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: 1, no: 5 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AI97
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.404 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.663 |
DEG_ODPH_VHL_1 | 286 | 299 | PF01847 | 0.475 |
DEG_SPOP_SBC_1 | 339 | 343 | PF00917 | 0.449 |
DOC_MAPK_MEF2A_6 | 383 | 390 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.534 |
DOC_PP1_RVXF_1 | 347 | 354 | PF00149 | 0.394 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.392 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.462 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.423 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 11 | 19 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.551 |
LIG_Actin_WH2_2 | 174 | 190 | PF00022 | 0.414 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.458 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.361 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.377 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.323 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.567 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.377 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.661 |
LIG_LIR_Apic_2 | 177 | 182 | PF02991 | 0.318 |
LIG_LIR_Apic_2 | 264 | 270 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 352 | 356 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 369 | 375 | PF02991 | 0.616 |
LIG_LIR_Apic_2 | 60 | 65 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.373 |
LIG_Pex14_2 | 385 | 389 | PF04695 | 0.558 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.333 |
LIG_Rb_LxCxE_1 | 331 | 346 | PF01857 | 0.524 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.374 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.356 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.374 |
LIG_SH2_PTP2 | 407 | 410 | PF00017 | 0.399 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.466 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.580 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.625 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.353 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.523 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.572 |
LIG_TRFH_1 | 284 | 288 | PF08558 | 0.390 |
LIG_TYR_ITIM | 328 | 333 | PF00017 | 0.429 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.315 |
LIG_WW_1 | 288 | 291 | PF00397 | 0.481 |
MOD_CDK_SPK_2 | 192 | 197 | PF00069 | 0.448 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.485 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.498 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.610 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.588 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.531 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.550 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.539 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.737 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.431 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.536 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.609 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.482 |
MOD_CMANNOS | 148 | 151 | PF00535 | 0.593 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.572 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.456 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.481 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.572 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.591 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.689 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.502 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.578 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.557 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.772 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.458 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.540 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.515 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.617 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.387 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.510 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.660 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.485 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.730 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.522 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.685 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.752 |
MOD_PKA_1 | 50 | 56 | PF00069 | 0.291 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.646 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.506 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.543 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.289 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.371 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.412 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.395 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.406 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.507 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.402 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.534 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.364 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.455 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.413 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.655 |
MOD_SUMO_rev_2 | 91 | 98 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_1 | 261 | 266 | PF01217 | 0.409 |
TRG_DiLeu_BaEn_1 | 369 | 374 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_2 | 380 | 386 | PF01217 | 0.416 |
TRG_DiLeu_BaLyEn_6 | 251 | 256 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIQ0 | Leptomonas seymouri | 49% | 100% |
A0A3S7WVU6 | Leishmania donovani | 73% | 100% |
A4HYN2 | Leishmania infantum | 72% | 100% |
E9AUI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QD02 | Leishmania major | 74% | 100% |