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: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005635 | nuclear envelope | 4 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0031967 | organelle envelope | 3 | 4 |
GO:0031975 | envelope | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: A4HMD6
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0043413 | macromolecule glycosylation | 3 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0070085 | glycosylation | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004576 | oligosaccharyl transferase activity | 5 | 27 |
GO:0004579 | dolichyl-diphosphooligosaccharide-protein glycotransferase activity | 6 | 27 |
GO:0005488 | binding | 1 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016757 | glycosyltransferase activity | 3 | 27 |
GO:0016758 | hexosyltransferase activity | 4 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043169 | cation binding | 3 | 27 |
GO:0046872 | metal ion binding | 4 | 27 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.268 |
CLV_C14_Caspase3-7 | 806 | 810 | PF00656 | 0.339 |
CLV_MEL_PAP_1 | 524 | 530 | PF00089 | 0.167 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 681 | 683 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 752 | 756 | PF00082 | 0.613 |
DEG_ODPH_VHL_1 | 684 | 695 | PF01847 | 0.348 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.475 |
DOC_AGCK_PIF_2 | 93 | 98 | PF00069 | 0.295 |
DOC_MAPK_DCC_7 | 540 | 549 | PF00069 | 0.162 |
DOC_MAPK_gen_1 | 213 | 222 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 56 | 64 | PF00069 | 0.217 |
DOC_MAPK_HePTP_8 | 512 | 524 | PF00069 | 0.167 |
DOC_MAPK_MEF2A_6 | 515 | 524 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 540 | 549 | PF00069 | 0.230 |
DOC_PP1_RVXF_1 | 579 | 586 | PF00149 | 0.281 |
DOC_PP4_FxxP_1 | 355 | 358 | PF00568 | 0.304 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.186 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.270 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 649 | 654 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.338 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 259 | 263 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 324 | 333 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.252 |
LIG_14-3-3_CanoR_1 | 598 | 602 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 657 | 663 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 800 | 805 | PF00244 | 0.441 |
LIG_AP2alpha_2 | 73 | 75 | PF02296 | 0.281 |
LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.382 |
LIG_DLG_GKlike_1 | 800 | 807 | PF00625 | 0.296 |
LIG_eIF4E_1 | 464 | 470 | PF01652 | 0.408 |
LIG_eIF4E_1 | 710 | 716 | PF01652 | 0.294 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.314 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.603 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.278 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.377 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.395 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.308 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.421 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.311 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.339 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.292 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.259 |
LIG_FHA_2 | 732 | 738 | PF00498 | 0.342 |
LIG_LIR_Apic_2 | 40 | 46 | PF02991 | 0.167 |
LIG_LIR_Apic_2 | 780 | 784 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 173 | 184 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 204 | 212 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 421 | 431 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 502 | 512 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 635 | 644 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 661 | 671 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 737 | 747 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 584 | 588 | PF02991 | 0.222 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 635 | 639 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 661 | 666 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 73 | 78 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 737 | 743 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.276 |
LIG_LYPXL_yS_3 | 113 | 116 | PF13949 | 0.377 |
LIG_MLH1_MIPbox_1 | 89 | 93 | PF16413 | 0.382 |
LIG_NRBOX | 300 | 306 | PF00104 | 0.384 |
LIG_NRBOX | 520 | 526 | PF00104 | 0.326 |
LIG_PCNA_PIPBox_1 | 404 | 413 | PF02747 | 0.167 |
LIG_Pex14_1 | 586 | 590 | PF04695 | 0.270 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.281 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.217 |
LIG_PTB_Apo_2 | 657 | 664 | PF02174 | 0.320 |
LIG_PTB_Phospho_1 | 657 | 663 | PF10480 | 0.317 |
LIG_REV1ctd_RIR_1 | 353 | 357 | PF16727 | 0.217 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.305 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.295 |
LIG_SH2_CRK | 801 | 805 | PF00017 | 0.307 |
LIG_SH2_PTP2 | 238 | 241 | PF00017 | 0.353 |
LIG_SH2_PTP2 | 636 | 639 | PF00017 | 0.282 |
LIG_SH2_SRC | 710 | 713 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.214 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.504 |
LIG_SH2_STAT3 | 588 | 591 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 744 | 747 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 801 | 804 | PF00017 | 0.505 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.377 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.403 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.366 |
LIG_SH3_3 | 771 | 777 | PF00018 | 0.370 |
LIG_SUMO_SIM_anti_2 | 326 | 334 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 20 | 27 | PF11976 | 0.557 |
LIG_TRAF2_1 | 482 | 485 | PF00917 | 0.511 |
LIG_TYR_ITIM | 426 | 431 | PF00017 | 0.250 |
LIG_TYR_ITSM | 202 | 209 | PF00017 | 0.318 |
LIG_UBA3_1 | 49 | 56 | PF00899 | 0.290 |
LIG_UBA3_1 | 750 | 755 | PF00899 | 0.312 |
LIG_WRC_WIRS_1 | 202 | 207 | PF05994 | 0.318 |
LIG_WRC_WIRS_1 | 415 | 420 | PF05994 | 0.414 |
MOD_CDC14_SPxK_1 | 290 | 293 | PF00782 | 0.382 |
MOD_CDK_SPxK_1 | 287 | 293 | PF00069 | 0.281 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.254 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.323 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.353 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.504 |
MOD_CK1_1 | 760 | 766 | PF00069 | 0.338 |
MOD_CK2_1 | 809 | 815 | PF00069 | 0.367 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.485 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.426 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.336 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.592 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.563 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.621 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.574 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.534 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.571 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.374 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.316 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.523 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.213 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.299 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.362 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.584 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.418 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.680 |
MOD_GSK3_1 | 807 | 814 | PF00069 | 0.329 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.351 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.468 |
MOD_N-GLC_1 | 757 | 762 | PF02516 | 0.536 |
MOD_N-GLC_2 | 138 | 140 | PF02516 | 0.437 |
MOD_N-GLC_2 | 193 | 195 | PF02516 | 0.281 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.334 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.392 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.334 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.357 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.215 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.459 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.308 |
MOD_NEK2_1 | 716 | 721 | PF00069 | 0.311 |
MOD_NEK2_1 | 807 | 812 | PF00069 | 0.310 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.318 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.605 |
MOD_NEK2_2 | 34 | 39 | PF00069 | 0.520 |
MOD_NEK2_2 | 436 | 441 | PF00069 | 0.294 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.291 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.244 |
MOD_PIKK_1 | 702 | 708 | PF00454 | 0.348 |
MOD_PK_1 | 510 | 516 | PF00069 | 0.383 |
MOD_PK_1 | 58 | 64 | PF00069 | 0.359 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.317 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.533 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.507 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.429 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.349 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.270 |
MOD_PKA_2 | 799 | 805 | PF00069 | 0.330 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.184 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.412 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.279 |
MOD_Plk_2-3 | 731 | 737 | PF00069 | 0.255 |
MOD_Plk_2-3 | 809 | 815 | PF00069 | 0.319 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.323 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.661 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.318 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.425 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.425 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.433 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.446 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.366 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.249 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.437 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.269 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.278 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.364 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.305 |
MOD_Plk_4 | 716 | 722 | PF00069 | 0.350 |
MOD_Plk_4 | 777 | 783 | PF00069 | 0.373 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.281 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.281 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.270 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.619 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.311 |
MOD_ProDKin_1 | 649 | 655 | PF00069 | 0.328 |
MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.330 |
MOD_SUMO_rev_2 | 21 | 31 | PF00179 | 0.542 |
TRG_DiLeu_BaEn_1 | 328 | 333 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_1 | 625 | 630 | PF01217 | 0.322 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 801 | 804 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.352 |
TRG_NES_CRM1_1 | 296 | 311 | PF08389 | 0.382 |
TRG_NLS_MonoCore_2 | 496 | 501 | PF00514 | 0.362 |
TRG_NLS_MonoExtC_3 | 496 | 502 | PF00514 | 0.425 |
TRG_NLS_MonoExtN_4 | 495 | 501 | PF00514 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 43% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 49% | 97% |
A0A3Q8IHT0 | Leishmania donovani | 54% | 95% |
A0A3Q8II34 | Leishmania donovani | 80% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 57% | 100% |
A0A3Q8IV37 | Leishmania donovani | 55% | 98% |
A0A422MX14 | Trypanosoma rangeli | 49% | 99% |
A4HFF9 | Leishmania braziliensis | 57% | 100% |
A4HMD5 | Leishmania braziliensis | 59% | 100% |
A4HMD7 | Leishmania braziliensis | 58% | 96% |
A4IB08 | Leishmania infantum | 53% | 95% |
A4IB09 | Leishmania infantum | 57% | 100% |
A4IB10 | Leishmania infantum | 80% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E2RG47 | Canis lupus familiaris | 30% | 100% |
E9AET6 | Leishmania major | 54% | 100% |
E9AET7 | Leishmania major | 57% | 100% |
E9AET8 | Leishmania major | 79% | 100% |
E9AET9 | Leishmania major | 55% | 100% |
E9AHU4 | Leishmania infantum | 56% | 98% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 95% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 98% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 97% |
F1PJP5 | Canis lupus familiaris | 27% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P46975 | Caenorhabditis elegans | 31% | 100% |
P46977 | Homo sapiens | 28% | 100% |
P46978 | Mus musculus | 27% | 100% |
Q2KJI2 | Bos taurus | 28% | 100% |
Q3TDQ1 | Mus musculus | 30% | 100% |
Q54NM9 | Dictyostelium discoideum | 29% | 100% |
Q5RCE2 | Pongo abelii | 28% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 28% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 31% | 100% |
Q8TCJ2 | Homo sapiens | 31% | 100% |
Q93ZY3 | Arabidopsis thaliana | 30% | 100% |
Q9FX21 | Arabidopsis thaliana | 28% | 100% |
V5BDM6 | Trypanosoma cruzi | 49% | 99% |