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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HQ14
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.577 |
CLV_PCSK_FUR_1 | 116 | 120 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 347 | 349 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.688 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.541 |
DOC_CYCLIN_RxL_1 | 18 | 26 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 155 | 161 | PF00134 | 0.415 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.484 |
DOC_MAPK_gen_1 | 291 | 301 | PF00069 | 0.622 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.517 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 167 | 172 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 332 | 339 | PF00244 | 0.516 |
LIG_BIR_III_4 | 94 | 98 | PF00653 | 0.518 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.470 |
LIG_deltaCOP1_diTrp_1 | 282 | 290 | PF00928 | 0.607 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.573 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.634 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.614 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.436 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.403 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.521 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.375 |
LIG_LIR_Apic_2 | 289 | 293 | PF02991 | 0.658 |
LIG_LIR_Apic_2 | 84 | 88 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 137 | 144 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.381 |
LIG_MAD2 | 21 | 29 | PF02301 | 0.536 |
LIG_MLH1_MIPbox_1 | 165 | 169 | PF16413 | 0.455 |
LIG_NRBOX | 306 | 312 | PF00104 | 0.630 |
LIG_PCNA_yPIPBox_3 | 304 | 316 | PF02747 | 0.636 |
LIG_PDZ_Class_1 | 348 | 353 | PF00595 | 0.448 |
LIG_Pex14_1 | 283 | 287 | PF04695 | 0.664 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.394 |
LIG_PTB_Apo_2 | 66 | 73 | PF02174 | 0.385 |
LIG_PTB_Phospho_1 | 66 | 72 | PF10480 | 0.382 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.421 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.573 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.579 |
LIG_SH2_GRB2like | 343 | 346 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 72 | 76 | PF00017 | 0.504 |
LIG_SH2_NCK_1 | 85 | 89 | PF00017 | 0.659 |
LIG_SH2_STAT3 | 295 | 298 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.389 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.526 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.569 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.625 |
LIG_SUMO_SIM_par_1 | 146 | 154 | PF11976 | 0.443 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.540 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.470 |
LIG_TYR_ITSM | 174 | 181 | PF00017 | 0.436 |
LIG_TYR_ITSM | 68 | 75 | PF00017 | 0.502 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.391 |
MOD_CDK_SPK_2 | 311 | 316 | PF00069 | 0.677 |
MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.406 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.538 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.678 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.638 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.695 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.610 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.522 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.397 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.641 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.484 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.381 |
MOD_DYRK1A_RPxSP_1 | 30 | 34 | PF00069 | 0.410 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.689 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.700 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.643 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.478 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.548 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.388 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.585 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.610 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.596 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.483 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.464 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.646 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.637 |
MOD_LATS_1 | 165 | 171 | PF00433 | 0.437 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.567 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.495 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.477 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.587 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.496 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.791 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.424 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.420 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.640 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.519 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.666 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.375 |
MOD_Plk_2-3 | 148 | 154 | PF00069 | 0.644 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.375 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.397 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.686 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.742 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.406 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.680 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 148 | 158 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_4 | 302 | 308 | PF01217 | 0.585 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.366 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.545 |
TRG_NLS_Bipartite_1 | 332 | 351 | PF00514 | 0.490 |
TRG_PTS1 | 350 | 353 | PF00515 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P554 | Leptomonas seymouri | 67% | 94% |
A0A1X0P394 | Trypanosomatidae | 40% | 89% |
A0A3Q8IRL6 | Leishmania donovani | 81% | 100% |
A0A3R7NA51 | Trypanosoma rangeli | 48% | 99% |
A4ICE4 | Leishmania infantum | 81% | 100% |
D0A8V6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9ATT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q0R5 | Leishmania major | 82% | 98% |
V5BDN3 | Trypanosoma cruzi | 47% | 100% |