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:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q888
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006265 | DNA topological change | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0071103 | DNA conformation change | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003916 | DNA topoisomerase activity | 3 | 12 |
GO:0003917 | DNA topoisomerase type I (single strand cut, ATP-independent) activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 737 | 741 | PF00656 | 0.421 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 835 | 837 | PF00675 | 0.541 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 835 | 837 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 800 | 804 | PF00082 | 0.530 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.400 |
DEG_APCC_DBOX_1 | 565 | 573 | PF00400 | 0.352 |
DEG_SCF_FBW7_1 | 379 | 386 | PF00400 | 0.400 |
DEG_SPOP_SBC_1 | 52 | 56 | PF00917 | 0.431 |
DOC_ANK_TNKS_1 | 302 | 309 | PF00023 | 0.292 |
DOC_CKS1_1 | 380 | 385 | PF01111 | 0.259 |
DOC_MAPK_gen_1 | 269 | 279 | PF00069 | 0.262 |
DOC_MAPK_gen_1 | 29 | 36 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 416 | 426 | PF00069 | 0.259 |
DOC_MAPK_gen_1 | 524 | 533 | PF00069 | 0.352 |
DOC_MAPK_gen_1 | 585 | 593 | PF00069 | 0.397 |
DOC_MAPK_HePTP_8 | 169 | 181 | PF00069 | 0.274 |
DOC_MAPK_JIP1_4 | 527 | 533 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 172 | 181 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 272 | 281 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 419 | 426 | PF00069 | 0.285 |
DOC_MAPK_MEF2A_6 | 527 | 535 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 540 | 548 | PF00069 | 0.200 |
DOC_MAPK_MEF2A_6 | 763 | 770 | PF00069 | 0.430 |
DOC_MAPK_NFAT4_5 | 172 | 180 | PF00069 | 0.259 |
DOC_MAPK_RevD_3 | 792 | 807 | PF00069 | 0.370 |
DOC_PP2B_LxvP_1 | 546 | 549 | PF13499 | 0.259 |
DOC_PP4_FxxP_1 | 641 | 644 | PF00568 | 0.383 |
DOC_PP4_FxxP_1 | 655 | 658 | PF00568 | 0.258 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.431 |
DOC_PP4_FxxP_1 | 815 | 818 | PF00568 | 0.349 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.218 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.365 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.413 |
LIG_14-3-3_CanoR_1 | 322 | 328 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 515 | 521 | PF00244 | 0.400 |
LIG_Actin_WH2_2 | 162 | 180 | PF00022 | 0.274 |
LIG_APCC_ABBAyCdc20_2 | 251 | 257 | PF00400 | 0.259 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_1 | 745 | 749 | PF00533 | 0.385 |
LIG_Clathr_ClatBox_1 | 244 | 248 | PF01394 | 0.295 |
LIG_deltaCOP1_diTrp_1 | 248 | 255 | PF00928 | 0.259 |
LIG_deltaCOP1_diTrp_1 | 395 | 400 | PF00928 | 0.344 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.439 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.268 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.521 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.259 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.400 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.285 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.443 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.323 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.330 |
LIG_FHA_1 | 730 | 736 | PF00498 | 0.344 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.484 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.399 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.469 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.272 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.431 |
LIG_FHA_2 | 778 | 784 | PF00498 | 0.432 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.431 |
LIG_GBD_Chelix_1 | 14 | 22 | PF00786 | 0.220 |
LIG_LIR_Apic_2 | 638 | 644 | PF02991 | 0.323 |
LIG_LIR_Apic_2 | 653 | 658 | PF02991 | 0.348 |
LIG_LIR_Apic_2 | 77 | 83 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 149 | 158 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 440 | 450 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 514 | 525 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 578 | 587 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 592 | 602 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 660 | 669 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 592 | 597 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 601 | 605 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 660 | 665 | PF02991 | 0.291 |
LIG_LYPXL_SIV_4 | 635 | 643 | PF13949 | 0.367 |
LIG_MYND_1 | 818 | 822 | PF01753 | 0.413 |
LIG_NRP_CendR_1 | 865 | 866 | PF00754 | 0.620 |
LIG_PCNA_yPIPBox_3 | 266 | 277 | PF02747 | 0.188 |
LIG_Pex14_2 | 139 | 143 | PF04695 | 0.487 |
LIG_Pex14_2 | 580 | 584 | PF04695 | 0.288 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.420 |
LIG_PTB_Apo_2 | 681 | 688 | PF02174 | 0.332 |
LIG_REV1ctd_RIR_1 | 578 | 587 | PF16727 | 0.304 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.276 |
LIG_SH2_CRK | 682 | 686 | PF00017 | 0.336 |
LIG_SH2_NCK_1 | 682 | 686 | PF00017 | 0.336 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 734 | 737 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.387 |
LIG_SH3_1 | 673 | 679 | PF00018 | 0.301 |
LIG_SH3_2 | 380 | 385 | PF14604 | 0.259 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.259 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.274 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.318 |
LIG_SH3_3 | 673 | 679 | PF00018 | 0.301 |
LIG_SUMO_SIM_anti_2 | 294 | 299 | PF11976 | 0.259 |
LIG_SUMO_SIM_par_1 | 4 | 10 | PF11976 | 0.271 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.369 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.440 |
LIG_TRAF2_1 | 780 | 783 | PF00917 | 0.375 |
LIG_UBA3_1 | 263 | 272 | PF00899 | 0.343 |
LIG_UBA3_1 | 430 | 436 | PF00899 | 0.460 |
LIG_UBA3_1 | 490 | 496 | PF00899 | 0.259 |
LIG_UBA3_1 | 535 | 540 | PF00899 | 0.293 |
LIG_WRC_WIRS_1 | 652 | 657 | PF05994 | 0.379 |
LIG_WW_1 | 481 | 484 | PF00397 | 0.293 |
MOD_CDK_SPxK_1 | 379 | 385 | PF00069 | 0.259 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.259 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.460 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.542 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.308 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.502 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.325 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.394 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.386 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.360 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.443 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.337 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.420 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.471 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.400 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.318 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.259 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.449 |
MOD_CK2_1 | 777 | 783 | PF00069 | 0.365 |
MOD_DYRK1A_RPxSP_1 | 385 | 389 | PF00069 | 0.400 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.220 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.298 |
MOD_GlcNHglycan | 391 | 395 | PF01048 | 0.249 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.331 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.350 |
MOD_GlcNHglycan | 88 | 92 | PF01048 | 0.246 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.426 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.268 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.263 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.285 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.270 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.400 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.448 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.323 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.461 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.551 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.376 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.386 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.282 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.474 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.501 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.272 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.309 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.344 |
MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.292 |
MOD_N-GLC_2 | 119 | 121 | PF02516 | 0.220 |
MOD_N-GLC_2 | 762 | 764 | PF02516 | 0.353 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.503 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.308 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.379 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.410 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.262 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.297 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.323 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.428 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.274 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.329 |
MOD_OFUCOSY | 721 | 726 | PF10250 | 0.347 |
MOD_OFUCOSY | 736 | 743 | PF10250 | 0.348 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.259 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.529 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.400 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.521 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.259 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.274 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.400 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.293 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.259 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.259 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.259 |
MOD_Plk_1 | 637 | 643 | PF00069 | 0.329 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.474 |
MOD_Plk_2-3 | 10 | 16 | PF00069 | 0.420 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.431 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.481 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.302 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.266 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.279 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.257 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.400 |
MOD_Plk_4 | 798 | 804 | PF00069 | 0.524 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.259 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.259 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.259 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.515 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.410 |
MOD_SUMO_for_1 | 226 | 229 | PF00179 | 0.259 |
MOD_SUMO_rev_2 | 174 | 179 | PF00179 | 0.264 |
MOD_SUMO_rev_2 | 793 | 802 | PF00179 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.274 |
TRG_DiLeu_BaLyEn_6 | 413 | 418 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.259 |
TRG_ER_diArg_1 | 286 | 289 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 551 | 554 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 827 | 830 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 834 | 836 | PF00400 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 261 | 265 | PF00026 | 0.261 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0L0P6P7 | Candida auris | 34% | 100% |
A0A0N1I0P1 | Leptomonas seymouri | 87% | 100% |
A0A0N1PAL1 | Leptomonas seymouri | 31% | 90% |
A0A0S4J933 | Bodo saltans | 68% | 99% |
A0A0S4JI21 | Bodo saltans | 31% | 89% |
A0A1X0NSK9 | Trypanosomatidae | 74% | 100% |
A0A1X0P3I0 | Trypanosomatidae | 32% | 93% |
A0A3R7KDV1 | Trypanosoma rangeli | 33% | 94% |
A0A3S7WW83 | Leishmania donovani | 23% | 100% |
A0A3S7X1K1 | Leishmania donovani | 98% | 100% |
A0A3S7XB89 | Leishmania donovani | 32% | 91% |
A0A422NYW0 | Trypanosoma rangeli | 72% | 100% |
A0R5D9 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 26% | 93% |
A4HGN1 | Leishmania braziliensis | 92% | 100% |
A4HPI6 | Leishmania braziliensis | 32% | 91% |
A4HZ99 | Leishmania infantum | 23% | 100% |
A4I3Q5 | Leishmania infantum | 98% | 100% |
A4IDA8 | Leishmania infantum | 32% | 91% |
C7J0A2 | Oryza sativa subsp. japonica | 35% | 93% |
D0A8A5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 100% |
D0A8E9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 94% |
E9AT98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 91% |
E9AUX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AZZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
F4ISQ7 | Arabidopsis thaliana | 48% | 100% |
O27661 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 27% | 100% |
O28469 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 28% | 100% |
O34204 | Fervidobacterium islandicum | 23% | 100% |
O51934 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 22% | 78% |
O58356 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 25% | 100% |
O60126 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
O61660 | Caenorhabditis elegans | 36% | 100% |
O67037 | Aquifex aeolicus (strain VF5) | 24% | 76% |
O69548 | Mycobacterium leprae (strain TN) | 26% | 91% |
O70157 | Mus musculus | 36% | 86% |
O95985 | Homo sapiens | 48% | 100% |
O96651 | Drosophila melanogaster | 45% | 99% |
P0A621 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 25% | 93% |
P0C2W6 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 24% | 100% |
P13099 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P14294 | Escherichia coli (strain K12) | 24% | 100% |
P34185 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 24% | 98% |
P40687 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 23% | 100% |
P43704 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 24% | 100% |
P46799 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 23% | 100% |
P47368 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 22% | 100% |
P78032 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 24% | 100% |
P9WG48 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 25% | 93% |
P9WG49 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 25% | 93% |
Q08582 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 22% | 69% |
Q0J0S6 | Oryza sativa subsp. japonica | 47% | 100% |
Q13472 | Homo sapiens | 35% | 87% |
Q2FEN5 | Staphylococcus aureus (strain USA300) | 24% | 100% |
Q2FW03 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 24% | 100% |
Q49ZH2 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 22% | 100% |
Q4L8B8 | Staphylococcus haemolyticus (strain JCSC1435) | 23% | 100% |
Q4Q199 | Leishmania major | 33% | 100% |
Q4QCK3 | Leishmania major | 23% | 100% |
Q59046 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 25% | 100% |
Q5HDV4 | Staphylococcus aureus (strain COL) | 24% | 100% |
Q5HLZ4 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 22% | 100% |
Q5HPU2 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 25% | 100% |
Q5WAX6 | Alkalihalobacillus clausii (strain KSM-K16) | 23% | 100% |
Q6G767 | Staphylococcus aureus (strain MSSA476) | 24% | 100% |
Q6GEH9 | Staphylococcus aureus (strain MRSA252) | 23% | 100% |
Q7A075 | Staphylococcus aureus (strain MW2) | 24% | 100% |
Q7A455 | Staphylococcus aureus (strain N315) | 24% | 100% |
Q8CRF7 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 22% | 100% |
Q8CSU3 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 25% | 100% |
Q8T2T7 | Dictyostelium discoideum | 36% | 100% |
Q8Z6F5 | Salmonella typhi | 23% | 100% |
Q8ZXT5 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 23% | 71% |
Q99S17 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 24% | 100% |
Q9CP53 | Pasteurella multocida (strain Pm70) | 23% | 100% |
Q9HM08 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 29% | 100% |
Q9KA23 | Halalkalibacterium halodurans (strain ATCC BAA-125 / DSM 18197 / FERM 7344 / JCM 9153 / C-125) | 24% | 100% |
Q9KQF5 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 22% | 100% |
Q9LVP1 | Arabidopsis thaliana | 36% | 94% |
Q9NG98 | Drosophila melanogaster | 36% | 69% |
Q9PHK2 | Xylella fastidiosa (strain 9a5c) | 23% | 100% |
Q9UYS8 | Pyrococcus abyssi (strain GE5 / Orsay) | 26% | 100% |
Q9UZ86 | Pyrococcus abyssi (strain GE5 / Orsay) | 22% | 71% |
Q9YB01 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 26% | 100% |
Q9Z321 | Mus musculus | 48% | 100% |
V5AV88 | Trypanosoma cruzi | 73% | 100% |