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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005811 | lipid droplet | 5 | 12 |
GO:0016020 | membrane | 2 | 11 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H5R6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006720 | isoprenoid metabolic process | 4 | 12 |
GO:0006721 | terpenoid metabolic process | 5 | 12 |
GO:0006722 | triterpenoid metabolic process | 6 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008299 | isoprenoid biosynthetic process | 4 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016104 | triterpenoid biosynthetic process | 6 | 12 |
GO:0016114 | terpenoid biosynthetic process | 5 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0016871 | cycloartenol synthase activity | 5 | 6 |
GO:0031559 | oxidosqualene cyclase activity | 4 | 7 |
GO:0000250 | lanosterol synthase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 905 | 909 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 743 | 745 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 1000 | 1002 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 743 | 745 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 818 | 820 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 1000 | 1002 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 269 | 271 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.673 |
CLV_PCSK_PC7_1 | 99 | 105 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 730 | 734 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.521 |
CLV_Separin_Metazoa | 190 | 194 | PF03568 | 0.488 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.620 |
DEG_APCC_DBOX_1 | 463 | 471 | PF00400 | 0.331 |
DEG_SPOP_SBC_1 | 288 | 292 | PF00917 | 0.399 |
DOC_CKS1_1 | 555 | 560 | PF01111 | 0.293 |
DOC_PP1_RVXF_1 | 877 | 884 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 343 | 346 | PF13499 | 0.367 |
DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 434 | 437 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 733 | 736 | PF13499 | 0.331 |
DOC_PP4_FxxP_1 | 121 | 124 | PF00568 | 0.332 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.451 |
DOC_SPAK_OSR1_1 | 301 | 305 | PF12202 | 0.345 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 910 | 914 | PF00917 | 0.445 |
DOC_USP7_MATH_2 | 965 | 971 | PF00917 | 0.522 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.245 |
DOC_WW_Pin1_4 | 906 | 911 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 289 | 296 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 517 | 521 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 824 | 833 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 903 | 907 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 941 | 951 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 501 | 519 | PF00022 | 0.331 |
LIG_Actin_WH2_2 | 742 | 758 | PF00022 | 0.286 |
LIG_AP2alpha_2 | 308 | 310 | PF02296 | 0.370 |
LIG_APCC_ABBA_1 | 344 | 349 | PF00400 | 0.382 |
LIG_APCC_ABBA_1 | 807 | 812 | PF00400 | 0.270 |
LIG_APCC_ABBAyCdc20_2 | 530 | 536 | PF00400 | 0.270 |
LIG_BIR_III_2 | 539 | 543 | PF00653 | 0.294 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_1 | 598 | 602 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 624 | 628 | PF00533 | 0.345 |
LIG_BRCT_BRCA1_1 | 969 | 973 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_2 | 624 | 630 | PF00533 | 0.318 |
LIG_CSL_BTD_1 | 257 | 260 | PF09270 | 0.466 |
LIG_deltaCOP1_diTrp_1 | 490 | 494 | PF00928 | 0.286 |
LIG_eIF4E_1 | 428 | 434 | PF01652 | 0.270 |
LIG_EVH1_1 | 344 | 348 | PF00568 | 0.396 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.337 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.279 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.338 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.686 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.350 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.309 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.264 |
LIG_FHA_1 | 804 | 810 | PF00498 | 0.253 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.609 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.426 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.442 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.316 |
LIG_FHA_2 | 903 | 909 | PF00498 | 0.550 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.583 |
LIG_KLC1_Yacidic_2 | 637 | 642 | PF13176 | 0.312 |
LIG_LIR_Apic_2 | 532 | 537 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 535 | 546 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 599 | 608 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 793 | 798 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 918 | 928 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 474 | 478 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.213 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 545 | 549 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 599 | 605 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 637 | 641 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 763 | 769 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 785 | 790 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 793 | 797 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 812 | 817 | PF02991 | 0.133 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.459 |
LIG_NRBOX | 728 | 734 | PF00104 | 0.306 |
LIG_PAM2_1 | 710 | 722 | PF00658 | 0.322 |
LIG_PDZ_Class_2 | 1002 | 1007 | PF00595 | 0.584 |
LIG_Pex14_1 | 314 | 318 | PF04695 | 0.273 |
LIG_Pex14_1 | 657 | 661 | PF04695 | 0.245 |
LIG_Pex14_1 | 847 | 851 | PF04695 | 0.297 |
LIG_Pex14_1 | 999 | 1003 | PF04695 | 0.519 |
LIG_Pex14_2 | 115 | 119 | PF04695 | 0.387 |
LIG_Pex14_2 | 310 | 314 | PF04695 | 0.363 |
LIG_Pex14_2 | 843 | 847 | PF04695 | 0.256 |
LIG_PTB_Apo_2 | 754 | 761 | PF02174 | 0.311 |
LIG_Rb_LxCxE_1 | 779 | 798 | PF01857 | 0.306 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.374 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.247 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 534 | 538 | PF00017 | 0.261 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.574 |
LIG_SH2_PTP2 | 428 | 431 | PF00017 | 0.286 |
LIG_SH2_PTP2 | 685 | 688 | PF00017 | 0.245 |
LIG_SH2_SRC | 685 | 688 | PF00017 | 0.245 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.630 |
LIG_SH2_STAP1 | 851 | 855 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 1003 | 1006 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 685 | 688 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 777 | 780 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 796 | 799 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 851 | 854 | PF00017 | 0.201 |
LIG_SH3_1 | 342 | 348 | PF00018 | 0.436 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.391 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.712 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.482 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.436 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.434 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.256 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.311 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.296 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.537 |
LIG_SH3_3 | 904 | 910 | PF00018 | 0.456 |
LIG_TRAF2_1 | 393 | 396 | PF00917 | 0.322 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.294 |
LIG_TYR_ITIM | 426 | 431 | PF00017 | 0.286 |
LIG_TYR_ITIM | 792 | 797 | PF00017 | 0.350 |
LIG_WW_3 | 40 | 44 | PF00397 | 0.582 |
MOD_CDC14_SPxK_1 | 18 | 21 | PF00782 | 0.714 |
MOD_CDK_SPxK_1 | 15 | 21 | PF00069 | 0.723 |
MOD_CDK_SPxxK_3 | 557 | 564 | PF00069 | 0.306 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.552 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.392 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.486 |
MOD_CK1_1 | 722 | 728 | PF00069 | 0.248 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.397 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.303 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.310 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.541 |
MOD_CK2_1 | 792 | 798 | PF00069 | 0.305 |
MOD_CMANNOS | 123 | 126 | PF00535 | 0.418 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.560 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.709 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.747 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.494 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.457 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.531 |
MOD_GlcNHglycan | 623 | 627 | PF01048 | 0.501 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.479 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.534 |
MOD_GlcNHglycan | 896 | 901 | PF01048 | 0.288 |
MOD_GlcNHglycan | 944 | 947 | PF01048 | 0.341 |
MOD_GlcNHglycan | 960 | 963 | PF01048 | 0.265 |
MOD_GlcNHglycan | 969 | 972 | PF01048 | 0.208 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.755 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.245 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.309 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.203 |
MOD_GSK3_1 | 799 | 806 | PF00069 | 0.250 |
MOD_GSK3_1 | 892 | 899 | PF00069 | 0.543 |
MOD_GSK3_1 | 902 | 909 | PF00069 | 0.482 |
MOD_LATS_1 | 352 | 358 | PF00433 | 0.530 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.684 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.520 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.601 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.464 |
MOD_N-GLC_1 | 710 | 715 | PF02516 | 0.445 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.351 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.539 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.753 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.318 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.243 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.309 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.265 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.298 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.194 |
MOD_NEK2_1 | 755 | 760 | PF00069 | 0.338 |
MOD_NEK2_1 | 843 | 848 | PF00069 | 0.267 |
MOD_NEK2_1 | 883 | 888 | PF00069 | 0.478 |
MOD_NEK2_1 | 953 | 958 | PF00069 | 0.456 |
MOD_NEK2_2 | 542 | 547 | PF00069 | 0.325 |
MOD_OFUCOSY | 108 | 113 | PF10250 | 0.245 |
MOD_PIKK_1 | 651 | 657 | PF00454 | 0.245 |
MOD_PIKK_1 | 910 | 916 | PF00454 | 0.445 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.552 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.367 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.306 |
MOD_PKA_2 | 755 | 761 | PF00069 | 0.334 |
MOD_PKA_2 | 902 | 908 | PF00069 | 0.550 |
MOD_PKA_2 | 967 | 973 | PF00069 | 0.441 |
MOD_PKB_1 | 220 | 228 | PF00069 | 0.474 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.289 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.245 |
MOD_Plk_1 | 792 | 798 | PF00069 | 0.286 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.541 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.245 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.318 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.373 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.329 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.570 |
MOD_Plk_4 | 792 | 798 | PF00069 | 0.338 |
MOD_Plk_4 | 805 | 811 | PF00069 | 0.248 |
MOD_Plk_4 | 902 | 908 | PF00069 | 0.550 |
MOD_Plk_4 | 986 | 992 | PF00069 | 0.493 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.723 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.414 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.331 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.245 |
MOD_ProDKin_1 | 906 | 912 | PF00069 | 0.531 |
TRG_DiLeu_BaEn_2 | 597 | 603 | PF01217 | 0.276 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.606 |
TRG_DiLeu_BaEn_4 | 196 | 202 | PF01217 | 0.348 |
TRG_DiLeu_BaLyEn_6 | 429 | 434 | PF01217 | 0.306 |
TRG_DiLeu_BaLyEn_6 | 558 | 563 | PF01217 | 0.294 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 777 | 780 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 794 | 797 | PF00928 | 0.199 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 702 | 705 | PF00400 | 0.251 |
TRG_ER_diArg_1 | 742 | 744 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 817 | 820 | PF00400 | 0.256 |
TRG_Pf-PMV_PEXEL_1 | 141 | 146 | PF00026 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 743 | 747 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 824 | 828 | PF00026 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0E0SP71 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 35% | 100% |
A0A0N0P5W0 | Leptomonas seymouri | 74% | 100% |
A0A0S2IHL6 | Kalopanax septemlobus | 36% | 100% |
A0A0S4JCG8 | Bodo saltans | 52% | 100% |
A0A0U2U4F3 | Barbarea vulgaris | 36% | 100% |
A0A125SXN1 | Lycopodium clavatum | 33% | 100% |
A0A125SXN2 | Lycopodium clavatum | 32% | 100% |
A0A125SXN3 | Lycopodium clavatum | 39% | 100% |
A0A1X0NL88 | Trypanosomatidae | 55% | 100% |
A0A3R7KVQ6 | Trypanosoma rangeli | 57% | 100% |
A0A455LN86 | Arthrinium sp. | 31% | 100% |
A0A455LRW3 | Nectria sp. | 32% | 100% |
A1CVK0 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 35% | 100% |
A4H4N0 | Leishmania braziliensis | 82% | 100% |
A4HSV6 | Leishmania infantum | 99% | 100% |
A8C980 | Rhizophora stylosa | 36% | 100% |
A8C981 | Rhizophora stylosa | 33% | 100% |
A8CDT2 | Bruguiera gymnorhiza | 37% | 100% |
A8CDT3 | Bruguiera gymnorhiza | 34% | 100% |
B0Y5B4 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 36% | 100% |
B6EXY6 | Arabidopsis thaliana | 37% | 100% |
B9X0J1 | Stevia rebaudiana | 36% | 100% |
C9ZTG7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
D7NJ68 | Ganoderma lucidum | 39% | 100% |
E2IUA6 | Kalanchoe daigremontiana | 36% | 100% |
E2IUA7 | Kalanchoe daigremontiana | 38% | 100% |
E2IUA8 | Kalanchoe daigremontiana | 38% | 100% |
E2IUA9 | Kalanchoe daigremontiana | 37% | 100% |
E2IUB0 | Kalanchoe daigremontiana | 40% | 100% |
E4V6I8 | Arthroderma gypseum (strain ATCC MYA-4604 / CBS 118893) | 31% | 100% |
E7DN63 | Solanum lycopersicum | 37% | 100% |
E7DN64 | Solanum lycopersicum | 35% | 100% |
E9AKU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
F8WQD0 | Aster tataricus | 37% | 100% |
H2KWF1 | Oryza sativa subsp. japonica | 37% | 100% |
K7NBZ9 | Siraitia grosvenorii | 39% | 100% |
O23390 | Arabidopsis thaliana | 32% | 100% |
O82139 | Panax ginseng | 39% | 100% |
O82140 | Panax ginseng | 36% | 100% |
O82146 | Panax ginseng | 35% | 100% |
P0C8Y0 | Arabidopsis thaliana | 35% | 100% |
P38604 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P38605 | Arabidopsis thaliana | 39% | 100% |
Q10231 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
Q1G1A4 | Arabidopsis thaliana | 38% | 100% |
Q2R712 | Oryza sativa subsp. japonica | 34% | 100% |
Q2XPU6 | Ricinus communis | 40% | 100% |
Q2XPU7 | Ricinus communis | 35% | 100% |
Q4QJ13 | Leishmania major | 95% | 100% |
Q4WES9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 37% | 100% |
Q4WQ95 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 35% | 100% |
Q4WR16 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 36% | 100% |
Q55D85 | Dictyostelium discoideum | 40% | 100% |
Q6BE23 | Cucurbita pepo | 39% | 100% |
Q6BE25 | Cucurbita pepo | 40% | 100% |
Q6Z2X6 | Oryza sativa subsp. japonica | 39% | 100% |
Q8RWT0 | Arabidopsis thaliana | 37% | 100% |
Q8W3Z1 | Betula platyphylla | 37% | 100% |
Q8W3Z2 | Betula platyphylla | 35% | 100% |
Q8W3Z3 | Betula platyphylla | 41% | 100% |
Q8W3Z4 | Betula platyphylla | 40% | 100% |
Q948R6 | Luffa aegyptiaca | 35% | 100% |
Q96WJ0 | Pneumocystis carinii | 38% | 100% |
Q9C5M3 | Arabidopsis thaliana | 36% | 100% |
Q9FI37 | Arabidopsis thaliana | 33% | 100% |
Q9FJV8 | Arabidopsis thaliana | 31% | 100% |
Q9FR95 | Arabidopsis thaliana | 34% | 100% |
Q9FZI2 | Arabidopsis thaliana | 34% | 100% |
Q9LRH8 | Pisum sativum | 37% | 100% |
Q9LS68 | Arabidopsis thaliana | 31% | 100% |
Q9LVY2 | Arabidopsis thaliana | 32% | 100% |
Q9MB42 | Glycyrrhiza glabra | 38% | 100% |
Q9SLP9 | Luffa aegyptiaca | 40% | 100% |
Q9SXV6 | Glycyrrhiza glabra | 39% | 100% |
Q9SYN1 | Arabidopsis thaliana | 35% | 100% |
V5DPI3 | Trypanosoma cruzi | 57% | 100% |