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: 16 |
NetGPI | no | yes: 0, no: 16 |
Related structures:
AlphaFold database: A4HM43
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 17 |
GO:0007165 | signal transduction | 2 | 17 |
GO:0008152 | metabolic process | 1 | 17 |
GO:0009056 | catabolic process | 2 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0016042 | lipid catabolic process | 4 | 17 |
GO:0035556 | intracellular signal transduction | 3 | 17 |
GO:0044238 | primary metabolic process | 2 | 17 |
GO:0050789 | regulation of biological process | 2 | 17 |
GO:0050794 | regulation of cellular process | 3 | 17 |
GO:0065007 | biological regulation | 1 | 17 |
GO:0071704 | organic substance metabolic process | 2 | 17 |
GO:1901575 | organic substance catabolic process | 3 | 17 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 2 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004435 | phosphatidylinositol phospholipase C activity | 7 | 17 |
GO:0004620 | phospholipase activity | 5 | 17 |
GO:0004629 | phospholipase C activity | 6 | 17 |
GO:0005488 | binding | 1 | 15 |
GO:0005509 | calcium ion binding | 5 | 15 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 17 |
GO:0016298 | lipase activity | 4 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 17 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 17 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043169 | cation binding | 3 | 15 |
GO:0046872 | metal ion binding | 4 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.176 |
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.176 |
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.357 |
CLV_C14_Caspase3-7 | 615 | 619 | PF00656 | 0.596 |
CLV_MEL_PAP_1 | 172 | 178 | PF00089 | 0.306 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.176 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.176 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.442 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.364 |
DEG_COP1_1 | 634 | 646 | PF00400 | 0.283 |
DEG_MDM2_SWIB_1 | 104 | 111 | PF02201 | 0.472 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.391 |
DOC_CKS1_1 | 431 | 436 | PF01111 | 0.287 |
DOC_CYCLIN_yCln2_LP_2 | 431 | 437 | PF00134 | 0.176 |
DOC_MAPK_gen_1 | 25 | 33 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 38 | 47 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 415 | 424 | PF00069 | 0.176 |
DOC_MAPK_gen_1 | 660 | 669 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 27 | 36 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 390 | 398 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 41 | 49 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 662 | 671 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 157 | 163 | PF00149 | 0.445 |
DOC_PP1_RVXF_1 | 359 | 365 | PF00149 | 0.347 |
DOC_SPAK_OSR1_1 | 236 | 240 | PF12202 | 0.465 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.432 |
DOC_USP7_MATH_2 | 710 | 716 | PF00917 | 0.268 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.315 |
DOC_USP7_UBL2_3 | 440 | 444 | PF12436 | 0.346 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.176 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 137 | 142 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 17 | 26 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 266 | 270 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.430 |
LIG_Actin_WH2_2 | 19 | 37 | PF00022 | 0.514 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.642 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.331 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 384 | 392 | PF00928 | 0.244 |
LIG_DLG_GKlike_1 | 251 | 258 | PF00625 | 0.376 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.593 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.446 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.328 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.552 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.314 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.402 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.474 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.385 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.406 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.415 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.380 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.440 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.391 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.385 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.420 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.391 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.393 |
LIG_LIR_Apic_2 | 341 | 346 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 119 | 125 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 161 | 169 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 179 | 185 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 232 | 240 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 67 | 78 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 695 | 705 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 107 | 111 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 721 | 725 | PF02991 | 0.277 |
LIG_MLH1_MIPbox_1 | 300 | 304 | PF16413 | 0.331 |
LIG_PCNA_yPIPBox_3 | 137 | 149 | PF02747 | 0.408 |
LIG_PCNA_yPIPBox_3 | 35 | 46 | PF02747 | 0.325 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.436 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.424 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.365 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.379 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.529 |
LIG_RPA_C_Fungi | 142 | 154 | PF08784 | 0.296 |
LIG_SH2_GRB2like | 207 | 210 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 432 | 436 | PF00017 | 0.178 |
LIG_SH2_SRC | 503 | 506 | PF00017 | 0.287 |
LIG_SH2_SRC | 58 | 61 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 218 | 221 | PF00017 | 0.383 |
LIG_SH2_STAT3 | 374 | 377 | PF00017 | 0.336 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.424 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.357 |
LIG_SUMO_SIM_par_1 | 391 | 397 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 45 | 50 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 473 | 478 | PF11976 | 0.508 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.463 |
LIG_TRFH_1 | 275 | 279 | PF08558 | 0.500 |
LIG_TRFH_1 | 582 | 586 | PF08558 | 0.347 |
LIG_UBA3_1 | 33 | 41 | PF00899 | 0.364 |
LIG_UBA3_1 | 716 | 723 | PF00899 | 0.225 |
MOD_CDK_SPxK_1 | 245 | 251 | PF00069 | 0.449 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.569 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.346 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.312 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.347 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.322 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.328 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.361 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.391 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.433 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.280 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.385 |
MOD_CK1_1 | 721 | 727 | PF00069 | 0.338 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.426 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.486 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.433 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.475 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.418 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.531 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.364 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.326 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.371 |
MOD_Cter_Amidation | 213 | 216 | PF01082 | 0.262 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.431 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.359 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.623 |
MOD_GlcNHglycan | 476 | 480 | PF01048 | 0.480 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.557 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.526 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.594 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.499 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.524 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.472 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.338 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.222 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.427 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.674 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.397 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.356 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.383 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.479 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.547 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.446 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.458 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.524 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.391 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.176 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.505 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.459 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.387 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.350 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.356 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.489 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.371 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.324 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.257 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.280 |
MOD_NEK2_2 | 718 | 723 | PF00069 | 0.341 |
MOD_OFUCOSY | 188 | 195 | PF10250 | 0.371 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.513 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.271 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.295 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.568 |
MOD_PK_1 | 147 | 153 | PF00069 | 0.284 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.456 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.496 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.494 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.377 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.524 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.302 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.571 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.462 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.534 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.528 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.489 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.445 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.193 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.303 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.367 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.462 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.380 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.468 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.497 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.328 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.328 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.276 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.403 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.461 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.422 |
MOD_Plk_4 | 667 | 673 | PF00069 | 0.400 |
MOD_Plk_4 | 712 | 718 | PF00069 | 0.448 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.458 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.176 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.287 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.348 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.486 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.538 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.466 |
MOD_SUMO_rev_2 | 453 | 458 | PF00179 | 0.559 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.337 |
TRG_DiLeu_BaLyEn_6 | 467 | 472 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 603 | 608 | PF01217 | 0.313 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.176 |
TRG_Pf-PMV_PEXEL_1 | 123 | 127 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1N0 | Leptomonas seymouri | 31% | 99% |
A0A0N1IKD7 | Leptomonas seymouri | 61% | 97% |
A0A0S4ITT3 | Bodo saltans | 31% | 84% |
A0A0S4J9Y4 | Bodo saltans | 32% | 100% |
A0A0S4JUS2 | Bodo saltans | 32% | 100% |
A0A1X0P2K1 | Trypanosomatidae | 33% | 99% |
A0A3Q8IF05 | Leishmania donovani | 32% | 99% |
A0A3S7X8U7 | Leishmania donovani | 79% | 100% |
A0A422N571 | Trypanosoma rangeli | 35% | 100% |
A4HCK9 | Leishmania braziliensis | 32% | 100% |
A4I027 | Leishmania infantum | 33% | 93% |
A4I5X4 | Leishmania infantum | 32% | 99% |
A4IAQ5 | Leishmania infantum | 79% | 100% |
A5D6R3 | Danio rerio | 29% | 93% |
E9AEI1 | Leishmania major | 79% | 100% |
E9B168 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 99% |
E9B5P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
P10688 | Rattus norvegicus | 32% | 96% |
P40977 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 81% |
P51178 | Homo sapiens | 30% | 96% |
Q15111 | Homo sapiens | 29% | 67% |
Q1RML2 | Bos taurus | 27% | 100% |
Q2VRL0 | Gallus gallus | 31% | 100% |
Q32NH8 | Xenopus laevis | 30% | 96% |
Q39032 | Arabidopsis thaliana | 27% | 100% |
Q3USB7 | Mus musculus | 29% | 67% |
Q4Q6Z7 | Leishmania major | 33% | 100% |
Q4QBH9 | Leishmania major | 31% | 100% |
Q56W08 | Arabidopsis thaliana | 29% | 100% |
Q5FX52 | Rattus norvegicus | 27% | 100% |
Q5RET0 | Pongo abelii | 30% | 96% |
Q62688 | Rattus norvegicus | 29% | 67% |
Q62711 | Rattus norvegicus | 31% | 94% |
Q7YRU3 | Sus scrofa | 27% | 100% |
Q86YW0 | Homo sapiens | 28% | 100% |
Q8GV43 | Arabidopsis thaliana | 28% | 100% |
Q8K2J0 | Mus musculus | 31% | 93% |
Q8K4D7 | Mus musculus | 29% | 100% |
Q8N3E9 | Homo sapiens | 32% | 92% |
Q8R3B1 | Mus musculus | 31% | 96% |
Q944C2 | Arabidopsis thaliana | 27% | 100% |
Q9BRC7 | Homo sapiens | 31% | 96% |