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. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3Q8I917
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006090 | pyruvate metabolic process | 7 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006091 | generation of precursor metabolites and energy | 3 | 1 |
GO:0006096 | glycolytic process | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
GO:0006165 | obsolete nucleoside diphosphate phosphorylation | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006757 | obsolete ATP generation from ADP | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009117 | nucleotide metabolic process | 5 | 1 |
GO:0009132 | nucleoside diphosphate metabolic process | 5 | 1 |
GO:0009135 | purine nucleoside diphosphate metabolic process | 6 | 1 |
GO:0009141 | nucleoside triphosphate metabolic process | 5 | 1 |
GO:0009144 | purine nucleoside triphosphate metabolic process | 6 | 1 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 1 |
GO:0009179 | purine ribonucleoside diphosphate metabolic process | 7 | 1 |
GO:0009185 | ribonucleoside diphosphate metabolic process | 6 | 1 |
GO:0009199 | ribonucleoside triphosphate metabolic process | 6 | 1 |
GO:0009205 | purine ribonucleoside triphosphate metabolic process | 7 | 1 |
GO:0009259 | ribonucleotide metabolic process | 5 | 1 |
GO:0016052 | carbohydrate catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046031 | ADP metabolic process | 7 | 1 |
GO:0046034 | ATP metabolic process | 7 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046939 | obsolete nucleotide phosphorylation | 6 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016781 | phosphotransferase activity, paired acceptors | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0050242 | pyruvate, phosphate dikinase activity | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.578 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.371 |
CLV_PCSK_FUR_1 | 315 | 319 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 904 | 906 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 904 | 906 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 773 | 777 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 845 | 849 | PF00082 | 0.378 |
CLV_Separin_Metazoa | 770 | 774 | PF03568 | 0.564 |
DEG_APCC_DBOX_1 | 870 | 878 | PF00400 | 0.658 |
DEG_APCC_KENBOX_2 | 70 | 74 | PF00400 | 0.639 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.629 |
DOC_CKS1_1 | 290 | 295 | PF01111 | 0.553 |
DOC_MAPK_gen_1 | 386 | 396 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 735 | 741 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 845 | 855 | PF00069 | 0.580 |
DOC_MAPK_MEF2A_6 | 450 | 457 | PF00069 | 0.557 |
DOC_PP1_RVXF_1 | 862 | 869 | PF00149 | 0.635 |
DOC_PP2B_LxvP_1 | 645 | 648 | PF13499 | 0.553 |
DOC_PP4_FxxP_1 | 882 | 885 | PF00568 | 0.578 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 824 | 828 | PF00917 | 0.578 |
DOC_USP7_UBL2_3 | 168 | 172 | PF12436 | 0.590 |
DOC_USP7_UBL2_3 | 418 | 422 | PF12436 | 0.565 |
DOC_USP7_UBL2_3 | 533 | 537 | PF12436 | 0.612 |
DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 848 | 852 | PF12436 | 0.578 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 877 | 882 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 477 | 487 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 539 | 544 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 694 | 700 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 773 | 781 | PF00244 | 0.573 |
LIG_AP2alpha_2 | 204 | 206 | PF02296 | 0.639 |
LIG_AP2alpha_2 | 823 | 825 | PF02296 | 0.578 |
LIG_APCC_ABBA_1 | 143 | 148 | PF00400 | 0.553 |
LIG_APCC_ABBA_1 | 379 | 384 | PF00400 | 0.658 |
LIG_APCC_ABBA_1 | 652 | 657 | PF00400 | 0.594 |
LIG_APCC_ABBA_1 | 811 | 816 | PF00400 | 0.589 |
LIG_CtBP_PxDLS_1 | 461 | 465 | PF00389 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 204 | 210 | PF00928 | 0.639 |
LIG_EH1_1 | 762 | 770 | PF00400 | 0.564 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.553 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.461 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.614 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.578 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.548 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.542 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.562 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.560 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.553 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.555 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.642 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.564 |
LIG_FHA_2 | 765 | 771 | PF00498 | 0.592 |
LIG_Integrin_RGD_1 | 625 | 627 | PF01839 | 0.378 |
LIG_LIR_Apic_2 | 219 | 223 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 880 | 885 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 187 | 193 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 204 | 213 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 823 | 833 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 544 | 550 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 627 | 631 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 698 | 702 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 784 | 790 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 823 | 828 | PF02991 | 0.578 |
LIG_LYPXL_yS_3 | 319 | 322 | PF13949 | 0.564 |
LIG_LYPXL_yS_3 | 699 | 702 | PF13949 | 0.553 |
LIG_PCNA_yPIPBox_3 | 633 | 645 | PF02747 | 0.631 |
LIG_PDZ_Class_1 | 909 | 914 | PF00595 | 0.730 |
LIG_Pex14_1 | 206 | 210 | PF04695 | 0.639 |
LIG_Pex14_2 | 628 | 632 | PF04695 | 0.564 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.564 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.550 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.553 |
LIG_SH2_STAT3 | 703 | 706 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 763 | 766 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 820 | 823 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 876 | 879 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.488 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.553 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.461 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.526 |
LIG_SH3_4 | 418 | 425 | PF00018 | 0.539 |
LIG_SH3_4 | 848 | 855 | PF00018 | 0.578 |
LIG_SUMO_SIM_par_1 | 520 | 525 | PF11976 | 0.639 |
LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.571 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.528 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.518 |
LIG_TRAF2_1 | 659 | 662 | PF00917 | 0.600 |
LIG_TRAF2_2 | 622 | 627 | PF00917 | 0.553 |
LIG_TRAF2_2 | 824 | 829 | PF00917 | 0.578 |
LIG_TYR_ITIM | 697 | 702 | PF00017 | 0.405 |
LIG_TYR_ITSM | 142 | 149 | PF00017 | 0.405 |
LIG_UBA3_1 | 728 | 736 | PF00899 | 0.421 |
LIG_WRC_WIRS_1 | 787 | 792 | PF05994 | 0.440 |
MOD_CDC14_SPxK_1 | 880 | 883 | PF00782 | 0.440 |
MOD_CDK_SPxK_1 | 877 | 883 | PF00069 | 0.440 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.421 |
MOD_CK1_1 | 789 | 795 | PF00069 | 0.440 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.405 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.413 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.392 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.513 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.485 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.535 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.479 |
MOD_CK2_1 | 764 | 770 | PF00069 | 0.460 |
MOD_Cter_Amidation | 366 | 369 | PF01082 | 0.421 |
MOD_Cter_Amidation | 733 | 736 | PF01082 | 0.421 |
MOD_GlcNHglycan | 254 | 258 | PF01048 | 0.406 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.507 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.402 |
MOD_GlcNHglycan | 656 | 660 | PF01048 | 0.554 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.466 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.405 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.421 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.405 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.424 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.549 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.496 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.604 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.380 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.405 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.487 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.571 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.473 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.405 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.440 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.539 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.755 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.367 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.475 |
MOD_PIKK_1 | 793 | 799 | PF00454 | 0.440 |
MOD_PK_1 | 597 | 603 | PF00069 | 0.475 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.440 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.507 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.660 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.506 |
MOD_PKB_1 | 316 | 324 | PF00069 | 0.417 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.455 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.442 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.405 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.440 |
MOD_Plk_1 | 793 | 799 | PF00069 | 0.440 |
MOD_Plk_2-3 | 520 | 526 | PF00069 | 0.405 |
MOD_Plk_2-3 | 862 | 868 | PF00069 | 0.526 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.400 |
MOD_Plk_4 | 764 | 770 | PF00069 | 0.421 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.552 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.402 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.400 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.517 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.405 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.405 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.552 |
MOD_ProDKin_1 | 877 | 883 | PF00069 | 0.440 |
MOD_SUMO_rev_2 | 16 | 24 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 164 | 171 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 176 | 185 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 542 | 550 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 78 | 84 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 328 | 333 | PF01217 | 0.421 |
TRG_DiLeu_BaEn_1 | 831 | 836 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 640 | 645 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 699 | 702 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 814 | 817 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 674 | 677 | PF00400 | 0.421 |
TRG_NES_CRM1_1 | 181 | 194 | PF08389 | 0.527 |
TRG_NES_CRM1_1 | 596 | 608 | PF08389 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 679 | 683 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 708 | 712 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 752 | 756 | PF00026 | 0.436 |
TRG_PTS1 | 911 | 914 | PF00515 | 0.686 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I112 | Leptomonas seymouri | 87% | 100% |
A0A0S4IJT3 | Bodo saltans | 71% | 100% |
A0A1X0NUY0 | Trypanosomatidae | 79% | 100% |
A0A3R7KK46 | Trypanosoma rangeli | 77% | 100% |
A4H6M6 | Leishmania braziliensis | 93% | 100% |
A4HV09 | Leishmania infantum | 100% | 100% |
D0A7D9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 76% | 100% |
E9ANP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O23404 | Arabidopsis thaliana | 53% | 95% |
O27190 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 28% | 100% |
O29548 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 27% | 100% |
O57830 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 27% | 100% |
O83026 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 25% | 100% |
O83728 | Treponema pallidum (strain Nichols) | 33% | 100% |
P11155 | Zea mays | 53% | 97% |
P22221 | Flaveria trinervia | 54% | 96% |
P22983 | Clostridium symbiosum | 57% | 100% |
P23538 | Escherichia coli (strain K12) | 24% | 100% |
P37213 | Entamoeba histolytica | 49% | 100% |
P42850 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 28% | 100% |
P46893 | Staphylothermus marinus (strain ATCC 43588 / DSM 3639 / JCM 9404 / F1) | 25% | 100% |
P51776 | Giardia intestinalis | 51% | 100% |
P56070 | Helicobacter pylori (strain ATCC 700392 / 26695) | 24% | 100% |
Q1RH78 | Rickettsia bellii (strain RML369-C) | 46% | 100% |
Q39734 | Flaveria brownii | 54% | 96% |
Q39735 | Flaveria bidentis | 54% | 96% |
Q42368 | Zea mays | 53% | 100% |
Q42736 | Flaveria pringlei | 54% | 96% |
Q42910 | Mesembryanthemum crystallinum | 53% | 96% |
Q4QGX9 | Leishmania major | 99% | 100% |
Q4ULI7 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 46% | 100% |
Q55905 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 23% | 100% |
Q59754 | Rhizobium meliloti (strain 1021) | 55% | 100% |
Q68WP2 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 46% | 100% |
Q6AVA8 | Oryza sativa subsp. japonica | 54% | 97% |
Q75KR1 | Oryza sativa subsp. japonica | 53% | 100% |
Q92HI8 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 47% | 100% |
Q9K0I2 | Neisseria meningitidis serogroup B (strain MC58) | 25% | 100% |
Q9V2H7 | Pyrococcus abyssi (strain GE5 / Orsay) | 27% | 100% |
Q9YEC5 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 25% | 100% |
Q9ZD55 | Rickettsia prowazekii (strain Madrid E) | 46% | 100% |
Q9ZMV4 | Helicobacter pylori (strain J99 / ATCC 700824) | 24% | 100% |
V5BBD4 | Trypanosoma cruzi | 79% | 100% |