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: 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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: E9ASL0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 4 |
GO:0006793 | phosphorus metabolic process | 3 | 4 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016310 | phosphorylation | 5 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0036211 | protein modification process | 4 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0043412 | macromolecule modification | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 4 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004672 | protein kinase activity | 3 | 4 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0005488 | binding | 1 | 4 |
GO:0005524 | ATP binding | 5 | 4 |
GO:0016301 | kinase activity | 4 | 4 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 4 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 4 |
GO:0032553 | ribonucleotide binding | 3 | 4 |
GO:0032555 | purine ribonucleotide binding | 4 | 4 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 4 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 4 |
GO:0036094 | small molecule binding | 2 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:0097367 | carbohydrate derivative binding | 2 | 4 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 40 | 46 | PF00089 | 0.597 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.314 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.335 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.454 |
DEG_Nend_Nbox_1 | 1 | 2 | PF02207 | 0.766 |
DOC_CKS1_1 | 402 | 407 | PF01111 | 0.627 |
DOC_CYCLIN_RxL_1 | 146 | 156 | PF00134 | 0.454 |
DOC_CYCLIN_RxL_1 | 302 | 311 | PF00134 | 0.530 |
DOC_MAPK_DCC_7 | 400 | 408 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 116 | 124 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 92 | 102 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 116 | 125 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 70 | 77 | PF00069 | 0.454 |
DOC_MAPK_NFAT4_5 | 118 | 126 | PF00069 | 0.366 |
DOC_SPAK_OSR1_1 | 345 | 349 | PF12202 | 0.639 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.760 |
DOC_USP7_MATH_2 | 350 | 356 | PF00917 | 0.640 |
DOC_USP7_UBL2_3 | 432 | 436 | PF12436 | 0.627 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.387 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.288 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.541 |
LIG_14-3-3_CanoR_1 | 164 | 174 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 289 | 293 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 322 | 328 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 368 | 377 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.759 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.413 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.674 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.454 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.314 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.454 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.624 |
LIG_LIR_Apic_2 | 209 | 215 | PF02991 | 0.280 |
LIG_LIR_Apic_2 | 261 | 267 | PF02991 | 0.318 |
LIG_LIR_Apic_2 | 399 | 405 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 311 | 318 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 391 | 401 | PF02991 | 0.659 |
LIG_LIR_Gen_1 | 57 | 65 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 421 | 426 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.354 |
LIG_MYND_1 | 299 | 303 | PF01753 | 0.454 |
LIG_PCNA_yPIPBox_3 | 275 | 289 | PF02747 | 0.454 |
LIG_PDZ_Class_2 | 481 | 486 | PF00595 | 0.722 |
LIG_PTB_Apo_2 | 442 | 449 | PF02174 | 0.757 |
LIG_Rb_pABgroove_1 | 106 | 114 | PF01858 | 0.366 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.314 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.314 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.366 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.414 |
LIG_SH2_CRK | 393 | 397 | PF00017 | 0.658 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.606 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.474 |
LIG_SH2_GRB2like | 31 | 34 | PF00017 | 0.705 |
LIG_SH2_GRB2like | 393 | 396 | PF00017 | 0.573 |
LIG_SH2_NCK_1 | 212 | 216 | PF00017 | 0.314 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.366 |
LIG_SH2_PTP2 | 426 | 429 | PF00017 | 0.663 |
LIG_SH2_SRC | 264 | 267 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.723 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.314 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.177 |
LIG_SUMO_SIM_anti_2 | 120 | 126 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 120 | 126 | PF11976 | 0.366 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.611 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.429 |
LIG_TRAF2_1 | 438 | 441 | PF00917 | 0.753 |
LIG_TRAF2_2 | 46 | 51 | PF00917 | 0.454 |
LIG_TYR_ITIM | 236 | 241 | PF00017 | 0.314 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.407 |
LIG_TYR_ITIM | 424 | 429 | PF00017 | 0.520 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.758 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.342 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.265 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.454 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.680 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.599 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.758 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.314 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.548 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.498 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.611 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.688 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.314 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.314 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.757 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.454 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.454 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.104 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.532 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.554 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.640 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.562 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.567 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.337 |
MOD_N-GLC_1 | 477 | 482 | PF02516 | 0.646 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.314 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.314 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.387 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.341 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.576 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.647 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.568 |
MOD_NEK2_2 | 182 | 187 | PF00069 | 0.404 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.451 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.672 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.741 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.454 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.314 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.314 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.761 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.586 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.645 |
MOD_Plk_2-3 | 288 | 294 | PF00069 | 0.314 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.619 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.652 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.567 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.607 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.288 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.366 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.636 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.540 |
MOD_SUMO_for_1 | 172 | 175 | PF00179 | 0.314 |
MOD_SUMO_for_1 | 93 | 96 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 394 | 401 | PF00179 | 0.576 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.654 |
TRG_NES_CRM1_1 | 337 | 352 | PF08389 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZY0 | Leptomonas seymouri | 28% | 81% |
A0A0N1I6Q7 | Leptomonas seymouri | 29% | 100% |
A0A0S4JNA1 | Bodo saltans | 26% | 98% |
A0A1X0NUQ4 | Trypanosomatidae | 29% | 100% |
A0A3Q8IAQ1 | Leishmania donovani | 29% | 100% |
A0A3Q8IB30 | Leishmania donovani | 28% | 100% |
A0A3Q8IB74 | Leishmania donovani | 26% | 100% |
A0A3Q8IC87 | Leishmania donovani | 34% | 100% |
A0A3Q8IHH8 | Leishmania donovani | 28% | 97% |
A0A3Q8II44 | Leishmania donovani | 28% | 100% |
A0A3Q8IJ66 | Leishmania donovani | 27% | 100% |
A0A3Q8INQ4 | Leishmania donovani | 33% | 100% |
A0A3R7KDE9 | Trypanosoma rangeli | 59% | 67% |
A0A3S5H5G0 | Leishmania donovani | 28% | 100% |
A0A3S5H5U5 | Leishmania donovani | 26% | 100% |
A0A3S7WRG1 | Leishmania donovani | 27% | 100% |
A0A3S7WTN9 | Leishmania donovani | 33% | 100% |
A0A3S7WWE7 | Leishmania donovani | 26% | 100% |
A0A3S7X2W9 | Leishmania donovani | 27% | 100% |
A0A3S7X7D5 | Leishmania donovani | 27% | 100% |
A0A3S7X7Y2 | Leishmania donovani | 28% | 100% |
A0A3S7X9R4 | Leishmania donovani | 30% | 100% |
A0A3S7X9S2 | Leishmania donovani | 30% | 100% |
A0A451EJH2 | Leishmania donovani | 26% | 100% |
A2ZVI7 | Oryza sativa subsp. japonica | 33% | 94% |
A4H3D2 | Leishmania braziliensis | 25% | 100% |
A4H436 | Leishmania braziliensis | 24% | 100% |
A4H459 | Leishmania braziliensis | 28% | 100% |
A4H4S9 | Leishmania braziliensis | 26% | 100% |
A4H8C4 | Leishmania braziliensis | 33% | 100% |
A4H9L8 | Leishmania braziliensis | 28% | 100% |
A4H9U7 | Leishmania braziliensis | 27% | 100% |
A4H9X5 | Leishmania braziliensis | 25% | 100% |
A4HAS1 | Leishmania braziliensis | 26% | 100% |
A4HBL4 | Leishmania braziliensis | 25% | 100% |
A4HCE6 | Leishmania braziliensis | 29% | 100% |
A4HED7 | Leishmania braziliensis | 32% | 100% |
A4HFI2 | Leishmania braziliensis | 27% | 100% |
A4HH03 | Leishmania braziliensis | 28% | 100% |
A4HHS9 | Leishmania braziliensis | 26% | 100% |
A4HMD1 | Leishmania braziliensis | 27% | 100% |
A4HN71 | Leishmania braziliensis | 29% | 100% |
A4HQG8 | Leishmania braziliensis | 27% | 100% |
A4HRN3 | Leishmania infantum | 26% | 100% |
A4HSE2 | Leishmania infantum | 28% | 100% |
A4HUS3 | Leishmania infantum | 27% | 100% |
A4HWP5 | Leishmania infantum | 33% | 100% |
A4HXY2 | Leishmania infantum | 28% | 100% |
A4HZA2 | Leishmania infantum | 26% | 100% |
A4HZV1 | Leishmania infantum | 34% | 100% |
A4HZW8 | Leishmania infantum | 29% | 100% |
A4I1T4 | Leishmania infantum | 33% | 100% |
A4I4X0 | Leishmania infantum | 28% | 97% |
A4I4Y0 | Leishmania infantum | 27% | 100% |
A4I9H1 | Leishmania infantum | 27% | 100% |
A4I9Y5 | Leishmania infantum | 28% | 100% |
A4IAZ8 | Leishmania infantum | 27% | 100% |
A4IBT4 | Leishmania infantum | 29% | 100% |
A4IBT9 | Leishmania infantum | 29% | 100% |
A4ICA4 | Leishmania infantum | 28% | 100% |
D0A2R8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 67% |
E8NHS0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ACB1 | Leishmania major | 25% | 100% |
E9AEB9 | Leishmania major | 28% | 97% |
E9AED4 | Leishmania major | 28% | 100% |
E9AFM1 | Leishmania major | 29% | 100% |
E9AG71 | Leishmania infantum | 26% | 100% |
E9AGS0 | Leishmania infantum | 25% | 100% |
E9AJJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ALU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 83% |
E9ANF7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AQF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9ARP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ARW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AUY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B4G9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B5Y1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B6S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B6S9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
O94168 | Candida tropicalis | 47% | 79% |
P06782 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 46% | 77% |
P28582 | Daucus carota | 29% | 91% |
P49101 | Zea mays | 31% | 95% |
P53682 | Oryza sativa subsp. japonica | 29% | 91% |
P53683 | Oryza sativa subsp. japonica | 29% | 91% |
P54645 | Rattus norvegicus | 46% | 87% |
Q00372 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 46% | 79% |
Q13131 | Homo sapiens | 46% | 87% |
Q27687 | Leishmania major | 28% | 100% |
Q2QQR2 | Oryza sativa subsp. japonica | 29% | 79% |
Q2QY37 | Oryza sativa subsp. japonica | 33% | 90% |
Q2RAV0 | Oryza sativa subsp. japonica | 33% | 90% |
Q38871 | Arabidopsis thaliana | 29% | 87% |
Q38872 | Arabidopsis thaliana | 30% | 89% |
Q42396 | Arabidopsis thaliana | 32% | 99% |
Q42438 | Arabidopsis thaliana | 32% | 91% |
Q42479 | Arabidopsis thaliana | 32% | 92% |
Q4Q0B0 | Leishmania major | 28% | 100% |
Q4Q2Z2 | Leishmania major | 28% | 100% |
Q4Q5T9 | Leishmania major | 26% | 100% |
Q4Q9K2 | Leishmania major | 33% | 100% |
Q4QBQ2 | Leishmania major | 28% | 100% |
Q4QBR6 | Leishmania major | 33% | 100% |
Q4QCK0 | Leishmania major | 25% | 100% |
Q4QCR3 | Leishmania major | 26% | 100% |
Q4QDK3 | Leishmania major | 25% | 100% |
Q4QF23 | Leishmania major | 33% | 100% |
Q4QH69 | Leishmania major | 26% | 100% |
Q4QIV8 | Leishmania major | 27% | 100% |
Q4QJJ0 | Leishmania major | 27% | 100% |
Q54YF2 | Dictyostelium discoideum | 43% | 67% |
Q5EG47 | Mus musculus | 46% | 87% |
Q5RDH5 | Pongo abelii | 46% | 88% |
Q6NLQ6 | Arabidopsis thaliana | 32% | 90% |
Q6ZI44 | Oryza sativa subsp. japonica | 38% | 100% |
Q75GE8 | Oryza sativa subsp. japonica | 35% | 90% |
Q7XJR9 | Arabidopsis thaliana | 31% | 85% |
Q965G5 | Caenorhabditis elegans | 30% | 100% |
Q9FIM9 | Arabidopsis thaliana | 33% | 82% |
Q9FX86 | Arabidopsis thaliana | 30% | 80% |
Q9GNR4 | Leishmania major | 29% | 100% |
Q9LJL9 | Arabidopsis thaliana | 32% | 81% |
Q9NHE1 | Leishmania major | 27% | 100% |
Q9SG12 | Arabidopsis thaliana | 33% | 82% |
Q9SJ61 | Arabidopsis thaliana | 29% | 93% |