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:0005835 | fatty acid synthase complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
Related structures:
AlphaFold database: E9B6M6
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 3 |
GO:0006629 | lipid metabolic process | 3 | 3 |
GO:0006631 | fatty acid metabolic process | 4 | 3 |
GO:0006633 | fatty acid biosynthetic process | 5 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0008610 | lipid biosynthetic process | 4 | 3 |
GO:0009058 | biosynthetic process | 2 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016053 | organic acid biosynthetic process | 4 | 3 |
GO:0019752 | carboxylic acid metabolic process | 5 | 3 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 3 |
GO:0043436 | oxoacid metabolic process | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044249 | cellular biosynthetic process | 3 | 3 |
GO:0044255 | cellular lipid metabolic process | 3 | 3 |
GO:0044281 | small molecule metabolic process | 2 | 3 |
GO:0044283 | small molecule biosynthetic process | 3 | 3 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 3 |
GO:1901576 | organic substance biosynthetic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0004312 | fatty acid synthase activity | 5 | 3 |
GO:0004314 | [acyl-carrier-protein] S-malonyltransferase activity | 6 | 1 |
GO:0016417 | S-acyltransferase activity | 5 | 1 |
GO:0016419 | S-malonyltransferase activity | 6 | 1 |
GO:0016420 | malonyltransferase activity | 5 | 1 |
GO:0016746 | acyltransferase activity | 3 | 3 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 275 | 279 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.378 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.441 |
CLV_PCSK_PC7_1 | 303 | 309 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.505 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.503 |
DEG_SPOP_SBC_1 | 213 | 217 | PF00917 | 0.411 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.266 |
DOC_CYCLIN_RxL_1 | 159 | 167 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 22 | 28 | PF00134 | 0.399 |
DOC_MAPK_gen_1 | 338 | 346 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 394 | 401 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 435 | 444 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 514 | 522 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 339 | 348 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 514 | 522 | PF00069 | 0.528 |
DOC_MAPK_RevD_3 | 147 | 162 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 197 | 203 | PF00149 | 0.305 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.369 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.412 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 497 | 503 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 504 | 509 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 517 | 521 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 72 | 80 | PF00244 | 0.401 |
LIG_Actin_WH2_2 | 343 | 360 | PF00022 | 0.443 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.441 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.559 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.519 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.483 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.195 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.424 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.441 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.394 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.573 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.460 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.441 |
LIG_IRF3_LxIS_1 | 378 | 385 | PF10401 | 0.380 |
LIG_LIR_Apic_2 | 341 | 345 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 215 | 226 | PF02991 | 0.364 |
LIG_LIR_LC3C_4 | 439 | 444 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.377 |
LIG_LRP6_Inhibitor_1 | 221 | 227 | PF00058 | 0.402 |
LIG_NRBOX | 377 | 383 | PF00104 | 0.425 |
LIG_PALB2_WD40_1 | 338 | 346 | PF16756 | 0.484 |
LIG_PCNA_TLS_4 | 358 | 365 | PF02747 | 0.435 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 126 | 129 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 48 | 51 | PF00017 | 0.188 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.274 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.355 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.517 |
LIG_SUMO_SIM_anti_2 | 215 | 223 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 380 | 385 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 439 | 446 | PF11976 | 0.574 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.599 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.625 |
LIG_TRAF2_1 | 477 | 480 | PF00917 | 0.524 |
LIG_TYR_ITIM | 113 | 118 | PF00017 | 0.451 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.556 |
MOD_CDC14_SPxK_1 | 184 | 187 | PF00782 | 0.476 |
MOD_CDC14_SPxK_1 | 494 | 497 | PF00782 | 0.524 |
MOD_CDK_SPK_2 | 491 | 496 | PF00069 | 0.489 |
MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.476 |
MOD_CDK_SPxK_1 | 491 | 497 | PF00069 | 0.503 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.402 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.520 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.675 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.487 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.537 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.335 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.333 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.582 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.594 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.494 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.560 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.522 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.587 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.618 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.491 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.537 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.483 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.335 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.371 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.437 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.538 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.381 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.428 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.375 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.527 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.368 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.333 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.541 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.382 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.478 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.406 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.327 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.548 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.341 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.474 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.399 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.262 |
MOD_NEK2_2 | 268 | 273 | PF00069 | 0.486 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.367 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.447 |
MOD_PKA_1 | 496 | 502 | PF00069 | 0.501 |
MOD_PKA_1 | 504 | 510 | PF00069 | 0.410 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.585 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.383 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.487 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.438 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.518 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.346 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.150 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.595 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.359 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.546 |
MOD_Plk_2-3 | 374 | 380 | PF00069 | 0.352 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.419 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.309 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.498 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.447 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.549 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.572 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.389 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.355 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.475 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.551 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.503 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.315 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.412 |
TRG_DiLeu_BaEn_4 | 322 | 328 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 162 | 167 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJM7 | Leptomonas seymouri | 67% | 94% |
A0A0S4IR28 | Bodo saltans | 38% | 99% |
A0A1X0P5F7 | Trypanosomatidae | 52% | 97% |
A0A3Q8IGH2 | Leishmania donovani | 93% | 100% |
A0A422NRA5 | Trypanosoma rangeli | 51% | 99% |
A4HN14 | Leishmania braziliensis | 82% | 100% |
A4IBN7 | Leishmania infantum | 94% | 100% |
C9ZYZ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 97% |
E9AFH1 | Leishmania major | 92% | 100% |