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: A4HLN2
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:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
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:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.274 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.255 |
CLV_C14_Caspase3-7 | 449 | 453 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.305 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.241 |
CLV_PCSK_FUR_1 | 516 | 520 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.179 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.299 |
CLV_Separin_Metazoa | 627 | 631 | PF03568 | 0.344 |
CLV_Separin_Metazoa | 86 | 90 | PF03568 | 0.225 |
DEG_APCC_DBOX_1 | 370 | 378 | PF00400 | 0.240 |
DOC_CYCLIN_RxL_1 | 461 | 473 | PF00134 | 0.305 |
DOC_CYCLIN_RxL_1 | 546 | 558 | PF00134 | 0.468 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 107 | 115 | PF00134 | 0.334 |
DOC_MAPK_gen_1 | 158 | 167 | PF00069 | 0.240 |
DOC_MAPK_gen_1 | 461 | 469 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 57 | 64 | PF00069 | 0.240 |
DOC_MAPK_gen_1 | 582 | 589 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 89 | 99 | PF00069 | 0.240 |
DOC_MAPK_MEF2A_6 | 463 | 471 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 509 | 517 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 57 | 66 | PF00069 | 0.239 |
DOC_MAPK_MEF2A_6 | 582 | 591 | PF00069 | 0.379 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.212 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.470 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.596 |
DOC_USP7_UBL2_3 | 461 | 465 | PF12436 | 0.385 |
DOC_USP7_UBL2_3 | 65 | 69 | PF12436 | 0.246 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 283 | 293 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 402 | 410 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 533 | 537 | PF00244 | 0.463 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.596 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.245 |
LIG_BRCT_BRCA1_1 | 491 | 495 | PF00533 | 0.305 |
LIG_BRCT_BRCA1_1 | 560 | 564 | PF00533 | 0.320 |
LIG_deltaCOP1_diTrp_1 | 222 | 231 | PF00928 | 0.288 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.274 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.602 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.363 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.362 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.385 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.332 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.323 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.377 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 106 | 117 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 120 | 126 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 193 | 203 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 437 | 448 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 477 | 486 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 437 | 443 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.263 |
LIG_PALB2_WD40_1 | 612 | 620 | PF16756 | 0.342 |
LIG_Pex14_2 | 391 | 395 | PF04695 | 0.240 |
LIG_Pex14_2 | 408 | 412 | PF04695 | 0.334 |
LIG_Pex14_2 | 613 | 617 | PF04695 | 0.326 |
LIG_PTB_Apo_2 | 316 | 323 | PF02174 | 0.580 |
LIG_Rb_LxCxE_1 | 626 | 644 | PF01857 | 0.417 |
LIG_REV1ctd_RIR_1 | 505 | 511 | PF16727 | 0.511 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.240 |
LIG_SH2_CRK | 598 | 602 | PF00017 | 0.294 |
LIG_SH2_NCK_1 | 540 | 544 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 598 | 602 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 139 | 142 | PF00017 | 0.240 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.240 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.305 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.573 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.193 |
LIG_TRAF2_1 | 384 | 387 | PF00917 | 0.274 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.119 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.522 |
LIG_TRAF2_1 | 563 | 566 | PF00917 | 0.461 |
LIG_TRAF2_2 | 265 | 270 | PF00917 | 0.305 |
LIG_UBA3_1 | 87 | 92 | PF00899 | 0.322 |
LIG_UBA3_1 | 99 | 107 | PF00899 | 0.334 |
MOD_CDK_SPK_2 | 325 | 330 | PF00069 | 0.681 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.255 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.463 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.470 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.577 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.340 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.333 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.516 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.481 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.271 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.298 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.382 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.294 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.299 |
MOD_DYRK1A_RPxSP_1 | 325 | 329 | PF00069 | 0.583 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.343 |
MOD_GlcNHglycan | 454 | 458 | PF01048 | 0.334 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.385 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.301 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.278 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.308 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.620 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.170 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.323 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.367 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.400 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.382 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.385 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.343 |
MOD_N-GLC_2 | 378 | 380 | PF02516 | 0.269 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.322 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.244 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.163 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.414 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.535 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.194 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.358 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.385 |
MOD_OFUCOSY | 221 | 226 | PF10250 | 0.240 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.214 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.518 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.240 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.299 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.255 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.554 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.370 |
MOD_PKB_1 | 249 | 257 | PF00069 | 0.359 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.435 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.410 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.269 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.263 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.540 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.632 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.626 |
MOD_SUMO_for_1 | 160 | 163 | PF00179 | 0.240 |
MOD_SUMO_for_1 | 624 | 627 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 385 | 391 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 481 | 490 | PF00179 | 0.279 |
TRG_DiLeu_BaEn_2 | 386 | 392 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 587 | 592 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.334 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.262 |
TRG_ER_diArg_1 | 515 | 518 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 620 | 622 | PF00400 | 0.354 |
TRG_NES_CRM1_1 | 439 | 454 | PF08389 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 251 | 256 | PF00026 | 0.220 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.280 |
TRG_Pf-PMV_PEXEL_1 | 621 | 626 | PF00026 | 0.332 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMD1 | Leptomonas seymouri | 80% | 100% |
A0A0S4IPB3 | Bodo saltans | 30% | 95% |
A0A0S4JIY0 | Bodo saltans | 54% | 100% |
A0A1X0NJJ7 | Trypanosomatidae | 30% | 86% |
A0A1X0P150 | Trypanosomatidae | 57% | 100% |
A0A2I0BVG8 | Plasmodium falciparum (isolate NF54) | 28% | 100% |
A0A3Q8IU22 | Leishmania donovani | 92% | 100% |
A0A3S5H5G0 | Leishmania donovani | 25% | 100% |
A0A3S5H5U5 | Leishmania donovani | 25% | 100% |
A0A3S5IQS7 | Trypanosoma rangeli | 30% | 87% |
A0A422N215 | Trypanosoma rangeli | 54% | 100% |
A0A509AHB6 | Plasmodium berghei (strain Anka) | 28% | 100% |
A0A509AQE6 | Plasmodium berghei (strain Anka) | 29% | 100% |
A0A5K1K8H0 | Plasmodium falciparum (isolate 3D7) | 26% | 100% |
A0AAR7 | Lotus japonicus | 26% | 100% |
A2ZVI7 | Oryza sativa subsp. japonica | 30% | 100% |
A4H459 | Leishmania braziliensis | 25% | 100% |
A4H4S9 | Leishmania braziliensis | 25% | 100% |
A4HCD7 | Leishmania braziliensis | 29% | 100% |
A4HFF3 | Leishmania braziliensis | 27% | 100% |
A4HSE2 | Leishmania infantum | 25% | 100% |
A4I967 | Leishmania infantum | 92% | 100% |
A5A7I7 | Solanum tuberosum | 28% | 100% |
A5A7I8 | Solanum tuberosum | 28% | 100% |
B9FKW9 | Oryza sativa subsp. japonica | 31% | 100% |
C9ZIW2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
D0A2A6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 87% |
E9AET0 | Leishmania major | 25% | 100% |
E9AG71 | Leishmania infantum | 25% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B408 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O49717 | Arabidopsis thaliana | 30% | 100% |
P28582 | Daucus carota | 30% | 100% |
P28583 | Glycine max | 29% | 100% |
P49101 | Zea mays | 29% | 100% |
P53681 | Daucus carota | 29% | 100% |
P53683 | Oryza sativa subsp. japonica | 30% | 100% |
P53684 | Oryza sativa subsp. japonica | 28% | 100% |
P62343 | Plasmodium falciparum (isolate K1 / Thailand) | 28% | 100% |
P62344 | Plasmodium falciparum (isolate 3D7) | 28% | 100% |
P62345 | Plasmodium berghei (strain Anka) | 28% | 100% |
P93759 | Arabidopsis thaliana | 30% | 100% |
Q06850 | Arabidopsis thaliana | 28% | 100% |
Q0D715 | Oryza sativa subsp. japonica | 30% | 100% |
Q0DYK7 | Oryza sativa subsp. japonica | 29% | 100% |
Q1PE17 | Arabidopsis thaliana | 29% | 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 | 30% | 100% |
Q2RAV0 | Oryza sativa subsp. japonica | 30% | 100% |
Q38868 | Arabidopsis thaliana | 31% | 100% |
Q38869 | Arabidopsis thaliana | 29% | 100% |
Q38870 | Arabidopsis thaliana | 28% | 100% |
Q38871 | Arabidopsis thaliana | 29% | 100% |
Q38872 | Arabidopsis thaliana | 29% | 100% |
Q38873 | Arabidopsis thaliana | 30% | 100% |
Q39016 | Arabidopsis thaliana | 28% | 100% |
Q3E9C0 | Arabidopsis thaliana | 32% | 100% |
Q42396 | Arabidopsis thaliana | 28% | 100% |
Q42438 | Arabidopsis thaliana | 28% | 100% |
Q42479 | Arabidopsis thaliana | 31% | 100% |
Q43531 | Lilium longiflorum | 30% | 100% |
Q4Q416 | Leishmania major | 91% | 99% |
Q4QIV8 | Leishmania major | 25% | 100% |
Q4QJJ0 | Leishmania major | 25% | 100% |
Q53P85 | Oryza sativa subsp. japonica | 28% | 100% |
Q5VQQ5 | Oryza sativa subsp. japonica | 31% | 100% |
Q60806 | Mus musculus | 28% | 100% |
Q69IM9 | Oryza sativa subsp. japonica | 30% | 100% |
Q6AVI8 | Oryza sativa subsp. japonica | 29% | 100% |
Q6F3A6 | Oryza sativa subsp. japonica | 29% | 100% |
Q6I587 | Oryza sativa subsp. japonica | 30% | 100% |
Q6I5I8 | Oryza sativa subsp. japonica | 29% | 100% |
Q6K968 | Oryza sativa subsp. japonica | 29% | 100% |
Q6NLQ6 | Arabidopsis thaliana | 30% | 100% |
Q6RET6 | Pisum sativum | 26% | 100% |
Q6Z2M9 | Oryza sativa subsp. japonica | 30% | 100% |
Q75GE8 | Oryza sativa subsp. japonica | 29% | 100% |
Q7RAH3 | Plasmodium yoelii yoelii | 28% | 100% |
Q7RJG2 | Plasmodium yoelii yoelii | 28% | 100% |
Q7XIM0 | Oryza sativa subsp. japonica | 28% | 100% |
Q7XJR9 | Arabidopsis thaliana | 31% | 100% |
Q7XSQ5 | Oryza sativa subsp. japonica | 29% | 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 | 31% | 100% |
Q9FJ54 | Arabidopsis thaliana | 32% | 100% |
Q9FKW4 | Arabidopsis thaliana | 30% | 100% |
Q9FMP5 | Arabidopsis thaliana | 32% | 100% |
Q9FXQ3 | Oryza sativa subsp. japonica | 30% | 100% |
Q9LJL9 | Arabidopsis thaliana | 28% | 100% |
Q9M101 | Arabidopsis thaliana | 29% | 100% |
Q9S9V0 | Arabidopsis thaliana | 27% | 100% |
Q9SCS2 | Arabidopsis thaliana | 27% | 100% |
Q9SSF8 | Arabidopsis thaliana | 29% | 100% |
Q9SZM3 | Arabidopsis thaliana | 28% | 100% |
Q9XF67 | Arabidopsis thaliana | 27% | 100% |
Q9ZSA2 | Arabidopsis thaliana | 30% | 100% |
Q9ZSA3 | Arabidopsis thaliana | 29% | 100% |
Q9ZSA4 | Arabidopsis thaliana | 28% | 100% |
Q9ZV15 | Arabidopsis thaliana | 27% | 100% |
V5BCN4 | Trypanosoma cruzi | 60% | 100% |
V5BN97 | Trypanosoma cruzi | 30% | 87% |