An enormously expanded group of various amino acid transporters.. Localization: Cell surface (by feature)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 8 |
Forrest at al. (procyclic) | no | yes: 8 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 63 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 88 |
NetGPI | no | yes: 0, no: 89 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 76 |
GO:0110165 | cellular anatomical entity | 1 | 76 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9B1Y0
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 16 |
GO:0006810 | transport | 3 | 16 |
GO:0006865 | amino acid transport | 5 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0015849 | organic acid transport | 5 | 16 |
GO:0051179 | localization | 1 | 16 |
GO:0051234 | establishment of localization | 2 | 16 |
GO:0055085 | transmembrane transport | 2 | 16 |
GO:0071702 | organic substance transport | 4 | 16 |
GO:0071705 | nitrogen compound transport | 4 | 16 |
GO:1903825 | organic acid transmembrane transport | 3 | 16 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 16 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006820 | monoatomic anion transport | 5 | 1 |
GO:0015711 | organic anion transport | 5 | 1 |
GO:0015802 | basic amino acid transport | 6 | 1 |
GO:0015819 | lysine transport | 6 | 1 |
GO:0046942 | carboxylic acid transport | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 16 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 16 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 16 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 16 |
GO:0022857 | transmembrane transporter activity | 2 | 16 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 16 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 1 |
GO:0008514 | organic anion transmembrane transporter activity | 5 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015174 | basic amino acid transmembrane transporter activity | 6 | 1 |
GO:0015189 | L-lysine transmembrane transporter activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.444 |
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.476 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.551 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.444 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.528 |
DOC_AGCK_PIF_2 | 367 | 372 | PF00069 | 0.449 |
DOC_MAPK_FxFP_2 | 560 | 563 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 71 | 78 | PF00069 | 0.754 |
DOC_MAPK_MEF2A_6 | 229 | 237 | PF00069 | 0.270 |
DOC_MAPK_MEF2A_6 | 253 | 262 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 215 | 222 | PF00149 | 0.366 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.348 |
DOC_PP2B_LxvP_1 | 538 | 541 | PF13499 | 0.375 |
DOC_PP4_FxxP_1 | 560 | 563 | PF00568 | 0.392 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 376 | 380 | PF12436 | 0.220 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.484 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 253 | 262 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 417 | 421 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 431 | 438 | PF00244 | 0.580 |
LIG_Actin_WH2_2 | 238 | 255 | PF00022 | 0.360 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.788 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.592 |
LIG_BRCT_BRCA1_1 | 553 | 557 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 569 | 573 | PF00533 | 0.572 |
LIG_eIF4E_1 | 583 | 589 | PF01652 | 0.445 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.409 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.332 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.444 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.420 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.551 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.390 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.429 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.731 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.543 |
LIG_KLC1_Yacidic_2 | 510 | 515 | PF13176 | 0.564 |
LIG_LIR_Gen_1 | 138 | 148 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 554 | 565 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 586 | 595 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 604 | 609 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 419 | 424 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 586 | 590 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.529 |
LIG_LYPXL_SIV_4 | 397 | 405 | PF13949 | 0.342 |
LIG_PALB2_WD40_1 | 576 | 584 | PF16756 | 0.557 |
LIG_PDZ_Class_2 | 604 | 609 | PF00595 | 0.549 |
LIG_Pex14_1 | 184 | 188 | PF04695 | 0.424 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.375 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.271 |
LIG_Pex14_2 | 262 | 266 | PF04695 | 0.396 |
LIG_Pex14_2 | 562 | 566 | PF04695 | 0.433 |
LIG_PTB_Apo_2 | 513 | 520 | PF02174 | 0.566 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.352 |
LIG_SH2_GRB2like | 583 | 586 | PF00017 | 0.395 |
LIG_SH2_NCK_1 | 409 | 413 | PF00017 | 0.221 |
LIG_SH2_PTP2 | 361 | 364 | PF00017 | 0.392 |
LIG_SH2_PTP2 | 398 | 401 | PF00017 | 0.394 |
LIG_SH2_PTP2 | 606 | 609 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.531 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.377 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.625 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.567 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.427 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 323 | 326 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.682 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.431 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.420 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.653 |
LIG_Sin3_3 | 408 | 415 | PF02671 | 0.424 |
LIG_SUMO_SIM_anti_2 | 381 | 386 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 586 | 592 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 146 | 153 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 525 | 530 | PF11976 | 0.459 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.375 |
LIG_TRAF2_2 | 490 | 495 | PF00917 | 0.434 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.416 |
LIG_TYR_ITIM | 396 | 401 | PF00017 | 0.378 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.383 |
LIG_TYR_ITSM | 357 | 364 | PF00017 | 0.383 |
LIG_TYR_ITSM | 602 | 609 | PF00017 | 0.438 |
LIG_UBA3_1 | 240 | 247 | PF00899 | 0.422 |
LIG_WRC_WIRS_1 | 157 | 162 | PF05994 | 0.575 |
MOD_CDC14_SPxK_1 | 35 | 38 | PF00782 | 0.625 |
MOD_CDK_SPxK_1 | 32 | 38 | PF00069 | 0.628 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.438 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.574 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.799 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.389 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.405 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.562 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.469 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.384 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.660 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.391 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.483 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.361 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.436 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.630 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.372 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.536 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.355 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.702 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.529 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.484 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.712 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.569 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.579 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.559 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.775 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.381 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.445 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.245 |
MOD_N-GLC_1 | 571 | 576 | PF02516 | 0.301 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.411 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.319 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.256 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.350 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.571 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.449 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.340 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.311 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.574 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.254 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.443 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.777 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.516 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.602 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.791 |
MOD_PKB_1 | 429 | 437 | PF00069 | 0.557 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.458 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.525 |
MOD_Plk_1 | 571 | 577 | PF00069 | 0.507 |
MOD_Plk_2-3 | 509 | 515 | PF00069 | 0.580 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.376 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.366 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.344 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.342 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.320 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.596 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.507 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.421 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.339 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.405 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.302 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.688 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.484 |
MOD_SUMO_rev_2 | 211 | 219 | PF00179 | 0.220 |
MOD_SUMO_rev_2 | 289 | 298 | PF00179 | 0.362 |
TRG_DiLeu_BaEn_2 | 439 | 445 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_3 | 390 | 396 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.639 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.772 |
TRG_NLS_MonoExtC_3 | 46 | 51 | PF00514 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P285 | Leptomonas seymouri | 29% | 100% |
A0A0N0P8T9 | Leptomonas seymouri | 34% | 100% |
A0A0N1I2L5 | Leptomonas seymouri | 32% | 100% |
A0A0N1IJ81 | Leptomonas seymouri | 21% | 100% |
A0A0N1PA98 | Leptomonas seymouri | 63% | 99% |
A0A0S4IV32 | Bodo saltans | 23% | 100% |
A0A3Q8ICL1 | Leishmania donovani | 86% | 100% |
A0A3Q8ID74 | Leishmania donovani | 34% | 100% |
A0A3Q8IDG8 | Leishmania donovani | 34% | 100% |
A0A3Q8IG00 | Leishmania donovani | 38% | 100% |
A0A3Q8IGE6 | Leishmania donovani | 85% | 100% |
A0A3Q8IHG8 | Leishmania donovani | 33% | 100% |
A0A3Q8IHH7 | Leishmania donovani | 22% | 100% |
A0A3Q8IJH2 | Leishmania donovani | 32% | 100% |
A0A3Q8IJX8 | Leishmania donovani | 33% | 100% |
A0A3Q8ILE0 | Leishmania donovani | 33% | 100% |
A0A3Q8IQG8 | Leishmania donovani | 23% | 100% |
A0A3R7MQD8 | Trypanosoma rangeli | 22% | 100% |
A0A3R7MWF1 | Trypanosoma rangeli | 22% | 100% |
A0A3S5H6T4 | Leishmania donovani | 35% | 100% |
A0A3S5H7P4 | Leishmania donovani | 32% | 100% |
A0A3S7WQ39 | Leishmania donovani | 35% | 100% |
A0A3S7X443 | Leishmania donovani | 32% | 100% |
A0A3S7X458 | Leishmania donovani | 32% | 100% |
A0A3S7X4A1 | Leishmania donovani | 33% | 100% |
A0A3S7X4L2 | Leishmania donovani | 87% | 100% |
A0A3S7X4N4 | Leishmania donovani | 86% | 100% |
A0A3S7X4P0 | Leishmania donovani | 86% | 100% |
A0A3S7XA86 | Leishmania donovani | 23% | 100% |
A0A422NZS1 | Trypanosoma rangeli | 33% | 100% |
A4H565 | Leishmania braziliensis | 35% | 100% |
A4HC75 | Leishmania braziliensis | 36% | 100% |
A4HFT5 | Leishmania braziliensis | 36% | 100% |
A4HJ07 | Leishmania braziliensis | 37% | 100% |
A4HJ09 | Leishmania braziliensis | 37% | 100% |
A4HJ35 | Leishmania braziliensis | 37% | 100% |
A4HJ36 | Leishmania braziliensis | 31% | 100% |
A4HJ63 | Leishmania braziliensis | 36% | 100% |
A4HJF8 | Leishmania braziliensis | 74% | 100% |
A4HJF9 | Leishmania braziliensis | 77% | 100% |
A4HJG1 | Leishmania braziliensis | 75% | 100% |
A4HJG3 | Leishmania braziliensis | 74% | 100% |
A4HJG5 | Leishmania braziliensis | 74% | 100% |
A4HKQ7 | Leishmania braziliensis | 31% | 100% |
A4HNJ6 | Leishmania braziliensis | 21% | 100% |
A4HNQ0 | Leishmania braziliensis | 25% | 100% |
A4HTE2 | Leishmania infantum | 36% | 100% |
A4HZQ0 | Leishmania infantum | 33% | 100% |
A4I6F1 | Leishmania infantum | 32% | 100% |
A4I6I1 | Leishmania infantum | 33% | 100% |
A4I6J8 | Leishmania infantum | 34% | 100% |
A4I6J9 | Leishmania infantum | 33% | 100% |
A4I6L3 | Leishmania infantum | 38% | 100% |
A4I6L4 | Leishmania infantum | 33% | 100% |
A4I6W4 | Leishmania infantum | 86% | 100% |
A4I887 | Leishmania infantum | 31% | 100% |
A4I914 | Leishmania infantum | 22% | 100% |
A4IC53 | Leishmania infantum | 23% | 100% |
A4ICU5 | Leishmania infantum | 23% | 100% |
C9ZMD1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZMD3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0AAF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0AAF8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E8NHF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AD44 | Leishmania major | 32% | 100% |
E9AD45 | Leishmania major | 34% | 100% |
E9ADD7 | Leishmania major | 33% | 100% |
E9AG08 | Leishmania major | 21% | 100% |
E9AG09 | Leishmania major | 23% | 100% |
E9AHD7 | Leishmania infantum | 33% | 100% |
E9AHD9 | Leishmania infantum | 34% | 100% |
E9AHL1 | Leishmania infantum | 86% | 100% |
E9AHL2 | Leishmania infantum | 85% | 100% |
E9AHL3 | Leishmania infantum | 87% | 100% |
E9ALD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9ASF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AVK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AYW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AYW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AZ62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1I4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1I6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B1N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B345 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B3X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B761 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B762 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
P40074 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
Q4Q236 | Leishmania major | 24% | 100% |
Q4Q445 | Leishmania major | 21% | 96% |
Q4Q509 | Leishmania major | 31% | 100% |
Q4Q680 | Leishmania major | 86% | 98% |
Q4Q682 | Leishmania major | 82% | 97% |
Q4Q683 | Leishmania major | 86% | 98% |
Q4Q6H5 | Leishmania major | 34% | 100% |
Q4Q6K5 | Leishmania major | 31% | 100% |
Q4Q6K6 | Leishmania major | 39% | 100% |
Q4Q6M9 | Leishmania major | 32% | 100% |
Q4Q6N0 | Leishmania major | 32% | 100% |
Q4Q6N1 | Leishmania major | 34% | 100% |
Q4QBX3 | Leishmania major | 37% | 100% |
Q4QIH0 | Leishmania major | 35% | 100% |
V5AXD0 | Trypanosoma cruzi | 23% | 100% |
V5BIJ1 | Trypanosoma cruzi | 35% | 100% |