DCC_7 | 102 | 110 | PF00069 | 0.522 |
DOC_MAPK_DCC_7 | 68 | 77 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 418 | 426 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 636 | 643 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 66 | 73 | PF00069 | 0.565 |
DOC_MAPK_JIP1_4 | 437 | 443 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 565 | 574 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 598 | 604 | PF00149 | 0.545 |
DOC_PP1_RVXF_1 | 801 | 808 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.313 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 745 | 749 | PF00917 | 0.244 |
DOC_USP7_MATH_1 | 770 | 774 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 836 | 840 | PF00917 | 0.540 |
DOC_USP7_UBL2_3 | 391 | 395 | PF12436 | 0.274 |
DOC_USP7_UBL2_3 | 918 | 922 | PF12436 | 0.489 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 805 | 810 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 933 | 938 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 12 | 19 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 228 | 237 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 339 | 347 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 521 | 531 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 802 | 806 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 912 | 920 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 70 | 86 | PF00022 | 0.495 |
LIG_AP2alpha_1 | 702 | 706 | PF02296 | 0.244 |
LIG_BRCT_BRCA1_1 | 788 | 792 | PF00533 | 0.528 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.426 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.565 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.409 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.530 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.428 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.370 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.563 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.351 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.244 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.244 |
LIG_FHA_1 | 830 | 836 | PF00498 | 0.390 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.483 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.279 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.334 |
LIG_FHA_2 | 806 | 812 | PF00498 | 0.369 |
LIG_FHA_2 | 846 | 852 | PF00498 | 0.537 |
LIG_FHA_2 | 914 | 920 | PF00498 | 0.385 |
LIG_GBD_Chelix_1 | 357 | 365 | PF00786 | 0.429 |
LIG_GBD_Chelix_1 | 724 | 732 | PF00786 | 0.287 |
LIG_LIR_Gen_1 | 444 | 452 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 602 | 609 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 615 | 624 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 704 | 711 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 902 | 913 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 548 | 553 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 584 | 588 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 602 | 606 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 615 | 620 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 673 | 678 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 704 | 709 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 902 | 908 | PF02991 | 0.438 |
LIG_NRBOX | 780 | 786 | PF00104 | 0.482 |
LIG_Pex14_2 | 476 | 480 | PF04695 | 0.333 |
LIG_Pex14_2 | 69 | 73 | PF04695 | 0.528 |
LIG_Pex14_2 | 702 | 706 | PF04695 | 0.244 |
LIG_PTB_Apo_2 | 821 | 828 | PF02174 | 0.470 |
LIG_SH2_CRK | 617 | 621 | PF00017 | 0.321 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.427 |
LIG_SH2_SRC | 731 | 734 | PF00017 | 0.244 |
LIG_SH2_SRC | 79 | 82 | PF00017 | 0.377 |
LIG_SH2_STAT3 | 678 | 681 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.244 |
LIG_SH3_2 | 146 | 151 | PF14604 | 0.442 |
LIG_SH3_2 | 40 | 45 | PF14604 | 0.388 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.456 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.456 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.493 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.435 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.512 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.313 |
LIG_SH3_3 | 935 | 941 | PF00018 | 0.735 |
LIG_SUMO_SIM_anti_2 | 274 | 280 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 773 | 783 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 106 | 114 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 137 | 143 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 273 | 280 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 410 | 415 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 439 | 444 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 487 | 493 | PF11976 | 0.278 |
LIG_SUMO_SIM_par_1 | 512 | 517 | PF11976 | 0.474 |
LIG_TRAF2_1 | 288 | 291 | PF00917 | 0.682 |
LIG_TRAF2_1 | 452 | 455 | PF00917 | 0.348 |
LIG_TRAF2_1 | 793 | 796 | PF00917 | 0.468 |
LIG_UBA3_1 | 629 | 636 | PF00899 | 0.404 |
LIG_UBA3_1 | 780 | 787 | PF00899 | 0.400 |
LIG_WRC_WIRS_1 | 582 | 587 | PF05994 | 0.316 |
MOD_CDK_SPxxK_3 | 933 | 940 | PF00069 | 0.479 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.572 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.389 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.651 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.212 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.359 |
MOD_CK1_1 | 718 | 724 | PF00069 | 0.257 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.451 |
MOD_CK1_1 | 907 | 913 | PF00069 | 0.552 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.503 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.518 |
MOD_CK2_1 | 790 | 796 | PF00069 | 0.379 |
MOD_CK2_1 | 911 | 917 | PF00069 | 0.474 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.255 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.630 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.439 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.768 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.731 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.516 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.549 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.225 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.594 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.319 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.264 |
MOD_GlcNHglycan | 716 | 720 | PF01048 | 0.257 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.406 |
MOD_GlcNHglycan | 811 | 815 | PF01048 | 0.383 |
MOD_GlcNHglycan | 817 | 820 | PF01048 | 0.352 |
MOD_GlcNHglycan | 845 | 848 | PF01048 | 0.619 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.521 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.427 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.522 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.404 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.653 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.460 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.443 |
MOD_GSK3_1 | 801 | 808 | PF00069 | 0.302 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.333 |
MOD_GSK3_1 | 904 | 911 | PF00069 | 0.487 |
MOD_GSK3_1 | 941 | 948 | PF00069 | 0.710 |
MOD_LATS_1 | 238 | 244 | PF00433 | 0.418 |
MOD_LATS_1 | 269 | 275 | PF00433 | 0.423 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.376 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.398 |
MOD_N-GLC_1 | 805 | 810 | PF02516 | 0.442 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.539 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.439 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.654 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.543 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.478 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.379 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.379 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.270 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.369 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.347 |
MOD_NEK2_1 | 785 | 790 | PF00069 | 0.354 |
MOD_NEK2_1 | 815 | 820 | PF00069 | 0.330 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.385 |
MOD_NEK2_1 | 908 | 913 | PF00069 | 0.477 |
MOD_NEK2_2 | 478 | 483 | PF00069 | 0.391 |
MOD_NEK2_2 | 570 | 575 | PF00069 | 0.388 |
MOD_NEK2_2 | 612 | 617 | PF00069 | 0.346 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.585 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.557 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.269 |
MOD_PIKK_1 | 941 | 947 | PF00454 | 0.500 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.560 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.512 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.442 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.438 |
MOD_PKA_2 | 801 | 807 | PF00069 | 0.473 |
MOD_PKA_2 | 911 | 917 | PF00069 | 0.450 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.309 |
MOD_PKB_1 | 228 | 236 | PF00069 | 0.458 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.312 |
MOD_Plk_1 | 810 | 816 | PF00069 | 0.460 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.537 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.513 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.515 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.378 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.456 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.482 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.380 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.250 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.370 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.303 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.498 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.518 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.381 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.358 |
MOD_ProDKin_1 | 805 | 811 | PF00069 | 0.342 |
MOD_ProDKin_1 | 933 | 939 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 161 | 166 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 548 | 558 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 605 | 615 | PF00179 | 0.386 |
MOD_SUMO_rev_2 | 682 | 686 | PF00179 | 0.244 |
MOD_SUMO_rev_2 | 733 | 741 | PF00179 | 0.269 |
TRG_DiLeu_BaEn_2 | 174 | 180 | PF01217 | 0.439 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.327 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.454 |
TRG_NES_CRM1_1 | 404 | 415 | PF08389 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I568 | Leptomonas seymouri | 75% | 99% |
A0A0S4IKL1 | Bodo saltans | 42% | 100% |
A0A1X0PA10 | Trypanosomatidae | 47% | 100% |
A0A3Q8IIU8 | Leishmania donovani | 84% | 99% |
A0A3R7MK02 | Trypanosoma rangeli | 48% | 100% |
A4IAB8 | Leishmania infantum | 84% | 99% |
C9ZLX8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AD83 | Leishmania major | 32% | 100% |
E9B5E1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
Q4Q2J2 | Leishmania major | 84% | 100% |
V5BKY8 | Trypanosoma cruzi | 47% | 100% |