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: A4H342
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_NRD_NRD_1 | 356 | 358 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 744 | 746 | PF00675 | 0.364 |
CLV_PCSK_FUR_1 | 733 | 737 | PF00082 | 0.464 |
CLV_PCSK_FUR_1 | 740 | 744 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 735 | 737 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 194 | 196 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.341 |
CLV_PCSK_PC7_1 | 47 | 53 | PF00082 | 0.340 |
CLV_PCSK_PC7_1 | 740 | 746 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 700 | 704 | PF00082 | 0.243 |
DEG_SCF_FBW7_1 | 382 | 387 | PF00400 | 0.301 |
DOC_AGCK_PIF_1 | 429 | 434 | PF00069 | 0.297 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.282 |
DOC_CYCLIN_RxL_1 | 680 | 690 | PF00134 | 0.503 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 659 | 668 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 362 | 371 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 562 | 569 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 623 | 631 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 710 | 716 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 221 | 228 | PF00069 | 0.237 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.282 |
DOC_PP4_FxxP_1 | 327 | 330 | PF00568 | 0.237 |
DOC_PP4_FxxP_1 | 381 | 384 | PF00568 | 0.298 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.194 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.571 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.370 |
DOC_USP7_UBL2_3 | 572 | 576 | PF12436 | 0.428 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.253 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.212 |
LIG_14-3-3_CanoR_1 | 416 | 422 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 646 | 651 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 754 | 761 | PF00244 | 0.506 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.258 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_1 | 472 | 476 | PF00533 | 0.263 |
LIG_Clathr_ClatBox_1 | 672 | 676 | PF01394 | 0.603 |
LIG_deltaCOP1_diTrp_1 | 29 | 38 | PF00928 | 0.488 |
LIG_eIF4E_1 | 283 | 289 | PF01652 | 0.479 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.603 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.342 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.293 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.220 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.384 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.373 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.238 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.291 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.425 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.522 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.501 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.534 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.592 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.651 |
LIG_KLC1_Yacidic_2 | 564 | 568 | PF13176 | 0.627 |
LIG_LIR_Apic_2 | 520 | 526 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 29 | 38 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 344 | 353 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 546 | 551 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 564 | 574 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 642 | 651 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 656 | 667 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 712 | 719 | PF02991 | 0.527 |
LIG_LIR_LC3C_4 | 21 | 25 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 546 | 550 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 642 | 647 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 656 | 662 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 712 | 716 | PF02991 | 0.497 |
LIG_MYND_1 | 557 | 561 | PF01753 | 0.494 |
LIG_Pex14_1 | 101 | 105 | PF04695 | 0.319 |
LIG_Pex14_1 | 134 | 138 | PF04695 | 0.300 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.417 |
LIG_Pex14_2 | 565 | 569 | PF04695 | 0.615 |
LIG_PTB_Apo_2 | 574 | 581 | PF02174 | 0.601 |
LIG_REV1ctd_RIR_1 | 135 | 145 | PF16727 | 0.321 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.282 |
LIG_SH2_CRK | 523 | 527 | PF00017 | 0.531 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 491 | 495 | PF00017 | 0.282 |
LIG_SH2_SRC | 491 | 494 | PF00017 | 0.282 |
LIG_SH2_SRC | 547 | 550 | PF00017 | 0.494 |
LIG_SH2_SRC | 558 | 561 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 547 | 551 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 586 | 589 | PF00017 | 0.590 |
LIG_SH2_STAT3 | 71 | 74 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.522 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.591 |
LIG_SUMO_SIM_anti_2 | 368 | 373 | PF11976 | 0.377 |
LIG_TRAF2_1 | 465 | 468 | PF00917 | 0.262 |
LIG_UBA3_1 | 527 | 535 | PF00899 | 0.372 |
LIG_UBA3_1 | 684 | 689 | PF00899 | 0.513 |
LIG_Vh1_VBS_1 | 493 | 511 | PF01044 | 0.298 |
LIG_WRC_WIRS_1 | 436 | 441 | PF05994 | 0.318 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.287 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.418 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.647 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.568 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.487 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.529 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.295 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.560 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.216 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.313 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.486 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.483 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.262 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.206 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.282 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.527 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.454 |
MOD_GlcNHglycan | 568 | 572 | PF01048 | 0.233 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.279 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.492 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.293 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.342 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.262 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.269 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.317 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.262 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.659 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.458 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.501 |
MOD_N-GLC_1 | 600 | 605 | PF02516 | 0.391 |
MOD_N-GLC_1 | 662 | 667 | PF02516 | 0.285 |
MOD_N-GLC_2 | 126 | 128 | PF02516 | 0.618 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.290 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.311 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.298 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.314 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.249 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.289 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.342 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.342 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.314 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.437 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.491 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.540 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.523 |
MOD_NEK2_2 | 677 | 682 | PF00069 | 0.576 |
MOD_PIKK_1 | 651 | 657 | PF00454 | 0.526 |
MOD_PKA_1 | 52 | 58 | PF00069 | 0.714 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.654 |
MOD_PKA_2 | 753 | 759 | PF00069 | 0.502 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.515 |
MOD_PKB_1 | 635 | 643 | PF00069 | 0.461 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.327 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.218 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.258 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.524 |
MOD_Plk_1 | 637 | 643 | PF00069 | 0.565 |
MOD_Plk_1 | 677 | 683 | PF00069 | 0.573 |
MOD_Plk_2-3 | 130 | 136 | PF00069 | 0.381 |
MOD_Plk_2-3 | 31 | 37 | PF00069 | 0.560 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.531 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.192 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.318 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.249 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.530 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.536 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.282 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.253 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.640 |
MOD_SUMO_for_1 | 561 | 564 | PF00179 | 0.534 |
MOD_SUMO_for_1 | 702 | 705 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 177 | 187 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 548 | 557 | PF00179 | 0.538 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.597 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 634 | 637 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 740 | 743 | PF00400 | 0.573 |
TRG_NLS_MonoExtN_4 | 355 | 361 | PF00514 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 464 | 468 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 591 | 595 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 736 | 741 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6P9 | Leptomonas seymouri | 78% | 100% |
A0A0N1IHR6 | Leptomonas seymouri | 28% | 66% |
A0A0N1IJL2 | Leptomonas seymouri | 24% | 87% |
A0A0S4IKD3 | Bodo saltans | 57% | 100% |
A0A0S4IL39 | Bodo saltans | 54% | 100% |
A0A0S4JG93 | Bodo saltans | 24% | 90% |
A0A1X0NKT6 | Trypanosomatidae | 26% | 80% |
A0A1X0NSH7 | Trypanosomatidae | 25% | 83% |
A0A1X0P2R6 | Trypanosomatidae | 63% | 100% |
A0A3Q8IH43 | Leishmania donovani | 24% | 87% |
A0A3R7KRB4 | Trypanosoma rangeli | 23% | 85% |
A0A3S5IRJ9 | Trypanosoma rangeli | 26% | 78% |
A0A422NY59 | Trypanosoma rangeli | 66% | 100% |
A0A451EJ75 | Leishmania donovani | 87% | 100% |
A4HKY2 | Leishmania braziliensis | 22% | 87% |
A4HRD9 | Leishmania infantum | 87% | 100% |
C9ZY92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 82% |
D0AAR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 83% |
E9AC07 | Leishmania major | 86% | 100% |
E9AHM3 | Leishmania infantum | 24% | 87% |
E9AJA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AK82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 68% |
E9B3C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 87% |
O18894 | Oryctolagus cuniculus | 32% | 94% |
O35454 | Mus musculus | 29% | 88% |
O60159 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
O70496 | Mus musculus | 27% | 96% |
O94287 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
P0C197 | Ustilago maydis (strain 521 / FGSC 9021) | 33% | 68% |
P35523 | Homo sapiens | 27% | 78% |
P35524 | Rattus norvegicus | 27% | 77% |
P35525 | Rattus norvegicus | 27% | 85% |
P37020 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 99% |
P51788 | Homo sapiens | 27% | 86% |
P51789 | Oryctolagus cuniculus | 27% | 86% |
P51790 | Homo sapiens | 32% | 94% |
P51791 | Mus musculus | 32% | 94% |
P51792 | Rattus norvegicus | 33% | 94% |
P51793 | Homo sapiens | 32% | 100% |
P51794 | Rattus norvegicus | 32% | 100% |
P51795 | Homo sapiens | 32% | 94% |
P51796 | Rattus norvegicus | 32% | 94% |
P51797 | Homo sapiens | 30% | 88% |
P51798 | Homo sapiens | 28% | 95% |
P51799 | Rattus norvegicus | 27% | 96% |
P51800 | Homo sapiens | 26% | 100% |
P51801 | Homo sapiens | 26% | 100% |
P51802 | Rattus norvegicus | 26% | 100% |
P51803 | Oryctolagus cuniculus | 25% | 100% |
P51804 | Oryctolagus cuniculus | 26% | 100% |
P60300 | Arabidopsis thaliana | 25% | 100% |
P92941 | Arabidopsis thaliana | 24% | 99% |
P92942 | Arabidopsis thaliana | 23% | 98% |
P92943 | Arabidopsis thaliana | 26% | 97% |
Q06393 | Rattus norvegicus | 26% | 100% |
Q4PKH3 | Bos taurus | 28% | 95% |
Q4Q4T5 | Leishmania major | 25% | 87% |
Q54AX6 | Dictyostelium discoideum | 27% | 89% |
Q54C67 | Dictyostelium discoideum | 27% | 95% |
Q54LQ4 | Dictyostelium discoideum | 25% | 77% |
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 | 28% | 94% |
Q96282 | Arabidopsis thaliana | 25% | 99% |
Q99P66 | Cavia porcellus | 34% | 100% |
Q9BMK9 | Caenorhabditis elegans | 29% | 77% |
Q9GKE7 | Sus scrofa | 33% | 94% |
Q9MZT1 | Canis lupus familiaris | 27% | 79% |
Q9R0A1 | Mus musculus | 27% | 85% |
Q9R279 | Cavia porcellus | 32% | 94% |
Q9TT16 | Oryctolagus cuniculus | 29% | 88% |
Q9TTU3 | Oryctolagus cuniculus | 32% | 94% |
Q9W701 | Xenopus laevis | 26% | 100% |
Q9WU45 | Cavia porcellus | 28% | 85% |
Q9WUB6 | Mus musculus | 26% | 100% |
Q9WUB7 | Mus musculus | 25% | 100% |
Q9WVD4 | Mus musculus | 32% | 94% |
V5AY77 | Trypanosoma cruzi | 25% | 79% |
V5BEI7 | Trypanosoma cruzi | 66% | 100% |
V5BVK3 | Trypanosoma cruzi | 24% | 85% |