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: 8 |
NetGPI | no | yes: 0, no: 8 |
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: A4ID42
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 8 |
GO:0009058 | biosynthetic process | 2 | 8 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010257 | NADH dehydrogenase complex assembly | 6 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0032981 | mitochondrial respiratory chain complex I assembly | 7 | 1 |
GO:0033108 | mitochondrial respiratory chain complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.390 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.500 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.251 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.502 |
DOC_CYCLIN_RxL_1 | 262 | 272 | PF00134 | 0.251 |
DOC_MAPK_gen_1 | 229 | 236 | PF00069 | 0.229 |
DOC_MAPK_gen_1 | 262 | 271 | PF00069 | 0.271 |
DOC_MAPK_gen_1 | 92 | 100 | PF00069 | 0.325 |
DOC_PP1_RVXF_1 | 112 | 119 | PF00149 | 0.229 |
DOC_PP1_RVXF_1 | 231 | 237 | PF00149 | 0.285 |
DOC_PP1_RVXF_1 | 265 | 272 | PF00149 | 0.271 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.464 |
LIG_14-3-3_CanoR_1 | 104 | 113 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 162 | 171 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 233 | 239 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 94 | 98 | PF00244 | 0.293 |
LIG_14-3-3_CterR_2 | 389 | 392 | PF00244 | 0.582 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.344 |
LIG_EH1_1 | 270 | 278 | PF00400 | 0.285 |
LIG_eIF4E_1 | 191 | 197 | PF01652 | 0.229 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.228 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.285 |
LIG_FXI_DFP_1 | 56 | 60 | PF00024 | 0.297 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 46 | 56 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.256 |
LIG_MYND_1 | 141 | 145 | PF01753 | 0.229 |
LIG_Pex14_2 | 160 | 164 | PF04695 | 0.229 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.271 |
LIG_PTB_Apo_2 | 327 | 334 | PF02174 | 0.357 |
LIG_PTB_Apo_2 | 361 | 368 | PF02174 | 0.463 |
LIG_Rb_pABgroove_1 | 176 | 184 | PF01858 | 0.229 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.447 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.229 |
LIG_SH2_GRB2like | 304 | 307 | PF00017 | 0.251 |
LIG_SH2_GRB2like | 362 | 365 | PF00017 | 0.473 |
LIG_SH2_PTP2 | 49 | 52 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.251 |
LIG_SH2_STAT3 | 71 | 74 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.333 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.229 |
LIG_SUMO_SIM_par_1 | 195 | 200 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.330 |
LIG_TYR_ITIM | 47 | 52 | PF00017 | 0.332 |
LIG_UBA3_1 | 270 | 278 | PF00899 | 0.271 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.251 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.341 |
MOD_GlcNHglycan | 29 | 33 | PF01048 | 0.435 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.343 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.524 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.599 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.366 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.228 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.630 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.483 |
MOD_LATS_1 | 373 | 379 | PF00433 | 0.411 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.224 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.435 |
MOD_N-GLC_2 | 222 | 224 | PF02516 | 0.271 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.271 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.229 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.233 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.271 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.322 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.310 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.371 |
MOD_PK_1 | 346 | 352 | PF00069 | 0.332 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.271 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.388 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.298 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.285 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.322 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.426 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.251 |
MOD_SUMO_for_1 | 202 | 205 | PF00179 | 0.251 |
MOD_SUMO_for_1 | 277 | 280 | PF00179 | 0.251 |
MOD_SUMO_for_1 | 50 | 53 | PF00179 | 0.284 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.267 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.251 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P3G5 | Trypanosomatidae | 75% | 68% |
A0A422N197 | Trypanosoma rangeli | 64% | 100% |
A2AIL4 | Mus musculus | 24% | 100% |
A4HPM3 | Leishmania braziliensis | 94% | 100% |
A7YVD7 | Bos taurus | 26% | 100% |
D0A8J3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 74% | 71% |
D3ZN43 | Rattus norvegicus | 24% | 100% |
E9ATD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
Q330K2 | Homo sapiens | 24% | 100% |
Q4Q162 | Leishmania major | 99% | 100% |
V5B709 | Trypanosoma cruzi | 74% | 84% |