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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 33 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 64 |
NetGPI | no | yes: 0, no: 64 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4Q1S4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 65 |
GO:0006793 | phosphorus metabolic process | 3 | 65 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 65 |
GO:0006807 | nitrogen compound metabolic process | 2 | 65 |
GO:0008152 | metabolic process | 1 | 65 |
GO:0009987 | cellular process | 1 | 65 |
GO:0016310 | phosphorylation | 5 | 65 |
GO:0019538 | protein metabolic process | 3 | 65 |
GO:0036211 | protein modification process | 4 | 65 |
GO:0043170 | macromolecule metabolic process | 3 | 65 |
GO:0043412 | macromolecule modification | 4 | 65 |
GO:0044237 | cellular metabolic process | 2 | 65 |
GO:0044238 | primary metabolic process | 2 | 65 |
GO:0071704 | organic substance metabolic process | 2 | 65 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 65 |
GO:0000281 | mitotic cytokinesis | 4 | 1 |
GO:0000910 | cytokinesis | 3 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 65 |
GO:0003824 | catalytic activity | 1 | 65 |
GO:0004672 | protein kinase activity | 3 | 65 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 49 |
GO:0005488 | binding | 1 | 65 |
GO:0005524 | ATP binding | 5 | 65 |
GO:0016301 | kinase activity | 4 | 65 |
GO:0016740 | transferase activity | 2 | 65 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 65 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 65 |
GO:0017076 | purine nucleotide binding | 4 | 65 |
GO:0030554 | adenyl nucleotide binding | 5 | 65 |
GO:0032553 | ribonucleotide binding | 3 | 65 |
GO:0032555 | purine ribonucleotide binding | 4 | 65 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 65 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 65 |
GO:0036094 | small molecule binding | 2 | 65 |
GO:0043167 | ion binding | 2 | 65 |
GO:0043168 | anion binding | 3 | 65 |
GO:0097159 | organic cyclic compound binding | 2 | 65 |
GO:0097367 | carbohydrate derivative binding | 2 | 65 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 65 |
GO:1901265 | nucleoside phosphate binding | 3 | 65 |
GO:1901363 | heterocyclic compound binding | 2 | 65 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.429 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.386 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.197 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 335 | 337 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.476 |
DEG_SCF_FBW7_2 | 436 | 442 | PF00400 | 0.455 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.551 |
DOC_CKS1_1 | 436 | 441 | PF01111 | 0.475 |
DOC_CYCLIN_RxL_1 | 467 | 478 | PF00134 | 0.454 |
DOC_MAPK_gen_1 | 169 | 178 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 394 | 400 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 416 | 424 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 418 | 426 | PF00069 | 0.402 |
DOC_MAPK_RevD_3 | 231 | 245 | PF00069 | 0.348 |
DOC_PP1_RVXF_1 | 468 | 475 | PF00149 | 0.392 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.334 |
DOC_PP4_FxxP_1 | 447 | 450 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.289 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.461 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 289 | 299 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 336 | 345 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 471 | 475 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 55 | 62 | PF00244 | 0.368 |
LIG_AP2alpha_1 | 18 | 22 | PF02296 | 0.385 |
LIG_APCC_ABBAyCdc20_2 | 164 | 170 | PF00400 | 0.340 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BIR_III_2 | 445 | 449 | PF00653 | 0.268 |
LIG_BRCT_BRCA1_1 | 436 | 440 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.446 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.333 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.565 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.496 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.543 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.361 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.382 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.377 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.520 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.486 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.351 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.491 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.456 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.488 |
LIG_IRF3_LxIS_1 | 420 | 427 | PF10401 | 0.451 |
LIG_LIR_Apic_2 | 210 | 216 | PF02991 | 0.333 |
LIG_LIR_Apic_2 | 444 | 450 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 437 | 448 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 91 | 100 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 437 | 443 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.311 |
LIG_NRBOX | 151 | 157 | PF00104 | 0.205 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.306 |
LIG_NRBOX | 305 | 311 | PF00104 | 0.509 |
LIG_PCNA_yPIPBox_3 | 104 | 116 | PF02747 | 0.300 |
LIG_PCNA_yPIPBox_3 | 295 | 305 | PF02747 | 0.318 |
LIG_PCNA_yPIPBox_3 | 77 | 88 | PF02747 | 0.288 |
LIG_Pex14_1 | 393 | 397 | PF04695 | 0.391 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.428 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.369 |
LIG_PTB_Apo_2 | 411 | 418 | PF02174 | 0.582 |
LIG_PTB_Apo_2 | 86 | 93 | PF02174 | 0.322 |
LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.382 |
LIG_SH2_GRB2like | 195 | 198 | PF00017 | 0.467 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 213 | 216 | PF00017 | 0.364 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.411 |
LIG_SUMO_SIM_par_1 | 421 | 427 | PF11976 | 0.414 |
LIG_TYR_ITIM | 236 | 241 | PF00017 | 0.351 |
LIG_UBA3_1 | 236 | 244 | PF00899 | 0.336 |
LIG_UBA3_1 | 296 | 303 | PF00899 | 0.283 |
MOD_CDK_SPxxK_3 | 269 | 276 | PF00069 | 0.457 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.348 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.466 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.579 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.460 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.317 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.503 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.407 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.477 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.495 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.348 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.437 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.382 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.283 |
MOD_Cter_Amidation | 287 | 290 | PF01082 | 0.194 |
MOD_Cter_Amidation | 468 | 471 | PF01082 | 0.435 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.674 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.359 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.336 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.357 |
MOD_GlcNHglycan | 350 | 355 | PF01048 | 0.532 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.330 |
MOD_GlcNHglycan | 499 | 505 | PF01048 | 0.744 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.403 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.345 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.356 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.526 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.582 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.489 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.410 |
MOD_N-GLC_1 | 456 | 461 | PF02516 | 0.502 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.319 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.314 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.356 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.349 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.418 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.509 |
MOD_NEK2_2 | 375 | 380 | PF00069 | 0.391 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.433 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.475 |
MOD_PKA_1 | 289 | 295 | PF00069 | 0.348 |
MOD_PKA_1 | 385 | 391 | PF00069 | 0.424 |
MOD_PKA_1 | 470 | 476 | PF00069 | 0.265 |
MOD_PKA_1 | 54 | 60 | PF00069 | 0.354 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.334 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.457 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.532 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.345 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.542 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.471 |
MOD_Plk_2-3 | 406 | 412 | PF00069 | 0.566 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.357 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.526 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.548 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.492 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.342 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.339 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.303 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.585 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.466 |
MOD_SUMO_for_1 | 23 | 26 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 127 | 134 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 328 | 337 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 333 | 338 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.348 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.457 |
TRG_DiLeu_LyEn_5 | 333 | 338 | PF01217 | 0.304 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.371 |
TRG_NES_CRM1_1 | 111 | 121 | PF08389 | 0.205 |
TRG_Pf-PMV_PEXEL_1 | 336 | 341 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 482 | 487 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N5 | Leptomonas seymouri | 34% | 100% |
A0A0N0P953 | Leptomonas seymouri | 35% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 30% | 78% |
A0A0N1PD05 | Leptomonas seymouri | 35% | 100% |
A0A0S4IMB7 | Bodo saltans | 37% | 100% |
A0A0S4IRZ7 | Bodo saltans | 34% | 100% |
A0A0S4IVW1 | Bodo saltans | 27% | 81% |
A0A0S4IX86 | Bodo saltans | 37% | 100% |
A0A0S4J804 | Bodo saltans | 37% | 97% |
A0A0S4JIJ6 | Bodo saltans | 27% | 90% |
A0A0S4JPZ1 | Bodo saltans | 32% | 100% |
A0A0S4JQN5 | Bodo saltans | 28% | 72% |
A0A0S4JWD5 | Bodo saltans | 24% | 100% |
A0A1X0NIA0 | Trypanosomatidae | 37% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 34% | 100% |
A0A1X0NTL6 | Trypanosomatidae | 33% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 30% | 88% |
A0A1X0P022 | Trypanosomatidae | 25% | 79% |
A0A1X0P527 | Trypanosomatidae | 37% | 100% |
A0A1X0P549 | Trypanosomatidae | 37% | 100% |
A0A1X0P863 | Trypanosomatidae | 76% | 100% |
A0A1X0P994 | Trypanosomatidae | 70% | 100% |
A0A3Q8IAQ1 | Leishmania donovani | 42% | 100% |
A0A3Q8IC87 | Leishmania donovani | 27% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 34% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 34% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 32% | 100% |
A0A3Q8IJM9 | Leishmania donovani | 34% | 100% |
A0A3R7KCZ4 | Trypanosoma rangeli | 36% | 100% |
A0A3R7KDE9 | Trypanosoma rangeli | 25% | 70% |
A0A3R7MKG5 | Trypanosoma rangeli | 34% | 100% |
A0A3S5H528 | Leishmania donovani | 27% | 100% |
A0A3S7WTN9 | Leishmania donovani | 26% | 100% |
A0A3S7X5M4 | Leishmania donovani | 30% | 78% |
A0A3S7X6T8 | Leishmania donovani | 35% | 100% |
A0A3S7X9R4 | Leishmania donovani | 29% | 100% |
A0A3S7X9S2 | Leishmania donovani | 28% | 100% |
A0A3S7XAL3 | Leishmania donovani | 72% | 100% |
A0A3S7XAT9 | Leishmania donovani | 58% | 100% |
A0A422NCP0 | Trypanosoma rangeli | 75% | 100% |
A0A422NH41 | Trypanosoma rangeli | 30% | 88% |
A4H3J3 | Leishmania braziliensis | 26% | 100% |
A4HCD7 | Leishmania braziliensis | 27% | 100% |
A4HCE6 | Leishmania braziliensis | 40% | 100% |
A4HFA1 | Leishmania braziliensis | 27% | 100% |
A4HH03 | Leishmania braziliensis | 31% | 100% |
A4HHN1 | Leishmania braziliensis | 27% | 100% |
A4HHQ5 | Leishmania braziliensis | 29% | 100% |
A4HJT5 | Leishmania braziliensis | 34% | 100% |
A4HJW2 | Leishmania braziliensis | 33% | 100% |
A4HKG9 | Leishmania braziliensis | 30% | 78% |
A4HLR0 | Leishmania braziliensis | 35% | 100% |
A4HN71 | Leishmania braziliensis | 29% | 100% |
A4HNI1 | Leishmania braziliensis | 35% | 100% |
A4HP12 | Leishmania braziliensis | 97% | 100% |
A4HP13 | Leishmania braziliensis | 59% | 100% |
A4HRT2 | Leishmania infantum | 27% | 100% |
A4HWP5 | Leishmania infantum | 26% | 100% |
A4HZV1 | Leishmania infantum | 27% | 100% |
A4HZW8 | Leishmania infantum | 42% | 100% |
A4I435 | Leishmania infantum | 31% | 100% |
A4I7A1 | Leishmania infantum | 34% | 100% |
A4I7C4 | Leishmania infantum | 34% | 100% |
A4I7Z6 | Leishmania infantum | 30% | 78% |
A4I960 | Leishmania infantum | 35% | 100% |
A4IBT4 | Leishmania infantum | 27% | 100% |
A4IBT9 | Leishmania infantum | 29% | 100% |
A4IC37 | Leishmania infantum | 34% | 100% |
A4IDC1 | Leishmania infantum | 98% | 100% |
A4IDC2 | Leishmania infantum | 58% | 100% |
C9ZMH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZUU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 77% |
C9ZWI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZWK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A2Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 100% |
D0A2Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 100% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 89% |
E9ACG8 | Leishmania major | 27% | 100% |
E9AFM1 | Leishmania major | 29% | 100% |
E9AFZ2 | Leishmania major | 34% | 97% |
E9AII8 | Leishmania braziliensis | 25% | 100% |
E9ASS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E9ASS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AUS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 78% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B6S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B6S9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B745 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
P28867 | Mus musculus | 27% | 76% |
P45894 | Caenorhabditis elegans | 27% | 86% |
Q03428 | Trypanosoma brucei brucei | 35% | 100% |
Q08942 | Trypanosoma brucei brucei | 36% | 100% |
Q4Q1S3 | Leishmania major | 58% | 100% |
Q4Q3Y9 | Leishmania major | 35% | 100% |
Q4Q598 | Leishmania major | 30% | 78% |
Q4Q5T9 | Leishmania major | 34% | 100% |
Q4Q5W2 | Leishmania major | 35% | 96% |
Q4Q7W2 | Leishmania major | 31% | 100% |
Q4Q9K2 | Leishmania major | 32% | 100% |
Q4QBQ2 | Leishmania major | 41% | 100% |
Q4QBR6 | Leishmania major | 26% | 100% |
Q4QF23 | Leishmania major | 26% | 100% |
Q5PU49 | Canis lupus familiaris | 28% | 76% |
Q86IX1 | Dictyostelium discoideum | 30% | 69% |
Q8RXT4 | Arabidopsis thaliana | 26% | 92% |
Q9GNR4 | Leishmania major | 29% | 100% |
Q9R0A5 | Mus musculus | 32% | 100% |
V5BC28 | Trypanosoma cruzi | 33% | 100% |
V5BL06 | Trypanosoma cruzi | 24% | 79% |
V5BPJ0 | Trypanosoma cruzi | 75% | 100% |
V5D579 | Trypanosoma cruzi | 37% | 100% |
V5DFW9 | Trypanosoma cruzi | 31% | 87% |
V5DKY9 | Trypanosoma cruzi | 34% | 82% |