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:0005737 | cytoplasm | 2 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q2S8
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003958 | NADPH-hemoprotein reductase activity | 5 | 8 |
GO:0005488 | binding | 1 | 12 |
GO:0010181 | FMN binding | 4 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016651 | oxidoreductase activity, acting on NAD(P)H | 3 | 8 |
GO:0016653 | oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor | 4 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 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 | 130 | 134 | PF00656 | 0.322 |
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 250 | 254 | PF00656 | 0.234 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.427 |
CLV_PCSK_FUR_1 | 364 | 368 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.412 |
DEG_APCC_DBOX_1 | 342 | 350 | PF00400 | 0.318 |
DEG_APCC_DBOX_1 | 476 | 484 | PF00400 | 0.427 |
DEG_SCF_FBW7_1 | 191 | 197 | PF00400 | 0.508 |
DEG_SCF_FBW7_1 | 281 | 288 | PF00400 | 0.364 |
DOC_CDC14_PxL_1 | 521 | 529 | PF14671 | 0.415 |
DOC_CKS1_1 | 191 | 196 | PF01111 | 0.512 |
DOC_CKS1_1 | 282 | 287 | PF01111 | 0.454 |
DOC_CKS1_1 | 389 | 394 | PF01111 | 0.395 |
DOC_CKS1_1 | 421 | 426 | PF01111 | 0.307 |
DOC_CKS1_1 | 458 | 463 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 297 | 308 | PF00134 | 0.427 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 366 | 373 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 455 | 461 | PF00134 | 0.469 |
DOC_MAPK_DCC_7 | 519 | 529 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 271 | 282 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 377 | 385 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 411 | 418 | PF00069 | 0.454 |
DOC_PP2B_LxvP_1 | 455 | 458 | PF13499 | 0.397 |
DOC_PP4_FxxP_1 | 300 | 303 | PF00568 | 0.364 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.364 |
DOC_PP4_FxxP_1 | 557 | 560 | PF00568 | 0.427 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.460 |
DOC_USP7_UBL2_3 | 577 | 581 | PF12436 | 0.364 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.322 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.367 |
LIG_14-3-3_CanoR_1 | 221 | 231 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 302 | 307 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 552 | 558 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 71 | 75 | PF00244 | 0.307 |
LIG_Actin_WH2_2 | 514 | 530 | PF00022 | 0.337 |
LIG_BIR_III_4 | 133 | 137 | PF00653 | 0.322 |
LIG_BIR_III_4 | 253 | 257 | PF00653 | 0.322 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.343 |
LIG_DLG_GKlike_1 | 302 | 309 | PF00625 | 0.454 |
LIG_FAT_LD_1 | 266 | 274 | PF03623 | 0.427 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.376 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.376 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.369 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.364 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.444 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.493 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.470 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.376 |
LIG_GBD_Chelix_1 | 265 | 273 | PF00786 | 0.415 |
LIG_LIR_Apic_2 | 388 | 392 | PF02991 | 0.364 |
LIG_LIR_Apic_2 | 420 | 424 | PF02991 | 0.324 |
LIG_LIR_Apic_2 | 554 | 560 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 147 | 155 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 321 | 332 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 488 | 499 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 513 | 523 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 98 | 108 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 513 | 518 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.314 |
LIG_NRBOX | 305 | 311 | PF00104 | 0.392 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.540 |
LIG_REV1ctd_RIR_1 | 297 | 302 | PF16727 | 0.322 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.454 |
LIG_SH2_STAT3 | 8 | 11 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.345 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.624 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.536 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.684 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.568 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.390 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.395 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.354 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.400 |
LIG_SUMO_SIM_anti_2 | 2 | 8 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 382 | 388 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 279 | 284 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 302 | 308 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 53 | 59 | PF11976 | 0.344 |
LIG_WRC_WIRS_1 | 386 | 391 | PF05994 | 0.341 |
MOD_CDK_SPxK_1 | 420 | 426 | PF00069 | 0.322 |
MOD_CDK_SPxxK_3 | 420 | 427 | PF00069 | 0.307 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.508 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.391 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.429 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.349 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.276 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.423 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.412 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.444 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.463 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.535 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.679 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.454 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.367 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.661 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.360 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.351 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.300 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.279 |
MOD_LATS_1 | 550 | 556 | PF00433 | 0.427 |
MOD_N-GLC_2 | 368 | 370 | PF02516 | 0.427 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.294 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.348 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.349 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.427 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.414 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.322 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.373 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.392 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.403 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.337 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.310 |
MOD_PK_1 | 396 | 402 | PF00069 | 0.322 |
MOD_PKA_1 | 221 | 227 | PF00069 | 0.392 |
MOD_PKA_1 | 503 | 509 | PF00069 | 0.220 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.341 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.422 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.396 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.220 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.465 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.297 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.307 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.323 |
MOD_Plk_1 | 591 | 597 | PF00069 | 0.566 |
MOD_Plk_2-3 | 514 | 520 | PF00069 | 0.376 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.391 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.415 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.354 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.388 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.421 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.351 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.322 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.392 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.660 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.643 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.364 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.322 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.392 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.362 |
MOD_SUMO_rev_2 | 130 | 137 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 371 | 379 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 534 | 541 | PF00179 | 0.360 |
TRG_DiLeu_BaEn_4 | 513 | 519 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.220 |
TRG_DiLeu_BaLyEn_6 | 460 | 465 | PF01217 | 0.360 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.220 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.427 |
TRG_NES_CRM1_1 | 16 | 29 | PF08389 | 0.407 |
TRG_NLS_MonoExtN_4 | 424 | 430 | PF00514 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 271 | 276 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.376 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7X2 | Leptomonas seymouri | 25% | 97% |
A0A0N1I491 | Leptomonas seymouri | 70% | 99% |
A0A0S4KLI2 | Bodo saltans | 34% | 100% |
A0A1X0NZ83 | Trypanosomatidae | 27% | 99% |
A0A1X0P5U2 | Trypanosomatidae | 24% | 90% |
A0A1X0P9S6 | Trypanosomatidae | 45% | 100% |
A0A2U1KZS6 | Artemisia annua | 30% | 88% |
A0A2U1LIM9 | Artemisia annua | 28% | 89% |
A0A3R7K908 | Trypanosoma rangeli | 25% | 87% |
A0A3S7X1H9 | Leishmania donovani | 27% | 97% |
A0A3S7X872 | Leishmania donovani | 95% | 100% |
A0A422N1R6 | Trypanosoma rangeli | 26% | 96% |
A0A422NS70 | Trypanosoma rangeli | 48% | 100% |
A0KTH4 | Shewanella sp. (strain ANA-3) | 28% | 100% |
A1AEV0 | Escherichia coli O1:K1 / APEC | 27% | 100% |
A1JJS2 | Yersinia enterocolitica serotype O:8 / biotype 1B (strain NCTC 13174 / 8081) | 28% | 100% |
A1KU06 | Neisseria meningitidis serogroup C / serotype 2a (strain ATCC 700532 / DSM 15464 / FAM18) | 26% | 100% |
A2AI05 | Mus musculus | 30% | 100% |
A2QS05 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 90% |
A4HAY4 | Leishmania braziliensis | 86% | 100% |
A4HGH1 | Leishmania braziliensis | 26% | 96% |
A4HMS7 | Leishmania braziliensis | 23% | 75% |
A4I3K3 | Leishmania infantum | 27% | 97% |
A4IA43 | Leishmania infantum | 95% | 100% |
A4TPY5 | Yersinia pestis (strain Pestoides F) | 26% | 100% |
A4WDW1 | Enterobacter sp. (strain 638) | 27% | 100% |
A5F3I4 | Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) | 29% | 100% |
A6TD49 | Klebsiella pneumoniae subsp. pneumoniae (strain ATCC 700721 / MGH 78578) | 27% | 100% |
A7FLZ0 | Yersinia pseudotuberculosis serotype O:1b (strain IP 31758) | 26% | 100% |
A7MJ63 | Cronobacter sakazakii (strain ATCC BAA-894) | 28% | 100% |
A7ZQK7 | Escherichia coli O139:H28 (strain E24377A / ETEC) | 27% | 100% |
A8A3P5 | Escherichia coli O9:H4 (strain HS) | 28% | 100% |
A8ANX1 | Citrobacter koseri (strain ATCC BAA-895 / CDC 4225-83 / SGSC4696) | 27% | 100% |
A8G9X6 | Serratia proteamaculans (strain 568) | 28% | 100% |
A9LZ73 | Neisseria meningitidis serogroup C (strain 053442) | 27% | 100% |
A9MF16 | Salmonella arizonae (strain ATCC BAA-731 / CDC346-86 / RSK2980) | 28% | 100% |
A9N2E6 | Salmonella paratyphi B (strain ATCC BAA-1250 / SPB7) | 27% | 100% |
B1IU77 | Escherichia coli (strain ATCC 8739 / DSM 1576 / NBRC 3972 / NCIMB 8545 / WDCM 00012 / Crooks) | 27% | 100% |
C5YJG8 | Sorghum bicolor | 32% | 88% |
C9ZM57 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZZA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 90% |
D0A7U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 99% |
D0A835 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 98% |
E9AZU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 97% |
E9B557 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B6D5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 75% |
O32214 | Bacillus subtilis (strain 168) | 30% | 100% |
O94613 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
P00388 | Rattus norvegicus | 30% | 92% |
P00389 | Oryctolagus cuniculus | 30% | 92% |
P04175 | Sus scrofa | 30% | 92% |
P0CP12 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 30% | 100% |
P0CP13 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 30% | 100% |
P16435 | Homo sapiens | 31% | 92% |
P16603 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 90% |
P19618 | Salmo trutta | 26% | 100% |
P36587 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 92% |
P37039 | Cavia porcellus | 30% | 92% |
P37040 | Mus musculus | 30% | 92% |
P37116 | Vigna radiata var. radiata | 28% | 90% |
P37201 | Candida tropicalis | 23% | 92% |
P38038 | Escherichia coli (strain K12) | 27% | 100% |
P38039 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 27% | 100% |
P50126 | Candida maltosa | 24% | 92% |
P57503 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 23% | 100% |
Q00141 | Aspergillus niger | 26% | 90% |
Q05001 | Catharanthus roseus | 30% | 87% |
Q07994 | Musca domestica | 26% | 93% |
Q0CMM0 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 26% | 90% |
Q0HFL6 | Shewanella sp. (strain MR-4) | 27% | 100% |
Q0HYB4 | Shewanella sp. (strain MR-7) | 27% | 100% |
Q0J705 | Oryza sativa subsp. japonica | 30% | 87% |
Q0T1I8 | Shigella flexneri serotype 5b (strain 8401) | 28% | 100% |
Q0TEA2 | Escherichia coli O6:K15:H31 (strain 536 / UPEC) | 27% | 100% |
Q12181 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
Q17574 | Caenorhabditis elegans | 24% | 91% |
Q1C3Z0 | Yersinia pestis bv. Antiqua (strain Antiqua) | 26% | 100% |
Q1CLS8 | Yersinia pestis bv. Antiqua (strain Nepal516) | 26% | 100% |
Q1JPJ0 | Bos taurus | 30% | 100% |
Q1LTP1 | Baumannia cicadellinicola subsp. Homalodisca coagulata | 25% | 100% |
Q1R7T4 | Escherichia coli (strain UTI89 / UPEC) | 27% | 100% |
Q27597 | Drosophila melanogaster | 27% | 92% |
Q2NVN4 | Sodalis glossinidius (strain morsitans) | 27% | 100% |
Q2UHA7 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 25% | 90% |
Q31XM4 | Shigella boydii serotype 4 (strain Sb227) | 27% | 100% |
Q32CG3 | Shigella dysenteriae serotype 1 (strain Sd197) | 27% | 100% |
Q3SYT8 | Bos taurus | 30% | 92% |
Q3YY94 | Shigella sonnei (strain Ss046) | 27% | 100% |
Q498R1 | Rattus norvegicus | 25% | 89% |
Q4HZQ1 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 100% |
Q4JIJ2 | Bos taurus | 27% | 90% |
Q4P3D8 | Ustilago maydis (strain 521 / FGSC 9021) | 28% | 95% |
Q4Q8E2 | Leishmania major | 27% | 97% |
Q4WM67 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 90% |
Q4WU59 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 29% | 95% |
Q54B10 | Dictyostelium discoideum | 26% | 99% |
Q54JL0 | Dictyostelium discoideum | 26% | 99% |
Q55CT1 | Dictyostelium discoideum | 28% | 94% |
Q57KH7 | Salmonella choleraesuis (strain SC-B67) | 27% | 100% |
Q5AD27 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 100% |
Q5BB41 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 29% | 95% |
Q5BFT5 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 90% |
Q5E841 | Aliivibrio fischeri (strain ATCC 700601 / ES114) | 26% | 100% |
Q5NRM1 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 27% | 100% |
Q5PEH7 | Salmonella paratyphi A (strain ATCC 9150 / SARB42) | 27% | 100% |
Q653S9 | Oryza sativa subsp. japonica | 29% | 87% |
Q66ED4 | Yersinia pseudotuberculosis serotype I (strain IP32953) | 27% | 100% |
Q6BR77 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 28% | 100% |
Q6CCH0 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 91% |
Q6CVG8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 23% | 100% |
Q6D1A1 | Pectobacterium atrosepticum (strain SCRI 1043 / ATCC BAA-672) | 28% | 100% |
Q6FRH1 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 100% |
Q6LM58 | Photobacterium profundum (strain SS9) | 27% | 100% |
Q6NPS8 | Arabidopsis thaliana | 32% | 100% |
Q6NRG5 | Xenopus laevis | 29% | 100% |
Q6PFP6 | Danio rerio | 32% | 100% |
Q75B78 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
Q7MHA5 | Vibrio vulnificus (strain YJ016) | 28% | 100% |
Q7N8L6 | Photorhabdus laumondii subsp. laumondii (strain DSM 15139 / CIP 105565 / TT01) | 27% | 100% |
Q7X7K8 | Oryza sativa subsp. japonica | 30% | 90% |
Q83QD9 | Shigella flexneri | 28% | 100% |
Q87L90 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 27% | 100% |
Q8C1A3 | Mus musculus | 26% | 90% |
Q8DCK2 | Vibrio vulnificus (strain CMCP6) | 28% | 100% |
Q8EAZ9 | Shewanella oneidensis (strain MR-1) | 28% | 100% |
Q8FEI7 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 27% | 100% |
Q8K9D3 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 25% | 100% |
Q8X7U1 | Escherichia coli O157:H7 | 27% | 100% |
Q8Z458 | Salmonella typhi | 27% | 100% |
Q8ZBN6 | Yersinia pestis | 26% | 100% |
Q9HDG2 | Phanerodontia chrysosporium | 24% | 85% |
Q9JS45 | Neisseria meningitidis serogroup B (strain MC58) | 27% | 100% |
Q9JUD8 | Neisseria meningitidis serogroup A / serotype 4A (strain DSM 15465 / Z2491) | 26% | 100% |
Q9KUX4 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 29% | 100% |
Q9SB48 | Arabidopsis thaliana | 27% | 90% |
Q9SUM3 | Arabidopsis thaliana | 29% | 88% |
Q9UBK8 | Homo sapiens | 25% | 89% |
Q9UHB4 | Homo sapiens | 31% | 100% |
Q9US28 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
V5BUZ5 | Trypanosoma cruzi | 48% | 100% |
V5DK85 | Trypanosoma cruzi | 24% | 89% |