Protein kinase, serine/threonine- 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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
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 | 1 |
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: A4I649
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0000245 | spliceosomal complex assembly | 7 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0050684 | regulation of mRNA processing | 7 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 371 | 375 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 587 | 591 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 695 | 699 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.405 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.718 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.704 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.229 |
DEG_SCF_FBW7_1 | 298 | 305 | PF00400 | 0.308 |
DOC_ANK_TNKS_1 | 107 | 114 | PF00023 | 0.617 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.308 |
DOC_CKS1_1 | 429 | 434 | PF01111 | 0.207 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.276 |
DOC_MAPK_gen_1 | 416 | 425 | PF00069 | 0.215 |
DOC_MAPK_HePTP_8 | 413 | 425 | PF00069 | 0.215 |
DOC_MAPK_MEF2A_6 | 416 | 425 | PF00069 | 0.215 |
DOC_PP1_RVXF_1 | 163 | 170 | PF00149 | 0.215 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.621 |
DOC_PP4_FxxP_1 | 313 | 316 | PF00568 | 0.431 |
DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.215 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.564 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.584 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.622 |
DOC_USP7_UBL2_3 | 330 | 334 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 342 | 346 | PF12436 | 0.378 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.592 |
DOC_USP7_UBL2_3 | 519 | 523 | PF12436 | 0.228 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.468 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.274 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.217 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.377 |
LIG_14-3-3_CanoR_1 | 321 | 329 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 349 | 353 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 671 | 680 | PF00244 | 0.482 |
LIG_APCC_ABBA_1 | 244 | 249 | PF00400 | 0.229 |
LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.623 |
LIG_Clathr_ClatBox_1 | 276 | 280 | PF01394 | 0.229 |
LIG_CtBP_PxDLS_1 | 478 | 482 | PF00389 | 0.229 |
LIG_deltaCOP1_diTrp_1 | 383 | 391 | PF00928 | 0.516 |
LIG_deltaCOP1_diTrp_1 | 434 | 443 | PF00928 | 0.265 |
LIG_EH1_1 | 303 | 311 | PF00400 | 0.354 |
LIG_eIF4E_1 | 203 | 209 | PF01652 | 0.215 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.215 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.469 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.215 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.541 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.567 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.423 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.609 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.479 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.217 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.648 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.458 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.351 |
LIG_FHA_2 | 733 | 739 | PF00498 | 0.608 |
LIG_Integrin_RGD_1 | 363 | 365 | PF01839 | 0.612 |
LIG_LIR_Apic_2 | 415 | 421 | PF02991 | 0.215 |
LIG_LIR_Apic_2 | 427 | 432 | PF02991 | 0.215 |
LIG_LIR_Apic_2 | 530 | 534 | PF02991 | 0.229 |
LIG_LIR_Gen_1 | 184 | 191 | PF02991 | 0.229 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.185 |
LIG_LIR_Gen_1 | 389 | 399 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.159 |
LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.354 |
LIG_MAD2 | 716 | 724 | PF02301 | 0.508 |
LIG_MYND_3 | 533 | 537 | PF01753 | 0.207 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.215 |
LIG_PTB_Apo_2 | 155 | 162 | PF02174 | 0.369 |
LIG_PTB_Apo_2 | 631 | 638 | PF02174 | 0.487 |
LIG_PTB_Phospho_1 | 155 | 161 | PF10480 | 0.374 |
LIG_PTB_Phospho_1 | 631 | 637 | PF10480 | 0.493 |
LIG_Rb_pABgroove_1 | 238 | 246 | PF01858 | 0.276 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.281 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.215 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.371 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.207 |
LIG_SH2_CRK | 564 | 568 | PF00017 | 0.462 |
LIG_SH2_GRB2like | 492 | 495 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.229 |
LIG_SH2_NCK_1 | 598 | 602 | PF00017 | 0.662 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.215 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.215 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.468 |
LIG_SUMO_SIM_anti_2 | 284 | 291 | PF11976 | 0.229 |
LIG_SUMO_SIM_anti_2 | 305 | 311 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 463 | 472 | PF11976 | 0.215 |
LIG_SUMO_SIM_par_1 | 249 | 256 | PF11976 | 0.215 |
LIG_SUMO_SIM_par_1 | 430 | 437 | PF11976 | 0.207 |
LIG_TRAF2_1 | 345 | 348 | PF00917 | 0.518 |
LIG_TRAF2_1 | 582 | 585 | PF00917 | 0.616 |
LIG_TRAF2_1 | 736 | 739 | PF00917 | 0.580 |
LIG_TYR_ITIM | 505 | 510 | PF00017 | 0.360 |
LIG_UBA3_1 | 306 | 311 | PF00899 | 0.329 |
MOD_CDK_SPK_2 | 298 | 303 | PF00069 | 0.229 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.360 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.447 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.514 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.638 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.215 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.612 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.683 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.508 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.662 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.474 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.360 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.232 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.514 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.253 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.510 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.594 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.489 |
MOD_CK2_1 | 732 | 738 | PF00069 | 0.605 |
MOD_CMANNOS | 176 | 179 | PF00535 | 0.215 |
MOD_Cter_Amidation | 68 | 71 | PF01082 | 0.495 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.215 |
MOD_GlcNHglycan | 571 | 576 | PF01048 | 0.558 |
MOD_GlcNHglycan | 577 | 582 | PF01048 | 0.603 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.638 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.669 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.693 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.343 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.558 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.469 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.630 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.628 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.601 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.514 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.673 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.278 |
MOD_N-GLC_1 | 633 | 638 | PF02516 | 0.484 |
MOD_N-GLC_2 | 220 | 222 | PF02516 | 0.340 |
MOD_N-GLC_2 | 401 | 403 | PF02516 | 0.215 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.690 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.253 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.394 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.215 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.484 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.536 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.409 |
MOD_PIKK_1 | 592 | 598 | PF00454 | 0.567 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.715 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.724 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.623 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.522 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.630 |
MOD_Plk_1 | 633 | 639 | PF00069 | 0.439 |
MOD_Plk_2-3 | 586 | 592 | PF00069 | 0.766 |
MOD_Plk_2-3 | 733 | 739 | PF00069 | 0.706 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.215 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.231 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.376 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.460 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.514 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.274 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.217 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.377 |
MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.215 |
MOD_SUMO_for_1 | 345 | 348 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 199 | 209 | PF00179 | 0.233 |
MOD_SUMO_rev_2 | 286 | 294 | PF00179 | 0.229 |
MOD_SUMO_rev_2 | 326 | 332 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 347 | 352 | PF00179 | 0.453 |
MOD_SUMO_rev_2 | 355 | 362 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 55 | 63 | PF00179 | 0.598 |
TRG_DiLeu_BaEn_1 | 348 | 353 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_1 | 668 | 673 | PF01217 | 0.379 |
TRG_DiLeu_BaEn_2 | 526 | 532 | PF01217 | 0.229 |
TRG_DiLeu_BaEn_4 | 628 | 634 | PF01217 | 0.497 |
TRG_DiLeu_BaEn_4 | 675 | 681 | PF01217 | 0.593 |
TRG_DiLeu_LyEn_5 | 668 | 673 | PF01217 | 0.423 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.215 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.148 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.443 |
TRG_NLS_Bipartite_1 | 16 | 30 | PF00514 | 0.636 |
TRG_NLS_MonoExtC_3 | 24 | 29 | PF00514 | 0.619 |
TRG_NLS_MonoExtC_3 | 521 | 526 | PF00514 | 0.273 |
TRG_NLS_MonoExtC_3 | 66 | 71 | PF00514 | 0.613 |
TRG_NLS_MonoExtN_4 | 23 | 30 | PF00514 | 0.621 |
TRG_NLS_MonoExtN_4 | 519 | 526 | PF00514 | 0.273 |
TRG_NLS_MonoExtN_4 | 65 | 71 | PF00514 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.229 |
TRG_Pf-PMV_PEXEL_1 | 500 | 504 | PF00026 | 0.229 |
TRG_Pf-PMV_PEXEL_1 | 671 | 675 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1H8 | Leptomonas seymouri | 82% | 100% |
A0A0S4JMD1 | Bodo saltans | 55% | 97% |
A0A1X0P1B0 | Trypanosomatidae | 60% | 100% |
A0A3R7KF70 | Trypanosoma rangeli | 58% | 100% |
A0A3S7X404 | Leishmania donovani | 99% | 100% |
A4HIU4 | Leishmania braziliensis | 83% | 100% |
C9ZRG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9B1D2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q6T0 | Leishmania major | 94% | 100% |
V5B752 | Trypanosoma cruzi | 63% | 100% |