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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0031965 | nuclear membrane | 4 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q7Q3
Term | Name | Level | Count |
---|---|---|---|
GO:0006488 | dolichol-linked oligosaccharide biosynthetic process | 5 | 12 |
GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 12 |
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004577 | N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase activity | 6 | 9 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 9 |
GO:0008375 | acetylglucosaminyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016757 | glycosyltransferase activity | 3 | 12 |
GO:0016758 | hexosyltransferase activity | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 269 | 275 | PF00089 | 0.325 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.313 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.327 |
CLV_PCSK_PC7_1 | 204 | 210 | PF00082 | 0.366 |
CLV_PCSK_PC7_1 | 272 | 278 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.353 |
CLV_Separin_Metazoa | 51 | 55 | PF03568 | 0.501 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.600 |
DEG_APCC_DBOX_1 | 326 | 334 | PF00400 | 0.487 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.612 |
DEG_MDM2_SWIB_1 | 195 | 202 | PF02201 | 0.517 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.340 |
DOC_CYCLIN_yCln2_LP_2 | 186 | 192 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 295 | 301 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 208 | 218 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.568 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.501 |
DOC_SPAK_OSR1_1 | 272 | 276 | PF12202 | 0.525 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.581 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 120 | 124 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 127 | 137 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 224 | 230 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 335 | 340 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 365 | 375 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 54 | 63 | PF00244 | 0.553 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.476 |
LIG_EH1_1 | 2 | 10 | PF00400 | 0.281 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.552 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.703 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.509 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.556 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.476 |
LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 172 | 182 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 241 | 248 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 250 | 261 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.562 |
LIG_NRBOX | 3 | 9 | PF00104 | 0.399 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.508 |
LIG_PTB_Apo_2 | 378 | 385 | PF02174 | 0.553 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.501 |
LIG_SH2_CRK | 243 | 247 | PF00017 | 0.562 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.528 |
LIG_SH2_NCK_1 | 243 | 247 | PF00017 | 0.562 |
LIG_SH2_PTP2 | 24 | 27 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.480 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.292 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.553 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.525 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.435 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.502 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.517 |
LIG_Sin3_3 | 337 | 344 | PF02671 | 0.476 |
LIG_SUMO_SIM_par_1 | 244 | 251 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 337 | 342 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.630 |
LIG_SxIP_EBH_1 | 54 | 65 | PF03271 | 0.510 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.693 |
LIG_TYR_ITIM | 22 | 27 | PF00017 | 0.637 |
LIG_WRC_WIRS_1 | 171 | 176 | PF05994 | 0.487 |
MOD_CDC14_SPxK_1 | 31 | 34 | PF00782 | 0.669 |
MOD_CDK_SPxK_1 | 28 | 34 | PF00069 | 0.649 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.306 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.562 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.587 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.572 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.476 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.562 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.495 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.300 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.266 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.251 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.468 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.311 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.430 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.490 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.696 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.483 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.542 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.549 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.498 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.487 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.411 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.489 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.479 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.606 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.652 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.525 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.581 |
MOD_PKA_1 | 211 | 217 | PF00069 | 0.550 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.398 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.540 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.610 |
MOD_PKB_1 | 209 | 217 | PF00069 | 0.581 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.571 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.587 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.476 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.417 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.457 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.521 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.532 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.563 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.508 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.439 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.562 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.649 |
TRG_DiLeu_BaEn_1 | 241 | 246 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 418 | 423 | PF01217 | 0.628 |
TRG_DiLeu_LyEn_5 | 395 | 400 | PF01217 | 0.643 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.633 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 234 | 239 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 54 | 58 | PF00026 | 0.307 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7X1 | Leptomonas seymouri | 62% | 100% |
A0A0S4IKP3 | Bodo saltans | 40% | 100% |
A0A1X0P2G9 | Trypanosomatidae | 48% | 100% |
A0A3Q8IBT8 | Leishmania donovani | 95% | 100% |
A0A422NIG8 | Trypanosoma rangeli | 48% | 100% |
A4HI04 | Leishmania braziliensis | 84% | 100% |
A4I581 | Leishmania infantum | 95% | 100% |
C9ZQL0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 96% |
E9B0H8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BC77 | Trypanosoma cruzi | 48% | 100% |