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:0008303 | caspase complex | 5 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0042765 | GPI-anchor transamidase complex | 3 | 11 |
GO:0098796 | membrane protein complex | 2 | 11 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:1905368 | peptidase complex | 3 | 11 |
GO:1905369 | endopeptidase complex | 4 | 11 |
Related structures:
AlphaFold database: A4HLC3
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016255 | attachment of GPI anchor to protein | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.590 |
CLV_PCSK_FUR_1 | 75 | 79 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.449 |
DEG_APCC_DBOX_1 | 429 | 437 | PF00400 | 0.528 |
DEG_COP1_1 | 243 | 253 | PF00400 | 0.181 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.582 |
DEG_ODPH_VHL_1 | 17 | 28 | PF01847 | 0.349 |
DOC_CDC14_PxL_1 | 29 | 37 | PF14671 | 0.404 |
DOC_CKS1_1 | 327 | 332 | PF01111 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 327 | 333 | PF00134 | 0.349 |
DOC_MAPK_DCC_7 | 315 | 324 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 136 | 143 | PF00069 | 0.236 |
DOC_MAPK_MEF2A_6 | 16 | 24 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 364 | 371 | PF00069 | 0.434 |
DOC_MAPK_NFAT4_5 | 136 | 144 | PF00069 | 0.331 |
DOC_MAPK_NFAT4_5 | 364 | 372 | PF00069 | 0.429 |
DOC_MAPK_RevD_3 | 24 | 39 | PF00069 | 0.349 |
DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.193 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.181 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.360 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.181 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.181 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 242 | 246 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.296 |
LIG_14-3-3_CterR_2 | 458 | 463 | PF00244 | 0.236 |
LIG_Actin_WH2_2 | 273 | 288 | PF00022 | 0.181 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.196 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 439 | 443 | PF00533 | 0.360 |
LIG_CSL_BTD_1 | 278 | 281 | PF09270 | 0.236 |
LIG_deltaCOP1_diTrp_1 | 199 | 204 | PF00928 | 0.181 |
LIG_eIF4E_1 | 134 | 140 | PF01652 | 0.282 |
LIG_eIF4E_1 | 428 | 434 | PF01652 | 0.421 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.221 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.314 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.277 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.503 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.259 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.435 |
LIG_GBD_Chelix_1 | 374 | 382 | PF00786 | 0.314 |
LIG_IRF3_LxIS_1 | 139 | 144 | PF10401 | 0.181 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.314 |
LIG_LIR_Apic_2 | 243 | 248 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 275 | 285 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 320 | 331 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 349 | 360 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 365 | 376 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 440 | 450 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.365 |
LIG_LYPXL_SIV_4 | 133 | 141 | PF13949 | 0.282 |
LIG_LYPXL_SIV_4 | 205 | 213 | PF13949 | 0.282 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.335 |
LIG_PTB_Apo_2 | 87 | 94 | PF02174 | 0.337 |
LIG_PTB_Phospho_1 | 87 | 93 | PF10480 | 0.372 |
LIG_SH2_GRB2like | 167 | 170 | PF00017 | 0.282 |
LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.270 |
LIG_SH2_NCK_1 | 134 | 138 | PF00017 | 0.397 |
LIG_SH2_NCK_1 | 290 | 294 | PF00017 | 0.236 |
LIG_SH2_PTP2 | 150 | 153 | PF00017 | 0.173 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.331 |
LIG_SH2_SRC | 290 | 293 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.379 |
LIG_SH2_STAT3 | 184 | 187 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.202 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.275 |
LIG_SH3_2 | 281 | 286 | PF14604 | 0.181 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.263 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.181 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.236 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.404 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.419 |
LIG_SH3_5 | 163 | 167 | PF00018 | 0.282 |
LIG_SUMO_SIM_par_1 | 229 | 236 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 323 | 329 | PF11976 | 0.381 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.428 |
LIG_TYR_ITIM | 421 | 426 | PF00017 | 0.404 |
LIG_UBA3_1 | 103 | 111 | PF00899 | 0.292 |
LIG_UBA3_1 | 31 | 39 | PF00899 | 0.419 |
LIG_WRC_WIRS_1 | 443 | 448 | PF05994 | 0.289 |
MOD_CDC14_SPxK_1 | 283 | 286 | PF00782 | 0.181 |
MOD_CDK_SPxK_1 | 280 | 286 | PF00069 | 0.181 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.311 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.271 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.346 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.407 |
MOD_CMANNOS | 201 | 204 | PF00535 | 0.531 |
MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.580 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.329 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.277 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.328 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.264 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.315 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.276 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.339 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.400 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.341 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.525 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.350 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.306 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.395 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.302 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.261 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.287 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.569 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.527 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.283 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.309 |
MOD_NEK2_2 | 237 | 242 | PF00069 | 0.339 |
MOD_PK_1 | 315 | 321 | PF00069 | 0.482 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.347 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.317 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.236 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.333 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.296 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.331 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.248 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.281 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.190 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.320 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.349 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.181 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.181 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.271 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.271 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.457 |
MOD_SUMO_rev_2 | 264 | 272 | PF00179 | 0.327 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 107 | 110 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2W7 | Leptomonas seymouri | 65% | 100% |
A0A1X0NIY4 | Trypanosomatidae | 40% | 100% |
A0A3R7N823 | Trypanosoma rangeli | 39% | 99% |
A0A3S7WWY8 | Leishmania donovani | 83% | 100% |
A4HZI7 | Leishmania infantum | 83% | 100% |
D0A0Y9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AVH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QC02 | Leishmania major | 85% | 100% |
V5DID2 | Trypanosoma cruzi | 38% | 96% |