Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 6 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7WZA2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 15 |
GO:0006793 | phosphorus metabolic process | 3 | 15 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 15 |
GO:0006807 | nitrogen compound metabolic process | 2 | 15 |
GO:0008152 | metabolic process | 1 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016310 | phosphorylation | 5 | 15 |
GO:0019538 | protein metabolic process | 3 | 15 |
GO:0036211 | protein modification process | 4 | 15 |
GO:0043170 | macromolecule metabolic process | 3 | 15 |
GO:0043412 | macromolecule modification | 4 | 15 |
GO:0044237 | cellular metabolic process | 2 | 15 |
GO:0044238 | primary metabolic process | 2 | 15 |
GO:0071704 | organic substance metabolic process | 2 | 15 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 15 |
GO:0006810 | transport | 3 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0004672 | protein kinase activity | 3 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0016301 | kinase activity | 4 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 15 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.484 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 349 | 351 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 503 | 505 | PF00082 | 0.638 |
CLV_PCSK_PC7_1 | 345 | 351 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.567 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.377 |
DEG_APCC_DBOX_1 | 263 | 271 | PF00400 | 0.428 |
DEG_SCF_FBW7_2 | 304 | 310 | PF00400 | 0.343 |
DOC_CKS1_1 | 304 | 309 | PF01111 | 0.443 |
DOC_CKS1_1 | 414 | 419 | PF01111 | 0.635 |
DOC_CYCLIN_RxL_1 | 324 | 332 | PF00134 | 0.469 |
DOC_CYCLIN_RxL_1 | 345 | 354 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 379 | 385 | PF00134 | 0.632 |
DOC_MAPK_gen_1 | 125 | 132 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 210 | 218 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 231 | 238 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 349 | 355 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 42 | 52 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 125 | 134 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 43 | 52 | PF00069 | 0.452 |
DOC_PP1_RVXF_1 | 223 | 229 | PF00149 | 0.377 |
DOC_PP1_RVXF_1 | 325 | 332 | PF00149 | 0.461 |
DOC_PP2B_LxvP_1 | 353 | 356 | PF13499 | 0.462 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.600 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.610 |
DOC_PP4_FxxP_1 | 507 | 510 | PF00568 | 0.614 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.880 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.566 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.614 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.439 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 125 | 129 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 169 | 174 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 350 | 356 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 396 | 401 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 409 | 413 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 475 | 481 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 504 | 510 | PF00244 | 0.588 |
LIG_AP2alpha_1 | 33 | 37 | PF02296 | 0.462 |
LIG_APCC_ABBAyCdc20_2 | 193 | 199 | PF00400 | 0.377 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.377 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.567 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.616 |
LIG_deltaCOP1_diTrp_1 | 439 | 445 | PF00928 | 0.516 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.418 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.343 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.665 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.606 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.519 |
LIG_LIR_Apic_2 | 411 | 417 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 269 | 278 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 336 | 344 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 439 | 450 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 318 | 322 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 32 | 36 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.480 |
LIG_LYPXL_yS_3 | 59 | 62 | PF13949 | 0.476 |
LIG_MYND_3 | 425 | 429 | PF01753 | 0.613 |
LIG_Pex14_2 | 33 | 37 | PF04695 | 0.580 |
LIG_PTB_Apo_2 | 27 | 34 | PF02174 | 0.484 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.548 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.459 |
LIG_SH3_2 | 510 | 515 | PF14604 | 0.578 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.448 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.611 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.650 |
LIG_SUMO_SIM_anti_2 | 129 | 134 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 175 | 181 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 393 | 405 | PF11976 | 0.774 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.374 |
LIG_UBA3_1 | 343 | 349 | PF00899 | 0.421 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.606 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.400 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.689 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.629 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.656 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.400 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.591 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.371 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.687 |
MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.400 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.742 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.605 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.729 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.615 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.544 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.348 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.419 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.714 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.803 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.758 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.590 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.748 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.608 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.573 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.486 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.705 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.621 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.609 |
MOD_N-GLC_2 | 165 | 167 | PF02516 | 0.329 |
MOD_N-GLC_2 | 321 | 323 | PF02516 | 0.348 |
MOD_N-GLC_2 | 364 | 366 | PF02516 | 0.586 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.499 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.464 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.446 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.343 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.473 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.594 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.795 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.408 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.554 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.616 |
MOD_PK_1 | 396 | 402 | PF00069 | 0.646 |
MOD_PKA_1 | 169 | 175 | PF00069 | 0.392 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.348 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.570 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.382 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.676 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.566 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.498 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.625 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.596 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.435 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.759 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.587 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.616 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.441 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.594 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.631 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.648 |
MOD_SUMO_for_1 | 200 | 203 | PF00179 | 0.370 |
MOD_SUMO_for_1 | 50 | 53 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 35 | 44 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 63 | 68 | PF00179 | 0.402 |
TRG_DiLeu_BaEn_2 | 267 | 273 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.638 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 515 | 518 | PF00400 | 0.606 |
TRG_NLS_Bipartite_1 | 42 | 59 | PF00514 | 0.434 |
TRG_NLS_MonoExtN_4 | 54 | 59 | PF00514 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 341 | 346 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.471 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F5 | Leptomonas seymouri | 40% | 100% |
A0A0N1I2H3 | Leptomonas seymouri | 31% | 100% |
A0A0N1IKB0 | Leptomonas seymouri | 31% | 91% |
A0A1X0NZS9 | Trypanosomatidae | 46% | 100% |
A0A3Q8IJ66 | Leishmania donovani | 46% | 100% |
A0A3Q8ISA0 | Leishmania donovani | 42% | 100% |
A0A3R7K1Y6 | Trypanosoma rangeli | 27% | 78% |
A0A3S7WNZ6 | Leishmania donovani | 33% | 100% |
A0A422NL83 | Trypanosoma rangeli | 52% | 100% |
A4H436 | Leishmania braziliensis | 33% | 100% |
A4HEI6 | Leishmania braziliensis | 79% | 99% |
A4HFV0 | Leishmania braziliensis | 31% | 93% |
A4HMD1 | Leishmania braziliensis | 46% | 100% |
A4HSC0 | Leishmania infantum | 33% | 100% |
A4I1K4 | Leishmania infantum | 100% | 100% |
A4I638 | Leishmania infantum | 42% | 100% |
A4IAZ8 | Leishmania infantum | 46% | 100% |
A7E3X2 | Bos taurus | 42% | 100% |
C9ZK43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZM31 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 75% |
E9AKA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AXN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AZ78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1C3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B5Y1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
O96999 | Leishmania major | 32% | 100% |
P39962 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 99% |
Q4Q6U1 | Leishmania major | 41% | 100% |
Q4Q9T3 | Leishmania major | 93% | 97% |
Q62761 | Rattus norvegicus | 41% | 100% |
Q8BN21 | Mus musculus | 28% | 100% |
Q8BTH8 | Mus musculus | 41% | 100% |
Q9NHE1 | Leishmania major | 46% | 100% |