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. | no | yes: 15 |
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: 25 |
NetGPI | no | yes: 0, no: 25 |
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: A0A3Q8IIH5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 26 |
GO:0006793 | phosphorus metabolic process | 3 | 26 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 26 |
GO:0006807 | nitrogen compound metabolic process | 2 | 26 |
GO:0008152 | metabolic process | 1 | 26 |
GO:0009987 | cellular process | 1 | 26 |
GO:0016310 | phosphorylation | 5 | 26 |
GO:0019538 | protein metabolic process | 3 | 26 |
GO:0036211 | protein modification process | 4 | 26 |
GO:0043170 | macromolecule metabolic process | 3 | 26 |
GO:0043412 | macromolecule modification | 4 | 26 |
GO:0044237 | cellular metabolic process | 2 | 26 |
GO:0044238 | primary metabolic process | 2 | 26 |
GO:0071704 | organic substance metabolic process | 2 | 26 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 26 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 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: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 | 26 |
GO:0003824 | catalytic activity | 1 | 26 |
GO:0004672 | protein kinase activity | 3 | 26 |
GO:0005488 | binding | 1 | 26 |
GO:0005524 | ATP binding | 5 | 26 |
GO:0016301 | kinase activity | 4 | 26 |
GO:0016740 | transferase activity | 2 | 26 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 26 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 26 |
GO:0017076 | purine nucleotide binding | 4 | 26 |
GO:0030554 | adenyl nucleotide binding | 5 | 26 |
GO:0032553 | ribonucleotide binding | 3 | 26 |
GO:0032555 | purine ribonucleotide binding | 4 | 26 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 26 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 26 |
GO:0036094 | small molecule binding | 2 | 26 |
GO:0043167 | ion binding | 2 | 26 |
GO:0043168 | anion binding | 3 | 26 |
GO:0097159 | organic cyclic compound binding | 2 | 26 |
GO:0097367 | carbohydrate derivative binding | 2 | 26 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 26 |
GO:1901265 | nucleoside phosphate binding | 3 | 26 |
GO:1901363 | heterocyclic compound binding | 2 | 26 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 365 | 369 | PF00656 | 0.775 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.259 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.510 |
DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.235 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.336 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.468 |
DEG_SPOP_SBC_1 | 362 | 366 | PF00917 | 0.520 |
DOC_ANK_TNKS_1 | 521 | 528 | PF00023 | 0.477 |
DOC_CDC14_PxL_1 | 385 | 393 | PF14671 | 0.602 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.349 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 178 | 184 | PF00134 | 0.295 |
DOC_CYCLIN_yCln2_LP_2 | 201 | 207 | PF00134 | 0.215 |
DOC_CYCLIN_yCln2_LP_2 | 531 | 537 | PF00134 | 0.494 |
DOC_MAPK_DCC_7 | 383 | 393 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 129 | 138 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 248 | 257 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 73 | 80 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 93 | 102 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 250 | 259 | PF00069 | 0.241 |
DOC_MAPK_MEF2A_6 | 73 | 82 | PF00069 | 0.378 |
DOC_MAPK_RevD_3 | 112 | 125 | PF00069 | 0.295 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.295 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.562 |
DOC_PP2B_LxvP_1 | 531 | 534 | PF13499 | 0.499 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.469 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.636 |
DOC_PP4_FxxP_1 | 423 | 426 | PF00568 | 0.540 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.543 |
DOC_PP4_FxxP_1 | 458 | 461 | PF00568 | 0.490 |
DOC_PP4_FxxP_1 | 518 | 521 | PF00568 | 0.598 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.295 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.304 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 317 | 324 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 45 | 50 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.259 |
LIG_Actin_RPEL_3 | 236 | 255 | PF02755 | 0.274 |
LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.202 |
LIG_APCC_ABBAyCdc20_2 | 124 | 130 | PF00400 | 0.341 |
LIG_BRCT_BRCA1_1 | 419 | 423 | PF00533 | 0.546 |
LIG_eIF4E_1 | 171 | 177 | PF01652 | 0.295 |
LIG_EVH1_1 | 535 | 539 | PF00568 | 0.458 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.310 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.252 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.567 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.767 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.330 |
LIG_LIR_Apic_2 | 420 | 426 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 469 | 475 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 510 | 516 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.303 |
LIG_LYPXL_S_1 | 406 | 410 | PF13949 | 0.487 |
LIG_LYPXL_yS_3 | 407 | 410 | PF13949 | 0.487 |
LIG_MAD2 | 216 | 224 | PF02301 | 0.335 |
LIG_MAD2 | 53 | 61 | PF02301 | 0.295 |
LIG_MYND_1 | 380 | 384 | PF01753 | 0.498 |
LIG_MYND_1 | 480 | 484 | PF01753 | 0.474 |
LIG_MYND_1 | 512 | 516 | PF01753 | 0.520 |
LIG_MYND_1 | 533 | 537 | PF01753 | 0.482 |
LIG_NRP_CendR_1 | 552 | 555 | PF00754 | 0.489 |
LIG_Pex14_2 | 423 | 427 | PF04695 | 0.499 |
LIG_PTB_Apo_2 | 512 | 519 | PF02174 | 0.603 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.244 |
LIG_SH2_CRK | 385 | 389 | PF00017 | 0.538 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.244 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.546 |
LIG_SH2_GRB2like | 385 | 388 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 513 | 516 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 472 | 476 | PF00017 | 0.508 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.526 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.295 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 120 | 123 | PF00017 | 0.215 |
LIG_SH2_STAT3 | 399 | 402 | PF00017 | 0.634 |
LIG_SH2_STAT3 | 476 | 479 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.382 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.379 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.313 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.627 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.550 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.614 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.637 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.498 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.451 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.632 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.646 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.329 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.215 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.454 |
LIG_TRFH_1 | 170 | 174 | PF08558 | 0.379 |
LIG_TYR_ITIM | 194 | 199 | PF00017 | 0.384 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.344 |
LIG_UBA3_1 | 198 | 202 | PF00899 | 0.233 |
LIG_WRC_WIRS_1 | 67 | 72 | PF05994 | 0.302 |
LIG_WW_2 | 533 | 536 | PF00397 | 0.471 |
MOD_CDC14_SPxK_1 | 418 | 421 | PF00782 | 0.506 |
MOD_CDK_SPxK_1 | 415 | 421 | PF00069 | 0.506 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.636 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.606 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.729 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.775 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.656 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.529 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.761 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.265 |
MOD_DYRK1A_RPxSP_1 | 415 | 419 | PF00069 | 0.504 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.347 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.477 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.751 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.700 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.609 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.525 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.639 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.544 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.254 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.271 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.405 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.563 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.594 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.714 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.544 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.648 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.597 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.593 |
MOD_N-GLC_2 | 77 | 79 | PF02516 | 0.333 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.600 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.295 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.564 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.537 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.330 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.679 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.516 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.295 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.459 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.312 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.295 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.254 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.295 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.345 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.561 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.684 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.519 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.491 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.508 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.524 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 552 | 555 | PF00400 | 0.580 |
TRG_NES_CRM1_1 | 106 | 119 | PF08389 | 0.374 |
TRG_NES_CRM1_1 | 209 | 223 | PF08389 | 0.215 |
TRG_NES_CRM1_1 | 232 | 244 | PF08389 | 0.223 |
TRG_Pf-PMV_PEXEL_1 | 239 | 244 | PF00026 | 0.341 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9A0 | Leptomonas seymouri | 27% | 85% |
A0A0N1IHM7 | Leptomonas seymouri | 54% | 94% |
A0A0S4JIJ6 | Bodo saltans | 29% | 98% |
A0A3Q8IC87 | Leishmania donovani | 30% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 37% | 100% |
A0A3Q8INQ4 | Leishmania donovani | 29% | 100% |
A0A3S5H789 | Leishmania donovani | 23% | 100% |
A0A3S7X2W3 | Leishmania donovani | 27% | 100% |
A0A3S7X5M4 | Leishmania donovani | 27% | 85% |
A0A3S7X7Y2 | Leishmania donovani | 28% | 100% |
A4H7W1 | Leishmania braziliensis | 77% | 100% |
A4HAS1 | Leishmania braziliensis | 29% | 100% |
A4HH03 | Leishmania braziliensis | 31% | 100% |
A4HHN1 | Leishmania braziliensis | 27% | 100% |
A4HJT5 | Leishmania braziliensis | 37% | 100% |
A4HKG9 | Leishmania braziliensis | 27% | 85% |
A4HW88 | Leishmania infantum | 100% | 100% |
A4HYX6 | Leishmania infantum | 23% | 100% |
A4HZV1 | Leishmania infantum | 30% | 100% |
A4I1T4 | Leishmania infantum | 29% | 100% |
A4I4U6 | Leishmania infantum | 28% | 100% |
A4I7A1 | Leishmania infantum | 37% | 100% |
A4I7Z6 | Leishmania infantum | 27% | 85% |
A4I9Y5 | Leishmania infantum | 28% | 100% |
E9ALJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9APY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AUS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 85% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P53351 | Mus musculus | 29% | 81% |
Q4Q2Z2 | Leishmania major | 28% | 100% |
Q4Q3K6 | Leishmania major | 26% | 100% |
Q4Q598 | Leishmania major | 27% | 85% |
Q4Q5T9 | Leishmania major | 40% | 100% |
Q4Q5W2 | Leishmania major | 38% | 100% |
Q4Q9K2 | Leishmania major | 29% | 100% |
Q4QBR6 | Leishmania major | 30% | 100% |
Q4QCR3 | Leishmania major | 23% | 100% |
Q4QFJ2 | Leishmania major | 92% | 100% |
Q6CSX2 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 27% | 67% |
Q9Y077 | Leishmania major | 27% | 100% |
V5B141 | Trypanosoma cruzi | 30% | 100% |
V5BAZ8 | Trypanosoma cruzi | 26% | 100% |