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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005768 | endosome | 7 | 1 |
GO:0005769 | early endosome | 8 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 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: E9AJA4
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 12 |
GO:0005216 | monoatomic ion channel activity | 4 | 12 |
GO:0005244 | voltage-gated monoatomic ion channel activity | 4 | 12 |
GO:0005247 | voltage-gated chloride channel activity | 6 | 12 |
GO:0005253 | monoatomic anion channel activity | 5 | 12 |
GO:0005254 | chloride channel activity | 6 | 12 |
GO:0008308 | voltage-gated monoatomic anion channel activity | 5 | 12 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 12 |
GO:0015108 | chloride transmembrane transporter activity | 5 | 12 |
GO:0015267 | channel activity | 4 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0022803 | passive transmembrane transporter activity | 3 | 12 |
GO:0022832 | voltage-gated channel activity | 6 | 12 |
GO:0022836 | gated channel activity | 5 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0005451 | obsolete monoatomic cation:proton antiporter activity | 5 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0015078 | proton transmembrane transporter activity | 5 | 1 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 1 |
GO:0015297 | antiporter activity | 5 | 1 |
GO:0015298 | obsolete solute:monoatomic cation antiporter activity | 5 | 1 |
GO:0015299 | obsolete solute:proton antiporter activity | 6 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 1 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 357 | 363 | PF00089 | 0.138 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 743 | 745 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 751 | 753 | PF00675 | 0.378 |
CLV_PCSK_FUR_1 | 741 | 745 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.214 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 743 | 745 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.239 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.231 |
CLV_PCSK_PC7_1 | 55 | 61 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.342 |
DEG_SCF_FBW7_1 | 390 | 395 | PF00400 | 0.281 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.577 |
DOC_CKS1_1 | 389 | 394 | PF01111 | 0.252 |
DOC_CYCLIN_RxL_1 | 688 | 698 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 570 | 577 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 718 | 724 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 229 | 236 | PF00069 | 0.214 |
DOC_PP1_RVXF_1 | 318 | 325 | PF00149 | 0.209 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.252 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.214 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.268 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.145 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.557 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.252 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.246 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 643 | 649 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 654 | 659 | PF00244 | 0.540 |
LIG_APCC_ABBA_1 | 99 | 104 | PF00400 | 0.264 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.584 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.138 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.241 |
LIG_Clathr_ClatBox_1 | 680 | 684 | PF01394 | 0.586 |
LIG_eIF4E_1 | 291 | 297 | PF01652 | 0.457 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.312 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.586 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.262 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.199 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.346 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.260 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.404 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.504 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.519 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.576 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.656 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.664 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.642 |
LIG_KLC1_Yacidic_2 | 572 | 576 | PF13176 | 0.615 |
LIG_LIR_Apic_2 | 528 | 534 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 164 | 173 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.230 |
LIG_LIR_Gen_1 | 331 | 340 | PF02991 | 0.166 |
LIG_LIR_Gen_1 | 352 | 361 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 37 | 46 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 572 | 582 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 651 | 659 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 664 | 675 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 720 | 727 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 84 | 95 | PF02991 | 0.283 |
LIG_LIR_LC3C_4 | 29 | 33 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 179 | 183 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.166 |
LIG_LIR_Nem_3 | 345 | 349 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 651 | 655 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 664 | 670 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 710 | 715 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 720 | 724 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.660 |
LIG_MYND_1 | 565 | 569 | PF01753 | 0.470 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.299 |
LIG_Pex14_1 | 142 | 146 | PF04695 | 0.276 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.398 |
LIG_Pex14_2 | 573 | 577 | PF04695 | 0.601 |
LIG_PTB_Apo_2 | 582 | 589 | PF02174 | 0.589 |
LIG_REV1ctd_RIR_1 | 143 | 153 | PF16727 | 0.297 |
LIG_RPA_C_Fungi | 55 | 67 | PF08784 | 0.449 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.252 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.395 |
LIG_SH2_NCK_1 | 499 | 503 | PF00017 | 0.252 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.145 |
LIG_SH2_SRC | 499 | 502 | PF00017 | 0.252 |
LIG_SH2_SRC | 555 | 558 | PF00017 | 0.335 |
LIG_SH2_SRC | 566 | 569 | PF00017 | 0.347 |
LIG_SH2_SRC | 627 | 630 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 478 | 482 | PF00017 | 0.264 |
LIG_SH2_STAP1 | 488 | 492 | PF00017 | 0.264 |
LIG_SH2_STAT3 | 594 | 597 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.369 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.289 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.486 |
LIG_SUMO_SIM_anti_2 | 376 | 381 | PF11976 | 0.350 |
LIG_SUMO_SIM_anti_2 | 397 | 404 | PF11976 | 0.289 |
LIG_TRAF2_1 | 473 | 476 | PF00917 | 0.287 |
LIG_UBA3_1 | 692 | 697 | PF00899 | 0.357 |
LIG_Vh1_VBS_1 | 501 | 519 | PF01044 | 0.268 |
LIG_WRC_WIRS_1 | 162 | 167 | PF05994 | 0.269 |
LIG_WRC_WIRS_1 | 343 | 348 | PF05994 | 0.259 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.287 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.479 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.395 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.275 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.398 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.569 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.429 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.374 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.549 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.332 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.261 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.448 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.530 |
MOD_CK2_1 | 707 | 713 | PF00069 | 0.368 |
MOD_Cter_Amidation | 749 | 752 | PF01082 | 0.344 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.331 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.317 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.500 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.517 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.304 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.225 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.252 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.377 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.247 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.278 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.478 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.341 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.182 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.312 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.287 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.373 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.287 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.433 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.551 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.330 |
MOD_N-GLC_1 | 608 | 613 | PF02516 | 0.475 |
MOD_N-GLC_2 | 127 | 129 | PF02516 | 0.443 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.305 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.303 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.268 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.274 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.259 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.252 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.339 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.318 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.330 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.252 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.397 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.370 |
MOD_NEK2_2 | 685 | 690 | PF00069 | 0.459 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.145 |
MOD_PKA_1 | 60 | 66 | PF00069 | 0.597 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.489 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.419 |
MOD_PKA_2 | 707 | 713 | PF00069 | 0.344 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.369 |
MOD_Plk_1 | 663 | 669 | PF00069 | 0.554 |
MOD_Plk_1 | 685 | 691 | PF00069 | 0.452 |
MOD_Plk_2-3 | 138 | 144 | PF00069 | 0.397 |
MOD_Plk_2-3 | 39 | 45 | PF00069 | 0.404 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.409 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.269 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.287 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.288 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.369 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.398 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.477 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.252 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.297 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.306 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.405 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 569 | 572 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 185 | 195 | PF00179 | 0.327 |
MOD_SUMO_rev_2 | 556 | 565 | PF00179 | 0.395 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 709 | 712 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.501 |
TRG_NLS_MonoExtN_4 | 363 | 369 | PF00514 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 472 | 476 | PF00026 | 0.268 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6P9 | Leptomonas seymouri | 78% | 100% |
A0A0N1IHR6 | Leptomonas seymouri | 27% | 66% |
A0A0N1IJL2 | Leptomonas seymouri | 24% | 87% |
A0A0S4IKD3 | Bodo saltans | 58% | 100% |
A0A0S4IL39 | Bodo saltans | 54% | 100% |
A0A0S4JG93 | Bodo saltans | 24% | 91% |
A0A0S4JSW7 | Bodo saltans | 25% | 89% |
A0A1X0NSH7 | Trypanosomatidae | 26% | 83% |
A0A1X0P2R6 | Trypanosomatidae | 64% | 100% |
A0A3Q8IH43 | Leishmania donovani | 24% | 87% |
A0A3R7KRB4 | Trypanosoma rangeli | 24% | 85% |
A0A422NY59 | Trypanosoma rangeli | 67% | 100% |
A0A451EJ75 | Leishmania donovani | 96% | 100% |
A4H342 | Leishmania braziliensis | 86% | 100% |
A4HKY2 | Leishmania braziliensis | 23% | 87% |
A4HRD9 | Leishmania infantum | 96% | 100% |
C9ZY92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 82% |
D0AAR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 84% |
E9AC07 | Leishmania major | 95% | 100% |
E9AHM3 | Leishmania infantum | 24% | 87% |
E9B3C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 87% |
O18894 | Oryctolagus cuniculus | 33% | 94% |
O35454 | Mus musculus | 28% | 89% |
O60159 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
O70496 | Mus musculus | 27% | 96% |
O94287 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P21564 | Torpedo marmorata | 26% | 96% |
P35522 | Tetronarce californica | 26% | 95% |
P35523 | Homo sapiens | 28% | 78% |
P35524 | Rattus norvegicus | 28% | 77% |
P35525 | Rattus norvegicus | 28% | 85% |
P37020 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 99% |
P51788 | Homo sapiens | 28% | 86% |
P51789 | Oryctolagus cuniculus | 27% | 86% |
P51790 | Homo sapiens | 33% | 94% |
P51791 | Mus musculus | 33% | 94% |
P51792 | Rattus norvegicus | 33% | 94% |
P51793 | Homo sapiens | 32% | 100% |
P51794 | Rattus norvegicus | 32% | 100% |
P51795 | Homo sapiens | 32% | 94% |
P51796 | Rattus norvegicus | 31% | 94% |
P51797 | Homo sapiens | 27% | 89% |
P51798 | Homo sapiens | 28% | 96% |
P51799 | Rattus norvegicus | 27% | 96% |
P51800 | Homo sapiens | 28% | 100% |
P51801 | Homo sapiens | 27% | 100% |
P51802 | Rattus norvegicus | 27% | 100% |
P51803 | Oryctolagus cuniculus | 26% | 100% |
P51804 | Oryctolagus cuniculus | 27% | 100% |
P60300 | Arabidopsis thaliana | 25% | 100% |
P92941 | Arabidopsis thaliana | 26% | 99% |
P92942 | Arabidopsis thaliana | 25% | 99% |
P92943 | Arabidopsis thaliana | 27% | 97% |
Q06393 | Rattus norvegicus | 27% | 100% |
Q4PKH3 | Bos taurus | 28% | 95% |
Q4Q4T5 | Leishmania major | 24% | 88% |
Q54AX6 | Dictyostelium discoideum | 27% | 89% |
Q54C67 | Dictyostelium discoideum | 26% | 95% |
Q5RBK4 | Pongo abelii | 32% | 94% |
Q5RDJ7 | Pongo abelii | 32% | 96% |
Q61418 | Mus musculus | 32% | 100% |
Q64347 | Mus musculus | 28% | 77% |
Q75JF3 | Dictyostelium discoideum | 29% | 100% |
Q86AZ6 | Dictyostelium discoideum | 29% | 94% |
Q96282 | Arabidopsis thaliana | 25% | 99% |
Q99P66 | Cavia porcellus | 32% | 100% |
Q9BMK9 | Caenorhabditis elegans | 30% | 77% |
Q9GKE7 | Sus scrofa | 32% | 94% |
Q9MZT1 | Canis lupus familiaris | 28% | 79% |
Q9R0A1 | Mus musculus | 28% | 85% |
Q9R279 | Cavia porcellus | 33% | 94% |
Q9TT16 | Oryctolagus cuniculus | 27% | 89% |
Q9TTU3 | Oryctolagus cuniculus | 32% | 94% |
Q9W701 | Xenopus laevis | 26% | 100% |
Q9WU45 | Cavia porcellus | 28% | 85% |
Q9WUB6 | Mus musculus | 28% | 100% |
Q9WUB7 | Mus musculus | 27% | 100% |
Q9WVD4 | Mus musculus | 32% | 94% |
V5AY77 | Trypanosoma cruzi | 27% | 79% |
V5BEI7 | Trypanosoma cruzi | 66% | 100% |
V5BVK3 | Trypanosoma cruzi | 23% | 85% |