A large and apprently artificial collection of diverse kinetoplastid protein kinases. None of them appear to be TM.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 3 |
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 |
Related structures:
AlphaFold database: Q4Q416
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.337 |
CLV_C14_Caspase3-7 | 365 | 369 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 445 | 449 | PF00656 | 0.513 |
CLV_C14_Caspase3-7 | 468 | 472 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.594 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.303 |
CLV_PCSK_FUR_1 | 512 | 516 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.345 |
CLV_Separin_Metazoa | 623 | 627 | PF03568 | 0.506 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.303 |
DEG_ODPH_VHL_1 | 111 | 124 | PF01847 | 0.350 |
DEG_SCF_FBW7_1 | 322 | 328 | PF00400 | 0.694 |
DOC_CKS1_1 | 306 | 311 | PF01111 | 0.667 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.642 |
DOC_CYCLIN_RxL_1 | 457 | 469 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 542 | 554 | PF00134 | 0.511 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 103 | 111 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 154 | 163 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 457 | 465 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 54 | 60 | PF00069 | 0.309 |
DOC_MAPK_gen_1 | 578 | 585 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 85 | 95 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 459 | 467 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 505 | 513 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 54 | 62 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 578 | 587 | PF00069 | 0.387 |
DOC_PP1_RVXF_1 | 603 | 610 | PF00149 | 0.476 |
DOC_PP2B_LxvP_1 | 271 | 274 | PF13499 | 0.372 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.421 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.490 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.763 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.423 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.307 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 279 | 289 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 398 | 406 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 529 | 533 | PF00244 | 0.512 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.774 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.664 |
LIG_BRCT_BRCA1_1 | 487 | 491 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 556 | 560 | PF00533 | 0.391 |
LIG_deltaCOP1_diTrp_1 | 218 | 227 | PF00928 | 0.303 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.337 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.372 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.447 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.399 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.423 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.360 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.365 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.402 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.727 |
LIG_LIR_Apic_2 | 198 | 204 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 102 | 113 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 116 | 124 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 433 | 444 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.366 |
LIG_PALB2_WD40_1 | 608 | 616 | PF16756 | 0.408 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.303 |
LIG_Pex14_2 | 404 | 408 | PF04695 | 0.435 |
LIG_Pex14_2 | 609 | 613 | PF04695 | 0.388 |
LIG_PTB_Apo_2 | 312 | 319 | PF02174 | 0.698 |
LIG_Rb_LxCxE_1 | 622 | 640 | PF01857 | 0.571 |
LIG_REV1ctd_RIR_1 | 501 | 507 | PF16727 | 0.550 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.303 |
LIG_SH2_CRK | 594 | 598 | PF00017 | 0.394 |
LIG_SH2_NCK_1 | 536 | 540 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 594 | 598 | PF00017 | 0.429 |
LIG_SH2_STAT3 | 135 | 138 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.303 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.464 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.600 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.677 |
LIG_TRAF2_1 | 380 | 383 | PF00917 | 0.337 |
LIG_TRAF2_1 | 400 | 403 | PF00917 | 0.360 |
LIG_TRAF2_1 | 551 | 554 | PF00917 | 0.552 |
LIG_TRAF2_1 | 559 | 562 | PF00917 | 0.528 |
LIG_TRAF2_2 | 261 | 266 | PF00917 | 0.450 |
LIG_UBA3_1 | 117 | 125 | PF00899 | 0.411 |
LIG_UBA3_1 | 83 | 88 | PF00899 | 0.366 |
LIG_UBA3_1 | 95 | 103 | PF00899 | 0.384 |
MOD_CDK_SPK_2 | 20 | 25 | PF00069 | 0.596 |
MOD_CDK_SPK_2 | 5 | 10 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 20 | 26 | PF00069 | 0.464 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.318 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.688 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.592 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.440 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.450 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.185 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.568 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.498 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.330 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.318 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.725 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.535 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.401 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.353 |
MOD_DYRK1A_RPxSP_1 | 321 | 325 | PF00069 | 0.641 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.394 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.659 |
MOD_GlcNHglycan | 450 | 454 | PF01048 | 0.388 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.372 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.423 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.293 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.312 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.384 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.550 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.617 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.648 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.211 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.337 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.383 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.478 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.410 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.423 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.354 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.377 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.317 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.558 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.571 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.441 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.412 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.423 |
MOD_OFUCOSY | 217 | 222 | PF10250 | 0.303 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.529 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.303 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.360 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.318 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.558 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.413 |
MOD_PKB_1 | 245 | 253 | PF00069 | 0.406 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.563 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.463 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.326 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.587 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.596 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.678 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.671 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.673 |
MOD_SUMO_for_1 | 156 | 159 | PF00179 | 0.303 |
MOD_SUMO_for_1 | 620 | 623 | PF00179 | 0.518 |
MOD_SUMO_for_1 | 633 | 636 | PF00179 | 0.608 |
MOD_SUMO_rev_2 | 119 | 127 | PF00179 | 0.355 |
MOD_SUMO_rev_2 | 381 | 387 | PF00179 | 0.433 |
MOD_SUMO_rev_2 | 477 | 486 | PF00179 | 0.341 |
TRG_DiLeu_BaEn_1 | 442 | 447 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_2 | 382 | 388 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 91 | 96 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 511 | 514 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 616 | 618 | PF00400 | 0.521 |
TRG_NES_CRM1_1 | 435 | 450 | PF08389 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 154 | 159 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 617 | 622 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMD1 | Leptomonas seymouri | 81% | 100% |
A0A0S4IPB3 | Bodo saltans | 30% | 95% |
A0A0S4JIY0 | Bodo saltans | 52% | 99% |
A0A1X0NJJ7 | Trypanosomatidae | 29% | 85% |
A0A1X0P150 | Trypanosomatidae | 56% | 100% |
A0A2I0BVG8 | Plasmodium falciparum (isolate NF54) | 27% | 100% |
A0A3Q8IIY5 | Leishmania donovani | 24% | 100% |
A0A3Q8IU22 | Leishmania donovani | 98% | 100% |
A0A3S5H5G0 | Leishmania donovani | 25% | 100% |
A0A3S5H5U5 | Leishmania donovani | 26% | 100% |
A0A3S5IQS7 | Trypanosoma rangeli | 30% | 87% |
A0A422N215 | Trypanosoma rangeli | 54% | 100% |
A0A509AHB6 | Plasmodium berghei (strain Anka) | 28% | 100% |
A0A509AQE6 | Plasmodium berghei (strain Anka) | 28% | 100% |
A0A5K1K8H0 | Plasmodium falciparum (isolate 3D7) | 27% | 100% |
A0AAR7 | Lotus japonicus | 26% | 100% |
A2ZVI7 | Oryza sativa subsp. japonica | 30% | 100% |
A4H459 | Leishmania braziliensis | 25% | 100% |
A4H4S9 | Leishmania braziliensis | 26% | 100% |
A4HCD7 | Leishmania braziliensis | 29% | 100% |
A4HFF3 | Leishmania braziliensis | 27% | 100% |
A4HLN2 | Leishmania braziliensis | 91% | 99% |
A4HSE2 | Leishmania infantum | 25% | 100% |
A4I967 | Leishmania infantum | 98% | 100% |
A5A7I7 | Solanum tuberosum | 28% | 100% |
A5A7I8 | Solanum tuberosum | 28% | 100% |
B9FKW9 | Oryza sativa subsp. japonica | 30% | 100% |
C9ZIW2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
D0A2A6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 86% |
E9AE77 | Leishmania major | 24% | 100% |
E9AG71 | Leishmania infantum | 26% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B408 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O49717 | Arabidopsis thaliana | 30% | 100% |
O80673 | Arabidopsis thaliana | 28% | 100% |
P28582 | Daucus carota | 29% | 100% |
P28583 | Glycine max | 29% | 100% |
P49101 | Zea mays | 30% | 100% |
P53681 | Daucus carota | 28% | 100% |
P53683 | Oryza sativa subsp. japonica | 30% | 100% |
P53684 | Oryza sativa subsp. japonica | 28% | 100% |
P62343 | Plasmodium falciparum (isolate K1 / Thailand) | 27% | 100% |
P62344 | Plasmodium falciparum (isolate 3D7) | 27% | 100% |
P93759 | Arabidopsis thaliana | 31% | 100% |
Q06850 | Arabidopsis thaliana | 28% | 100% |
Q0D715 | Oryza sativa subsp. japonica | 29% | 100% |
Q0DYK7 | Oryza sativa subsp. japonica | 29% | 100% |
Q10KY3 | Oryza sativa subsp. japonica | 29% | 100% |
Q1PE17 | Arabidopsis thaliana | 31% | 100% |
Q1PFH8 | Arabidopsis thaliana | 29% | 100% |
Q2QQR2 | Oryza sativa subsp. japonica | 28% | 100% |
Q2QVG8 | Oryza sativa subsp. japonica | 31% | 100% |
Q2QX45 | Oryza sativa subsp. japonica | 28% | 100% |
Q2QY37 | Oryza sativa subsp. japonica | 31% | 100% |
Q2RAV0 | Oryza sativa subsp. japonica | 31% | 100% |
Q38868 | Arabidopsis thaliana | 31% | 100% |
Q38869 | Arabidopsis thaliana | 29% | 100% |
Q38870 | Arabidopsis thaliana | 28% | 99% |
Q38871 | Arabidopsis thaliana | 28% | 100% |
Q38872 | Arabidopsis thaliana | 28% | 100% |
Q38873 | Arabidopsis thaliana | 29% | 100% |
Q39016 | Arabidopsis thaliana | 28% | 100% |
Q3E9C0 | Arabidopsis thaliana | 31% | 100% |
Q42396 | Arabidopsis thaliana | 28% | 100% |
Q42438 | Arabidopsis thaliana | 29% | 100% |
Q42479 | Arabidopsis thaliana | 32% | 100% |
Q4QIV8 | Leishmania major | 26% | 100% |
Q4QJJ0 | Leishmania major | 25% | 100% |
Q53P85 | Oryza sativa subsp. japonica | 29% | 100% |
Q5VQQ5 | Oryza sativa subsp. japonica | 30% | 100% |
Q69IM9 | Oryza sativa subsp. japonica | 30% | 100% |
Q6AVI8 | Oryza sativa subsp. japonica | 29% | 100% |
Q6F3A6 | Oryza sativa subsp. japonica | 30% | 100% |
Q6I587 | Oryza sativa subsp. japonica | 29% | 100% |
Q6I5I8 | Oryza sativa subsp. japonica | 29% | 100% |
Q6K968 | Oryza sativa subsp. japonica | 29% | 100% |
Q6NLQ6 | Arabidopsis thaliana | 30% | 100% |
Q6Z2M9 | Oryza sativa subsp. japonica | 30% | 100% |
Q6ZIU9 | Oryza sativa subsp. japonica | 30% | 100% |
Q75GE8 | Oryza sativa subsp. japonica | 30% | 100% |
Q7RAH3 | Plasmodium yoelii yoelii | 28% | 100% |
Q7XIM0 | Oryza sativa subsp. japonica | 28% | 100% |
Q7XJR9 | Arabidopsis thaliana | 30% | 100% |
Q7XSQ5 | Oryza sativa subsp. japonica | 30% | 100% |
Q84SL0 | Oryza sativa subsp. japonica | 29% | 100% |
Q852N6 | Oryza sativa subsp. japonica | 28% | 100% |
Q8IBS5 | Plasmodium falciparum (isolate 3D7) | 27% | 100% |
Q8LPZ7 | Oryza sativa subsp. japonica | 30% | 100% |
Q8RWL2 | Arabidopsis thaliana | 31% | 100% |
Q8W4I7 | Arabidopsis thaliana | 29% | 100% |
Q9C6P3 | Arabidopsis thaliana | 30% | 100% |
Q9FKW4 | Arabidopsis thaliana | 29% | 100% |
Q9FMP5 | Arabidopsis thaliana | 30% | 100% |
Q9FX86 | Arabidopsis thaliana | 28% | 100% |
Q9FXQ3 | Oryza sativa subsp. japonica | 30% | 100% |
Q9LET1 | Arabidopsis thaliana | 27% | 100% |
Q9M101 | Arabidopsis thaliana | 28% | 100% |
Q9S9V0 | Arabidopsis thaliana | 28% | 100% |
Q9SIQ7 | Arabidopsis thaliana | 31% | 100% |
Q9SSF8 | Arabidopsis thaliana | 30% | 100% |
Q9SZM3 | Arabidopsis thaliana | 28% | 100% |
Q9ZSA2 | Arabidopsis thaliana | 30% | 100% |
Q9ZSA3 | Arabidopsis thaliana | 30% | 100% |
Q9ZSA4 | Arabidopsis thaliana | 28% | 100% |
Q9ZV15 | Arabidopsis thaliana | 27% | 100% |
V5BCN4 | Trypanosoma cruzi | 60% | 100% |
V5BN97 | Trypanosoma cruzi | 30% | 87% |