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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4H349
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0051213 | dioxygenase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0015616 | DNA translocase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 586 | 590 | PF00656 | 0.374 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.217 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.258 |
CLV_PCSK_FUR_1 | 391 | 395 | PF00082 | 0.216 |
CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.186 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.224 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.162 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.166 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.488 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 540 | 548 | PF00400 | 0.388 |
DEG_APCC_DBOX_1 | 574 | 582 | PF00400 | 0.383 |
DEG_SCF_FBW7_1 | 610 | 617 | PF00400 | 0.514 |
DOC_CYCLIN_RxL_1 | 382 | 392 | PF00134 | 0.436 |
DOC_MAPK_DCC_7 | 101 | 111 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 247 | 255 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 383 | 389 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 391 | 401 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 103 | 111 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 247 | 255 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 36 | 44 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 368 | 377 | PF00069 | 0.287 |
DOC_MAPK_RevD_3 | 369 | 384 | PF00069 | 0.222 |
DOC_PP1_RVXF_1 | 383 | 390 | PF00149 | 0.423 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.506 |
DOC_PP2B_LxvP_1 | 718 | 721 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 721 | 725 | PF00917 | 0.675 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 711 | 716 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 213 | 223 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 228 | 233 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 256 | 264 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 378 | 387 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 489 | 496 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 569 | 578 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 723 | 728 | PF00244 | 0.574 |
LIG_BIR_III_4 | 650 | 654 | PF00653 | 0.508 |
LIG_BRCT_BRCA1_1 | 712 | 716 | PF00533 | 0.503 |
LIG_deltaCOP1_diTrp_1 | 172 | 180 | PF00928 | 0.423 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.445 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.506 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.506 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.423 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.438 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.423 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.612 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.474 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.474 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.496 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.295 |
LIG_IBAR_NPY_1 | 351 | 353 | PF08397 | 0.452 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 283 | 291 | PF02991 | 0.358 |
LIG_LIR_LC3C_4 | 55 | 60 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 534 | 539 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.455 |
LIG_MYND_2 | 61 | 65 | PF01753 | 0.366 |
LIG_NRBOX | 324 | 330 | PF00104 | 0.366 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.432 |
LIG_PCNA_PIPBox_1 | 174 | 183 | PF02747 | 0.506 |
LIG_PCNA_yPIPBox_3 | 478 | 491 | PF02747 | 0.415 |
LIG_Pex14_1 | 68 | 72 | PF04695 | 0.474 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.453 |
LIG_PTB_Apo_2 | 500 | 507 | PF02174 | 0.356 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.451 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.408 |
LIG_SH2_PTP2 | 131 | 134 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 48 | 51 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 501 | 504 | PF00017 | 0.348 |
LIG_SH2_STAT3 | 6 | 9 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.439 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.715 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.506 |
LIG_SUMO_SIM_anti_2 | 455 | 461 | PF11976 | 0.424 |
LIG_SUMO_SIM_anti_2 | 55 | 61 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 560 | 566 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 184 | 189 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 318 | 326 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 455 | 461 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 716 | 722 | PF11976 | 0.488 |
LIG_TRAF2_1 | 495 | 498 | PF00917 | 0.292 |
LIG_TYR_ITIM | 129 | 134 | PF00017 | 0.375 |
LIG_WRC_WIRS_1 | 398 | 403 | PF05994 | 0.331 |
MOD_CDK_SPxxK_3 | 414 | 421 | PF00069 | 0.331 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.406 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.218 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.179 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.531 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.628 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.249 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.503 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.331 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.218 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.328 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.292 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.570 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.461 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.214 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.288 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.331 |
MOD_GlcNHglycan | 207 | 211 | PF01048 | 0.222 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.383 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.346 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.329 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.288 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.263 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.252 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.647 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.670 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.685 |
MOD_GlcNHglycan | 722 | 726 | PF01048 | 0.652 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.263 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.232 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.186 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.343 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.321 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.274 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.422 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.649 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.596 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.622 |
MOD_N-GLC_1 | 608 | 613 | PF02516 | 0.510 |
MOD_N-GLC_2 | 590 | 592 | PF02516 | 0.388 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.276 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.364 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.329 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.289 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.259 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.267 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.331 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.283 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.319 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.386 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.259 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.646 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.179 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.331 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.259 |
MOD_PIKK_1 | 569 | 575 | PF00454 | 0.322 |
MOD_PIKK_1 | 629 | 635 | PF00454 | 0.728 |
MOD_PIKK_1 | 689 | 695 | PF00454 | 0.528 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.623 |
MOD_PKA_1 | 383 | 389 | PF00069 | 0.179 |
MOD_PKA_1 | 94 | 100 | PF00069 | 0.179 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.375 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.301 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.449 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.179 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.509 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.615 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.331 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.143 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.259 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.259 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.295 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.428 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.278 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.304 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.323 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.249 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.565 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.259 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.259 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.448 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.665 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.629 |
MOD_ProDKin_1 | 711 | 717 | PF00069 | 0.666 |
TRG_DiLeu_BaEn_1 | 560 | 565 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 318 | 323 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 391 | 396 | PF01217 | 0.208 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.259 |
TRG_ER_diArg_1 | 644 | 647 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 659 | 662 | PF00400 | 0.498 |
TRG_NLS_MonoExtN_4 | 98 | 104 | PF00514 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5A7 | Leptomonas seymouri | 23% | 66% |
A0A0N0P8H3 | Leptomonas seymouri | 27% | 66% |
A0A0N1HYE0 | Leptomonas seymouri | 66% | 75% |
A0A0P0WGX7 | Oryza sativa subsp. japonica | 30% | 74% |
A0A0S4JCY2 | Bodo saltans | 23% | 100% |
A0A0S4JHP8 | Bodo saltans | 24% | 81% |
A0A1X0NIN9 | Trypanosomatidae | 25% | 70% |
A0A1X0NNS9 | Trypanosomatidae | 21% | 67% |
A0A1X0NY53 | Trypanosomatidae | 29% | 75% |
A0A1X0P3S9 | Trypanosomatidae | 50% | 100% |
A0A3Q8IGW7 | Leishmania donovani | 27% | 66% |
A0A3R7M571 | Trypanosoma rangeli | 24% | 100% |
A0A3R7MS90 | Trypanosoma rangeli | 50% | 100% |
A0A3R7MWL4 | Trypanosoma rangeli | 23% | 77% |
A0A422MV13 | Trypanosoma rangeli | 27% | 71% |
A0A422P4R6 | Trypanosoma rangeli | 29% | 79% |
A0A451EJ80 | Leishmania donovani | 79% | 79% |
A4HDB9 | Leishmania braziliensis | 22% | 67% |
A4HLN1 | Leishmania braziliensis | 27% | 66% |
A4HRE5 | Leishmania infantum | 79% | 94% |
A4I966 | Leishmania infantum | 27% | 66% |
A4PBL4 | Oryza sativa subsp. japonica | 29% | 75% |
A6ZL17 | Saccharomyces cerevisiae (strain YJM789) | 25% | 79% |
A7ZI07 | Escherichia coli O139:H28 (strain E24377A / ETEC) | 26% | 68% |
B0R061 | Danio rerio | 24% | 75% |
B3LN76 | Saccharomyces cerevisiae (strain RM11-1a) | 25% | 79% |
B3MMA5 | Drosophila ananassae | 27% | 92% |
B3NAN8 | Drosophila erecta | 26% | 93% |
B4GS98 | Drosophila persimilis | 27% | 93% |
B4JCS7 | Drosophila grimshawi | 26% | 93% |
B4KHL5 | Drosophila mojavensis | 27% | 93% |
B4M9A8 | Drosophila virilis | 26% | 93% |
B4MX21 | Drosophila willistoni | 27% | 93% |
B4NXB8 | Drosophila yakuba | 26% | 93% |
B5VE38 | Saccharomyces cerevisiae (strain AWRI1631) | 25% | 79% |
C7GQI8 | Saccharomyces cerevisiae (strain JAY291) | 25% | 79% |
C9ZKA7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 77% |
C9ZT80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 68% |
D0A725 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 76% |
D0A743 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
D0A772 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 68% |
D0A7Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 96% |
E7F1C4 | Danio rerio | 25% | 77% |
E9AC13 | Leishmania major | 79% | 100% |
E9AJB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 79% |
E9AWQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 67% |
E9B407 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 67% |
F1Q8K0 | Danio rerio | 25% | 99% |
F4I2H2 | Arabidopsis thaliana | 28% | 85% |
F4IV45 | Arabidopsis thaliana | 25% | 83% |
F4J9M5 | Arabidopsis thaliana | 29% | 66% |
F4JY24 | Arabidopsis thaliana | 27% | 68% |
F4K128 | Arabidopsis thaliana | 27% | 69% |
O10302 | Orgyia pseudotsugata multicapsid polyhedrosis virus | 27% | 100% |
O12944 | Gallus gallus | 26% | 100% |
O16102 | Drosophila melanogaster | 26% | 82% |
O42861 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 79% |
O60264 | Homo sapiens | 29% | 69% |
O76460 | Drosophila melanogaster | 26% | 93% |
P28370 | Homo sapiens | 27% | 69% |
P31244 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 93% |
P32863 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 81% |
P34739 | Drosophila melanogaster | 22% | 69% |
P38086 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 76% |
P40352 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 67% |
P41410 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 86% |
P41447 | Autographa californica nuclear polyhedrosis virus | 24% | 100% |
P41877 | Caenorhabditis elegans | 28% | 72% |
P43610 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 86% |
P47264 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 27% | 71% |
P70270 | Mus musculus | 26% | 98% |
P75093 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 26% | 71% |
P87114 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 77% |
P94593 | Bacillus subtilis (strain 168) | 26% | 79% |
Q04692 | Mus musculus | 26% | 72% |
Q09772 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 90% |
Q0PCS3 | Arabidopsis thaliana | 30% | 80% |
Q24368 | Drosophila melanogaster | 29% | 71% |
Q29KH2 | Drosophila pseudoobscura pseudoobscura | 27% | 93% |
Q3B7N1 | Bos taurus | 28% | 81% |
Q4Q417 | Leishmania major | 27% | 66% |
Q57X81 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 22% | 68% |
Q5A310 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 69% |
Q5FWR0 | Xenopus tropicalis | 25% | 73% |
Q60848 | Mus musculus | 27% | 89% |
Q6PFE3 | Mus musculus | 25% | 83% |
Q6PGB8 | Mus musculus | 28% | 70% |
Q7G8Y3 | Oryza sativa subsp. japonica | 28% | 66% |
Q7ZU90 | Danio rerio | 27% | 71% |
Q86WJ1 | Homo sapiens | 27% | 81% |
Q8RWY3 | Arabidopsis thaliana | 27% | 69% |
Q8W103 | Arabidopsis thaliana | 31% | 67% |
Q91ZW3 | Mus musculus | 29% | 70% |
Q92698 | Homo sapiens | 26% | 98% |
Q95216 | Oryctolagus cuniculus | 24% | 73% |
Q9CXF7 | Mus musculus | 28% | 81% |
Q9DG67 | Gallus gallus | 26% | 80% |
Q9NRZ9 | Homo sapiens | 26% | 87% |
Q9UR24 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 75% |
Q9VL72 | Drosophila melanogaster | 28% | 87% |
Q9XFH4 | Arabidopsis thaliana | 25% | 96% |
Q9Y620 | Homo sapiens | 26% | 80% |
V5B5G3 | Trypanosoma cruzi | 51% | 100% |
V5BVU6 | Trypanosoma cruzi | 28% | 85% |
V5DIY2 | Trypanosoma cruzi | 29% | 79% |
V5DSK3 | Trypanosoma cruzi | 22% | 82% |