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: 6 |
Forrest at al. (procyclic) | no | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 48 |
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: 90 |
NetGPI | no | yes: 0, no: 90 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 79 |
GO:0110165 | cellular anatomical entity | 1 | 79 |
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: A0A3Q8IGE6
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 11 |
GO:0006810 | transport | 3 | 11 |
GO:0006865 | amino acid transport | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015849 | organic acid transport | 5 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0055085 | transmembrane transport | 2 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:1903825 | organic acid transmembrane transport | 3 | 11 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 11 |
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:0003824 | catalytic activity | 1 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0005215 | transporter activity | 1 | 11 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 11 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 11 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 11 |
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 | 0.619 |
CLV_C14_Caspase3-7 | 446 | 450 | PF00656 | 0.388 |
CLV_C14_Caspase3-7 | 480 | 484 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.454 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.557 |
CLV_PCSK_PC7_1 | 38 | 44 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.451 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.455 |
DEG_SPOP_SBC_1 | 19 | 23 | PF00917 | 0.612 |
DOC_AGCK_PIF_2 | 338 | 343 | PF00069 | 0.354 |
DOC_MAPK_FxFP_2 | 538 | 541 | PF00069 | 0.361 |
DOC_MAPK_gen_1 | 42 | 49 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 200 | 208 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 186 | 193 | PF00149 | 0.188 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.300 |
DOC_PP2B_LxvP_1 | 516 | 519 | PF13499 | 0.323 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.364 |
DOC_PP4_FxxP_1 | 538 | 541 | PF00568 | 0.322 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.312 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 143 | 149 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 209 | 226 | PF00022 | 0.317 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.704 |
LIG_BRCT_BRCA1_1 | 531 | 535 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_1 | 547 | 551 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.349 |
LIG_eIF4E_1 | 561 | 567 | PF01652 | 0.554 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.374 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.338 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.341 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.284 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.513 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.320 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.672 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.525 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.498 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.248 |
LIG_Integrin_RGD_1 | 8 | 10 | PF01839 | 0.402 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 330 | 340 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 532 | 543 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 564 | 573 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 582 | 587 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 564 | 568 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 582 | 587 | PF02991 | 0.511 |
LIG_PALB2_WD40_1 | 554 | 562 | PF16756 | 0.563 |
LIG_PDZ_Class_3 | 582 | 587 | PF00595 | 0.466 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.342 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.343 |
LIG_Pex14_2 | 540 | 544 | PF04695 | 0.385 |
LIG_PTB_Apo_2 | 491 | 498 | PF02174 | 0.544 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.276 |
LIG_SH2_GRB2like | 561 | 564 | PF00017 | 0.554 |
LIG_SH2_PTP2 | 332 | 335 | PF00017 | 0.331 |
LIG_SH2_PTP2 | 369 | 372 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.474 |
LIG_SH2_SRC | 165 | 168 | PF00017 | 0.304 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.545 |
LIG_SH2_SRC | 481 | 484 | PF00017 | 0.375 |
LIG_SH2_SRC | 62 | 65 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 488 | 492 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 294 | 297 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.501 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.425 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.572 |
LIG_Sin3_3 | 379 | 386 | PF02671 | 0.417 |
LIG_SUMO_SIM_anti_2 | 352 | 357 | PF11976 | 0.235 |
LIG_SUMO_SIM_anti_2 | 564 | 570 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 117 | 124 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 502 | 508 | PF11976 | 0.293 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.352 |
LIG_TRAF2_2 | 463 | 468 | PF00917 | 0.378 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.339 |
LIG_TYR_ITIM | 367 | 372 | PF00017 | 0.362 |
LIG_TYR_ITIM | 378 | 383 | PF00017 | 0.334 |
LIG_TYR_ITSM | 328 | 335 | PF00017 | 0.412 |
LIG_TYR_ITSM | 580 | 587 | PF00017 | 0.397 |
LIG_UBA3_1 | 211 | 218 | PF00899 | 0.369 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.533 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.355 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.498 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.662 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.368 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.599 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.373 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.337 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.578 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.365 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.360 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.299 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.293 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.318 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.316 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.467 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.489 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.343 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.529 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.598 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.541 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.495 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.496 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.295 |
MOD_LATS_1 | 18 | 24 | PF00433 | 0.609 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.189 |
MOD_N-GLC_1 | 549 | 554 | PF02516 | 0.298 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.318 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.351 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.274 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.520 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.342 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.328 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.382 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.346 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.295 |
MOD_NEK2_2 | 387 | 392 | PF00069 | 0.514 |
MOD_NEK2_2 | 439 | 444 | PF00069 | 0.373 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.367 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.711 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.648 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.541 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.733 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.488 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.524 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.719 |
MOD_PKB_1 | 400 | 408 | PF00069 | 0.537 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.551 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.382 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.546 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.466 |
MOD_Plk_2-3 | 487 | 493 | PF00069 | 0.555 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.326 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.301 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.347 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.329 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.299 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.271 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.491 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.502 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.334 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.301 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.508 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.254 |
MOD_SUMO_rev_2 | 260 | 269 | PF00179 | 0.333 |
TRG_DiLeu_BaEn_2 | 410 | 416 | PF01217 | 0.388 |
TRG_DiLeu_BaEn_3 | 361 | 367 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.636 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.646 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2L5 | Leptomonas seymouri | 32% | 100% |
A0A0N1IJ81 | Leptomonas seymouri | 20% | 100% |
A0A0N1PA98 | Leptomonas seymouri | 65% | 96% |
A0A0S4IV32 | Bodo saltans | 23% | 100% |
A0A0S4JU02 | Bodo saltans | 34% | 100% |
A0A3Q8ICL1 | Leishmania donovani | 91% | 100% |
A0A3Q8IDG8 | Leishmania donovani | 35% | 100% |
A0A3Q8IG00 | Leishmania donovani | 40% | 100% |
A0A3Q8IHH7 | Leishmania donovani | 20% | 100% |
A0A3Q8IJH2 | Leishmania donovani | 34% | 100% |
A0A3Q8IJX8 | Leishmania donovani | 34% | 100% |
A0A3Q8ILE0 | Leishmania donovani | 34% | 100% |
A0A3Q8IQG8 | Leishmania donovani | 25% | 100% |
A0A3R7JSA0 | Trypanosoma rangeli | 44% | 100% |
A0A3R7MWF1 | Trypanosoma rangeli | 22% | 100% |
A0A3R7N1H9 | Trypanosoma rangeli | 43% | 100% |
A0A3S7WQ39 | Leishmania donovani | 36% | 100% |
A0A3S7X443 | Leishmania donovani | 35% | 100% |
A0A3S7X4A1 | Leishmania donovani | 34% | 100% |
A0A3S7X4L2 | Leishmania donovani | 92% | 97% |
A0A3S7X4N4 | Leishmania donovani | 92% | 97% |
A0A3S7X4P0 | Leishmania donovani | 91% | 97% |
A0A3S7XA86 | Leishmania donovani | 23% | 100% |
A0A3S7XCE3 | Leishmania donovani | 22% | 100% |
A0A422MW74 | Trypanosoma rangeli | 37% | 100% |
A0A422N608 | Trypanosoma rangeli | 43% | 100% |
A4H565 | Leishmania braziliensis | 35% | 100% |
A4HC75 | Leishmania braziliensis | 35% | 100% |
A4HFJ2 | Leishmania braziliensis | 32% | 100% |
A4HFT5 | Leishmania braziliensis | 37% | 100% |
A4HJ06 | Leishmania braziliensis | 32% | 100% |
A4HJ07 | Leishmania braziliensis | 35% | 100% |
A4HJ09 | Leishmania braziliensis | 34% | 100% |
A4HJ35 | Leishmania braziliensis | 38% | 100% |
A4HJ37 | Leishmania braziliensis | 36% | 100% |
A4HJ63 | Leishmania braziliensis | 33% | 100% |
A4HJF8 | Leishmania braziliensis | 77% | 100% |
A4HJF9 | Leishmania braziliensis | 75% | 99% |
A4HJG1 | Leishmania braziliensis | 76% | 99% |
A4HJG3 | Leishmania braziliensis | 77% | 100% |
A4HJG5 | Leishmania braziliensis | 76% | 100% |
A4HKQ7 | Leishmania braziliensis | 33% | 100% |
A4HNJ6 | Leishmania braziliensis | 24% | 100% |
A4HNJ7 | Leishmania braziliensis | 23% | 100% |
A4HNQ0 | Leishmania braziliensis | 24% | 100% |
A4HTE2 | Leishmania infantum | 36% | 100% |
A4HZQ0 | Leishmania infantum | 34% | 100% |
A4I6I1 | Leishmania infantum | 34% | 100% |
A4I6J9 | Leishmania infantum | 34% | 100% |
A4I6L3 | Leishmania infantum | 40% | 100% |
A4I6L4 | Leishmania infantum | 34% | 100% |
A4I6W4 | Leishmania infantum | 93% | 100% |
A4I887 | Leishmania infantum | 34% | 100% |
A4I914 | Leishmania infantum | 20% | 95% |
A4IC53 | Leishmania infantum | 23% | 100% |
A4IC66 | Leishmania infantum | 22% | 100% |
A4ICC3 | Leishmania infantum | 23% | 100% |
A4ICU5 | Leishmania infantum | 25% | 100% |
C9ZMB9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZMD2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZMD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZWQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZWQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZWR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D0AAF6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0AAF8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E8NHF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
E9ADD7 | Leishmania major | 34% | 100% |
E9AG08 | Leishmania major | 22% | 100% |
E9AG09 | Leishmania major | 22% | 100% |
E9AHL1 | Leishmania infantum | 92% | 100% |
E9AHL2 | Leishmania infantum | 99% | 100% |
E9AHL3 | Leishmania infantum | 91% | 100% |
E9ALD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9ASF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AUB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AVK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AZ62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1I4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1I6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B1K8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B1N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B1X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B1Y0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9B345 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B3X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 20% | 95% |
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) | 23% | 100% |
P40501 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 100% |
Q4Q072 | Leishmania major | 23% | 100% |
Q4Q236 | Leishmania major | 26% | 100% |
Q4Q509 | Leishmania major | 34% | 100% |
Q4Q680 | Leishmania major | 87% | 100% |
Q4Q682 | Leishmania major | 91% | 100% |
Q4Q683 | Leishmania major | 87% | 100% |
Q4Q6H5 | Leishmania major | 34% | 100% |
Q4Q6K6 | Leishmania major | 40% | 100% |
Q4Q6M9 | Leishmania major | 35% | 100% |
Q4QBX3 | Leishmania major | 34% | 100% |
Q4QIH0 | Leishmania major | 33% | 100% |
Q8R1S9 | Mus musculus | 22% | 100% |
V5BA72 | Trypanosoma cruzi | 31% | 100% |
V5BH70 | Trypanosoma cruzi | 33% | 100% |