Acyltransferase involved in GPI anchor remodelling (homologue of yeast GUP1)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HFC9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 5 |
GO:0004707 | MAP kinase activity | 5 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.311 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.651 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.333 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.333 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.418 |
DEG_SPOP_SBC_1 | 388 | 392 | PF00917 | 0.624 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.670 |
DOC_AGCK_PIF_2 | 77 | 82 | PF00069 | 0.333 |
DOC_CYCLIN_RxL_1 | 212 | 221 | PF00134 | 0.333 |
DOC_CYCLIN_RxL_1 | 433 | 442 | PF00134 | 0.512 |
DOC_CYCLIN_yClb1_LxF_4 | 73 | 79 | PF00134 | 0.333 |
DOC_CYCLIN_yCln2_LP_2 | 464 | 470 | PF00134 | 0.483 |
DOC_MAPK_gen_1 | 138 | 147 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 181 | 190 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 491 | 500 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 650 | 658 | PF00069 | 0.593 |
DOC_MAPK_HePTP_8 | 178 | 190 | PF00069 | 0.387 |
DOC_MAPK_JIP1_4 | 141 | 147 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.387 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.476 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.202 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.333 |
DOC_USP7_UBL2_3 | 34 | 38 | PF12436 | 0.333 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 253 | 257 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 291 | 298 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 354 | 361 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 493 | 498 | PF00244 | 0.504 |
LIG_eIF4E_1 | 183 | 189 | PF01652 | 0.333 |
LIG_eIF4E_1 | 82 | 88 | PF01652 | 0.333 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.387 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.398 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.214 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.333 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.660 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.202 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.596 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.372 |
LIG_LIR_Apic_2 | 180 | 186 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.387 |
LIG_LYPXL_yS_3 | 113 | 116 | PF13949 | 0.333 |
LIG_NRBOX | 643 | 649 | PF00104 | 0.579 |
LIG_PTB_Apo_2 | 585 | 592 | PF02174 | 0.635 |
LIG_PTB_Apo_2 | 597 | 604 | PF02174 | 0.536 |
LIG_PTB_Phospho_1 | 585 | 591 | PF10480 | 0.637 |
LIG_REV1ctd_RIR_1 | 300 | 308 | PF16727 | 0.330 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.321 |
LIG_SH2_NCK_1 | 468 | 472 | PF00017 | 0.704 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 468 | 472 | PF00017 | 0.497 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.496 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.333 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.333 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.631 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.333 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.515 |
LIG_SH3_5 | 173 | 177 | PF00018 | 0.333 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.510 |
LIG_SUMO_SIM_anti_2 | 50 | 55 | PF11976 | 0.333 |
LIG_SUMO_SIM_anti_2 | 86 | 92 | PF11976 | 0.202 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.333 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.333 |
LIG_TYR_ITIM | 111 | 116 | PF00017 | 0.369 |
LIG_UBA3_1 | 123 | 132 | PF00899 | 0.379 |
LIG_UBA3_1 | 87 | 95 | PF00899 | 0.369 |
MOD_CDC14_SPxK_1 | 365 | 368 | PF00782 | 0.464 |
MOD_CDC14_SPxK_1 | 404 | 407 | PF00782 | 0.624 |
MOD_CDK_SPK_2 | 362 | 367 | PF00069 | 0.618 |
MOD_CDK_SPK_2 | 633 | 638 | PF00069 | 0.515 |
MOD_CDK_SPxK_1 | 362 | 368 | PF00069 | 0.481 |
MOD_CDK_SPxK_1 | 401 | 407 | PF00069 | 0.626 |
MOD_CDK_SPxxK_3 | 505 | 512 | PF00069 | 0.531 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.278 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.333 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.686 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.569 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.632 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.688 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.580 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.579 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.450 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.425 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.372 |
MOD_Cter_Amidation | 434 | 437 | PF01082 | 0.654 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.475 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.298 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.337 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.377 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.548 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.566 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.462 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.732 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.631 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.621 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.658 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.609 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.517 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.462 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.317 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.471 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.621 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.748 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.610 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.792 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.647 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.724 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.700 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.674 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.571 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.559 |
MOD_N-GLC_1 | 567 | 572 | PF02516 | 0.522 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.692 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.644 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.487 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.555 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.633 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.642 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.526 |
MOD_PIKK_1 | 570 | 576 | PF00454 | 0.645 |
MOD_PK_1 | 229 | 235 | PF00069 | 0.333 |
MOD_PKA_1 | 148 | 154 | PF00069 | 0.202 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.202 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.362 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.387 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.656 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.671 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.617 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.558 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.647 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.650 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.607 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.650 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.720 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.321 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.516 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.600 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.202 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.438 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.619 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.606 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.711 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.667 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.596 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.703 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.803 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.538 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.649 |
MOD_SUMO_for_1 | 140 | 143 | PF00179 | 0.333 |
MOD_SUMO_for_1 | 531 | 534 | PF00179 | 0.618 |
TRG_DiLeu_BaEn_4 | 43 | 49 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 106 | 111 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.362 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.333 |
TRG_NES_CRM1_1 | 296 | 309 | PF08389 | 0.333 |
TRG_NLS_MonoExtN_4 | 247 | 254 | PF00514 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 437 | 441 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4E3 | Leptomonas seymouri | 55% | 98% |
A0A3Q8IE25 | Leishmania donovani | 82% | 100% |
A0A3Q8IND3 | Leishmania donovani | 27% | 100% |
A0A3Q8IVR8 | Leishmania donovani | 34% | 100% |
A0A3S5H5U5 | Leishmania donovani | 24% | 100% |
A0A3S5H6C8 | Leishmania donovani | 27% | 100% |
A0A3S7WQK7 | Leishmania donovani | 27% | 100% |
A0A3S7X8Z8 | Leishmania donovani | 23% | 100% |
A4H4S9 | Leishmania braziliensis | 26% | 100% |
A4H5L7 | Leishmania braziliensis | 26% | 100% |
A4H7W1 | Leishmania braziliensis | 25% | 100% |
A4H9U7 | Leishmania braziliensis | 26% | 100% |
A4HEA1 | Leishmania braziliensis | 24% | 100% |
A4HFF3 | Leishmania braziliensis | 25% | 100% |
A4HNT2 | Leishmania braziliensis | 35% | 100% |
A4HNU6 | Leishmania braziliensis | 26% | 100% |
A4HTV4 | Leishmania infantum | 27% | 100% |
A4HTV5 | Leishmania infantum | 27% | 100% |
A4I2K6 | Leishmania infantum | 82% | 100% |
A4IB02 | Leishmania infantum | 23% | 100% |
A4ICP8 | Leishmania infantum | 27% | 100% |
A4ICR2 | Leishmania infantum | 34% | 100% |
E9ACY7 | Leishmania major | 82% | 100% |
E9AET0 | Leishmania major | 24% | 100% |
E9AG71 | Leishmania infantum | 24% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ASJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AYR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q1Z0 | Leishmania major | 28% | 100% |
Q4QIV8 | Leishmania major | 24% | 100% |
Q4R7T5 | Macaca fascicularis | 31% | 100% |
Q5R754 | Pongo abelii | 32% | 100% |
Q92772 | Homo sapiens | 31% | 100% |