Acidocalcisome, Low affinity phosphate Pho91 sodium/sulphate symporter
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000331 | contractile vacuole | 6 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
Related structures:
AlphaFold database: A4I428
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006797 | polyphosphate metabolic process | 4 | 1 |
GO:0006810 | transport | 3 | 4 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006817 | phosphate ion transport | 7 | 1 |
GO:0006820 | monoatomic anion transport | 5 | 1 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 4 |
GO:0015698 | inorganic anion transport | 6 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030002 | intracellular monoatomic anion homeostasis | 5 | 1 |
GO:0030643 | intracellular phosphate ion homeostasis | 7 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
GO:0055062 | phosphate ion homeostasis | 8 | 1 |
GO:0055081 | monoatomic anion homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 4 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072502 | obsolete cellular trivalent inorganic anion homeostasis | 6 | 1 |
GO:0072506 | obsolete trivalent inorganic anion homeostasis | 7 | 1 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 7 |
GO:0022857 | transmembrane transporter activity | 2 | 7 |
GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 1 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.765 |
CLV_C14_Caspase3-7 | 604 | 608 | PF00656 | 0.370 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.375 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.653 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.582 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.565 |
DEG_APCC_DBOX_1 | 224 | 232 | PF00400 | 0.563 |
DEG_APCC_DBOX_1 | 381 | 389 | PF00400 | 0.287 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.601 |
DOC_CYCLIN_RxL_1 | 160 | 171 | PF00134 | 0.630 |
DOC_CYCLIN_RxL_1 | 222 | 232 | PF00134 | 0.627 |
DOC_MAPK_DCC_7 | 494 | 504 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 142 | 149 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 223 | 231 | PF00069 | 0.578 |
DOC_MAPK_gen_1 | 237 | 243 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 5 | 13 | PF00069 | 0.660 |
DOC_MAPK_gen_1 | 71 | 81 | PF00069 | 0.646 |
DOC_MAPK_HePTP_8 | 340 | 352 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 223 | 231 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 343 | 352 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 74 | 81 | PF00069 | 0.658 |
DOC_PP1_RVXF_1 | 462 | 468 | PF00149 | 0.332 |
DOC_PP1_RVXF_1 | 641 | 647 | PF00149 | 0.348 |
DOC_PP4_FxxP_1 | 239 | 242 | PF00568 | 0.624 |
DOC_PP4_FxxP_1 | 315 | 318 | PF00568 | 0.416 |
DOC_PP4_FxxP_1 | 646 | 649 | PF00568 | 0.287 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 689 | 693 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.564 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.266 |
LIG_14-3-3_CanoR_1 | 131 | 141 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 377 | 385 | PF00244 | 0.269 |
LIG_Actin_WH2_2 | 22 | 37 | PF00022 | 0.598 |
LIG_BIR_III_2 | 127 | 131 | PF00653 | 0.630 |
LIG_BRCT_BRCA1_1 | 231 | 235 | PF00533 | 0.617 |
LIG_deltaCOP1_diTrp_1 | 254 | 259 | PF00928 | 0.604 |
LIG_EH1_1 | 629 | 637 | PF00400 | 0.323 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.792 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.692 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.572 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.331 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.279 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.482 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.630 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.490 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.283 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.348 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.311 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.352 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.337 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.309 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.514 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.323 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.469 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.519 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.370 |
LIG_GBD_Chelix_1 | 525 | 533 | PF00786 | 0.387 |
LIG_LIR_Apic_2 | 236 | 242 | PF02991 | 0.622 |
LIG_LIR_Apic_2 | 417 | 422 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 532 | 537 | PF02991 | 0.464 |
LIG_LIR_Apic_2 | 720 | 724 | PF02991 | 0.324 |
LIG_LIR_Apic_2 | 726 | 731 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 244 | 251 | PF02991 | 0.671 |
LIG_LIR_Gen_1 | 266 | 277 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 55 | 65 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 565 | 575 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 608 | 619 | PF02991 | 0.381 |
LIG_LIR_LC3C_4 | 613 | 617 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 14 | 18 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 461 | 465 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 498 | 504 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 565 | 570 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 679 | 684 | PF02991 | 0.323 |
LIG_NRBOX | 136 | 142 | PF00104 | 0.671 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.651 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.626 |
LIG_NRBOX | 573 | 579 | PF00104 | 0.323 |
LIG_PCNA_PIPBox_1 | 338 | 347 | PF02747 | 0.522 |
LIG_Pex14_1 | 15 | 19 | PF04695 | 0.547 |
LIG_Pex14_1 | 259 | 263 | PF04695 | 0.465 |
LIG_Pex14_1 | 572 | 576 | PF04695 | 0.323 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.606 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.548 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.626 |
LIG_SH2_GRB2like | 246 | 249 | PF00017 | 0.675 |
LIG_SH2_NCK_1 | 246 | 250 | PF00017 | 0.679 |
LIG_SH2_PTP2 | 261 | 264 | PF00017 | 0.380 |
LIG_SH2_PTP2 | 501 | 504 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 728 | 731 | PF00017 | 0.399 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.675 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.640 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.370 |
LIG_SH3_1 | 74 | 80 | PF00018 | 0.716 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.771 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.500 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.318 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.346 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.193 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.469 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.633 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.660 |
LIG_SUMO_SIM_anti_2 | 613 | 619 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 708 | 715 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 145 | 152 | PF11976 | 0.715 |
LIG_SUMO_SIM_par_1 | 227 | 232 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 291 | 296 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 475 | 481 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 661 | 666 | PF11976 | 0.300 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.767 |
LIG_TRAF2_1 | 510 | 513 | PF00917 | 0.570 |
LIG_TYR_ITIM | 20 | 25 | PF00017 | 0.539 |
LIG_TYR_ITIM | 499 | 504 | PF00017 | 0.540 |
LIG_UBA3_1 | 593 | 602 | PF00899 | 0.340 |
LIG_UBA3_1 | 635 | 643 | PF00899 | 0.325 |
LIG_Vh1_VBS_1 | 617 | 635 | PF01044 | 0.318 |
LIG_WRC_WIRS_1 | 624 | 629 | PF05994 | 0.469 |
LIG_WRPW_2 | 493 | 496 | PF00400 | 0.452 |
MOD_CDK_SPK_2 | 158 | 163 | PF00069 | 0.605 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.766 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.581 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.295 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.501 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.267 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.370 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.514 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.305 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.469 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.540 |
MOD_Cter_Amidation | 3 | 6 | PF01082 | 0.378 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.409 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.319 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.540 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.340 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.423 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.473 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.306 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.318 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.580 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.733 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.567 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.323 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.481 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.323 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.301 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.350 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.408 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.771 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.596 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.251 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.338 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.290 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.348 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.341 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.408 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.180 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.269 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.323 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.300 |
MOD_NEK2_1 | 712 | 717 | PF00069 | 0.300 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.671 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.683 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.535 |
MOD_PKA_1 | 327 | 333 | PF00069 | 0.487 |
MOD_PKA_1 | 94 | 100 | PF00069 | 0.742 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.576 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.583 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.487 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.618 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.255 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.270 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.564 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.612 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.730 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.563 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.337 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.234 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.280 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.345 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.323 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.287 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.469 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.310 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.349 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.601 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.307 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.310 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.266 |
MOD_SUMO_for_1 | 52 | 55 | PF00179 | 0.624 |
MOD_SUMO_rev_2 | 230 | 239 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.638 |
TRG_DiLeu_BaEn_2 | 105 | 111 | PF01217 | 0.710 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 589 | 594 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.533 |
TRG_NES_CRM1_1 | 175 | 185 | PF08389 | 0.593 |
TRG_NLS_Bipartite_1 | 5 | 27 | PF00514 | 0.583 |
TRG_NLS_MonoExtC_3 | 191 | 196 | PF00514 | 0.581 |
TRG_NLS_MonoExtN_4 | 189 | 196 | PF00514 | 0.573 |
TRG_NLS_MonoExtN_4 | 92 | 97 | PF00514 | 0.759 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 416 | 420 | PF00026 | 0.309 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWP2 | Leptomonas seymouri | 81% | 99% |
A0A1X0NQK1 | Trypanosomatidae | 64% | 100% |
A0A3Q8IB88 | Leishmania donovani | 100% | 100% |
A0A422NG32 | Trypanosoma rangeli | 71% | 100% |
A4HGZ6 | Leishmania braziliensis | 91% | 100% |
D0A8X9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9B0B5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P27514 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 82% |
Q21339 | Caenorhabditis elegans | 25% | 100% |
Q4Q7W9 | Leishmania major | 98% | 100% |
Q93655 | Caenorhabditis elegans | 21% | 100% |
Q9ES88 | Mus musculus | 22% | 100% |