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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 33 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 65 |
NetGPI | no | yes: 0, no: 65 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HKG9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 66 |
GO:0006793 | phosphorus metabolic process | 3 | 66 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 66 |
GO:0006807 | nitrogen compound metabolic process | 2 | 66 |
GO:0008152 | metabolic process | 1 | 66 |
GO:0009987 | cellular process | 1 | 66 |
GO:0016310 | phosphorylation | 5 | 66 |
GO:0019538 | protein metabolic process | 3 | 66 |
GO:0036211 | protein modification process | 4 | 66 |
GO:0043170 | macromolecule metabolic process | 3 | 66 |
GO:0043412 | macromolecule modification | 4 | 66 |
GO:0044237 | cellular metabolic process | 2 | 66 |
GO:0044238 | primary metabolic process | 2 | 66 |
GO:0071704 | organic substance metabolic process | 2 | 66 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 66 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 66 |
GO:0003824 | catalytic activity | 1 | 66 |
GO:0004672 | protein kinase activity | 3 | 66 |
GO:0005488 | binding | 1 | 66 |
GO:0005524 | ATP binding | 5 | 66 |
GO:0016301 | kinase activity | 4 | 66 |
GO:0016740 | transferase activity | 2 | 66 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 66 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 66 |
GO:0017076 | purine nucleotide binding | 4 | 66 |
GO:0030554 | adenyl nucleotide binding | 5 | 66 |
GO:0032553 | ribonucleotide binding | 3 | 66 |
GO:0032555 | purine ribonucleotide binding | 4 | 66 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 66 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 66 |
GO:0036094 | small molecule binding | 2 | 66 |
GO:0043167 | ion binding | 2 | 66 |
GO:0043168 | anion binding | 3 | 66 |
GO:0097159 | organic cyclic compound binding | 2 | 66 |
GO:0097367 | carbohydrate derivative binding | 2 | 66 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 66 |
GO:1901265 | nucleoside phosphate binding | 3 | 66 |
GO:1901363 | heterocyclic compound binding | 2 | 66 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 39 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.579 |
CLV_PCSK_FUR_1 | 581 | 585 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 371 | 373 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.372 |
CLV_PCSK_PC7_1 | 252 | 258 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.304 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.292 |
DEG_APCC_DBOX_1 | 583 | 591 | PF00400 | 0.293 |
DEG_SPOP_SBC_1 | 68 | 72 | PF00917 | 0.705 |
DOC_CKS1_1 | 357 | 362 | PF01111 | 0.364 |
DOC_CYCLIN_RxL_1 | 553 | 563 | PF00134 | 0.287 |
DOC_CYCLIN_yCln2_LP_2 | 357 | 363 | PF00134 | 0.392 |
DOC_MAPK_gen_1 | 317 | 326 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 581 | 589 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 581 | 589 | PF00069 | 0.334 |
DOC_MAPK_RevD_3 | 300 | 313 | PF00069 | 0.340 |
DOC_PP1_RVXF_1 | 499 | 505 | PF00149 | 0.279 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.366 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.520 |
DOC_PP4_FxxP_1 | 633 | 636 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.731 |
DOC_USP7_MATH_2 | 396 | 402 | PF00917 | 0.307 |
DOC_USP7_UBL2_3 | 28 | 32 | PF12436 | 0.445 |
DOC_USP7_UBL2_3 | 371 | 375 | PF12436 | 0.276 |
DOC_USP7_UBL2_3 | 452 | 456 | PF12436 | 0.199 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 202 | 211 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 529 | 538 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 584 | 590 | PF00244 | 0.395 |
LIG_Actin_RPEL_3 | 306 | 325 | PF02755 | 0.423 |
LIG_Actin_WH2_2 | 242 | 258 | PF00022 | 0.167 |
LIG_APCC_ABBA_1 | 265 | 270 | PF00400 | 0.199 |
LIG_APCC_ABBAyCdc20_2 | 312 | 318 | PF00400 | 0.316 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 629 | 633 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_2 | 327 | 333 | PF00533 | 0.337 |
LIG_Clathr_ClatBox_1 | 473 | 477 | PF01394 | 0.348 |
LIG_EH1_1 | 297 | 305 | PF00400 | 0.293 |
LIG_eIF4E_1 | 298 | 304 | PF01652 | 0.327 |
LIG_EVH1_2 | 617 | 621 | PF00568 | 0.423 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.832 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.415 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.303 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.468 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.738 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.564 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.546 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.367 |
LIG_Integrin_isoDGR_2 | 120 | 122 | PF01839 | 0.432 |
LIG_Integrin_RGD_1 | 252 | 254 | PF01839 | 0.172 |
LIG_Integrin_RGD_1 | 61 | 63 | PF01839 | 0.463 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 411 | 417 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 612 | 618 | PF02991 | 0.356 |
LIG_LIR_Apic_2 | 630 | 636 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 142 | 150 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 157 | 167 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 297 | 306 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 328 | 339 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 555 | 565 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 642 | 652 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 555 | 560 | PF02991 | 0.207 |
LIG_LIR_Nem_3 | 642 | 647 | PF02991 | 0.419 |
LIG_LYPXL_SIV_4 | 23 | 31 | PF13949 | 0.451 |
LIG_MAD2 | 408 | 416 | PF02301 | 0.237 |
LIG_Pex14_1 | 553 | 557 | PF04695 | 0.319 |
LIG_PTB_Apo_2 | 161 | 168 | PF02174 | 0.391 |
LIG_PTB_Phospho_1 | 161 | 167 | PF10480 | 0.384 |
LIG_SH2_CRK | 615 | 619 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 167 | 171 | PF00017 | 0.537 |
LIG_SH2_PTP2 | 144 | 147 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 619 | 623 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 298 | 301 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.334 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.553 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.237 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.613 |
LIG_SUMO_SIM_par_1 | 237 | 248 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 563 | 568 | PF11976 | 0.402 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.436 |
LIG_TRAF2_1 | 637 | 640 | PF00917 | 0.258 |
LIG_TRFH_1 | 361 | 365 | PF08558 | 0.305 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.575 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.352 |
LIG_UBA3_1 | 445 | 452 | PF00899 | 0.294 |
MOD_CDC14_SPxK_1 | 453 | 456 | PF00782 | 0.167 |
MOD_CDC14_SPxK_1 | 92 | 95 | PF00782 | 0.480 |
MOD_CDK_SPxK_1 | 450 | 456 | PF00069 | 0.167 |
MOD_CDK_SPxK_1 | 89 | 95 | PF00069 | 0.480 |
MOD_CDK_SPxxK_3 | 450 | 457 | PF00069 | 0.473 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.739 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.336 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.468 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.555 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.352 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.417 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.679 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.268 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.423 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.348 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.355 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.386 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.555 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.366 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.383 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.293 |
MOD_Cter_Amidation | 369 | 372 | PF01082 | 0.290 |
MOD_Cter_Amidation | 373 | 376 | PF01082 | 0.266 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.582 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.545 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.381 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.345 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.671 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.272 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.699 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.402 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.523 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.329 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.725 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.326 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.323 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.459 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.641 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.608 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.333 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.329 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.610 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.548 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.697 |
MOD_LATS_1 | 602 | 608 | PF00433 | 0.168 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.451 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.182 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.364 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.260 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.315 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.307 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.208 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.331 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.748 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.439 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.294 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.377 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.308 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.594 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.531 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.213 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.315 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.335 |
MOD_PK_1 | 146 | 152 | PF00069 | 0.543 |
MOD_PKA_1 | 456 | 462 | PF00069 | 0.333 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.293 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.167 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.319 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.595 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.629 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.434 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.281 |
MOD_Plk_2-3 | 398 | 404 | PF00069 | 0.342 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.391 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.312 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.325 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.390 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.392 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.372 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.331 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.330 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.543 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.631 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.334 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.314 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.361 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.581 |
MOD_SUMO_rev_2 | 25 | 33 | PF00179 | 0.450 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.325 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.318 |
TRG_NES_CRM1_1 | 643 | 655 | PF08389 | 0.243 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 530 | 534 | PF00026 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 556 | 561 | PF00026 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 650 | 655 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P953 | Leptomonas seymouri | 30% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 68% | 100% |
A0A0N1PD05 | Leptomonas seymouri | 34% | 100% |
A0A0S4IMB7 | Bodo saltans | 34% | 100% |
A0A0S4IRZ7 | Bodo saltans | 39% | 100% |
A0A0S4J804 | Bodo saltans | 30% | 100% |
A0A0S4JPZ1 | Bodo saltans | 28% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 28% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 47% | 100% |
A0A1X0P527 | Trypanosomatidae | 32% | 100% |
A0A1X0P549 | Trypanosomatidae | 30% | 100% |
A0A1X0P863 | Trypanosomatidae | 29% | 100% |
A0A1X0P8W3 | Trypanosomatidae | 24% | 88% |
A0A1X0P994 | Trypanosomatidae | 29% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 26% | 100% |
A0A3Q8IHH8 | Leishmania donovani | 33% | 100% |
A0A3Q8IIH5 | Leishmania donovani | 27% | 100% |
A0A3Q8IJM9 | Leishmania donovani | 30% | 100% |
A0A3R7MKG5 | Trypanosoma rangeli | 28% | 100% |
A0A3S7X5M4 | Leishmania donovani | 74% | 100% |
A0A3S7X6T8 | Leishmania donovani | 32% | 100% |
A0A3S7XAL3 | Leishmania donovani | 30% | 100% |
A0A3S7XAT9 | Leishmania donovani | 31% | 100% |
A0A422NCP0 | Trypanosoma rangeli | 30% | 100% |
A0A422NH41 | Trypanosoma rangeli | 46% | 100% |
A4HHQ5 | Leishmania braziliensis | 34% | 100% |
A4HJT5 | Leishmania braziliensis | 27% | 85% |
A4HLR0 | Leishmania braziliensis | 32% | 100% |
A4HNI1 | Leishmania braziliensis | 29% | 100% |
A4HP12 | Leishmania braziliensis | 30% | 100% |
A4HP13 | Leishmania braziliensis | 29% | 100% |
A4HW88 | Leishmania infantum | 27% | 100% |
A4I4X0 | Leishmania infantum | 33% | 100% |
A4I7A1 | Leishmania infantum | 26% | 100% |
A4I7Z6 | Leishmania infantum | 74% | 100% |
A4I960 | Leishmania infantum | 32% | 100% |
A4IC37 | Leishmania infantum | 29% | 100% |
A4IDC1 | Leishmania infantum | 30% | 100% |
A4IDC2 | Leishmania infantum | 31% | 100% |
C9ZMH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZWK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A2Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0A2Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AEB9 | Leishmania major | 33% | 100% |
E9AFZ2 | Leishmania major | 30% | 100% |
E9ALG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9ASS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ASS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B745 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q1S3 | Leishmania major | 29% | 98% |
Q4Q1S4 | Leishmania major | 30% | 100% |
Q4Q3Y9 | Leishmania major | 32% | 85% |
Q4Q598 | Leishmania major | 72% | 100% |
Q4Q5W2 | Leishmania major | 26% | 81% |
Q4QFJ2 | Leishmania major | 27% | 100% |
V5BC28 | Trypanosoma cruzi | 28% | 100% |
V5BPJ0 | Trypanosoma cruzi | 31% | 100% |
V5D7G4 | Trypanosoma cruzi | 31% | 79% |
V5DFW9 | Trypanosoma cruzi | 46% | 100% |
V5DKY9 | Trypanosoma cruzi | 25% | 100% |