Helicases, DEAD/DEAH box helicase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 3 |
Forrest at al. (metacyclic) | no | yes: 5 |
Forrest at al. (procyclic) | no | yes: 5 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 22 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0005634 | nucleus | 5 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0034399 | nuclear periphery | 2 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
Related structures:
AlphaFold database: A4ICF9
Term | Name | Level | Count |
---|---|---|---|
GO:0002183 | cytoplasmic translational initiation | 4 | 1 |
GO:0006412 | translation | 4 | 1 |
GO:0006413 | translational initiation | 3 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902775 | mitochondrial large ribosomal subunit assembly | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 24 |
GO:0003676 | nucleic acid binding | 3 | 24 |
GO:0003824 | catalytic activity | 1 | 24 |
GO:0004386 | helicase activity | 2 | 24 |
GO:0005488 | binding | 1 | 24 |
GO:0005524 | ATP binding | 5 | 24 |
GO:0017076 | purine nucleotide binding | 4 | 24 |
GO:0030554 | adenyl nucleotide binding | 5 | 24 |
GO:0032553 | ribonucleotide binding | 3 | 24 |
GO:0032555 | purine ribonucleotide binding | 4 | 24 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 24 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 24 |
GO:0036094 | small molecule binding | 2 | 24 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043168 | anion binding | 3 | 24 |
GO:0097159 | organic cyclic compound binding | 2 | 24 |
GO:0097367 | carbohydrate derivative binding | 2 | 24 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 24 |
GO:0140657 | ATP-dependent activity | 1 | 24 |
GO:1901265 | nucleoside phosphate binding | 3 | 24 |
GO:1901363 | heterocyclic compound binding | 2 | 24 |
GO:0003724 | RNA helicase activity | 3 | 9 |
GO:0003743 | translation initiation factor activity | 4 | 9 |
GO:0008135 | translation factor activity, RNA binding | 3 | 9 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 9 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0045182 | translation regulator activity | 1 | 9 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0003723 | RNA binding | 4 | 3 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.172 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.732 |
CLV_PCSK_FUR_1 | 562 | 566 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.334 |
CLV_PCSK_PC7_1 | 162 | 168 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.180 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 24 | 32 | PF00400 | 0.288 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.336 |
DEG_APCC_DBOX_1 | 373 | 381 | PF00400 | 0.452 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.446 |
DOC_CYCLIN_RxL_1 | 288 | 298 | PF00134 | 0.401 |
DOC_CYCLIN_RxL_1 | 307 | 315 | PF00134 | 0.349 |
DOC_CYCLIN_yClb1_LxF_4 | 290 | 295 | PF00134 | 0.375 |
DOC_CYCLIN_yCln2_LP_2 | 323 | 329 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 535 | 538 | PF00134 | 0.380 |
DOC_MAPK_gen_1 | 162 | 171 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 285 | 295 | PF00069 | 0.418 |
DOC_MAPK_JIP1_4 | 289 | 295 | PF00069 | 0.403 |
DOC_PP1_RVXF_1 | 290 | 296 | PF00149 | 0.371 |
DOC_PP1_RVXF_1 | 376 | 383 | PF00149 | 0.345 |
DOC_PP1_RVXF_1 | 390 | 396 | PF00149 | 0.238 |
DOC_PP1_RVXF_1 | 405 | 412 | PF00149 | 0.482 |
DOC_PP1_RVXF_1 | 467 | 474 | PF00149 | 0.395 |
DOC_PP1_SILK_1 | 21 | 26 | PF00149 | 0.309 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.403 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.342 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.453 |
DOC_PP4_FxxP_1 | 513 | 516 | PF00568 | 0.282 |
DOC_PP4_FxxP_1 | 557 | 560 | PF00568 | 0.424 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.542 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 248 | 254 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 454 | 462 | PF00244 | 0.500 |
LIG_Actin_WH2_2 | 69 | 84 | PF00022 | 0.414 |
LIG_AP2alpha_1 | 548 | 552 | PF02296 | 0.432 |
LIG_APCC_ABBA_1 | 128 | 133 | PF00400 | 0.477 |
LIG_BRCT_BRCA1_1 | 196 | 200 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.300 |
LIG_EH1_1 | 206 | 214 | PF00400 | 0.403 |
LIG_eIF4E_1 | 71 | 77 | PF01652 | 0.477 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.463 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.474 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.616 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.458 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.451 |
LIG_LIR_Apic_2 | 145 | 150 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 512 | 516 | PF02991 | 0.276 |
LIG_LIR_Apic_2 | 555 | 560 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 12 | 21 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 315 | 326 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 547 | 556 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 472 | 476 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 547 | 551 | PF02991 | 0.541 |
LIG_NRBOX | 75 | 81 | PF00104 | 0.477 |
LIG_OCRL_FandH_1 | 199 | 211 | PF00620 | 0.403 |
LIG_PCNA_PIPBox_1 | 588 | 597 | PF02747 | 0.498 |
LIG_Pex14_2 | 548 | 552 | PF04695 | 0.432 |
LIG_PTB_Apo_2 | 551 | 558 | PF02174 | 0.460 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.486 |
LIG_SH2_CRK | 482 | 486 | PF00017 | 0.451 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 482 | 486 | PF00017 | 0.451 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 528 | 531 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 543 | 546 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.441 |
LIG_SH3_2 | 560 | 565 | PF14604 | 0.511 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.470 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.513 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.522 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.520 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.696 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.449 |
LIG_SUMO_SIM_par_1 | 14 | 20 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 48 | 53 | PF11976 | 0.414 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.416 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.321 |
LIG_TYR_ITIM | 52 | 57 | PF00017 | 0.477 |
LIG_UBA3_1 | 242 | 250 | PF00899 | 0.403 |
LIG_UBA3_1 | 279 | 285 | PF00899 | 0.431 |
LIG_UBA3_1 | 76 | 82 | PF00899 | 0.477 |
LIG_WRC_WIRS_1 | 115 | 120 | PF05994 | 0.403 |
LIG_WRC_WIRS_1 | 510 | 515 | PF05994 | 0.342 |
LIG_WW_3 | 536 | 540 | PF00397 | 0.307 |
MOD_CDC14_SPxK_1 | 345 | 348 | PF00782 | 0.493 |
MOD_CDK_SPxK_1 | 342 | 348 | PF00069 | 0.492 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.415 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.403 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.562 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.424 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.451 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.420 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.405 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.409 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.465 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.440 |
MOD_DYRK1A_RPxSP_1 | 38 | 42 | PF00069 | 0.312 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.192 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.202 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.241 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.249 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.419 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.627 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.530 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.401 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.483 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.467 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.422 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.306 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.701 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.462 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.466 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.494 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.489 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.482 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.451 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.496 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.419 |
MOD_NEK2_2 | 509 | 514 | PF00069 | 0.253 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.405 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.309 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.498 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.408 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.456 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.524 |
MOD_Plk_2-3 | 483 | 489 | PF00069 | 0.422 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.403 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.427 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.411 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.490 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.493 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.310 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.394 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.406 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.405 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.435 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.493 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.640 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.285 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.544 |
TRG_DiLeu_BaEn_1 | 180 | 185 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 562 | 565 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.637 |
TRG_NLS_MonoExtN_4 | 34 | 39 | PF00514 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 201 | 206 | PF00026 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWK5 | Leptomonas seymouri | 20% | 76% |
A0A0N1I1U1 | Leptomonas seymouri | 23% | 77% |
A0A0N1I458 | Leptomonas seymouri | 73% | 100% |
A0A0N1I5R1 | Leptomonas seymouri | 20% | 75% |
A0A0N1I7N1 | Leptomonas seymouri | 24% | 96% |
A0A0S4IX79 | Bodo saltans | 24% | 82% |
A0A0S4JPF4 | Bodo saltans | 39% | 86% |
A0A1X0P7J3 | Trypanosomatidae | 56% | 86% |
A0A3Q8ID91 | Leishmania donovani | 26% | 100% |
A0A3Q8IEU7 | Leishmania donovani | 25% | 100% |
A0A3Q8IF94 | Leishmania donovani | 26% | 97% |
A0A3Q8IG57 | Leishmania donovani | 100% | 76% |
A0A3S5H4X0 | Leishmania donovani | 27% | 100% |
A1D405 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 25% | 100% |
A4HGR1 | Leishmania braziliensis | 27% | 100% |
A4HK20 | Leishmania braziliensis | 26% | 100% |
A4HPB9 | Leishmania braziliensis | 88% | 100% |
A4HRK0 | Leishmania infantum | 27% | 100% |
A4I3T6 | Leishmania infantum | 26% | 100% |
A4I7K4 | Leishmania infantum | 26% | 100% |
A4IAT7 | Leishmania infantum | 25% | 100% |
A7EML8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 25% | 100% |
B1KQF6 | Shewanella woodyi (strain ATCC 51908 / MS32) | 22% | 100% |
C9ZNU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 93% |
D0A127 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 21% | 100% |
D0A3C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 87% |
E9AEL4 | Leishmania major | 25% | 100% |
E9AJG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AT30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B5S5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
O13370 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 94% |
O62591 | Leishmania major | 27% | 100% |
Q0DB53 | Oryza sativa subsp. japonica | 26% | 99% |
Q1DMX8 | Coccidioides immitis (strain RS) | 26% | 73% |
Q1E1N5 | Coccidioides immitis (strain RS) | 25% | 100% |
Q25225 | Leishmania braziliensis | 26% | 100% |
Q2UH00 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 26% | 74% |
Q3MSQ8 | Pelophylax lessonae | 23% | 83% |
Q4I7F9 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 25% | 83% |
Q4JG17 | Penaeus vannamei | 25% | 85% |
Q4Q1G8 | Leishmania major | 95% | 100% |
Q4Q5P5 | Leishmania major | 26% | 100% |
Q4Q858 | Leishmania major | 26% | 100% |
Q4R5S7 | Macaca fascicularis | 23% | 82% |
Q4WJE9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 100% |
Q53RK8 | Oryza sativa subsp. japonica | 26% | 81% |
Q5BCU6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 76% |
Q5W5U4 | Bos taurus | 24% | 82% |
Q61496 | Mus musculus | 24% | 85% |
Q64060 | Rattus norvegicus | 23% | 84% |
Q6CXB7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 23% | 100% |
Q6GWX0 | Sus scrofa | 24% | 83% |
Q6YS30 | Oryza sativa subsp. japonica | 23% | 100% |
Q7S5R1 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 97% |
Q814I2 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 24% | 100% |
Q8TFK8 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 97% |
Q91372 | Xenopus laevis | 25% | 85% |
Q91VN6 | Mus musculus | 24% | 96% |
Q9NQI0 | Homo sapiens | 24% | 83% |
Q9UJV9 | Homo sapiens | 24% | 96% |
V5D8J9 | Trypanosoma cruzi | 57% | 93% |