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: 63 |
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: 92 |
NetGPI | no | yes: 0, no: 92 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 78 |
GO:0110165 | cellular anatomical entity | 1 | 78 |
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: A4HJG5
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 14 |
GO:0006810 | transport | 3 | 14 |
GO:0006865 | amino acid transport | 5 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0015849 | organic acid transport | 5 | 14 |
GO:0051179 | localization | 1 | 14 |
GO:0051234 | establishment of localization | 2 | 14 |
GO:0055085 | transmembrane transport | 2 | 14 |
GO:0071702 | organic substance transport | 4 | 14 |
GO:0071705 | nitrogen compound transport | 4 | 14 |
GO:1903825 | organic acid transmembrane transport | 3 | 14 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 14 |
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 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0005215 | transporter activity | 1 | 14 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 14 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 14 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 14 |
GO:0022857 | transmembrane transporter activity | 2 | 14 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 14 |
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 | 120 | 124 | PF00656 | 0.317 |
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.507 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.427 |
DEG_SPOP_SBC_1 | 45 | 49 | PF00917 | 0.602 |
DOC_CDC14_PxL_1 | 238 | 246 | PF14671 | 0.180 |
DOC_MAPK_FxFP_2 | 565 | 568 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 37 | 45 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 71 | 78 | PF00069 | 0.628 |
DOC_MAPK_MEF2A_6 | 229 | 237 | PF00069 | 0.219 |
DOC_MAPK_MEF2A_6 | 253 | 262 | PF00069 | 0.501 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.329 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.334 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.332 |
DOC_PP4_FxxP_1 | 565 | 568 | PF00568 | 0.337 |
DOC_PP4_FxxP_1 | 62 | 65 | PF00568 | 0.612 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.215 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.209 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.759 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.715 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 24 | 33 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 253 | 262 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 37 | 43 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 417 | 421 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 64 | 70 | PF00244 | 0.716 |
LIG_Actin_WH2_2 | 238 | 255 | PF00022 | 0.301 |
LIG_ActinCP_TwfCPI_2 | 62 | 72 | PF01115 | 0.585 |
LIG_APCC_ABBA_1 | 386 | 391 | PF00400 | 0.186 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.636 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 558 | 562 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 563 | 567 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 574 | 578 | PF00533 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 331 | 336 | PF00928 | 0.423 |
LIG_EH_1 | 386 | 390 | PF12763 | 0.185 |
LIG_eIF4E_1 | 588 | 594 | PF01652 | 0.517 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.321 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.383 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.341 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.330 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.478 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.306 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.597 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.515 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.359 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.750 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.421 |
LIG_GBD_Chelix_1 | 271 | 279 | PF00786 | 0.183 |
LIG_GBD_Chelix_1 | 348 | 356 | PF00786 | 0.190 |
LIG_HP1_1 | 462 | 466 | PF01393 | 0.376 |
LIG_KLC1_Yacidic_2 | 515 | 520 | PF13176 | 0.499 |
LIG_LIR_Apic_2 | 564 | 568 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 559 | 570 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 591 | 600 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 609 | 614 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 419 | 424 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 591 | 595 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 609 | 614 | PF02991 | 0.537 |
LIG_MYND_1 | 242 | 246 | PF01753 | 0.180 |
LIG_PALB2_WD40_1 | 581 | 589 | PF16756 | 0.530 |
LIG_PCNA_yPIPBox_3 | 341 | 352 | PF02747 | 0.381 |
LIG_Pex14_1 | 184 | 188 | PF04695 | 0.436 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.329 |
LIG_Pex14_2 | 262 | 266 | PF04695 | 0.377 |
LIG_Pex14_2 | 567 | 571 | PF04695 | 0.381 |
LIG_PTB_Apo_2 | 518 | 525 | PF02174 | 0.501 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.324 |
LIG_SH2_GRB2like | 588 | 591 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 398 | 401 | PF00017 | 0.368 |
LIG_SH2_SRC | 133 | 136 | PF00017 | 0.210 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.316 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.291 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 323 | 326 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.338 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.433 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.617 |
LIG_Sin3_3 | 408 | 415 | PF02671 | 0.352 |
LIG_SUMO_SIM_anti_2 | 256 | 262 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 381 | 386 | PF11976 | 0.253 |
LIG_SUMO_SIM_anti_2 | 390 | 396 | PF11976 | 0.259 |
LIG_SUMO_SIM_anti_2 | 468 | 475 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 591 | 597 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.295 |
LIG_SUMO_SIM_par_1 | 530 | 535 | PF11976 | 0.327 |
LIG_SxIP_EBH_1 | 88 | 100 | PF03271 | 0.542 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.440 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.365 |
LIG_TYR_ITIM | 263 | 268 | PF00017 | 0.363 |
LIG_TYR_ITIM | 396 | 401 | PF00017 | 0.373 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.365 |
LIG_TYR_ITSM | 129 | 136 | PF00017 | 0.201 |
LIG_TYR_ITSM | 357 | 364 | PF00017 | 0.332 |
LIG_TYR_ITSM | 607 | 614 | PF00017 | 0.479 |
LIG_UBA3_1 | 240 | 247 | PF00899 | 0.341 |
LIG_WRC_WIRS_1 | 157 | 162 | PF05994 | 0.493 |
LIG_WRC_WIRS_1 | 562 | 567 | PF05994 | 0.233 |
MOD_CDC14_SPxK_1 | 35 | 38 | PF00782 | 0.587 |
MOD_CDK_SPK_2 | 32 | 37 | PF00069 | 0.585 |
MOD_CDK_SPxK_1 | 32 | 38 | PF00069 | 0.587 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.290 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.676 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.652 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.684 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.404 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.594 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.354 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.330 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.289 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.493 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.481 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.404 |
MOD_GlcNHglycan | 215 | 219 | PF01048 | 0.490 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.316 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.464 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.550 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.255 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.353 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.269 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.272 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.478 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.400 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.390 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.288 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.747 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.690 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.593 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.497 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.485 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.467 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.411 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.228 |
MOD_N-GLC_1 | 510 | 515 | PF02516 | 0.176 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.283 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.281 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.332 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.329 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.296 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.510 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.205 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.758 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.604 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.185 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.680 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.503 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.628 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.586 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.191 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.441 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.496 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.503 |
MOD_Plk_2-3 | 510 | 516 | PF00069 | 0.494 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.334 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.379 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.326 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.287 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.283 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.314 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.291 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.596 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.476 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.498 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.358 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.272 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.499 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.335 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.511 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.303 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.716 |
MOD_SUMO_rev_2 | 289 | 298 | PF00179 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.350 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.740 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8W4 | Leptomonas seymouri | 26% | 100% |
A0A0N1I9T3 | Leptomonas seymouri | 31% | 100% |
A0A0N1IJ81 | Leptomonas seymouri | 22% | 100% |
A0A0N1PA98 | Leptomonas seymouri | 62% | 100% |
A0A0N1PBP2 | Leptomonas seymouri | 32% | 100% |
A0A0N1PFD1 | Leptomonas seymouri | 32% | 100% |
A0A0S4IV32 | Bodo saltans | 24% | 100% |
A0A1X0NKV2 | Trypanosomatidae | 33% | 100% |
A0A1X0P0B5 | Trypanosomatidae | 23% | 100% |
A0A3Q8ICL1 | Leishmania donovani | 73% | 100% |
A0A3Q8IDG8 | Leishmania donovani | 36% | 100% |
A0A3Q8IFZ0 | Leishmania donovani | 34% | 100% |
A0A3Q8IG00 | Leishmania donovani | 38% | 100% |
A0A3Q8IGE6 | Leishmania donovani | 76% | 100% |
A0A3Q8IHH7 | Leishmania donovani | 22% | 100% |
A0A3Q8IJH2 | Leishmania donovani | 32% | 100% |
A0A3Q8IJX8 | Leishmania donovani | 33% | 100% |
A0A3Q8ILE0 | Leishmania donovani | 39% | 100% |
A0A3Q8IQG8 | Leishmania donovani | 28% | 100% |
A0A3S5H6T4 | Leishmania donovani | 34% | 100% |
A0A3S5H7P4 | Leishmania donovani | 34% | 100% |
A0A3S7WQ39 | Leishmania donovani | 35% | 100% |
A0A3S7X443 | Leishmania donovani | 38% | 100% |
A0A3S7X4A1 | Leishmania donovani | 33% | 100% |
A0A3S7X4L2 | Leishmania donovani | 74% | 100% |
A0A3S7X4N4 | Leishmania donovani | 73% | 100% |
A0A3S7X4P0 | Leishmania donovani | 74% | 100% |
A0A3S7XA86 | Leishmania donovani | 26% | 100% |
A0A422P566 | Trypanosoma rangeli | 21% | 100% |
A4H565 | Leishmania braziliensis | 37% | 100% |
A4HC75 | Leishmania braziliensis | 38% | 100% |
A4HFJ2 | Leishmania braziliensis | 33% | 100% |
A4HFT5 | Leishmania braziliensis | 37% | 100% |
A4HJ06 | Leishmania braziliensis | 32% | 100% |
A4HJ07 | Leishmania braziliensis | 39% | 100% |
A4HJ09 | Leishmania braziliensis | 40% | 100% |
A4HJ10 | Leishmania braziliensis | 33% | 100% |
A4HJ35 | Leishmania braziliensis | 38% | 100% |
A4HJ36 | Leishmania braziliensis | 34% | 100% |
A4HJ63 | Leishmania braziliensis | 35% | 100% |
A4HJF8 | Leishmania braziliensis | 98% | 100% |
A4HJF9 | Leishmania braziliensis | 95% | 100% |
A4HJG1 | Leishmania braziliensis | 95% | 100% |
A4HJG3 | Leishmania braziliensis | 99% | 100% |
A4HKQ7 | Leishmania braziliensis | 32% | 100% |
A4HLK3 | Leishmania braziliensis | 21% | 100% |
A4HNJ6 | Leishmania braziliensis | 24% | 100% |
A4HNQ0 | Leishmania braziliensis | 25% | 100% |
A4HTE2 | Leishmania infantum | 35% | 100% |
A4HZQ0 | Leishmania infantum | 39% | 100% |
A4I6F1 | Leishmania infantum | 34% | 100% |
A4I6I1 | Leishmania infantum | 33% | 100% |
A4I6J9 | Leishmania infantum | 38% | 100% |
A4I6K0 | Leishmania infantum | 36% | 100% |
A4I6L3 | Leishmania infantum | 38% | 100% |
A4I6L4 | Leishmania infantum | 33% | 100% |
A4I6W4 | Leishmania infantum | 74% | 100% |
A4I887 | Leishmania infantum | 31% | 100% |
A4I914 | Leishmania infantum | 22% | 100% |
A4IC53 | Leishmania infantum | 26% | 100% |
A4ICC3 | Leishmania infantum | 22% | 100% |
A4ICU5 | Leishmania infantum | 28% | 100% |
C9ZWR1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E8NHF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9ADD7 | Leishmania major | 35% | 100% |
E9AG08 | Leishmania major | 24% | 100% |
E9AHD7 | Leishmania infantum | 33% | 100% |
E9AHL1 | Leishmania infantum | 74% | 100% |
E9AHL2 | Leishmania infantum | 75% | 100% |
E9AHL3 | Leishmania infantum | 73% | 100% |
E9ALD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9ASF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AUB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AVK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AYW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AZ62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1I4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B1I6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1K8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 79% |
E9B1Y0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9B345 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B3X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B761 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
P40074 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
Q4Q072 | Leishmania major | 23% | 100% |
Q4Q236 | Leishmania major | 27% | 100% |
Q4Q445 | Leishmania major | 22% | 95% |
Q4Q509 | Leishmania major | 31% | 100% |
Q4Q680 | Leishmania major | 74% | 98% |
Q4Q682 | Leishmania major | 77% | 100% |
Q4Q683 | Leishmania major | 74% | 98% |
Q4Q6H5 | Leishmania major | 34% | 100% |
Q4Q6K5 | Leishmania major | 34% | 100% |
Q4Q6K6 | Leishmania major | 37% | 100% |
Q4Q6M8 | Leishmania major | 36% | 100% |
Q4Q6M9 | Leishmania major | 37% | 100% |
Q4QBX3 | Leishmania major | 39% | 100% |
Q4QIH0 | Leishmania major | 34% | 100% |