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: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 15 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HHE4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 24 |
GO:0006793 | phosphorus metabolic process | 3 | 24 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 24 |
GO:0006807 | nitrogen compound metabolic process | 2 | 24 |
GO:0008152 | metabolic process | 1 | 24 |
GO:0009987 | cellular process | 1 | 24 |
GO:0016310 | phosphorylation | 5 | 24 |
GO:0019538 | protein metabolic process | 3 | 24 |
GO:0036211 | protein modification process | 4 | 24 |
GO:0043170 | macromolecule metabolic process | 3 | 24 |
GO:0043412 | macromolecule modification | 4 | 24 |
GO:0044237 | cellular metabolic process | 2 | 24 |
GO:0044238 | primary metabolic process | 2 | 24 |
GO:0071704 | organic substance metabolic process | 2 | 24 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 24 |
GO:0007165 | signal transduction | 2 | 3 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 3 |
GO:0046777 | protein autophosphorylation | 6 | 2 |
GO:0050789 | regulation of biological process | 2 | 3 |
GO:0050794 | regulation of cellular process | 3 | 3 |
GO:0065007 | biological regulation | 1 | 3 |
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 1 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 24 |
GO:0003824 | catalytic activity | 1 | 24 |
GO:0004672 | protein kinase activity | 3 | 24 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 19 |
GO:0005488 | binding | 1 | 24 |
GO:0005524 | ATP binding | 5 | 24 |
GO:0016301 | kinase activity | 4 | 24 |
GO:0016740 | transferase activity | 2 | 24 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 24 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 24 |
GO:0017076 | purine nucleotide binding | 4 | 24 |
GO:0030554 | adenyl nucleotide binding | 5 | 24 |
GO:0032553 | ribonucleotide binding | 3 | 24 |
GO:0032555 | purine ribonucleotide binding | 4 | 24 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 24 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 24 |
GO:0036094 | small molecule binding | 2 | 24 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043168 | anion binding | 3 | 24 |
GO:0097159 | organic cyclic compound binding | 2 | 24 |
GO:0097367 | carbohydrate derivative binding | 2 | 24 |
GO:0106310 | protein serine kinase activity | 4 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 24 |
GO:1901265 | nucleoside phosphate binding | 3 | 24 |
GO:1901363 | heterocyclic compound binding | 2 | 24 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005516 | calmodulin binding | 3 | 2 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 2 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.272 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.215 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.512 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.523 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.314 |
DOC_CYCLIN_yCln2_LP_2 | 545 | 551 | PF00134 | 0.244 |
DOC_MAPK_gen_1 | 315 | 325 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 386 | 395 | PF00069 | 0.461 |
DOC_PP1_RVXF_1 | 295 | 301 | PF00149 | 0.244 |
DOC_PP4_FxxP_1 | 329 | 332 | PF00568 | 0.244 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.256 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.222 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.222 |
DOC_USP7_MATH_2 | 44 | 50 | PF00917 | 0.523 |
DOC_USP7_UBL2_3 | 584 | 588 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 172 | 182 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 324 | 329 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 456 | 460 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 570 | 580 | PF00244 | 0.266 |
LIG_14-3-3_CterR_2 | 587 | 589 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 245 | 260 | PF00022 | 0.413 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.531 |
LIG_BIR_III_4 | 396 | 400 | PF00653 | 0.254 |
LIG_BRCT_BRCA1_1 | 283 | 287 | PF00533 | 0.213 |
LIG_CtBP_PxDLS_1 | 200 | 204 | PF00389 | 0.473 |
LIG_CtBP_PxDLS_1 | 515 | 519 | PF00389 | 0.244 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.504 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.489 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.244 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.502 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.282 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.244 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.231 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.267 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.481 |
LIG_LIR_Apic_2 | 212 | 217 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 327 | 332 | PF02991 | 0.244 |
LIG_LIR_Apic_2 | 405 | 411 | PF02991 | 0.234 |
LIG_LIR_Apic_2 | 462 | 468 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 270 | 279 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.203 |
LIG_MAD2 | 218 | 226 | PF02301 | 0.501 |
LIG_REV1ctd_RIR_1 | 285 | 295 | PF16727 | 0.210 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.491 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 273 | 277 | PF00017 | 0.244 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.244 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.321 |
LIG_SH3_1 | 36 | 42 | PF00018 | 0.527 |
LIG_SH3_1 | 525 | 531 | PF00018 | 0.210 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.540 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.533 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.531 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.248 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.210 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.524 |
LIG_SUMO_SIM_par_1 | 118 | 127 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 230 | 238 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 547 | 552 | PF11976 | 0.242 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.523 |
LIG_UBA3_1 | 286 | 291 | PF00899 | 0.215 |
LIG_UBA3_1 | 558 | 565 | PF00899 | 0.288 |
LIG_WRC_WIRS_1 | 137 | 142 | PF05994 | 0.480 |
LIG_WW_1 | 497 | 500 | PF00397 | 0.244 |
MOD_CDC14_SPxK_1 | 22 | 25 | PF00782 | 0.534 |
MOD_CDC14_SPxK_1 | 94 | 97 | PF00782 | 0.539 |
MOD_CDK_SPK_2 | 156 | 161 | PF00069 | 0.518 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.540 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.537 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.538 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.538 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.522 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.534 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.538 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.560 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.494 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.514 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.484 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.255 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.246 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.256 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.237 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.244 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.229 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.272 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.544 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.531 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.507 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.215 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.231 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.344 |
MOD_Cter_Amidation | 454 | 457 | PF01082 | 0.244 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.552 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.556 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.511 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.551 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.498 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.516 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.498 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.282 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.247 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.261 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.336 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.288 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.222 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.257 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.348 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.556 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.513 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.542 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.497 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.591 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.583 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.518 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.509 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.245 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.248 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.295 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.491 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.244 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.252 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.243 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.300 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.578 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.531 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.503 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.277 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.548 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.537 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.520 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.566 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.346 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.310 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.302 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.508 |
MOD_NEK2_2 | 541 | 546 | PF00069 | 0.210 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.543 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.319 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.244 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.210 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.263 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.408 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.541 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.276 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.523 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.280 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.503 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.541 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.290 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.268 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.245 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.316 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.524 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.540 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.541 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.489 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.314 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.382 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.539 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.587 |
MOD_SUMO_for_1 | 388 | 391 | PF00179 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 8 | 13 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.293 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 301 | 306 | PF00026 | 0.277 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8INQ4 | Leishmania donovani | 27% | 100% |
A0A3S5H5G0 | Leishmania donovani | 27% | 100% |
A0A3S7WY10 | Leishmania donovani | 27% | 100% |
A0A3S7X2F1 | Leishmania donovani | 74% | 100% |
A4H459 | Leishmania braziliensis | 27% | 100% |
A4HA97 | Leishmania braziliensis | 25% | 100% |
A4HCD7 | Leishmania braziliensis | 27% | 100% |
A4HD79 | Leishmania braziliensis | 28% | 100% |
A4HED7 | Leishmania braziliensis | 28% | 100% |
A4HHQ5 | Leishmania braziliensis | 24% | 100% |
A4HSE2 | Leishmania infantum | 27% | 100% |
A4I1T4 | Leishmania infantum | 27% | 100% |
E9ADZ1 | Leishmania major | 74% | 100% |
E9AET0 | Leishmania major | 27% | 100% |
E9AH34 | Leishmania infantum | 27% | 100% |
E9AHI7 | Leishmania infantum | 74% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ALU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AWL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4QAV8 | Leishmania major | 27% | 100% |
Q4QJJ0 | Leishmania major | 26% | 100% |