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. | yes | 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: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 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 |
Related structures:
AlphaFold database: A4I349
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 23 |
GO:0006793 | phosphorus metabolic process | 3 | 23 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 23 |
GO:0006807 | nitrogen compound metabolic process | 2 | 23 |
GO:0008152 | metabolic process | 1 | 23 |
GO:0009987 | cellular process | 1 | 23 |
GO:0016310 | phosphorylation | 5 | 23 |
GO:0019538 | protein metabolic process | 3 | 23 |
GO:0036211 | protein modification process | 4 | 23 |
GO:0043170 | macromolecule metabolic process | 3 | 23 |
GO:0043412 | macromolecule modification | 4 | 23 |
GO:0044237 | cellular metabolic process | 2 | 23 |
GO:0044238 | primary metabolic process | 2 | 23 |
GO:0071704 | organic substance metabolic process | 2 | 23 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 23 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0000281 | mitotic cytokinesis | 4 | 1 |
GO:0000910 | cytokinesis | 3 | 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 | 23 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0004672 | protein kinase activity | 3 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0005524 | ATP binding | 5 | 23 |
GO:0016301 | kinase activity | 4 | 23 |
GO:0016740 | transferase activity | 2 | 23 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 23 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 23 |
GO:0017076 | purine nucleotide binding | 4 | 23 |
GO:0030554 | adenyl nucleotide binding | 5 | 23 |
GO:0032553 | ribonucleotide binding | 3 | 23 |
GO:0032555 | purine ribonucleotide binding | 4 | 23 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 23 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 23 |
GO:0036094 | small molecule binding | 2 | 23 |
GO:0043167 | ion binding | 2 | 23 |
GO:0043168 | anion binding | 3 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0097367 | carbohydrate derivative binding | 2 | 23 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 23 |
GO:1901265 | nucleoside phosphate binding | 3 | 23 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 16 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.216 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 549 | 551 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.216 |
CLV_PCSK_PC1ET2_1 | 408 | 410 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 549 | 551 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 56 | 58 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.552 |
DEG_APCC_DBOX_1 | 127 | 135 | PF00400 | 0.338 |
DEG_APCC_DBOX_1 | 440 | 448 | PF00400 | 0.346 |
DEG_SCF_FBW7_1 | 537 | 542 | PF00400 | 0.553 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.338 |
DEG_SPOP_SBC_1 | 532 | 536 | PF00917 | 0.552 |
DOC_CYCLIN_yCln2_LP_2 | 287 | 293 | PF00134 | 0.252 |
DOC_MAPK_gen_1 | 145 | 154 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 313 | 322 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 43 | 53 | PF00069 | 0.238 |
DOC_MAPK_gen_1 | 94 | 102 | PF00069 | 0.274 |
DOC_MAPK_JIP1_4 | 148 | 154 | PF00069 | 0.285 |
DOC_MAPK_JIP1_4 | 280 | 286 | PF00069 | 0.229 |
DOC_MAPK_MEF2A_6 | 94 | 102 | PF00069 | 0.285 |
DOC_MAPK_NFAT4_5 | 95 | 103 | PF00069 | 0.301 |
DOC_SPAK_OSR1_1 | 95 | 99 | PF12202 | 0.214 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.804 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 52 | 56 | PF12436 | 0.331 |
DOC_USP7_UBL2_3 | 540 | 544 | PF12436 | 0.560 |
DOC_USP7_UBL2_3 | 58 | 62 | PF12436 | 0.331 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.274 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 250 | 254 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 344 | 352 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 479 | 483 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 550 | 555 | PF00244 | 0.524 |
LIG_14-3-3_CterR_2 | 562 | 564 | PF00244 | 0.553 |
LIG_APCC_ABBA_1 | 413 | 418 | PF00400 | 0.473 |
LIG_APCC_ABBAyCdc20_2 | 140 | 146 | PF00400 | 0.227 |
LIG_deltaCOP1_diTrp_1 | 334 | 342 | PF00928 | 0.478 |
LIG_EH1_1 | 96 | 104 | PF00400 | 0.227 |
LIG_eIF4E_1 | 97 | 103 | PF01652 | 0.237 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.270 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.222 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.450 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.299 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.241 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.255 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.303 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.412 |
LIG_LIR_Apic_2 | 190 | 196 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 334 | 338 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 241 | 247 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 336 | 343 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 346 | 353 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 402 | 411 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.222 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 402 | 406 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 481 | 486 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.380 |
LIG_LYPXL_S_1 | 413 | 417 | PF13949 | 0.341 |
LIG_LYPXL_yS_3 | 414 | 417 | PF13949 | 0.336 |
LIG_Pex14_1 | 335 | 339 | PF04695 | 0.482 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.349 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.278 |
LIG_SH2_NCK_1 | 275 | 279 | PF00017 | 0.244 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.237 |
LIG_SH2_PTP2 | 193 | 196 | PF00017 | 0.271 |
LIG_SH2_PTP2 | 225 | 228 | PF00017 | 0.305 |
LIG_SH2_PTP2 | 97 | 100 | PF00017 | 0.418 |
LIG_SH2_SRC | 181 | 184 | PF00017 | 0.338 |
LIG_SH2_SRC | 275 | 278 | PF00017 | 0.222 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.237 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.330 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.283 |
LIG_SH3_4 | 540 | 547 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 282 | 288 | PF11976 | 0.229 |
LIG_SUMO_SIM_anti_2 | 70 | 75 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.373 |
LIG_TYR_ITIM | 223 | 228 | PF00017 | 0.351 |
LIG_TYR_ITIM | 273 | 278 | PF00017 | 0.222 |
LIG_UBA3_1 | 108 | 116 | PF00899 | 0.311 |
MOD_CDK_SPK_2 | 535 | 540 | PF00069 | 0.549 |
MOD_CDK_SPxK_1 | 556 | 562 | PF00069 | 0.541 |
MOD_CDK_SPxxK_3 | 259 | 266 | PF00069 | 0.278 |
MOD_CDK_SPxxK_3 | 533 | 540 | PF00069 | 0.724 |
MOD_CDK_SPxxK_3 | 556 | 563 | PF00069 | 0.523 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.246 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.250 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.224 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.281 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.452 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.518 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.546 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.558 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.608 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.254 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.325 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.246 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.471 |
MOD_Cter_Amidation | 406 | 409 | PF01082 | 0.375 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.348 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.331 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.265 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.535 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.283 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.281 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.256 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.345 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.273 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.520 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.366 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.498 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.530 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.758 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.661 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.222 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.429 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.442 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.259 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.478 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.499 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.468 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.572 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.418 |
MOD_PKA_1 | 549 | 555 | PF00069 | 0.527 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.386 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.255 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.515 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.264 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.590 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.526 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.323 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.418 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.259 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.269 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.457 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.333 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.553 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.274 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.326 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.302 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.434 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.638 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.640 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.538 |
MOD_SUMO_for_1 | 147 | 150 | PF00179 | 0.331 |
MOD_SUMO_rev_2 | 357 | 364 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 368 | 378 | PF00179 | 0.447 |
TRG_DiLeu_BaEn_1 | 241 | 246 | PF01217 | 0.222 |
TRG_DiLeu_BaEn_2 | 411 | 417 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.224 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 441 | 444 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.214 |
TRG_NLS_MonoExtC_3 | 312 | 317 | PF00514 | 0.388 |
TRG_NLS_MonoExtN_4 | 313 | 318 | PF00514 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 145 | 150 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE80 | Leptomonas seymouri | 71% | 100% |
A0A0S4J7K4 | Bodo saltans | 60% | 100% |
A0A1X0NJV4 | Trypanosomatidae | 60% | 100% |
A0A1X0P1A2 | Trypanosomatidae | 60% | 100% |
A0A2I0BVG8 | Plasmodium falciparum (isolate NF54) | 28% | 100% |
A0A3Q8IDK8 | Leishmania donovani | 100% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 27% | 100% |
A0A3Q8INQ4 | Leishmania donovani | 30% | 100% |
A0A3Q8IVR8 | Leishmania donovani | 26% | 100% |
A0A3S5H5G0 | Leishmania donovani | 28% | 100% |
A0A3S5H5U5 | Leishmania donovani | 23% | 100% |
A0A3S7WTN9 | Leishmania donovani | 25% | 100% |
A0A509AHB6 | Plasmodium berghei (strain Anka) | 28% | 100% |
A4H459 | Leishmania braziliensis | 29% | 100% |
A4H4S9 | Leishmania braziliensis | 25% | 100% |
A4H8C4 | Leishmania braziliensis | 26% | 100% |
A4HC27 | Leishmania braziliensis | 24% | 100% |
A4HCD7 | Leishmania braziliensis | 33% | 100% |
A4HED7 | Leishmania braziliensis | 29% | 100% |
A4HG27 | Leishmania braziliensis | 84% | 100% |
A4HJT5 | Leishmania braziliensis | 27% | 100% |
A4HJW2 | Leishmania braziliensis | 24% | 100% |
A4HNT2 | Leishmania braziliensis | 26% | 100% |
A4HP12 | Leishmania braziliensis | 27% | 100% |
A4HSE2 | Leishmania infantum | 28% | 100% |
A4HWP5 | Leishmania infantum | 25% | 100% |
A4I1T4 | Leishmania infantum | 30% | 100% |
A4I7A1 | Leishmania infantum | 27% | 100% |
A4IBT4 | Leishmania infantum | 27% | 100% |
A4ICR2 | Leishmania infantum | 26% | 100% |
C9ZN29 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9ACW7 | Leishmania major | 92% | 100% |
E9AG71 | Leishmania infantum | 23% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AQF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AZF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B6S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P62343 | Plasmodium falciparum (isolate K1 / Thailand) | 28% | 100% |
P62344 | Plasmodium falciparum (isolate 3D7) | 28% | 100% |
Q4Q204 | Leishmania major | 26% | 100% |
Q4Q5W2 | Leishmania major | 28% | 100% |
Q4Q9K2 | Leishmania major | 31% | 100% |
Q4QF23 | Leishmania major | 25% | 100% |
Q4QIV8 | Leishmania major | 25% | 100% |
Q4QJJ0 | Leishmania major | 28% | 100% |
Q6C7U0 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 79% |
Q7RAH3 | Plasmodium yoelii yoelii | 28% | 100% |