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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4Q5U4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 9 |
GO:0006644 | phospholipid metabolic process | 4 | 9 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 9 |
GO:0006656 | phosphatidylcholine biosynthetic process | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008610 | lipid biosynthetic process | 4 | 9 |
GO:0008654 | phospholipid biosynthetic process | 5 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0019637 | organophosphate metabolic process | 3 | 9 |
GO:0032259 | methylation | 2 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 9 |
GO:0044255 | cellular lipid metabolic process | 3 | 9 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 9 |
GO:0046470 | phosphatidylcholine metabolic process | 4 | 9 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 9 |
GO:0046486 | glycerolipid metabolic process | 4 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090407 | organophosphate biosynthetic process | 4 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004608 | phosphatidylethanolamine N-methyltransferase activity | 6 | 6 |
GO:0008168 | methyltransferase activity | 4 | 9 |
GO:0008170 | N-methyltransferase activity | 5 | 6 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 6 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 401 | 403 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.418 |
DOC_CKS1_1 | 44 | 49 | PF01111 | 0.639 |
DOC_CYCLIN_RxL_1 | 122 | 131 | PF00134 | 0.567 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 408 | 417 | PF00134 | 0.409 |
DOC_CYCLIN_yCln2_LP_2 | 183 | 189 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 349 | 355 | PF00134 | 0.366 |
DOC_MAPK_gen_1 | 31 | 40 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 332 | 340 | PF00069 | 0.495 |
DOC_PIKK_1 | 159 | 167 | PF02985 | 0.555 |
DOC_PP1_RVXF_1 | 227 | 234 | PF00149 | 0.272 |
DOC_PP2B_LxvP_1 | 349 | 352 | PF13499 | 0.366 |
DOC_PP4_FxxP_1 | 240 | 243 | PF00568 | 0.272 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.527 |
DOC_SPAK_OSR1_1 | 31 | 35 | PF12202 | 0.544 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.440 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.361 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 332 | 340 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.552 |
LIG_AP2alpha_1 | 145 | 149 | PF02296 | 0.500 |
LIG_APCC_ABBA_1 | 324 | 329 | PF00400 | 0.523 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.409 |
LIG_Clathr_ClatBox_1 | 325 | 329 | PF01394 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 215 | 225 | PF00928 | 0.272 |
LIG_eIF4E_1 | 344 | 350 | PF01652 | 0.406 |
LIG_eIF4E_1 | 501 | 507 | PF01652 | 0.328 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.591 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.472 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.409 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.555 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.436 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.336 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.739 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.592 |
LIG_GBD_Chelix_1 | 338 | 346 | PF00786 | 0.409 |
LIG_LIR_Apic_2 | 30 | 35 | PF02991 | 0.538 |
LIG_LIR_Apic_2 | 387 | 393 | PF02991 | 0.589 |
LIG_LIR_Apic_2 | 424 | 428 | PF02991 | 0.506 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 109 | 118 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 188 | 197 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 261 | 270 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.488 |
LIG_LIR_LC3C_4 | 321 | 324 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 454 | 458 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 463 | 467 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.388 |
LIG_NRBOX | 345 | 351 | PF00104 | 0.376 |
LIG_NRBOX | 372 | 378 | PF00104 | 0.463 |
LIG_Pex14_1 | 220 | 224 | PF04695 | 0.272 |
LIG_Pex14_1 | 400 | 404 | PF04695 | 0.498 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.328 |
LIG_Pex14_2 | 145 | 149 | PF04695 | 0.500 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.284 |
LIG_Pex14_2 | 216 | 220 | PF04695 | 0.330 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.272 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.370 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.475 |
LIG_Pex14_2 | 82 | 86 | PF04695 | 0.343 |
LIG_PTB_Apo_2 | 409 | 416 | PF02174 | 0.328 |
LIG_PTB_Phospho_1 | 409 | 415 | PF10480 | 0.328 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.601 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.540 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.560 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.272 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.328 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.652 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.511 |
LIG_SH2_CRK | 482 | 486 | PF00017 | 0.472 |
LIG_SH2_GRB2like | 488 | 491 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 458 | 462 | PF00017 | 0.480 |
LIG_SH2_SRC | 316 | 319 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.272 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 565 | 569 | PF00017 | 0.550 |
LIG_SH2_STAT3 | 540 | 543 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.346 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.472 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.472 |
LIG_SUMO_SIM_anti_2 | 321 | 327 | PF11976 | 0.534 |
LIG_SUMO_SIM_anti_2 | 510 | 516 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 334 | 341 | PF11976 | 0.372 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.584 |
LIG_TYR_ITIM | 168 | 173 | PF00017 | 0.511 |
LIG_TYR_ITIM | 264 | 269 | PF00017 | 0.328 |
LIG_TYR_ITIM | 480 | 485 | PF00017 | 0.472 |
LIG_WRC_WIRS_1 | 107 | 112 | PF05994 | 0.539 |
MOD_CDK_SPK_2 | 43 | 48 | PF00069 | 0.643 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.691 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.530 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.700 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.636 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.534 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.744 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.632 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.401 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.383 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.602 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.230 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.484 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.643 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.296 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.321 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.297 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.686 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.537 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.318 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.472 |
MOD_LATS_1 | 104 | 110 | PF00433 | 0.606 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.569 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.334 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.313 |
MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.288 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.688 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.510 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.328 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.328 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.409 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.381 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.474 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.239 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.646 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.366 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.582 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.496 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.607 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.507 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.337 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.472 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.334 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.283 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.459 |
MOD_Plk_2-3 | 36 | 42 | PF00069 | 0.633 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.534 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.542 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.503 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.328 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.385 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.332 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.561 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.403 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.486 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.496 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.641 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.585 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.590 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.361 |
MOD_SUMO_for_1 | 377 | 380 | PF00179 | 0.556 |
MOD_SUMO_for_1 | 574 | 577 | PF00179 | 0.627 |
MOD_SUMO_rev_2 | 136 | 143 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 561 | 569 | PF00179 | 0.610 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.574 |
TRG_DiLeu_BaEn_1 | 318 | 323 | PF01217 | 0.576 |
TRG_DiLeu_BaEn_2 | 433 | 439 | PF01217 | 0.296 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 536 | 539 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.588 |
TRG_NLS_MonoExtN_4 | 534 | 541 | PF00514 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1S1 | Leptomonas seymouri | 79% | 100% |
A0A0S4ITN2 | Bodo saltans | 53% | 100% |
A0A1X0NK27 | Trypanosomatidae | 59% | 97% |
A0A3Q8IF60 | Leishmania donovani | 97% | 100% |
A3LQW6 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 30% | 68% |
A4HJV7 | Leishmania braziliensis | 86% | 100% |
A4I7B9 | Leishmania infantum | 97% | 100% |
A5DL79 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 31% | 67% |
A6ZUG8 | Saccharomyces cerevisiae (strain YJM789) | 30% | 67% |
A7TLA7 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 33% | 69% |
A7TNI7 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 33% | 69% |
B3LI73 | Saccharomyces cerevisiae (strain RM11-1a) | 30% | 67% |
B5VJA0 | Saccharomyces cerevisiae (strain AWRI1631) | 30% | 67% |
C4Y206 | Clavispora lusitaniae (strain ATCC 42720) | 30% | 68% |
C5DGB6 | Lachancea thermotolerans (strain ATCC 56472 / CBS 6340 / NRRL Y-8284) | 34% | 69% |
C5DZU3 | Zygosaccharomyces rouxii (strain ATCC 2623 / CBS 732 / NBRC 1130 / NCYC 568 / NRRL Y-229) | 31% | 70% |
C5M4D4 | Candida tropicalis (strain ATCC MYA-3404 / T1) | 30% | 67% |
C7GQ65 | Saccharomyces cerevisiae (strain JAY291) | 30% | 67% |
C8Z951 | Saccharomyces cerevisiae (strain Lalvin EC1118 / Prise de mousse) | 30% | 67% |
E9B2B2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P05374 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 67% |
Q6BY28 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 31% | 67% |
Q6CJI9 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 69% |
Q6FVB6 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 32% | 68% |
Q754G0 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 32% | 69% |