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: 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: 24 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 3 |
GO:0032991 | protein-containing complex | 1 | 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:0045239 | tricarboxylic acid cycle enzyme complex | 3 | 3 |
GO:0045240 | dihydrolipoyl dehydrogenase complex | 4 | 3 |
GO:0045252 | oxoglutarate dehydrogenase complex | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
GO:1990204 | oxidoreductase complex | 3 | 3 |
GO:1990234 | transferase complex | 3 | 3 |
Related structures:
AlphaFold database: A4HJQ3
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 31 |
GO:0019725 | cellular homeostasis | 2 | 31 |
GO:0042592 | homeostatic process | 3 | 31 |
GO:0045454 | cell redox homeostasis | 3 | 31 |
GO:0050789 | regulation of biological process | 2 | 31 |
GO:0050794 | regulation of cellular process | 3 | 31 |
GO:0065007 | biological regulation | 1 | 31 |
GO:0065008 | regulation of biological quality | 2 | 31 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 31 |
GO:0003824 | catalytic activity | 1 | 31 |
GO:0005488 | binding | 1 | 31 |
GO:0016491 | oxidoreductase activity | 2 | 31 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 4 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 4 |
GO:0019152 | acetoin dehydrogenase activity | 5 | 4 |
GO:0036094 | small molecule binding | 2 | 31 |
GO:0043167 | ion binding | 2 | 31 |
GO:0043168 | anion binding | 3 | 31 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 31 |
GO:0052587 | diacetyl reductase ((R)-acetoin forming) activity | 6 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 31 |
GO:1901265 | nucleoside phosphate binding | 3 | 31 |
GO:1901363 | heterocyclic compound binding | 2 | 31 |
GO:0004148 | dihydrolipoyl dehydrogenase activity | 5 | 12 |
GO:0016667 | oxidoreductase activity, acting on a sulfur group of donors | 3 | 12 |
GO:0016668 | oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor | 4 | 12 |
GO:0004591 | oxoglutarate dehydrogenase (succinyl-transferring) activity | 5 | 4 |
GO:0016624 | oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor | 4 | 4 |
GO:0016903 | oxidoreductase activity, acting on the aldehyde or oxo group of donors | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.206 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.438 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 236 | 238 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.372 |
DEG_APCC_DBOX_1 | 88 | 96 | PF00400 | 0.409 |
DOC_MAPK_gen_1 | 12 | 22 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 208 | 217 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 270 | 279 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 407 | 415 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 66 | 74 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 726 | 734 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 436 | 445 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 13 | 19 | PF00149 | 0.404 |
DOC_PP2B_LxvP_1 | 695 | 698 | PF13499 | 0.337 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.332 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.412 |
LIG_14-3-3_CanoR_1 | 114 | 123 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 15 | 21 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 156 | 165 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 296 | 300 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 326 | 330 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 346 | 355 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 372 | 381 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 488 | 494 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 589 | 595 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 612 | 616 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 66 | 70 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 676 | 683 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 726 | 734 | PF00244 | 0.571 |
LIG_APCC_ABBA_1 | 277 | 282 | PF00400 | 0.237 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.151 |
LIG_BRCT_BRCA1_1 | 582 | 586 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 683 | 687 | PF00533 | 0.286 |
LIG_DLG_GKlike_1 | 32 | 39 | PF00625 | 0.395 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.573 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.263 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.408 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.370 |
LIG_FHA_1 | 727 | 733 | PF00498 | 0.558 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.294 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.307 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.355 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.321 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.321 |
LIG_GBD_Chelix_1 | 430 | 438 | PF00786 | 0.302 |
LIG_IRF3_LxIS_1 | 11 | 17 | PF10401 | 0.393 |
LIG_LIR_Apic_2 | 120 | 126 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 104 | 112 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 177 | 188 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 263 | 271 | PF02991 | 0.213 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 507 | 513 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 614 | 623 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 627 | 636 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 507 | 511 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 678 | 683 | PF02991 | 0.251 |
LIG_LYPXL_yS_3 | 680 | 683 | PF13949 | 0.300 |
LIG_MLH1_MIPbox_1 | 34 | 38 | PF16413 | 0.395 |
LIG_NRBOX | 35 | 41 | PF00104 | 0.393 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.450 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.420 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.655 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.316 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.256 |
LIG_SH2_SRC | 565 | 568 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.227 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 452 | 455 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.364 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.325 |
LIG_SUMO_SIM_anti_2 | 159 | 168 | PF11976 | 0.410 |
LIG_SUMO_SIM_anti_2 | 388 | 393 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 411 | 417 | PF11976 | 0.312 |
LIG_TRAF2_1 | 456 | 459 | PF00917 | 0.358 |
LIG_TRAF2_1 | 686 | 689 | PF00917 | 0.427 |
LIG_TRFH_1 | 172 | 176 | PF08558 | 0.381 |
LIG_TRFH_1 | 195 | 199 | PF08558 | 0.389 |
LIG_TRFH_1 | 83 | 87 | PF08558 | 0.387 |
LIG_TRFH_1 | 90 | 94 | PF08558 | 0.403 |
LIG_TYR_ITIM | 178 | 183 | PF00017 | 0.380 |
LIG_TYR_ITSM | 676 | 683 | PF00017 | 0.229 |
LIG_UBA3_1 | 310 | 315 | PF00899 | 0.225 |
LIG_UBA3_1 | 404 | 412 | PF00899 | 0.416 |
LIG_UBA3_1 | 72 | 76 | PF00899 | 0.393 |
LIG_ULM_U2AF65_1 | 131 | 136 | PF00076 | 0.411 |
LIG_WRC_WIRS_1 | 490 | 495 | PF05994 | 0.427 |
MOD_CDK_SPxxK_3 | 90 | 97 | PF00069 | 0.417 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.454 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.410 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.409 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.381 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.606 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.448 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.396 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.428 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.249 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.297 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.267 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.306 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.292 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.284 |
MOD_Cter_Amidation | 129 | 132 | PF01082 | 0.412 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.448 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.353 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.365 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.441 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.421 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.483 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.380 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.407 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.430 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.603 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.577 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.396 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.390 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.347 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.343 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.441 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.416 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.569 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.396 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.313 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.405 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.323 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.383 |
MOD_N-GLC_1 | 666 | 671 | PF02516 | 0.320 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.407 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.585 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.327 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.391 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.315 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.342 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.338 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.493 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.346 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.706 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.381 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.442 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.237 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.384 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.298 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.436 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.411 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.407 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.351 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.379 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.373 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.339 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.435 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.398 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.411 |
MOD_PKA_2 | 675 | 681 | PF00069 | 0.370 |
MOD_PKA_2 | 732 | 738 | PF00069 | 0.624 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.407 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.376 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.468 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.396 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.404 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.344 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.339 |
MOD_Plk_1 | 666 | 672 | PF00069 | 0.397 |
MOD_Plk_2-3 | 263 | 269 | PF00069 | 0.461 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.584 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.286 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.396 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.300 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.383 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.321 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.302 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.151 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.312 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.300 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.576 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.644 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.640 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.414 |
MOD_SUMO_rev_2 | 289 | 295 | PF00179 | 0.355 |
MOD_SUMO_rev_2 | 564 | 574 | PF00179 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 615 | 618 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 680 | 683 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 641 | 643 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 286 | 291 | PF00026 | 0.333 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUA4 | Leptomonas seymouri | 79% | 100% |
A0A0N1IHT7 | Leptomonas seymouri | 37% | 100% |
A0A0N1IIN8 | Leptomonas seymouri | 37% | 100% |
A0A0S4J6A3 | Bodo saltans | 20% | 100% |
A0A0S4KLJ6 | Bodo saltans | 37% | 100% |
A0A1X0NJ18 | Trypanosomatidae | 51% | 100% |
A0A1X0NK15 | Trypanosomatidae | 45% | 100% |
A0A1X0NZX1 | Trypanosomatidae | 41% | 100% |
A0A3Q8IDT8 | Leishmania donovani | 39% | 100% |
A0A3Q8IF30 | Leishmania donovani | 85% | 100% |
A0A3R7NSH5 | Trypanosoma rangeli | 43% | 100% |
A0A3S7X4X4 | Leishmania donovani | 35% | 100% |
A0A422NPA5 | Trypanosoma rangeli | 52% | 100% |
A0A422NPB5 | Trypanosoma rangeli | 42% | 100% |
A4HIY7 | Leishmania braziliensis | 40% | 98% |
A4HJQ2 | Leishmania braziliensis | 35% | 100% |
A4I4P1 | Leishmania infantum | 39% | 100% |
A8MS68 | Arabidopsis thaliana | 25% | 100% |
C9ZLC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZMF4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
C9ZWN2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
D0A4H8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 21% | 100% |
E9AE44 | Leishmania major | 39% | 99% |
E9AHL8 | Leishmania infantum | 85% | 100% |
E9ALP1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B263 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B264 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
F4JLP5 | Arabidopsis thaliana | 24% | 100% |
G0SB20 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 26% | 100% |
O00087 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O04955 | Brassica rapa subsp. pekinensis | 22% | 100% |
O15770 | Plasmodium falciparum (isolate 3D7) | 22% | 100% |
O17953 | Caenorhabditis elegans | 27% | 100% |
P09624 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P0A0E4 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 22% | 100% |
P0A0E5 | Staphylococcus aureus | 22% | 100% |
P16171 | Bacillus cereus | 23% | 100% |
P17239 | Acidithiobacillus ferrooxidans | 26% | 100% |
P28593 | Trypanosoma cruzi | 21% | 100% |
P30635 | Caenorhabditis elegans | 22% | 100% |
P31023 | Pisum sativum | 28% | 100% |
P39051 | Trypanosoma brucei brucei | 21% | 100% |
P47791 | Mus musculus | 25% | 100% |
P48641 | Arabidopsis thaliana | 22% | 100% |
P61076 | Plasmodium falciparum (isolate 3D7) | 24% | 100% |
P80461 | Nicotiana tabacum | 22% | 100% |
P91938 | Drosophila melanogaster | 22% | 100% |
P9WHH6 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 27% | 100% |
P9WHH7 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 27% | 100% |
Q02733 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
Q25861 | Plasmodium falciparum (isolate FCH-5) | 24% | 100% |
Q4Q5Z6 | Leishmania major | 84% | 100% |
Q4Q5Z7 | Leishmania major | 34% | 100% |
Q94655 | Plasmodium falciparum (isolate K1 / Thailand) | 22% | 100% |
Q9JMH6 | Mus musculus | 22% | 100% |
Q9M5K2 | Arabidopsis thaliana | 26% | 100% |
Q9M5K3 | Arabidopsis thaliana | 26% | 100% |
Q9N2I8 | Bos taurus | 21% | 100% |
Q9VNT5 | Drosophila melanogaster | 23% | 100% |
V5AJG2 | Trypanosoma cruzi | 21% | 100% |
V5B6P6 | Trypanosoma cruzi | 43% | 100% |
V5BB90 | Trypanosoma cruzi | 52% | 100% |
V5BDX2 | Trypanosoma cruzi | 42% | 100% |