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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4QDZ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0006644 | phospholipid metabolic process | 4 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044255 | cellular lipid metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0008195 | phosphatidate phosphatase activity | 6 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.361 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.245 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.700 |
DOC_CYCLIN_yCln2_LP_2 | 350 | 356 | PF00134 | 0.390 |
DOC_MAPK_DCC_7 | 342 | 352 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 331 | 340 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 241 | 250 | PF00069 | 0.457 |
DOC_PP1_RVXF_1 | 302 | 308 | PF00149 | 0.286 |
DOC_PP2B_LxvP_1 | 350 | 353 | PF13499 | 0.390 |
DOC_PP2B_PxIxI_1 | 66 | 72 | PF00149 | 0.281 |
DOC_SPAK_OSR1_1 | 11 | 15 | PF12202 | 0.548 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.299 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.297 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 304 | 308 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.325 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.681 |
LIG_BIR_III_2 | 214 | 218 | PF00653 | 0.686 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.428 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.619 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.390 |
LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.382 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.633 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.470 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.529 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.336 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.703 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.297 |
LIG_LIR_Apic_2 | 45 | 49 | PF02991 | 0.358 |
LIG_LIR_Apic_2 | 63 | 67 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 232 | 238 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 252 | 263 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 295 | 300 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 313 | 324 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.573 |
LIG_MLH1_MIPbox_1 | 12 | 16 | PF16413 | 0.428 |
LIG_OCRL_FandH_1 | 14 | 26 | PF00620 | 0.294 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.532 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.340 |
LIG_PTB_Apo_2 | 281 | 288 | PF02174 | 0.314 |
LIG_PTB_Phospho_1 | 281 | 287 | PF10480 | 0.280 |
LIG_REV1ctd_RIR_1 | 13 | 21 | PF16727 | 0.469 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 287 | 290 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.354 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.653 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.262 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.668 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.667 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.568 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.700 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.285 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.434 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.390 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.526 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.634 |
MOD_Cter_Amidation | 88 | 91 | PF01082 | 0.438 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.568 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.606 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.249 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.322 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.348 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.248 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.322 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.269 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.561 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.614 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.580 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.544 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.378 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.342 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.390 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.371 |
MOD_LATS_1 | 40 | 46 | PF00433 | 0.362 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.605 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.324 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.338 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.344 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.293 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.344 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.629 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.711 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.314 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.314 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.482 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.307 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.511 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.355 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.417 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.662 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.690 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.342 |
MOD_SUMO_rev_2 | 99 | 107 | PF00179 | 0.524 |
TRG_DiLeu_BaEn_1 | 144 | 149 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_1 | 154 | 159 | PF01217 | 0.660 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.318 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 273 | 276 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I046 | Leptomonas seymouri | 46% | 91% |
A0A3S7WUU8 | Leishmania donovani | 79% | 100% |
A4H9E7 | Leishmania braziliensis | 53% | 100% |
A4H9F0 | Leishmania braziliensis | 53% | 100% |
A4HXR9 | Leishmania infantum | 79% | 100% |
E9ARI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |