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: 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:0005737 | cytoplasm | 2 | 2 |
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 |
Related structures:
AlphaFold database: Q4QJ13
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:0000250 | lanosterol synthase activity | 5 | 3 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 900 | 904 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 665 | 667 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 939 | 941 | PF00675 | 0.207 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 665 | 667 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 813 | 815 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 939 | 941 | PF00082 | 0.208 |
CLV_PCSK_KEX2_1 | 995 | 997 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 995 | 997 | PF00082 | 0.384 |
CLV_PCSK_PC7_1 | 99 | 105 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.496 |
CLV_Separin_Metazoa | 190 | 194 | PF03568 | 0.404 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.599 |
DEG_APCC_DBOX_1 | 458 | 466 | PF00400 | 0.310 |
DEG_SPOP_SBC_1 | 283 | 287 | PF00917 | 0.333 |
DOC_CKS1_1 | 550 | 555 | PF01111 | 0.259 |
DOC_MAPK_gen_1 | 108 | 117 | PF00069 | 0.497 |
DOC_MAPK_RevD_3 | 127 | 142 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 872 | 879 | PF00149 | 0.424 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.311 |
DOC_PP2B_LxvP_1 | 369 | 372 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.325 |
DOC_PP2B_LxvP_1 | 728 | 731 | PF13499 | 0.310 |
DOC_PP4_FxxP_1 | 121 | 124 | PF00568 | 0.279 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.360 |
DOC_SPAK_OSR1_1 | 296 | 300 | PF12202 | 0.280 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 905 | 909 | PF00917 | 0.408 |
DOC_USP7_MATH_2 | 960 | 966 | PF00917 | 0.497 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.208 |
DOC_WW_Pin1_4 | 901 | 906 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 284 | 291 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 357 | 365 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 43 | 53 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 512 | 516 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 819 | 828 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 898 | 902 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 251 | 266 | PF00022 | 0.251 |
LIG_Actin_WH2_2 | 496 | 514 | PF00022 | 0.310 |
LIG_Actin_WH2_2 | 600 | 617 | PF00022 | 0.228 |
LIG_Actin_WH2_2 | 737 | 753 | PF00022 | 0.250 |
LIG_AP2alpha_2 | 303 | 305 | PF02296 | 0.356 |
LIG_APCC_ABBA_1 | 802 | 807 | PF00400 | 0.232 |
LIG_APCC_ABBAyCdc20_2 | 525 | 531 | PF00400 | 0.232 |
LIG_BIR_III_2 | 534 | 538 | PF00653 | 0.227 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.292 |
LIG_BRCT_BRCA1_1 | 593 | 597 | PF00533 | 0.322 |
LIG_BRCT_BRCA1_1 | 619 | 623 | PF00533 | 0.308 |
LIG_BRCT_BRCA1_1 | 964 | 968 | PF00533 | 0.408 |
LIG_BRCT_BRCA1_2 | 619 | 625 | PF00533 | 0.257 |
LIG_CSL_BTD_1 | 252 | 255 | PF09270 | 0.413 |
LIG_deltaCOP1_diTrp_1 | 485 | 489 | PF00928 | 0.250 |
LIG_eIF4E_1 | 423 | 429 | PF01652 | 0.232 |
LIG_EVH1_1 | 339 | 343 | PF00568 | 0.346 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.440 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.285 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.348 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.245 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.320 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.270 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.279 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.227 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.557 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.215 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.583 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.356 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.441 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.289 |
LIG_FHA_2 | 898 | 904 | PF00498 | 0.462 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.540 |
LIG_KLC1_Yacidic_2 | 632 | 637 | PF13176 | 0.244 |
LIG_LIR_Apic_2 | 527 | 532 | PF02991 | 0.220 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 530 | 541 | PF02991 | 0.232 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 594 | 603 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 788 | 793 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 913 | 923 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 454 | 460 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 469 | 473 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 506 | 511 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 530 | 536 | PF02991 | 0.219 |
LIG_LIR_Nem_3 | 540 | 544 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.205 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 632 | 636 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 758 | 764 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 780 | 785 | PF02991 | 0.213 |
LIG_LIR_Nem_3 | 788 | 792 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 807 | 812 | PF02991 | 0.126 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.413 |
LIG_NRBOX | 723 | 729 | PF00104 | 0.275 |
LIG_PAM2_1 | 705 | 717 | PF00658 | 0.297 |
LIG_PDZ_Class_2 | 997 | 1002 | PF00595 | 0.499 |
LIG_Pex14_1 | 309 | 313 | PF04695 | 0.234 |
LIG_Pex14_1 | 652 | 656 | PF04695 | 0.208 |
LIG_Pex14_1 | 842 | 846 | PF04695 | 0.245 |
LIG_Pex14_1 | 994 | 998 | PF04695 | 0.472 |
LIG_Pex14_2 | 117 | 121 | PF04695 | 0.340 |
LIG_Pex14_2 | 305 | 309 | PF04695 | 0.347 |
LIG_Pex14_2 | 838 | 842 | PF04695 | 0.218 |
LIG_PTB_Apo_2 | 749 | 756 | PF02174 | 0.289 |
LIG_Rb_LxCxE_1 | 774 | 793 | PF01857 | 0.275 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.320 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.210 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 529 | 533 | PF00017 | 0.224 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.519 |
LIG_SH2_PTP2 | 423 | 426 | PF00017 | 0.250 |
LIG_SH2_PTP2 | 680 | 683 | PF00017 | 0.208 |
LIG_SH2_SRC | 680 | 683 | PF00017 | 0.208 |
LIG_SH2_SRC | 764 | 767 | PF00017 | 0.210 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 846 | 850 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.208 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.193 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.208 |
LIG_SH2_STAT5 | 772 | 775 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 791 | 794 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 827 | 830 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 846 | 849 | PF00017 | 0.168 |
LIG_SH2_STAT5 | 998 | 1001 | PF00017 | 0.506 |
LIG_SH3_1 | 337 | 343 | PF00018 | 0.415 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.360 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.650 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.317 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.422 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.412 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.415 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.245 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.282 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.263 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.495 |
LIG_SH3_3 | 899 | 905 | PF00018 | 0.418 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.297 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.227 |
LIG_TYR_ITIM | 421 | 426 | PF00017 | 0.250 |
LIG_TYR_ITIM | 787 | 792 | PF00017 | 0.262 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.477 |
LIG_WW_2 | 340 | 343 | PF00397 | 0.310 |
MOD_CDC14_SPxK_1 | 18 | 21 | PF00782 | 0.652 |
MOD_CDK_SPxK_1 | 15 | 21 | PF00069 | 0.658 |
MOD_CDK_SPxxK_3 | 552 | 559 | PF00069 | 0.275 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.480 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.211 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.708 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.381 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.336 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.280 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.485 |
MOD_CK2_1 | 787 | 793 | PF00069 | 0.273 |
MOD_CMANNOS | 123 | 126 | PF00535 | 0.388 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.556 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.673 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.467 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.429 |
MOD_GlcNHglycan | 351 | 355 | PF01048 | 0.696 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.744 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.474 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.510 |
MOD_GlcNHglycan | 618 | 622 | PF01048 | 0.459 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.441 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.514 |
MOD_GlcNHglycan | 891 | 896 | PF01048 | 0.275 |
MOD_GlcNHglycan | 955 | 958 | PF01048 | 0.227 |
MOD_GlcNHglycan | 964 | 967 | PF01048 | 0.176 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.713 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.208 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.279 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.172 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.213 |
MOD_GSK3_1 | 887 | 894 | PF00069 | 0.504 |
MOD_GSK3_1 | 897 | 904 | PF00069 | 0.444 |
MOD_LATS_1 | 347 | 353 | PF00433 | 0.455 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.582 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.451 |
MOD_N-GLC_1 | 646 | 651 | PF02516 | 0.426 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.408 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.300 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.462 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.297 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.730 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.294 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.428 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.208 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.279 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.225 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.259 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.165 |
MOD_NEK2_1 | 750 | 755 | PF00069 | 0.321 |
MOD_NEK2_1 | 838 | 843 | PF00069 | 0.229 |
MOD_NEK2_1 | 878 | 883 | PF00069 | 0.446 |
MOD_NEK2_1 | 948 | 953 | PF00069 | 0.418 |
MOD_NEK2_2 | 537 | 542 | PF00069 | 0.302 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.208 |
MOD_PIKK_1 | 905 | 911 | PF00454 | 0.408 |
MOD_PKA_1 | 356 | 362 | PF00069 | 0.378 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.463 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.335 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.542 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.275 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.314 |
MOD_PKA_2 | 897 | 903 | PF00069 | 0.462 |
MOD_PKA_2 | 962 | 968 | PF00069 | 0.408 |
MOD_PKB_1 | 220 | 228 | PF00069 | 0.395 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.252 |
MOD_Plk_1 | 652 | 658 | PF00069 | 0.208 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.543 |
MOD_Plk_1 | 787 | 793 | PF00069 | 0.250 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.485 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.208 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.323 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.366 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.295 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.537 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.321 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.211 |
MOD_Plk_4 | 897 | 903 | PF00069 | 0.462 |
MOD_Plk_4 | 981 | 987 | PF00069 | 0.459 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.674 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.400 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.310 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.208 |
MOD_ProDKin_1 | 901 | 907 | PF00069 | 0.510 |
TRG_DiLeu_BaEn_2 | 592 | 598 | PF01217 | 0.238 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.584 |
TRG_DiLeu_BaEn_4 | 196 | 202 | PF01217 | 0.345 |
TRG_DiLeu_BaLyEn_6 | 424 | 429 | PF01217 | 0.275 |
TRG_DiLeu_BaLyEn_6 | 553 | 558 | PF01217 | 0.227 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.218 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.216 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.221 |
TRG_ENDOCYTIC_2 | 680 | 683 | PF00928 | 0.209 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.212 |
TRG_ENDOCYTIC_2 | 789 | 792 | PF00928 | 0.208 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.263 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.246 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.232 |
TRG_ER_diArg_1 | 697 | 700 | PF00400 | 0.213 |
TRG_ER_diArg_1 | 737 | 739 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 812 | 815 | PF00400 | 0.218 |
TRG_ER_diArg_1 | 938 | 940 | PF00400 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 141 | 146 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 738 | 742 | PF00026 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 819 | 823 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0E0SP71 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 34% | 100% |
A0A0N0P5W0 | Leptomonas seymouri | 75% | 100% |
A0A0S2IHL6 | Kalopanax septemlobus | 35% | 100% |
A0A0S4JCG8 | Bodo saltans | 52% | 100% |
A0A0U2U4F3 | Barbarea vulgaris | 34% | 100% |
A0A125SXN1 | Lycopodium clavatum | 32% | 100% |
A0A125SXN2 | Lycopodium clavatum | 33% | 100% |
A0A125SXN3 | Lycopodium clavatum | 39% | 100% |
A0A1X0NL88 | Trypanosomatidae | 55% | 100% |
A0A3R7KVQ6 | Trypanosoma rangeli | 57% | 100% |
A0A3S5H5R6 | Leishmania donovani | 95% | 100% |
A0A455LN86 | Arthrinium sp. | 31% | 100% |
A0A455LRW3 | Nectria sp. | 31% | 100% |
A1CVK0 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 36% | 100% |
A4H4N0 | Leishmania braziliensis | 83% | 100% |
A4HSV6 | Leishmania infantum | 95% | 100% |
A8C980 | Rhizophora stylosa | 35% | 100% |
A8C981 | Rhizophora stylosa | 32% | 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 | 36% | 100% |
B9X0J1 | Stevia rebaudiana | 36% | 100% |
C9ZTG7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
D7NJ68 | Ganoderma lucidum | 38% | 100% |
E2IUA6 | Kalanchoe daigremontiana | 35% | 100% |
E2IUA7 | Kalanchoe daigremontiana | 36% | 100% |
E2IUA8 | Kalanchoe daigremontiana | 37% | 100% |
E2IUA9 | Kalanchoe daigremontiana | 36% | 100% |
E2IUB0 | Kalanchoe daigremontiana | 40% | 100% |
E4V6I8 | Arthroderma gypseum (strain ATCC MYA-4604 / CBS 118893) | 32% | 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) | 35% | 100% |
Q1G1A4 | Arabidopsis thaliana | 38% | 100% |
Q2R712 | Oryza sativa subsp. japonica | 34% | 100% |
Q2XPU6 | Ricinus communis | 40% | 100% |
Q2XPU7 | Ricinus communis | 35% | 100% |
Q4WES9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 36% | 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 | 38% | 100% |
Q6BE24 | Cucurbita pepo | 38% | 100% |
Q6BE25 | Cucurbita pepo | 40% | 100% |
Q6Z2X6 | Oryza sativa subsp. japonica | 40% | 100% |
Q8RWT0 | Arabidopsis thaliana | 36% | 100% |
Q8W3Z1 | Betula platyphylla | 36% | 100% |
Q8W3Z2 | Betula platyphylla | 35% | 100% |
Q8W3Z3 | Betula platyphylla | 41% | 100% |
Q8W3Z4 | Betula platyphylla | 40% | 100% |
Q948R6 | Luffa aegyptiaca | 34% | 100% |
Q96WJ0 | Pneumocystis carinii | 37% | 100% |
Q9C5M3 | Arabidopsis thaliana | 36% | 100% |
Q9FI37 | Arabidopsis thaliana | 32% | 100% |
Q9FJV8 | Arabidopsis thaliana | 29% | 100% |
Q9FR95 | Arabidopsis thaliana | 33% | 100% |
Q9FZI2 | Arabidopsis thaliana | 34% | 100% |
Q9LRH8 | Pisum sativum | 36% | 100% |
Q9LS68 | Arabidopsis thaliana | 31% | 100% |
Q9LVY2 | Arabidopsis thaliana | 32% | 100% |
Q9SLP9 | Luffa aegyptiaca | 40% | 100% |
Q9SXV6 | Glycyrrhiza glabra | 39% | 100% |
Q9SYN1 | Arabidopsis thaliana | 33% | 100% |
V5DPI3 | Trypanosoma cruzi | 57% | 100% |