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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0010008 | endosome membrane | 5 | 11 |
GO:0012506 | vesicle membrane | 4 | 11 |
GO:0016020 | membrane | 2 | 11 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 11 |
GO:0030666 | endocytic vesicle membrane | 5 | 11 |
GO:0030670 | phagocytic vesicle membrane | 6 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0031901 | early endosome membrane | 6 | 11 |
GO:0098588 | bounding membrane of organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4H885
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006644 | phospholipid metabolic process | 4 | 11 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0007165 | signal transduction | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016311 | dephosphorylation | 5 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0030258 | lipid modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0046486 | glycerolipid metabolic process | 4 | 11 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 11 |
GO:0046839 | phospholipid dephosphorylation | 5 | 11 |
GO:0046856 | phosphatidylinositol dephosphorylation | 6 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0043647 | inositol phosphate metabolic process | 4 | 1 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046164 | alcohol catabolic process | 4 | 1 |
GO:0046174 | polyol catabolic process | 5 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046838 | obsolete phosphorylated carbohydrate dephosphorylation | 4 | 1 |
GO:0046855 | obsolete inositol phosphate dephosphorylation | 5 | 1 |
GO:0071545 | inositol phosphate catabolic process | 5 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016791 | phosphatase activity | 5 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0004439 | phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity | 8 | 2 |
GO:0034593 | phosphatidylinositol bisphosphate phosphatase activity | 7 | 2 |
GO:0034595 | phosphatidylinositol phosphate 5-phosphatase activity | 7 | 2 |
GO:0052866 | phosphatidylinositol phosphate phosphatase activity | 6 | 2 |
GO:0106019 | phosphatidylinositol-4,5-bisphosphate phosphatase activity | 8 | 2 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004519 | endonuclease activity | 5 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004445 | inositol-polyphosphate 5-phosphatase activity | 8 | 1 |
GO:0046030 | inositol trisphosphate phosphatase activity | 7 | 1 |
GO:0052658 | inositol-1,4,5-trisphosphate 5-phosphatase activity | 8 | 1 |
GO:0052659 | inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity | 8 | 1 |
GO:0052743 | inositol tetrakisphosphate phosphatase activity | 7 | 1 |
GO:0052745 | inositol phosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.304 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.310 |
CLV_PCSK_PC1ET2_1 | 359 | 361 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.548 |
CLV_Separin_Metazoa | 591 | 595 | PF03568 | 0.538 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.353 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.422 |
DEG_SCF_FBW7_2 | 574 | 581 | PF00400 | 0.261 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.426 |
DOC_CKS1_1 | 327 | 332 | PF01111 | 0.422 |
DOC_CKS1_1 | 575 | 580 | PF01111 | 0.445 |
DOC_CKS1_1 | 781 | 786 | PF01111 | 0.546 |
DOC_CYCLIN_RxL_1 | 179 | 189 | PF00134 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 664 | 670 | PF00134 | 0.305 |
DOC_CYCLIN_yCln2_LP_2 | 724 | 730 | PF00134 | 0.273 |
DOC_MAPK_gen_1 | 383 | 393 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 682 | 691 | PF00069 | 0.377 |
DOC_MAPK_gen_1 | 79 | 85 | PF00069 | 0.505 |
DOC_MAPK_JIP1_4 | 104 | 110 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 169 | 178 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 406 | 413 | PF00069 | 0.486 |
DOC_MAPK_RevD_3 | 67 | 80 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 445 | 451 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 295 | 298 | PF13499 | 0.422 |
DOC_PP2B_LxvP_1 | 724 | 727 | PF13499 | 0.182 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.656 |
DOC_PP4_FxxP_1 | 9 | 12 | PF00568 | 0.389 |
DOC_SPAK_OSR1_1 | 346 | 350 | PF12202 | 0.422 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.505 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.205 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 182 | 191 | PF00244 | 0.234 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 386 | 393 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 394 | 401 | PF00244 | 0.124 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.187 |
LIG_14-3-3_CanoR_1 | 518 | 522 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 715 | 724 | PF00244 | 0.419 |
LIG_Actin_WH2_2 | 699 | 717 | PF00022 | 0.305 |
LIG_BIR_III_4 | 743 | 747 | PF00653 | 0.422 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.422 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.202 |
LIG_CaM_NSCaTE_8 | 134 | 141 | PF13499 | 0.353 |
LIG_deltaCOP1_diTrp_1 | 13 | 21 | PF00928 | 0.572 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.396 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.299 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.403 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.468 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.306 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.380 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.410 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.265 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.445 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.532 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.491 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.359 |
LIG_GBD_Chelix_1 | 287 | 295 | PF00786 | 0.383 |
LIG_LIR_Apic_2 | 161 | 167 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 13 | 21 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 271 | 279 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 308 | 316 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 488 | 499 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 588 | 596 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 603 | 609 | PF02991 | 0.457 |
LIG_LYPXL_S_1 | 1 | 5 | PF13949 | 0.644 |
LIG_LYPXL_yS_3 | 2 | 5 | PF13949 | 0.640 |
LIG_NRBOX | 170 | 176 | PF00104 | 0.310 |
LIG_NRBOX | 709 | 715 | PF00104 | 0.324 |
LIG_Pex14_1 | 605 | 609 | PF04695 | 0.245 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.329 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.486 |
LIG_SH2_SRC | 609 | 612 | PF00017 | 0.241 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 671 | 675 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 779 | 782 | PF00017 | 0.390 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.202 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.348 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.494 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.447 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.405 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.353 |
LIG_SH3_3 | 664 | 670 | PF00018 | 0.305 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.513 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.631 |
LIG_SUMO_SIM_anti_2 | 106 | 112 | PF11976 | 0.386 |
LIG_SUMO_SIM_anti_2 | 283 | 288 | PF11976 | 0.310 |
LIG_SUMO_SIM_anti_2 | 498 | 503 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 569 | 577 | PF11976 | 0.364 |
LIG_SUMO_SIM_anti_2 | 769 | 778 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 407 | 412 | PF11976 | 0.473 |
LIG_TRAF2_1 | 495 | 498 | PF00917 | 0.323 |
LIG_TRFH_1 | 712 | 716 | PF08558 | 0.305 |
LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.281 |
LIG_UBA3_1 | 633 | 640 | PF00899 | 0.419 |
LIG_UBA3_1 | 657 | 662 | PF00899 | 0.419 |
LIG_WRC_WIRS_1 | 71 | 76 | PF05994 | 0.330 |
LIG_WRPW_2 | 526 | 529 | PF00400 | 0.331 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.450 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.422 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.422 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.468 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.442 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.526 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.484 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.329 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.374 |
MOD_GlcNHglycan | 117 | 121 | PF01048 | 0.312 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.442 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.422 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.374 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.306 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.202 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.672 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.454 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.403 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.458 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.591 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.210 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.338 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.357 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.379 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.310 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.350 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.432 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.277 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.292 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.522 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.456 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.465 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.454 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.499 |
MOD_N-GLC_1 | 717 | 722 | PF02516 | 0.182 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.310 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.301 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.202 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.457 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.436 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.411 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.353 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.202 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.505 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.518 |
MOD_PKA_1 | 374 | 380 | PF00069 | 0.353 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.522 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.329 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.439 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.353 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.353 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.353 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.449 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.425 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.450 |
MOD_PKA_2 | 739 | 745 | PF00069 | 0.528 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.264 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.454 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.372 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.446 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.353 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.530 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.547 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.408 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.338 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.379 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.516 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.297 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.205 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.355 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.320 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.302 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.294 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.558 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.459 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.384 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.536 |
MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.310 |
MOD_SUMO_rev_2 | 318 | 327 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 392 | 401 | PF00179 | 0.310 |
MOD_SUMO_rev_2 | 635 | 642 | PF00179 | 0.419 |
TRG_DiLeu_BaEn_1 | 569 | 574 | PF01217 | 0.330 |
TRG_DiLeu_BaEn_1 | 603 | 608 | PF01217 | 0.229 |
TRG_DiLeu_BaLyEn_6 | 180 | 185 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 724 | 729 | PF01217 | 0.182 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 631 | 635 | PF00026 | 0.182 |
TRG_Pf-PMV_PEXEL_1 | 662 | 666 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E8 | Leptomonas seymouri | 77% | 100% |
A0A1X0NU91 | Trypanosomatidae | 51% | 100% |
A0A3S5H6V6 | Leishmania donovani | 87% | 100% |
A0A422NRC5 | Trypanosoma rangeli | 49% | 100% |
C9ZXT0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D3ZGS3 | Rattus norvegicus | 25% | 88% |
E9AGM3 | Leishmania infantum | 87% | 100% |
E9AQB3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P32019 | Homo sapiens | 28% | 80% |
Q01968 | Homo sapiens | 26% | 88% |
Q4QF61 | Leishmania major | 86% | 100% |
Q6NVF0 | Mus musculus | 26% | 88% |
Q8K337 | Mus musculus | 28% | 80% |
V5DL78 | Trypanosoma cruzi | 49% | 100% |