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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HN45
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.458 |
CLV_PCSK_FUR_1 | 89 | 93 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.449 |
CLV_PCSK_PC7_1 | 284 | 290 | PF00082 | 0.534 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.489 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.507 |
DEG_SCF_FBW7_2 | 337 | 342 | PF00400 | 0.494 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.417 |
DOC_CDC14_PxL_1 | 192 | 200 | PF14671 | 0.442 |
DOC_CYCLIN_yCln2_LP_2 | 272 | 278 | PF00134 | 0.495 |
DOC_PP1_RVXF_1 | 186 | 193 | PF00149 | 0.359 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.461 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.448 |
DOC_PP4_FxxP_1 | 172 | 175 | PF00568 | 0.386 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.536 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.561 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 132 | 142 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 253 | 259 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.585 |
LIG_AP2alpha_2 | 64 | 66 | PF02296 | 0.424 |
LIG_APCC_ABBAyCdc20_2 | 188 | 194 | PF00400 | 0.350 |
LIG_Clathr_ClatBox_1 | 145 | 149 | PF01394 | 0.307 |
LIG_deltaCOP1_diTrp_1 | 270 | 276 | PF00928 | 0.587 |
LIG_DLG_GKlike_1 | 42 | 49 | PF00625 | 0.589 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.557 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.616 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.445 |
LIG_HCF-1_HBM_1 | 13 | 16 | PF13415 | 0.441 |
LIG_Integrin_isoDGR_2 | 103 | 105 | PF01839 | 0.482 |
LIG_LIR_Apic_2 | 169 | 175 | PF02991 | 0.409 |
LIG_LIR_Apic_2 | 200 | 205 | PF02991 | 0.417 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 13 | 23 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 45 | 52 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.355 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.361 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.409 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.383 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.429 |
LIG_SH2_SRC | 16 | 19 | PF00017 | 0.446 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.469 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.415 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.495 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.349 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.358 |
LIG_SH3_4 | 174 | 181 | PF00018 | 0.494 |
LIG_SUMO_SIM_anti_2 | 321 | 326 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 320 | 326 | PF11976 | 0.404 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.330 |
LIG_TYR_ITIM | 206 | 211 | PF00017 | 0.480 |
LIG_UBA3_1 | 70 | 76 | PF00899 | 0.619 |
LIG_WRPW_2 | 273 | 276 | PF00400 | 0.573 |
LIG_WW_1 | 383 | 386 | PF00397 | 0.413 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.462 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.641 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.294 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.367 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.463 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.546 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.501 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.698 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.521 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.468 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.581 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.474 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.413 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.578 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.557 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.382 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.549 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.385 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.425 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.441 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.654 |
MOD_NEK2_2 | 134 | 139 | PF00069 | 0.513 |
MOD_NEK2_2 | 263 | 268 | PF00069 | 0.513 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.490 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.455 |
MOD_PKA_1 | 42 | 48 | PF00069 | 0.393 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.346 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.652 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.478 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.623 |
MOD_PKB_1 | 289 | 297 | PF00069 | 0.311 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.523 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.416 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.424 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.367 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.416 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.378 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.382 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.522 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.284 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.410 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.575 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.519 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.404 |
TRG_DiLeu_BaEn_4 | 113 | 119 | PF01217 | 0.341 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.561 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.492 |
TRG_NLS_Bipartite_1 | 76 | 95 | PF00514 | 0.510 |
TRG_NLS_MonoExtC_3 | 90 | 95 | PF00514 | 0.573 |
TRG_NLS_MonoExtN_4 | 88 | 95 | PF00514 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF2 | Leptomonas seymouri | 71% | 100% |
A0A0S4J0E9 | Bodo saltans | 34% | 96% |
A0A1X0P564 | Trypanosomatidae | 49% | 100% |
A0A3Q8IJC4 | Leishmania donovani | 87% | 100% |
A0A3R7R9I8 | Trypanosoma rangeli | 49% | 100% |
A4IBR3 | Leishmania infantum | 87% | 100% |
C9ZYW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AFJ8 | Leishmania major | 87% | 100% |
E9B6Q2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5BCU7 | Trypanosoma cruzi | 48% | 100% |