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: 1, no: 33 |
NetGPI | no | yes: 0, no: 34 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
GO:0005737 | cytoplasm | 2 | 2 |
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 |
Related structures:
AlphaFold database: A4HDP2
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:0030497 | fatty acid elongation | 6 | 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 | 4 |
GO:0004312 | fatty acid synthase activity | 5 | 3 |
GO:0004316 | 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity | 5 | 3 |
GO:0016491 | oxidoreductase activity | 2 | 4 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 3 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016746 | acyltransferase activity | 3 | 3 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 3 |
GO:0008667 | 2,3-dihydro-2,3-dihydroxybenzoate dehydrogenase activity | 5 | 1 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 1 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.291 |
CLV_PCSK_PC7_1 | 201 | 207 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.377 |
DOC_MAPK_gen_1 | 229 | 239 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 414 | 423 | PF00069 | 0.235 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.297 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.364 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 33 | 42 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 388 | 396 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.550 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.557 |
LIG_CSL_BTD_1 | 289 | 292 | PF09270 | 0.542 |
LIG_eIF4E_1 | 417 | 423 | PF01652 | 0.276 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.591 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.467 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.531 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.455 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.452 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.534 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.667 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.320 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.343 |
LIG_HCF-1_HBM_1 | 57 | 60 | PF13415 | 0.539 |
LIG_LIR_Apic_2 | 322 | 326 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 195 | 203 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.372 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.423 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.530 |
LIG_PTB_Apo_2 | 442 | 449 | PF02174 | 0.297 |
LIG_PTB_Phospho_1 | 442 | 448 | PF10480 | 0.298 |
LIG_RPA_C_Fungi | 110 | 122 | PF08784 | 0.504 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.490 |
LIG_SH2_GRB2like | 449 | 452 | PF00017 | 0.346 |
LIG_SH2_NCK_1 | 358 | 362 | PF00017 | 0.572 |
LIG_SH2_PTP2 | 420 | 423 | PF00017 | 0.478 |
LIG_SH2_SRC | 418 | 421 | PF00017 | 0.224 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.374 |
LIG_SH3_1 | 39 | 45 | PF00018 | 0.437 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.479 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.437 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.433 |
LIG_SUMO_SIM_anti_2 | 157 | 162 | PF11976 | 0.370 |
LIG_SUMO_SIM_anti_2 | 213 | 218 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 250 | 258 | PF11976 | 0.414 |
LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.324 |
LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.169 |
MOD_CDK_SPK_2 | 28 | 33 | PF00069 | 0.670 |
MOD_CDK_SPK_2 | 288 | 293 | PF00069 | 0.422 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.461 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.598 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.543 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.704 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.169 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.476 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.390 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.350 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.537 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.521 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.315 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.635 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.323 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.482 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.586 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.629 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.664 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.611 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.521 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.286 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.554 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.435 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.617 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.430 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.643 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.277 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.491 |
MOD_N-GLC_1 | 464 | 469 | PF02516 | 0.248 |
MOD_N-GLC_2 | 123 | 125 | PF02516 | 0.325 |
MOD_N-GLC_2 | 436 | 438 | PF02516 | 0.321 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.330 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.213 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.459 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.298 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.521 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.382 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.477 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.709 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.310 |
MOD_PIKK_1 | 473 | 479 | PF00454 | 0.251 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.463 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.533 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.370 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.186 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.636 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.676 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.369 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.423 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.314 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.439 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.561 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.292 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.209 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.169 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.370 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.316 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.514 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.445 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.482 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.633 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.376 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.334 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.456 |
TRG_NES_CRM1_1 | 150 | 164 | PF08389 | 0.250 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2S5 | Leptomonas seymouri | 27% | 100% |
A0A0N0P2S7 | Leptomonas seymouri | 32% | 95% |
A0A0N1HZ81 | Leptomonas seymouri | 67% | 87% |
A0A0S4IWT0 | Bodo saltans | 31% | 100% |
A0A0S4IZG2 | Bodo saltans | 35% | 100% |
A0A0S4J1I6 | Bodo saltans | 41% | 100% |
A0A1X0NVT8 | Trypanosomatidae | 34% | 98% |
A0A1X0NVV6 | Trypanosomatidae | 51% | 95% |
A0A3Q8ID46 | Leishmania donovani | 34% | 96% |
A0A3Q8IM89 | Leishmania donovani | 26% | 100% |
A0A3R7K071 | Trypanosoma rangeli | 51% | 100% |
A0A3R7N7S2 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H7D5 | Leishmania donovani | 86% | 100% |
A0A3S7X986 | Leishmania donovani | 23% | 100% |
A0A422N2B6 | Trypanosoma rangeli | 33% | 100% |
A4HDP3 | Leishmania braziliensis | 32% | 100% |
A4HMN7 | Leishmania braziliensis | 24% | 100% |
C9ZWC0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 98% |
C9ZZF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AF41 | Leishmania major | 24% | 100% |
E9AH88 | Leishmania infantum | 86% | 97% |
E9AH89 | Leishmania infantum | 33% | 96% |
E9AHV6 | Leishmania infantum | 25% | 100% |
E9AHV8 | Leishmania infantum | 23% | 100% |
E9AX26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AX27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 96% |
E9B694 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B696 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4QAE9 | Leishmania major | 33% | 100% |
Q4QAF0 | Leishmania major | 85% | 100% |
V5BAF4 | Trypanosoma cruzi | 34% | 100% |
V5BNY6 | Trypanosoma cruzi | 28% | 100% |