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: E9ANP5
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016311 | dephosphorylation | 5 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0019932 | second-messenger-mediated signaling | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043647 | inositol phosphate metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 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:0048016 | inositol phosphate-mediated signaling | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071545 | inositol phosphate catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 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 | 7 |
GO:0004445 | inositol-polyphosphate 5-phosphatase activity | 8 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0046030 | inositol trisphosphate phosphatase activity | 7 | 7 |
GO:0052658 | inositol-1,4,5-trisphosphate 5-phosphatase activity | 8 | 6 |
GO:0052659 | inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity | 8 | 6 |
GO:0052743 | inositol tetrakisphosphate phosphatase activity | 7 | 6 |
GO:0052745 | inositol phosphate phosphatase activity | 6 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.610 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.670 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.831 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.637 |
CLV_PCSK_PC7_1 | 459 | 465 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.423 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.644 |
DEG_SCF_FBW7_2 | 64 | 70 | PF00400 | 0.565 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.476 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.510 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.608 |
DEG_SPOP_SBC_1 | 582 | 586 | PF00917 | 0.515 |
DOC_AGCK_PIF_3 | 684 | 687 | PF00069 | 0.649 |
DOC_CKS1_1 | 64 | 69 | PF01111 | 0.565 |
DOC_CYCLIN_yCln2_LP_2 | 427 | 433 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 365 | 375 | PF00069 | 0.568 |
DOC_MAPK_JIP1_4 | 33 | 39 | PF00069 | 0.610 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.642 |
DOC_MAPK_MEF2A_6 | 367 | 375 | PF00069 | 0.553 |
DOC_MAPK_NFAT4_5 | 368 | 376 | PF00069 | 0.554 |
DOC_PP1_RVXF_1 | 614 | 620 | PF00149 | 0.468 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.491 |
DOC_PP2B_PxIxI_1 | 189 | 195 | PF00149 | 0.455 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 475 | 478 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.729 |
DOC_SPAK_OSR1_1 | 20 | 24 | PF12202 | 0.666 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.825 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.690 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.627 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 109 | 119 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 125 | 129 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 181 | 186 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 20 | 24 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 251 | 258 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 631 | 636 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 661 | 670 | PF00244 | 0.591 |
LIG_APCC_ABBA_1 | 387 | 392 | PF00400 | 0.562 |
LIG_APCC_ABBA_1 | 431 | 436 | PF00400 | 0.436 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.711 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.598 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.700 |
LIG_deltaCOP1_diTrp_1 | 469 | 475 | PF00928 | 0.527 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.339 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.668 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.627 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.407 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.761 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.754 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.538 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.394 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.696 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.507 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.797 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.369 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.632 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.754 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.732 |
LIG_FHA_2 | 676 | 682 | PF00498 | 0.569 |
LIG_GSK3_LRP6_1 | 163 | 168 | PF00069 | 0.772 |
LIG_LIR_Apic_2 | 315 | 321 | PF02991 | 0.489 |
LIG_LIR_Apic_2 | 473 | 478 | PF02991 | 0.544 |
LIG_LIR_Apic_2 | 84 | 89 | PF02991 | 0.721 |
LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 469 | 478 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 517 | 523 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 681 | 687 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 76 | 86 | PF02991 | 0.738 |
LIG_LIR_Gen_1 | 90 | 98 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 517 | 521 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 665 | 670 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 681 | 687 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.716 |
LIG_Pex14_2 | 21 | 25 | PF04695 | 0.598 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.496 |
LIG_Pex14_2 | 471 | 475 | PF04695 | 0.586 |
LIG_PTB_Apo_2 | 205 | 212 | PF02174 | 0.550 |
LIG_Rb_LxCxE_1 | 461 | 483 | PF01857 | 0.639 |
LIG_SH2_CRK | 518 | 522 | PF00017 | 0.626 |
LIG_SH2_NCK_1 | 518 | 522 | PF00017 | 0.626 |
LIG_SH2_NCK_1 | 670 | 674 | PF00017 | 0.587 |
LIG_SH2_PTP2 | 337 | 340 | PF00017 | 0.513 |
LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.667 |
LIG_SH2_SRC | 337 | 340 | PF00017 | 0.513 |
LIG_SH2_SRC | 668 | 671 | PF00017 | 0.622 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.714 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 668 | 672 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.724 |
LIG_SH3_1 | 633 | 639 | PF00018 | 0.753 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.720 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.641 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.544 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.754 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.655 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.627 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.793 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.706 |
LIG_SUMO_SIM_anti_2 | 193 | 198 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 35 | 40 | PF11976 | 0.534 |
LIG_SUMO_SIM_anti_2 | 497 | 504 | PF11976 | 0.611 |
LIG_SUMO_SIM_par_1 | 35 | 40 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 422 | 429 | PF11976 | 0.576 |
LIG_TRAF2_1 | 480 | 483 | PF00917 | 0.581 |
LIG_WW_2 | 6 | 9 | PF00397 | 0.750 |
MOD_CDC14_SPxK_1 | 599 | 602 | PF00782 | 0.664 |
MOD_CDK_SPK_2 | 317 | 322 | PF00069 | 0.504 |
MOD_CDK_SPxK_1 | 596 | 602 | PF00069 | 0.668 |
MOD_CDK_SPxxK_3 | 102 | 109 | PF00069 | 0.592 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.520 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.475 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.551 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.645 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.719 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.567 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.492 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.521 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.647 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.584 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.627 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.772 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.368 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.563 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.519 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.784 |
MOD_Cter_Amidation | 407 | 410 | PF01082 | 0.571 |
MOD_DYRK1A_RPxSP_1 | 63 | 67 | PF00069 | 0.696 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.608 |
MOD_GlcNHglycan | 137 | 141 | PF01048 | 0.561 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.690 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.680 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.483 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.562 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.815 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.676 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.733 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.507 |
MOD_GlcNHglycan | 420 | 424 | PF01048 | 0.486 |
MOD_GlcNHglycan | 552 | 556 | PF01048 | 0.581 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.573 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.709 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.752 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.669 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.579 |
MOD_GlcNHglycan | 74 | 78 | PF01048 | 0.764 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.676 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.692 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.686 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.472 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.749 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.554 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.407 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.603 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.704 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.784 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.702 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.582 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.645 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.720 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.749 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.786 |
MOD_N-GLC_2 | 383 | 385 | PF02516 | 0.442 |
MOD_N-GLC_2 | 604 | 606 | PF02516 | 0.709 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.836 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.550 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.482 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.596 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.453 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.629 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.543 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.437 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.523 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.652 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.834 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.539 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.661 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.576 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.751 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.730 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.398 |
MOD_PKB_1 | 251 | 259 | PF00069 | 0.755 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.483 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.539 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.529 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.481 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.567 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.504 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.611 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.598 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.807 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.703 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.499 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.565 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.506 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.521 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.695 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.782 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.576 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.704 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.660 |
MOD_SUMO_rev_2 | 436 | 446 | PF00179 | 0.445 |
MOD_SUMO_rev_2 | 448 | 454 | PF00179 | 0.611 |
TRG_DiLeu_BaEn_1 | 491 | 496 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.590 |
TRG_DiLeu_BaLyEn_6 | 573 | 578 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.714 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.795 |
TRG_ER_diArg_1 | 409 | 412 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 484 | 487 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.828 |
TRG_NLS_MonoExtN_4 | 460 | 467 | PF00514 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E4 | Leptomonas seymouri | 51% | 100% |
A0A3S5H6J4 | Leishmania donovani | 89% | 100% |
A4H6M7 | Leishmania braziliensis | 72% | 100% |
A4HV10 | Leishmania infantum | 88% | 100% |
Q4QGX8 | Leishmania major | 87% | 99% |