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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030117 | membrane coat | 3 | 12 |
GO:0030120 | vesicle coat | 4 | 12 |
GO:0030127 | COPII vesicle coat | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0005794 | Golgi apparatus | 5 | 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:0070971 | endoplasmic reticulum exit site | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HE50
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 11 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 11 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0048193 | Golgi vesicle transport | 5 | 11 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0035459 | vesicle cargo loading | 4 | 1 |
GO:0090110 | COPII-coated vesicle cargo loading | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005515 | protein binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 810 | 816 | PF00089 | 0.304 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 769 | 771 | PF00675 | 0.389 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 769 | 771 | PF00082 | 0.389 |
CLV_PCSK_PC7_1 | 514 | 520 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 786 | 790 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.429 |
CLV_Separin_Metazoa | 369 | 373 | PF03568 | 0.340 |
DEG_APCC_DBOX_1 | 231 | 239 | PF00400 | 0.426 |
DEG_APCC_DBOX_1 | 611 | 619 | PF00400 | 0.340 |
DEG_APCC_DBOX_1 | 754 | 762 | PF00400 | 0.436 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.496 |
DOC_CDC14_PxL_1 | 302 | 310 | PF14671 | 0.200 |
DOC_CYCLIN_RxL_1 | 365 | 375 | PF00134 | 0.340 |
DOC_CYCLIN_RxL_1 | 688 | 697 | PF00134 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 608 | 611 | PF00134 | 0.426 |
DOC_MAPK_DCC_7 | 262 | 271 | PF00069 | 0.242 |
DOC_MAPK_DCC_7 | 612 | 620 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 452 | 461 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 526 | 535 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 612 | 620 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 86 | 95 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 262 | 271 | PF00069 | 0.205 |
DOC_MAPK_MEF2A_6 | 528 | 537 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 612 | 620 | PF00069 | 0.340 |
DOC_PP1_RVXF_1 | 244 | 250 | PF00149 | 0.306 |
DOC_PP1_RVXF_1 | 415 | 422 | PF00149 | 0.200 |
DOC_PP1_RVXF_1 | 689 | 696 | PF00149 | 0.474 |
DOC_PP1_SILK_1 | 448 | 453 | PF00149 | 0.321 |
DOC_PP2B_LxvP_1 | 269 | 272 | PF13499 | 0.335 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.306 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.508 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.426 |
DOC_PP4_FxxP_1 | 73 | 76 | PF00568 | 0.377 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.200 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 128 | 138 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 168 | 172 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 452 | 461 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 521 | 529 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 566 | 574 | PF00244 | 0.383 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.303 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 727 | 731 | PF00533 | 0.480 |
LIG_Clathr_ClatBox_1 | 210 | 214 | PF01394 | 0.306 |
LIG_Clathr_ClatBox_1 | 663 | 667 | PF01394 | 0.356 |
LIG_EH_1 | 275 | 279 | PF12763 | 0.306 |
LIG_eIF4E_1 | 658 | 664 | PF01652 | 0.277 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.453 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.317 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.368 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.321 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.413 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.493 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.376 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.352 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.321 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.426 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.273 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.401 |
LIG_Integrin_isoDGR_2 | 415 | 417 | PF01839 | 0.340 |
LIG_LIR_Apic_2 | 71 | 76 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 248 | 256 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 285 | 295 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 391 | 398 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 399 | 407 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 485 | 492 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 53 | 64 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 592 | 600 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 643 | 652 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 592 | 596 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 643 | 648 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 782 | 788 | PF02991 | 0.394 |
LIG_LYPXL_S_1 | 659 | 663 | PF13949 | 0.322 |
LIG_LYPXL_yS_3 | 660 | 663 | PF13949 | 0.323 |
LIG_MAD2 | 23 | 31 | PF02301 | 0.571 |
LIG_MLH1_MIPbox_1 | 484 | 488 | PF16413 | 0.340 |
LIG_MLH1_MIPbox_1 | 70 | 74 | PF16413 | 0.511 |
LIG_PCNA_yPIPBox_3 | 204 | 217 | PF02747 | 0.200 |
LIG_PCNA_yPIPBox_3 | 538 | 546 | PF02747 | 0.200 |
LIG_Pex14_2 | 487 | 491 | PF04695 | 0.321 |
LIG_PTB_Apo_2 | 654 | 661 | PF02174 | 0.225 |
LIG_PTB_Apo_2 | 753 | 760 | PF02174 | 0.414 |
LIG_PTB_Phospho_1 | 654 | 660 | PF10480 | 0.226 |
LIG_PTB_Phospho_1 | 753 | 759 | PF10480 | 0.413 |
LIG_Rb_LxCxE_1 | 701 | 720 | PF01857 | 0.310 |
LIG_REV1ctd_RIR_1 | 71 | 75 | PF16727 | 0.381 |
LIG_REV1ctd_RIR_1 | 782 | 790 | PF16727 | 0.376 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.410 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.306 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.293 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.546 |
LIG_SH2_SRC | 227 | 230 | PF00017 | 0.291 |
LIG_SH2_SRC | 593 | 596 | PF00017 | 0.453 |
LIG_SH2_SRC | 658 | 661 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 759 | 763 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 799 | 803 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 468 | 471 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 802 | 805 | PF00017 | 0.454 |
LIG_SH3_2 | 118 | 123 | PF14604 | 0.554 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.550 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.494 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.315 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.489 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.325 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.624 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.426 |
LIG_SH3_3 | 739 | 745 | PF00018 | 0.296 |
LIG_SUMO_SIM_anti_2 | 531 | 537 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 211 | 216 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 403 | 408 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 676 | 682 | PF11976 | 0.554 |
LIG_TRAF2_1 | 745 | 748 | PF00917 | 0.510 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.417 |
LIG_TYR_ITIM | 713 | 718 | PF00017 | 0.344 |
LIG_UBA3_1 | 620 | 625 | PF00899 | 0.341 |
LIG_WRC_WIRS_1 | 249 | 254 | PF05994 | 0.426 |
LIG_WW_3 | 609 | 613 | PF00397 | 0.426 |
MOD_CDK_SPxxK_3 | 239 | 246 | PF00069 | 0.426 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.269 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.391 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.418 |
MOD_CK1_1 | 780 | 786 | PF00069 | 0.280 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.306 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.284 |
MOD_Cter_Amidation | 140 | 143 | PF01082 | 0.426 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.680 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.604 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.470 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.395 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.406 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.387 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.615 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.381 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.391 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.452 |
MOD_GSK3_1 | 809 | 816 | PF00069 | 0.448 |
MOD_N-GLC_2 | 409 | 411 | PF02516 | 0.426 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.754 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.293 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.436 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.426 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.330 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.350 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.469 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.321 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.340 |
MOD_OFUCOSY | 127 | 133 | PF10250 | 0.321 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.426 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.306 |
MOD_PK_1 | 640 | 646 | PF00069 | 0.426 |
MOD_PKA_1 | 603 | 609 | PF00069 | 0.426 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.461 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.416 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.583 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.306 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.363 |
MOD_PKA_2 | 812 | 818 | PF00069 | 0.352 |
MOD_PKB_1 | 452 | 460 | PF00069 | 0.291 |
MOD_PKB_1 | 519 | 527 | PF00069 | 0.306 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.488 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.565 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.467 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.391 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.376 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.306 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.392 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.393 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.380 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.331 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.168 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.439 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.512 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.463 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.280 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.426 |
MOD_SUMO_for_1 | 788 | 791 | PF00179 | 0.367 |
MOD_SUMO_rev_2 | 592 | 599 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_1 | 709 | 714 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 569 | 574 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 767 | 772 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 660 | 663 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 759 | 762 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 526 | 529 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 768 | 770 | PF00400 | 0.397 |
TRG_NES_CRM1_1 | 752 | 766 | PF08389 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 14 | 19 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 691 | 696 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 786 | 790 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P662 | Leptomonas seymouri | 77% | 79% |
A0A0N1PA55 | Leptomonas seymouri | 24% | 84% |
A0A0S4KJI0 | Bodo saltans | 47% | 74% |
A0A1X0NMN7 | Trypanosomatidae | 54% | 82% |
A0A1X0NZG8 | Trypanosomatidae | 26% | 88% |
A0A3Q8IF67 | Leishmania donovani | 23% | 85% |
A0A3R7KKF1 | Trypanosoma rangeli | 26% | 90% |
A0A3R7MV46 | Trypanosoma rangeli | 53% | 84% |
A0A3S7WZ57 | Leishmania donovani | 90% | 81% |
A1CUC3 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 27% | 89% |
A1DP06 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 26% | 89% |
A2QSG6 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 27% | 89% |
A3LRW3 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 24% | 90% |
A4HH30 | Leishmania braziliensis | 23% | 85% |
A4I1H8 | Leishmania infantum | 90% | 81% |
A4I475 | Leishmania infantum | 23% | 85% |
A4QUL1 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 27% | 85% |
A5DPC0 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 25% | 89% |
A5DSK2 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 25% | 85% |
A6QNT8 | Bos taurus | 26% | 74% |
C9ZJZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 84% |
C9ZKQ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 91% |
E9ADM4 | Leishmania major | 23% | 100% |
E9AM57 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 84% |
E9AXL3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 80% |
O94855 | Homo sapiens | 26% | 79% |
O95486 | Homo sapiens | 26% | 75% |
P0CR40 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 25% | 89% |
P0CR41 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 25% | 89% |
P38810 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 88% |
P40482 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 88% |
P53953 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 93% |
P53992 | Homo sapiens | 27% | 75% |
Q0CSL7 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 26% | 90% |
Q0PVD8 | Komagataella pastoris | 24% | 85% |
Q1E6U9 | Coccidioides immitis (strain RS) | 28% | 88% |
Q2HH63 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 27% | 86% |
Q2ULI0 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 27% | 90% |
Q3U2P1 | Mus musculus | 27% | 75% |
Q4P9K4 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 82% |
Q4Q9V9 | Leishmania major | 89% | 100% |
Q4WLP1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 89% |
Q54U61 | Dictyostelium discoideum | 27% | 81% |
Q5AQ76 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 26% | 88% |
Q5B6W0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 90% |
Q6BT80 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 24% | 89% |
Q6C2T4 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 25% | 88% |
Q6CLE0 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 89% |
Q6FWD3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 90% |
Q6FX11 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 91% |
Q75B16 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 92% |
Q7S4P3 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 86% |
Q86ZK8 | Podospora anserina | 27% | 86% |
Q875Q0 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 25% | 92% |
Q875V7 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 25% | 90% |
Q875V8 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 24% | 90% |
Q876F4 | Saccharomyces uvarum (strain ATCC 76518 / CBS 7001 / CLIB 283 / NBRC 10550 / MCYC 623 / NCYC 2669 / NRRL Y-11845) | 23% | 92% |
Q876F5 | Saccharomyces uvarum (strain ATCC 76518 / CBS 7001 / CLIB 283 / NBRC 10550 / MCYC 623 / NCYC 2669 / NRRL Y-11845) | 25% | 88% |
Q9M081 | Arabidopsis thaliana | 27% | 76% |
Q9M291 | Arabidopsis thaliana | 27% | 75% |
Q9SFU0 | Arabidopsis thaliana | 27% | 79% |
Q9USS7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 92% |
Q9UUI5 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 88% |
V5D902 | Trypanosoma cruzi | 54% | 80% |
V5DLD4 | Trypanosoma cruzi | 25% | 90% |