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: 45 |
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: 1, no: 83 |
NetGPI | no | yes: 0, no: 84 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 72 |
GO:0110165 | cellular anatomical entity | 1 | 72 |
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: A0A3S7X4N4
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 | 464 | 468 | PF00656 | 0.390 |
CLV_C14_Caspase3-7 | 498 | 502 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.455 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.541 |
CLV_PCSK_PC7_1 | 56 | 62 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.511 |
DEG_APCC_DBOX_1 | 405 | 413 | PF00400 | 0.516 |
DEG_SPOP_SBC_1 | 25 | 29 | PF00917 | 0.609 |
DOC_AGCK_PIF_2 | 356 | 361 | PF00069 | 0.374 |
DOC_MAPK_FxFP_2 | 556 | 559 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 60 | 67 | PF00069 | 0.734 |
DOC_MAPK_MEF2A_6 | 218 | 226 | PF00069 | 0.317 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.485 |
DOC_PP1_RVXF_1 | 204 | 211 | PF00149 | 0.204 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.282 |
DOC_PP2B_LxvP_1 | 534 | 537 | PF13499 | 0.307 |
DOC_PP4_FxxP_1 | 556 | 559 | PF00568 | 0.333 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.344 |
LIG_14-3-3_CanoR_1 | 145 | 150 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 218 | 223 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 242 | 251 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 26 | 31 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.796 |
LIG_Actin_WH2_2 | 227 | 244 | PF00022 | 0.302 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.728 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 565 | 569 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.301 |
LIG_eIF4E_1 | 579 | 585 | PF01652 | 0.405 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.321 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.345 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.708 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.301 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.400 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.520 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.320 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.601 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.481 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.237 |
LIG_KLC1_Yacidic_2 | 506 | 511 | PF13176 | 0.535 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 348 | 358 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 550 | 561 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 582 | 591 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 600 | 605 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 250 | 254 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 582 | 586 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 600 | 605 | PF02991 | 0.438 |
LIG_PALB2_WD40_1 | 572 | 580 | PF16756 | 0.556 |
LIG_PDZ_Class_3 | 600 | 605 | PF00595 | 0.445 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.352 |
LIG_Pex14_2 | 251 | 255 | PF04695 | 0.315 |
LIG_Pex14_2 | 558 | 562 | PF04695 | 0.378 |
LIG_PTB_Apo_2 | 509 | 516 | PF02174 | 0.536 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.284 |
LIG_SH2_GRB2like | 579 | 582 | PF00017 | 0.422 |
LIG_SH2_PTP2 | 350 | 353 | PF00017 | 0.344 |
LIG_SH2_PTP2 | 387 | 390 | PF00017 | 0.311 |
LIG_SH2_PTP2 | 80 | 83 | PF00017 | 0.466 |
LIG_SH2_SRC | 183 | 186 | PF00017 | 0.296 |
LIG_SH2_SRC | 411 | 414 | PF00017 | 0.537 |
LIG_SH2_SRC | 499 | 502 | PF00017 | 0.539 |
LIG_SH2_SRC | 80 | 83 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.307 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.486 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.439 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.536 |
LIG_Sin3_3 | 397 | 404 | PF02671 | 0.405 |
LIG_SUMO_SIM_anti_2 | 370 | 375 | PF11976 | 0.230 |
LIG_SUMO_SIM_anti_2 | 582 | 588 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 135 | 142 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 520 | 526 | PF11976 | 0.325 |
LIG_TRAF2_1 | 377 | 380 | PF00917 | 0.344 |
LIG_TRAF2_2 | 481 | 486 | PF00917 | 0.379 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.321 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.330 |
LIG_TYR_ITIM | 396 | 401 | PF00017 | 0.319 |
LIG_TYR_ITSM | 346 | 353 | PF00017 | 0.358 |
LIG_TYR_ITSM | 598 | 605 | PF00017 | 0.365 |
LIG_UBA3_1 | 229 | 236 | PF00899 | 0.317 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.490 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.396 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.531 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.706 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.714 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.372 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.597 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.359 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.466 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.340 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.497 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.331 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.605 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.628 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.368 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.275 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.389 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.329 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.478 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.696 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.362 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.505 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.689 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.663 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.684 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.534 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.499 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.508 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.298 |
MOD_LATS_1 | 24 | 30 | PF00433 | 0.607 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.476 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.191 |
MOD_N-GLC_1 | 567 | 572 | PF02516 | 0.280 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.282 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.335 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.274 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.525 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.417 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.310 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.384 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.274 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.325 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.330 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.540 |
MOD_NEK2_2 | 457 | 462 | PF00069 | 0.374 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.361 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.726 |
MOD_PIKK_1 | 479 | 485 | PF00454 | 0.389 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.792 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.740 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.457 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.537 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.804 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.740 |
MOD_PKB_1 | 418 | 426 | PF00069 | 0.528 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.543 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.384 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.538 |
MOD_Plk_1 | 567 | 573 | PF00069 | 0.452 |
MOD_Plk_2-3 | 505 | 511 | PF00069 | 0.547 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.305 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.320 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.322 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.318 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.312 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.276 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.514 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.490 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.342 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.274 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.345 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.258 |
MOD_SUMO_rev_2 | 278 | 287 | PF00179 | 0.358 |
TRG_DiLeu_BaEn_2 | 428 | 434 | PF01217 | 0.390 |
TRG_DiLeu_BaEn_3 | 379 | 385 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.594 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.767 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ81 | Leptomonas seymouri | 21% | 100% |
A0A0N1PA98 | Leptomonas seymouri | 65% | 99% |
A0A0S4IV32 | Bodo saltans | 23% | 100% |
A0A0S4JU02 | Bodo saltans | 33% | 100% |
A0A1X0NR26 | Trypanosomatidae | 31% | 100% |
A0A1X0NRL7 | Trypanosomatidae | 41% | 100% |
A0A3Q8ICL1 | Leishmania donovani | 97% | 100% |
A0A3Q8IDG8 | Leishmania donovani | 35% | 100% |
A0A3Q8IG00 | Leishmania donovani | 40% | 100% |
A0A3Q8IGE6 | Leishmania donovani | 92% | 98% |
A0A3Q8IHH7 | Leishmania donovani | 20% | 95% |
A0A3Q8IJH2 | Leishmania donovani | 34% | 100% |
A0A3Q8IJX8 | Leishmania donovani | 34% | 100% |
A0A3Q8ILE0 | Leishmania donovani | 38% | 100% |
A0A3Q8IQG8 | Leishmania donovani | 25% | 100% |
A0A3R7JSA0 | Trypanosoma rangeli | 43% | 100% |
A0A3R7MWF1 | Trypanosoma rangeli | 22% | 100% |
A0A3R7N1H9 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WQ39 | Leishmania donovani | 37% | 100% |
A0A3S7X443 | Leishmania donovani | 36% | 100% |
A0A3S7X4A1 | Leishmania donovani | 34% | 100% |
A0A3S7X4L2 | Leishmania donovani | 100% | 100% |
A0A3S7X4P0 | Leishmania donovani | 98% | 100% |
A0A3S7XA86 | Leishmania donovani | 23% | 100% |
A0A3S7XCE3 | Leishmania donovani | 23% | 100% |
A0A422MW74 | Trypanosoma rangeli | 37% | 100% |
A0A422N608 | Trypanosoma rangeli | 44% | 100% |
A0A422NZS1 | Trypanosoma rangeli | 34% | 100% |
A4H565 | Leishmania braziliensis | 36% | 100% |
A4HC75 | Leishmania braziliensis | 36% | 100% |
A4HFT5 | Leishmania braziliensis | 36% | 100% |
A4HJ07 | Leishmania braziliensis | 36% | 100% |
A4HJ09 | Leishmania braziliensis | 36% | 100% |
A4HJ35 | Leishmania braziliensis | 39% | 100% |
A4HJ63 | Leishmania braziliensis | 36% | 100% |
A4HJF8 | Leishmania braziliensis | 74% | 99% |
A4HJF9 | Leishmania braziliensis | 73% | 96% |
A4HJG1 | Leishmania braziliensis | 72% | 96% |
A4HJG3 | Leishmania braziliensis | 74% | 99% |
A4HJG5 | Leishmania braziliensis | 73% | 99% |
A4HKQ7 | Leishmania braziliensis | 34% | 100% |
A4HLK3 | Leishmania braziliensis | 20% | 93% |
A4HNJ6 | Leishmania braziliensis | 24% | 100% |
A4HNJ7 | Leishmania braziliensis | 22% | 100% |
A4HNQ0 | Leishmania braziliensis | 25% | 100% |
A4HTE2 | Leishmania infantum | 37% | 100% |
A4HZQ0 | Leishmania infantum | 38% | 100% |
A4I6I1 | Leishmania infantum | 34% | 100% |
A4I6J9 | Leishmania infantum | 36% | 100% |
A4I6L3 | Leishmania infantum | 40% | 100% |
A4I6L4 | Leishmania infantum | 34% | 100% |
A4I6W4 | Leishmania infantum | 99% | 100% |
A4I887 | Leishmania infantum | 33% | 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% |
C9ZWR1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZWR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 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) | 35% | 100% |
E8NHS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
E9ADD7 | Leishmania major | 33% | 100% |
E9AG08 | Leishmania major | 22% | 100% |
E9AG09 | Leishmania major | 23% | 100% |
E9AHL1 | Leishmania infantum | 98% | 100% |
E9AHL2 | Leishmania infantum | 90% | 97% |
E9AHL3 | Leishmania infantum | 97% | 100% |
E9ALD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 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% |
E9AYW9 | 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) | 36% | 100% |
E9B1K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B1N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9B1Y0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
E9B345 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B3X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 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% |
Q4Q072 | Leishmania major | 23% | 100% |
Q4Q236 | Leishmania major | 26% | 100% |
Q4Q509 | Leishmania major | 34% | 100% |
Q4Q680 | Leishmania major | 92% | 100% |
Q4Q682 | Leishmania major | 88% | 99% |
Q4Q683 | Leishmania major | 92% | 100% |
Q4Q6H5 | Leishmania major | 34% | 100% |
Q4Q6K6 | Leishmania major | 40% | 100% |
Q4Q6M9 | Leishmania major | 35% | 100% |
Q4QBX3 | Leishmania major | 38% | 100% |
Q4QIH0 | Leishmania major | 37% | 100% |
Q969I6 | Homo sapiens | 23% | 100% |
V5BIJ1 | Trypanosoma cruzi | 36% | 100% |
V5D7K9 | Trypanosoma cruzi | 34% | 100% |