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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0009331 | glycerol-3-phosphate dehydrogenase complex | 4 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:1902494 | catalytic complex | 2 | 10 |
GO:1990204 | oxidoreductase complex | 3 | 10 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AUI7
Term | Name | Level | Count |
---|---|---|---|
GO:0006072 | glycerol-3-phosphate metabolic process | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019637 | organophosphate metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0052646 | alditol phosphate metabolic process | 4 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004368 | glycerol-3-phosphate dehydrogenase (quinone) activity | 5 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 10 |
GO:0016901 | oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor | 4 | 10 |
GO:0052590 | sn-glycerol-3-phosphate:ubiquinone oxidoreductase activity | 6 | 5 |
GO:0052591 | sn-glycerol-3-phosphate:ubiquinone-8 oxidoreductase activity | 7 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.591 |
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.398 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.290 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 666 | 668 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 774 | 776 | PF00675 | 0.518 |
CLV_PCSK_FUR_1 | 174 | 178 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 741 | 743 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.518 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.508 |
DEG_APCC_DBOX_1 | 224 | 232 | PF00400 | 0.183 |
DEG_APCC_DBOX_1 | 719 | 727 | PF00400 | 0.336 |
DEG_SCF_FBW7_1 | 708 | 714 | PF00400 | 0.183 |
DEG_SPOP_SBC_1 | 343 | 347 | PF00917 | 0.466 |
DEG_SPOP_SBC_1 | 416 | 420 | PF00917 | 0.551 |
DOC_CDC14_PxL_1 | 534 | 542 | PF14671 | 0.480 |
DOC_CDC14_PxL_1 | 754 | 762 | PF14671 | 0.361 |
DOC_CKS1_1 | 702 | 707 | PF01111 | 0.472 |
DOC_CKS1_1 | 708 | 713 | PF01111 | 0.320 |
DOC_CYCLIN_RxL_1 | 693 | 704 | PF00134 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 463 | 469 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 702 | 708 | PF00134 | 0.418 |
DOC_MAPK_DCC_7 | 649 | 657 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 3 | 12 | PF00069 | 0.656 |
DOC_MAPK_gen_1 | 649 | 657 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 694 | 702 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 299 | 307 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.656 |
DOC_MAPK_MEF2A_6 | 309 | 318 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 352 | 360 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 512 | 520 | PF00069 | 0.194 |
DOC_MAPK_MEF2A_6 | 649 | 657 | PF00069 | 0.442 |
DOC_MAPK_RevD_3 | 652 | 667 | PF00069 | 0.404 |
DOC_PP1_RVXF_1 | 510 | 516 | PF00149 | 0.444 |
DOC_PP2B_LxvP_1 | 260 | 263 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 373 | 376 | PF13499 | 0.383 |
DOC_PP2B_LxvP_1 | 463 | 466 | PF13499 | 0.508 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.401 |
DOC_PP4_FxxP_1 | 508 | 511 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.221 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 707 | 712 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.278 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 348 | 356 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 388 | 398 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 408 | 414 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 512 | 516 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 562 | 567 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 580 | 589 | PF00244 | 0.237 |
LIG_14-3-3_CanoR_1 | 67 | 74 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 701 | 705 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 741 | 747 | PF00244 | 0.307 |
LIG_Actin_WH2_2 | 83 | 100 | PF00022 | 0.290 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.681 |
LIG_BIR_III_4 | 639 | 643 | PF00653 | 0.528 |
LIG_CtBP_PxDLS_1 | 630 | 634 | PF00389 | 0.455 |
LIG_deltaCOP1_diTrp_1 | 135 | 140 | PF00928 | 0.327 |
LIG_eIF4E_1 | 658 | 664 | PF01652 | 0.427 |
LIG_eIF4E_1 | 678 | 684 | PF01652 | 0.292 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.336 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.356 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.317 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.600 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.434 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.557 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.494 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.589 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.293 |
LIG_FHA_1 | 695 | 701 | PF00498 | 0.383 |
LIG_FHA_1 | 746 | 752 | PF00498 | 0.308 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.567 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.497 |
LIG_FHA_2 | 708 | 714 | PF00498 | 0.336 |
LIG_FHA_2 | 728 | 734 | PF00498 | 0.358 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.287 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 149 | 160 | PF02991 | 0.207 |
LIG_LIR_Gen_1 | 514 | 522 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 59 | 70 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 72 | 79 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 320 | 324 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.296 |
LIG_MYND_1 | 117 | 121 | PF01753 | 0.194 |
LIG_MYND_1 | 272 | 276 | PF01753 | 0.536 |
LIG_PDZ_Class_2 | 788 | 793 | PF00595 | 0.479 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.492 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.561 |
LIG_SH2_CRK | 747 | 751 | PF00017 | 0.313 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.194 |
LIG_SH2_NCK_1 | 321 | 325 | PF00017 | 0.492 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.290 |
LIG_SH2_SRC | 321 | 324 | PF00017 | 0.561 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.194 |
LIG_SH2_STAP1 | 423 | 427 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 609 | 613 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 731 | 735 | PF00017 | 0.308 |
LIG_SH2_STAT3 | 558 | 561 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 747 | 750 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.290 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.371 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.389 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.536 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.455 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.422 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.421 |
LIG_SUMO_SIM_anti_2 | 514 | 520 | PF11976 | 0.398 |
LIG_SUMO_SIM_anti_2 | 628 | 635 | PF11976 | 0.533 |
LIG_SUMO_SIM_anti_2 | 75 | 80 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 143 | 151 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 301 | 306 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.551 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.588 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.537 |
LIG_TYR_ITIM | 319 | 324 | PF00017 | 0.369 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.194 |
MOD_CDK_SPK_2 | 507 | 512 | PF00069 | 0.444 |
MOD_CDK_SPxxK_3 | 218 | 225 | PF00069 | 0.194 |
MOD_CDK_SPxxK_3 | 51 | 58 | PF00069 | 0.603 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.408 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.589 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.307 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.349 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.321 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.482 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.459 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.414 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.342 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.522 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.319 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.524 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.485 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.444 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.445 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.405 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.378 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.285 |
MOD_CK2_1 | 727 | 733 | PF00069 | 0.452 |
MOD_CK2_1 | 746 | 752 | PF00069 | 0.174 |
MOD_CK2_1 | 774 | 780 | PF00069 | 0.484 |
MOD_CMANNOS | 170 | 173 | PF00535 | 0.485 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.432 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.396 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.369 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.314 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.467 |
MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.466 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.464 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.443 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.426 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.421 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.531 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.452 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.513 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.455 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.410 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.320 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.378 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.407 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.378 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.424 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.427 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.329 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.470 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.480 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.304 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.309 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.269 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.354 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.368 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.532 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.406 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.482 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.513 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.330 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.444 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.380 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.468 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.485 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.455 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.477 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.401 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.411 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.551 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.335 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.488 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.488 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.496 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.439 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.462 |
MOD_NEK2_1 | 785 | 790 | PF00069 | 0.452 |
MOD_NEK2_2 | 434 | 439 | PF00069 | 0.485 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.554 |
MOD_PKA_1 | 774 | 780 | PF00069 | 0.571 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.490 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.465 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.408 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.446 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.529 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.540 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.300 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.369 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.571 |
MOD_PKB_1 | 30 | 38 | PF00069 | 0.420 |
MOD_PKB_1 | 562 | 570 | PF00069 | 0.603 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.444 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.472 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.494 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.412 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.326 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.485 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.369 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.371 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.545 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.689 |
MOD_Plk_4 | 759 | 765 | PF00069 | 0.408 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.362 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.404 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.392 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.446 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.194 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.415 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.437 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.394 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.565 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.474 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.600 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.327 |
TRG_DiLeu_BaEn_1 | 629 | 634 | PF01217 | 0.693 |
TRG_DiLeu_BaEn_1 | 72 | 77 | PF01217 | 0.238 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.287 |
TRG_DiLeu_BaLyEn_6 | 492 | 497 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 577 | 582 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 650 | 655 | PF01217 | 0.550 |
TRG_DiLeu_BaLyEn_6 | 659 | 664 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 8 | 13 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 666 | 668 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 720 | 723 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 774 | 776 | PF00400 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 666 | 670 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 774 | 778 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4L0 | Leptomonas seymouri | 46% | 94% |
A0A1X0NY01 | Trypanosomatidae | 33% | 100% |
A0A3Q8IDJ7 | Leishmania donovani | 85% | 100% |
A4HYM4 | Leishmania infantum | 86% | 100% |
C9ZI64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AIA2 | Leishmania braziliensis | 75% | 99% |
Q4QCZ7 | Leishmania major | 86% | 100% |
V5BVH7 | Trypanosoma cruzi | 33% | 100% |