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: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: E9AWC2
Term | Name | Level | Count |
---|---|---|---|
GO:0006575 | cellular modified amino acid metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006730 | one-carbon metabolic process | 3 | 1 |
GO:0006760 | folic acid-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009396 | folic acid-containing compound biosynthetic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035999 | tetrahydrofolate interconversion | 4 | 1 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 1 |
GO:0042558 | pteridine-containing compound metabolic process | 4 | 1 |
GO:0042559 | pteridine-containing compound biosynthetic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046653 | tetrahydrofolate metabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016874 | ligase activity | 2 | 2 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
GO:0016882 | cyclo-ligase activity | 4 | 1 |
GO:0030272 | 5-formyltetrahydrofolate cyclo-ligase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 71 | 75 | PF00656 | 0.423 |
CLV_MEL_PAP_1 | 353 | 359 | PF00089 | 0.538 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.372 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.399 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.578 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.310 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.486 |
DOC_CKS1_1 | 118 | 123 | PF01111 | 0.454 |
DOC_CYCLIN_yCln2_LP_2 | 202 | 208 | PF00134 | 0.482 |
DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 10 | 21 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 169 | 177 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 302 | 311 | PF00069 | 0.367 |
DOC_MAPK_RevD_3 | 7 | 23 | PF00069 | 0.428 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.598 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.470 |
DOC_PP2B_PxIxI_1 | 409 | 415 | PF00149 | 0.519 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.486 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.505 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 60 | 67 | PF00244 | 0.613 |
LIG_AP2alpha_1 | 332 | 336 | PF02296 | 0.492 |
LIG_APCC_ABBA_1 | 92 | 97 | PF00400 | 0.327 |
LIG_BIR_III_2 | 374 | 378 | PF00653 | 0.493 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.390 |
LIG_eIF4E_1 | 270 | 276 | PF01652 | 0.501 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.395 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.654 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.456 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.428 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.358 |
LIG_HCF-1_HBM_1 | 41 | 44 | PF13415 | 0.452 |
LIG_LIR_Gen_1 | 236 | 243 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 256 | 263 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 277 | 285 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 41 | 51 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 277 | 281 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.321 |
LIG_MYND_2 | 84 | 88 | PF01753 | 0.201 |
LIG_Pex14_2 | 332 | 336 | PF04695 | 0.492 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.356 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.338 |
LIG_SH2_SRC | 44 | 47 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.348 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.374 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.745 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.476 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.471 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.420 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.450 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.397 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 305 | 311 | PF11976 | 0.367 |
LIG_TYR_ITIM | 276 | 281 | PF00017 | 0.350 |
LIG_TYR_ITIM | 89 | 94 | PF00017 | 0.370 |
LIG_UBA3_1 | 18 | 26 | PF00899 | 0.492 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.612 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.720 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.418 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.607 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.704 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.678 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.538 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.587 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.406 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.469 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.278 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.484 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.488 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.456 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.506 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.508 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.582 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.619 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.376 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.494 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.462 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.495 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.568 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.496 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.498 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.527 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.535 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.381 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.540 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.507 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.516 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.542 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.364 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.614 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.512 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.619 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.437 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.623 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.422 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 25 | 28 | PF00179 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.300 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 346 | 351 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1K4 | Leptomonas seymouri | 41% | 100% |
A0A1X0NWU1 | Trypanosomatidae | 27% | 100% |
A0A3Q8IEK9 | Leishmania donovani | 86% | 100% |
A0A3R7KPU1 | Trypanosoma rangeli | 28% | 100% |
A4HCX6 | Leishmania braziliensis | 71% | 100% |
A4I0F9 | Leishmania infantum | 86% | 100% |
C9ZV81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4QB50 | Leishmania major | 85% | 100% |
V5DFL5 | Trypanosoma cruzi | 29% | 100% |