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: 27 |
NetGPI | no | yes: 0, no: 27 |
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: A0A3Q8IDK8
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 28 |
GO:0006793 | phosphorus metabolic process | 3 | 28 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 28 |
GO:0006807 | nitrogen compound metabolic process | 2 | 28 |
GO:0008152 | metabolic process | 1 | 28 |
GO:0009987 | cellular process | 1 | 28 |
GO:0016310 | phosphorylation | 5 | 28 |
GO:0019538 | protein metabolic process | 3 | 28 |
GO:0036211 | protein modification process | 4 | 28 |
GO:0043170 | macromolecule metabolic process | 3 | 28 |
GO:0043412 | macromolecule modification | 4 | 28 |
GO:0044237 | cellular metabolic process | 2 | 28 |
GO:0044238 | primary metabolic process | 2 | 28 |
GO:0071704 | organic substance metabolic process | 2 | 28 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 28 |
GO:0007165 | signal transduction | 2 | 2 |
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 | 2 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
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 | 28 |
GO:0003824 | catalytic activity | 1 | 28 |
GO:0004672 | protein kinase activity | 3 | 28 |
GO:0005488 | binding | 1 | 28 |
GO:0005524 | ATP binding | 5 | 28 |
GO:0016301 | kinase activity | 4 | 28 |
GO:0016740 | transferase activity | 2 | 28 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 28 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 28 |
GO:0017076 | purine nucleotide binding | 4 | 28 |
GO:0030554 | adenyl nucleotide binding | 5 | 28 |
GO:0032553 | ribonucleotide binding | 3 | 28 |
GO:0032555 | purine ribonucleotide binding | 4 | 28 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 28 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 28 |
GO:0036094 | small molecule binding | 2 | 28 |
GO:0043167 | ion binding | 2 | 28 |
GO:0043168 | anion binding | 3 | 28 |
GO:0097159 | organic cyclic compound binding | 2 | 28 |
GO:0097367 | carbohydrate derivative binding | 2 | 28 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 28 |
GO:1901265 | nucleoside phosphate binding | 3 | 28 |
GO:1901363 | heterocyclic compound binding | 2 | 28 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 21 |
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 | 202 | 204 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.291 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.437 |
CLV_PCSK_PC1ET2_1 | 545 | 547 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.405 |
DEG_APCC_DBOX_1 | 436 | 444 | PF00400 | 0.428 |
DEG_SCF_FBW7_1 | 533 | 538 | PF00400 | 0.621 |
DEG_SPOP_SBC_1 | 178 | 182 | PF00917 | 0.405 |
DEG_SPOP_SBC_1 | 528 | 532 | PF00917 | 0.621 |
DOC_CYCLIN_yCln2_LP_2 | 283 | 289 | PF00134 | 0.323 |
DOC_MAPK_gen_1 | 141 | 150 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 309 | 318 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 39 | 49 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 90 | 98 | PF00069 | 0.347 |
DOC_MAPK_JIP1_4 | 144 | 150 | PF00069 | 0.362 |
DOC_MAPK_JIP1_4 | 276 | 282 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 90 | 98 | PF00069 | 0.354 |
DOC_MAPK_NFAT4_5 | 91 | 99 | PF00069 | 0.370 |
DOC_SPAK_OSR1_1 | 91 | 95 | PF12202 | 0.288 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.871 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 48 | 52 | PF12436 | 0.404 |
DOC_USP7_UBL2_3 | 536 | 540 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 54 | 58 | PF12436 | 0.404 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 340 | 348 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 475 | 479 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 546 | 551 | PF00244 | 0.596 |
LIG_14-3-3_CterR_2 | 558 | 560 | PF00244 | 0.617 |
LIG_APCC_ABBA_1 | 409 | 414 | PF00400 | 0.533 |
LIG_APCC_ABBAyCdc20_2 | 136 | 142 | PF00400 | 0.300 |
LIG_deltaCOP1_diTrp_1 | 330 | 338 | PF00928 | 0.568 |
LIG_EH1_1 | 92 | 100 | PF00400 | 0.300 |
LIG_eIF4E_1 | 93 | 99 | PF01652 | 0.310 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.349 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.310 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.494 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.367 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.307 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.325 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.372 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.497 |
LIG_LIR_Apic_2 | 186 | 192 | PF02991 | 0.404 |
LIG_LIR_Apic_2 | 330 | 334 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 237 | 243 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 251 | 261 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 332 | 339 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 342 | 349 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.444 |
LIG_LYPXL_S_1 | 409 | 413 | PF13949 | 0.422 |
LIG_LYPXL_yS_3 | 410 | 413 | PF13949 | 0.415 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.571 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.428 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 271 | 275 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 30 | 34 | PF00017 | 0.310 |
LIG_SH2_PTP2 | 189 | 192 | PF00017 | 0.341 |
LIG_SH2_PTP2 | 221 | 224 | PF00017 | 0.380 |
LIG_SH2_PTP2 | 93 | 96 | PF00017 | 0.494 |
LIG_SH2_SRC | 177 | 180 | PF00017 | 0.405 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.403 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.363 |
LIG_SH3_4 | 536 | 543 | PF00018 | 0.608 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.301 |
LIG_SUMO_SIM_anti_2 | 66 | 71 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 94 | 100 | PF11976 | 0.445 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.424 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.295 |
LIG_UBA3_1 | 104 | 112 | PF00899 | 0.380 |
MOD_CDK_SPK_2 | 531 | 536 | PF00069 | 0.623 |
MOD_CDK_SPxK_1 | 552 | 558 | PF00069 | 0.611 |
MOD_CDK_SPxxK_3 | 255 | 262 | PF00069 | 0.348 |
MOD_CDK_SPxxK_3 | 529 | 536 | PF00069 | 0.791 |
MOD_CDK_SPxxK_3 | 552 | 559 | PF00069 | 0.595 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.321 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.316 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.304 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.594 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.531 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.579 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.618 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.627 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.675 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.325 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.383 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.300 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.553 |
MOD_Cter_Amidation | 402 | 405 | PF01082 | 0.468 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.383 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.336 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.369 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.353 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.483 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.337 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.384 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.382 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.579 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.403 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.578 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.604 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.825 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.724 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.295 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.442 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.588 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.499 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.577 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.560 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.661 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.482 |
MOD_PKA_1 | 545 | 551 | PF00069 | 0.599 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.454 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.334 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.538 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.334 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.649 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.598 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.383 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.474 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.327 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.340 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.511 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.401 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.602 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.320 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.395 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.359 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.528 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.705 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.707 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.614 |
MOD_SUMO_for_1 | 143 | 146 | PF00179 | 0.404 |
MOD_SUMO_rev_2 | 353 | 360 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 364 | 374 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 237 | 242 | PF01217 | 0.295 |
TRG_DiLeu_BaEn_2 | 407 | 413 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.288 |
TRG_NLS_MonoExtC_3 | 308 | 313 | PF00514 | 0.479 |
TRG_NLS_MonoExtN_4 | 309 | 314 | PF00514 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 141 | 146 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE80 | Leptomonas seymouri | 71% | 99% |
A0A0S4J7K4 | Bodo saltans | 60% | 100% |
A0A1X0NJV4 | Trypanosomatidae | 60% | 100% |
A0A1X0P1A2 | Trypanosomatidae | 60% | 100% |
A0A2I0BVG8 | Plasmodium falciparum (isolate NF54) | 28% | 100% |
A0A3Q8IC87 | Leishmania donovani | 33% | 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% |
A0A3S7X9R4 | Leishmania donovani | 28% | 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% |
A4HN71 | Leishmania braziliensis | 27% | 100% |
A4HNT2 | Leishmania braziliensis | 26% | 100% |
A4HP12 | Leishmania braziliensis | 27% | 100% |
A4HSE2 | Leishmania infantum | 28% | 100% |
A4HWP5 | Leishmania infantum | 25% | 100% |
A4HZV1 | Leishmania infantum | 33% | 100% |
A4I1T4 | Leishmania infantum | 30% | 100% |
A4I349 | Leishmania infantum | 100% | 100% |
A4I7A1 | Leishmania infantum | 27% | 100% |
A4IBT4 | Leishmania infantum | 27% | 100% |
A4IBT9 | 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% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 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% |
E9B6S9 | 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% |
Q4QBR6 | Leishmania major | 33% | 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% |
Q9GNR4 | Leishmania major | 28% | 100% |