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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HGG0
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006631 | fatty acid metabolic process | 4 | 1 |
GO:0006633 | fatty acid biosynthetic process | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016053 | organic acid biosynthetic process | 4 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004467 | long-chain fatty acid-CoA ligase activity | 3 | 5 |
GO:0015645 | fatty acid ligase activity | 2 | 5 |
GO:0016405 | CoA-ligase activity | 4 | 5 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 5 |
GO:0016878 | acid-thiol ligase activity | 4 | 5 |
GO:0140657 | ATP-dependent activity | 1 | 5 |
GO:0031957 | very long-chain fatty acid-CoA ligase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.355 |
CLV_MEL_PAP_1 | 454 | 460 | PF00089 | 0.174 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 679 | 683 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.526 |
CLV_Separin_Metazoa | 41 | 45 | PF03568 | 0.292 |
CLV_Separin_Metazoa | 721 | 725 | PF03568 | 0.273 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.508 |
DEG_ODPH_VHL_1 | 707 | 719 | PF01847 | 0.331 |
DOC_ANK_TNKS_1 | 586 | 593 | PF00023 | 0.174 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.541 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 730 | 739 | PF00134 | 0.405 |
DOC_CYCLIN_yCln2_LP_2 | 140 | 146 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 513 | 519 | PF00134 | 0.273 |
DOC_MAPK_gen_1 | 343 | 353 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 628 | 637 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 700 | 706 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 732 | 741 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 35 | 42 | PF00069 | 0.238 |
DOC_MAPK_NFAT4_5 | 35 | 43 | PF00069 | 0.250 |
DOC_PP1_RVXF_1 | 677 | 684 | PF00149 | 0.331 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.266 |
DOC_PP2B_LxvP_1 | 484 | 487 | PF13499 | 0.273 |
DOC_PP2B_LxvP_1 | 706 | 709 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 739 | 742 | PF13499 | 0.335 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.254 |
DOC_PP4_FxxP_1 | 5 | 8 | PF00568 | 0.552 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.386 |
DOC_USP7_UBL2_3 | 235 | 239 | PF12436 | 0.678 |
DOC_USP7_UBL2_3 | 729 | 733 | PF12436 | 0.433 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.256 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 503 | 513 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 619 | 623 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 679 | 684 | PF00244 | 0.248 |
LIG_Actin_WH2_2 | 215 | 232 | PF00022 | 0.414 |
LIG_APCC_ABBAyCdc20_2 | 644 | 650 | PF00400 | 0.299 |
LIG_BRCT_BRCA1_1 | 213 | 217 | PF00533 | 0.599 |
LIG_Clathr_ClatBox_1 | 318 | 322 | PF01394 | 0.331 |
LIG_deltaCOP1_diTrp_1 | 381 | 385 | PF00928 | 0.362 |
LIG_EH1_1 | 397 | 405 | PF00400 | 0.273 |
LIG_eIF4E_1 | 223 | 229 | PF01652 | 0.586 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.376 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.668 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.532 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.476 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.523 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.250 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.285 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.236 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.198 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.354 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.273 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.515 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.331 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.273 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.273 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.273 |
LIG_FHA_2 | 680 | 686 | PF00498 | 0.246 |
LIG_IRF3_LxIS_1 | 561 | 567 | PF10401 | 0.174 |
LIG_LIR_Apic_2 | 27 | 32 | PF02991 | 0.250 |
LIG_LIR_Apic_2 | 83 | 87 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 438 | 447 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 714 | 723 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 51 | 55 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 714 | 719 | PF02991 | 0.318 |
LIG_PCNA_yPIPBox_3 | 20 | 29 | PF02747 | 0.374 |
LIG_Pex14_2 | 572 | 576 | PF04695 | 0.255 |
LIG_PTB_Apo_2 | 44 | 51 | PF02174 | 0.308 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.330 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.448 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.307 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.197 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.383 |
LIG_SH2_CRK | 614 | 618 | PF00017 | 0.386 |
LIG_SH2_CRK | 710 | 714 | PF00017 | 0.273 |
LIG_SH2_GRB2like | 575 | 578 | PF00017 | 0.386 |
LIG_SH2_PTP2 | 716 | 719 | PF00017 | 0.334 |
LIG_SH2_SRC | 716 | 719 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 347 | 351 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 447 | 451 | PF00017 | 0.168 |
LIG_SH2_STAP1 | 649 | 653 | PF00017 | 0.386 |
LIG_SH2_STAT3 | 538 | 541 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.334 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.415 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.273 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.273 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.263 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.273 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.556 |
LIG_SH3_5 | 104 | 108 | PF00018 | 0.555 |
LIG_SUMO_SIM_anti_2 | 620 | 627 | PF11976 | 0.431 |
LIG_SUMO_SIM_anti_2 | 663 | 670 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 224 | 231 | PF11976 | 0.588 |
LIG_TRAF2_1 | 582 | 585 | PF00917 | 0.174 |
LIG_TYR_ITIM | 13 | 18 | PF00017 | 0.510 |
LIG_UBA3_1 | 228 | 235 | PF00899 | 0.444 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.355 |
MOD_CDK_SPxxK_3 | 456 | 463 | PF00069 | 0.334 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.632 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.267 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.273 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.326 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.416 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.604 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.256 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.273 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.273 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.364 |
MOD_CK2_1 | 679 | 685 | PF00069 | 0.249 |
MOD_GlcNHglycan | 159 | 163 | PF01048 | 0.600 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.561 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.544 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.562 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.270 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.264 |
MOD_GlcNHglycan | 494 | 498 | PF01048 | 0.289 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.470 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.342 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.608 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.319 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.615 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.273 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.318 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.382 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.433 |
MOD_N-GLC_1 | 724 | 729 | PF02516 | 0.304 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.574 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.577 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.573 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.639 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.277 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.314 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.278 |
MOD_NEK2_2 | 14 | 19 | PF00069 | 0.443 |
MOD_NEK2_2 | 240 | 245 | PF00069 | 0.467 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.174 |
MOD_NEK2_2 | 435 | 440 | PF00069 | 0.386 |
MOD_NEK2_2 | 470 | 475 | PF00069 | 0.331 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.535 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.412 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.299 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.295 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.393 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.409 |
MOD_PKB_1 | 677 | 685 | PF00069 | 0.246 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.633 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.278 |
MOD_Plk_1 | 690 | 696 | PF00069 | 0.306 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.530 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.334 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.438 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.564 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.464 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.320 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.269 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.255 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.285 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.346 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.259 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.411 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.377 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.436 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.684 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.532 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.256 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.334 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.531 |
MOD_SUMO_rev_2 | 175 | 184 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 231 | 241 | PF00179 | 0.665 |
MOD_SUMO_rev_2 | 692 | 702 | PF00179 | 0.291 |
TRG_DiLeu_BaEn_1 | 638 | 643 | PF01217 | 0.174 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.627 |
TRG_NES_CRM1_1 | 316 | 327 | PF08389 | 0.174 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 279 | 284 | PF00026 | 0.709 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IL67 | Bodo saltans | 42% | 96% |
A0A1X0NYK4 | Trypanosomatidae | 52% | 100% |
A0A3Q8ID29 | Leishmania donovani | 82% | 100% |
A0A3R7KRF3 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WVH9 | Leishmania donovani | 21% | 100% |
A0A3S7WVL1 | Leishmania donovani | 22% | 100% |
A4HA52 | Leishmania braziliensis | 21% | 100% |
A4HYA8 | Leishmania infantum | 22% | 100% |
A4HYB7 | Leishmania infantum | 21% | 100% |
A4I3J3 | Leishmania infantum | 82% | 100% |
D0A7V2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AGS6 | Leishmania infantum | 22% | 100% |
E9AZT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
O24146 | Nicotiana tabacum | 24% | 100% |
Q4Q8F1 | Leishmania major | 81% | 100% |
Q4QDB5 | Leishmania major | 22% | 100% |
Q4QDB6 | Leishmania major | 22% | 100% |
V5AUI9 | Trypanosoma cruzi | 52% | 100% |