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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: Q4Q4T5
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 16 |
GO:0005216 | monoatomic ion channel activity | 4 | 16 |
GO:0005244 | voltage-gated monoatomic ion channel activity | 4 | 16 |
GO:0005247 | voltage-gated chloride channel activity | 6 | 16 |
GO:0005253 | monoatomic anion channel activity | 5 | 16 |
GO:0005254 | chloride channel activity | 6 | 16 |
GO:0008308 | voltage-gated monoatomic anion channel activity | 5 | 16 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 16 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 16 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 16 |
GO:0015108 | chloride transmembrane transporter activity | 5 | 16 |
GO:0015267 | channel activity | 4 | 16 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 16 |
GO:0022803 | passive transmembrane transporter activity | 3 | 16 |
GO:0022832 | voltage-gated channel activity | 6 | 16 |
GO:0022836 | gated channel activity | 5 | 16 |
GO:0022857 | transmembrane transporter activity | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 726 | 730 | PF00656 | 0.387 |
CLV_C14_Caspase3-7 | 741 | 745 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.534 |
CLV_MEL_PAP_1 | 860 | 866 | PF00089 | 0.489 |
CLV_MEL_PAP_1 | 88 | 94 | PF00089 | 0.340 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.339 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 774 | 776 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.442 |
DEG_APCC_DBOX_1 | 711 | 719 | PF00400 | 0.247 |
DEG_MDM2_SWIB_1 | 361 | 368 | PF02201 | 0.314 |
DOC_CDC14_PxL_1 | 834 | 842 | PF14671 | 0.311 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.631 |
DOC_CKS1_1 | 462 | 467 | PF01111 | 0.388 |
DOC_CYCLIN_RxL_1 | 429 | 438 | PF00134 | 0.463 |
DOC_CYCLIN_RxL_1 | 509 | 519 | PF00134 | 0.315 |
DOC_MAPK_gen_1 | 474 | 484 | PF00069 | 0.220 |
DOC_MAPK_MEF2A_6 | 103 | 110 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 476 | 484 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 595 | 604 | PF00069 | 0.272 |
DOC_MAPK_MEF2A_6 | 690 | 699 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 712 | 721 | PF00069 | 0.245 |
DOC_MAPK_NFAT4_5 | 103 | 111 | PF00069 | 0.406 |
DOC_MAPK_NFAT4_5 | 712 | 720 | PF00069 | 0.246 |
DOC_PP1_RVXF_1 | 105 | 112 | PF00149 | 0.247 |
DOC_PP1_RVXF_1 | 180 | 187 | PF00149 | 0.331 |
DOC_PP1_RVXF_1 | 337 | 343 | PF00149 | 0.477 |
DOC_PP1_RVXF_1 | 510 | 516 | PF00149 | 0.250 |
DOC_PP1_RVXF_1 | 593 | 599 | PF00149 | 0.241 |
DOC_PP1_RVXF_1 | 850 | 856 | PF00149 | 0.359 |
DOC_PP2B_LxvP_1 | 212 | 215 | PF13499 | 0.299 |
DOC_PP4_FxxP_1 | 14 | 17 | PF00568 | 0.614 |
DOC_PP4_FxxP_1 | 296 | 299 | PF00568 | 0.219 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.272 |
DOC_PP4_FxxP_1 | 570 | 573 | PF00568 | 0.275 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.194 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 798 | 802 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.716 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.274 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 665 | 670 | PF00397 | 0.250 |
LIG_14-3-3_CanoR_1 | 145 | 154 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 182 | 187 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 517 | 521 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 595 | 599 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 765 | 773 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.601 |
LIG_Actin_WH2_2 | 761 | 776 | PF00022 | 0.339 |
LIG_APCC_ABBA_1 | 805 | 810 | PF00400 | 0.255 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_BIR_III_4 | 101 | 105 | PF00653 | 0.593 |
LIG_BIR_III_4 | 759 | 763 | PF00653 | 0.372 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.412 |
LIG_Clathr_ClatBox_1 | 326 | 330 | PF01394 | 0.272 |
LIG_EH1_1 | 237 | 245 | PF00400 | 0.409 |
LIG_eIF4E_1 | 508 | 514 | PF01652 | 0.250 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.301 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.315 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.338 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.335 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.409 |
LIG_FHA_1 | 665 | 671 | PF00498 | 0.279 |
LIG_FHA_1 | 841 | 847 | PF00498 | 0.361 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.230 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.565 |
LIG_FHA_2 | 659 | 665 | PF00498 | 0.312 |
LIG_FHA_2 | 669 | 675 | PF00498 | 0.336 |
LIG_FHA_2 | 767 | 773 | PF00498 | 0.320 |
LIG_GBD_Chelix_1 | 244 | 252 | PF00786 | 0.311 |
LIG_LIR_Apic_2 | 11 | 17 | PF02991 | 0.615 |
LIG_LIR_Apic_2 | 294 | 299 | PF02991 | 0.219 |
LIG_LIR_Apic_2 | 315 | 321 | PF02991 | 0.272 |
LIG_LIR_Apic_2 | 455 | 461 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 363 | 373 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 483 | 492 | PF02991 | 0.221 |
LIG_LIR_Gen_1 | 505 | 515 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 527 | 537 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 597 | 605 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 801 | 809 | PF02991 | 0.294 |
LIG_LIR_LC3C_4 | 597 | 602 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 597 | 601 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 801 | 805 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 823 | 829 | PF02991 | 0.274 |
LIG_MYND_3 | 645 | 649 | PF01753 | 0.286 |
LIG_NRBOX | 201 | 207 | PF00104 | 0.304 |
LIG_NRBOX | 411 | 417 | PF00104 | 0.279 |
LIG_NRBOX | 509 | 515 | PF00104 | 0.322 |
LIG_NRBOX | 618 | 624 | PF00104 | 0.388 |
LIG_NRBOX | 714 | 720 | PF00104 | 0.241 |
LIG_PALB2_WD40_1 | 29 | 37 | PF16756 | 0.599 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.409 |
LIG_Pex14_2 | 361 | 365 | PF04695 | 0.314 |
LIG_Pex14_2 | 449 | 453 | PF04695 | 0.366 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.388 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.209 |
LIG_SH2_GRB2like | 228 | 231 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 77 | 81 | PF00017 | 0.489 |
LIG_SH2_PTP2 | 458 | 461 | PF00017 | 0.334 |
LIG_SH2_PTP2 | 802 | 805 | PF00017 | 0.277 |
LIG_SH2_SRC | 228 | 231 | PF00017 | 0.431 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.309 |
LIG_SH2_STAT3 | 815 | 818 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 802 | 805 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 808 | 811 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 815 | 818 | PF00017 | 0.266 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.463 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.425 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.263 |
LIG_SH3_3 | 783 | 789 | PF00018 | 0.310 |
LIG_Sin3_3 | 598 | 605 | PF02671 | 0.334 |
LIG_SUMO_SIM_anti_2 | 122 | 128 | PF11976 | 0.312 |
LIG_SUMO_SIM_anti_2 | 667 | 675 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 122 | 128 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 393 | 400 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 667 | 675 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 681 | 687 | PF11976 | 0.239 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.522 |
LIG_UBA3_1 | 617 | 625 | PF00899 | 0.336 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.614 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.274 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.249 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.276 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.258 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.430 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.276 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.285 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.273 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.339 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.297 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.309 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.423 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.710 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.388 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.400 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.312 |
MOD_CK2_1 | 766 | 772 | PF00069 | 0.508 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.712 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.710 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.571 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.387 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.293 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.304 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.236 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.282 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.146 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.231 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.325 |
MOD_GlcNHglycan | 369 | 373 | PF01048 | 0.325 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.388 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.651 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.610 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.433 |
MOD_GlcNHglycan | 810 | 814 | PF01048 | 0.385 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.623 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.445 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.697 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.557 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.250 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.288 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.241 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.284 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.308 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.347 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.304 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.255 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.241 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.358 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.637 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.505 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.641 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.516 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.625 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.647 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.700 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.448 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.250 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.271 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.301 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.292 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.262 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.416 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.318 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.514 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.288 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.515 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.452 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.453 |
MOD_NEK2_2 | 17 | 22 | PF00069 | 0.538 |
MOD_NEK2_2 | 387 | 392 | PF00069 | 0.259 |
MOD_NEK2_2 | 524 | 529 | PF00069 | 0.171 |
MOD_NEK2_2 | 631 | 636 | PF00069 | 0.384 |
MOD_NEK2_2 | 650 | 655 | PF00069 | 0.482 |
MOD_PIKK_1 | 840 | 846 | PF00454 | 0.316 |
MOD_PIKK_1 | 863 | 869 | PF00454 | 0.420 |
MOD_PK_1 | 379 | 385 | PF00069 | 0.270 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.563 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.647 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.398 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.285 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.272 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.618 |
MOD_PKB_1 | 145 | 153 | PF00069 | 0.587 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.551 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.395 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.375 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.389 |
MOD_Plk_1 | 609 | 615 | PF00069 | 0.241 |
MOD_Plk_1 | 702 | 708 | PF00069 | 0.204 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.379 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.277 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.398 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.257 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.297 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.256 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.368 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.279 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.301 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.371 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.314 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.407 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.566 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.274 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.420 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.310 |
MOD_ProDKin_1 | 665 | 671 | PF00069 | 0.299 |
MOD_SUMO_rev_2 | 130 | 137 | PF00179 | 0.465 |
MOD_SUMO_rev_2 | 170 | 178 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 639 | 645 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 766 | 776 | PF00179 | 0.407 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 104 | 109 | PF01217 | 0.237 |
TRG_DiLeu_BaLyEn_6 | 509 | 514 | PF01217 | 0.325 |
TRG_DiLeu_BaLyEn_6 | 561 | 566 | PF01217 | 0.274 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.709 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 706 | 709 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 802 | 805 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 826 | 829 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.390 |
TRG_NES_CRM1_1 | 127 | 138 | PF08389 | 0.446 |
TRG_NES_CRM1_1 | 714 | 726 | PF08389 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 572 | 577 | PF00026 | 0.179 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHR6 | Leptomonas seymouri | 34% | 76% |
A0A0N1IJL2 | Leptomonas seymouri | 75% | 99% |
A0A0S4IKD3 | Bodo saltans | 24% | 100% |
A0A0S4IL39 | Bodo saltans | 23% | 100% |
A0A0S4JG93 | Bodo saltans | 47% | 100% |
A0A0S4JSW7 | Bodo saltans | 26% | 100% |
A0A1X0NSH7 | Trypanosomatidae | 54% | 95% |
A0A3Q8IH43 | Leishmania donovani | 95% | 99% |
A0A3R7KRB4 | Trypanosoma rangeli | 51% | 97% |
A0A3S7WNV9 | Leishmania donovani | 35% | 75% |
A0A422NY59 | Trypanosoma rangeli | 24% | 100% |
A0A451EJ75 | Leishmania donovani | 25% | 100% |
A4H342 | Leishmania braziliensis | 25% | 100% |
A4HKY2 | Leishmania braziliensis | 86% | 99% |
A4HRD9 | Leishmania infantum | 25% | 100% |
A4HS98 | Leishmania infantum | 35% | 75% |
D0A4W6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 89% |
D0AAR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 96% |
E9AC07 | Leishmania major | 25% | 100% |
E9AHM3 | Leishmania infantum | 95% | 99% |
E9AJA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AK82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 77% |
E9B3C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
O18894 | Oryctolagus cuniculus | 25% | 100% |
O70496 | Mus musculus | 30% | 100% |
P0C197 | Ustilago maydis (strain 521 / FGSC 9021) | 24% | 78% |
P21564 | Torpedo marmorata | 26% | 100% |
P51790 | Homo sapiens | 25% | 100% |
P51791 | Mus musculus | 26% | 100% |
P51792 | Rattus norvegicus | 26% | 100% |
P51793 | Homo sapiens | 25% | 100% |
P51794 | Rattus norvegicus | 25% | 100% |
P51798 | Homo sapiens | 30% | 100% |
P51799 | Rattus norvegicus | 30% | 100% |
P51801 | Homo sapiens | 25% | 100% |
P51803 | Oryctolagus cuniculus | 25% | 100% |
P51804 | Oryctolagus cuniculus | 24% | 100% |
P60300 | Arabidopsis thaliana | 27% | 100% |
P92941 | Arabidopsis thaliana | 28% | 100% |
P92942 | Arabidopsis thaliana | 31% | 100% |
P92943 | Arabidopsis thaliana | 26% | 100% |
Q4PKH3 | Bos taurus | 31% | 100% |
Q54AX6 | Dictyostelium discoideum | 28% | 100% |
Q5RDJ7 | Pongo abelii | 25% | 100% |
Q61418 | Mus musculus | 26% | 100% |
Q75JF3 | Dictyostelium discoideum | 28% | 100% |
Q86AZ6 | Dictyostelium discoideum | 28% | 100% |
Q96282 | Arabidopsis thaliana | 29% | 100% |
Q9R279 | Cavia porcellus | 26% | 100% |
Q9TTU3 | Oryctolagus cuniculus | 27% | 100% |
V5BEI7 | Trypanosoma cruzi | 25% | 100% |
V5BPC2 | Trypanosoma cruzi | 28% | 100% |
V5BVK3 | Trypanosoma cruzi | 52% | 97% |