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: 18 |
NetGPI | no | yes: 0, no: 18 |
Related structures:
AlphaFold database: E9AEI1
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 19 |
GO:0007165 | signal transduction | 2 | 19 |
GO:0008152 | metabolic process | 1 | 19 |
GO:0009056 | catabolic process | 2 | 19 |
GO:0009987 | cellular process | 1 | 19 |
GO:0016042 | lipid catabolic process | 4 | 19 |
GO:0035556 | intracellular signal transduction | 3 | 19 |
GO:0044238 | primary metabolic process | 2 | 19 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 3 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 3 |
GO:0050789 | regulation of biological process | 2 | 19 |
GO:0050794 | regulation of cellular process | 3 | 19 |
GO:0065007 | biological regulation | 1 | 19 |
GO:0071704 | organic substance metabolic process | 2 | 19 |
GO:1901575 | organic substance catabolic process | 3 | 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 19 |
GO:0004435 | phosphatidylinositol phospholipase C activity | 7 | 19 |
GO:0004620 | phospholipase activity | 5 | 19 |
GO:0004629 | phospholipase C activity | 6 | 19 |
GO:0005488 | binding | 1 | 17 |
GO:0005509 | calcium ion binding | 5 | 17 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 19 |
GO:0016298 | lipase activity | 4 | 19 |
GO:0016787 | hydrolase activity | 2 | 19 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 19 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 19 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043169 | cation binding | 3 | 17 |
GO:0046872 | metal ion binding | 4 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 618 | 622 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.461 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.360 |
DEG_MDM2_SWIB_1 | 104 | 111 | PF02201 | 0.472 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.509 |
DOC_CKS1_1 | 722 | 727 | PF01111 | 0.372 |
DOC_MAPK_gen_1 | 27 | 36 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 38 | 47 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 436 | 443 | PF00069 | 0.337 |
DOC_MAPK_gen_1 | 660 | 669 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 390 | 398 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 41 | 49 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 662 | 671 | PF00069 | 0.441 |
DOC_PP1_RVXF_1 | 157 | 163 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 359 | 365 | PF00149 | 0.348 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.388 |
DOC_PP4_FxxP_1 | 722 | 725 | PF00568 | 0.485 |
DOC_SPAK_OSR1_1 | 236 | 240 | PF12202 | 0.486 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.381 |
DOC_USP7_UBL2_3 | 436 | 440 | PF12436 | 0.363 |
DOC_USP7_UBL2_3 | 84 | 88 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 721 | 726 | PF00397 | 0.445 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 17 | 26 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 220 | 229 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 487 | 492 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 521 | 530 | PF00244 | 0.416 |
LIG_Actin_WH2_2 | 19 | 37 | PF00022 | 0.509 |
LIG_Actin_WH2_2 | 440 | 458 | PF00022 | 0.389 |
LIG_APCC_ABBA_1 | 629 | 634 | PF00400 | 0.522 |
LIG_APCC_ABBAyCdc20_2 | 628 | 634 | PF00400 | 0.334 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.604 |
LIG_BRCT_BRCA1_1 | 613 | 617 | PF00533 | 0.296 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.514 |
LIG_DLG_GKlike_1 | 251 | 258 | PF00625 | 0.365 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.568 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.448 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.319 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.570 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.296 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.436 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.421 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.459 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.369 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.389 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.419 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.370 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.439 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.475 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.665 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.458 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.406 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.400 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.368 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.574 |
LIG_LIR_Apic_2 | 341 | 346 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 721 | 725 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 119 | 125 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 161 | 168 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 232 | 239 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 254 | 260 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 270 | 279 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 695 | 705 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 107 | 111 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.376 |
LIG_PCNA_yPIPBox_3 | 135 | 149 | PF02747 | 0.575 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.439 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.430 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.380 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.507 |
LIG_PTB_Apo_2 | 167 | 174 | PF02174 | 0.368 |
LIG_REV1ctd_RIR_1 | 202 | 210 | PF16727 | 0.273 |
LIG_SH2_GRB2like | 207 | 210 | PF00017 | 0.421 |
LIG_SH2_SRC | 503 | 506 | PF00017 | 0.282 |
LIG_SH2_SRC | 58 | 61 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 374 | 377 | PF00017 | 0.355 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.423 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.352 |
LIG_SUMO_SIM_par_1 | 391 | 397 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 473 | 478 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 639 | 646 | PF11976 | 0.349 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.481 |
LIG_TRFH_1 | 275 | 279 | PF08558 | 0.435 |
LIG_TRFH_1 | 582 | 586 | PF08558 | 0.333 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.471 |
MOD_CDK_SPxK_1 | 245 | 251 | PF00069 | 0.501 |
MOD_CDK_SPxK_1 | 430 | 436 | PF00069 | 0.388 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.627 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.421 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.455 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.309 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.319 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.406 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.423 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.344 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.508 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.480 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.519 |
MOD_CK1_1 | 721 | 727 | PF00069 | 0.329 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.624 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.531 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.414 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.421 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.514 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.418 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.400 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.343 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.417 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.626 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.471 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.392 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.528 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.523 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.505 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.403 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.604 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.347 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.421 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.622 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.418 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.326 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.373 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.499 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.538 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.403 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.576 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.390 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.356 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.606 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.479 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.507 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.351 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.268 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.353 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.458 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.379 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.598 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.366 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.470 |
MOD_NEK2_2 | 718 | 723 | PF00069 | 0.335 |
MOD_OFUCOSY | 188 | 195 | PF10250 | 0.366 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.374 |
MOD_PKA_1 | 17 | 23 | PF00069 | 0.330 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.435 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.468 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.361 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.562 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.463 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.510 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.576 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.659 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.479 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.527 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.486 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.466 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.324 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.428 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.329 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.459 |
MOD_Plk_2-3 | 7 | 13 | PF00069 | 0.431 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.451 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.500 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.407 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.392 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.333 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.446 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.497 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.450 |
MOD_Plk_4 | 712 | 718 | PF00069 | 0.444 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.588 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.490 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.282 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.323 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.496 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.248 |
MOD_ProDKin_1 | 721 | 727 | PF00069 | 0.460 |
MOD_SUMO_rev_2 | 10 | 20 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 453 | 458 | PF00179 | 0.574 |
TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 467 | 472 | PF01217 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 603 | 608 | PF01217 | 0.311 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 627 | 630 | PF00400 | 0.245 |
TRG_NES_CRM1_1 | 412 | 428 | PF08389 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.433 |
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 | 31% | 100% |
A0A1X0P2K1 | Trypanosomatidae | 34% | 99% |
A0A3Q8IF05 | Leishmania donovani | 33% | 99% |
A0A3S7X8U7 | Leishmania donovani | 92% | 100% |
A0A422N571 | Trypanosoma rangeli | 35% | 100% |
A4HCK9 | Leishmania braziliensis | 30% | 100% |
A4HM43 | Leishmania braziliensis | 79% | 100% |
A4I027 | Leishmania infantum | 32% | 93% |
A4I5X4 | Leishmania infantum | 33% | 99% |
A4IAQ5 | Leishmania infantum | 92% | 100% |
A5D6R3 | Danio rerio | 30% | 93% |
E9B168 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 99% |
E9B5P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
P10688 | Rattus norvegicus | 30% | 96% |
P10895 | Bos taurus | 31% | 96% |
P40977 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 81% |
Q15111 | Homo sapiens | 29% | 67% |
Q1RML2 | Bos taurus | 27% | 100% |
Q2VRL0 | Gallus gallus | 29% | 100% |
Q32NH8 | Xenopus laevis | 29% | 96% |
Q39032 | Arabidopsis thaliana | 25% | 100% |
Q39033 | Arabidopsis thaliana | 26% | 100% |
Q3USB7 | Mus musculus | 28% | 67% |
Q4Q6Z7 | Leishmania major | 33% | 99% |
Q4QBH9 | Leishmania major | 30% | 100% |
Q5RET0 | Pongo abelii | 29% | 96% |
Q62688 | Rattus norvegicus | 28% | 67% |
Q62711 | Rattus norvegicus | 28% | 94% |
Q6NMA7 | Arabidopsis thaliana | 23% | 100% |
Q7YRU3 | Sus scrofa | 31% | 100% |
Q86YW0 | Homo sapiens | 28% | 100% |
Q8GV43 | Arabidopsis thaliana | 27% | 100% |
Q8K2J0 | Mus musculus | 31% | 93% |
Q8K4D7 | Mus musculus | 27% | 100% |
Q8N3E9 | Homo sapiens | 31% | 92% |
Q8R3B1 | Mus musculus | 29% | 96% |
Q944C2 | Arabidopsis thaliana | 27% | 100% |
Q9BRC7 | Homo sapiens | 29% | 96% |