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: 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: 99 |
NetGPI | no | yes: 0, no: 99 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 85 |
GO:0110165 | cellular anatomical entity | 1 | 85 |
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: E8NHS7
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 15 |
GO:0006810 | transport | 3 | 15 |
GO:0006865 | amino acid transport | 5 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0015849 | organic acid transport | 5 | 15 |
GO:0051179 | localization | 1 | 15 |
GO:0051234 | establishment of localization | 2 | 15 |
GO:0055085 | transmembrane transport | 2 | 15 |
GO:0071702 | organic substance transport | 4 | 15 |
GO:0071705 | nitrogen compound transport | 4 | 15 |
GO:1903825 | organic acid transmembrane transport | 3 | 15 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 15 |
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 | 15 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 15 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 15 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 15 |
GO:0022857 | transmembrane transporter activity | 2 | 15 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 15 |
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 | 22 | 26 | PF00656 | 0.879 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.440 |
CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.581 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.526 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.345 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.547 |
DEG_SPOP_SBC_1 | 19 | 23 | PF00917 | 0.653 |
DOC_AGCK_PIF_2 | 338 | 343 | PF00069 | 0.443 |
DOC_MAPK_FxFP_2 | 531 | 534 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 42 | 49 | PF00069 | 0.613 |
DOC_MAPK_MEF2A_6 | 200 | 208 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 186 | 193 | PF00149 | 0.415 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.368 |
DOC_PP2B_LxvP_1 | 509 | 512 | PF13499 | 0.374 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.391 |
DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.396 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.215 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 143 | 149 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 402 | 409 | PF00244 | 0.574 |
LIG_Actin_WH2_2 | 209 | 226 | PF00022 | 0.366 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.693 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_1 | 524 | 528 | PF00533 | 0.376 |
LIG_BRCT_BRCA1_1 | 540 | 544 | PF00533 | 0.499 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.391 |
LIG_eIF4E_1 | 554 | 560 | PF01652 | 0.488 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.401 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.385 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.358 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.710 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.415 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.573 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.383 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.764 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.578 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.301 |
LIG_Integrin_RGD_1 | 8 | 10 | PF01839 | 0.451 |
LIG_KLC1_Yacidic_2 | 481 | 486 | PF13176 | 0.596 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 525 | 536 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 557 | 566 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 575 | 580 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 557 | 561 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 575 | 580 | PF02991 | 0.432 |
LIG_PALB2_WD40_1 | 547 | 555 | PF16756 | 0.619 |
LIG_PDZ_Class_3 | 575 | 580 | PF00595 | 0.523 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.417 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.368 |
LIG_Pex14_2 | 533 | 537 | PF04695 | 0.467 |
LIG_PTB_Apo_2 | 484 | 491 | PF02174 | 0.597 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.281 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.355 |
LIG_SH2_GRB2like | 554 | 557 | PF00017 | 0.486 |
LIG_SH2_PTP2 | 369 | 372 | PF00017 | 0.365 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.530 |
LIG_SH2_SRC | 165 | 168 | PF00017 | 0.356 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.561 |
LIG_SH2_SRC | 469 | 472 | PF00017 | 0.422 |
LIG_SH2_SRC | 62 | 65 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.394 |
LIG_SH2_STAT3 | 294 | 297 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.564 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.665 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.468 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.415 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.628 |
LIG_Sin3_3 | 379 | 386 | PF02671 | 0.471 |
LIG_SUMO_SIM_anti_2 | 352 | 357 | PF11976 | 0.288 |
LIG_SUMO_SIM_anti_2 | 557 | 563 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 104 | 109 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 117 | 124 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 496 | 501 | PF11976 | 0.336 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.404 |
LIG_TRAF2_2 | 461 | 466 | PF00917 | 0.429 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.426 |
LIG_TYR_ITIM | 367 | 372 | PF00017 | 0.378 |
LIG_TYR_ITIM | 378 | 383 | PF00017 | 0.366 |
LIG_TYR_ITSM | 328 | 335 | PF00017 | 0.392 |
LIG_TYR_ITSM | 573 | 580 | PF00017 | 0.431 |
LIG_UBA3_1 | 211 | 218 | PF00899 | 0.378 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.568 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.450 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.593 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.420 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.398 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.427 |
MOD_DYRK1A_RPxSP_1 | 14 | 18 | PF00069 | 0.783 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.399 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.591 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.440 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.393 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.392 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.313 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.366 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.537 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.545 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.772 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.392 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.541 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.517 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.599 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.522 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.504 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.346 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.241 |
MOD_N-GLC_1 | 542 | 547 | PF02516 | 0.388 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.410 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.351 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.343 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.565 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.413 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.377 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.359 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.298 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.420 |
MOD_NEK2_2 | 387 | 392 | PF00069 | 0.544 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.433 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.439 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.749 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.531 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.547 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.752 |
MOD_PKB_1 | 400 | 408 | PF00069 | 0.590 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.600 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.566 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.555 |
MOD_Plk_2-3 | 480 | 486 | PF00069 | 0.607 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.382 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.338 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.386 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.360 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.339 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.321 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.532 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.549 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.377 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.335 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.395 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.292 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.742 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.517 |
MOD_SUMO_rev_2 | 182 | 190 | PF00179 | 0.215 |
MOD_SUMO_rev_2 | 260 | 269 | PF00179 | 0.417 |
TRG_DiLeu_BaEn_2 | 410 | 416 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_3 | 361 | 367 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.678 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.674 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2L5 | Leptomonas seymouri | 32% | 100% |
A0A0N1I9T3 | Leptomonas seymouri | 30% | 100% |
A0A0N1IJ81 | Leptomonas seymouri | 21% | 100% |
A0A0N1PA98 | Leptomonas seymouri | 64% | 94% |
A0A0S4IV32 | Bodo saltans | 23% | 100% |
A0A0S4JU02 | Bodo saltans | 33% | 100% |
A0A1X0NRL7 | Trypanosomatidae | 40% | 100% |
A0A3Q8ICL1 | Leishmania donovani | 84% | 96% |
A0A3Q8ID74 | Leishmania donovani | 33% | 100% |
A0A3Q8IDG8 | Leishmania donovani | 35% | 100% |
A0A3Q8IFZ0 | Leishmania donovani | 34% | 100% |
A0A3Q8IG00 | Leishmania donovani | 39% | 100% |
A0A3Q8IGE6 | Leishmania donovani | 89% | 99% |
A0A3Q8IHG8 | Leishmania donovani | 33% | 100% |
A0A3Q8IHH7 | Leishmania donovani | 21% | 100% |
A0A3Q8IJH2 | Leishmania donovani | 34% | 100% |
A0A3Q8IJX8 | Leishmania donovani | 32% | 100% |
A0A3Q8ILE0 | Leishmania donovani | 33% | 100% |
A0A3Q8IQG8 | Leishmania donovani | 24% | 100% |
A0A3R7MWF1 | Trypanosoma rangeli | 22% | 100% |
A0A3R7N1H9 | Trypanosoma rangeli | 43% | 100% |
A0A3R7RFB5 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H6T4 | Leishmania donovani | 34% | 100% |
A0A3S5H7P4 | Leishmania donovani | 33% | 100% |
A0A3S7WQ39 | Leishmania donovani | 36% | 100% |
A0A3S7X443 | Leishmania donovani | 34% | 100% |
A0A3S7X458 | Leishmania donovani | 34% | 100% |
A0A3S7X4A1 | Leishmania donovani | 32% | 100% |
A0A3S7X4L2 | Leishmania donovani | 90% | 96% |
A0A3S7X4N4 | Leishmania donovani | 86% | 96% |
A0A3S7X4P0 | Leishmania donovani | 89% | 96% |
A0A3S7XA86 | Leishmania donovani | 23% | 100% |
A0A3S7XCE3 | Leishmania donovani | 22% | 100% |
A0A422N608 | Trypanosoma rangeli | 43% | 100% |
A4H565 | Leishmania braziliensis | 36% | 100% |
A4HC75 | Leishmania braziliensis | 35% | 100% |
A4HFT5 | Leishmania braziliensis | 36% | 100% |
A4HJ06 | Leishmania braziliensis | 31% | 100% |
A4HJ07 | Leishmania braziliensis | 36% | 100% |
A4HJ09 | Leishmania braziliensis | 35% | 100% |
A4HJ35 | Leishmania braziliensis | 38% | 100% |
A4HJ36 | Leishmania braziliensis | 30% | 100% |
A4HJ37 | Leishmania braziliensis | 34% | 100% |
A4HJ63 | Leishmania braziliensis | 32% | 100% |
A4HJF8 | Leishmania braziliensis | 76% | 100% |
A4HJF9 | Leishmania braziliensis | 75% | 100% |
A4HJG1 | Leishmania braziliensis | 75% | 100% |
A4HJG3 | Leishmania braziliensis | 76% | 100% |
A4HJG5 | Leishmania braziliensis | 76% | 100% |
A4HKQ7 | Leishmania braziliensis | 32% | 100% |
A4HNJ6 | Leishmania braziliensis | 21% | 100% |
A4HNQ0 | Leishmania braziliensis | 24% | 100% |
A4HTE2 | Leishmania infantum | 37% | 100% |
A4HZQ0 | Leishmania infantum | 33% | 100% |
A4I6F1 | Leishmania infantum | 33% | 100% |
A4I6I1 | Leishmania infantum | 32% | 100% |
A4I6J8 | Leishmania infantum | 33% | 100% |
A4I6J9 | Leishmania infantum | 34% | 100% |
A4I6K0 | Leishmania infantum | 34% | 100% |
A4I6L3 | Leishmania infantum | 39% | 100% |
A4I6L4 | Leishmania infantum | 32% | 100% |
A4I6W4 | Leishmania infantum | 90% | 96% |
A4I887 | Leishmania infantum | 33% | 100% |
A4I914 | Leishmania infantum | 21% | 100% |
A4IC53 | Leishmania infantum | 23% | 100% |
A4ICC3 | Leishmania infantum | 22% | 100% |
A4ICU5 | Leishmania infantum | 24% | 100% |
C9ZMD2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZMD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZWR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 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) | 31% | 100% |
D0AAF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0AAF8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0AAG8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E8NHF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AD44 | Leishmania major | 33% | 100% |
E9ADD7 | Leishmania major | 32% | 100% |
E9AG09 | Leishmania major | 23% | 100% |
E9AHD7 | Leishmania infantum | 33% | 100% |
E9AHD9 | Leishmania infantum | 33% | 100% |
E9AHL1 | Leishmania infantum | 85% | 96% |
E9AHL2 | Leishmania infantum | 89% | 100% |
E9AHL3 | Leishmania infantum | 84% | 96% |
E9ALD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9ASF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AVK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AYW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 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) | 35% | 100% |
E9B1K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B1N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 75% |
E9B1Y0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 95% |
E9B345 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B3X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9B761 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B762 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
P40074 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P40501 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 100% |
Q4Q236 | Leishmania major | 24% | 100% |
Q4Q445 | Leishmania major | 20% | 96% |
Q4Q509 | Leishmania major | 32% | 100% |
Q4Q680 | Leishmania major | 84% | 100% |
Q4Q682 | Leishmania major | 87% | 100% |
Q4Q683 | Leishmania major | 84% | 100% |
Q4Q6H5 | Leishmania major | 32% | 100% |
Q4Q6K5 | Leishmania major | 31% | 100% |
Q4Q6K6 | Leishmania major | 40% | 100% |
Q4Q6M8 | Leishmania major | 34% | 100% |
Q4Q6M9 | Leishmania major | 33% | 100% |
Q4Q6N0 | Leishmania major | 33% | 100% |
Q4Q6N1 | Leishmania major | 33% | 100% |
Q4QBX3 | Leishmania major | 33% | 100% |
Q4QIH0 | Leishmania major | 34% | 100% |
V5AXD0 | Trypanosoma cruzi | 23% | 100% |
V5DCG4 | Trypanosoma cruzi | 36% | 100% |