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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AWR1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.793 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.666 |
CLV_PCSK_FUR_1 | 364 | 368 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.777 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.777 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.521 |
DEG_APCC_DBOX_1 | 144 | 152 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.611 |
DEG_SCF_FBW7_1 | 268 | 273 | PF00400 | 0.418 |
DEG_SPOP_SBC_1 | 301 | 305 | PF00917 | 0.465 |
DOC_CKS1_1 | 36 | 41 | PF01111 | 0.694 |
DOC_CYCLIN_yCln2_LP_2 | 91 | 97 | PF00134 | 0.411 |
DOC_MAPK_DCC_7 | 77 | 86 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 5 | 14 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 109 | 116 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 77 | 86 | PF00069 | 0.617 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.411 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 46 | 54 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 98 | 108 | PF00244 | 0.347 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.644 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.378 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.568 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.436 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.553 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.713 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.709 |
LIG_NRBOX | 233 | 239 | PF00104 | 0.416 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.338 |
LIG_SH2_NCK_1 | 213 | 217 | PF00017 | 0.416 |
LIG_SH2_SRC | 264 | 267 | PF00017 | 0.642 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.535 |
LIG_SH3_2 | 144 | 149 | PF14604 | 0.411 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.411 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.416 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.684 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.692 |
LIG_SUMO_SIM_anti_2 | 123 | 128 | PF11976 | 0.222 |
LIG_SUMO_SIM_par_1 | 80 | 87 | PF11976 | 0.474 |
LIG_UBA3_1 | 237 | 242 | PF00899 | 0.338 |
LIG_WRC_WIRS_1 | 28 | 33 | PF05994 | 0.410 |
LIG_WRC_WIRS_1 | 393 | 398 | PF05994 | 0.499 |
MOD_CDK_SPK_2 | 35 | 40 | PF00069 | 0.597 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.471 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.494 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.520 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.536 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.650 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.499 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.527 |
MOD_Cter_Amidation | 296 | 299 | PF01082 | 0.793 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.342 |
MOD_GlcNHglycan | 202 | 206 | PF01048 | 0.513 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.411 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.633 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.689 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.353 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.494 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.411 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.375 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.460 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.481 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.602 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.562 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.701 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.462 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.443 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.716 |
MOD_N-GLC_2 | 282 | 284 | PF02516 | 0.731 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.478 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.530 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.456 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.562 |
MOD_PIKK_1 | 406 | 412 | PF00454 | 0.563 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.384 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.641 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.573 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.730 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.513 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.436 |
MOD_Plk_2-3 | 358 | 364 | PF00069 | 0.529 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.472 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.411 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.276 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.377 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.411 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.590 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.689 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.629 |
MOD_SUMO_for_1 | 191 | 194 | PF00179 | 0.319 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_1 | 206 | 211 | PF01217 | 0.265 |
TRG_DiLeu_BaLyEn_6 | 109 | 114 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.433 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.612 |
TRG_NES_CRM1_1 | 123 | 135 | PF08389 | 0.411 |
TRG_NLS_Bipartite_1 | 366 | 380 | PF00514 | 0.447 |
TRG_NLS_MonoCore_2 | 374 | 379 | PF00514 | 0.591 |
TRG_NLS_MonoExtN_4 | 373 | 380 | PF00514 | 0.752 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 354 | 358 | PF00026 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3F4 | Leptomonas seymouri | 42% | 100% |
A0A3S7WY61 | Leishmania donovani | 87% | 94% |
A4HDC8 | Leishmania braziliensis | 75% | 100% |
A4I0Q9 | Leishmania infantum | 87% | 94% |
Q4QAR2 | Leishmania major | 89% | 100% |