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:0005768 | endosome | 7 | 2 |
GO:0005769 | early endosome | 8 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 12 |
GO:0031410 | cytoplasmic vesicle | 6 | 2 |
GO:0031982 | vesicle | 4 | 2 |
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:0097708 | intracellular vesicle | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AC07
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:0005451 | obsolete monoatomic cation:proton antiporter activity | 5 | 2 |
GO:0008308 | voltage-gated monoatomic anion channel activity | 5 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 2 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015078 | proton transmembrane transporter activity | 5 | 2 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 12 |
GO:0015108 | chloride transmembrane transporter activity | 5 | 12 |
GO:0015267 | channel activity | 4 | 12 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 2 |
GO:0015297 | antiporter activity | 5 | 2 |
GO:0015298 | obsolete solute:monoatomic cation antiporter activity | 5 | 2 |
GO:0015299 | obsolete solute:proton antiporter activity | 6 | 2 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0022803 | passive transmembrane transporter activity | 3 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 2 |
GO:0022832 | voltage-gated channel activity | 6 | 12 |
GO:0022836 | gated channel activity | 5 | 12 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.207 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.436 |
CLV_PCSK_FUR_1 | 743 | 747 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 665 | 669 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.329 |
DEG_SCF_FBW7_1 | 392 | 397 | PF00400 | 0.274 |
DEG_SPOP_SBC_1 | 69 | 73 | PF00917 | 0.571 |
DOC_CKS1_1 | 391 | 396 | PF01111 | 0.241 |
DOC_CYCLIN_RxL_1 | 690 | 700 | PF00134 | 0.469 |
DOC_MAPK_gen_1 | 367 | 379 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 572 | 579 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 633 | 641 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 720 | 726 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 231 | 238 | PF00069 | 0.207 |
DOC_MAPK_MEF2A_6 | 372 | 381 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 665 | 674 | PF00069 | 0.594 |
DOC_PP1_RVXF_1 | 320 | 327 | PF00149 | 0.202 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.241 |
DOC_PP4_FxxP_1 | 337 | 340 | PF00568 | 0.207 |
DOC_PP4_FxxP_1 | 391 | 394 | PF00568 | 0.256 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.310 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.249 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.547 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.241 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.207 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 426 | 432 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 645 | 651 | PF00244 | 0.603 |
LIG_APCC_ABBA_1 | 101 | 106 | PF00400 | 0.252 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.510 |
LIG_BRCT_BRCA1_1 | 482 | 486 | PF00533 | 0.232 |
LIG_Clathr_ClatBox_1 | 682 | 686 | PF01394 | 0.574 |
LIG_eIF4E_1 | 293 | 299 | PF01652 | 0.449 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.300 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.568 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.251 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.192 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.389 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.335 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.249 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.397 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.523 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.488 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.569 |
LIG_FHA_1 | 757 | 763 | PF00498 | 0.654 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.630 |
LIG_KLC1_Yacidic_2 | 574 | 578 | PF13176 | 0.600 |
LIG_LIR_Apic_2 | 530 | 536 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.207 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 436 | 446 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 574 | 584 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 653 | 661 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 666 | 677 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 722 | 729 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 86 | 97 | PF02991 | 0.262 |
LIG_LIR_LC3C_4 | 31 | 35 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.207 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 574 | 579 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 712 | 717 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 722 | 726 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.656 |
LIG_MYND_1 | 567 | 571 | PF01753 | 0.462 |
LIG_Pex14_1 | 111 | 115 | PF04695 | 0.291 |
LIG_Pex14_1 | 144 | 148 | PF04695 | 0.267 |
LIG_Pex14_2 | 469 | 473 | PF04695 | 0.390 |
LIG_Pex14_2 | 575 | 579 | PF04695 | 0.588 |
LIG_PTB_Apo_2 | 584 | 591 | PF02174 | 0.578 |
LIG_REV1ctd_RIR_1 | 145 | 155 | PF16727 | 0.289 |
LIG_RPA_C_Fungi | 58 | 70 | PF08784 | 0.441 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.241 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.386 |
LIG_SH2_CRK | 629 | 633 | PF00017 | 0.223 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.241 |
LIG_SH2_SRC | 501 | 504 | PF00017 | 0.241 |
LIG_SH2_SRC | 557 | 560 | PF00017 | 0.323 |
LIG_SH2_SRC | 568 | 571 | PF00017 | 0.336 |
LIG_SH2_SRC | 629 | 632 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 480 | 484 | PF00017 | 0.252 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.252 |
LIG_SH2_STAT3 | 596 | 599 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 654 | 657 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 696 | 699 | PF00017 | 0.353 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.467 |
LIG_SUMO_SIM_anti_2 | 378 | 383 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 399 | 406 | PF11976 | 0.277 |
LIG_SUMO_SIM_anti_2 | 622 | 628 | PF11976 | 0.241 |
LIG_TRAF2_1 | 475 | 478 | PF00917 | 0.275 |
LIG_TYR_ITIM | 627 | 632 | PF00017 | 0.214 |
LIG_UBA3_1 | 694 | 699 | PF00899 | 0.340 |
LIG_Vh1_VBS_1 | 503 | 521 | PF01044 | 0.256 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.258 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.275 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.262 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.245 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.386 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.402 |
MOD_CK1_1 | 700 | 706 | PF00069 | 0.358 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.502 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.318 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.250 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.385 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.504 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.360 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.312 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.304 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.275 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.204 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.241 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.380 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.259 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.283 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.460 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.321 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.299 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.162 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.256 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.276 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.504 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.479 |
MOD_LATS_1 | 663 | 669 | PF00433 | 0.438 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.482 |
MOD_N-GLC_1 | 610 | 615 | PF02516 | 0.448 |
MOD_N-GLC_2 | 129 | 131 | PF02516 | 0.430 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.545 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.251 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.268 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.256 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.262 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.248 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.241 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.300 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.300 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.281 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.241 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.368 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.355 |
MOD_NEK2_2 | 687 | 692 | PF00069 | 0.445 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.582 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.480 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.412 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.329 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.544 |
MOD_Plk_1 | 622 | 628 | PF00069 | 0.342 |
MOD_Plk_1 | 665 | 671 | PF00069 | 0.529 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.437 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.368 |
MOD_Plk_2-3 | 41 | 47 | PF00069 | 0.401 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.386 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.254 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.275 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.258 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.342 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.383 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.450 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.241 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.241 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.460 |
MOD_SUMO_for_1 | 571 | 574 | PF00179 | 0.373 |
MOD_SUMO_rev_2 | 187 | 197 | PF00179 | 0.300 |
MOD_SUMO_rev_2 | 558 | 567 | PF00179 | 0.384 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.208 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 61 | 63 | PF00400 | 0.497 |
TRG_NLS_MonoExtN_4 | 365 | 371 | PF00514 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 474 | 478 | PF00026 | 0.256 |
TRG_Pf-PMV_PEXEL_1 | 601 | 605 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6P9 | Leptomonas seymouri | 78% | 100% |
A0A0N1IHR6 | Leptomonas seymouri | 29% | 66% |
A0A0N1IJL2 | Leptomonas seymouri | 25% | 87% |
A0A0S4IKD3 | Bodo saltans | 59% | 100% |
A0A0S4IL39 | Bodo saltans | 54% | 100% |
A0A0S4JG93 | Bodo saltans | 24% | 91% |
A0A0S4JSW7 | Bodo saltans | 26% | 89% |
A0A1X0NSH7 | Trypanosomatidae | 26% | 83% |
A0A1X0P2R6 | Trypanosomatidae | 64% | 100% |
A0A3Q8IH43 | Leishmania donovani | 24% | 87% |
A0A3R7KRB4 | Trypanosoma rangeli | 24% | 85% |
A0A422NY59 | Trypanosoma rangeli | 66% | 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) | 26% | 82% |
D0AAR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 84% |
E9AHM3 | Leishmania infantum | 24% | 87% |
E9AJA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9B3C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 87% |
O18894 | Oryctolagus cuniculus | 32% | 94% |
O35454 | Mus musculus | 28% | 89% |
O60159 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
O70496 | Mus musculus | 27% | 96% |
O94287 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P0C197 | Ustilago maydis (strain 521 / FGSC 9021) | 33% | 68% |
P35523 | Homo sapiens | 28% | 78% |
P35524 | Rattus norvegicus | 28% | 78% |
P35525 | Rattus norvegicus | 28% | 85% |
P37020 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 99% |
P51788 | Homo sapiens | 29% | 86% |
P51789 | Oryctolagus cuniculus | 28% | 86% |
P51790 | Homo sapiens | 32% | 94% |
P51791 | Mus musculus | 32% | 94% |
P51792 | Rattus norvegicus | 32% | 94% |
P51793 | Homo sapiens | 31% | 100% |
P51794 | Rattus norvegicus | 32% | 100% |
P51795 | Homo sapiens | 31% | 95% |
P51796 | Rattus norvegicus | 31% | 95% |
P51797 | Homo sapiens | 27% | 89% |
P51798 | Homo sapiens | 28% | 96% |
P51799 | Rattus norvegicus | 27% | 96% |
P51800 | Homo sapiens | 27% | 100% |
P51801 | Homo sapiens | 26% | 100% |
P51802 | Rattus norvegicus | 27% | 100% |
P51803 | Oryctolagus cuniculus | 25% | 100% |
P51804 | Oryctolagus cuniculus | 26% | 100% |
P60300 | Arabidopsis thaliana | 25% | 100% |
P92941 | Arabidopsis thaliana | 25% | 100% |
P92942 | Arabidopsis thaliana | 25% | 99% |
P92943 | Arabidopsis thaliana | 26% | 97% |
Q06393 | Rattus norvegicus | 27% | 100% |
Q4PKH3 | Bos taurus | 29% | 95% |
Q4Q4T5 | Leishmania major | 25% | 88% |
Q54AX6 | Dictyostelium discoideum | 28% | 89% |
Q5RBK4 | Pongo abelii | 31% | 95% |
Q5RDJ7 | Pongo abelii | 32% | 96% |
Q61418 | Mus musculus | 32% | 100% |
Q64347 | Mus musculus | 28% | 78% |
Q75JF3 | Dictyostelium discoideum | 29% | 100% |
Q86AZ6 | Dictyostelium discoideum | 29% | 95% |
Q96282 | Arabidopsis thaliana | 25% | 99% |
Q99P66 | Cavia porcellus | 32% | 100% |
Q9BMK9 | Caenorhabditis elegans | 30% | 77% |
Q9GKE7 | Sus scrofa | 31% | 95% |
Q9MZT1 | Canis lupus familiaris | 27% | 79% |
Q9R0A1 | Mus musculus | 28% | 85% |
Q9R279 | Cavia porcellus | 32% | 94% |
Q9TT16 | Oryctolagus cuniculus | 27% | 89% |
Q9TTU3 | Oryctolagus cuniculus | 31% | 95% |
Q9W701 | Xenopus laevis | 25% | 100% |
Q9WU45 | Cavia porcellus | 28% | 86% |
Q9WUB6 | Mus musculus | 28% | 100% |
Q9WUB7 | Mus musculus | 27% | 100% |
Q9WVD4 | Mus musculus | 31% | 95% |
V5AY77 | Trypanosoma cruzi | 26% | 79% |
V5BEI7 | Trypanosoma cruzi | 66% | 100% |