Phospholipid biosynthesis, inositol/phosphatidylinositol phosphatase
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: E9AGM3
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_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.404 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.303 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 359 | 361 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.454 |
CLV_Separin_Metazoa | 591 | 595 | PF03568 | 0.533 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.352 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.421 |
DEG_APCC_DBOX_1 | 533 | 541 | PF00400 | 0.405 |
DEG_COP1_1 | 355 | 365 | PF00400 | 0.306 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.425 |
DOC_CKS1_1 | 327 | 332 | PF01111 | 0.421 |
DOC_CKS1_1 | 781 | 786 | PF01111 | 0.524 |
DOC_CYCLIN_RxL_1 | 179 | 189 | PF00134 | 0.421 |
DOC_CYCLIN_RxL_1 | 659 | 666 | PF00134 | 0.376 |
DOC_CYCLIN_yCln2_LP_2 | 664 | 670 | PF00134 | 0.304 |
DOC_MAPK_gen_1 | 22 | 29 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 255 | 261 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 383 | 393 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 684 | 691 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 79 | 85 | PF00069 | 0.421 |
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 | 0.309 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 406 | 413 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 493 | 501 | PF00069 | 0.505 |
DOC_MAPK_RevD_3 | 67 | 80 | PF00069 | 0.352 |
DOC_PP1_RVXF_1 | 445 | 451 | PF00149 | 0.506 |
DOC_PP2B_LxvP_1 | 295 | 298 | PF13499 | 0.421 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.681 |
DOC_SPAK_OSR1_1 | 346 | 350 | PF12202 | 0.421 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.435 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 386 | 393 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 394 | 401 | PF00244 | 0.124 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.183 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 532 | 538 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 623 | 629 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 715 | 724 | PF00244 | 0.418 |
LIG_Actin_WH2_2 | 699 | 717 | PF00022 | 0.304 |
LIG_BIR_III_2 | 159 | 163 | PF00653 | 0.240 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.421 |
LIG_CaM_NSCaTE_8 | 134 | 141 | PF13499 | 0.352 |
LIG_CtBP_PxDLS_1 | 496 | 500 | PF00389 | 0.434 |
LIG_deltaCOP1_diTrp_1 | 13 | 21 | PF00928 | 0.559 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.395 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.321 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.402 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.467 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.305 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.450 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.509 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.451 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.337 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.308 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.565 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.530 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.360 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.490 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.359 |
LIG_GBD_Chelix_1 | 287 | 295 | PF00786 | 0.382 |
LIG_LIR_Apic_2 | 161 | 167 | PF02991 | 0.329 |
LIG_LIR_Apic_2 | 28 | 32 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 12 | 21 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 271 | 279 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 588 | 596 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 12 | 17 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.525 |
LIG_LYPXL_S_1 | 1 | 5 | PF13949 | 0.621 |
LIG_LYPXL_yS_3 | 2 | 5 | PF13949 | 0.616 |
LIG_NRBOX | 170 | 176 | PF00104 | 0.309 |
LIG_NRBOX | 660 | 666 | PF00104 | 0.376 |
LIG_NRBOX | 709 | 715 | PF00104 | 0.323 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.329 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 674 | 678 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 674 | 677 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 779 | 782 | PF00017 | 0.377 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.347 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.488 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.442 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.406 |
LIG_SH3_3 | 664 | 670 | PF00018 | 0.304 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.421 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.435 |
LIG_SUMO_SIM_anti_2 | 106 | 112 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 283 | 288 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 471 | 477 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 498 | 503 | PF11976 | 0.488 |
LIG_SUMO_SIM_anti_2 | 569 | 576 | PF11976 | 0.363 |
LIG_SUMO_SIM_anti_2 | 734 | 740 | PF11976 | 0.286 |
LIG_SUMO_SIM_anti_2 | 769 | 778 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 407 | 412 | PF11976 | 0.467 |
LIG_TRFH_1 | 712 | 716 | PF08558 | 0.304 |
LIG_TYR_ITIM | 315 | 320 | PF00017 | 0.376 |
LIG_UBA3_1 | 633 | 640 | PF00899 | 0.418 |
LIG_UBA3_1 | 657 | 662 | PF00899 | 0.418 |
LIG_WRC_WIRS_1 | 657 | 662 | PF05994 | 0.267 |
LIG_WRC_WIRS_1 | 71 | 76 | PF05994 | 0.309 |
LIG_WRPW_2 | 526 | 529 | PF00400 | 0.322 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.447 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.421 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.454 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.408 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.587 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.421 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.406 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.457 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.412 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.524 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.482 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.328 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.240 |
MOD_GlcNHglycan | 117 | 121 | PF01048 | 0.312 |
MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.425 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.445 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.421 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.374 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.305 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.689 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.454 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.421 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.401 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.458 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.420 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.353 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.365 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.356 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.413 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.376 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.612 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.309 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.350 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.432 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.289 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.501 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.562 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.465 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.412 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.699 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.454 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.497 |
MOD_N-GLC_2 | 68 | 70 | PF02516 | 0.403 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.309 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.300 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.454 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.212 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.468 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.349 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.411 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.240 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.526 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.509 |
MOD_PKA_1 | 374 | 380 | PF00069 | 0.352 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.421 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.329 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.352 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.352 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.352 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.410 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.449 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.454 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.444 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.556 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.352 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.551 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.519 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.540 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.400 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.334 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.427 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.378 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.484 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.355 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.317 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.294 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.556 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.455 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.513 |
MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.309 |
MOD_SUMO_rev_2 | 318 | 327 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 392 | 401 | PF00179 | 0.309 |
MOD_SUMO_rev_2 | 635 | 642 | PF00179 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 180 | 185 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.309 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 532 | 535 | PF00400 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 662 | 666 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E8 | Leptomonas seymouri | 77% | 100% |
A0A1X0NU91 | Trypanosomatidae | 52% | 100% |
A0A3S5H6V6 | Leishmania donovani | 99% | 100% |
A0A422NRC5 | Trypanosoma rangeli | 48% | 100% |
A4H885 | Leishmania braziliensis | 87% | 100% |
C9ZXT0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
D3ZGS3 | Rattus norvegicus | 26% | 88% |
E9AQB3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
P32019 | Homo sapiens | 27% | 80% |
Q01968 | Homo sapiens | 26% | 88% |
Q4QF61 | Leishmania major | 95% | 100% |
Q6NVF0 | Mus musculus | 27% | 88% |
Q8K337 | Mus musculus | 27% | 80% |
V5DL78 | Trypanosoma cruzi | 50% | 100% |