A large and apprently artificial collection of diverse kinetoplastid protein kinases. A subfamily has 2TM regions, but the majority is cytoplasmic.
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HNU6
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 26 |
GO:0006793 | phosphorus metabolic process | 3 | 26 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 26 |
GO:0006807 | nitrogen compound metabolic process | 2 | 26 |
GO:0008152 | metabolic process | 1 | 26 |
GO:0009987 | cellular process | 1 | 26 |
GO:0016310 | phosphorylation | 5 | 26 |
GO:0019538 | protein metabolic process | 3 | 26 |
GO:0036211 | protein modification process | 4 | 26 |
GO:0043170 | macromolecule metabolic process | 3 | 26 |
GO:0043412 | macromolecule modification | 4 | 26 |
GO:0044237 | cellular metabolic process | 2 | 26 |
GO:0044238 | primary metabolic process | 2 | 26 |
GO:0071704 | organic substance metabolic process | 2 | 26 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 26 |
GO:0000165 | MAPK cascade | 4 | 1 |
GO:0001932 | regulation of protein phosphorylation | 7 | 1 |
GO:0001934 | positive regulation of protein phosphorylation | 8 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0009967 | positive regulation of signal transduction | 5 | 1 |
GO:0010562 | positive regulation of phosphorus metabolic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0010647 | positive regulation of cell communication | 5 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0023056 | positive regulation of signaling | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0031401 | positive regulation of protein modification process | 7 | 1 |
GO:0033674 | positive regulation of kinase activity | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0042325 | regulation of phosphorylation | 7 | 1 |
GO:0042327 | positive regulation of phosphorylation | 8 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0043405 | regulation of MAP kinase activity | 8 | 1 |
GO:0043406 | positive regulation of MAP kinase activity | 8 | 1 |
GO:0043408 | regulation of MAPK cascade | 6 | 1 |
GO:0043410 | positive regulation of MAPK cascade | 7 | 1 |
GO:0043549 | regulation of kinase activity | 5 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045859 | regulation of protein kinase activity | 6 | 1 |
GO:0045860 | positive regulation of protein kinase activity | 7 | 1 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0048584 | positive regulation of response to stimulus | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0071900 | regulation of protein serine/threonine kinase activity | 7 | 1 |
GO:0071902 | positive regulation of protein serine/threonine kinase activity | 8 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
GO:1902533 | positive regulation of intracellular signal transduction | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 26 |
GO:0003824 | catalytic activity | 1 | 26 |
GO:0004672 | protein kinase activity | 3 | 26 |
GO:0005488 | binding | 1 | 26 |
GO:0005524 | ATP binding | 5 | 26 |
GO:0016301 | kinase activity | 4 | 26 |
GO:0016740 | transferase activity | 2 | 26 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 26 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 26 |
GO:0017076 | purine nucleotide binding | 4 | 26 |
GO:0030554 | adenyl nucleotide binding | 5 | 26 |
GO:0032553 | ribonucleotide binding | 3 | 26 |
GO:0032555 | purine ribonucleotide binding | 4 | 26 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 26 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 26 |
GO:0036094 | small molecule binding | 2 | 26 |
GO:0043167 | ion binding | 2 | 26 |
GO:0043168 | anion binding | 3 | 26 |
GO:0097159 | organic cyclic compound binding | 2 | 26 |
GO:0097367 | carbohydrate derivative binding | 2 | 26 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 26 |
GO:1901265 | nucleoside phosphate binding | 3 | 26 |
GO:1901363 | heterocyclic compound binding | 2 | 26 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 12 |
GO:0004707 | MAP kinase activity | 5 | 4 |
GO:0004708 | MAP kinase kinase activity | 5 | 1 |
GO:0004712 | protein serine/threonine/tyrosine kinase activity | 4 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0019900 | kinase binding | 4 | 1 |
GO:0019901 | protein kinase binding | 5 | 1 |
GO:0051019 | mitogen-activated protein kinase binding | 6 | 1 |
GO:0004140 | dephospho-CoA kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.212 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.231 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.232 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.230 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.236 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.448 |
CLV_PCSK_PC7_1 | 416 | 422 | PF00082 | 0.400 |
CLV_PCSK_PC7_1 | 75 | 81 | PF00082 | 0.174 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.176 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.266 |
DEG_APCC_DBOX_1 | 101 | 109 | PF00400 | 0.214 |
DEG_APCC_DBOX_1 | 158 | 166 | PF00400 | 0.212 |
DEG_APCC_DBOX_1 | 431 | 439 | PF00400 | 0.479 |
DEG_SCF_TRCP1_1 | 483 | 488 | PF00400 | 0.496 |
DOC_CKS1_1 | 113 | 118 | PF01111 | 0.221 |
DOC_CYCLIN_yClb1_LxF_4 | 521 | 526 | PF00134 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 145 | 151 | PF00134 | 0.221 |
DOC_CYCLIN_yCln2_LP_2 | 345 | 348 | PF00134 | 0.496 |
DOC_MAPK_MEF2A_6 | 451 | 460 | PF00069 | 0.485 |
DOC_PP2B_LxvP_1 | 280 | 283 | PF13499 | 0.280 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.221 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.555 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.234 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 370 | 380 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 506 | 512 | PF00244 | 0.505 |
LIG_Actin_WH2_2 | 244 | 260 | PF00022 | 0.251 |
LIG_APCC_ABBAyCdc20_2 | 172 | 178 | PF00400 | 0.275 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.489 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.333 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.377 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.364 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.404 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.765 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.515 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.484 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.241 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.320 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.380 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.499 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.522 |
LIG_GBD_Chelix_1 | 406 | 414 | PF00786 | 0.315 |
LIG_LIR_Apic_2 | 112 | 116 | PF02991 | 0.240 |
LIG_LIR_Apic_2 | 217 | 223 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 130 | 138 | PF02991 | 0.212 |
LIG_LIR_LC3C_4 | 239 | 244 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 229 | 233 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.240 |
LIG_NRBOX | 520 | 526 | PF00104 | 0.486 |
LIG_PDZ_Class_2 | 521 | 526 | PF00595 | 0.488 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.212 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.221 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.350 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.292 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.280 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 52 | 61 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 46 | 53 | PF11976 | 0.356 |
MOD_CDC14_SPxK_1 | 222 | 225 | PF00782 | 0.280 |
MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.221 |
MOD_CDK_SPxK_1 | 219 | 225 | PF00069 | 0.280 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.221 |
MOD_CDK_SPxxK_3 | 298 | 305 | PF00069 | 0.221 |
MOD_CDK_SPxxK_3 | 384 | 391 | PF00069 | 0.522 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.533 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.657 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.495 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.231 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.305 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.486 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.253 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.528 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.591 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.328 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.352 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.497 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.603 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.636 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.345 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.329 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.312 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.373 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.542 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.546 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.663 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.688 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.461 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.598 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.588 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.522 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.514 |
MOD_N-GLC_2 | 187 | 189 | PF02516 | 0.174 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.269 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.370 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.260 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.272 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.374 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.507 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.379 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.513 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.320 |
MOD_PKA_1 | 304 | 310 | PF00069 | 0.232 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.319 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.687 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.357 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.512 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.584 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.525 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.232 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.310 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.479 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.425 |
MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.393 |
MOD_Plk_2-3 | 393 | 399 | PF00069 | 0.393 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.227 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.333 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.374 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.472 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.330 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.248 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.304 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.234 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.551 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.581 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.523 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.618 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.592 |
MOD_SUMO_for_1 | 414 | 417 | PF00179 | 0.323 |
MOD_SUMO_rev_2 | 188 | 196 | PF00179 | 0.284 |
TRG_DiLeu_BaEn_1 | 520 | 525 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_2 | 127 | 133 | PF01217 | 0.212 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.222 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.253 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.223 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.235 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0B6 | Leptomonas seymouri | 57% | 98% |
A0A0N1I0C1 | Leptomonas seymouri | 28% | 100% |
A0A0S4J7K5 | Bodo saltans | 24% | 89% |
A0A1X0P919 | Trypanosomatidae | 56% | 100% |
A0A3Q8IND3 | Leishmania donovani | 77% | 100% |
A0A3S5IRC3 | Trypanosoma rangeli | 56% | 100% |
A0A3S7WYP4 | Leishmania donovani | 34% | 100% |
A0A3S7X2W3 | Leishmania donovani | 35% | 100% |
A0A3S7X7Y2 | Leishmania donovani | 34% | 100% |
A0A422NT49 | Trypanosoma rangeli | 27% | 74% |
A4HAS1 | Leishmania braziliensis | 34% | 100% |
A4HDU3 | Leishmania braziliensis | 34% | 100% |
A4HFA1 | Leishmania braziliensis | 30% | 100% |
A4HFC9 | Leishmania braziliensis | 26% | 80% |
A4HHN1 | Leishmania braziliensis | 35% | 100% |
A4I140 | Leishmania infantum | 34% | 100% |
A4I4U6 | Leishmania infantum | 35% | 100% |
A4I9Y5 | Leishmania infantum | 34% | 100% |
A4ICP8 | Leishmania infantum | 77% | 100% |
B4HBU3 | Drosophila persimilis | 28% | 68% |
E9ALJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9APX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 74% |
E9ASK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
E9AX78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AYN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
P54739 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 28% | 97% |
Q0PKV7 | Leishmania mexicana | 77% | 100% |
Q2LYK3 | Drosophila pseudoobscura pseudoobscura | 28% | 68% |
Q4Q1Z0 | Leishmania major | 77% | 98% |
Q4Q2Z2 | Leishmania major | 33% | 100% |
Q4QA98 | Leishmania major | 33% | 100% |
Q4QFK4 | Leishmania major | 28% | 84% |
Q9Y077 | Leishmania major | 35% | 100% |
V5C234 | Trypanosoma cruzi | 27% | 97% |
V5DCD4 | Trypanosoma cruzi | 24% | 90% |