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: 18 |
NetGPI | no | yes: 0, no: 18 |
Related structures:
AlphaFold database: E9APD8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016787 | hydrolase activity | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.375 |
CLV_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.323 |
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.343 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.274 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 265 | 269 | PF03568 | 0.169 |
DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.181 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.669 |
DEG_SCF_TRCP1_1 | 204 | 209 | PF00400 | 0.197 |
DOC_MAPK_DCC_7 | 3 | 12 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.411 |
DOC_MAPK_HePTP_8 | 213 | 225 | PF00069 | 0.246 |
DOC_MAPK_HePTP_8 | 56 | 68 | PF00069 | 0.274 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 336 | 344 | PF00069 | 0.286 |
DOC_MAPK_MEF2A_6 | 59 | 68 | PF00069 | 0.289 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.402 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.391 |
DOC_USP7_UBL2_3 | 289 | 293 | PF12436 | 0.425 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.296 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 195 | 201 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 336 | 341 | PF00244 | 0.361 |
LIG_Actin_WH2_2 | 118 | 135 | PF00022 | 0.321 |
LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.203 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.274 |
LIG_CtBP_PxDLS_1 | 65 | 69 | PF00389 | 0.169 |
LIG_eIF4E_1 | 31 | 37 | PF01652 | 0.274 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.298 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.307 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.375 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.428 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.197 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.298 |
LIG_LIR_Apic_2 | 103 | 107 | PF02991 | 0.222 |
LIG_LIR_Apic_2 | 350 | 355 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.336 |
LIG_MLH1_MIPbox_1 | 361 | 365 | PF16413 | 0.274 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.274 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.335 |
LIG_SUMO_SIM_par_1 | 221 | 226 | PF11976 | 0.305 |
LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.412 |
LIG_WRC_WIRS_1 | 308 | 313 | PF05994 | 0.411 |
MOD_CDK_SPxxK_3 | 223 | 230 | PF00069 | 0.357 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.461 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.456 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.545 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.387 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.378 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.374 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.300 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.344 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.249 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.296 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.339 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.508 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.423 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.313 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.383 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.439 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.211 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.384 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.357 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.264 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.401 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.305 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.287 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.407 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.237 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.335 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.203 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.270 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.357 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.203 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.341 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.415 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.374 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.308 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.361 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.320 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.439 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.370 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.448 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.442 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.296 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.378 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.243 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.240 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.246 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.411 |
MOD_Plk_2-3 | 255 | 261 | PF00069 | 0.370 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.451 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.510 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.373 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.286 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.296 |
TRG_DiLeu_BaEn_2 | 274 | 280 | PF01217 | 0.211 |
TRG_DiLeu_BaLyEn_6 | 136 | 141 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 209 | 214 | PF01217 | 0.246 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.278 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.189 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.428 |
TRG_NES_CRM1_1 | 243 | 255 | PF08389 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 48 | 52 | PF00026 | 0.333 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8L5 | Leptomonas seymouri | 65% | 100% |
A0A0N1I6V6 | Leptomonas seymouri | 23% | 100% |
A0A0S4J886 | Bodo saltans | 32% | 97% |
A0A0S4JJG1 | Bodo saltans | 26% | 100% |
A0A1X0NNK2 | Trypanosomatidae | 41% | 100% |
A0A3Q8I9M0 | Leishmania donovani | 91% | 100% |
A0A3Q8IDU3 | Leishmania donovani | 23% | 100% |
A0A3R7LZE9 | Trypanosoma rangeli | 45% | 100% |
A4H7A0 | Leishmania braziliensis | 78% | 100% |
A4HF07 | Leishmania braziliensis | 24% | 100% |
A4HVP2 | Leishmania infantum | 91% | 100% |
A4I286 | Leishmania infantum | 23% | 100% |
D0A6K3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AYD1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q942 | Leishmania major | 24% | 100% |
Q4QG40 | Leishmania major | 89% | 100% |
V5ARR6 | Trypanosoma cruzi | 45% | 94% |