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: 15 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 11 |
GO:0012506 | vesicle membrane | 4 | 10 |
GO:0016020 | membrane | 2 | 11 |
GO:0030117 | membrane coat | 3 | 11 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 10 |
GO:0030660 | Golgi-associated vesicle membrane | 5 | 10 |
GO:0030662 | coated vesicle membrane | 5 | 10 |
GO:0030663 | COPI-coated vesicle membrane | 6 | 10 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0098588 | bounding membrane of organelle | 4 | 11 |
GO:0098796 | membrane protein complex | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0030120 | vesicle coat | 4 | 1 |
GO:0030126 | COPI vesicle coat | 5 | 1 |
Related structures:
AlphaFold database: A0A3Q8IGV8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0006886 | intracellular protein transport | 4 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0016192 | vesicle-mediated transport | 4 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 1 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.366 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.339 |
DEG_APCC_KENBOX_2 | 569 | 573 | PF00400 | 0.490 |
DEG_SCF_FBW7_2 | 334 | 340 | PF00400 | 0.508 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.480 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.508 |
DOC_CKS1_1 | 175 | 180 | PF01111 | 0.539 |
DOC_CKS1_1 | 334 | 339 | PF01111 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 788 | 794 | PF00134 | 0.539 |
DOC_MAPK_gen_1 | 282 | 289 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 414 | 423 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 644 | 652 | PF00069 | 0.551 |
DOC_MAPK_HePTP_8 | 430 | 442 | PF00069 | 0.527 |
DOC_MAPK_HePTP_8 | 626 | 638 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 417 | 425 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 629 | 638 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 644 | 652 | PF00069 | 0.432 |
DOC_PP1_RVXF_1 | 524 | 531 | PF00149 | 0.460 |
DOC_PP1_RVXF_1 | 60 | 67 | PF00149 | 0.354 |
DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.540 |
DOC_PP2B_LxvP_1 | 806 | 809 | PF13499 | 0.576 |
DOC_PP2B_PxIxI_1 | 611 | 617 | PF00149 | 0.563 |
DOC_PP4_FxxP_1 | 435 | 438 | PF00568 | 0.460 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 782 | 786 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 825 | 829 | PF00917 | 0.732 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.437 |
LIG_14-3-3_CanoR_1 | 263 | 273 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 385 | 390 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 422 | 428 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 443 | 449 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 69 | 74 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 775 | 779 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 783 | 791 | PF00244 | 0.472 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.554 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.486 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.540 |
LIG_Clathr_ClatBox_1 | 574 | 578 | PF01394 | 0.530 |
LIG_deltaCOP1_diTrp_1 | 128 | 133 | PF00928 | 0.380 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.510 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.455 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.460 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.406 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.474 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.441 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.512 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.512 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.457 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.563 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.460 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.432 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.463 |
LIG_FHA_2 | 837 | 843 | PF00498 | 0.744 |
LIG_Integrin_isoDGR_2 | 313 | 315 | PF01839 | 0.522 |
LIG_Integrin_RGD_1 | 197 | 199 | PF01839 | 0.339 |
LIG_LIR_Gen_1 | 373 | 384 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 401 | 408 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 512 | 521 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 512 | 518 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 669 | 674 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 696 | 700 | PF02991 | 0.525 |
LIG_LYPXL_yS_3 | 794 | 797 | PF13949 | 0.471 |
LIG_MYND_1 | 795 | 799 | PF01753 | 0.470 |
LIG_Pex14_2 | 487 | 491 | PF04695 | 0.460 |
LIG_PTB_Apo_2 | 429 | 436 | PF02174 | 0.438 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.474 |
LIG_SH2_CRK | 704 | 708 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 537 | 540 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 758 | 762 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 42 | 45 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 499 | 502 | PF00017 | 0.540 |
LIG_SH2_STAT3 | 537 | 540 | PF00017 | 0.540 |
LIG_SH2_STAT3 | 586 | 589 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 683 | 686 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 762 | 765 | PF00017 | 0.452 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.402 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.366 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.508 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.474 |
LIG_SH3_3 | 801 | 807 | PF00018 | 0.496 |
LIG_SH3_3 | 811 | 817 | PF00018 | 0.680 |
LIG_SH3_3 | 819 | 825 | PF00018 | 0.743 |
LIG_SH3_3 | 848 | 854 | PF00018 | 0.688 |
LIG_SH3_3 | 855 | 861 | PF00018 | 0.717 |
LIG_SUMO_SIM_anti_2 | 455 | 460 | PF11976 | 0.540 |
LIG_SUMO_SIM_anti_2 | 476 | 485 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 698 | 706 | PF11976 | 0.515 |
LIG_SUMO_SIM_anti_2 | 741 | 747 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 112 | 117 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 438 | 447 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 476 | 485 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 612 | 617 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 698 | 706 | PF11976 | 0.471 |
LIG_TRAF2_1 | 875 | 878 | PF00917 | 0.714 |
LIG_TYR_ITIM | 702 | 707 | PF00017 | 0.386 |
LIG_UBA3_1 | 378 | 387 | PF00899 | 0.332 |
LIG_UBA3_1 | 564 | 570 | PF00899 | 0.348 |
LIG_UBA3_1 | 574 | 581 | PF00899 | 0.217 |
LIG_WRC_WIRS_1 | 225 | 230 | PF05994 | 0.524 |
LIG_WRC_WIRS_1 | 50 | 55 | PF05994 | 0.383 |
LIG_WRC_WIRS_1 | 70 | 75 | PF05994 | 0.157 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.570 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.511 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.200 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.354 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.326 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.485 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.360 |
MOD_CK1_1 | 777 | 783 | PF00069 | 0.553 |
MOD_CK1_1 | 866 | 872 | PF00069 | 0.714 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.448 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.307 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.511 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.366 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.420 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.442 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.620 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.422 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.313 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.356 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.414 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.370 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.386 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.453 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.446 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.313 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.425 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.437 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.217 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.403 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.380 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.276 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.456 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.358 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.366 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.712 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.389 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.496 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.360 |
MOD_N-GLC_1 | 471 | 476 | PF02516 | 0.457 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.457 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.146 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.490 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.425 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.313 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.516 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.478 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.356 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.448 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.386 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.289 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.349 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.191 |
MOD_NEK2_1 | 831 | 836 | PF00069 | 0.693 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.400 |
MOD_NEK2_2 | 409 | 414 | PF00069 | 0.411 |
MOD_NEK2_2 | 827 | 832 | PF00069 | 0.695 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.509 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.391 |
MOD_PIKK_1 | 733 | 739 | PF00454 | 0.457 |
MOD_PIKK_1 | 782 | 788 | PF00454 | 0.554 |
MOD_PK_1 | 579 | 585 | PF00069 | 0.360 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.426 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.426 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.411 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.524 |
MOD_PKA_2 | 782 | 788 | PF00069 | 0.489 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.313 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.356 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.262 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.313 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.332 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.310 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.403 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.146 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.347 |
MOD_Plk_1 | 614 | 620 | PF00069 | 0.457 |
MOD_Plk_2-3 | 348 | 354 | PF00069 | 0.411 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.485 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.313 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.189 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.358 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.366 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.306 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.244 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.369 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.456 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.431 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.468 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.386 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.442 |
MOD_SUMO_rev_2 | 323 | 332 | PF00179 | 0.313 |
MOD_SUMO_rev_2 | 516 | 525 | PF00179 | 0.425 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_1 | 476 | 481 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_1 | 627 | 632 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_1 | 741 | 746 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 435 | 440 | PF01217 | 0.332 |
TRG_DiLeu_LyEn_5 | 260 | 265 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.127 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 704 | 707 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 794 | 797 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 644 | 646 | PF00400 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 629 | 633 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2R6 | Leptomonas seymouri | 24% | 74% |
A0A0N1HWQ8 | Leptomonas seymouri | 79% | 98% |
A0A0S4IPS1 | Bodo saltans | 25% | 73% |
A0A0S4J4T7 | Bodo saltans | 42% | 89% |
A0A1X0NT50 | Trypanosomatidae | 61% | 92% |
A0A3S7X8J8 | Leishmania donovani | 22% | 74% |
A0A422N6J5 | Trypanosoma rangeli | 61% | 96% |
A4HBF3 | Leishmania braziliensis | 23% | 74% |
A4HM28 | Leishmania braziliensis | 84% | 100% |
A4I9G2 | Leishmania infantum | 99% | 100% |
A4IAK2 | Leishmania infantum | 22% | 74% |
C9ZJT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9B4G0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B5M6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 74% |
O35142 | Rattus norvegicus | 41% | 98% |
O42937 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
O55029 | Mus musculus | 41% | 98% |
O62621 | Drosophila melanogaster | 42% | 97% |
P35605 | Bos taurus | 41% | 98% |
P35606 | Homo sapiens | 41% | 98% |
P41811 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 99% |
P53621 | Homo sapiens | 24% | 72% |
P53622 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 74% |
Q0J3D9 | Oryza sativa subsp. japonica | 25% | 73% |
Q20168 | Caenorhabditis elegans | 38% | 88% |
Q27954 | Bos taurus | 24% | 72% |
Q4Q2B0 | Leishmania major | 23% | 74% |
Q4Q3L5 | Leishmania major | 95% | 100% |
Q4R4I8 | Macaca fascicularis | 41% | 98% |
Q54YD8 | Dictyostelium discoideum | 42% | 88% |
Q5R664 | Pongo abelii | 41% | 98% |
Q5VQ78 | Oryza sativa subsp. japonica | 43% | 97% |
Q6H8D5 | Oryza sativa subsp. japonica | 42% | 97% |
Q6H8D6 | Oryza sativa subsp. japonica | 44% | 97% |
Q8CIE6 | Mus musculus | 24% | 72% |
Q8L828 | Arabidopsis thaliana | 43% | 97% |
Q94A40 | Arabidopsis thaliana | 26% | 73% |
Q96WV5 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 73% |
Q9AUR7 | Oryza sativa subsp. japonica | 25% | 73% |
Q9AUR8 | Oryza sativa subsp. japonica | 25% | 73% |
Q9C827 | Arabidopsis thaliana | 43% | 95% |
Q9CAA0 | Arabidopsis thaliana | 42% | 96% |
Q9SJT9 | Arabidopsis thaliana | 26% | 73% |
V5AUU0 | Trypanosoma cruzi | 59% | 97% |