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: 6 |
Forrest at al. (procyclic) | no | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 30 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 75 |
NetGPI | no | yes: 0, no: 75 |
Related structures:
AlphaFold database: A0A3S7XAT9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 76 |
GO:0006793 | phosphorus metabolic process | 3 | 76 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 76 |
GO:0006807 | nitrogen compound metabolic process | 2 | 76 |
GO:0008152 | metabolic process | 1 | 76 |
GO:0009987 | cellular process | 1 | 76 |
GO:0016310 | phosphorylation | 5 | 76 |
GO:0019538 | protein metabolic process | 3 | 76 |
GO:0036211 | protein modification process | 4 | 76 |
GO:0043170 | macromolecule metabolic process | 3 | 76 |
GO:0043412 | macromolecule modification | 4 | 76 |
GO:0044237 | cellular metabolic process | 2 | 76 |
GO:0044238 | primary metabolic process | 2 | 76 |
GO:0071704 | organic substance metabolic process | 2 | 76 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 76 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 76 |
GO:0003824 | catalytic activity | 1 | 76 |
GO:0004672 | protein kinase activity | 3 | 76 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 49 |
GO:0005488 | binding | 1 | 76 |
GO:0005524 | ATP binding | 5 | 76 |
GO:0016301 | kinase activity | 4 | 76 |
GO:0016740 | transferase activity | 2 | 76 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 76 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 76 |
GO:0017076 | purine nucleotide binding | 4 | 76 |
GO:0030554 | adenyl nucleotide binding | 5 | 76 |
GO:0032553 | ribonucleotide binding | 3 | 76 |
GO:0032555 | purine ribonucleotide binding | 4 | 76 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 76 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 76 |
GO:0036094 | small molecule binding | 2 | 76 |
GO:0043167 | ion binding | 2 | 76 |
GO:0043168 | anion binding | 3 | 76 |
GO:0097159 | organic cyclic compound binding | 2 | 76 |
GO:0097367 | carbohydrate derivative binding | 2 | 76 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 76 |
GO:1901265 | nucleoside phosphate binding | 3 | 76 |
GO:1901363 | heterocyclic compound binding | 2 | 76 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.409 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.374 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.182 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.234 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 394 | 396 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.231 |
CLV_Separin_Metazoa | 81 | 85 | PF03568 | 0.163 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.546 |
DOC_ANK_TNKS_1 | 27 | 34 | PF00023 | 0.684 |
DOC_CKS1_1 | 302 | 307 | PF01111 | 0.262 |
DOC_CKS1_1 | 437 | 442 | PF01111 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.293 |
DOC_MAPK_gen_1 | 174 | 183 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 339 | 347 | PF00069 | 0.554 |
DOC_MAPK_gen_1 | 394 | 400 | PF00069 | 0.265 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 361 | 368 | PF00069 | 0.634 |
DOC_MAPK_RevD_3 | 155 | 170 | PF00069 | 0.306 |
DOC_MAPK_RevD_3 | 236 | 250 | PF00069 | 0.300 |
DOC_PP1_RVXF_1 | 372 | 378 | PF00149 | 0.509 |
DOC_PP1_RVXF_1 | 469 | 476 | PF00149 | 0.276 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.246 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.275 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.276 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 361 | 365 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 488 | 494 | PF00244 | 0.327 |
LIG_APCC_ABBA_1 | 398 | 403 | PF00400 | 0.165 |
LIG_APCC_ABBAyCdc20_2 | 169 | 175 | PF00400 | 0.306 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.536 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.343 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.343 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 437 | 441 | PF00533 | 0.428 |
LIG_CaM_IQ_9 | 421 | 437 | PF13499 | 0.393 |
LIG_Clathr_ClatBox_1 | 418 | 422 | PF01394 | 0.165 |
LIG_deltaCOP1_diTrp_1 | 484 | 493 | PF00928 | 0.362 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.429 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.228 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.539 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.567 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.306 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.326 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.516 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.447 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.393 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.357 |
LIG_Integrin_isoDGR_2 | 469 | 471 | PF01839 | 0.165 |
LIG_IRF3_LxIS_1 | 305 | 312 | PF10401 | 0.221 |
LIG_LIR_Apic_2 | 215 | 221 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 438 | 449 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.280 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.250 |
LIG_PCNA_PIPBox_1 | 487 | 496 | PF02747 | 0.165 |
LIG_PCNA_yPIPBox_3 | 278 | 288 | PF02747 | 0.162 |
LIG_Pex14_1 | 393 | 397 | PF04695 | 0.274 |
LIG_Pex14_2 | 16 | 20 | PF04695 | 0.373 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.282 |
LIG_SH2_GRB2like | 127 | 130 | PF00017 | 0.337 |
LIG_SH2_NCK_1 | 127 | 131 | PF00017 | 0.324 |
LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.321 |
LIG_SH2_PTP2 | 310 | 313 | PF00017 | 0.220 |
LIG_SH2_PTP2 | 397 | 400 | PF00017 | 0.165 |
LIG_SH2_SRC | 127 | 130 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 200 | 204 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.166 |
LIG_SH2_STAT3 | 77 | 80 | PF00017 | 0.163 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.335 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.677 |
LIG_SUMO_SIM_anti_2 | 420 | 425 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.363 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.533 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.163 |
LIG_TYR_ITIM | 241 | 246 | PF00017 | 0.317 |
LIG_UBA3_1 | 241 | 249 | PF00899 | 0.290 |
LIG_WRC_WIRS_1 | 490 | 495 | PF05994 | 0.165 |
MOD_CDC14_SPxK_1 | 371 | 374 | PF00782 | 0.538 |
MOD_CDK_SPxK_1 | 368 | 374 | PF00069 | 0.548 |
MOD_CDK_SPxxK_3 | 301 | 308 | PF00069 | 0.165 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.176 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.519 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.362 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.291 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.259 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.433 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.282 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.523 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.407 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.312 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.445 |
MOD_Cter_Amidation | 469 | 472 | PF01082 | 0.300 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.326 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.304 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.457 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.284 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.392 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.304 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.399 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.501 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.342 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.365 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.304 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.353 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.173 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.286 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.283 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.308 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.332 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.531 |
MOD_OFUCOSY | 90 | 95 | PF10250 | 0.163 |
MOD_PKA_1 | 294 | 300 | PF00069 | 0.307 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.295 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.599 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.564 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.166 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.163 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.183 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.489 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.317 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.334 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.287 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.353 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.336 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.306 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.307 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.309 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.652 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.248 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.508 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.307 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.276 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.300 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.325 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 471 | 473 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.409 |
TRG_NLS_MonoExtN_4 | 292 | 297 | PF00514 | 0.194 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 472 | 476 | PF00026 | 0.259 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N5 | Leptomonas seymouri | 35% | 100% |
A0A0N0P953 | Leptomonas seymouri | 35% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 30% | 77% |
A0A0N1PD05 | Leptomonas seymouri | 33% | 100% |
A0A0N1PE80 | Leptomonas seymouri | 26% | 89% |
A0A0S4IMB7 | Bodo saltans | 38% | 100% |
A0A0S4IQ75 | Bodo saltans | 33% | 99% |
A0A0S4IRZ7 | Bodo saltans | 33% | 100% |
A0A0S4IVW1 | Bodo saltans | 24% | 80% |
A0A0S4IX86 | Bodo saltans | 33% | 100% |
A0A0S4J7K4 | Bodo saltans | 25% | 100% |
A0A0S4J804 | Bodo saltans | 38% | 96% |
A0A0S4JIJ6 | Bodo saltans | 28% | 89% |
A0A0S4JPZ1 | Bodo saltans | 32% | 100% |
A0A0S4JQN5 | Bodo saltans | 28% | 71% |
A0A1X0NFW4 | Trypanosomatidae | 27% | 100% |
A0A1X0NIA0 | Trypanosomatidae | 33% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 31% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 31% | 86% |
A0A1X0P527 | Trypanosomatidae | 33% | 100% |
A0A1X0P549 | Trypanosomatidae | 36% | 100% |
A0A1X0P863 | Trypanosomatidae | 57% | 100% |
A0A1X0P994 | Trypanosomatidae | 56% | 100% |
A0A3Q8IAQ1 | Leishmania donovani | 40% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 36% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 33% | 94% |
A0A3Q8IIG1 | Leishmania donovani | 30% | 100% |
A0A3Q8IJM9 | Leishmania donovani | 35% | 96% |
A0A3Q8INQ4 | Leishmania donovani | 30% | 100% |
A0A3R7KCZ4 | Trypanosoma rangeli | 34% | 100% |
A0A3R7MKG5 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X5M4 | Leishmania donovani | 31% | 100% |
A0A3S7X9R4 | Leishmania donovani | 28% | 100% |
A0A3S7X9S2 | Leishmania donovani | 28% | 100% |
A0A3S7XAL3 | Leishmania donovani | 85% | 100% |
A0A422NCP0 | Trypanosoma rangeli | 57% | 100% |
A0A422NH41 | Trypanosoma rangeli | 29% | 87% |
A0A422NIF0 | Trypanosoma rangeli | 25% | 70% |
A0A422NT89 | Trypanosoma rangeli | 24% | 76% |
A4HCE6 | Leishmania braziliensis | 39% | 100% |
A4HED7 | Leishmania braziliensis | 30% | 100% |
A4HJT5 | Leishmania braziliensis | 30% | 93% |
A4HJW2 | Leishmania braziliensis | 33% | 92% |
A4HKG9 | Leishmania braziliensis | 31% | 100% |
A4HLR0 | Leishmania braziliensis | 35% | 100% |
A4HN71 | Leishmania braziliensis | 28% | 100% |
A4HNI1 | Leishmania braziliensis | 35% | 97% |
A4HP12 | Leishmania braziliensis | 58% | 100% |
A4HP13 | Leishmania braziliensis | 90% | 100% |
A4HZW8 | Leishmania infantum | 40% | 100% |
A4I1T4 | Leishmania infantum | 30% | 100% |
A4I435 | Leishmania infantum | 30% | 100% |
A4I7A1 | Leishmania infantum | 36% | 100% |
A4I7C4 | Leishmania infantum | 33% | 94% |
A4I7Z6 | Leishmania infantum | 31% | 100% |
A4IBT4 | Leishmania infantum | 28% | 100% |
A4IBT9 | Leishmania infantum | 28% | 100% |
A4IC37 | Leishmania infantum | 36% | 99% |
A4IDC1 | Leishmania infantum | 58% | 100% |
A4IDC2 | Leishmania infantum | 100% | 100% |
C9ZMH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZWI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A2Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
D0A2Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 87% |
E9AFM1 | Leishmania major | 27% | 100% |
E9AFZ2 | Leishmania major | 35% | 96% |
E9ASS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9ASS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 93% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 93% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B6S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B6S9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B745 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
O13839 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 69% |
P11837 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 72% |
P49071 | Drosophila melanogaster | 28% | 100% |
Q03428 | Trypanosoma brucei brucei | 32% | 100% |
Q08942 | Trypanosoma brucei brucei | 33% | 100% |
Q0VD22 | Bos taurus | 26% | 100% |
Q4Q1S3 | Leishmania major | 97% | 100% |
Q4Q1S4 | Leishmania major | 58% | 100% |
Q4Q598 | Leishmania major | 31% | 100% |
Q4Q5T9 | Leishmania major | 33% | 94% |
Q4Q5W2 | Leishmania major | 36% | 100% |
Q4Q7W2 | Leishmania major | 30% | 100% |
Q4QBQ2 | Leishmania major | 39% | 100% |
Q5KQF5 | Oryza sativa subsp. japonica | 29% | 100% |
Q9GNR4 | Leishmania major | 28% | 100% |
V5BHW8 | Trypanosoma cruzi | 24% | 79% |
V5BPJ0 | Trypanosoma cruzi | 58% | 100% |
V5D579 | Trypanosoma cruzi | 33% | 100% |
V5DFW9 | Trypanosoma cruzi | 30% | 86% |
V5DKY9 | Trypanosoma cruzi | 34% | 81% |