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: 3, no: 4 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 7 |
GO:0004568 | chitinase activity | 5 | 5 |
GO:0005488 | binding | 1 | 8 |
GO:0008061 | chitin binding | 3 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.197 |
CLV_PCSK_FUR_1 | 116 | 120 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.197 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.285 |
DEG_APCC_DBOX_1 | 3 | 11 | PF00400 | 0.394 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 307 | 316 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 307 | 316 | PF00069 | 0.282 |
DOC_MAPK_NFAT4_5 | 307 | 315 | PF00069 | 0.337 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.278 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.810 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.387 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 357 | 365 | PF00244 | 0.277 |
LIG_Actin_WH2_2 | 87 | 102 | PF00022 | 0.354 |
LIG_APCC_ABBA_1 | 281 | 286 | PF00400 | 0.330 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.278 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.320 |
LIG_Clathr_ClatBox_1 | 101 | 105 | PF01394 | 0.306 |
LIG_deltaCOP1_diTrp_1 | 182 | 189 | PF00928 | 0.280 |
LIG_deltaCOP1_diTrp_1 | 332 | 341 | PF00928 | 0.337 |
LIG_EH1_1 | 123 | 131 | PF00400 | 0.251 |
LIG_eIF4E_1 | 331 | 337 | PF01652 | 0.245 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.365 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.281 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.337 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.278 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.278 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.448 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.281 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.463 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.149 |
LIG_LIR_Apic_2 | 171 | 177 | PF02991 | 0.278 |
LIG_LIR_Apic_2 | 434 | 440 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 138 | 149 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 73 | 84 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.353 |
LIG_NRBOX | 21 | 27 | PF00104 | 0.230 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.314 |
LIG_REV1ctd_RIR_1 | 77 | 85 | PF16727 | 0.330 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.568 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.306 |
LIG_SH2_NCK_1 | 437 | 441 | PF00017 | 0.568 |
LIG_SH2_PTP2 | 251 | 254 | PF00017 | 0.306 |
LIG_SH2_SRC | 257 | 260 | PF00017 | 0.337 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.265 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.306 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 271 | 275 | PF00017 | 0.228 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.278 |
LIG_SH3_1 | 437 | 443 | PF00018 | 0.545 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.545 |
LIG_TYR_ITIM | 249 | 254 | PF00017 | 0.306 |
LIG_TYR_ITSM | 366 | 373 | PF00017 | 0.354 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.342 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.387 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.551 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.337 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.337 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.337 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.463 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.201 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.349 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.202 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.354 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.351 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.312 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.547 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.332 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.331 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.354 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.524 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.476 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.388 |
MOD_LATS_1 | 297 | 303 | PF00433 | 0.281 |
MOD_LATS_1 | 306 | 312 | PF00433 | 0.354 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.354 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.328 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.306 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.352 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.259 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.337 |
MOD_PKA_1 | 308 | 314 | PF00069 | 0.362 |
MOD_PKA_1 | 70 | 76 | PF00069 | 0.197 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.306 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.449 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.434 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.243 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.402 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.337 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.306 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.491 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.542 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.582 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.440 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 97 | 102 | PF01217 | 0.306 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 215 | 218 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 291 | 293 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.224 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 324 | 329 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.306 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A072VEP0 | Medicago truncatula | 22% | 100% |
A0A0N0P753 | Leptomonas seymouri | 56% | 93% |
A0A0S4J833 | Bodo saltans | 32% | 100% |
A4H8K3 | Leishmania braziliensis | 78% | 100% |
A4HWX6 | Leishmania infantum | 99% | 100% |
E9AQN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QEU0 | Leishmania major | 94% | 100% |