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. | no | yes: 21 |
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: 65 |
NetGPI | no | yes: 0, no: 65 |
Related structures:
AlphaFold database: A0A3S7XAL3
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 66 |
GO:0006793 | phosphorus metabolic process | 3 | 66 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 66 |
GO:0006807 | nitrogen compound metabolic process | 2 | 66 |
GO:0008152 | metabolic process | 1 | 66 |
GO:0009987 | cellular process | 1 | 66 |
GO:0016310 | phosphorylation | 5 | 66 |
GO:0019538 | protein metabolic process | 3 | 66 |
GO:0036211 | protein modification process | 4 | 66 |
GO:0043170 | macromolecule metabolic process | 3 | 66 |
GO:0043412 | macromolecule modification | 4 | 66 |
GO:0044237 | cellular metabolic process | 2 | 66 |
GO:0044238 | primary metabolic process | 2 | 66 |
GO:0071704 | organic substance metabolic process | 2 | 66 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 66 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 66 |
GO:0003824 | catalytic activity | 1 | 66 |
GO:0004672 | protein kinase activity | 3 | 66 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 47 |
GO:0005488 | binding | 1 | 66 |
GO:0005524 | ATP binding | 5 | 66 |
GO:0016301 | kinase activity | 4 | 66 |
GO:0016740 | transferase activity | 2 | 66 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 66 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 66 |
GO:0017076 | purine nucleotide binding | 4 | 66 |
GO:0030554 | adenyl nucleotide binding | 5 | 66 |
GO:0032553 | ribonucleotide binding | 3 | 66 |
GO:0032555 | purine ribonucleotide binding | 4 | 66 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 66 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 66 |
GO:0036094 | small molecule binding | 2 | 66 |
GO:0043167 | ion binding | 2 | 66 |
GO:0043168 | anion binding | 3 | 66 |
GO:0097159 | organic cyclic compound binding | 2 | 66 |
GO:0097367 | carbohydrate derivative binding | 2 | 66 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 66 |
GO:1901265 | nucleoside phosphate binding | 3 | 66 |
GO:1901363 | heterocyclic compound binding | 2 | 66 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.406 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.362 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.168 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.259 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.265 |
DOC_CKS1_1 | 297 | 302 | PF01111 | 0.295 |
DOC_CKS1_1 | 432 | 437 | PF01111 | 0.330 |
DOC_MAPK_gen_1 | 169 | 178 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 334 | 342 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 389 | 395 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 344 | 351 | PF00069 | 0.634 |
DOC_MAPK_MEF2A_6 | 356 | 363 | PF00069 | 0.560 |
DOC_MAPK_RevD_3 | 231 | 245 | PF00069 | 0.315 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.494 |
DOC_PP1_RVXF_1 | 464 | 471 | PF00149 | 0.290 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.340 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 356 | 360 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 55 | 62 | PF00244 | 0.302 |
LIG_AP2alpha_1 | 18 | 22 | PF02296 | 0.352 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.171 |
LIG_APCC_ABBAyCdc20_2 | 164 | 170 | PF00400 | 0.311 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.626 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.454 |
LIG_CaM_IQ_9 | 416 | 432 | PF13499 | 0.403 |
LIG_Clathr_ClatBox_1 | 413 | 417 | PF01394 | 0.171 |
LIG_deltaCOP1_diTrp_1 | 479 | 488 | PF00928 | 0.374 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.434 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.526 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.517 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.368 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.318 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.391 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.340 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.404 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.461 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.403 |
LIG_Integrin_isoDGR_2 | 464 | 466 | PF01839 | 0.171 |
LIG_IRF3_LxIS_1 | 300 | 307 | PF10401 | 0.222 |
LIG_LIR_Apic_2 | 210 | 216 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 433 | 444 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 91 | 100 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.297 |
LIG_NRBOX | 151 | 157 | PF00104 | 0.168 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.266 |
LIG_PCNA_PIPBox_1 | 482 | 491 | PF02747 | 0.171 |
LIG_PCNA_yPIPBox_3 | 104 | 116 | PF02747 | 0.271 |
LIG_PCNA_yPIPBox_3 | 273 | 283 | PF02747 | 0.170 |
LIG_PCNA_yPIPBox_3 | 77 | 88 | PF02747 | 0.255 |
LIG_Pex14_1 | 388 | 392 | PF04695 | 0.295 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.395 |
LIG_Pex14_2 | 458 | 462 | PF04695 | 0.324 |
LIG_PTB_Apo_2 | 86 | 93 | PF02174 | 0.289 |
LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.338 |
LIG_SH2_GRB2like | 195 | 198 | PF00017 | 0.430 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.327 |
LIG_SH2_PTP2 | 213 | 216 | PF00017 | 0.301 |
LIG_SH2_PTP2 | 305 | 308 | PF00017 | 0.223 |
LIG_SH2_PTP2 | 392 | 395 | PF00017 | 0.171 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.293 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 415 | 420 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 411 | 417 | PF11976 | 0.171 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.549 |
LIG_TYR_ITIM | 236 | 241 | PF00017 | 0.306 |
LIG_UBA3_1 | 236 | 244 | PF00899 | 0.299 |
LIG_WRC_WIRS_1 | 485 | 490 | PF05994 | 0.171 |
MOD_CDC14_SPxK_1 | 366 | 369 | PF00782 | 0.530 |
MOD_CDK_SPxK_1 | 363 | 369 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 296 | 303 | PF00069 | 0.403 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.454 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.519 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.361 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.305 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.304 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.302 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.439 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.363 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.415 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.431 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.340 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.244 |
MOD_Cter_Amidation | 464 | 467 | PF01082 | 0.315 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.709 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.333 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.345 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.458 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.320 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.381 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.294 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.393 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.486 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.354 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.365 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.433 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.287 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.282 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.312 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.337 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.482 |
MOD_PKA_1 | 289 | 295 | PF00069 | 0.342 |
MOD_PKA_1 | 54 | 60 | PF00069 | 0.282 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.307 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.496 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.175 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.294 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.537 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.331 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.325 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.277 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.372 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.306 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.376 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.296 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.258 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.509 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.340 |
MOD_SUMO_for_1 | 23 | 26 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 127 | 134 | PF00179 | 0.295 |
TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.298 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.368 |
TRG_NES_CRM1_1 | 111 | 121 | PF08389 | 0.168 |
TRG_NLS_MonoExtN_4 | 287 | 292 | PF00514 | 0.171 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 331 | 335 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 467 | 471 | PF00026 | 0.275 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N5 | Leptomonas seymouri | 35% | 100% |
A0A0N0P953 | Leptomonas seymouri | 34% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 30% | 76% |
A0A0N1PD05 | Leptomonas seymouri | 34% | 100% |
A0A0S4IMB7 | Bodo saltans | 39% | 100% |
A0A0S4IQ75 | Bodo saltans | 33% | 98% |
A0A0S4IRZ7 | Bodo saltans | 33% | 100% |
A0A0S4IVW1 | Bodo saltans | 26% | 79% |
A0A0S4IX86 | Bodo saltans | 34% | 100% |
A0A0S4J7K4 | Bodo saltans | 27% | 100% |
A0A0S4J804 | Bodo saltans | 38% | 95% |
A0A0S4JIJ6 | Bodo saltans | 30% | 88% |
A0A0S4JPZ1 | Bodo saltans | 33% | 100% |
A0A0S4JQN5 | Bodo saltans | 29% | 71% |
A0A1X0NFW4 | Trypanosomatidae | 27% | 100% |
A0A1X0NIA0 | Trypanosomatidae | 35% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 32% | 100% |
A0A1X0NTL6 | Trypanosomatidae | 33% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 31% | 85% |
A0A1X0P527 | Trypanosomatidae | 34% | 100% |
A0A1X0P549 | Trypanosomatidae | 36% | 100% |
A0A1X0P863 | Trypanosomatidae | 65% | 100% |
A0A1X0P994 | Trypanosomatidae | 65% | 99% |
A0A3Q8IAQ1 | Leishmania donovani | 42% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 38% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 35% | 93% |
A0A3Q8IIG1 | Leishmania donovani | 29% | 100% |
A0A3Q8IJM9 | Leishmania donovani | 36% | 98% |
A0A3R7KCZ4 | Trypanosoma rangeli | 35% | 100% |
A0A3R7MKG5 | Trypanosoma rangeli | 32% | 100% |
A0A3R7RIN5 | Trypanosoma rangeli | 34% | 99% |
A0A3S5H528 | Leishmania donovani | 26% | 100% |
A0A3S7X5M4 | Leishmania donovani | 31% | 100% |
A0A3S7X9R4 | Leishmania donovani | 29% | 100% |
A0A3S7X9S2 | Leishmania donovani | 29% | 100% |
A0A3S7XAT9 | Leishmania donovani | 85% | 99% |
A0A422NCP0 | Trypanosoma rangeli | 65% | 100% |
A0A422NH41 | Trypanosoma rangeli | 29% | 86% |
A0A422NT89 | Trypanosoma rangeli | 26% | 75% |
A4HCE6 | Leishmania braziliensis | 40% | 100% |
A4HJT5 | Leishmania braziliensis | 32% | 96% |
A4HJW2 | Leishmania braziliensis | 34% | 92% |
A4HKG9 | Leishmania braziliensis | 30% | 100% |
A4HLR0 | Leishmania braziliensis | 37% | 100% |
A4HN71 | Leishmania braziliensis | 29% | 100% |
A4HNI1 | Leishmania braziliensis | 36% | 100% |
A4HP12 | Leishmania braziliensis | 71% | 100% |
A4HP13 | Leishmania braziliensis | 79% | 100% |
A4HRT2 | Leishmania infantum | 26% | 100% |
A4HZW8 | Leishmania infantum | 42% | 100% |
A4I435 | Leishmania infantum | 29% | 100% |
A4I7A1 | Leishmania infantum | 38% | 100% |
A4I7C4 | Leishmania infantum | 35% | 93% |
A4I7Z6 | Leishmania infantum | 31% | 100% |
A4IBT4 | Leishmania infantum | 28% | 100% |
A4IBT9 | Leishmania infantum | 29% | 100% |
A4IC37 | Leishmania infantum | 36% | 99% |
A4IDC1 | Leishmania infantum | 73% | 100% |
A4IDC2 | Leishmania infantum | 85% | 100% |
C9ZUU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 75% |
C9ZWI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZWK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A2Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
D0A2Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 87% |
E9ACG8 | Leishmania major | 26% | 100% |
E9AFM1 | Leishmania major | 30% | 100% |
E9AFZ2 | Leishmania major | 35% | 97% |
E9AII8 | Leishmania braziliensis | 25% | 100% |
E9ALF7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ASS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9ASS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9AUS3 | 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) | 29% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 96% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 93% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B6S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B6S9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B745 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 99% |
O13839 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 69% |
O35942 | Mus musculus | 30% | 100% |
O74426 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P10665 | Xenopus laevis | 26% | 68% |
P18653 | Mus musculus | 25% | 69% |
Q03428 | Trypanosoma brucei brucei | 35% | 100% |
Q08942 | Trypanosoma brucei brucei | 35% | 100% |
Q15418 | Homo sapiens | 25% | 67% |
Q4Q1S3 | Leishmania major | 83% | 100% |
Q4Q1S4 | Leishmania major | 72% | 100% |
Q4Q598 | Leishmania major | 31% | 100% |
Q4Q5T9 | Leishmania major | 35% | 93% |
Q4Q5W2 | Leishmania major | 38% | 100% |
Q4Q7W2 | Leishmania major | 29% | 100% |
Q4Q9K2 | Leishmania major | 30% | 100% |
Q4QBQ2 | Leishmania major | 41% | 100% |
Q5KQF5 | Oryza sativa subsp. japonica | 28% | 100% |
Q63531 | Rattus norvegicus | 25% | 67% |
Q9GNR4 | Leishmania major | 30% | 100% |
V5BHW8 | Trypanosoma cruzi | 25% | 78% |
V5BPJ0 | Trypanosoma cruzi | 66% | 100% |
V5C224 | Trypanosoma cruzi | 35% | 99% |
V5D579 | Trypanosoma cruzi | 35% | 100% |
V5DFW9 | Trypanosoma cruzi | 30% | 85% |
V5DKY9 | Trypanosoma cruzi | 34% | 80% |