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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B2D6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 275 | 279 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.797 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.839 |
CLV_PCSK_FUR_1 | 197 | 201 | PF00082 | 0.720 |
CLV_PCSK_FUR_1 | 70 | 74 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.831 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.802 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 346 | 348 | PF00082 | 0.831 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.802 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.753 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.580 |
CLV_PCSK_PC7_1 | 76 | 82 | PF00082 | 0.803 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.743 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.706 |
DOC_ANK_TNKS_1 | 143 | 150 | PF00023 | 0.740 |
DOC_MAPK_MEF2A_6 | 171 | 179 | PF00069 | 0.727 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.788 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.743 |
DOC_USP7_UBL2_3 | 234 | 238 | PF12436 | 0.593 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.847 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.810 |
LIG_14-3-3_CanoR_1 | 183 | 193 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.660 |
LIG_APCC_ABBA_1 | 125 | 130 | PF00400 | 0.533 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.574 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.492 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.548 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.655 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.566 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.548 |
LIG_LIR_Gen_1 | 271 | 279 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.647 |
LIG_MYND_1 | 60 | 64 | PF01753 | 0.762 |
LIG_SH2_NCK_1 | 274 | 278 | PF00017 | 0.779 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.776 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.711 |
LIG_SH3_2 | 64 | 69 | PF14604 | 0.715 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.750 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.762 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.699 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.754 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.546 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.671 |
LIG_SUMO_SIM_par_1 | 175 | 180 | PF11976 | 0.797 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.745 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.653 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.821 |
LIG_WW_3 | 239 | 243 | PF00397 | 0.704 |
MOD_CDK_SPxxK_3 | 306 | 313 | PF00069 | 0.849 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.623 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.551 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.775 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.601 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.583 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.770 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.711 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.730 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.768 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.609 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.564 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.627 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.751 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.660 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.711 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.645 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.720 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.686 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.796 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.598 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.761 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.808 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.664 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.680 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.607 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.691 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.646 |
MOD_LATS_1 | 99 | 105 | PF00433 | 0.757 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.810 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.795 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.851 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.681 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.690 |
MOD_NEK2_2 | 269 | 274 | PF00069 | 0.763 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.839 |
MOD_PKA_1 | 346 | 352 | PF00069 | 0.553 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.821 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.848 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.574 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.762 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.765 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.684 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.675 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.469 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.547 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.807 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.638 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.824 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.819 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.848 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.804 |
MOD_SUMO_rev_2 | 252 | 262 | PF00179 | 0.702 |
MOD_SUMO_rev_2 | 341 | 348 | PF00179 | 0.756 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.824 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.754 |
TRG_NLS_MonoExtC_3 | 68 | 73 | PF00514 | 0.664 |
TRG_NLS_MonoExtN_4 | 66 | 73 | PF00514 | 0.728 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICV9 | Leishmania donovani | 82% | 100% |
A4HJZ6 | Leishmania braziliensis | 63% | 100% |
A4I7H9 | Leishmania infantum | 81% | 100% |
Q4Q5S0 | Leishmania major | 83% | 100% |