Phospholipid biosynthesis, diacylglycerol kinase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A0A3Q8IAN3
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0007165 | signal transduction | 2 | 10 |
GO:0007186 | G protein-coupled receptor signaling pathway | 3 | 10 |
GO:0007205 | protein kinase C-activating G protein-coupled receptor signaling pathway | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0050789 | regulation of biological process | 2 | 10 |
GO:0050794 | regulation of cellular process | 3 | 10 |
GO:0065007 | biological regulation | 1 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004143 | diacylglycerol kinase activity | 5 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.642 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 571 | 573 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 212 | 218 | PF00082 | 0.398 |
CLV_PCSK_PC7_1 | 328 | 334 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.340 |
DEG_COP1_1 | 102 | 110 | PF00400 | 0.716 |
DEG_COP1_1 | 52 | 64 | PF00400 | 0.520 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.677 |
DEG_SCF_FBW7_1 | 587 | 592 | PF00400 | 0.360 |
DEG_SCF_TRCP1_1 | 157 | 163 | PF00400 | 0.456 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.720 |
DOC_CKS1_1 | 600 | 605 | PF01111 | 0.371 |
DOC_CKS1_1 | 606 | 611 | PF01111 | 0.336 |
DOC_CKS1_1 | 654 | 659 | PF01111 | 0.435 |
DOC_CYCLIN_RxL_1 | 548 | 556 | PF00134 | 0.438 |
DOC_MAPK_DCC_7 | 365 | 375 | PF00069 | 0.437 |
DOC_MAPK_DCC_7 | 507 | 517 | PF00069 | 0.361 |
DOC_MAPK_gen_1 | 506 | 517 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 95 | 103 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 510 | 517 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 539 | 546 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 690 | 697 | PF00069 | 0.445 |
DOC_PP2B_LxvP_1 | 544 | 547 | PF13499 | 0.353 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.381 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.353 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.712 |
DOC_USP7_UBL2_3 | 506 | 510 | PF12436 | 0.341 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.238 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 500 | 504 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 578 | 583 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 690 | 694 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 724 | 731 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.634 |
LIG_APCC_ABBA_1 | 275 | 280 | PF00400 | 0.321 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.700 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.662 |
LIG_deltaCOP1_diTrp_1 | 330 | 334 | PF00928 | 0.444 |
LIG_EH1_1 | 164 | 172 | PF00400 | 0.368 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.462 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.268 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.406 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.417 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.368 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.344 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.518 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.395 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.297 |
LIG_FHA_2 | 654 | 660 | PF00498 | 0.435 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.690 |
LIG_LIR_Apic_2 | 203 | 208 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 442 | 448 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 538 | 547 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 647 | 657 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 668 | 675 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 454 | 458 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 647 | 653 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 668 | 673 | PF02991 | 0.542 |
LIG_MYND_1 | 301 | 305 | PF01753 | 0.396 |
LIG_PCNA_yPIPBox_3 | 485 | 497 | PF02747 | 0.400 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.396 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.429 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.420 |
LIG_SH2_CRK | 455 | 459 | PF00017 | 0.314 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.263 |
LIG_SH2_CRK | 577 | 581 | PF00017 | 0.377 |
LIG_SH2_CRK | 630 | 634 | PF00017 | 0.396 |
LIG_SH2_CRK | 670 | 674 | PF00017 | 0.506 |
LIG_SH2_GRB2like | 314 | 317 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 679 | 683 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 670 | 673 | PF00017 | 0.501 |
LIG_SH3_2 | 397 | 402 | PF14604 | 0.552 |
LIG_SH3_2 | 567 | 572 | PF14604 | 0.360 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.659 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.357 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.611 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.362 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.396 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.294 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.685 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 250 | 256 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 610 | 616 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 99 | 104 | PF11976 | 0.718 |
LIG_TRAF2_2 | 145 | 150 | PF00917 | 0.501 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.301 |
LIG_TYR_ITIM | 458 | 463 | PF00017 | 0.297 |
LIG_TYR_ITIM | 575 | 580 | PF00017 | 0.396 |
LIG_TYR_ITIM | 628 | 633 | PF00017 | 0.396 |
LIG_WW_3 | 81 | 85 | PF00397 | 0.580 |
MOD_CDC14_SPxK_1 | 81 | 84 | PF00782 | 0.542 |
MOD_CDK_SPxK_1 | 78 | 84 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 78 | 85 | PF00069 | 0.546 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.457 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.474 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.649 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.597 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.603 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.319 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.404 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.438 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.451 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.537 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.488 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.653 |
MOD_CK2_1 | 678 | 684 | PF00069 | 0.523 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.674 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.635 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.673 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.611 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.424 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.683 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.430 |
MOD_GlcNHglycan | 280 | 284 | PF01048 | 0.345 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.666 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.449 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.439 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.667 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.424 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.438 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.694 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.531 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.484 |
MOD_GlcNHglycan | 726 | 729 | PF01048 | 0.468 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.541 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.360 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.404 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.780 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.381 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.670 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.634 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.320 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.359 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.722 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.458 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.531 |
MOD_LATS_1 | 576 | 582 | PF00433 | 0.360 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.786 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.636 |
MOD_N-GLC_2 | 615 | 617 | PF02516 | 0.321 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.371 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.420 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.438 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.524 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.332 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.297 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.396 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.375 |
MOD_NEK2_2 | 90 | 95 | PF00069 | 0.509 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.376 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.415 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.634 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.571 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.488 |
MOD_PK_1 | 726 | 732 | PF00069 | 0.504 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.297 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.440 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.349 |
MOD_PKA_2 | 689 | 695 | PF00069 | 0.468 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.611 |
MOD_PKB_1 | 724 | 732 | PF00069 | 0.492 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.475 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.436 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.425 |
MOD_Plk_1 | 685 | 691 | PF00069 | 0.488 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.540 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.297 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.297 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.420 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.685 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.450 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.219 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.740 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.600 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.653 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.387 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.238 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.405 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.547 |
TRG_DiLeu_BaEn_2 | 261 | 267 | PF01217 | 0.389 |
TRG_DiLeu_BaEn_2 | 279 | 285 | PF01217 | 0.389 |
TRG_DiLeu_BaEn_2 | 647 | 653 | PF01217 | 0.321 |
TRG_DiLeu_BaLyEn_6 | 209 | 214 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 723 | 726 | PF00400 | 0.389 |
TRG_NLS_MonoExtN_4 | 570 | 575 | PF00514 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRI7 | Leptomonas seymouri | 51% | 98% |
A0A3R7MJ80 | Trypanosoma rangeli | 32% | 100% |
A4H8Q7 | Leishmania braziliensis | 72% | 96% |
A4HX26 | Leishmania infantum | 100% | 100% |
C9ZVX0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AQU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QEN8 | Leishmania major | 91% | 99% |
V5DJ39 | Trypanosoma cruzi | 33% | 100% |