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. | no | yes: 69 |
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: 0, no: 106 |
NetGPI | no | yes: 0, no: 106 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 94 |
GO:0110165 | cellular anatomical entity | 1 | 94 |
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: A4HJG1
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 17 |
GO:0006810 | transport | 3 | 17 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006820 | monoatomic anion transport | 5 | 1 |
GO:0006865 | amino acid transport | 5 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0015711 | organic anion transport | 5 | 1 |
GO:0015802 | basic amino acid transport | 6 | 1 |
GO:0015819 | lysine transport | 6 | 1 |
GO:0015849 | organic acid transport | 5 | 17 |
GO:0046942 | carboxylic acid transport | 6 | 1 |
GO:0051179 | localization | 1 | 17 |
GO:0051234 | establishment of localization | 2 | 17 |
GO:0055085 | transmembrane transport | 2 | 17 |
GO:0071702 | organic substance transport | 4 | 17 |
GO:0071705 | nitrogen compound transport | 4 | 17 |
GO:1903825 | organic acid transmembrane transport | 3 | 17 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 17 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 17 |
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:0015171 | amino acid transmembrane transporter activity | 5 | 17 |
GO:0015174 | basic amino acid transmembrane transporter activity | 6 | 1 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 17 |
GO:0015189 | L-lysine transmembrane transporter activity | 5 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 17 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 478 | 482 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 488 | 492 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.325 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.498 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.464 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.466 |
DEG_Kelch_Keap1_1 | 6 | 11 | PF01344 | 0.591 |
DOC_CDC14_PxL_1 | 209 | 217 | PF14671 | 0.168 |
DOC_MAPK_FxFP_2 | 536 | 539 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 42 | 49 | PF00069 | 0.679 |
DOC_MAPK_MEF2A_6 | 200 | 208 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.480 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.308 |
DOC_PP2B_LxvP_1 | 514 | 517 | PF13499 | 0.316 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.383 |
DOC_PP4_FxxP_1 | 536 | 539 | PF00568 | 0.328 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.191 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.316 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.526 |
LIG_Actin_WH2_2 | 209 | 226 | PF00022 | 0.300 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.756 |
LIG_BRCT_BRCA1_1 | 529 | 533 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.323 |
LIG_BRCT_BRCA1_1 | 545 | 549 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.328 |
LIG_deltaCOP1_diTrp_1 | 302 | 307 | PF00928 | 0.476 |
LIG_eIF4E_1 | 559 | 565 | PF01652 | 0.403 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.355 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.322 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.355 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.340 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.692 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.527 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.307 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.504 |
LIG_GBD_Chelix_1 | 242 | 250 | PF00786 | 0.170 |
LIG_GBD_Chelix_1 | 319 | 327 | PF00786 | 0.224 |
LIG_HP1_1 | 433 | 437 | PF01393 | 0.364 |
LIG_KLC1_Yacidic_2 | 486 | 491 | PF13176 | 0.551 |
LIG_LIR_Apic_2 | 535 | 539 | PF02991 | 0.226 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 147 | 156 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 330 | 340 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 530 | 541 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 562 | 571 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 580 | 585 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 530 | 536 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 562 | 566 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 580 | 585 | PF02991 | 0.402 |
LIG_MYND_1 | 213 | 217 | PF01753 | 0.168 |
LIG_PALB2_WD40_1 | 552 | 560 | PF16756 | 0.572 |
LIG_PCNA_yPIPBox_3 | 312 | 323 | PF02747 | 0.569 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.379 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.320 |
LIG_Pex14_2 | 538 | 542 | PF04695 | 0.375 |
LIG_PTB_Apo_2 | 489 | 496 | PF02174 | 0.552 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.302 |
LIG_SH2_GRB2like | 559 | 562 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.499 |
LIG_SH2_PTP2 | 369 | 372 | PF00017 | 0.330 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.281 |
LIG_SH2_SRC | 165 | 168 | PF00017 | 0.298 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 294 | 297 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.309 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.721 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.450 |
LIG_Sin3_3 | 379 | 386 | PF02671 | 0.431 |
LIG_SUMO_SIM_anti_2 | 227 | 233 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 352 | 357 | PF11976 | 0.250 |
LIG_SUMO_SIM_anti_2 | 361 | 367 | PF11976 | 0.246 |
LIG_SUMO_SIM_anti_2 | 439 | 446 | PF11976 | 0.364 |
LIG_SUMO_SIM_anti_2 | 562 | 568 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 104 | 109 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 501 | 506 | PF11976 | 0.280 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.359 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.511 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.361 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.423 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.340 |
LIG_TYR_ITIM | 367 | 372 | PF00017 | 0.336 |
LIG_TYR_ITIM | 378 | 383 | PF00017 | 0.285 |
LIG_TYR_ITSM | 328 | 335 | PF00017 | 0.347 |
LIG_TYR_ITSM | 578 | 585 | PF00017 | 0.390 |
LIG_UBA3_1 | 211 | 218 | PF00899 | 0.333 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.491 |
LIG_WRC_WIRS_1 | 533 | 538 | PF05994 | 0.342 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.351 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.783 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.369 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.597 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.616 |
MOD_DYRK1A_RPxSP_1 | 14 | 18 | PF00069 | 0.582 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.289 |
MOD_GlcNHglycan | 186 | 190 | PF01048 | 0.468 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.315 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.537 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.323 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.343 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.256 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.312 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.295 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.326 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.481 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.477 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.401 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.804 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.361 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.598 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.539 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.703 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.465 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.461 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.306 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.297 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.591 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.235 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.164 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.291 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.277 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.280 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.374 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.337 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.257 |
MOD_NEK2_2 | 387 | 392 | PF00069 | 0.527 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.830 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.194 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.686 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.320 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.532 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.714 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.368 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.738 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.431 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.549 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.554 |
MOD_Plk_2-3 | 481 | 487 | PF00069 | 0.548 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.308 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.303 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.317 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.275 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.514 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.495 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.328 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.266 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.333 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.250 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.721 |
MOD_SUMO_rev_2 | 260 | 269 | PF00179 | 0.370 |
TRG_DiLeu_BaEn_3 | 361 | 367 | PF01217 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ81 | Leptomonas seymouri | 21% | 100% |
A0A0N1PA98 | Leptomonas seymouri | 63% | 95% |
A0A0N1PFD1 | Leptomonas seymouri | 32% | 100% |
A0A0S4IV32 | Bodo saltans | 24% | 100% |
A0A0S4JU02 | Bodo saltans | 34% | 100% |
A0A1X0NKV2 | Trypanosomatidae | 33% | 100% |
A0A1X0NPV3 | Trypanosomatidae | 34% | 100% |
A0A1X0NR26 | Trypanosomatidae | 33% | 100% |
A0A1X0P0B5 | Trypanosomatidae | 22% | 100% |
A0A3Q8ICL1 | Leishmania donovani | 71% | 97% |
A0A3Q8IDG8 | Leishmania donovani | 35% | 100% |
A0A3Q8IFZ0 | Leishmania donovani | 33% | 100% |
A0A3Q8IG00 | Leishmania donovani | 35% | 100% |
A0A3Q8IGE6 | Leishmania donovani | 76% | 100% |
A0A3Q8IHG8 | Leishmania donovani | 34% | 100% |
A0A3Q8IHH7 | Leishmania donovani | 21% | 100% |
A0A3Q8IJH2 | Leishmania donovani | 36% | 100% |
A0A3Q8IJX8 | Leishmania donovani | 31% | 100% |
A0A3Q8ILE0 | Leishmania donovani | 40% | 100% |
A0A3Q8IQG8 | Leishmania donovani | 26% | 100% |
A0A3R7N1H9 | Trypanosoma rangeli | 46% | 100% |
A0A3R7R2W8 | Trypanosoma rangeli | 31% | 100% |
A0A3R7RQX3 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H6T4 | Leishmania donovani | 34% | 100% |
A0A3S7WQ39 | Leishmania donovani | 34% | 100% |
A0A3S7X443 | Leishmania donovani | 34% | 100% |
A0A3S7X458 | Leishmania donovani | 34% | 100% |
A0A3S7X4A1 | Leishmania donovani | 31% | 100% |
A0A3S7X4L2 | Leishmania donovani | 72% | 97% |
A0A3S7X4N4 | Leishmania donovani | 72% | 97% |
A0A3S7X4P0 | Leishmania donovani | 73% | 97% |
A0A3S7XA86 | Leishmania donovani | 24% | 100% |
A0A3S7XCE3 | Leishmania donovani | 23% | 100% |
A0A422MW74 | Trypanosoma rangeli | 36% | 100% |
A0A422NZS1 | Trypanosoma rangeli | 34% | 100% |
A4H565 | Leishmania braziliensis | 36% | 100% |
A4HC75 | Leishmania braziliensis | 38% | 100% |
A4HFT5 | Leishmania braziliensis | 37% | 100% |
A4HJ06 | Leishmania braziliensis | 32% | 100% |
A4HJ07 | Leishmania braziliensis | 35% | 100% |
A4HJ09 | Leishmania braziliensis | 36% | 100% |
A4HJ35 | Leishmania braziliensis | 35% | 100% |
A4HJ36 | Leishmania braziliensis | 33% | 100% |
A4HJ37 | Leishmania braziliensis | 35% | 100% |
A4HJ63 | Leishmania braziliensis | 32% | 100% |
A4HJF8 | Leishmania braziliensis | 96% | 100% |
A4HJF9 | Leishmania braziliensis | 98% | 100% |
A4HJG3 | Leishmania braziliensis | 95% | 95% |
A4HJG5 | Leishmania braziliensis | 95% | 95% |
A4HKQ7 | Leishmania braziliensis | 33% | 100% |
A4HLK3 | Leishmania braziliensis | 21% | 100% |
A4HNJ6 | Leishmania braziliensis | 24% | 100% |
A4HNJ7 | Leishmania braziliensis | 24% | 100% |
A4HNQ0 | Leishmania braziliensis | 24% | 100% |
A4HTE2 | Leishmania infantum | 35% | 100% |
A4HZQ0 | Leishmania infantum | 40% | 100% |
A4I6I1 | Leishmania infantum | 31% | 100% |
A4I6J9 | Leishmania infantum | 35% | 100% |
A4I6K0 | Leishmania infantum | 33% | 100% |
A4I6L3 | Leishmania infantum | 35% | 100% |
A4I6L4 | Leishmania infantum | 31% | 100% |
A4I6W4 | Leishmania infantum | 72% | 97% |
A4I887 | Leishmania infantum | 35% | 100% |
A4I914 | Leishmania infantum | 21% | 100% |
A4IC53 | Leishmania infantum | 24% | 100% |
A4IC66 | Leishmania infantum | 23% | 100% |
A4ICC3 | Leishmania infantum | 23% | 100% |
A4ICU5 | Leishmania infantum | 26% | 100% |
C9ZMD2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZN59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZWQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZWQ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZWQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZWX3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0AAF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0AAF8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E8NHF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9AD44 | Leishmania major | 34% | 100% |
E9AD45 | Leishmania major | 33% | 100% |
E9ADD7 | Leishmania major | 34% | 100% |
E9AG08 | Leishmania major | 23% | 100% |
E9AG09 | Leishmania major | 24% | 100% |
E9AHD7 | Leishmania infantum | 34% | 100% |
E9AHL1 | Leishmania infantum | 72% | 97% |
E9AHL2 | Leishmania infantum | 74% | 100% |
E9AHL3 | Leishmania infantum | 71% | 97% |
E9ALD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9ASF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AUB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AVK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AYW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AYW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AZ62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1I4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1I6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 75% |
E9B1Y0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 96% |
E9B345 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B3X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9B761 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B762 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
P40074 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
P40501 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 100% |
Q4Q072 | Leishmania major | 23% | 100% |
Q4Q236 | Leishmania major | 27% | 100% |
Q4Q445 | Leishmania major | 21% | 93% |
Q4Q509 | Leishmania major | 34% | 100% |
Q4Q680 | Leishmania major | 73% | 100% |
Q4Q682 | Leishmania major | 76% | 100% |
Q4Q683 | Leishmania major | 73% | 100% |
Q4Q6H5 | Leishmania major | 31% | 100% |
Q4Q6K5 | Leishmania major | 34% | 100% |
Q4Q6K6 | Leishmania major | 36% | 100% |
Q4Q6M8 | Leishmania major | 34% | 100% |
Q4Q6M9 | Leishmania major | 34% | 100% |
Q4Q6N0 | Leishmania major | 34% | 100% |
Q4Q6N1 | Leishmania major | 33% | 100% |
Q4QBX3 | Leishmania major | 37% | 100% |
Q4QIH0 | Leishmania major | 32% | 100% |
V5BH70 | Trypanosoma cruzi | 33% | 100% |
V5BMG4 | Trypanosoma cruzi | 38% | 100% |