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: A0A3S7X5M4
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 | 46 | 50 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 581 | 585 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 371 | 373 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.321 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.268 |
DEG_APCC_DBOX_1 | 583 | 591 | PF00400 | 0.269 |
DOC_CKS1_1 | 357 | 362 | PF01111 | 0.340 |
DOC_CYCLIN_RxL_1 | 553 | 564 | PF00134 | 0.263 |
DOC_CYCLIN_yCln2_LP_2 | 357 | 363 | PF00134 | 0.368 |
DOC_MAPK_gen_1 | 317 | 326 | PF00069 | 0.300 |
DOC_MAPK_RevD_3 | 300 | 313 | PF00069 | 0.316 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.342 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.512 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.453 |
DOC_USP7_MATH_2 | 396 | 402 | PF00917 | 0.282 |
DOC_USP7_UBL2_3 | 371 | 375 | PF12436 | 0.252 |
DOC_USP7_UBL2_3 | 452 | 456 | PF12436 | 0.174 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.342 |
LIG_14-3-3_CanoR_1 | 101 | 110 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 202 | 211 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 54 | 59 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 584 | 593 | PF00244 | 0.371 |
LIG_Actin_RPEL_3 | 306 | 325 | PF02755 | 0.399 |
LIG_APCC_ABBA_1 | 265 | 270 | PF00400 | 0.174 |
LIG_APCC_ABBAyCdc20_2 | 312 | 318 | PF00400 | 0.292 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.622 |
LIG_BRCT_BRCA1_1 | 629 | 633 | PF00533 | 0.341 |
LIG_BRCT_BRCA1_2 | 327 | 333 | PF00533 | 0.313 |
LIG_EH1_1 | 297 | 305 | PF00400 | 0.269 |
LIG_EH1_1 | 642 | 650 | PF00400 | 0.160 |
LIG_eIF4E_1 | 298 | 304 | PF01652 | 0.303 |
LIG_EVH1_2 | 617 | 621 | PF00568 | 0.399 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.768 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.676 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.230 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.391 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.399 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.279 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.422 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.371 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.401 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.498 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.296 |
LIG_LIR_Apic_2 | 411 | 417 | PF02991 | 0.351 |
LIG_LIR_Apic_2 | 612 | 618 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 142 | 150 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 297 | 306 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 328 | 339 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 555 | 565 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 555 | 560 | PF02991 | 0.183 |
LIG_Pex14_1 | 553 | 557 | PF04695 | 0.285 |
LIG_PTB_Apo_2 | 161 | 168 | PF02174 | 0.378 |
LIG_PTB_Phospho_1 | 161 | 167 | PF10480 | 0.372 |
LIG_SH2_CRK | 615 | 619 | PF00017 | 0.399 |
LIG_SH2_NCK_1 | 167 | 171 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 486 | 490 | PF00017 | 0.496 |
LIG_SH2_PTP2 | 128 | 131 | PF00017 | 0.499 |
LIG_SH2_PTP2 | 144 | 147 | PF00017 | 0.523 |
LIG_SH2_SRC | 472 | 475 | PF00017 | 0.213 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.214 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 486 | 490 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 619 | 623 | PF00017 | 0.348 |
LIG_SH2_STAT3 | 298 | 301 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.675 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.299 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.566 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.225 |
LIG_SH3_4 | 466 | 473 | PF00018 | 0.230 |
LIG_SUMO_SIM_anti_2 | 237 | 248 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 237 | 248 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 42 | 49 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 563 | 568 | PF11976 | 0.377 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.412 |
LIG_TRAF2_1 | 637 | 640 | PF00917 | 0.234 |
LIG_TRFH_1 | 361 | 365 | PF08558 | 0.280 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.539 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.328 |
LIG_UBA3_1 | 445 | 452 | PF00899 | 0.271 |
LIG_UBA3_1 | 586 | 591 | PF00899 | 0.289 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.721 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.434 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.312 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.449 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.295 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.381 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.641 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.423 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.324 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.331 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.362 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.493 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.341 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.269 |
MOD_Cter_Amidation | 369 | 372 | PF01082 | 0.271 |
MOD_Cter_Amidation | 373 | 376 | PF01082 | 0.242 |
MOD_Cter_Amidation | 392 | 395 | PF01082 | 0.296 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.577 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.407 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.358 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.329 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.684 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.321 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.268 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.460 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.285 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.687 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.693 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.730 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.611 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.461 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.391 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.310 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.301 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.673 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.440 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.574 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.314 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.294 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.640 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.432 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.164 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.572 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.750 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.340 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.291 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.284 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.701 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.264 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.343 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.282 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.575 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.531 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.347 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.381 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.291 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.426 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.692 |
MOD_PK_1 | 146 | 152 | PF00069 | 0.513 |
MOD_PK_1 | 43 | 49 | PF00069 | 0.417 |
MOD_PKA_1 | 456 | 462 | PF00069 | 0.309 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.552 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.301 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.554 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.286 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.427 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.167 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.257 |
MOD_Plk_2-3 | 398 | 404 | PF00069 | 0.318 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.610 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.306 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.384 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.300 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.629 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.374 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.306 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.641 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.310 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.337 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.342 |
TRG_DiLeu_BaEn_1 | 555 | 560 | PF01217 | 0.325 |
TRG_DiLeu_BaEn_4 | 78 | 84 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.301 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.286 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 530 | 534 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 556 | 561 | PF00026 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 650 | 655 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P953 | Leptomonas seymouri | 30% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 68% | 100% |
A0A0N1PD05 | Leptomonas seymouri | 33% | 100% |
A0A0S4IMB7 | Bodo saltans | 34% | 100% |
A0A0S4IRZ7 | Bodo saltans | 40% | 100% |
A0A0S4J804 | Bodo saltans | 31% | 100% |
A0A0S4JPZ1 | Bodo saltans | 28% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 28% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 47% | 100% |
A0A1X0P527 | Trypanosomatidae | 31% | 100% |
A0A1X0P549 | Trypanosomatidae | 30% | 100% |
A0A1X0P863 | Trypanosomatidae | 30% | 100% |
A0A1X0P8W3 | Trypanosomatidae | 26% | 88% |
A0A1X0P994 | Trypanosomatidae | 30% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 31% | 100% |
A0A3Q8IHH8 | Leishmania donovani | 31% | 100% |
A0A3Q8IIH5 | Leishmania donovani | 27% | 100% |
A0A3Q8IJM9 | Leishmania donovani | 30% | 100% |
A0A3R7MKG5 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X6T8 | Leishmania donovani | 34% | 100% |
A0A3S7XAL3 | Leishmania donovani | 31% | 100% |
A0A3S7XAT9 | Leishmania donovani | 31% | 100% |
A0A422NCP0 | Trypanosoma rangeli | 32% | 100% |
A0A422NH41 | Trypanosoma rangeli | 45% | 100% |
A4HHQ5 | Leishmania braziliensis | 32% | 100% |
A4HJT5 | Leishmania braziliensis | 30% | 100% |
A4HKG9 | Leishmania braziliensis | 74% | 100% |
A4HLR0 | Leishmania braziliensis | 34% | 100% |
A4HNI1 | Leishmania braziliensis | 29% | 100% |
A4HP12 | Leishmania braziliensis | 30% | 100% |
A4HP13 | Leishmania braziliensis | 30% | 100% |
A4HW88 | Leishmania infantum | 27% | 100% |
A4I4X0 | Leishmania infantum | 31% | 100% |
A4I7A1 | Leishmania infantum | 31% | 100% |
A4I7Z6 | Leishmania infantum | 100% | 100% |
A4I960 | Leishmania infantum | 34% | 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) | 30% | 100% |
D0A2Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AEB9 | Leishmania major | 32% | 100% |
E9AFZ2 | Leishmania major | 29% | 100% |
E9ALG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 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) | 31% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B745 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4Q1S3 | Leishmania major | 30% | 100% |
Q4Q1S4 | Leishmania major | 30% | 100% |
Q4Q3Y9 | Leishmania major | 32% | 85% |
Q4Q598 | Leishmania major | 93% | 100% |
Q4Q5W2 | Leishmania major | 31% | 100% |
Q4QFJ2 | Leishmania major | 27% | 100% |
Q8N5S9 | Homo sapiens | 25% | 100% |
Q8VBY2 | Mus musculus | 25% | 100% |
V5BC28 | Trypanosoma cruzi | 28% | 100% |
V5BPJ0 | Trypanosoma cruzi | 32% | 100% |
V5D7G4 | Trypanosoma cruzi | 30% | 79% |
V5DFW9 | Trypanosoma cruzi | 46% | 100% |
V5DKY9 | Trypanosoma cruzi | 28% | 100% |