Homologous to animal CLCN-group H+/Cl- exchangers.. The family seems to have duplicated in Kinetoplastida
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
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 |
Related structures:
AlphaFold database: A0A3Q8IH43
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 17 |
GO:0005216 | monoatomic ion channel activity | 4 | 17 |
GO:0005244 | voltage-gated monoatomic ion channel activity | 4 | 17 |
GO:0005247 | voltage-gated chloride channel activity | 6 | 17 |
GO:0005253 | monoatomic anion channel activity | 5 | 17 |
GO:0005254 | chloride channel activity | 6 | 17 |
GO:0008308 | voltage-gated monoatomic anion channel activity | 5 | 17 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 17 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 17 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 17 |
GO:0015108 | chloride transmembrane transporter activity | 5 | 17 |
GO:0015267 | channel activity | 4 | 17 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 17 |
GO:0022803 | passive transmembrane transporter activity | 3 | 17 |
GO:0022832 | voltage-gated channel activity | 6 | 17 |
GO:0022836 | gated channel activity | 5 | 17 |
GO:0022857 | transmembrane transporter activity | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 727 | 731 | PF00656 | 0.383 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.525 |
CLV_MEL_PAP_1 | 855 | 861 | PF00089 | 0.441 |
CLV_MEL_PAP_1 | 88 | 94 | PF00089 | 0.341 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.349 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 780 | 782 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 780 | 782 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.424 |
DEG_APCC_DBOX_1 | 712 | 720 | PF00400 | 0.210 |
DEG_MDM2_SWIB_1 | 362 | 369 | PF02201 | 0.314 |
DOC_CDC14_PxL_1 | 840 | 848 | PF14671 | 0.314 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.620 |
DOC_CKS1_1 | 463 | 468 | PF01111 | 0.389 |
DOC_CYCLIN_RxL_1 | 430 | 440 | PF00134 | 0.465 |
DOC_CYCLIN_RxL_1 | 510 | 520 | PF00134 | 0.285 |
DOC_MAPK_gen_1 | 475 | 485 | PF00069 | 0.221 |
DOC_MAPK_MEF2A_6 | 103 | 110 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 477 | 485 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 596 | 605 | PF00069 | 0.263 |
DOC_MAPK_MEF2A_6 | 691 | 700 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 713 | 722 | PF00069 | 0.262 |
DOC_MAPK_NFAT4_5 | 103 | 111 | PF00069 | 0.398 |
DOC_MAPK_NFAT4_5 | 713 | 721 | PF00069 | 0.249 |
DOC_PP1_RVXF_1 | 105 | 112 | PF00149 | 0.249 |
DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.292 |
DOC_PP1_RVXF_1 | 338 | 344 | PF00149 | 0.476 |
DOC_PP1_RVXF_1 | 511 | 517 | PF00149 | 0.251 |
DOC_PP1_RVXF_1 | 594 | 600 | PF00149 | 0.243 |
DOC_PP1_RVXF_1 | 856 | 862 | PF00149 | 0.351 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.301 |
DOC_PP4_FxxP_1 | 14 | 17 | PF00568 | 0.603 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.220 |
DOC_PP4_FxxP_1 | 319 | 322 | PF00568 | 0.263 |
DOC_PP4_FxxP_1 | 571 | 574 | PF00568 | 0.276 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 804 | 808 | PF00917 | 0.261 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.277 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.243 |
LIG_14-3-3_CanoR_1 | 145 | 154 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 282 | 287 | PF00244 | 0.224 |
LIG_14-3-3_CanoR_1 | 518 | 525 | PF00244 | 0.242 |
LIG_14-3-3_CanoR_1 | 596 | 600 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 830 | 836 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 858 | 862 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.625 |
LIG_Actin_WH2_2 | 712 | 728 | PF00022 | 0.228 |
LIG_Actin_WH2_2 | 767 | 782 | PF00022 | 0.331 |
LIG_APCC_ABBA_1 | 811 | 816 | PF00400 | 0.257 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.651 |
LIG_BIR_III_4 | 101 | 105 | PF00653 | 0.590 |
LIG_BIR_III_4 | 765 | 769 | PF00653 | 0.367 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.655 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.413 |
LIG_Clathr_ClatBox_1 | 327 | 331 | PF01394 | 0.263 |
LIG_EH1_1 | 238 | 246 | PF00400 | 0.410 |
LIG_eIF4E_1 | 509 | 515 | PF01652 | 0.250 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.278 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.343 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.341 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.277 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.444 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.264 |
LIG_FHA_1 | 847 | 853 | PF00498 | 0.362 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.365 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.603 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.299 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.293 |
LIG_FHA_2 | 773 | 779 | PF00498 | 0.346 |
LIG_GBD_Chelix_1 | 245 | 253 | PF00786 | 0.314 |
LIG_LIR_Apic_2 | 11 | 17 | PF02991 | 0.606 |
LIG_LIR_Apic_2 | 295 | 300 | PF02991 | 0.220 |
LIG_LIR_Apic_2 | 316 | 322 | PF02991 | 0.263 |
LIG_LIR_Apic_2 | 456 | 462 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 291 | 300 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 484 | 493 | PF02991 | 0.220 |
LIG_LIR_Gen_1 | 506 | 516 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 598 | 606 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 807 | 815 | PF02991 | 0.305 |
LIG_LIR_LC3C_4 | 598 | 603 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 484 | 489 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 598 | 602 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 807 | 811 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 829 | 835 | PF02991 | 0.311 |
LIG_MYND_3 | 646 | 650 | PF01753 | 0.284 |
LIG_NRBOX | 202 | 208 | PF00104 | 0.258 |
LIG_NRBOX | 412 | 418 | PF00104 | 0.243 |
LIG_NRBOX | 510 | 516 | PF00104 | 0.309 |
LIG_NRBOX | 715 | 721 | PF00104 | 0.244 |
LIG_PALB2_WD40_1 | 29 | 37 | PF16756 | 0.589 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.410 |
LIG_Pex14_2 | 362 | 366 | PF04695 | 0.337 |
LIG_Pex14_2 | 450 | 454 | PF04695 | 0.368 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.389 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.217 |
LIG_SH2_GRB2like | 229 | 232 | PF00017 | 0.424 |
LIG_SH2_NCK_1 | 77 | 81 | PF00017 | 0.489 |
LIG_SH2_PTP2 | 459 | 462 | PF00017 | 0.336 |
LIG_SH2_PTP2 | 808 | 811 | PF00017 | 0.278 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.424 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 821 | 824 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 724 | 727 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 808 | 811 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 821 | 824 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 833 | 836 | PF00017 | 0.243 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.434 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.426 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.266 |
LIG_SH3_3 | 789 | 795 | PF00018 | 0.314 |
LIG_Sin3_3 | 599 | 606 | PF02671 | 0.336 |
LIG_SUMO_SIM_anti_2 | 668 | 676 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 250 | 256 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 394 | 401 | PF11976 | 0.198 |
LIG_SUMO_SIM_par_1 | 407 | 414 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 668 | 676 | PF11976 | 0.253 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.507 |
LIG_UBA3_1 | 618 | 626 | PF00899 | 0.338 |
LIG_WRC_WIRS_1 | 832 | 837 | PF05994 | 0.310 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.469 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.217 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.251 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.277 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.335 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.347 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.264 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.232 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.282 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.282 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.299 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.198 |
MOD_CK1_1 | 772 | 778 | PF00069 | 0.350 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.531 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.328 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.532 |
MOD_CK2_1 | 669 | 675 | PF00069 | 0.213 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.410 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.545 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.556 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.712 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.676 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.315 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.516 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.240 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.241 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.238 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.439 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.141 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.217 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.451 |
MOD_GlcNHglycan | 370 | 374 | PF01048 | 0.451 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.398 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.549 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.723 |
MOD_GlcNHglycan | 802 | 805 | PF01048 | 0.474 |
MOD_GlcNHglycan | 816 | 820 | PF01048 | 0.512 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.673 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.372 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.367 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.252 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.226 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.243 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.232 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.442 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.342 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.269 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.359 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.418 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.259 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.509 |
MOD_GSK3_1 | 800 | 807 | PF00069 | 0.388 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.703 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.588 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.581 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.479 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.513 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.352 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.238 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.258 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.254 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.267 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.255 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.255 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.425 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.396 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.230 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.341 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.386 |
MOD_NEK2_2 | 17 | 22 | PF00069 | 0.630 |
MOD_NEK2_2 | 632 | 637 | PF00069 | 0.312 |
MOD_NEK2_2 | 651 | 656 | PF00069 | 0.376 |
MOD_NEK2_2 | 831 | 836 | PF00069 | 0.286 |
MOD_OFUCOSY | 352 | 359 | PF10250 | 0.298 |
MOD_PIKK_1 | 846 | 852 | PF00454 | 0.256 |
MOD_PIKK_1 | 869 | 875 | PF00454 | 0.463 |
MOD_PK_1 | 380 | 386 | PF00069 | 0.220 |
MOD_PK_1 | 790 | 796 | PF00069 | 0.285 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.469 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.500 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.232 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.263 |
MOD_PKA_2 | 857 | 863 | PF00069 | 0.240 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.684 |
MOD_PKB_1 | 145 | 153 | PF00069 | 0.443 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.392 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.411 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.314 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.278 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.282 |
MOD_Plk_1 | 610 | 616 | PF00069 | 0.444 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.385 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.238 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.326 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.245 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.246 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.248 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.462 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.327 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.289 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.245 |
MOD_Plk_4 | 669 | 675 | PF00069 | 0.303 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.266 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.539 |
MOD_Plk_4 | 857 | 863 | PF00069 | 0.359 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.634 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.277 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.419 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.268 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.243 |
MOD_SUMO_rev_2 | 130 | 137 | PF00179 | 0.364 |
MOD_SUMO_rev_2 | 170 | 179 | PF00179 | 0.360 |
MOD_SUMO_rev_2 | 640 | 646 | PF00179 | 0.246 |
MOD_SUMO_rev_2 | 772 | 782 | PF00179 | 0.350 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.574 |
TRG_DiLeu_BaLyEn_6 | 104 | 109 | PF01217 | 0.227 |
TRG_DiLeu_BaLyEn_6 | 510 | 515 | PF01217 | 0.251 |
TRG_DiLeu_BaLyEn_6 | 562 | 567 | PF01217 | 0.277 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.217 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.210 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 808 | 811 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 832 | 835 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.545 |
TRG_NES_CRM1_1 | 127 | 138 | PF08389 | 0.348 |
TRG_NES_CRM1_1 | 715 | 727 | PF08389 | 0.355 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHR6 | Leptomonas seymouri | 35% | 76% |
A0A0N1IJL2 | Leptomonas seymouri | 75% | 100% |
A0A0S4IKD3 | Bodo saltans | 24% | 100% |
A0A0S4JG93 | Bodo saltans | 47% | 100% |
A0A0S4JSW7 | Bodo saltans | 26% | 100% |
A0A1X0NSH7 | Trypanosomatidae | 55% | 96% |
A0A3R7KRB4 | Trypanosoma rangeli | 52% | 97% |
A0A3S7WNV9 | Leishmania donovani | 36% | 75% |
A0A422NY59 | Trypanosoma rangeli | 24% | 100% |
A0A451EJ75 | Leishmania donovani | 24% | 100% |
A4H342 | Leishmania braziliensis | 24% | 100% |
A4HKY2 | Leishmania braziliensis | 87% | 100% |
A4HRD9 | Leishmania infantum | 24% | 100% |
A4HS98 | Leishmania infantum | 36% | 75% |
D0A4W6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 90% |
D0AAR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 96% |
E9AC07 | Leishmania major | 24% | 100% |
E9AHM3 | Leishmania infantum | 100% | 100% |
E9AJA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AK82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 78% |
E9B3C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O18894 | Oryctolagus cuniculus | 25% | 100% |
O70496 | Mus musculus | 30% | 100% |
P21564 | Torpedo marmorata | 26% | 100% |
P35522 | Tetronarce californica | 26% | 100% |
P51788 | Homo sapiens | 23% | 99% |
P51790 | Homo sapiens | 25% | 100% |
P51791 | Mus musculus | 26% | 100% |
P51792 | Rattus norvegicus | 25% | 100% |
P51793 | Homo sapiens | 25% | 100% |
P51794 | Rattus norvegicus | 25% | 100% |
P51798 | Homo sapiens | 29% | 100% |
P51799 | Rattus norvegicus | 30% | 100% |
P60300 | Arabidopsis thaliana | 28% | 100% |
P92941 | Arabidopsis thaliana | 29% | 100% |
P92942 | Arabidopsis thaliana | 31% | 100% |
P92943 | Arabidopsis thaliana | 27% | 100% |
Q4PKH3 | Bos taurus | 32% | 100% |
Q4Q4T5 | Leishmania major | 95% | 99% |
Q54AX6 | Dictyostelium discoideum | 28% | 100% |
Q5RDJ7 | Pongo abelii | 24% | 100% |
Q61418 | Mus musculus | 25% | 100% |
Q75JF3 | Dictyostelium discoideum | 31% | 100% |
Q86AZ6 | Dictyostelium discoideum | 28% | 100% |
Q96282 | Arabidopsis thaliana | 29% | 100% |
Q9R279 | Cavia porcellus | 25% | 100% |
Q9TTU3 | Oryctolagus cuniculus | 27% | 100% |
V5AY77 | Trypanosoma cruzi | 33% | 91% |
V5BEI7 | Trypanosoma cruzi | 25% | 100% |
V5BPC2 | Trypanosoma cruzi | 28% | 100% |
V5BVK3 | Trypanosoma cruzi | 53% | 98% |