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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4I027
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0007165 | signal transduction | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009056 | catabolic process | 2 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016042 | lipid catabolic process | 4 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901575 | organic substance catabolic process | 3 | 7 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 1 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004435 | phosphatidylinositol phospholipase C activity | 7 | 7 |
GO:0004620 | phospholipase activity | 5 | 7 |
GO:0004629 | phospholipase C activity | 6 | 7 |
GO:0005488 | binding | 1 | 5 |
GO:0005509 | calcium ion binding | 5 | 5 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 7 |
GO:0016298 | lipase activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 581 | 585 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 757 | 761 | PF00656 | 0.378 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 753 | 755 | PF00675 | 0.377 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 466 | 468 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.419 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.452 |
DEG_APCC_DBOX_1 | 716 | 724 | PF00400 | 0.298 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.564 |
DEG_SCF_FBW7_1 | 684 | 691 | PF00400 | 0.438 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.515 |
DOC_CYCLIN_RxL_1 | 352 | 359 | PF00134 | 0.313 |
DOC_MAPK_gen_1 | 195 | 203 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 505 | 514 | PF00069 | 0.651 |
DOC_MAPK_MEF2A_6 | 636 | 645 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 717 | 724 | PF00069 | 0.298 |
DOC_PP1_RVXF_1 | 385 | 391 | PF00149 | 0.313 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.278 |
DOC_PP4_FxxP_1 | 660 | 663 | PF00568 | 0.322 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.423 |
DOC_USP7_MATH_2 | 108 | 114 | PF00917 | 0.535 |
DOC_USP7_UBL2_3 | 160 | 164 | PF12436 | 0.526 |
DOC_USP7_UBL2_3 | 460 | 464 | PF12436 | 0.322 |
DOC_USP7_UBL2_3 | 751 | 755 | PF12436 | 0.432 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.412 |
LIG_14-3-3_CanoR_1 | 145 | 153 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 513 | 521 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 636 | 641 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 650 | 655 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 717 | 723 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 732 | 739 | PF00244 | 0.201 |
LIG_14-3-3_CanoR_1 | 754 | 759 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 87 | 92 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 96 | 103 | PF00244 | 0.488 |
LIG_Actin_RPEL_3 | 725 | 744 | PF02755 | 0.298 |
LIG_AP2alpha_2 | 672 | 674 | PF02296 | 0.396 |
LIG_APCC_ABBA_1 | 212 | 217 | PF00400 | 0.424 |
LIG_APCC_ABBA_1 | 302 | 307 | PF00400 | 0.559 |
LIG_APCC_ABBA_1 | 675 | 680 | PF00400 | 0.396 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.565 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 573 | 577 | PF00533 | 0.341 |
LIG_BRCT_BRCA1_1 | 607 | 611 | PF00533 | 0.333 |
LIG_Clathr_ClatBox_1 | 521 | 525 | PF01394 | 0.298 |
LIG_deltaCOP1_diTrp_1 | 270 | 276 | PF00928 | 0.386 |
LIG_deltaCOP1_diTrp_1 | 710 | 718 | PF00928 | 0.313 |
LIG_EH1_1 | 319 | 327 | PF00400 | 0.298 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.583 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.393 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.438 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.431 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.307 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.694 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.360 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.430 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.231 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.269 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.343 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.581 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.472 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.511 |
LIG_Integrin_RGD_1 | 467 | 469 | PF01839 | 0.602 |
LIG_LIR_Apic_2 | 367 | 372 | PF02991 | 0.396 |
LIG_LIR_Apic_2 | 435 | 441 | PF02991 | 0.278 |
LIG_LIR_Apic_2 | 55 | 59 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 658 | 663 | PF02991 | 0.313 |
LIG_LIR_Apic_2 | 761 | 767 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 316 | 326 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 496 | 502 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 596 | 603 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 672 | 682 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 237 | 241 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 596 | 601 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 647 | 652 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 672 | 677 | PF02991 | 0.356 |
LIG_LYPXL_yS_3 | 407 | 410 | PF13949 | 0.313 |
LIG_MLH1_MIPbox_1 | 302 | 306 | PF16413 | 0.425 |
LIG_NRBOX | 432 | 438 | PF00104 | 0.403 |
LIG_PDZ_Class_3 | 779 | 784 | PF00595 | 0.499 |
LIG_Pex14_1 | 272 | 276 | PF04695 | 0.386 |
LIG_Pex14_1 | 594 | 598 | PF04695 | 0.298 |
LIG_Pex14_2 | 16 | 20 | PF04695 | 0.497 |
LIG_Pex14_2 | 438 | 442 | PF04695 | 0.322 |
LIG_Pex14_2 | 674 | 678 | PF04695 | 0.396 |
LIG_Pex14_2 | 699 | 703 | PF04695 | 0.313 |
LIG_PTB_Apo_2 | 693 | 700 | PF02174 | 0.313 |
LIG_Rb_pABgroove_1 | 175 | 183 | PF01858 | 0.298 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.333 |
LIG_SH2_CRK | 764 | 768 | PF00017 | 0.523 |
LIG_SH2_GRB2like | 232 | 235 | PF00017 | 0.465 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.473 |
LIG_SH2_NCK_1 | 764 | 768 | PF00017 | 0.531 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 243 | 246 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 777 | 780 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.467 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.483 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.366 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.413 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.405 |
LIG_SH3_3 | 667 | 673 | PF00018 | 0.423 |
LIG_SUMO_SIM_anti_2 | 279 | 285 | PF11976 | 0.565 |
LIG_SUMO_SIM_anti_2 | 653 | 658 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 719 | 724 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 29 | 34 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 407 | 412 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 519 | 527 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 651 | 658 | PF11976 | 0.314 |
LIG_SxIP_EBH_1 | 86 | 98 | PF03271 | 0.398 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.582 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.333 |
LIG_TRFH_1 | 628 | 632 | PF08558 | 0.322 |
LIG_UBA3_1 | 743 | 751 | PF00899 | 0.335 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.423 |
MOD_CDK_SPK_2 | 684 | 689 | PF00069 | 0.298 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.440 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.548 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.322 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.284 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.514 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.608 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.295 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.356 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.298 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.356 |
MOD_CK1_1 | 658 | 664 | PF00069 | 0.372 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.396 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.575 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.372 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.514 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.356 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.474 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.392 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.298 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.452 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.434 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.527 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.454 |
MOD_GlcNHglycan | 184 | 188 | PF01048 | 0.325 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.446 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.439 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.481 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.447 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.333 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.320 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.326 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.440 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.481 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.462 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.403 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.356 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.123 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.433 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.464 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.533 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.322 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.322 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.356 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.651 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.424 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.322 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.356 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.439 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.386 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.362 |
MOD_LATS_1 | 634 | 640 | PF00433 | 0.367 |
MOD_LATS_1 | 730 | 736 | PF00433 | 0.298 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.541 |
MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.519 |
MOD_N-GLC_1 | 568 | 573 | PF02516 | 0.403 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.403 |
MOD_N-GLC_1 | 758 | 763 | PF02516 | 0.370 |
MOD_N-GLC_2 | 616 | 618 | PF02516 | 0.333 |
MOD_N-GLC_2 | 623 | 625 | PF02516 | 0.259 |
MOD_N-GLC_2 | 731 | 733 | PF02516 | 0.298 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.390 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.396 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.486 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.283 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.356 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.449 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.395 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.543 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.356 |
MOD_NEK2_2 | 673 | 678 | PF00069 | 0.396 |
MOD_NEK2_2 | 711 | 716 | PF00069 | 0.298 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.300 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.298 |
MOD_PIKK_1 | 733 | 739 | PF00454 | 0.298 |
MOD_PKA_1 | 313 | 319 | PF00069 | 0.453 |
MOD_PKA_1 | 754 | 760 | PF00069 | 0.355 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.448 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.488 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.502 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.283 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.479 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.479 |
MOD_PKA_2 | 716 | 722 | PF00069 | 0.446 |
MOD_PKA_2 | 731 | 737 | PF00069 | 0.201 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.533 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.403 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.322 |
MOD_Plk_1 | 568 | 574 | PF00069 | 0.403 |
MOD_Plk_2-3 | 481 | 487 | PF00069 | 0.592 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.425 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.343 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.452 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.322 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.362 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.316 |
MOD_Plk_4 | 766 | 772 | PF00069 | 0.418 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.426 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.536 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.550 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.379 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.298 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.412 |
MOD_SUMO_rev_2 | 188 | 197 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 525 | 535 | PF00179 | 0.397 |
TRG_DiLeu_BaEn_1 | 193 | 198 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_1 | 279 | 284 | PF01217 | 0.558 |
TRG_DiLeu_BaEn_3 | 133 | 139 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 587 | 592 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.503 |
TRG_NLS_MonoCore_2 | 310 | 315 | PF00514 | 0.276 |
TRG_NLS_MonoExtC_3 | 311 | 317 | PF00514 | 0.283 |
TRG_NLS_MonoExtN_4 | 311 | 316 | PF00514 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 650 | 655 | PF00026 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWX7 | Leptomonas seymouri | 66% | 100% |
A0A0N1I1N0 | Leptomonas seymouri | 33% | 100% |
A0A0N1IKD7 | Leptomonas seymouri | 29% | 100% |
A0A0S4ITT3 | Bodo saltans | 28% | 90% |
A0A0S4JUS2 | Bodo saltans | 30% | 100% |
A0A1X0P2K1 | Trypanosomatidae | 31% | 100% |
A0A3Q8IF05 | Leishmania donovani | 34% | 100% |
A0A3S7X8U7 | Leishmania donovani | 31% | 100% |
A0A422N571 | Trypanosoma rangeli | 46% | 100% |
A4HCK9 | Leishmania braziliensis | 72% | 100% |
A4HI17 | Leishmania braziliensis | 24% | 100% |
A4HM43 | Leishmania braziliensis | 33% | 100% |
A4I5X4 | Leishmania infantum | 34% | 100% |
A4IAQ5 | Leishmania infantum | 30% | 100% |
A5D6R3 | Danio rerio | 34% | 100% |
D0A7A3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AEI1 | Leishmania major | 32% | 100% |
E9B168 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B5P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
O13433 | Candida albicans | 28% | 71% |
O89040 | Rattus norvegicus | 34% | 66% |
P10688 | Rattus norvegicus | 33% | 100% |
P10895 | Bos taurus | 34% | 100% |
P21671 | Bos taurus | 33% | 99% |
P32383 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 90% |
P40977 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 87% |
P51178 | Homo sapiens | 33% | 100% |
Q00722 | Homo sapiens | 32% | 66% |
Q02158 | Dictyostelium discoideum | 32% | 98% |
Q15147 | Homo sapiens | 32% | 67% |
Q1RML2 | Bos taurus | 29% | 100% |
Q2VRL0 | Gallus gallus | 32% | 100% |
Q32NH8 | Xenopus laevis | 32% | 100% |
Q39032 | Arabidopsis thaliana | 30% | 100% |
Q39033 | Arabidopsis thaliana | 28% | 100% |
Q4Q6Z7 | Leishmania major | 33% | 100% |
Q4QBH9 | Leishmania major | 85% | 100% |
Q56W08 | Arabidopsis thaliana | 29% | 100% |
Q5FX52 | Rattus norvegicus | 30% | 100% |
Q5RET0 | Pongo abelii | 33% | 100% |
Q62711 | Rattus norvegicus | 32% | 100% |
Q86YW0 | Homo sapiens | 30% | 100% |
Q8K2J0 | Mus musculus | 33% | 100% |
Q8K394 | Mus musculus | 30% | 70% |
Q8K3R3 | Mus musculus | 32% | 97% |
Q8K4D7 | Mus musculus | 30% | 100% |
Q8N3E9 | Homo sapiens | 33% | 99% |
Q8R3B1 | Mus musculus | 32% | 100% |
Q8SPR7 | Sus scrofa | 33% | 100% |
Q944C1 | Arabidopsis thaliana | 28% | 100% |
Q944C2 | Arabidopsis thaliana | 27% | 100% |
Q95JS1 | Macaca fascicularis | 29% | 100% |
Q9BRC7 | Homo sapiens | 33% | 100% |
Q9LY51 | Arabidopsis thaliana | 27% | 100% |
Q9QW07 | Rattus norvegicus | 32% | 67% |
Q9UPR0 | Homo sapiens | 30% | 70% |