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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8IF05
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0007165 | signal transduction | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009056 | catabolic process | 2 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016042 | lipid catabolic process | 4 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901575 | organic substance catabolic process | 3 | 7 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 1 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004435 | phosphatidylinositol phospholipase C activity | 7 | 7 |
GO:0004620 | phospholipase activity | 5 | 7 |
GO:0004629 | phospholipase C activity | 6 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 7 |
GO:0016298 | lipase activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.551 |
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.694 |
CLV_C14_Caspase3-7 | 686 | 690 | PF00656 | 0.291 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.474 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 639 | 641 | PF00082 | 0.392 |
CLV_PCSK_PC7_1 | 37 | 43 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 407 | 415 | PF00400 | 0.392 |
DEG_SCF_TRCP1_1 | 459 | 465 | PF00400 | 0.580 |
DOC_CKS1_1 | 425 | 430 | PF01111 | 0.392 |
DOC_CYCLIN_RxL_1 | 511 | 522 | PF00134 | 0.346 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 21 | 30 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 108 | 117 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 176 | 184 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 362 | 371 | PF00069 | 0.256 |
DOC_MAPK_gen_1 | 46 | 52 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 65 | 74 | PF00069 | 0.283 |
DOC_MAPK_HePTP_8 | 170 | 182 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 173 | 182 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 670 | 679 | PF00069 | 0.346 |
DOC_PP1_RVXF_1 | 112 | 118 | PF00149 | 0.326 |
DOC_PP1_RVXF_1 | 267 | 273 | PF00149 | 0.346 |
DOC_PP1_RVXF_1 | 363 | 369 | PF00149 | 0.346 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.536 |
DOC_USP7_UBL2_3 | 169 | 173 | PF12436 | 0.468 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.437 |
DOC_USP7_UBL2_3 | 62 | 66 | PF12436 | 0.465 |
DOC_USP7_UBL2_3 | 88 | 92 | PF12436 | 0.468 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 269 | 279 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 377 | 387 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 47 | 53 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.401 |
LIG_Actin_WH2_2 | 23 | 39 | PF00022 | 0.349 |
LIG_Actin_WH2_2 | 687 | 704 | PF00022 | 0.346 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.368 |
LIG_BIR_III_2 | 499 | 503 | PF00653 | 0.346 |
LIG_BIR_III_4 | 199 | 203 | PF00653 | 0.459 |
LIG_deltaCOP1_diTrp_1 | 236 | 243 | PF00928 | 0.416 |
LIG_EVH1_1 | 10 | 14 | PF00568 | 0.471 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.500 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.463 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.394 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.485 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.384 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.306 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.564 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.346 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.288 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.386 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.201 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.449 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.430 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.532 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.415 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.359 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.392 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.392 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.346 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.495 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.573 |
LIG_IBAR_NPY_1 | 656 | 658 | PF08397 | 0.392 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 209 | 218 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 242 | 249 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 256 | 264 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 630 | 637 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 703 | 708 | PF02991 | 0.437 |
LIG_MAD2 | 434 | 442 | PF02301 | 0.286 |
LIG_MYND_1 | 282 | 286 | PF01753 | 0.535 |
LIG_NRBOX | 477 | 483 | PF00104 | 0.528 |
LIG_PCNA_yPIPBox_3 | 469 | 482 | PF02747 | 0.615 |
LIG_PCNA_yPIPBox_3 | 688 | 702 | PF02747 | 0.353 |
LIG_Pex14_1 | 113 | 117 | PF04695 | 0.398 |
LIG_Pex14_1 | 659 | 663 | PF04695 | 0.286 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.407 |
LIG_PTB_Apo_2 | 420 | 427 | PF02174 | 0.332 |
LIG_PTB_Phospho_1 | 420 | 426 | PF10480 | 0.332 |
LIG_SH2_CRK | 705 | 709 | PF00017 | 0.334 |
LIG_SH2_GRB2like | 636 | 639 | PF00017 | 0.353 |
LIG_SH2_PTP2 | 632 | 635 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 503 | 506 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.286 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.286 |
LIG_SH3_3 | 728 | 734 | PF00018 | 0.466 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.454 |
LIG_SH3_4 | 619 | 626 | PF00018 | 0.392 |
LIG_SH3_4 | 62 | 69 | PF00018 | 0.515 |
LIG_SH3_5 | 303 | 307 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 608 | 613 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 671 | 676 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 385 | 390 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 48 | 55 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 605 | 610 | PF11976 | 0.392 |
LIG_SxIP_EBH_1 | 610 | 624 | PF03271 | 0.346 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.499 |
LIG_TRFH_1 | 278 | 282 | PF08558 | 0.364 |
LIG_TRFH_1 | 586 | 590 | PF08558 | 0.286 |
LIG_TYR_ITSM | 701 | 708 | PF00017 | 0.392 |
LIG_UBA3_1 | 190 | 197 | PF00899 | 0.484 |
LIG_UBA3_1 | 258 | 266 | PF00899 | 0.488 |
LIG_UBA3_1 | 410 | 419 | PF00899 | 0.295 |
LIG_UBA3_1 | 577 | 582 | PF00899 | 0.392 |
LIG_WRC_WIRS_1 | 228 | 233 | PF05994 | 0.465 |
LIG_WRC_WIRS_1 | 660 | 665 | PF05994 | 0.392 |
MOD_CDK_SPxxK_3 | 462 | 469 | PF00069 | 0.681 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.510 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.366 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.297 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.377 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.504 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.449 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.389 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.349 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.392 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.392 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.346 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.403 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.442 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.545 |
MOD_GlcNHglycan | 199 | 203 | PF01048 | 0.400 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.393 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.660 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.499 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.346 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.403 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.677 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.363 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.458 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.353 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.605 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.517 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.392 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.372 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.317 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.396 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.297 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.403 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.308 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.575 |
MOD_N-GLC_1 | 687 | 692 | PF02516 | 0.353 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.500 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.529 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.499 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.305 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.371 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.392 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.444 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.269 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.346 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.464 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.429 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.361 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.712 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.562 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.346 |
MOD_PK_1 | 41 | 47 | PF00069 | 0.401 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.514 |
MOD_PKA_1 | 46 | 52 | PF00069 | 0.443 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.403 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.346 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.510 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.430 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.422 |
MOD_PKB_1 | 46 | 54 | PF00069 | 0.440 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.438 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.459 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.392 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.375 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.404 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.453 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.286 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.409 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.392 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.392 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.314 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.522 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.380 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.347 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.286 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.730 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.455 |
MOD_SUMO_rev_2 | 163 | 170 | PF00179 | 0.424 |
MOD_SUMO_rev_2 | 171 | 178 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 51 | 59 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 641 | 648 | PF00179 | 0.353 |
TRG_DiLeu_BaEn_2 | 241 | 247 | PF01217 | 0.332 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 705 | 708 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.501 |
TRG_NES_CRM1_1 | 207 | 220 | PF08389 | 0.467 |
TRG_NES_CRM1_1 | 405 | 420 | PF08389 | 0.247 |
TRG_NLS_Bipartite_1 | 47 | 69 | PF00514 | 0.529 |
TRG_NLS_MonoExtC_3 | 64 | 69 | PF00514 | 0.570 |
TRG_NLS_MonoExtN_4 | 62 | 69 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 88 | 95 | PF00514 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWX7 | Leptomonas seymouri | 35% | 100% |
A0A0N1I1N0 | Leptomonas seymouri | 63% | 100% |
A0A0N1IKD7 | Leptomonas seymouri | 33% | 98% |
A0A0S4ITT3 | Bodo saltans | 33% | 84% |
A0A0S4J9Y4 | Bodo saltans | 37% | 100% |
A0A0S4JUS2 | Bodo saltans | 35% | 100% |
A0A1X0P2K1 | Trypanosomatidae | 41% | 100% |
A0A3S7X8U7 | Leishmania donovani | 33% | 100% |
A0A422N571 | Trypanosoma rangeli | 34% | 100% |
A4HCK9 | Leishmania braziliensis | 34% | 100% |
A4HM43 | Leishmania braziliensis | 32% | 100% |
A4I027 | Leishmania infantum | 34% | 100% |
A4I5X4 | Leishmania infantum | 100% | 100% |
A4IAQ5 | Leishmania infantum | 33% | 100% |
A5D6R3 | Danio rerio | 34% | 94% |
D0A7A3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AEI1 | Leishmania major | 33% | 100% |
E9B168 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B5P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
P10688 | Rattus norvegicus | 33% | 97% |
P10895 | Bos taurus | 33% | 97% |
P40977 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 82% |
P51178 | Homo sapiens | 32% | 97% |
Q15111 | Homo sapiens | 28% | 67% |
Q1RML2 | Bos taurus | 32% | 100% |
Q2VRL0 | Gallus gallus | 33% | 100% |
Q32NH8 | Xenopus laevis | 35% | 97% |
Q39032 | Arabidopsis thaliana | 29% | 100% |
Q39033 | Arabidopsis thaliana | 29% | 100% |
Q3USB7 | Mus musculus | 27% | 67% |
Q4Q6Z7 | Leishmania major | 95% | 100% |
Q4QBH9 | Leishmania major | 31% | 100% |
Q56W08 | Arabidopsis thaliana | 28% | 100% |
Q5FX52 | Rattus norvegicus | 31% | 100% |
Q5RET0 | Pongo abelii | 32% | 97% |
Q62688 | Rattus norvegicus | 27% | 67% |
Q62711 | Rattus norvegicus | 35% | 95% |
Q7YRU3 | Sus scrofa | 31% | 100% |
Q86YW0 | Homo sapiens | 32% | 100% |
Q8GV43 | Arabidopsis thaliana | 29% | 100% |
Q8K2J0 | Mus musculus | 37% | 94% |
Q8K4D7 | Mus musculus | 31% | 100% |
Q8N3E9 | Homo sapiens | 38% | 93% |
Q8R3B1 | Mus musculus | 33% | 97% |
Q8SPR7 | Sus scrofa | 32% | 95% |
Q944C1 | Arabidopsis thaliana | 30% | 100% |
Q944C2 | Arabidopsis thaliana | 28% | 100% |
Q9BRC7 | Homo sapiens | 33% | 97% |
Q9LY51 | Arabidopsis thaliana | 29% | 100% |